Category: Health

  • Stephen Duckett. Health in 2016: a cheat sheet on hospitals, Medicare and private health insurance.

    We start 2016 as we started 2015 – with big challenges for the health system and uncertainty as to how governments will meet them.

    The health care headaches in 2016 are, in fact, the same ones we faced a decade ago, albeit different in severity and symptoms. They include population growth, ageing and the rise of chronic disease; inequality in access to care and health outcomes; technological change (the good, the bad and the expensive) and the seemingly inexorable rise in health costs.

    Circling for landing are three major reviews on private health insurance, primary care, and low-value care. Their recommendations, and the government’s response to them, are very much up in the air.

    Adding to the uncertainty is the broader review of federalism and its consequences for public hospital funding, along with speculation around the 2016 federal election date and what each party’s Santa sack of election promises might contain.

    Private health insurance

    The number of people with private health insurance continues to creep up but the market is not in good shape.

    The rebate is one of the fastest growing areas of government health expenditure and complaints about the product abound. High levels of coverage are being achieved throughcarrots (the rebate) and sticks (penalties for the uninsured) rather than genuine consumer appeal.

    One solution being floated is for the whole subsidy framework to be thrown out. Instead of subsidising private insurers, which pay private hospitals, the government could subsidise private hospitals directly.

    Government advisers are impressed by the efficiency gains that activity-based funding (paying hospitals per procedure rather than a lump sum) brought to public hospitals and believe similar improvement can be brought to the private sector.

    The mechanism to achieve this could be a Hospital Benefits Schedule which, like the Medicare Benefits Schedule, would prescribe a schedule fee for private hospital care, based on existing Commonwealth payments for public hospital services under activity-based funding. The same schedule may later be used for public hospitals, replacing grants to the states.

    However, it will only be politically palatable if it is cost neutral for consumers or comes with reduced private health insurance sticks.

    The devil is in the detail of a new policy such as this. Will payment be to the hospital or surgeon? Will it cover the surgeon’s fee, as in public hospitals? Will it cover diagnostics? Without this information it is impossible to forecast the impact of the shift.

    Public hospitals

    This will be a challenging year for public hospitals. Major reductions in Commonwealth funding for hospital admissions – which continue to grow – will kick in from 2017, and states are likely to start the belt-tightening early.

    The cuts far exceed the productivity gains that can be made, so a reduction in services is certainly possible. Efficiency may be improved somewhat by the ongoing expansion of activity-based funding to mental health and “sub-acute” care such as rehabilitation and palliative care.

    The possible changes to private health insurance and a Hospital Benefits Schedule may be one way to put money from the federal government back into the system, but there is no sign that Treasurer Scott Morrison is keen to loosen the purse strings.

    Hospitals will also be under pressure to lift quality. Hospitals face increasingly stringent “quality standards” with tougher monitoring covering a broader scope of issues, including access and timeliness.

    Meanwhile, the increasing array of publicly available data is putting variation in hospital performance under the spotlight more and more, with commensurate calls for greater accountability.

    Medicare

    Two independent reviews of Medicare are expected to land sometime in 2016.

    The first examines primary care. It could address any number of challenges, including chronic disease management, “six-minute medicine”, co-payments, frozen rebates, and the growing corporatisation of general practice.

    Management of chronic diseases such as diabetes, heart disease and cancer poses the main challenge. The rise of chronic disease is imposing big costs on a system that wasn’t designed to provide the complex, continuous and coordinated care now needed.

    The government will have to consider far-reaching reform with only limited and equivocal evidence to draw on. Options on the table include a shift in the balance of payments to practices, with less emphasis on payment for attendances (fee-for-service) and more emphasis on payment for care over the episode of illness or year (capitation payments).

    There may be other changes in payment structures. The government’s long-standing desire to reduce perceived incentives for six-minute medicine may see a minimum consultation time imposed on the standard (level B) fee.

    If sense prevails we won’t see a resurrection of the GP co-payment policy zombie. We should, however, see an end to the freeze on medical rebates; the only question being when and with what trade-offs.

    A further issue to be addressed is the shift toward practices owned by corporate chains that profit from referrals to and provision of diagnostic services, such as blood tests and X-rays. The implications of changed ownership structures for practice are not at the forefront of practice payment redesign but should be.

    The second review looks at quality and cost-effectiveness of items on the Medicare schedule. The review got off to a rocky start with wild claims about 30% waste in the system, and release of its first list of items targeted for delisting in the sleepy period between Christmas and New Year.

    The work on modernising the schedule will come to fruition in 2016. There will be individual and group losers in this process who undoubtedly will scream loudly with varying levels of effectiveness.

    What should you expect?

    It isn’t yet clear whether Health Minister Sussan Ley’s appetite for reviews portends massive reform to the sector, or simply a politically judicious preference for treading water in a portfolio still reeling from tumultuous management by her predecessor. However, the auguries are good for the former.

    The scene for change has been set, at least with the medical profession. Respectable leaders are engaged and leading some of the review processes. Hopefully this will be the year the health system rises to meet the big challenges of 21st-century health care.

     

    Stephen Duckett, Director, Health Program, Grattan Institute.  This article first appeared in The Conversation on February 1, 2016.

     

  • Ian McPhee. Let’s talk about dying.

    What does it mean to die well?

    We must acknowledge divergent views on assisted dying and start framing laws that will enable it, writes Ian McPhee.

    I am a medical specialist with advanced cancer. In a career begun more than 35 years ago, I have seen death in all its guises: in homes, at the roadside, in the emergency department, intensive care, operating theatres and on hospital wards. There has been no age limit on these experiences.

    I have gently taken a dead child from a mother after she travelled for an hour with him cradled in her arms following a farm accident. I have watched the slow, inexorable deterioration of ICU patients with multiple organ failure because of myriad causes.

    Inevitably, because it is the lot of a doctor whose practice has been predominantly hospital-based, I have also been present at countless attempts at resuscitation from cardiac arrest, the vast preponderance of which were unsuccessful – perhaps surprising news for regular viewers of medi-drama.

    The cult of survival, however, is extant and is sadly a feature of 21st century, Western medicine. Only a short while ago an intensive care colleague related the story of a call, generated by a senior doctor, to assist in the resuscitation and ICU admission of a patient whom he assessed on review as cadaveric, or dead.

    How can a system have evolved to deal so inhumanely with an individual at the end of life? How is it possible that doctors continue to administer futile care as if a “last right” for their patients, when for themselves they wish for no such thing. As recently as this month, in the Journal of the American Medical Association, this fact was again highlighted.

    The cult of survival, however, is extant and is sadly a feature of 21st century, Western medicine.

    Dr Ian McPhee

    The limitations of intervention are understood but this is not translated into the treatments administered to patients. In a 2014 paper, researchers from Stanford University reported that 88 per cent of more than 1000 US doctors surveyed indicated they would forgo high-intensity care for themselves at the end of life.

    To bring focus here, my colleague Peter Saul said recently that we are facing “a perfect storm of ageing and expanding population with a higher burden of chronic disease”. His call to us as a society has been: “Let’s talk about dying.” It is no less directed at health professionals as it is to the public at large.

    For me, the recent, wide public consideration and debate of end-of-life issues has taken on special significance. Eighteen months ago, at the age of 59, I was diagnosed with a rare, aggressive T-cell lymphoma. In the interim, multiple attempts to achieve remission have failed.

    At the time of original diagnosis I was reading Atul Gawande’s book Being Mortal. Gawande is an American surgeon, author and staff writer for The New Yorker. For those unfamiliar with this work, he has made the case for a patient’s wellbeing to be at the forefront of care considerations, for their wishes to be actively sought, and for medicine to move to helping them to not just live but also die with a sense of control.

    Within his narrative there was for me a special anecdote. Gawande’s father, himself a surgeon, developed a spinal-cord tumour. Treatment options were investigated, discussed openly, and evaluated for their potential impact on those things that held meaning within what had been a truly full and fulfilling life.

    Importantly, he made informed choices, not least among them to enter into the care of a neurosurgeon who took time to answer even the “annoying” questions.

    Their relationship became “informative”, as opposed to paternalistic. There was later surgery, and, beyond that, symptom management. And when a long-considered point was reached at which going on would have provided no benefit, treatment was ceased. Ultimately death was at home, surrounded by family.

    I too have actively sought an informative relationship with my own treating clinicians and given similar consideration to what I might expect from my treatment.

    Yet, while now inhabiting my end of life, do I wish to consider foreshortening it? And if not immediately, are there ever likely to be circumstances that are no longer tolerable in my view; according to my values, and determined by my own informed assessment of my situation?

    Intolerable enough, that is, to mean, in the absence of medically assisted dying, suicide.

    The counter argument to those in favour of assisted dying has tended in large part to be based on the notion that palliative care is the answer; that it is accessible to all, universally effective and, by implication, restorative. Of course, it may not be any of these.

    In my own border community of almost 200,000, there are no palliative-care specialist doctors in the public sector. The same is true for many non-metropolitan centres.

    The palliative-care clinician’s pharmacopoeia in many ways matches those that I have drawn on during a 30-year career in anaesthesia and acute pain. There are no magic bullets. I cannot accept that it might be otherwise.

    Palliative medicine is, however, a vital part of a “system” of care. I acknowledge that for many it is the difference between last months of extreme suffering, and the achieving of some respite.

    And while it might herald for some a meaningful end, and even approach the Gawande notion of a “good death”, there remain others, and I number among them, whose sense of what is meaningful carries with it vastly different connotations.

    It is past time to acknowledge the existence of such divergent views, accept that there is scope for regulation to reflect this, and move toward establishing the framework to enact it.

    To not do so will mean only a slow but steady growth in the number of people such as Peter and Pat Shaw, who determine that their last day will involve final, furtive visits to garden sheds. Most sadly of all, however, such passing will of necessity continue to mean the exclusion of immediate family, lest they should be seen as having acted criminally in assisting at a loved one’s entry to the Big Sleep.

    Dr Ian McPhee is a clinical senior lecturer at Sydney Medical School and an anaesthetist in provincial practice in NSW. This article was published by Sydney University.

  • Ian McAuley Private health insurance – does the lady protest too much?

    Sussan Ley, the Commonwealth Health Minister, has hit out at private health insurers’ bid for a six per cent price increase.

    In view of the strong support the Coalition has always given private health insurers, such public criticism from a Liberal Party minister may surprise us. As one-time Prime Minister Tony Abbott said “private health insurance is in our DNA”.

    It would be reassuring to believe that the Sussan Ley has come to recognise private health insurance (PHI) for what it is – a high-cost financial intermediary that does nothing to take pressure off public hospitals and that has been largely responsible for diverting scarce health care resources away from areas of need.

    As John Menadue, Jennifer Doggett and I have pointed out in conference papers, submissions to enquiries and a major study published by the Centre for Policy Development, PHI is an expensive, inequitable and inefficient way to share health costs. It does at high cost what Medicare and the Australian Tax Office (collecting taxes to fund Medicare) can do far better.

    Its bureaucratic overheads are high: only 86 cents in the dollar of insurers’ premiums are returned as benefits, compared with 95 cents for Medicare.

    It fails in its main avowed purpose to relieve pressure off public hospitals, because in channelling funds to private hospitals it has attracted resources – nurses and specialists – away from public hospitals. All it has done is to shuffle queues for access to limited resources, bringing insured patients to the front of the queue and pushing everyone else back.

    It fails to keep providers’ costs and patients’ usage under control. That’s because of what economists know as “moral hazard” – the tendency for people to over-use a service when it is free at the point of delivery. A single funder such as Medicare can control moral hazard through use of well-structured co-payments to impose some pricing discipline and through hospital staff allocating services on the basis of need. By contrast, when there are multiple insurers they necessarily have to be permissive in meeting the demands of service providers, particularly highly-paid medical specialists.

    That’s why PHI premiums have been rising at an average of 5.5 per cent a year since 2000, while general inflation has averaged only 2.9 per cent. Insurers claim that they are simply passing on costs incurred in hospitals, without acknowledging their own role in driving price inflation and over-usage in health care.

    Insurers may claim that in marshalling private funds for health care they have kept demands on the Commonwealth budget and therefore taxes in check, but even if this is the case, there is no virtue by any economic criterion, “right” or “left”, in substituting what is essentially a privatised tax (PHI) for an official tax. It’s a weird ideology that would find benefit in saving taxpayers $1.00 in official tax at the cost of their having to pay $1.10 or even $1.50 for the same or inferior service, because for most people the incentives for holding PHI come near to compulsion.

    Young people are cajoled into PHI through the penalties in “lifetime community rating”, and people with moderate and higher incomes are cajoled into PHI through exemption from the Medicare Levy Surcharge. While official taxes can incorporate progressivity, PHI, in its regulations designed to achieve “community rating”, builds in many injustices. For example, those who rely on PHI for private hospitalisation or dentistry are subsidised by the taxpayer up to 40 per cent, while those who pay from their own resources get no support.

    We don’t know the reasons for Susan Ley’s criticism of health insurers. Maybe it’s just clever politics, to distance herself and the government from another round of premium increases. Maybe it’s about her own constrained budget: because of the direct subsidies to PHI every one per cent premium rise means there is $60 million less for other health priorities. (In fact the total fiscal cost of supporting PHI, often reported at $6 billion a year, is more like $11 billion a year once tax expenditures (revenue forgone) are taken into account.)

    Or perhaps she realises that there are better ways to support private hospitals than channelling funds through PHI, and that scarce funds for health care are best directed at primary care and prevention, rather than subsidising the lifestyles of medical specialists and the well-off to jump the queue.

    (On my website are several papers on PHI. Those wishing to go further into the issues, or to find sources for the points covered in this article, will find a major study John Menadue and I conducted for the Centre for Policy Development in 2012. Late last year Jennifer Doggett and I made a submission, incorporating updated costing and other data, to a Departmental inquiry into health insurance.)

     

  • Ian Webster. Alcohol and Sport.

    The facts about alcohol should stop politicians in their tracks. But they are unmoved.

    A quarter to a third of the work of a general hospital is alcohol-related. On Australia Day one in seven ED attendances were caused by alcohol; in some EDs it was one in three. The Senior Australian of the Year, Gordian Fulde, time and time again, has described the carnage at St Vincent’s Hospital’s ED late on Thursday, Friday and Saturday nights; as many as 70 percent of cases at peak periods are intoxicated.

    That’s only part of the medical story. The alcohol load is massive in the trauma, orthopaedic and burns units and manifestly over-represented in suicide attempts, mental health, brain injury and in the general medical and surgical wards. Twenty to 40 percent of patients in general practice have had a serious alcohol problem at some time in their life. Globally, alcohol is the third most modifiable risk factor to prevent disability and death. Alcohol overshadows most contemporary public health problems.

    In the social story, alcohol outstrips the impact of other substances. One third of child protection cases, 40+ percent of domestic violence, 40+ percent of homicides, 45 percent of assaults attended by police and up to 60 percent of suicides – the list could go on. The police, courts and welfare agencies are tied up dealing with the consequences. Alcohol’s social impact dwarfs the anxieties about ICE and cannabis.

    It’s not that we can’t tackle alcohol; it’s the countervailing forces which stop us. Dealing with the health and social harms of alcohol is not straightforward public health as the strategies to reduce harm competes with commercial interests and politics.

    In the recent holiday period, the cricket season was awash with alcohol advertising, for all to see. Loopholes in legislation allowed alcohol advertising to subvert the measures designed to protect young minds. When alcohol is linked so convincingly to sporting success and peer-acceptance, young minds are too easily persuaded that being a drinker is OK.

    Since ancient Greece, sporting activities have celebrated athleticism, skills, teamwork and playing by the rules. Sporting heroes have been role models for youth. But the role models of today are seduced into colluding with the alcohol industry – for celebrity, money and power. The once noble traditions have been corrupted by the dollar.

    This collusion is not for the common good. With apologies to former US President Dwight Eisenhower, the alcohol industry and organised sport have established a powerful ‘industrial complex’ along with their bedfellows – the gaming and PR industries. The asymmetry of power and political influence, compared with the proponents for public health means that effective strategies such as reduced late-night trading hours for alcohol-outlets and evidence-based alcohol taxes struggle for a place in government policy.

    Michael Thorn, referring to the alcohol industry, wrote last week (Pearls and Irritations, 23/01/2016), “It’s an industry built on identifying, targeting and exploiting its best customers, and ensuring they continue to misuse and abuse alcohol.” He observed that 20 percent of Australians aged 14 years and above consume 74.2 percent of all the alcohol consumed in a year. As far back as 2006, a US study showed the alcohol industry’s revenue in that country was dependent on heavy and disordered drinkers (‘sick’ drinkers) and underage drinkers. (1) A degree of exploitation redolent of the gaming industry’s dependence on problem and addicted gamblers.

    Professor Robin Room and Dr Michael Livingstone, internationally recognised alcohol policy researchers from Latrobe University, and Michael Thorn, CEO, Foundation for Alcohol Research and Education, have said recently, that the alcohol industry’s interests run in the opposite direction to public health and effective alcohol policy and the industry should be excluded from alcohol policy decision-making. On the evidence, who can disagree?

    It is also in the community’s interest to warn sporting organisations, that partnership with the alcohol industry undermines sporting values and risks the health of future generations.

    ___________

    1. Foster SE, Vaughan RD, Foster WH and Califano JA Jr. Estimate of the commercial value of underage drinking and adult abusive and dependent drinking to the alcohol industry. Archives of Pediatric and Adolescent Medicine. 2006 May; 160(5): 473-8.

    Ian Webster is Emeritus Professor of Health and Community Medicine at UNSW and patron of the Alcohol and Other Drugs Council of Australia. He was formerly a National Mental Health Commissioner and Chair of the Australian Suicide Prevention Advisory Council.

  • John Dwyer. ‘Health’ products and treatments that are often unproven and sometimes dangerous.

                      Health Care Advertising and Consumer Protection

    There are far more irritations than pearls available currently to those of us trying to champion the importance of having our health care underpinned by credible scientific evidence of clinical effectiveness. Though we live in the most scientific of all ages it is cause for concern that practices based on “pseudoscience” remain so entrenched in our community. Consumer protection from misleading often-fraudulent advertising and unscientific ineffective practices is distressingly inadequate.

    For those concerned about this situation, the pleasure from watching the Australian Open Tennis championship on TV is diminished by the plethora of advertisements telling Australians that better health is available from vitamins and “supplements” that in fact offer no benefit to the average citizen. Swisse and Blackmores make a fortune selling a promise of a healthier you if you regularly consume their products. To prove this is so they have the likes of Lleyton Hewitt and Ricky Ponting telling you how they have benefitted from such consumption. I doubt that either of these fine athletes have independently pursued evidence to make sure what they are saying is true. What about all those fraudulent advertisements for painless quick weight loss products? You cannot watch the Sky News channel for very long before you are asked if you have had your “Inner Health” today! While there are definite indications for treatment with probiotics (“good bacteria”) to suggest that everyday everyone needs these good guys is indefensible.

    The truth is that with health literacy in short supply for many of us it is easy and convenient to believe that an unhealthy life style can be neutralised by pills from a bottle. Of course there are people in the community who do need vitamins and supplements for various conditions but such use should be planned and supervised by doctors and nutritionists. There has been much quality research that confirms the lack of benefit and occasional harm associated with excessive vitamin and “supplement” intake. Although companies marketing products for which they make a therapeutic claim are meant to hold evidence that their claim is supported by credible evidence, many just label their product with an “as traditionally used” label even when scientific studies have contradicted those traditional claims. This is big business with Australian’s spending at least three billion dollars a year on products that for the majority provide no benefit.

    Our universities are not doing enough to make sure that they do not give undeserved credibility to pseudoscience. Courses in Chiropractic, Osteopathy and Traditional Chinese medicine often include concepts that could be considered to represent pre-scientific beliefs. At a recent Open Day for a major university’s Traditional Chinese Medicine program, participants had the ancient art of “cupping” demonstrated and touted as a technique for countering lung disease and all who attended left with a artefact to place on a specific spot behind the ear to prevent depression.

    Two related matters received much mainstream publicity recently. The first involved the extraordinary decision of the University of Wollongong to award a PhD to a candidate who for the last decade or so had been a very public spokesperson for the anti-vaccination movement. She enrolled in a higher degree program in the Humanities and Social Science faculty with a supervisor who, as a champion of free speech, courted controversial students who had been criticised for their publicised opinions. The “research” for the thesis would focus on the safety or otherwise of our current vaccination policies.

    The candidate concluded that vaccines did far more harm than good, were not necessary and would not be forced upon an ignorant community if an international conglomeration of companies with a vested interest in the vaccine industry had not coerced the WHO into lying to the public about vaccine safety. Many with the appropriate expertise examined the thesis and found it to be riddled with errors particularly when discussing immunology and epidemiology. The official reviewers of the thesis were social not biological scientists. There has been a major effort both inside and outside of the University to have the thesis re-examined but to date the University maintains it is comfortable with the decision to grant the PhD. Meanwhile the supervisor has labelled criticisms as an attack on free speech seemingly dismissive of the fact that a PhD thesis is not a vehicle for opinion but rather a vigorous search for and presentation of verifiable facts.

    The second issue which provoked Editorials in the Fairfax and Murdoch media concerned reports that hundreds of Chiropractors across the nation were claiming to be able to assist patients with numerous problems beyond their traditional focus on musculoskeletal problems with one’s back and neck. Particularly objectionable is the targeting of care for neonates, children and pregnant women. Involved chiropractors support the totally discredited suggestion of their 19th century founder, that there is associated with the spinal column an invisible but potent energy force (“innate energy”) the integrity of which is essential for whole of body health. Even slight distortions of the bony spinal column (“subluxation”) can interfere with this energy flow and cause problems remote from the spine. Chiropractors can make “adjustments” to the spine to correct the defects. Some of the problems that can be addressed in this way include Autism, Asthma, bed-wetting, developmental delay and colic. Parents are advised to have all neonates see a chiropractor soon after birth so that any distortions that occurred during the birthing process and that could cause long-term problems are addressed. Some chiropractors claim that their pregnancy care can prevent the need for Caesarean births, others say they can cure cancer.. This in 2016!

    How can this be I hear many of you thinking? The previous government decided that consumers would be better protected if chiropractors, osteopaths and traditional Chinese Medicine practitioners were required to seek national registration and have their professional activities monitored by a federal Board for their specialty under the auspices of the Australian Health Professional Registration Agency (AHPRA). This organisation reports to the COAG Health Council set up Australia’s Health Ministers who appoint Board members. AHPRA and the Chiropractic Board of Australia have been totally ineffective in protecting consumers from fraudulent activities described above. The Board has even been populated with members who practiced subluxation chiropractic. It has taken up to two years to investigate complaints made to the Board and AHPRA claims they do not have the legislative power to limit the scope of practice of the profession. AHPRA claims that only a few chiropractors fail to modify their advertising and practises after a warning. This is not true and this week the Friends of Science in Medicine sent images from 400 chiropractic websites targeting children to the CBA, AHPRA and Minister Jack Snelling who heads the COAG Health council. I should emphasise that the chiropractic profession is polarised with many chiropractors that stick to an evidence based form of practice distressed by the behaviour of colleagues who bring the profession into disrepute.

    The government is not helping. When our NH&MRC concluded that homeopathy and 18 other “Alternative” practices (Iridology, Reflexology, Reiki etc.) were not supported by any evidence of effectiveness one would have expected the government to stop allowing tax-payer dollars to be used to subsidise such treatments. Not so! While Homeopathy has been declared to be of no value, despite protests, students studying Homeopathy at colleges of Natural Medicine receive an annual $6000 handout from the government.

    There are many other anomalies that compromise consumer protection in this area that we could discuss and in so doing acknowledge that there are some medical doctors who engage in health care fraud, but to summarise, our approach has been and continues to be one where the emphasis is on having after the fact complaints dealt with rather than legislating and organising to prevent the incidents that generate so many complaints from happening in the first place. True consumer protection must be based on the primacy of such a strategy.

    John Dwyer is Emeritus Professor of Medicine, UNSW.

  • Brad Chilcott. I donated a kidney to my son. Don’t tell me not to make it ‘political’.

    In early December, I went into surgery to give my eight-year-old son Harrison my left kidney. He heard me groaning in recovery as the anaesthetist put him to sleep a few hours later so that he could receive it. The operation was the first of my life and Harrison’s 13th. He’d experience his 14th general anaesthetic two weeks later when surgeons removed the vascular catheter that had been used to connect the dialysis machine into his heart three times a week for the five months leading up to the transplant.

    After a successful surgery, Harrison had a number of complications that meant an eight-day stay in the intensive care unit of the Women’s and Children’s Hospital in Adelaide, followed by another six days in the surgical ward. Daily blood tests, a Christmas Day virus that precipitated an extra five days of hospital hospitality, and then on Sunday, 3 January, our family enjoyed our first hospital-free day in well over a month.

    As is my wont, I covered the process extensively via my social media outlets, interspersed with the occasional comment on the social and political issues of the period – a Myefo update committed to balancing the budget on the backs of the poor here and abroad; welcoming refugees and asylum seekers; supporting my brilliant friend Wawira Njiru’s work in Kenya making sure kids don’t have to go to school on an empty stomach; protecting penalty rates from being cut by people wealthy enough not to be forced to rely on them.

    On Christmas Day, before the infection set in that evening, I took Harrison into hospital for an 8am blood test wearing the full Santa suit I’d donned to give our three children their presents early that morning. I figured if we had to be in hospital on such a day, we should at least make it memorable. We handed out candy canes to taxi drivers waiting at the rank outside, orderlies cleaning the halls and other families having a similar experience to our own. Driving home, I filled the car with petrol in full costume while commuters took photos and small children gawked in confusion. Harrison loved every moment.

    On Christmas Day, before the infection set in that evening, I took Harrison into hospital for an 8am blood test wearing the full Santa suit. That afternoon, resting after a hearty Christmas lunch with the in-laws, I posted on social media: “Trip to hospital – saw Drs, nurses, cleaners, servo staff, RAA and more helping folks enjoy Christmas. Of course they deserve penalty rates” to which one person responded, “Enough politics for the day”.

    It’s easy to understand the sentiment – why sully the joy of Christmas with “politics” when there’s backyard cricket to play and pudding to consume? But if you’re any kind of activist or political advocate, it’s a familiar response.

    Children spending their third Christmas in immigration prisons; Australian Aid set at the lowest level in Australia’s history; health and education budgets being slashed by billions of dollars; one in three Australian pensioners living below the poverty line; climate change; sexism; racism; recognition of Australia’s Indigenous people … the easiest way to avoid thinking too deeply about any issue that arises around the barbecue on the beach is to dismiss it as “politics”.

    This is nothing new – people have always employed the word “politics” in the work of absolving themselves of personal responsibility for addressing inequality, injustice and the exploitation of the earth and its people.

    For our family, however, there’s no amount of using the word “politics” that can distance us from the truth that government-funded healthcare has not only kept Harrison alive for eight-and-a-half years but has also enabled him to thrive despite a range of other physical challenges.

    He’s required a huge volume of medical supplies and medication that have been provided free of charge or heavily subsidised; publicly-funded in-school support services have allowed him to keep up with his peers educationally; 14 operations and more-than-regular appointments with physicians since birth would’ve attracted a financial cost I can’t even comprehend, entirely borne by the public purse.

    So, while it might be easy to dismiss $15bn of cuts to the annual health budget as “politics” when you read it as a headline in the paper, the reality is that those are dollars that may have been spent on a child like Harrison. Forcing people to pay for pap smears and other preventative procedures is either “politics” or it’s a change that will mean some people won’t have their illness diagnosed early or accurately enough with huge impact on them and their families.

    Similarly, cuts to the education budget and the cancellation of the Gonski funding model are either an ideological minefield to be avoided in polite conversation – or it’s $196m that won’t be spent in my electorate alone on making sure that every Australia child receives a quality education . It’s either “politics” or it’s some children missing out on the opportunity to achieve their full potential because of the economic circumstance of the family they were born into.

    For the nurses, service station staff, cleaners and other workers that helped millions of Australians, including Harrison and I, have a good Christmas, penalty rates can’t be dismissed as mere “politics”. They’re students, single parents, new Australians and more who rely on every dollar to make ends meet.

    Children in immigration prisons, women enduring the violence of men, pensioners below the poverty line, parents who can’t afford child care, Muslim Australians being vilified by politicians and abused in our streets, Aboriginal people being forced from their communities – while others treat their experiences as abstract, impersonal political concepts, these people have no such convenience. That which is derided as a topic that should not interrupt the Christmas cheer invades their lives without their consent.

    Harrison and I went back in to hospital last week for blood tests. He’s on a huge amount of anti-rejection medication. We’re in the hands of the best medical practitioners in the field, the nursing and other support staff at the hospital are wonderful and Harrison has all the social scaffolding he needs to thrive. But this situation didn’t happen by chance – throughout Australia’s history progressive people fought for this outcome, so successfully that it would be culturally unacceptable for us to be paying for this level of care. Australians naturally assume it’s what sick children deserve.

    We are living, and grateful, beneficiaries of those who valued other people enough to make politics personal.

    Brad Chilcott is the Founder of Welcome to Australia. This article was first published in The Guardian on 16 January 2016.

  • Robin Room and Michael Livingston. Alcohol companies target the 20% of Australians who drink 75% of the alcohol.

    Researchers have known for a long time that alcohol consumption is quite concentrated in a small part of the population. They argue about the exact distribution, but there is substantial agreement that, so long as alcohol sales are not heavily restricted, consumption is distributed in a quite predictable way. That is, there are many light and moderate consumers, along with a long tail of those drinking at heavier levels.

    In Australia, the top 20% of the drinking-age population in 2013 consumed around three-quarters of all the alcohol consumed. The top 5% consumed more than a third.

    The concentration of alcohol consumption among the heaviest drinkers has actually increased in recent years. The top 10% of consumers accounted for 49% of the consumption in 2001, and this had increased to 53% in 2013.

    The heaviest-drinking 20% of the population reported consuming a daily average equivalent to 43 grams of pure alcohol – a bit over four standard drinks. This is a substantial underestimate of their actual drinking.

    The total amount of drinking reported in such surveys is calculated to be about 55% of the alcohol sold in Australia, so their actual daily average is likely to be about 7.8 drinks. This is nearly four times the low-risk limit of two standard drinks per day recommended by the National Health and Medical Research Council.

    The dangers of alcohol

    If you drink enough alcohol, you get intoxicated, making you unfit for a lot of everyday activities. This includes, for instance, driving a car, most kinds of work or looking after children. Apart from these issues of injury and social functioning, alcohol also carries longer-term health risks.

    At an average of four drinks per day, the chances of dying of an alcohol-related cancer or other chronic disease are two in 100 for men and 2.5 in 100 for women. At 7.8 drinks a day, the chances are about five in 100 for men and eight in 100 for women.

    Adding in risks of dying from alcohol-related injuries more than doubles the risk for men, and increases the risk for women by more than 50%. Just considering the risks of health and injury harms, alcohol is by far the riskiest commodity that a majority of us regularly consume.

    The current guidelines “to reduce health risks from drinking alcohol” set upper limits calculated on lifetime death risks from drinking. These are around four times the rate National Road Safety Strategy aims for as an upper limit of lifetime rate of deaths from traffic collisions. They contrast, for instance, with the National Health and Medical Research Council (NHMRC) guidelines on water safety, which aim to keep the risk of death from contaminated drinking water below one in a million.

    Alcohol marketing

    Those in the business of selling alcohol have long known about the skewed distribution of alcohol consumption in the population. In meetings among people in the industry, those at the top end of the distribution are called the “super consumers“, and they are vital to maintaining or increasing sales.

    If all the “super consumers” reduced their drinking to the two-drinks-a-day average recommended by the NHMRC as an upper limit, it has been calculated, based on self-reported consumption, that alcohol sales would fall by 39%.

    In its public face, the alcohol industry takes the line that it is only seeking to protect and promote “responsible drinking”: how to “drink properly”, minimising risks of harm.

    But, in its internal discussions of the need for retailers to “identify and target super consumers”, the industry is acknowledging a large part of its sales are to drinkers who are taking substantial risks with their own lives and the lives of those around them. If all drinkers in Australia were to drink within the government guidelines for low-risk drinking, the alcohol market would shrink substantially.

    If governments want to reduce alcohol-related harms, they can’t rely on the industry’s commitment to responsible drinking. It’s directly against the industry’s interests for the heaviest drinkers (who make up the majority of their sales) to drink less.

    Given this inherent conflict, policymakers should focus on well-evaluated policies such as reduced late-night trading hours for pubs and nightclubs and smarter taxation of alcoholic products. Most importantly, governments should be sceptical of working in partnership with an industry whose interests are diametrically opposed to public health.


    Robin Room is Professor and Director, Centre for Alcohol Policy Research, Latrobe University.  Michael Livingston is Post-Doctoral Research Fellow at the Centre for Alcohol Policy Research, Latrobe University. This article was first published in The Conversation on January 20,2016.

  • Michael Thorn. Caught Out: How Cricket Australia maintains Aussies high drinking average.

     

    The runs are coming thick and fast in the current Victoria Bitter One Day International Series between Australia and India, bested only by the onslaught of alcohol advertising both on and off the pitch as well as in the commercial breaks in between the on field action.

    That barrage of alcohol ads on the telly are the result of an egregious loophole in Australia’s legislation that allows for alcohol advertising to be broadcast on television before 8:30pm during sporting broadcasts on weekends and public holidays.

    So while the Australian cricket team deservedly basks in the glow of its 4-0 series lead with only the fifth and final game of the series to be played; Cricket Australia and the alcohol companies that advertise during sporting events deserve only our disdain.

    Of course we know why the alcohol industry does it.

    Alcohol companies know only too well that the earlier children are exposed to alcohol branding, the more likely they are to commence drinking earlier and the more likely they are to drink to excess.

    And make no mistake. The Australian alcohol industry is absolutely dependent on not simply recruiting new drinkers but ensuring that its customers drink at levels harmful to their health.

    A new video produced by my organisation, the Foundation for Alcohol Research and Education (FARE), earlier this week exposed the Australian alcohol industry’s heavy reliance on risky drinkers, with over 3.8 million Aussies averaging more than four standard drinks of alcohol a day, twice the recommended health guidelines.

    Targeted by the alcohol industry and branded as ‘super consumers’, the industry’s best customers represent just 20 per cent of Australians aged 14 and above, yet they account for a staggering 74.2 per cent all the alcohol consumed as a nation each year.

    This is the alcohol industry’s dirty little secret. It’s an industry built on identifying, targeting and exploiting its best customers, and ensuring that they continue to misuse and abuse alcohol.

    So much so, that if the industry’s best customers were to drink within the guidelines, the total alcohol consumed as a nation would be reduced by a staggering 39 per cent or more than 38 million litres of pure alcohol.

    Unfortunately, we will all grow old waiting for the alcohol industry to ever agree to effective measures that would save lives and reduce harm, and to willingly stop exploiting these opportunities to link alcohol products with sport.

    It is government that must accept the ultimate responsibility to ensure that vested interests do not trump the health and welfare of our children, our families and our communities.

    The price we pay as a society is already too high; a heavy burden that extends beyond the 5,500 deaths and the 157,000 hospitalisations every year.

    It’s been almost ten months since Australia’s one-day cricket team won the 2015 ICC World Cup. Thanks to a series of unfortunate and embarrassing post-game interviews by Channel Nine’s Shane Warne and members of the cricket team, it was not the sporting victory that held the nation’s attention in the days to follow, but rather the communities building disappointment and outrage that alcohol and a culture of drinking to excess had literally drowned out and overwhelmed the sporting achievement.

    I said then that I hoped the strong reaction would make clear to sports administrators and those responsible in government that it was time for action.

    To date those calls have fallen on deaf ears.

    Today Cricket Australia still worships at the feet of Big Alcohol. Still accepts millions of dollars for the honour of a logo on a shirt and the naming rights to its contests. Still works hand-in-cricket glove with the alcohol industry with the knowledge that by doing so Cricket Australia is complicit in recruiting the risky drinkers so crucial to the alcohol industry’s bottom line and normalising the alcohol-drenched culture.

    Far from strengthening its code during its recent review, Free TV Australia failed to remove the sports loophole and relaxed its code even further.

    And while we can take comfort in changing community attitudes that recognise it is not acceptable that our children be exposed to a sporting code inextricably linked to big alcohol and a culture of risky drinking, it seems that Free TV Australia, Cricket Australia and our governments remain two steps behind and alarmingly out of touch.

    Michael Thorn is Chief Executive of the Foundation for Alcohol and Education Research.

     

     

     

     

     

     

  • Kim Oates. Excuse me doctor, have you washed your hands?

    Imagine you are a patient in hospital. The doctor draws back the bed sheet to examine your abdomen. Before you are touched, you say “Excuse me doctor, have you washed your hands?”

    Would you dare? Would you be too embarrassed, awkward or even afraid to ask? Would you worry that it would be rude to ask, or that it could undermine the doctor’s authority? Would you risk upsetting the person taking care of you if it led to your doctor taking offence? Or you might think it’s just not your role to ask this type of question.

    Hospitals can be dangerous places. Sometimes things go wrong and patients suffer. Dr Don Berwick from the Institute for Healthcare Improvement in Boston showed that the risk of death from hospital admission was the same as the risk of death from mountain climbing or bungy jumping. But of course, because hospital admissions are far more common than these sports, the actual number of deaths is far higher.

    One reason for this is that people admitted to hospital are often unhealthy to start with. They may have multiple health problems. Some have supressed immune systems, making them more susceptible to infection. They may undergo complex procedures where there are small margins for error.

    Another less apparent reason is that not all health professionals practise hand hygiene as well as they should.

    According to the Australian Commission on Safety and Quality in Healthcare, each year approximately 200,000 patients acquire an infection while they are in hospital, making hospital acquired infection the most common complication for hospitalised patients.

    Sometimes these infections can enter the blood stream, with the potential to cause death, particularly when the infection is from an organism resistant to most antibiotics. And hospitals are places where antibiotic resistant bacteria are more commonly found.

    Hand hygiene is probably the most important thing health workers can do to protect their patients from infection.

    But what can patients do to protect themselves? Asking health professionals if they have washed their hands is a good start.

    Studies show that a substantial minority of health professionals don’t wash their hands as often as they should, although concerted campaigns, coupled with surveillance, by Hand Hygiene Australia and other patient safety bodies show that compliance with hand washing is increasing.

    In 2010, 70% of nurses complied with hand washing regimes, the highest of all health professional groups surveyed. By 2105, their rate had risen to 86%. But would you rest easy if you knew that there was a 14% chance that your nurse was one of those who had not performed correct hand hygiene?

    Doctors comply less often. In 2010 the hand hygiene rate for doctors was just under half, a worrying 49%. By 2015 their rate had risen to 71%. It’s a big improvement but doesn’t help if you are the patient of one of the 29% who has not complied.

    What can you, the patient, do about this? The answer is simple in theory, but difficult in practice. Just ask: “Have you washed your hands?”

    However, studies show that 77% of patients would feel uncomfortable asking their doctors if they have washed their hands before examining them. Fifty seven per cent said that they would not ask, assuming the doctor had already washed. Twenty per cent worried that asking could be construed as questioning the doctor’s professionalism.

    Contrast this information with what health professionals think about being asked this question by patients. Twenty nine per cent said they would not like to be asked. Twenty seven per cent said they would find it humiliating if they were asked.

    This essential question is not the responsibility of the patient or of the health professional alone. The best health care occurs when there is a partnership between the patient and the health professional.

    Patients need to know it’s OK to ask the question. Health professionals need to encourage them to ask. Ninety two per cent of patients said they would be more likely to ask the question if the health professional invited them to ask the question, such as by wearing a badge saying “Ask me if I’ve washed my hands.”

    Patients need to be encouraged to ask and health professionals need to become more comfortable with patients who ask the question. If the aim of health care is to improve the health of the patient, rather than make it worse, it’s pretty obvious.

    Kim Oates is an Emeritus Professor at Sydney University and a clinical advisor to the Clinical Excellence Commission

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  • The policy scandal of a $11b taxpayer subsidy to private health insurance.

    I don’t think that I can recall a domestic policy that is so outrageous as the $11 b. annual cost to the taxpayer of the subsidy to private health insurance (PHI) companies. The subsidy is paid to policy holders, but it really means that PHI companies receive the benefit of the subsidy. For further explanation of the $11b figure see link to submission below. Repost from 08/12/2013

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  • John Duggan. Advice from expert clinicians or the AMA

    For those interested in the cost of health care the recently released interim report by the Medical Benefits Schedule (MBS) Review “obsolete MBS items track one” demonstrates the dawning recognition that there are procedures and tests that do not justify their existence or federal funding.

    The story begins with the decision of Ms Sussan Ley, Minister for Health to form the Medical Benefits Schedule Review taskforce, with a mandate to review the schedule in its entirety. The Task Force is ‘an expert clinician led Medicare Benefit Schedule (MBS) review … established to lead an accelerated program of MBS reviews to align MBS funding services with contemporary clinical evidence and improve health outcomes for patients’.

    The taskforce, chaired by Professor Bruce Robinson, Dean of the Sydney University Medical School, is an expert clinician-led group whose main duty is to align MBS funded services with contemporary clinical evidence and improve outcomes.

    One role of the taskforce of 13 members is to appoint chairs and members of working groups to progress the work using evidence based reviews and data and assessment of literature. Priority areas will include safety, clinically unnecessary service provision and accepted clinical guidelines. It also has the power to recommend adding new services to the MBS.

    Of the host of clinical committees created several have already reported on obsolete items – an interesting group. The strictures about kidney x-rays (MBS item number 58705) illustrate the problem and variety of obsolete and useless procedures recommended for abolition. The gastroenterology group reviewed the practice of treating gastric bleeding by infusing refrigerant fluid into the stomach, discarded soon after its initiation about 60 years ago and which was only used eight times in the last 11 years.

    It is evident to any medical scientist that the review is overdue and can only benefit both patients and the budget.

    Whether the AMA feels happy about the review will be reflected in its attitude to the recommendations of the Task Force.

    John Duggan is Conjoint Professor, School of Medicine and Public Health, University of Newcastle.

  • Ian McAuley, Jennifer Doggett, John Menadue. Private Health Insurance companies are price takers. Prices are set by doctors and hospitals.

    Repost from 22/10/2015

    On Tuesday the Australian Competition and Consumer Commission (ACCC) released its  report on private health insurance.

    Private health insurance (PHI) was also in the news a day later with the standing down of the CEO of Medibank Pte, the largest PHI company.

    The ACCC report has been a regular report since 1999, when the Howard Government introduced a swag of subsidies for private health insurance. It covers specific “consumer” issues, such as possible false or misleading representation of products, anti-competitive behaviour, and the incidence of unexpected out-of-pocket expenses.

    Because government policy is taken as a given condition, its recommendations are confined to administrative matters. In this year’s report they are largely about the need for insurers to use standardised terminology and clearer information on restrictions, exclusions and out-of-pocket costs.

    Although not explicitly stated, its concern seems to be to help consumers to make a choice within the range of products (more than 20 000 on offer) from 34 private insurers, rather than helping consumers make a choice whether to hold private insurance or not.

    Unsurprisingly, the report finds that consumers are faced with what the cartoonist Scott Adams (creator of the Dilbert character) calls “confusopoly”. The range of products is bewildering, different insurers use different language to describe similar products, and there  are subtle definitions in policy exclusions (who knows the difference between “obstetrics” and “gynaecology”, for instance?).

    Its most telling findings are that complaints are on the rise, and that the main concerns of complainants are the unpleasant surprises they get (exclusions, co-payments, restrictions on choice of providers) when they come to claim on a policy. The price of private insurance is only of minor concern, even though its price, in real (inflation-adjusted) terms has risen by 54 per cent since 2000.

    We don’t find that at all surprising.  Since the Howard Government introduced generous subsidies for private insurance in 1999, six million more people have taken some form of hospital cover. Many of these have been virtually forced into private insurance by the Medicare Levy Surcharge applying to those with high incomes, and many others were  enticed by the 1999 “Run for cover” scare campaign.

    Research in behavioral economics shows that people don’t make careful, rational choices about insurance. People tend to over-insure for small risks, while leaving themselves inadequately covered in other areas. People buy insurance because they believe it is a prudent thing to have, without giving it much consideration.

    This is confirmed by the ABS in its survey of reasons why people hold private health insurance. It has found that financial considerations hardly count, but that “security, protection, peace of mind” is the overwhelming reason for people to hold private insurance.

    It’s only when people come to make a significant claim, which can be many years down the track, that they realise that they have bought a dud product. Or, perhaps, after outlaying thousands of dollars for private insurance over many years, they have a medical emergency and discover, for the first time, that there is an efficient and responsive public hospital system covering their needs.

    What comes through in the ACCC’s report is a level of frustration. This is a body with a strong faith in the benefits of competition. It says “as a starting point, competition should be relied upon to drive efficient outcomes wherever possible”, but finds that even though there are plenty of players in the market the industry is not providing what consumers want.

    The problem the ACCC faces is that in private health insurance competition doesn’t work, mainly because the insurers are simply a financial intermediary between consumers and well-organised suppliers, as we have pointed our in our work on private insurance for the Centre for Policy Development. Insurers, are essentially price-takers in a market dominated by powerful suppliers.

    That power asymmetry was illustrated earlier this year in the dispute between Medibank Private, Australia’s largest health insurer and Canberra’s Calvary Hospital. The fact that MBF had to back down in this dispute may explain the standing down of the CEO of Medibank Private, George Savvides. He understood the power of providers, but his board didn’t.

    As we point out in our research, it takes the power of a single insurer, such as Medicare and similar bodies in other countries, to ensure that costs are controlled and to see that scarce resources are put to their best use. A case study in resource misallocation (the economists’ term for “waste”) driven by the perverse incentives in private insurance was provided by a recent ABC Four Corners program on over-servicing in private hospitals.

    While the ACCC is critical of some insurers’ practices, particularly some potentially misleading product descriptions, it does not claim that this industry is engaged in collusion or other systemic anti-consumer behaviour. It seems to be annoyed by consumers who do not do their homework and shop around for the best deal – this is a common grizzle by competition regulators, who seem to believe that we all have unlimited time to devote to comparison shopping.

    But even if we were all well-informed and diligent consumers, shopping around for the best products, this would still be a market subject to fundamental market failures that go well beyond the usual scope of competition regulators. Private health insurance is simply a high-cost financial intermediary that takes 14 cents in the dollar for management and profits, without adding any consumer value.

    The fundamental problem is that insurance of any form, be it public or private, by its very nature suppresses price signals – the very mechanism that makes markets work. When a service is free at the point of delivery the discipline of markets does not operate. Economists know this problem by the quaint term “moral hazard”.

    The ACCC acknowledges the existence of moral hazard in private insurance, but there is no way it can resolve the fundamental conflict: that is seeking to use market mechanisms to regulate an industry whose very raison d’etre is to allow people to buy out of the discipline of markets.

    Of course there is still moral hazard in single insurer systems, but a single national insurer can use its power as a strong purchaser to make sure suppliers operate efficiently. There are plenty of successful overseas models of single national insurers, particularly in Canada and the Nordic countries, but, closer to home state governments, particularly in Victoria, and the Commonwealth Department of Veterans’ Affairs, act as single purchasers of hospital services. And moral hazard on the part of consumers can be held in check by the use of judicious co-payments set at such a level to provide some market discipline but not so as to discourage those with limited means from seeking necessary care.

    Perhaps, when the ACCC produces its 2014-15 report for release this time next year, it could remember that competition is not the answer to all market failures. Competition is not an end in itself – it is one way, in some markets, whereby efficient and fair outcomes can be achieved. In some markets it doesn’t work.

     

     

  • Jennifer Doggett, Ian McAuley, John Menadue. Four Corners: No wonder we’re wasting money in health care – we got the incentives wrong

    Repost from 06/10/2015.

    A recently-aired ABC Four Corners program aptly titled “Wasted” exposed three areas of unnecessary, ineffective and outright dangerous health interventions, in knee, spinal and heart surgery.

    The show’s host, Norman Swan, presumably extrapolating from the findings in those three areas, claimed that waste could be as high as 30 percent of all health care expenditure.

    Perhaps that’s an overstatement, but the point made by Swan and by most of the ten other clinical experts who appeared on the program is that we just don’t know how much waste there is in health care because we lack the processes for evaluating the effectiveness of various interventions.

    We know what we pay for a knee replacement or a cardiac stent, but we do not systematically evaluate the outcomes of these procedures.

    Identifying and reducing or eliminating funding for low value services would save our health system billions every year.

    However, this would only address one area of waste and inefficiency within our health system. A less obvious but potentially more significant source of waste lies in the way in which health care is funded in Australia, in particular via fee-for-service payment mechanisms and private health insurance.

    These funding processes are driving unsustainable growth in health services consumption without meeting the needs of the community for efficient, preventative and coordinated care.

    Unless Australia’s health funding system is fundamentally reformed to discourage inefficient and provider-driven health expenditure, efforts to increase the efficiency and targeting of Medicare expenditure will be dwarfed by the growing waste associated with our current funding systems.

    The big picture

    Every year we spend around $160 billion on health care – two thirds through our taxes, and one third through private sources.

    At a macro level we can claim we spend that money well. At around ten per cent of GDP it’s in line with expenditure in similar countries, and by gross indicators such as infant mortality and life expectancy we’re among the high achievers.

    But within our health care arrangements – a complex mix of private and public funding and provision – there are areas of poor outcomes, such as indigenous health, youth suicide, and obesity, and there is evidence of resource misallocation, such as long waiting times for elective surgery in public hospitals while there are government subsidies encouraging queue-jumping for those with lesser needs to use private hospitals.

    The role of data

    It’s not that we fail to collect data in many areas of health care, but as Adam Elshaug, Associate Professor of Health Care Policy at Sydney University points out, all the data is kept in separate silos – some relating to the Pharmaceutical Benefits Scheme, some relating to the Medical Benefits Scheme (MBS), and some in state public hospitals just to name three of the non-interlinked sources.

    While we lack a systematic method of data analysis and feedback (which was one of the original purposes of Medicare), there are a some studies of cost effectiveness in specific areas of health care, upon which the experts were able to draw. In these three areas of health care, that make up a large proportion of surgical admissions in private hospitals, all the experts were able to identify evidence of ineffective treatment and over-servicing and where resources could be put to better use. As an example Swan pointed out:

    At least half of all back scans and X rays are of no value, and to put that into perspective, that’s at least half a billion dollars over ten years. Now that would buy you a regionally delivered national suicide prevention program that would save 1000 lives a year.

    The experts offered a number of explanations for this waste. One strong message was that the vast majority of the 5700 items on the MBS schedule had never been subject to any rigorous cost-effectiveness evaluation. As Elshaug reminded us, the MBS schedule dates back to the 1960s (when it had only 300 items), when the idea of “evidence based policy” as a standard was still some decades off. It has been easy for advocates, mainly in the medical profession, to add new items to the schedule, but it is very hard to have any removed. Professor Rachelle Buchbinder, Director of the Department of Clinical Epidemiology at Monash University, recounted the great difficulty she had experienced in having just one item removed from the MBS. She was confronted by well-funded corporate interests, and was subject to ad hominem vilification. (We wish Minister Ley the best of luck in her taking on the MBS schedule.)

    Drivers of growth

    Many referred to the availability of imaging technology, referring, for example, to the fact that GPs can now order knee MRIs without going through a specialist. Often discussions about technology in health care degenerate into a romantic and unrealistic call for the clock of technological advancement to be turned back. But Paul Glasziou, Director of the Centre for Research and Evidence Based Practice at Bond University pointed out that imaging and other diagnostic technology is here to stay and is becoming more widely available (have you noticed that “health” app on your smartphone?). As the Productivity Commission pointed out in its 2005 report on medical technology, IT-based technologies in most industries have reduced unit costs, and there is no reason why it should not do so in health care if used properly.

    The problem that Glasziou and others pointed out is that diagnostic technology has given us much more capacity to detect what is “abnormal” or supposedly “wrong” in our bodies. We misinterpret the normal changes associated with ageing, and, as a result otherwise healthy people are turned into “patients”. Our expectations and anxieties as consumers have interacted with GPs’ fear of missing a diagnosis and desire to do something tangible, in the form of delivering a “product” to the patient, leading to a detected abnormality and on to surgery, with all the attendant costs and the possibility of infection and other iatrogenic risks. (A similar motivation to provide some tangible product has been found to be a driver of pharmaceutical over-prescribing.) Doctors are generally dedicated professionals motivated by a strong desire to “do something” for those who turn up in their surgeries.

    But as Robyn Ward, Chair of the Medical Services Advisory Committee said, “often the best medicine is no medicine at all, often the best intervention is no intervention at all”.

    She said that if GPs could explain how certain procedures are ineffective, patients may make better decisions. And if GPs or other health professionals could help people understand that adopting a healthy lifestyle may be more effective (and certainly less costly) than going down the diagnosis-surgery path, there would be better outcomes all around.

    The problem with our current funding system

    But that’s not where the incentives lie in a fee-for-service system. Swan summarised the problem when he said “the way we pay for health services in Australia does not encourage good practice”. We pay for throughput, not for outcomes.

    One perverse consequence of these incentives for over-servicing is that early intervention at the primary care level, which is supposed to result in better health outcomes and financial savings, can actually worsen outcomes and cost money when the incentives are wrong.

    Cardiologists Richard Harper (of Monash University) and Andrew Macisaac (of St Vincent’s Hospital) noted that there was excessive use of angiograms (Harper suggested that up to 43 percent of invasive angiograms were unnecessary), and that these were most likely to occur in private hospitals. There is a confirmation of published findings by Monash University researchers that observed “startling variation” in the use of well-known procedures in Victorian hospitals. They found “in the 14 days following a heart attack, men and women admitted to a private hospital were 2.20 and 2.27 times more likely to receive angiography than their counter-parts in public hospitals”. They were 3.43 and 3.86 times more likely, respectively, “‘to undergo revascularisation” (coronary by-pass surgery, angioplasty and stent).

    That study was published in 2000, around the same time the Commonwealth was strengthening subsidies for private health insurance, in a set of arrangements that de facto linked funding of private hospitals to private insurance. At no time has the Commonwealth evaluated that policy, but independent research suggests that while it has injected a large amount of new money into private hospitals, and into the incomes of medical specialists, it has done nothing to achieve its avowed objective of “taking pressure off public hospitals”, because where the funds have gone, so too have the specialists. If anything the subsidies have sucked resources out of public hospitals and have put pressure on public hospitals to try to match the incomes specialist can enjoy when they work in private hospitals.

    If people who present to private hospitals get more treatment than those with similar conditions who present to public hospitals, then there is certainly some resource misallocation. Either public patients are being under-serviced, or private patients are being over-serviced. The Four Corners program strongly suggests the latter.

    The funding honeypot – private health insurance

    While there were frequent reference to the problems of fee-for-service medicine, the program only touched on the interaction of private health insurance and fee-for-service remuneration, which is where the root of the problem lies. Private health insurance is a major driver of resource misallocation and waste. But since 1997 the Commonwealth has had a policy of supporting private insurance, almost as an end in its own right.

    It is notable that not since 1969 – when the Nimmo Report paved the way for universal public health insurance – have governments subjected private health insurance to policy scrutiny. The principle of evidence-based medicine, and the general bipartisan disdain for industry subsidies, do not seem to apply to private health insurance.

    Although unquestioned support for private health insurance is normally associated with Coalition governments (“Private health insurance is in our DNA was Prime Minister Abbott’s justification), it has become bipartisan. When the Rudd Government set up the National Health and Hospitals Reform Commission it specifically ruled out any scrutiny of private health insurance. The Gillard Government strengthened the Medicare Levy Surcharge penalties for those higher income people without private insurance, and removed the 20 per cent tax offset for those who incur expenses not covered by private health insurance. Only the Greens seem to be committed to the original principles of Medicare as a single national insurer.

    Thanks to the Medicare Levy Surcharge, people on higher incomes (individuals with an income above $90 000 and families with an income above $180 000) are virtually conscripted into private insurance. Quite apart from the problem of promoting a two-tier health system, with the public system reduced to a residual “charity” system, the surcharge has strong incentives for people to use private insurance, and for opting out of sharing his or her health expenses with other Australians. Someone with an income of $150 000 can either buy top hospital cover for around $1300 or pay an extra $2250 in taxes, for example.

    The subsidy to private health insurance comes to more than $8 billion a year according to Commonwealth Budget papers, and is growing strongly. That figure does not include the effect of the Surcharge, which, if it is re-framed as a subsidy for having private insurance (rather than as a penalty for not having it), results in revenue forgone of around $3 billion a year, or a total subsidy of around 11 billion dollars a year. As Jeff Richardson of Monash University once said, not even in the days of high support of manufacturing were the rich actually provided with a taxpayer-funded Holden with change left over.

    With governments ready to provide such permissive access to public money to support private insurance, it is hardly surprising that private health insurance premiums have risen so strongly. Since 2000, while general prices (as measured by the CPI) have risen by 54 per cent, private health insurance premiums have risen by 133 percent – a 50 per cent real increase. As a source of ever-growing funds private insurance has been a honeypot for private hospitals and those who work in them (as well as directing public money that taxpayers may have believed were for health expenditure, to flybuy cards and Coles gift vouchers).

    So long as we have a highly-subsidised private health insurance industry, fee-for-service medicine, and a private hospital system with its own privileged source of funding, these problems will remain. In time we could head to the US system, where private health insurance has resulted in health costs approaching 20 per cent of GDP, and with only mediocre outcomes by the standards of most prosperous countries. (“Obamacare” will solve some coverage problems, but it will not solve the cost problem.)

    The real cost of private health insurance

    There are several independent analyses of the costs of private health insurance – Jeff Richardson’s “Private Health Insurance and the PBS: How effective has recent government policy been?”, an analysis by Don Hindle and Ian McAuley “The effects of increased private health insurance: a review of the evidence”, a Centre for Policy Development paper“Private health insurance: High in cost, and low in equity”, an article for The Conversation by Terence Cheung of the University of Adelaide “Why it’s time to remove private health insurance rebates”, and a chapter in the recently-published book Governomics: can we afford small government?

    A common theme of these works is that measures such as private health insurance, designed to shift costs off-budget, generally result in the public paying more for the same or worse services, with far less accountability or equity, and with much higher administrative costs as slimmed down public agencies (such as Medicare) are replaced by corporate bureaucracies duplicating competitors’ corporate bureaucracies.

    In fact, in the USA, reliance on private health insurance, far from saving public money, has resulted in a blowout in public expenditure. Because health costs are set in an undisciplined market between powerful service providers and comparatively weak health insurers, even the publicly-funded programs (Medicare and Medicaid) are now costing more than the comprehensive single insurer models in place in Canada, the UK and the Scandinavian countries.

    Outcomes, not volume

    In the Four Corners program Robyn Ward called for a system that pays for value and outcomes rather than activity or volume. It’s a view shared by many others.

    It is hard to see how such a system based on outcomes rather than outputs could be developed through any monetary incentive system. One basic problem is that in very few cases is it possible to link any specific health interventions unambiguously to outcomes. There are too many other variables leading to people’s health outcomes, and there is often a very large time lag between interventions and outcomes. When it comes to non-interventions (e,g, the decision not to have a knee reconstruction) the measurement and time lags are even more problematic.

    It is even harder to see how any private insurance-based system can deliver satisfactory consumer outcomes or any significant degree of cost control. The economics textbooks claim that businesses seek profit, while the business textbooks, based on empirical studies of organizational behaviour, see growth and expansion as the prime objective of firms (with profit as a constraint to be satisfied). That growth objective would surely dominate in any scheme relying on financial incentives, leading to over-servicing. The Four Corners program is an excellent exposition of the way private sector incentives lead to such poor outcomes. If costs rise because of over-servicing, the insurers can simply jack up their premiums.

    The benefit of a single public insurer is that Commonwealth Treasurers will always sustain pressure to keep expenditure in control and to achieve value for money. It’s easier for insurers to raise premiums than for governments to raise taxes.

    Public insurance, private and public delivery

    That is not to say the private sector should not be involved. It is simply to point out that private insurance should have no role in funding health care.

    There is clearly a role for personal out-of-pocket (i.e. uninsured) contributions to health care. In fact, such contributions are a feature even of the most generous single insurer models as operate in the Scandinavian countries, and, in a wealthy country such as Australia they should clearly pay their part. When Medicare was first designed we were much less prosperous, but now, on average, households now have around $300 000 in financial assets, a figure that has grown, in real terms, more than 60 per cent this century.

    While we all need to be covered for high health care expenses, we don’t need the “first dollar cover” provided by so many private insurers – the cover that drives us to over-use of health services. Both public and public insurance comes with the same incentive for over-use (“moral hazard” in the quaint language of economics) – there is no difference in the notion “Medicare will pay for it” and “BUPA/Medibank Private/HCF will pay for it”, but, as pointed out above, Medicare comes with the discipline and accountability of public finance, and it is easy for governments to build in compulsory out-of-pocket contributions to lessen moral hazard.

    Out-of-pocket payments provide some price signals to consumers, and they can be designed in such a way that most people who make light use of health services in any one year can be independent of any public funding support, so that public funding can be directed to serious acute and chronic conditions. We already spend around $27 billion a year in out-of-pocket contributions, but, as Jennifer Doggett points out, their incidence is haphazard, and do not adhere to good insurance principles: some health care programs are free at the point of service, while for some others the patient is left bearing open-ended risk. Ham-fisted ideas to bring in open-ended MBS co-payments, as proposed by the Abbott Government, understandably meet with community resistance.

    In the delivery of services the private sector has always played a central role, and will go on doing so. Alarmists often interpret any criticism of private health insurance as an attack on the “private system”, but that’s bunkum. There is no reason why private hospitals cannot be involved in delivering publicly-funded services.

    That model is already operating in Australia through the Department of Veterans’ Affairs, which acts as a single insurer for war veterans, while purchasing most services, including hospitalisation, from the private sector. At a state level there have been initiatives to break this dependence. Victoria, under the leadership of Premier Jeff Kennett first made the offer to private hospitals in the 1990s and the Tasmanian Government has recently offered $25 million of elective surgery cases to private providers. There’s nothing radical about such measures – in fact they are in line with national competition policy that calls for competitive neutrality between private and public sector providers.

    Future dangers – Medicare Select

    The Four Corners program has been a useful reminder of the problems we face in health care, particularly (but not only) the perverse outcomes when private insurance, fee-for-service payment, and a private hospital system separated from public hospitals interact. No doubt private insurers, who will be well aware of these perverse outcomes, will be presenting to government schemes which they claim will solve these problems. For example, arising out of the Health and Hospital Reform Commission’s work, the insurers put forward an idea called Medicare Select, which made great claims about consumer choice and cost control, but which was simply a way of churning even more public funds through health insurers, adding private sector administrative costs to public sector administrative costs, without demonstrating any value-added, other than offering consumers some “choice” of care plans – as if people are in a position to know their future health care needs.

    We could well see the private insurers offer Medicare Select, or some similar proposal, as a “solution” to our problems. Even if such schemes are put forward in good faith, we should heed the lessons from the USA, however, where private health insurers have been quite unable to contain health costs – or perhaps unwilling.

    There are too many parties – medical specialists, private hospital companies, appliance manufacturers, pharmaceutical firms – who would see cost containment as quite inimical to their interests. And there is the whole investment community – superannuation funds, banks stockbrokers, financial advisors – looking for a new growth industry, as profits in traditional industries such as airlines, newspapers and retailing are squeezed.

    Only a strong government can protect us from the economic and health costs of health care becoming a growth industry.

    Jenniffer Doggett is a consultant in the health sector. Ian McAuley is a Adjunct Lecturer, Canberra University. John Menadue chaired Health Enquiries in NSW and SA and was involved with Gough Whitlam in the creation of Medicare.  All three are Fellows of the Centre for Policy Development. 

    ********

    John Menadue posted three articles on health reform as part of the Policy Series ‘Fairness, Opportunity and Security’ which he edited with Michael Keating. Links to those three articles follow.

    Health Policy Reform: Part 1 – Why reform is needed.

    Health Policy Reform Part 2 – Why reform is difficult.Health ministers are in office but not in power.

    Health Policy Reform: Part 3 – Principles for reform.

  • Michael Thorn. The Australian cricket captain says its about the brand and not alcohol.

    Repost from 24/09/2015

    Premier Mike Baird’s public comments at last week’s Thomas Kelly Foundation event in Sydney wasn’t the first time he has questioned the extent of alcohol advertising in this country, particularly its strong association with big sport.

    Baird made the self-evident point that such alcohol advertising has become omni-present and spoke about the need to reduce its presence.

    I find it quite an incredible position where the captain of our cricket team sits there with a big VB on the middle [of his chest],” Mr Baird said.

    It would be a fair bet that there were more than few alcohol industry, advertising and sporting corporate types on the phone to the Premier’s office the next morning to set him straight.

    Indeed, Australian Cricket Captain Steve Smith was sent out to face the media and, attempting to play a dead bat, suggested that “we’re promoting the brand, not the consumption of alcohol”.

    Which would be all well and good if the two were not so inextricably linked.

    I dearly hope Mike Baird continues to be engaged in this issue because his leadership will be important for an issue most Australian’s want changed.

    The problem with alcohol advertising is threefold.

    First, child and adolescent exposure to alcohol advertising is associated with earlier initiation of drinking and greater consumption among existing drinkers.

    Second, alcohol advertising targets children. The industry does this because unless new drinkers are recruited they are out of business.

    Third, and most importantly, alcohol advertising confirms and reinforces the cultural norm about alcohol’s place in our society and overwhelms health and medical efforts to change this.

    It also fosters unhealthy politico-corporate behaviour. Time and again political leaders are either captured by these vested interests or too weak to resist their overtures. History is littered with examples of these private corporate interests being placed ahead of the public interest.

    These interests have enormous power, which they aren’t afraid to use. It takes a special kind of political leader to stand up to these corporate bullies.

    But the research evidence about the pervasiveness of alcohol advertising is clear. It is considerable in its breadth and it volume; and big sport, advertisers and the media barons are completely attached to the steady financial drip.

    New research from Monash University’s Professor Kerry O’Brien shows that Australian children and adolescents receive millions of exposures to alcohol advertising when watching AFL, NRL, and Cricket on television. It found that a cumulative audience of 26.9 million Australian children and adolescents watching these sports are exposed to 51 million instances of alcohol advertising, with nearly half (47%) of these broadcast during daytime programming between 6am and 8.30pm.

    This latest research once again demonstrates that existing alcohol advertising regulations are not protecting Australian children from exposure to unhealthy advertising during prominent televised sports.

    As NRL and AFL footy finals move towards their denouement, the egregious loophole that allows alcohol advertising to be broadcast during live sporting broadcasts in the daytime, on weekends and public holidays continues to expose millions of Australian children and adolescents to high levels of alcohol advertising.

    Premier Baird’s comments, timely as they are, come as FreeTV Australia seeks approval to relax restrictions that will allow for even more alcohol advertising on TV, a move that would be a backward and an enormously damaging step.

    The current self-regulatory alcohol advertising codes have not only failed to protect children and adolescents from exposure to alcohol messages. They have failed miserably to keep up with the rapidly shifting traditional and digital landscape and protect consumers of all ages from inappropriate advertising.

    Ideally, alcohol advertising should be banned from broadcast and online media, alcohol sponsorship of sport and cultural events should cease (using a replacement advertising scheme funded by a levy on alcohol sales), and health and safety counter-advertising should accompany print and outdoor advertising.

    In the meantime, the Commonwealth Government needs to establish an independent review of Australia’s broadcast and digital alcohol advertising guidelines. Such a government-instigated review could cut through the complexity, identify and resolve current failings and recommend the introduction of an effective alcohol advertising regulatory regime.

    Perhaps this is something Premier Baird could take up new Prime Minister Turnbull, whom I know has also expressed concern about the pervasiveness of alcohol advertising.

    The review could deal with the inconsistent approaches to alcohol advertising without having to lower the bar further on an already broken system. We must tighten the alcohol advertising guidelines and lift the advertising standards across all media including commercial television, Pay TV and online platforms.

    Meanwhile, Mike Baird continues to lead the way when it comes to speaking up about issues that damage and destroy too many lives.

    Michael Thorn is CEO of Foundation for Alcohol Research and Education.

     

  • Kim Oates. Don’t forget children when talking about domestic violence

    Children are victims of domestic violence too.

    Last week the Children’s Commissioner released this year’s children’s rights report. It provided new data about the prevalence of child physical and sexual abuse and their links with domestic violence.

    Christmas, traditionally a time of peace and goodwill is sadly, a time of increased domestic violence, thought to be due to increased alcohol consumption and family gatherings where there can be the potential to cause resentment and open old wounds.

    Our awareness of the extent of domestic violence has been slow in coming. It parallels the way awareness of child sexual abuse came about almost 40 years ago.

    When I was a medical student attending psychiatry lectures in 1966, our very eminent professor of psychiatry mentioned that sometimes men sexually abused girls, but that this was very rare. He explained to us that it often occurred at the instigation of the mother who, not wanting sex, pushed her daughter forward instead. Like good students we took notes and learned this “fact” in case it came up in an exam. We did not realise how outrageous and how wrong this teaching was.

    Then in 1977 a US paediatrician, Henry Kempe wrote a seminal paper “Sexual abuse, another hidden paediatric problem”. He documented what happens to these children, that it happens in outwardly respectable families, that it is not the child’s fault or the mother’s fault and that it is not rare. Kempe wasn’t the first to describe the sexual abuse of children but having described “The Battered Child Syndrome” 15 years earlier, his stature was such that when he wrote, people took notice.

    Brave victims came forward and spoke of their childhood experiences.  Other prominent women, social workers and concerned paediatricians spoke about the problem. A backlash followed. There was denial about its extent. Child victims were accused of fabricating stories. It took many years until the community became aware that this was a serious and widespread problem for the whole of society and that prevention as well as treatment and care for the victims was needed.

    The awareness of domestic violence has been similar, although occurring much later. For many years it was swept under the carpet,  considered to be family business, “better not to get involved”. Victims were blamed as if it was their fault. Police did not give it high priority.

    Like child sex abuse, it was a problem that made us feel uncomfortable, a problem we’d rather not know about, a problem that perhaps occurred in “other families”, but certainly not amongst people we knew.

    It took some horrific cases, it required concerned women who set up refuges, and it needed brave victims, such as Rosie Batty, to speak up. Only now are we becoming aware of the extent and seriousness of domestic violence, violence that on average causes the death of at least one woman each week and causes physical and psychological harm to countless others.

    So what about the link between domestic violence and the abuse of children? We used to teach that they had little in common. Now we know that domestic violence has very serious effects on children.

    Children who witness domestic violence can have a range of reactions. Some become fearful, living in constant anxiety, some may feel guilty that they are unable to protect their mother, some feel guilty because they still love their father and they just want him to stop.  Others become aggressive. Some learn that this is the way fathers behave towards their wives, leading to the possible intergenerational transmission of domestic violence if this is the only role model they are exposed to.

    And then there is the physical and sexual abuse of children in families where domestic violence occurs. Research has shown that between 45 per cent and 75 per cent of women living in refuges report some form of abuse to their children, whether it be physical, emotional or sexual. Other studies suggest that approximately 60 per cent of child physical abuse occurs in homes where there is family and domestic violence. Sometimes a perpetrator uses violence against his partner to prevent her from revealing that he is sexually abusing her child.

    It is ironic and sad that the home, where one expects to be safe, can be the most dangerous place of all for some women and children.

    With Christmas approaching, this is yet another reason not to forget the children.

    Kim Oates is an Emeritus Professor of Paediatrics at Sydney University and a past president of the International Society for the Prevention of Child Abuse and Neglect.

    This story was found at: http://www.smh.com.au/comment/dont-forget-children-when-talking-about-domestic-violence-20151216-glo9js.html

  • John Menadue. Cricket and the sound of summer.

    For me, the most memorable comment of the cricket season so far has been by Steve Smith, the Australian captain, explaining that the VB logo on their jackets wasn’t really advertising alcohol. It was only ‘branding’.

    I notice that he is now promoting Kentucky Fried Chicken.  I am waiting for his explanation of how that helps combat obesity.

    A sad feature of the current season was the untimely death of Phillip Hughes. There was much public sympathy from the players. It was surprising that they did not fund a memorial foundation. They could afford to. In 2014 out top five players had salaries of over $20 m between them.

    But the best cricket writing of the year was Geoff Lemon in his piece ‘Just not cricket – how Channel 9 is destroying a legacy’.  for his story about Slats, Heals, Tubby, Binga eta al, see link below.

    http://gu.com/p/45d92/sbl

  • John Duggan. The effect of healthcare privatisation on patient outcomes

    Recent actions by the Federal Minister of Health and her predecessors indicate the government’s aim to shift hospital care from the public to the private sector. Associated with this is the   developing perception that private hospitals are superior just as private schooling is increasingly held to be superior to publicly funded schooling.

    However, while there are massive data available comparing standards and outcomes in the school system, public, private and Catholic, there are virtually no Australian data comparing the two hospital systems; the only study found is a Productivity Commission report outlining the equal inefficiency of both systems.    http://www.pc.gov.au/inquiries/completed/hospitals/report

    The Federal, State and Territory Health Departments are treasuries of relevant data awaiting the will, finance and logistics to convert data to information and information into knowledge.. The absence of such  data comparing quality of care and outcomes in the two healthcare systems, contrasting with educational data may be attributed to apathy or to the power of vested interests ,.However, studies from the US and , Canada indicate that it can be done,. recognising that in Australia, as the Productivity Commission reported,, the data sources are multiple and ill-coordinated. and that both systems function at 20 % below best practice,.,

    To interpret the US data, it is necessary to understand that, at least until the Obama legislation, there were several hospital systems and funding mechanisms. There were the not-for-profit hospitals often run by religious or community//civic groups , for- profit institutions, generally investor owned and part of a chain, and thirdly, those owned by cities or universities.

    A detailed analysis of 14 studies in the US, totalling 36 million admissions to 26,399 US hospitals 1982 – 1995 http://www.ncbi.nlm.nih.gov/pubmed/12054406 .compared  for-profit versus not-for-profit hospitals .It showed  a small but statistically significant 2% elevation in mortality in for-profit hospitals. Six of the component studies showed a statistically significant advantage for not-for- profit institutions; while only one study           showed a similar advantage in for-profit hospitals. The only obstetric study, that of 1,642,002 patients in 241 hospitals showed a highly significant 9.5% increase in mortality rates for babies in for-profit hospitals.

    In another study the U.S. Health Care Financing Administration studied data on 3100 hospitals, adjusting for differing patient characteristics. Lower mortality rates were associated with teaching hospitals, a higher proportion of board-certified medical staff (specialist qualifications), a higher proportion of registered nurses and higher payroll expenses i.e. staffing levels. A higher mortality rate was associated with for profit and public (in Australian parlance state-owned) hospitals compared with not-for-profit hospitals .http://www.ncbi.nlm.nih.gov/pubmed/?term=NEJMED++19

    The U.S. Joint Commission on Accreditation of Healthcare Organisations and the Centers for Medicare and Medicaid Services studied data submitted in 2004 to the American Hospitals Association on coronary occlusion, heart failure and pneumonia. Detailed statistical analysis showed that “for-profit hospitals consistently underperformed not- for-profit hospitals”. The conclusion reached was that “Patients are more likely to receive high quality care in not-for -profit hospitals and in hospitals with high registered nurse staffing ratios and more investment in technology”.http://www.ncbi.nlm.nih.gov/pubmed/?term=landon+in+Arch

    Of several studies of specific conditions, one of the largest compared outcomes in for-profit and not-for-profit renal dialysis centres in the U.S http://jama.jamanetwork.com/article.aspx?articleid=195538. In a review based on 500,000 patient years from 1973 to 1997 in 1342 facilities, six of the eight studies showed a statistically significant increase in mortality in for-profit facilities, one only suggested the same and one suggested lower mortality in for- profit institutions. The authors conclude that “there are annually 2500 (with a plausible range of 1200-4000) excess deaths in U.S. for-profit centres”.

    Another study examined the evidence for performance differences between for-profit and not-for-profit psychiatric inpatient facilities since 1980. All but one of these

    studies found that not- for- profits performed as well as or better than the for-profit psychiatric organisations. http://www.ncbi.nlm.nih.gov/pubmed/12556598

    In view of the Federal government’s push for cost savings through efficiency we should compare health care administration costs in the U.S. and Canada (http://www.nejm.org/doi/full/10.1056/NEJMsa022033) .While the two countries share many social characteristics with excellent databases, their health care systems are quite different. Canada had a centrally funded health care system and a single payer – the government, while the U.S, .like Australia, had a multitude of health insurance systems with multiple payers. In 1999, health administration costs were at least   $1059 per head in the US compared with $307 per head in Canada. Thus, administration accounted for 31% of health care expenditure in the US but only 16.7% in Canada. In the 30 years to 1999 administration’s share of healthcare labour force expenditure went from18.2% to 27.3% in the US whereas in Canada it rose from 16.0% to 19.1%.

    Privatization also uses more doctor’s time. A recent study of treating doctors in the U.S. showed that they devote an average of one sixth of their time to administration; psychiatrists top the bill at 20% whereas paediatricians only spend 14%.http://www.ncbi.nlm.nih.gov/pubmed/25626223

    Only one study comparing Quality of Care issues in investor owned and not-for-profit Health Maintenance Organisations in the U.S. has been found. http://www.ncbi.nlm.nih.gov/pubmed/10411197 Data from the National Committee for Quality Assurance’s Quality Compass on 329 HM0 plans showed that the 248 investor owned plans had lower scores for all the quality of care indices than the 81 not- for- profit plans.

    There is, however, one aspect of the U.S. studies relevant to Australia. A recurrent theme there is the association of better outcomes with medium and large size hospitals, and for procedures performed by experienced doctors with specialist qualifications.http://www.nejm.org/doi/full/10.1056/NEJMsa0907130 http://www.nejm.org/doi/full/10.1056/NEJMsa012337 http://www.nejm.org/doi/full/10.1056/NEJMsa035205

    Whether there is significance in the fact that there are in NSW 380 public hospitals but more than 600private hospitals remains speculative.

    Overall, while the U.S. findings are relevant to the U.S,  their application to Australia is debatable; unfortunately we lack any data to indicate that the deplorable US system is replicated here. With the enormous and growing cost of Healthcare in Australia, surely the time has come to consider an analysis of the costs and patient benefits of the various healthcare systems in Australia , such as has been done in North America..

    Conjoint Professor John Duggan, School of Medicine and Public Health, University of Newcastle.

     

  • Peter Gibilisco. The standardisation of services for people with disabilities.

    WHAT IS MEANT BY EFFICIENCY IN THE PROVISION OF SERVICES FOR PEOPLE WITH DISABILITIES? IS IT JUST A COVER FOR GREATER STANDARDISATION? 

    The State Disability Plan is not the only endorsement of the need to emphasize the individualising of care for people with disabilities. We now hear of a profound development – person-centred planning is said to be the world-wide benchmarked best practice. This involves a highly individualised vision of the person with disabilities and the result is that care needs multiply into a kaleidoscopic variety of individually generated special needs and concerns.

    This attempt to generate a sensitive and compassionate approach nevertheless faces an ongoing dilemma. The costs associated with such an approach to provision of disability services continue to outstrip the services that can be provided by the pension. Moreover, the demands (and possibly the false needs as well) that are generated by this latest example of neo-liberal micro-reform of the “disability workplace”, has the effect of further transforming the already precarious environment for care-worker and the client.

    I continue to think about what happened at a recent meeting that was convened by my own “service provider” to discuss with us an increase in rent for residents.

    At this meeting, we were told of plans to sell the provider’s prime real estate in the Melbourne CBD. A question was asked about the way in which the provider was viewing this sale. The discussion seemed to be suggesting that the sale could assist the provider in overcoming its budget problems. That was why as a corporation it was considering divesting itself of one of its assets.

    So the suggestion was put to the provider that if the building in Flinders Street was being sold for budgetary purposes, a small amount of the profit from the sale could be used to help the pensioners among the residents overcome their budget problems that would accrue from an increase in the rent.

    After all, the service provider is keen to present itself to the community as an effective not-for-profit company, and so all of its profits are to be ploughed back into the community it is serving. And residents certainly wish to have their part in this community recognised. They are not merely rentiers; they are constitutive of the provider’s “community”.

    The assets held by the provider are retained by it to enable the provision of a service it is constituted to provide.

    I had assumed all this but those representing the provider’s main office did not seem to get these basic points. Do they understand what a not-for-profit service provider is? I asked myself. They gave the impression that the budgetary problems of the residents were completely different from the financial demands that are upon the provider as these are documented in the company’s official accounts.

    And of course, these budget stresses and strains are not exactly the same thing. We residents also have to be responsible for how we manage our finances and that in fact was why we had insisted upon having the conversation in the first place. But just because they are not the same thing, does not mean they are unrelated and their inter-dependence ignored. To dismiss the suggestion that the profits from the sale might be distributed in a way that helped ease the strain on the budgeting of residents, seemed to suggest that the provider’s budget issues are a completely different kind of responsibility to those residents have for their own finances. Moreover, the residents are part of a community comprising themselves and the workers at all levels.

    So I guess the result was somewhat inevitable. Disgruntled residents will be left wondering how the sale of this prime real estate shores up the company in a way that will enable top management to be paid at the level to which they have become accustomed. So where will the profits from this sale go? In ensuring the immediate “business prospects” of provider, the company will, I guess, reduce some of its current budget deficit. But at the same time, there is still unrequited budget pressure for residents due to rent increases.

    Let me change the topic slightly here and note how in these days of cut-throat public relations, the provider may be confusing the services it provides with replacing proper policy-development with slogans. Let me invent a possible slogan:

    ACE DISABILITY SERVICES – We are here to give independent and fulfilling lives to people with physical, intellectual and multiple disabilities. Lovely slogan isn’t it? But then reflect upon the efficiencies that are required in shared supported accommodation like my own. And now look carefully at that phrase: people with physical, intellectual and multiple disabilities. I am not criticizing the ethical intention; I am trying to draw attention to the inner organizational chaos that will result for workers and residents if a facility conflates physical and intellectual disabilities. And who can tell how care for those with “multiple disabilities” can emerge in the midst of such organizational blurring.

    There are many residents, perhaps an overwhelming majority of up to 80%, in supported accommodation with some form of intellectual disability. Therefore it can be expected that in shared support accommodation like the place where I reside, that a policy of taking on such high demand people will simply result in a standardization of disability care for many service providers. And don’t get me wrong. Such people are also my neighbours and deserve proper care. But by putting all disability together in one facility, even if there are different classifications on paper in a provider’s policy documents, there will be an inevitable drive toward standardized care and abstract efficiency, that may allow the provider to continue its “service provision” rather than actually looking to the individual care of people with disabilities.

    Quite seriously, this is what I fear will happen. Without a rediscovery of how residents are genuine members of the community that the service provider is maintaining, a policy will develop in favour of standardisation over the appropriately differentiated individual care needed for people with disabilities in shared supported accommodation.

    Service providers receive much money for the care of people with disabilities. These payments come in the form of funding, government payments, and donations from other for-profit companies and the general public. But among residents of such facilities in the disability sector the suspicion is deeply ingrained that these funds never seem to meet the need for which they were intended. And requiring service provision to be subject to a culture of competitive tendering processes means that what were once not-for-profit bodies are not driven by a non-charitable need to accumulate the accoutrements of “business success” coinciding it seems with the self-serving “need” to provide their own CEOs and senior management with wages or salaries or packages as if “management” is a sphere that floats high well above the reality of the people their company is supporting.

    Most people with disabilities are highly individual, not unlike the rest of humanity. And indeed it is from this individuality that life becomes extremely complex. So, when people with disabilities are recognised for their individuality and diverse needs then it becomes apparent what treatment they require. That then is the moment when due respect is needed.

    Recently, over the rents, we have witnessed a significant demise in the provider’s ethos; fairness has been jettisoned. This has been a harrowing experience for me. I am yet to feel that I have been treated according to the stated and published goals of the provider. And then when severe disability is added to the mix of this residence, I conclude that the appeals to standardization and the need to run an efficient enterprise are simply ridiculous.

    As a resident of the facility supported by this service provider, I am certainly NOT a ’customer’. This word and its usage has passed its “use-by date”. In this context ‘customer’ refers to a person who is vulnerable and inadequate. I am assured of my vulnerability; I quite literally feel it in my bones. But am I inadequate? That is what is being questioned in these efficiency policies? Does one have to be a celebrity like Stephen Hawking before one can qualify for non-stereotyping?

    Yes branding costs money, too. But it’s ok if the payoff of new logos is spent beneficially in not-for-profit service management, rather than in making more attractive packages for over the top management. It is surely the responsibility of any company’s management to ensure its good public image. But this is not merely a function of the sales of assets to wipe out a deficit. And appeal to a black ink entry on the bottom line of a company’s account books can always be heralded in way that diverts attention away from the inner organisation dysfunction, if not moral bankruptcy.

    Special thanks to Christina Irugalbandara,  Cunxia Li and Bruce Wearne.

    For some time now I have been discussing my deep concerns about the way my support facility is managed with Bruce Wearne who helps me by smoothing my English for publication. In this latest piece, the more we discussed the topic, the more it became obvious that my angle of vision was sharpened by Peter Sember whose encouragement has meant so much to me. He came along to the meeting I describe in this piece. He was the one who set the cat among the pigeons by asking the kinds of questions I now continue to ask in this article. Sadly, he died a short time after going out of his way for me on that occasion and I feel it a great honour to dedicate this article to his memory.

    Dr Peter Gibilisco, is Honorary Fellow, University of Melbourne. His new book is ‘The Politics of Disability’.

     

  • Why we don’t want private health insurance for primary care

    The worst possible outcome from the current review of Private Health Insurance would be changes that resulted in the best-resourced Primary Care being only available to those who have such insurance.

    (more…)

  • Sebastian Rosenberg. Mental health changes.

    Announcing the federal government’s response to the National Mental Health Commission’s review of mental health services today, Prime Minister Malcolm Turnbull emphasised the concept of patient choice.

    The commission’s review was the latest in a long line of reports showing that for many Australians needing mental health care, their current choice is between getting no care or getting poor care.

    The reforms announced today have the potential to change this appalling situation. But ultimately they should be judged on the outcomes they achieve for patients.

    Poor access to care

    Mental health is the third-biggest chronic disease in Australia behind cancer and heart disease, affecting 4-5 million people each year.

    Access rates to care are low. And once a person has seen their general practitioner or psychologist, if their condition deteriorates, they have few options but to seek care from their local hospital emergency department.

    Following deinstitutionalisation 30 years ago, which overturned the practice of sending people with severe mental illness to asylums, Australia largely failed to invest in a genuine system of community mental health care.

    The bar for entry into the state-run hospital system rose, so you must be sicker and sicker to qualify for care. Rates of access to state and territory mental health services have not changed in some years. Yet spending has increased by more than 50%.

    We are, in fact, over-reliant on hospitalisation and there is waste. An unpublished survey by state governments indicated that more than 40% of all hospital mental health beds were occupied by people who would be better off in other settings if there was anywhere to send them.

    Mental illness also has a colossal impact on productivity and economic participation. The OECD estimates the average overall cost of mental health to developed countries is about 4% of GDP. In Australia, this would equate to more than A$60 billion or about A$4,000 a year per individual taxpayer.

    Tailored responses

    The federal government’s announcements have the potential to address these problems by presenting two key structural changes.

    The first is the decision to use the new Primary Health Networks (PHNs) to keep people with mental health problems out of hospital, by building new, integrated and stepped approaches to primary and community mental health care. Under the Abbott government, PHNs replaced Medicare Locals. PHNs’ role is to both plan and commission (fund) primary and community care.

    This means having the capacity to respond to all the problems a person might have, including not just their mental illness, but drug and alcohol issues, physical problems, homelessness and other problems. It also means having a range of services available to match the intensity of the person’s needs.

    PHNs will be tasked with properly planning to meet the mental health needs of the regions they serve.

    Given the size of the PHNs, some may require multiple plans to ensure they understand and can respond to locals’ needs. One of the PHNs in Western Australia covers an area the size of much of Western Europe, so plans will need to cater for diversity within regions.

    The second key structural change offered under these reforms is to end the dependency on simplistic fee-based services. The government has recognised that just sending people off for a set number of psychology sessions is an inadequate response, particularly for people with more complex conditions.

    The suggestion is that people with less complex problems should access evidence-based mental health therapies and services online.

    For others, a continuation of the Better Access program, which subsidises ten sessions with a psychologist or psychiatrist, may be entirely suitable.

    For people with more complex problems, however, the government has flagged its intention to permit PHNs to cash out some of their Medicare Benefits Schedule payments into new pooled funding arrangements to meet locally identified needs. PHNs would have the capacity, for instance, to build further on successful programs such as headspace or the Mental Health Nurse Incentive Program.

    These reforms suggest that better understanding individual needs can lead the PHN to more intelligently plan individual responses, bringing together clinical care and social supports such as living skills, vocational training and education.

    Overcoming barriers

    The government’s changes to mental health are not without challenges. It’s unclear whether PHNs will be up to the job, and what support they need to make the scheme work.

    The changes don’t appear to be supported with any new funding, yet we know the mental health system is under-funded. Mental illness accounts for 13% of the burden of disease but receives only around 6% of the total health budget. It should be noted that the “cashing out” arrangements are uncapped, opening up the potential for new funding under Medicare.

    Most importantly, we need to ensure these changes marry up to commensurate reforms by the states and territories. The fifth national mental health planning process now underway has proven ineffective in joining up mental health approaches between governments. The Commonwealth has pledged new leadership and it is here that it is needed most.

    Finally, the Commonwealth must establish a new and robust approach to accountability. Regionalism cannot mean we let myriad programs start and go unevaluated. Instead we need strong and consistent approaches to data collection, providing real information about things that matter.

    Rather than reporting on bed numbers, these processes need to reveal the extent to which PHNs are actually working to help people with a mental illness stay out of hospital, recover from their illness, complete their education, resume employment, avoid homelessness and become healthy and productive members of the community. None of this information is currently available.

    Prime Minister Turnbull stated that these changes were about trying to make the most of Australia’s mental wealth and human capital. His goal is laudable. But the work starts now.

    Sebastian Rosenberg is Senior Lecturer, Brain and Mind Centre, University of Sydney. This article first appeared in The Conversation on 26 November, 2015.

  • John Thompson. The costly abolition of Medicare Locals

    Even when it had no clear policies or plans to replace them, the Abbott government seemed determined to undo many of the initiatives of the previous Labor government. This was certainly the case in relation to primary health care.

    In 2008, the then Labor government established the National Health and Hospital Reform Commission(link is external) (NHHRC) to conduct a comprehensive review of Australia’s health system. The review provided the basis for the National Health Reform Agreement (NHRA) signed by the Australian government and the states and territories in August 2011. The reforms set out in the NHRA had three main objectives:

    1. Reforming the fundamentals of our health and hospital system, including funding and governance, to provide a sustainable foundation for providing better services now and in the future.
    2. Changing the way health services are delivered, through better access to high quality integrated care designed around the needs of patients, and a greater focus on prevention, early intervention and the provision of care outside of hospitals.
    3. Providing better care and better access to services for patients, through increased investments to provide better hospitals, improved infrastructure, and more doctors and nurses.

    The establishment of 61 Medicare Locals across Australia was one of the key initiatives taken to address these objectives.These regional structures aimed to strengthen the primary care system (and thereby relieve pressure on hospitals and other acute providers) by integrating Commonwealth and state government health planning and service delivery and access.

    Medicare Locals were non-profit companies selected after a competitive application process and funded largely by the Commonwealth with $1.8 billion for the period 2011–12 to 2015–16. While the Commonwealth funding deed specified program schedules and reporting requirements, Medicare Locals were provided with considerable scope to arrange their structure, operations and relationships to reflect their local health environment.

    To provide this focus on primary care, Medicare Locals were required “to work with the full spectrum of general practice, allied health and community health care providers and improve access to care and drive integration between services.” They established collaboration with health care services and other community organisations in their region to develop strategies to meet the overall primary health care needs of their communities. Considerable effort was made to ensure that general practice had a central role in the work of Medicare Locals – with varying effectiveness.

    Medicare Locals worked at a regional level with state and local government in the planning of primary health care services and in the linking of these services with Local Hospital Networks and aged care programs to deliver improved integration and effective transitions for patients across the entire health care system.

    The Medicare Locals program was a contentious one, not just because it was a Labor government initiative, but many GPs saw it as a threat to their primacy in their local primary care market and saw the regional health planning activities of the Medicare Locals as an unnecessary additional layer of bureaucracy. This negative view was reinforced by the AMA, the doctors’ union, that lobbied the Coalition Opposition on the basis of the perceived threat to the GP small businesses. For this reason, the Coalition went to the 2013 election with a health policy that included brief mention of Medicare Locals as follows: “We will also review the Medicare Locals structure to ensure that funding is being spent as effectively as possible to support frontline services rather than administration.” However, the then Opposition Leader, Tony Abbott, made a promise that no Medicare Locals would be closed should the Coalition form government.

    About a month after coming into office, the new Minister for Health, Peter Dutton, announced a review(link is external) of Medicare Locals to be conducted by Professor John Horvath. The review was aimed at “reducing waste and spending on administration and bureaucracy, so that greater investment can be made in services that directly benefit patients and support health professionals who deliver those services to patients.” Comments from selected “stakeholders” were invited.

    Professor Horvath, previously Chief Medical Officer, was assisted in the review by two consulting firms: Ernst & Young provided advice on the current operations of Medicare Locals and future structure and governance options, and Deloitte Touche Tohmatsu (Deloitte), conducted an assessment of their financial performance and compliance to their Deed.

    The conduct of the review attracted substantial criticism, particularly for its lack of transparency. A Senate committee subsequently reported(link is external) that it had not been able to obtain much definitive information about the process and methodology used to conduct the review.

    More than 270 submissions were received, indicating a high level of interest in the review, but none was made available by the Department of Health or as supporting documents with the review as is the usual case. Horvath advised that he “personally conducted” interviews with key stakeholders but did not identify who they were. A small number of Medicare Locals were asked for input to the review but were restricted in the amount of information they could provide.

    It is understood that the Deloitte audit involved what the Department of Health called “a basic review” of the 2012–13 operations of the Medicare Locals functioning at that time, with a more considered audit of six of the 61 Medicare Locals. As most Medicare Locals had only just begun operating (setting up structures, employing staff, developing IT systems, etc.), it is not surprising that their audited financial and other achievements were not substantial, and the auditors were not interested in the future plans of the Medicare Locals.

    The review was completed in March 2014 and was highly critical of the performance of the Medicare Locals. Itrecommended(link is external) that the recently established Medicare Local system (one third of the Medicare Locals were only established as from July 2012) be replaced with a system comprising a smaller number of regional organisations called Primary Health Organisations.

    The Senate committee referred to above reported: “With limited information available publicly, and no detailed discussion of methodology in the Review report, it is difficult to understand the Review’s recommendations. Similarly, without the transparency that would have been achieved by the publication of the consultancy reports and the 270 submissions, the Review’s assertions that the Medicare Locals are ‘flawed’ cannot be tested.” The Senate Committee also stated that it could not reconcile the positive evidence it heard of the progress and achievements of Medicare Locals with the highly critical and negative findings of Horvath’s review of the work of the Medicare Locals.

    Notwithstandinga clear public statement by Tony Abbott that no Medicare Locals would be closed should the Coalition form government, when his government brought down the 2014-15 Budget in May 2014 it was announced that all Medicare Locals would cease operation on 30 June 2015 and a new network of Primary Health Networks(link is external) (PHNs) would be established.

    There have been substantial costs incurred in the closure of the 61newly established Medicare Locals, both financial and in terms of disruption or termination of valuable health services. In a relatively short time, boards had been established, staff had been recruited, premises and operating resources were acquired, relationships and collaborations established with local health organisations, and services and programs initiated. On the basis of government commitments, the Medicare Locals had entered into contracts, leases and employment obligations.

    The costs of winding up the Medicare Locals have been estimated at between $112 million to $200 million. The Health Department admitted that closing Medicare Locals would cost $112 million but refused a Freedom of Information request for details of this estimate claiming it would not be in the public interest to release these figures because it could jeopardise “its good relationship with Medicare Locals.” However, many Medicare Locals showed no reluctance to publicly announce their wind up costs at the Senate Committee hearing. The Barwon Medicare Local estimated their costs at $2 million; the North Adelaide Medicare Local’s estimated costs were $2.2 million.

    Skilled, and often very scarce, staff were lost as they became aware of the uncertainty of their future employment. These staff losses were felt most keenly in non-metropolitan areas where health workers are often difficult to find.

    Perhaps more crucially, many highly needed health services that had been recently begun were terminated.Although in their early stage of operation, Medicare Locals had established or funded a range of vital services, made important advances in population health, identified and filled key gaps in services, and begun the critical task of integrating primary care with hospital services. This momentum was lost and many communities lost the gains made. Furthermore, key health staff were lost, a particularly important factor in rural and remote areas.

    The Department of Health then announced that the new PHNs would be selected on the basis of a public tender process so that the new organisations could begin operations on 1 July 2015. This tender process was very poorly managed by the Department.

    The notice of tender for the PHN Program was issued on 28 November 2014, almost a month after the previously advised scheduled release date. The tender period was very short and conducted over the Christmas–New Year period with tenders to be submitted by 28 January 2015.This was an absurdly short time for major organisational relationships to be established and business structures and financial decisions to be made, particularly as the minister encouraged new private sector interests to participate.

    Although broad guidelines were provided to potential tenderers at the start of the process, major decisions and criteria such as the geographic boundaries of the proposed PHNs were drip fed to interested tenderers as the tenders were being prepared.

    State government officials advised that there was very little consultation with the key state health agencies to recognise and capitalise on existing health planning and coordination bodies.

    Information meetings for prospective tenderers were conducted in each state by Department of Health officials but the information provided was no more than that which already available on the Department’s website. The Department even refused to provide notes of the meetings or lists of attendees (which would have been of assistance to facilitate collaboration in the preparation of tenders).

    Horvarth’s review criticised Medicare Locals for focussing too much on service delivery, not entirely coincidentally a concern of GPs and other providers. His report recommended that PHNs “should only provide services where there is demonstrable market failure, significant economies of scale or absence of services”. However, he did not define “market failure” and the Department clearly had difficulty in providing potential tenderers any reasonable clarity on this matter. This certainly made the preparation of submissions very difficult, especially for tenderers in rural and regional areas where Medicare Locals had provided services to meet significant gaps in services.

    In summary, the tender process was very deficient. The Senate Committee noted the confusion surrounding the tender process and considered “flaws in the government’s PHN tender process raises doubts regarding any outcome of the tender process.”

    It is not surprising that about this time a poll of more than 1100 doctors across Australia conducted by the AMA declared the Minister for Health, Peter Dutton MP, the worst Minister for Health for 35 years.

    In April 2015 the Commonwealth government announced that 31 PHNs would be funded as from 1 July 2015. They would be required to establish Clinical Councils involving GPs, and Consumer Advisory Committees. Announcing the successful bidders, the Minister of Health, Sussan Ley, said the new PHNs would replace “Labor’s flawed Medicare Local system,” yet almost all PHNs selected (24 of the 28 PHNs) are either consortia of former Medicare Locals or have a Medicare Local as the lead applicant.

    The new PHNs will be responsible for populations and geographic areas that are much larger than those of the Medicare Locals. (For example, one PHN will now be responsible for all of Western Australia except the Perth metropolitan area.) Medicare Locals had an average population of 355,000; PHNs will service an average population of 738,000. Six PHNs will service populations of more than one million. Many health experts doubt the effectiveness and efficiency of such very large organisations, citing the failure of the NSW government’s establishment of mega health services.

    The substantial costs of establishing these new organisations are not known and it will be interesting to discover their operating costs when their first financial reports are made.

    The concerns of the Senate Committee that the inadequate Horvarth review and the Department’s inept tender process could lead to a poor result appear to be justified. Now, several months after the PHNs were formally established, there has been little progress in developing any useful operations. Many in the health system are of the view that the whole exercise is a very expensive ideological move that, despite very substantial financial resources and lengthy disruption and dislocation, may not achieve the results that the fledgling Medicare Locals were beginning to realise.

    John Thompson is an economist with experience in primary health. This article was first published in Australian Policy Online on 23 November 2015.

  • An Open Letter to the Minister for Health concerning Private Health Insurance.

    19 November 2015 

    Hon Sussan Ley M.P.,
    Minister for Health,
    Parliament House,
    ACT 2600

    Dear Minister

    (I have signed this letter on my behalf and also on behalf of the people listed below. I will be posting this ‘open letter’ on my blog early next week.)

    We are pleased to see that you are canvassing community and expert views on private health insurance.

    In discussing the community survey, recently on the ABC Breakfast Program, you said “We support the public system for those who can’t afford private health”.

    That is a long way from the idea of universal mutual support that has underpinned Medicare and public hospital arrangements. It assumes, incorrectly, that private health insurance, and the associated subsidised access to private hospitals, is something Australians see as desirable if only they could afford it.

    As you know, about half of Australians do not hold private health insurance. Many are driven to hold it by the Medicare Levy Surcharge – a coercive instrument that has little to do with choice. You would also be aware that 200 000 taxpayers pay the surcharge, rather than holding private insurance, even though almost all of them would be financially better off taking the cheapest hospital cover.

    For many, the main attraction of public hospitals is not that they are “free”, but rather that they offer a high standard of care. Most importantly the funding system for public hospitals, unlike the funding for private hospitals, does not carry an incentive for over-servicing. There is growing community awareness of the risks of over-diagnosis and of over-servicing.

    Some others, particularly older wealthy people whose income is below the MLS threshold, do the sums and work out that their best bet is to draw on their savings to finance any needed private hospitalisation, secure in the knowledge that if they need acute care they are served by public hospitals. In doing this they miss out on the subsidies, the benefits of which are go to pay for high administrative costs and the cross-subsidies associated with adverse selection. Thanks in part to superannuation, households with people in the 65-74 age range, have on average $500 000 in financial assets.

    It is ironic that, in spite of your Party’s commitment to self-reliance, those who pay for their own private hospitalisation, or who pay their own dental bills, receive no support, while those who hand over responsibility to insurance corporations receive a 30 per cent subsidy or a generous tax incentive in the form of exemption from the MLS.

    Then there are those community-minded people who value the idea of sharing their health care expenses with other Australians. They are morally repulsed by the idea of being corralled into the “gated community” of private health insurance. Also some people, aware of the way “charity” systems inevitably degenerate, see it as important that people with means who hold political influence have a stake in using and maintaining a high standard public hospital system.

    You, and your fellow health ministers in the states and territories, fund and operate an excellent public hospital system. We hope you take pride in a public service that serves all Australians so well, and do not let it degenerate into a charity system.  A way to prevent such degeneration would be to remove private hospitals’ de facto dependence on private insurance, and to bring them into the same funding arrangements as public hospitals, thus allowing them to provide the same high-standard of integrated care as public hospitals, allowing for remuneration models other than individual fee-for-service, and abolishing any suggestion that Australia has two health care systems – one for the affluent and one for those who are less fortunate.

    Yours sincerely,

    John Menadue

    Kerry Goulston, Emeritus Professor, Medicine, USyd
    Ian McAuley, Adjunct Lecturer, Canberra University
    Jennifer Doggett, Health Consultant,
    Stephen Leeder, Emeritus Professor of Public Health and Community Medicine, USyd.
    Karen Willis, Associate Dean, Learning & Teaching, Faculty of Health Sciences, ACU
    Arthur Chesterfield-Evans, Medical Practitioner and anti-tobacco activist
    Sebastian Rosenberg, Senior Lecturer, Brain and Mind Centre, USYD
    Jill White, Professor of Nursing and Midwifery, USYD
    John Dwyer, Emeritus Professor of Medicine, UNSW
    Fiona Armstrong, Executive Director, Climate and Health Alliance
    Tony McBride, President, Australian Health Care Reform Alliance
    Tim Woodruff, Vice President, Doctors’ Reform Society

  • Lesley Russell   Too high: the impact of specialists’ fees on patients’ health

    In today’s health care debates around the centrality of primary care, moving towards patient-centred medical homes, improving care coordination for people with chronic illnesses and whether private health insurance provides value for money, there is one element that is almost always missing – the role and the costs of specialist services.

    In 2014 over 28 million specialist services were billed to Medicare and 21 million of these were for out-of-hospital services. Only 30% of these services were bulk billed, and the average out-of-pocket cost for the remaining 70% of services was $70.89. However gaps of several hundred dollars are not uncommon.

    Specialist fees are the main driver of Medicare out-of-pocket costs and the main reason why people access the various Medicare safety nets (Extended Medicare Safety Net, the Original Medicare Safety Net and the Greatest Permissible Gap measure).

    The Government has moved to make changes to the Medicare safety nets in the name of ‘simplification’ and the Health Insurance Amendment (Safety Net) Bill 2015 is currently before the Senate where it has been sent to the Community Affairs Committee for review.

    Reforms to the Medicare safety nets are long overdue. There is considerable evidence that the current arrangements are inequitable, do not benefit those with the greatest need, and continue to be inflationary, despite legislative tweeks. This has led to increasing economic pressures on patients from their out-of-pocket costs with consequences for their health outcomes and quality of life. There are also pressures on hospital budgets from preventable admissions that can result when patients skip specialist appointments and fail to comply with treatment regimes because of cost.

    As federal parliament considers the new safety net legislation, it is crucial to ensure that this does not have the unintended consequences that were inherent in the Extended Medicare Safety Net (EMSN). One such consequence was that the EMSN actually increased the ability of specialists to charge higher fees, particularly in areas such as obstetrics and assisted-reproductive technology services. In 2009 it was estimated that for every dollar the government spent on the safety net, only 57 cents went towards reducing patients’ costs and the remainder went towards increased doctor fees.

    Preventing such problems will require an informed study of the impact of specialist fees and how specialists are likely to respond to efforts to limit reimbursements to patients of fees that are in excess of the Medicare Benefits Schedule (MBS). As it stands there is very little publicly available information in this area. Considerable work was done on a relative value study in the 1990s (regrettably with no outcomes) and the specialist medical colleges presumably have data from their members, but the Department of Health has shown no inclination to analyse their data or to make it available to academic centres for such work.

    Medicare data for the June quarter 2015 show the following:

    • The average bilk billing rate for specialists (for services in and out of hospital) is 30.2% although this varies dramatically by speciality.
    • The average fee observance for out of hospital services is slightly higher at 43.4%.
    • The average patient contribution for services that are provided out of hospital and are not bulk billed is $70.89. This varies considerably by state and territory – it is lowest in South Australia ($53.94) and highest in the Northern Territory ($89.38).

    Over the past decade there have been some interesting changes in these figures that tell a story of policy and community pressures and influences.

    Although the average bulk billing rate for specialist services delivered out of hospital has barely changed, the average out-of-pocket cost has more than doubled (from $32.66 to $70.89). For individual specialties there have been some dramatic changes. For example, the bulk billing rate for obstetrics, currently 51.5%, was only 21.8% in the June quarter of 2005. We can assume that the increase in bulk billing is due to the increases in Medicare reimbursements that were made as part of an effort to tackling the inappropriate use of the ESMN. But the bad news is that those obstetricians who don’t bulk bill have continued to increase their fees and the patient’s average contribution has risen from $51.75 in 2005 to $247.79 today. Moreover, my previous work on Medicare obstetric costs highlights that when loophole is closed, obstetricians look to shift their costs around between capped and uncapped and outpatient and inpatient billing items.

    Specialists who work in radiotherapy and nuclear medicine have also changed their billing behaviours over the past decade. While bulk billing rates have increased impressively from 13.3% in 2005 to 68.5 % in June 2015, presumably in response to government agreements and legislation, average out-of-pocket costs for patients who are not bulk billed have more than doubled, from $16.33 to $38.74.

    It’s important to think what the growing costs to see a specialist mean for patients such as older Australian with multiple chronic illnesses. A recent study shows 27% of older Australian reported having at least three chronic diseases, with high blood pressure, arthritis and cancer as the most prevalent diseases. Such patients may have a very competent bulk-billing GP coordinating their care, but in addition to the cost of specialist consultations there will be costs for diagnostic tests and monitoring, prescription medicines, over-the-counter medicines, and supplies for conditions such as diabetes, colostomies and incontinence.

    National Seniors Australia found that older Australians with five or more chronic conditions spend $3528 per year on out-of-pocket health care costs. Small wonder then that approximately 10% of adults referred to a specialist delay or do not keep their appointment because of cost. This proportion rises to over 12% in the most socioeconomically disadvantaged fifth of the population. The current freeze on Medicare rebates to doctors will only aggravate the growth in gap fees. The gap between what Medicare pays and the AMA-recommended fee for MBS item 104 (initial referral to a specialist) is now $97.72; the new safety net will ignore $40 of this.

    There are no Medicare incentives to encourage specialists to bulk bill. Because poorer Australians can’t afford to pay the gap fees to reach the safety net thresholds, less than 4% of EMSN benefits go to the most socioeconomically disadvantaged 20% of the population while over 50% of benefits go to the most advantaged 20% of Australians. This exemplifies the inverse care law – and poor public policy – as it is the poor who are most likely to suffer ill health, who have the lowest discretionary income, and who are most in need of protection from out-of-pocket costs.

    The government’s “simplification” of safety net arrangements, eliminates the confusion of multiple Medicare safety nets and caps on reimbursement for selected items and ostensibly will make it easier for people to qualify for support if they have high out-of-pocket expenses. But this comes at a cost for patients – the new safety net actually provides patients with less financial protection against high out-of-pocket costs – and a saving for government.

    It is estimated that new threshold levels will mean an additional 60,000 people will qualify each year for the Medicare safety net. The big question is whether the reforms will lead to a change in the type of people who qualify for safety net benefits and that is not easily answered. In testimony to the Senate Community Affairs Committee, Dr Kees Van Gool indicated that the answer depends on how many concession card families experience annual costs between $400 and $638 how many general families have out-of-pocket costs between $1,000 and $2,000 because these are the people who stand to benefit under the new arrangements. However he noted that concession card status is a poor proxy for household income. Capping the amount of out-of-pocket costs that contribute to the safety net threshold will have further implications for how many and what type of families qualify for the new benefits.

    This reform may invoke a number of behavioural changes by both doctors and patients seeking to derive maximum benefits from the safety net. There are clearly greater incentives for patients to seek out doctors who charge less than 150% of the MBS fee and this, in turn, may invoke price competition amongst doctors. Doctors may act to redistribute their fees across an episode of are, as obstetricians have done, or increase the volume of services they offer. The Minister for Health has indicated that she wants to prevent the inappropriate provision of complicated medical services outside of hospitals, although it is not clear how the safety net legislation will address this.

    In an era of budget restraint, what can be done to address the impact of rising specialists’ fees on the federal and individuals’ budgets in ways that do not undermine the business needs of the medical profession? In a paper written earlier this year, Jennifer Doggett and I proposed greater transparency around specialists’ outpatient fees and the out-of-pocket costs to the patient. This approach was also put forward by Dr van Gool in his testimony to the Senate Community Affairs Committee.

    Anecdotal evidence indicates a wide range of fees charged, with some specialists charging dramatically more than the Australian Medical Association recommended fee (which is itself higher than the MBS reimbursement). However there is no evidence that specialists charging the highest fees deliver the best outcomes and patients and referring GPs might make different choices about specialist care if they knew the costs involved. At the very least the major outliers should be named and shamed. It is also important that consumers are provided with comprehensive information about their health care choices and are made aware of options, such as public outpatient clinics, where they can receive specialist services at no (or lower) cost.

    There has been some support for this approach from the medical profession, perhaps driven to action by the fact that a few greedy colleagues are making life difficult for those doctors who bulk bill or have only a small gap fee. In July 2014, the Royal Australasian College of Surgeons spoke out against excessive fees, saying that the College “is highly concerned at the amount of reported out-of-pocket costs being incurred by patients in the health-care sector“ and further stating that the College “believes that extortionate fees, where they are manifestly excessive and bear little if any relationship to utilisation of skills, time or resources, are exploitative and unethical. As such, they are in breach of the College’s Code of Conduct and will be dealt with by the College”.

    An information sheet on the College website strongly supports full disclosure and transparency of fees as early as possible in the patient-doctor relationship, advocates that patients understand all available treatment options, and encourages concerned patients to seek second opinions on recommended treatments and the fees to be charged.

    Just recently, the Urological Society of Australia and New Zealand has been prompted by a study showing that out-of-pocket costs for prostate cancer can be in excess of $30,000 (this includes not just specialists fees but private hospital services, medicines and other costs) to talk to its members about the perils of extortionist fees and of not telling men about public health options for treatment.

    Most importantly, the issue of out-of-pocket costs for patients and the impact these have on health outcomes and costs elsewhere in the health care system and the federal budget needs to be addressed across a range of issues currently under consideration – not just Medicare safety nets, but the Medicare Benefits Schedule review, the mental health and primary care reforms, and welfare supports. Many people will predictably always have trouble meeting their health care costs, and the solutions will not always lie within the purview of the Health portfolio.

    There are branches within the Department of Health that deal with the medical profession, the pharmaceutical industry, and private health insurers; it’s time for a branch with specific responsibilities for consumers’ and patients’ needs. It’s an important part of the effective, efficient and equitable delivery of health care services.

    Dr Lesley Russell is an Adjunct Associate Professor at the Menzies Centre for Health Policy, University of Sydney.

     

     

  • John Dwyer. Wasting precious health dollars.

     

    In the last eighteen months our coalition government has repeatedly warned that the rate at which we are increasing health related expenditure is unsustainable. The attempt to extract a co-payment from Australians visiting their GP was justified using this concern. However it is the better use of the currently available health dollars that should be given priority rather than asking Australians pay more for a health system that no longer adequately meets contemporary need. It is true that a considerable amount of the cost ineffective expenditure on health is generated by members of my profession with low value and sometimes no value tests and procedures wasting at least 10 billion dollar a year. While there are vested interests hampering necessary reforms, progress is being made as critical pathways, generated from the best available evidence by independent and expert clinicians, are developed centrally for application locally. The Institute for Clinical Excellence in NSW is one organisation facilitating this type of reform which should improve the standardization of evidence based clinical decision making.

    Looking more broadly at the inefficient use of precious health dollars we could discuss the 600,000 or so avoidable and expensive admissions to public hospitals each year and the billions of dollars wasted as 24 million people are served by nine Departments of Health. However there are two other examples of cost ineffective expenditure that are in the news and worthy of further comment; the Private Health Insurance rebate and the subsidy tax-payers pay to the private heath industry as they pay for a raft of useless pseudo-scientific modalities. Both of these have been addressed recently and unsatisfactorily by health minister Sussan Lay.

    Interviewed on the 7.30 report Minister Lay defended the need for government to use six billion dollars of our money to reduce the cost of Private Health Insurance claiming it was needed to relieve the pressure on the demand for public hospital services. She has no doubt been told and believes that this is so. It is not.

    The Howard government introduced the taxpayer-funded rebate at a time when private health insurance rates were falling. In the ensuing twelve months private health insurance rates increased by only 2% and there was an almost negligible decrease in admission to public hospitals. After that year there was no noticeable effect even though additional strategies did significantly increase the uptake of private insurance. Making insurance more expensive as one aged and demanding a significant levy be paid by wealthier Australians who did not have private insurance, did have the desired effect on participation rates but not on helping public hospitals.

    Private and public hospitals operate in different health care universes. Both by and large offer excellent services but one has a fixed budget and an average annual increase of 3% in the demand for admission that is fiscally intolerable. The other makes more money when more patients are admitted. More than 70 % of the patients in public hospitals have serious and often chronic medical conditions while more than 70% of patients seeking private hospital care need day only procedures or surgery. As cash strapped public hospitals were forced to close beds without being able to escape the demands from sick medical patients, elective surgery became increasingly difficult to deliver in a reliable and timely matter and much surgery (and the surgeons needed for that surgery) moved to the private sector.

    Had the six billion dollars worth of subsidies been available to public hospitals many could have continued to offer more of the surgery required by patients who reluctantly paid for private insurance to get their operations in a timely manner. With the public sector increasingly unable to compete, volume wise, with the private sector surgical fees have skyrocketed contributing significantly to the 29 billion dollars of out-of-pocket expenses Australians fork out each year for their health care.

    A number of health insurers, responding, they say, to consumer demand, will pay for treatment from a range of “Alternative” practitioners. The Labor government concerned, at the growth in such payments, asked the Chief Health Officer and the NH&MRC to examine some 18 modalities to see if there was “credible scientific evidence for their clinical effectiveness”. The committee assembled looked at practices such as Iridology, Reflexology, Homeopathy, Reiki etc. and reported to the current government that there was no evidence that any of them offered clinical benefit. The government was urged to stop public subsidies for these pseudo-sciences and, in so doing send a message to the public emphasising the need to enquire about the evidence base for any care they receive. The report is “lying on the Minister’s table”. For decades I have been depressed by the influence the “Alternative” industry has on governments so I was not that surprised at the response when, at her Press Club presentation, reporter Sue Dunleavy asked her the following question.

    “Every year health insurers are paying $180 million for natural therapies for which there is no evidence,” she said.

    “You already have the review of the worth of those therapies conducted by the chief medical officer on your desk.

    Can you tell us what that report said and what you are doing about it?”

    The nonsensical and depressing response was “…the issue of complementary therapies is an issue of great interest to Australian patients and certainly to private health insurers and those concerns about the budgetary implications of which you speak.

    But I don’t propose to take any piece in isolation out of the complex mix of interests, stakeholders (for want of a better word) and, of course patients and taxpayers, when we look at the important issue of private health insurance.

    To pick up one report commissioned by a previous government (not that necessarily has to be an issue in itself) and make it something that this government has to respond to almost at the micro level, without regard to the intersecting policies issues and interests, I don’t believe is sensible public policy.”

    Many contributors to “Pearls and Irritations” have noted that for a cost effective sustainable health system providing better health care, we, as is the case in much of the developed world, must invest in Primary care that emphasises prevention, in house team management of chronic diseases and the ability to care for many in the community currently sent to hospital. Quality hospital care is totally dependent on our reducing the need for so much hospital care. The currently wasted dollars, if applied to fund needed reforms could provide us with the excellence we need without increasing the % of GDP we spend on health. Such reforms should be a major issue for the coming election.

     

     

  • Thanks to Jake Bailey and Christchurch Boys High School.

    Just one week before his final school assembly, Christchurch Boys High School’s Head Boy, Jake Bailey, was told that he may not have long to live.

    The 18 year old NZ student was bed-ridden and absent from school for three weeks while undergoing treatment for aggressive cancer.

    But during his final school prize-giving ceremony he managed to give an inspirational speech from his wheelchair.

    “None of us get out of life alive, so be gallant, be great, be gracious and be grateful for the opportunities you have” Jake told his audience.

    The school listened in silence as he told of his diagnosis with Burkitts non-Hodgkinson lymphoma, one of the fastest growing tumours.

    See link from The New Daily to story and video of speech below:

     

    http://thenewdaily.com.au/news/2015/11/09/dying-school-captain-speech/?utm_source=SilverpopMailing&utm_medium=email&utm_campaign=20151110%20The%20New%20Daily%20final%20(3)&utm_content=&spMailingID=23943738&spUserID=MTAyODk0Mjg4NDUzS0&spJobID=680889348&spReportId=NjgwODM2MjY0S0

  • Ian Marsh. Will privatised schools and hospital drive public sector efficiency?

    One of the first substantive announcements of Treasurer Scott Morrison concerned the privatisation of schools, hospitals and community services that are provided by State governments. He enthusiastically endorsed this 2012 Commission of Audit recommendation: ‘Given the size of the human services sector (which is set to increase further as Australia’s population ages), even small improvements will have profound impacts on people’s standard of living and quality of life.’ Morrison pointed to the greater efficiency and effectiveness that a competitive regime can deliver. There is no doubt that market mediated competition can drive performance. The private sector provides daily evidence of this.

    But the notion that these approaches can be readily transferred to public services like schools and hospitals and social services cries out for deconstruction. For a start schools, hospitals and social agencies serve many purposes that cannot be easily captured in a unified price measure. How are these more subtle and variegated outcomes, which can vary hugely between individuals and between places, to be incorporated in a contract design? No easy challenge in itself. For reasons the Harper review acknowledges, it is fanciful to imagine that consumer choice can be generally instituted. In it absence, who are the omniscient, all-knowing central agents who will define the precise outcomes that contracted services should deliver? Even assuming this is possible, in practice accountability systems that recognise these wider concerns increase the likelihood of micro-management. And then the alleged benefits of privatised or contract-based settings rapidly evaporate. Innovation or continuous improvement is stillborn. Transaction costs escalate.

    Is there an alternative to these dysfunctions? One approach might be to build on private sector practices that directly lead on to service or process innovation. Think of the Toyota just-in-time production system. Toyota deliberately jettisoned end-of-line capacities to repair or correct faults. It deliberately limited back up component reserves in case of supply chain hiccups. Production was stopped by every fault or flaw. But each of these stoppages became a key source of data in Toyota’s never ending quest for improved efficiency. This covered both the immediate production process as well as the wider system in which it nested. Unlike the aggregated information or ‘strong’ signal that is embodied in price data, this approach focused on the ‘weak’ signals that were critical to continuous improvement.

    Prices embody the outcomes of a multitude of these weak signals. Note Toyota’s rise to become the major global car company. This was an immediate consequence of the visible hand of management practice – only distantly that of the invisible hand of market forces.

    Or note the consistent stellar performance of the Finnish education system. Not one single school is privatised. Instead there is a deliberate focus on identifying obstacles to student performance at an individual level and from an early age. The system deploys more special education teachers than any comparable country. These work with mainline teachers and parents to identify under-performing or troubled children. They focus on these early ‘weak’ signals and initiate immediate remedial action. Approximately one third of the pupils in Finnish schools receive extra support in special education classes.

    So markets and contracting by all means. But if they are to work the invisible hand of the market need to be supplemented by the visible hand of ‘weak’ signals. These are the building blocks of continuous improvement. Of course the challenge to identify pertinent weak signals varies widely. The relevant indicators are not the same in routine or highly specialised surgery or in Accident and Emergency or routine hospital care.

    Translated to a contracting system, how can this be achieved? In principle the answer is simple. Contractors need to report not just on the outcomes that they believe they can achieve but also the means that they propose to use to achieve them. Then they need to be held to account for both outcomes and means. A central authority then needs to manage accountability and learning about these means. Its role is to learn and then to share this information amongst providers.

    The core ethos of such a system is learning about means as well as outcomes. Its unit of exchange is the means used by different providers who are working towards broadly similar ends. But these exchanges will typically not involve anything that could be described as ‘best practice’. Most service settings are too contextualised to allow codified or standardised service designs to be developed. Service decisions need to take into account the circumstances and needs of an individual person or a specific place. In a technical sense decisions are ‘transaction intensive’ – prioritising the needs of individuals or places and mostly blending the technical skills and the empathic judgements of practitioners. Thus a teacher must respond to the circumstances of her students, a doctor to the needs of her patients. In both instances, the hardest cases can provide the richest source of systemic learning.

    Indeed where services can be codified and standardised price mediated exchange will be a sufficient driver of performance. Where the latter is not possible, price mediated exchange will not by itself drive performance. Unless contracts or other systemic arrangements also disseminate learning about means, rhetorical promises of efficiency and continuous improvement will be misleading, indeed chimerical.

    In a justly celebrated book, The Visible Hand, the distinguished Harvard economic historian, Alfred Chandler, showed the extent to which business efficiency in the United States was the product of superior management not in the first instance price mediated exchange. In seeking efficiency and continuous improvement in the much more complex world of hospitals, schools and community services this visible hand is even more critical.

    Over the past thirty years, the discipline of economics has been a fertile source of models and frameworks for the redesign of government and of public services. But as more complex, transaction intensive services (‘wicked’ problems) have come increasingly to be the focus of attention, the limitations of price mediated exchanges need to be acknowledged. This is not the royal road to innovation and continuous improvement. Pace the Harper Review, the design of a functional innovation system is a more complex and more demanding challenge.

    Ian Marsh is a visiting professor at the University of Technology Sydney’s management school.

  • Peter Gibilisco. Friendship and Service Provision Ethos for People with Disabilities

    In this article I want to discuss an aspect of the standardised procedures set by service providers in facilities that serve people with disabilities. More to the point, I am keen to explore how this affects the ethos of service delivery for people with severe or profound physical disabilities within such shared supportive accommodation.

    Let me be utterly frank. The ethos of service delivery, in this house where I live, has lacked key attributes that are necessary for caring for people with disabilities. Admittedly, I have sought to draw attention to this deficit by a constant effort to raise awareness. And an organisation’s ethos takes time to change. Nevertheless, the jury is still out with respect to whether we are experiencing a positive change. I am concerned that the friendships that I have made with support staff be respected by a form of management that recognises the benefits that arise from the personal synergies that arise from the work done.

    There is a simple need of enjoying life as an individual, in a way that is like the individual aspects of dignity that are part and parcel of the much proclaimed “freedom of choice.” I want to ask: has the “right to choose” become a ploy of many service providers? The principle is conveniently displayed in marketing and other public relations material. But is it all a matter of staying on the politically right side of the Government and public opinion?  After all, it can be argued by many living in such supportive accommodation that the self-interest of top management has been placed well beyond the reach of the people with disabilities that these facilities are established to serve. But Personal Care Attendants (PCA) are not just an abstract function;  they are people just like the people they are employed to serve.

    This state of affairs is why I am taking the opportunity of writing this article. Our friendships with PCAs need to be defended. I am a little fired up although I guess some who know me will think that is rather strange. It is true: I cannot wave my arms around and bang my fist on the table. But I am just a little concerned that the message I have been putting for many years gets through. This is serious.

    I am a severely physically disabled person with Friedreich’s Ataxia, who presently lives in shared supported accommodation. This place can fail to administer appropriate assessment of my specialist medical and social needs, one of which is human companionship. This place needs to function in ways that allow the clients with disabilities to solve individual problems pertaining to their own problems even if the house is managed under the protocols of a service provider. And the workers should be respected as our friends.

    I am quite sure that those managing this place were not expecting me, and I too never expected to be here. But even though we have to make the most of this unfortunate state of affairs, it is not going to prevent me from saying what needs to be said.

    The service provider has a real problem. Rather than looking to a set of policies that emphasise procedures that are formed individually with the needs of the person front and centre, they seem to be stuck with operating in a standardised way that at the same time keeps the self-interest of top management of service providers out of sight, and makes continuity with workers difficult.

    The standardised procedures simply do not provide adequate support. Even if the standardised approach qualifies as “best practice” under some managerial criteria we, and our day-to-day relationships that sustain us, are simply too complex for an abstract modus operandi.

    As a matter of fact, I am not a person with a cognitive, behavioural or developmental disability. I do not take kindly to being treated like one, as I am also sure many people with intellectual disabilities do not take kindly to being treated like a semi-paralyzed person who has to live in a wheelchair. Mistreatment that ignores a person’s humanity, violates the person’s right to be given due respect.

    My complaint also has to do with the ethos of the place I live in. Let me tell you what I experience all too often. My friendships with my support workers are unfairly reduced in a variety of ways by the presumptions of management that fail to respect what is going on. Support workers are the first faces we see in the morning and last faces we see at night. It is as if our friendships are simply not part of the implementation of policy. I suspect that this kind of managerial presumption of the disposability of friendship is alive and well elsewhere in social welfare delivery. But I am keen to preserve the friendships that keep me going, even as I find my body slowing down.

    I am also not wanting to identify any individual manager – there are some I have come across who come to mind that possibly should be exposed for their blindness and self-interest, but I will restrain myself.

    My aim here is to suggest some sustained soul searching among those managing service provision for people with disabilities.

    I’m writing this against the background of a service delivery context that is simply not good enough.

    Dr Peter Gibilisco was assisted by Dr Bruce Wearne in the preparation of this article.

    Special thanks to Cunxia Li, Patrick Wleh and Christina Irugalbandara.

  • Michael Keating. The role of government in policy renewal.

    In thanking Ross Gittins for launching ‘Freedom, Opportunity and Security’, Mike Keating explains the reasons why he and I decided to launch this series, first online and now in a book. Mike Keating’s book launch notes follow. I will also be posting Ross Gittins’ comments. John Menadue.

    Thank you Ross Gittins and thanks to you all for coming

    Why we embarked on this project

    • Concern about the poor quality of public debate on many public issues
    • The failure of political leadership to change that situation, or even be willing to try

    Instead we think there is a role for public conversation in developing and prosecuting a genuine reform agenda

    • History of past reforms is a long gestation period, with expert opinion often playing a key role in establishing the policy agenda
      • Eg tariff reform and de-regulation of financial markets
    • Too often calls for reform these days are little more than slogans – tax reform; industrial relations reform – but no content.

    Have been fortunate in attracting people who are experts in their field and who are able to support their arguments with evidence. This evidence and logic is I hope one of the strengths of this book.

    Timing of the book is also fortuitous, coinciding with advent of a new and different government

    • More open, less negative and more optimistic
    • Most importantly good ideas are not being ruled out without any consideration

    Labor needs to respond accordingly. 

    The book itself

    Not my job to summarise the book.

    • Ross has done that, and we would rather you buy it now if you want to know more – as I am sure you do

    Just a couple of observations

    • Despite apparently deep divides between our political parties, judging by the articles in this book there is considerable consensus about the policy prescriptions for moving forward
    • This consensus may just reflect the company that John and I keep
      • Don’t think so
    • Foreign policy is a good example, of how there is more consensus than I expected
      • Used to think there were more opinions in DFAT than there were senior staff members
      • But the five different authors here – all former senior member of DFAT – agree that
        • we need to focus more on the opportunities and less on the threats – should appeal to Turnbull –
        • we need to achieve a more independent balance in our foreign policy
    • Most importantly, all the authors see an important role for government in our future
      • Consistent with past Australian traditions, general presumption among all the authors that we should maintain government responsibilities, even if we think their effective achievement requires changes in the means used
      • Want better government, not less government
      • Contrast with the US

    Given that conclusion, one issue in particular seems to me to be most important and that is taxation and the Budget

    • Perhaps I am biased, but naturally I don’t think so. Taxation and the Budget encompass so many of the other issues.
    • Critical issue is that we will need to raise more tax to preserve let alone enhance our sort of society
      • Market economy is likely to deliver greater inequality unless government acts to counter-act a wider distribution of earnings
      • State Premiers all want more tax beyond the cuts that the Australian Government has imposed.
      • Considerable expert opinion, including in this book, that Budget repair will require action on the revenue side as well as on the expenditure side, but hard to raise additional revenue if expenditure is not efficient, effective and equitable.
      • Do we think we can raise the additional revenue needed without increasing the GST?
        • Removal of tax concessions may not raise as much as some seem to expect
        • ALP proposal to reduce super concession will not raise much
      • My article in this book suggests that such actions will not be sufficient, and raises the option of increasing the GST to obtain the extra revenue needed. Progressive and even realistic thinkers need to support this option if it is the best way to obtain a consensus in favour of higher taxation
        • Can protect the poor
        • Income tax scales need adjustment to offset fiscal drag
  • John Menadue. The unfairness and waste in health. Private Health Insurance is the real culprit.

    Medibank Pte has been in dispute with the Calvary Hospital Group and now with UnitingCare over performance in their hospitals.

    At last our largest private health insurance company, MBP has come to understand that the private providers, hospitals and doctors, are really in control. These private providers determine the quality of care and its cost. The PHI companies like MBP are really powerless to control both the quality and cost of healthcare. They need to lift their game .But they are in a bind.

    The problem that the MBP faces is precisely the same problem as the US healthcare system faces. In the US hundreds of competing private health insurers do not have the power to control quality and price setting by providers. If a private insurance company is too tough the provider will take the business to a competitor. The worldwide lesson is that only a single insurer can have a real effect on costs and promote quality.

    The CEO of MBP has got into trouble by confronting the powerful providers, in this case Calvary and UnitingCare. He has resigned!  In his exit comments, the CEO of MBP, George Savvides said he was seeking to ‘reposition MBP from being a payer of bills, to a player in the health system’. He could not be more precise and correct. The private health insurance companies meekly accept the prices set by providers, both hospitals and doctors. I read Savvides’ comments to mean that the providers rebuffed him in his attempts to improve the quality and contain the cost of care. And his board did not support him. The providers have won again.

    Apparently Savvides was insisting on two things. The first was that MBP would refuse to pay when any of a list of 165 ‘highly preventable adverse events’ occurred, including preventable falls in hospital and presumably hospital-caused infections. Secondly he proposed that MBP would refuse to pay hospitals for unplanned patient readmissions that occur within 28 days of a procedure, compared with seven days previously.

    Good luck to PHI companies like MBP who refuse to be passive payers of bills and want to have a say in the cost and quality of care by private providers particularly in private hospitals.

    ‘Adverse events’ are a major cost in all health systems – mistakes, injury, infections and even death. Many are avoidable and many are not. Avoidable adverse events probably cost well over $ 5b p.a. in the Australian health sector. Good clinicians are caught up in a bad system. See link to my previous post ‘The personal, public and social costs of mistakes in health’.

    Other PHI companies like BUPA must similarly be concerned about the difficulty in controlling provider costs. That is the reason why PHI premiums rise significantly each year. Since John Howard introduced the rebate on PHI in 1999 the cost of PHI premiums has increased 150%.Overall prices have increased by less than 50%.Not surprisingly a reader panel in the Sydney Morning Herald has found that 64% of people don’t believe that PHI provides value for money. The Minister for Health describes many PHI policies as ‘junk’

    But PHI companies like MBP and Bupa contribute to high costs. Through GAP insurance that they provide they have underwritten an enormous increase in specialist fees in private hospitals. These specialists receive remuneration three to four times what is paid in public hospitals. And not to be out done on specialist fees the major private hospital; Ramsay Healthcare for example paid its CEO $31 m in 2014. No wonder MBP wants to get hospital costs down!

    In addition to the inability of PHI companies to put pressure on health costs, there is the problem of waste in the delivery of health care – excessive pathology and radiology tests, over-treatment and over-prescribing. In the recent Four Corners program we were told about a tsunami of over-diagnosis and treatment. We heard about

    • Care that is ineffective and sometimes unsafe;
    • That perhaps a half of MRIs, are unnecessary;
    • At least half arthroscopies are unnecessary;
    • At least 20% of knee replacements may be inappropriate;
    • The majority of MRI’s and CT’s for back pain are a complete waste;
    • The scientific evidence for spinal fusion is just not there;
    • As much as a third of money for stenting is potentially being wasted;
    • And up to 43% of invasive coronary angiograms are unnecessary.

    This waste is common across the health sector, both public and private, but I suggest that the problems are greater in the private sector and private hospitals in particular.

    The Four Corners program highlighted the particular problems in private hospitals.

    • ‘Stents are more likely to be given in the private sector than in the public’
    • ‘Most spinal fusion is done in private hospitals’
    • Angiograms are performed ‘more frequently in the private system’
    • ‘In the last ten years we have forked out nearly $486 m. for knee MRIs in the private sector alone.’
    • ‘It does seem that over-treatment is in the private sector’.

    Four Corners did not examine Work Cover and the cost of injuries in the workplace, particularly back injury when it is treated in private hospitals.

    Many clinicians and others in the Four Corners program pointed out that there is a great deal of data in all these areas but unfortunately it is invariably in silos and not readily accessible to the public so that we can effectively address the problems of ineffective, wasteful and sometimes harmful medical procedures. There are large variations in medical procedures between public and private hospitals and regions. We have a long way to go in rigorous evidence based care. Accreditation in itself does not tell us much about the quality of care.

    There are particular reasons why we should be concerned about what is happening in some private hospitals.

    • Fee for service in private hospitals and in the private sector generally provides a perverse incentive. Clinicians are rewarded for volume of work rather than the quality of care and patient outcomes. In the public sector, clinicians are more likely to be remunerated on a salaried or sessional basis without the financial incentives for over treatment.
    • In the public hospitals peer review is much more widely practiced with mistakes, adverse events and poor performance more readily corrected.
    • Dealing with less complicated cases, many private hospitals do not have the breadth and depth of experience and the skills that are found in public hospitals and particularly teaching hospitals. Some of the larger private hospitals are well run with peer review and strict accreditation. Some have training registrars and medical students. However the quality of care is patchy, particularly in smaller private hospitals.
    • I am also advised that private hospitals are much more likely to import minimally qualified nurses on temporary visas. This inevitably leads to more adverse events.
    • Private hospitals work much more on a cottage industry basis with visiting medical practitioners coming and going between the hospital and their private rooms. With hundreds of visiting specialists it is very difficult to develop professional collaboration and peer review and professional esprit des corps when they are coming and going on a part time basis.

    Australia is spending $10 b. to subsidise private health insurance. In 2014/15 this was made up as follows

    • $6.3 b for direct outlays as in Budget Paper 1
    • $1.5b tax free income rebate.
    • $1.0b benefit for exemption from Medicare levy surcharge.

    The total is $8.8 b for 2014/15. This year it would be higher and before we look at the inflation effects of PHI

    Most of the direct outlay of over $6b benefits higher income people accessing high cost private hospitals in the name of choice .In the process they jump the hospital queue.

    MBP’s attempt to address some of these problems in negotiations with Calvary Hospitals and UnitingCare is the first public sign that I have seen of PHI companies recognizing their serious problems. The ‘canary in the mine’ is warning us about the quality and cost of private hospital care that is   generously subsidised by the Australian taxpayer.

    PHI’s are financial intermediaries. They do not deliver healthcare. They are proving unable to effectively manage quality and contain costs in private hospitals. George Savvides has found out the hard way. But the government doesn’t care and diverts attention with nonsense about the unsustainability of our health system. Abolishing the $10b subsidy for PHI would greatly improve the quality of health care, reduce costs and make our health care system much more sustainable.

    But the lobbying power of PHI companies and private hospitals like Ramsay Healthcare frightens almost all politicians and particularly Commonwealth health ministers from both sides of politics.

    Taxpayer subsidised PHI will destroy our world class health system in the same way that PHI has caused disaster in the US.

  • Peter Gibilisco and assisted by Bruce Wearne. A Special Minister for Disability.

    Disability support and policy is currently undergoing much needed reform. Such reforms highlight the attenuated life chances of people with disabilities and how these can be mitigated by policies that emphasize the inclusion of people with disabilities into the social life of us all. There is much public money being spent on getting things right, and indeed many lives are at stake.

    The National Disability Insurance Scheme is a wide sweeping reform that seems to be trying its utmost to significantly improve the lives of all people with disabilities however severe or profound these may be. There is a constant need for significant government financial support for people with disabilities to promote their health and wellbeing.

    All this has led me in times past to ask: should there be a specific Government ministry for people with disabilities?

    But now I am wondering: how does this proposal relate to the recent change in Prime Minister and the Ministerial reshuffle? Should I be pleased?

    An article in the Sydney Morning Herald (21 September) discusses the new arrangement of Ministers with special attention to disability. The article’s headline suggests that the Turnbull Government’s reshuffle of portfolios amounts to a loss for disability. But it concludes with the statement of the new minister, Christian Porter (who has replaced Mitch Fifield), that “people can be absolutely assured that disabilities is going to have front and centre care inside portfolios.”

    The word “care” is interesting; it refers here to policies. In his portfolio statement it refers to people. This is a subtle reminder that policies need to be framed with care in order to care for people. But the statement on its own is ambiguous. My question is this: How can any one issue coming under Porter’s many-sided portfolio be “front and centre” when all the other issues to be dealt with under this “Social Welfare” portfolio also need to be addressed? I am not wanting to debate here. This is no quibble. The ambiguity confirms the suspicion that disability as a “front and centre” political issue may have lost ground in the ministerial reshuffle.

    And so to my point. I suggest that disability should be covered by one federal ministerial portfolio with one minister just as there is one Ministry for Indigenous Affairs.

    Of course the new Minister’s sincerity is not in doubt. I realise such an innovation would be difficult to implement. I also welcome his emphasis upon putting disability “front and centre”. That indeed affirms a principle of good ministerial oversight and what he has said should encourage people with disability to fight on for better outcomes. But as “disability minister” he is not simply the Minister for Disability Affairs; he is Minister for Social Services overseeing “Australian government social services, including Mental health, families and children’s policy, and support for carers and people with disabilities, and seniors.” (From the Minister’s web-site). And so the situation that confronts this minister is indeed complex with many issues “front and centre”.

    My point is that the social structural complexity confronting those with disability has to be the “front and centre” focus of a specially designated minister (and department). How else can he, or she, deal with all the other issues that have to be “front and centre” to other ministers and other departments?

    The people we are talking about are our fellow citizens who suffer from an infinite number of complex disabilities. It would make sense to have a Government minister who can articulate and define disability in human and medical discourse. It makes sense for a Government minister to be a political figurehead in overseeing impacts from legislation from other portfolios and ensuring appropriate adjustments. Such a ministry would be innovative with a massive work load. There are innumerable social issues to be addressed; the demographic features of disability across the country have to be regularly monitored.

    Australia has a diverse population, with approximately 20 per cent living with disability.

    There is also the shocking statistic that identifies that at least 45 per cent of these welfare recipients are living in poverty. This is  further suggesting that there is an appalling ignorance toward people with disabilities. Christian Porter has much work to do on this front. Australia, along with other OECD countries, should be developing a perspective on economic and social development that puts this fact “front and centre”.

    A Government ministerial innovation that I propose here will help to upgrade the professional and analytical skills of our public service to find a new path to reach out and include all of our society. This is something that a disability minister would seek to implement.

    Further: does the absence of such a specifically designated ministry already create an unfortunate stigma when it comes to the funding of disability services? Of course, this is a cultural problem even if many voices say there is a community-wide failure to acknowledge the problems confronting services to those with disabilities. How is this ignorance to be addressed without a Federal minister to give political clout to such a change in the general attitude?

    We note that many voices are suggesting that proposed funding for the National Disability Insurance Scheme will be inadequate. And indeed the appointment of a Minister for Disability Affairs, as I am proposing, would require wise guidance from those in public life (as well as parliamentarians) who are well versed about life and its struggles. This is but one step to support a move beyond mere coping with life’s struggles to embrace a national generosity that reckons with the pleasures of freedom for all.

    Peter Gibilisco was diagnosed with the progressive neurological condition called Friedreich’s Ataxia, at age 14. The disability has made his life painful and challenging. He rocks the boat substantially in the formation of needed attributes to succeed in life. For example, he successfully completed a PhD at the University of Melbourne, this was achieved late into the disability’s progression. However, he still performs research with the university, as an honorary fellow. Please read about his new book The Politics of Disability.

    Bruce Wearne was awarded a Ph.D. from LaTrobe University in Melbourne, Australia, in 1987, for a thesis examining the 20th–century history of American sociology. Having left university employment, he serves on the Editorial Board of The American Sociologist. He develops a perspective on South West Pacific politics at his blog: https://nurturingjustice.wordpress.com