Tuesday, November 26, 2019

Tuesday, November 5, 2019

Healthcare is in danger of becoming humanless

Two communication challenges that have hit the media recently should act as a warning for the increasing automation of communication for GPs.

First, there’s the mandatory new rules for referring patients to public hospital clinics in Victoria; and second, the ineffective management of patients supported by the National Disability Insurance Scheme (NDIS), which sees GPs’ involvement relegated to a form-filling exercise.
Australian Doctor reported last month that Victoria Health had introduced more formality in GPs’ referrals to specialist clinics, including vascular surgery, urology and adult ENT. Patients referred without ‘complete’ information — and the information required is extensive — will no longer be accepted, nor will patients whose referrals do not satisfy specific criteria.
For example, a patient referred for an aortic aneurysm requires radiological evidence that it is at least 4cm in diameter or is growing more than 1cm a year. And a patient for prostate cancer assessment must have a PSA level according to certain age criteria, a palpable prostatic abnormality or bone pain.
These stipulations for referral aim to make the best use of expensive medical care facilities. Sloppy referrals of patients probably not needing specialist attention should be reduced. But care is needed, as with any guideline, to allow clinical judgement to be the final arbiter. No guideline based on statistically grouped data can fit each case.
While guidelines for referral concentrate the mind, they should allow for exceptions based on clinical assessment that need human communication and interaction.
Do we really want to get to a situation where healthcare is as humanless as the likes of border control and modern retail?
Recently in the US, I was impressed (and greatly relieved) to discover that the previous immigration procedures on entry were now paperless, depending instead on facial recognition and fingerprints. But the humans, generally friendly, who had staffed the stalls were also gone.
Arriving at Atlanta, one of the biggest terminals in the country, we also found the coffee shop ominously quiet: orders were placed via an iPad at one’s seat and customers silently consumed refreshments while watching television.
Communications were once based on people speaking to one another rather than completing forms. In US medical circles, there is currently lively controversy and debate about what has been lost with the almost universal move to electronic medical records.
There is evidence of benefit in reducing medication errors, but it is sparse beyond that. Experienced clinicians complain about the opportunity cost of the time spent entering data and the subsequent loss of time for direct patient interaction.
Author John Banville recently reviewed the wide-ranging book The Unnamable Present by Roberto Calosso, an Italian polymath. Writing in the New York Review of Books, Banville quotes Calosso’s concern that, in the brave new world of the web, “information tends to replace not only knowledge, but thought in general”.
The internet leads to “disintermediation” — a loss of connection with others who can help and guide us — and becomes instead a place where “a man can entangle himself in a series of algorithms and imagine he is thinking”. Calosso hopes our preoccupation with digital data “may come to be regarded one day as an instance of mass delirium”.
Why not build into the stylised referral a two-minute (or maybe five-minute) phone conversation between the GP and the clinic to ensure everyone is in sync? This suggestion may provoke mirth because it is naive, but it could be done.
In the case of the NDIS, as with any new system, there will be discomfort. Management of the program in its early years has been unimpressive.
Although GPs fill out a bundle of forms to ensure patients can access the scheme, they’re not deeply involved in the planning of services and have no direct communication with the NDIS when they should have. The issue is now concerning both the AMA and the RACGP.

The tendency of communication based on templates, and information technology, is to reduce the human element and human interaction. This may be vital to the mechanised production of goods, but in the provision of collaborative medical services, it utterly misses the point.

Published in the Medical Observer 4 November 2019 https://bit.ly/33oXkS4

Saturday, October 26, 2019

Healthcare costs increasingly shifting to patients, study shows





13 September 2019

Out-of-pocket spending on health by households in Australia is rising faster than overall household spending on goods and services—and taking an increasingly bigger slice of the household budget, according to a research study published today in Australian Health Review, the journal of the Australian Healthcare and Hospitals Association (AHHA).
The study, by Sydney University researchers Professor Farhat Yusuf and Professor Stephen Leeder, uses consumer-reported data gathered by the Australian Bureau of Statistics Household Expenditure Survey.
Household out-of-pocket (OOP) spending on healthcare rose by more than 25% over a recent 6-year period while overall household spending on goods and services rose by 15%.
In 2015–16, the mean amount spent by households on healthcare out of their own pockets was $4,290, or 5.8% of total household expenditure.
The most expensive OOP item was private health insurance ($1,744), followed by non-PBS medicines ($585), specialists ($438) and dentists ($396). Spending on GPs was $96.
The biggest percentage rises in out-of-pocket healthcare costs between 2009–10 and 2015–16 were for health insurance (51% rise), co-payments to ‘other health professionals’ (42% rise), and co-payments to specialists (35% rise).
‘Out-of-pocket expenses on healthcare as a proportion of the total household budget has been rising in real terms since 1984’, said AHHA Chief Executive Alison Verhoeven.
‘This study notes that the progressive movement of healthcare costs “from public to person” has occurred “without policy debate, slowly and steadily, with small steps such as freezing Medicare rebates”.
‘Other more recent data suggest that OOP costs have continued rising right to the present day.’ The situation was brought to a head earlier this year with media reports of huge five-figure co-payments for some types of medical and surgical care, particularly cancer care, with dire financial consequences for individuals as a result.
‘Yet, there is no evidence that higher OOP costs are related to better quality of care or increased access to care.
‘This creeping burden on individuals challenges our notions of universal healthcare, a fair go, and care based on medical need rather than the depth of your pockets’, Ms Verhoeven said.
The study found that OOP costs were highest among affluent households, especially those holding private health insurance.
Correspondingly, OOP costs were lowest in low-income households, but no data were available on to what extent care was skipped because of the cost. Other studies show, however, that OOP costs weigh most heavily on individuals with low incomes and multiple health problems.
‘This individual upward drift in out-of-pocket health expenses deserves very serious policy attention before our nation’s health starts to drift downwards’, Ms Verhoeven said.
Recent estimates of out-of-pocket expenditure on health care in Australia is available at http://www.publish.csiro.au/ah/Fulltext/AH18191. This release is also available online.

The Australian Healthcare and Hospitals Association is the national peak body for public and not-for-profit hospitals, Primary Health Networks, and community and primary healthcare services.

Tuesday, October 22, 2019

A child shall lead them



Published in Australian Medicine 21 October 2019 https://bit.ly/2NhDL7B

Tuesday, September 17, 2019

Tuesday, August 27, 2019