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What matters in healthcare? Surrogate markers or patients?

In its latest Croakey update, the Primary Health Care Research and Information Service (better known as PHC RIS) highlights concerns about over-reliance on the use of surrogate markers in health research, practice and policy.

***

Diabetes care reveals the pitfalls of surrogate markers

Christina Hagger writes:

‘What works’ in evidence-influenced health care is being overshadowed by ‘What can be measured’.

In a recent article in the BMJ (extract free, pay for full access), Yudkin and colleagues argue that the quality of medical practice is being infiltrated by an over reliance on surrogates being used as substitute predictors for clinically meaningful endpoints.

The US Institute of Medicine defines surrogates as biomarkers (such as glucose, blood pressure or lipids) that are based on epidemiologic or other scientific evidence and used to predict clinical benefit or harm.

Using diabetes as an example, the authors observe that much of the evidence for clinical interventions is based on results drawn from such surrogate markers rather than outcomes central to the patient experience such as vision loss, amputation or quality of life.

Furthermore, as the surrogate markers are generally more responsive to interventions than such ‘hard’ end points as renal failure, the authors suggest that many of the widely accepted strategies for diabetes may be based on artificially inflated expectations.

Adding to these concerns are their observations that surrogate outcomes, despite their severe limitations as perfect surrogates for patient centred outcomes, are assuming their own mantles of importance as measurable reference points for both clinical research and evaluation of health care.

The findings of such research and evaluations are used to shape policy and practice as well as influence funding.

The result is that patients with diabetes may be treated to achieve target levels of surrogates. While the authors concede such actions are usually made in a patient’s best interests, these decisions carry no information to which patients can relate, thus withdrawing opportunities for personal engagement in their own treatment plans.  Such surrogate-centric rather than patient focused strategies are counter-productive to efforts to develop patient centred medicine.

The reliance on surrogate markers sees health care shift back to a disease management approach and away from people, their quality of life and their narratives.

A surrogate is a detached marker, it does not bleed, feel fear or pain. It does not communicate a story to the patient to engage them in their health care.

Yes, evidence-influenced health care is our goal, and we need to know how to measure it but the current over-reliance on surrogates is derailing our successes by diverting our attention to measure, fund and practise only that which can be readily measured and drawing our eye away from the living complexities that are our patients.

What are we really measuring, funding and doing?

• Christina Hagger is a Research Fellow, Primary Health Care Research & Information Service (PHC RIS)

***

The BMJ article cited is not freely available but Croakey is happy to provide a copy to interested readers. Leave your details below or send an email.

Yudkin JS, Lipska KJ, Montori VM, The idolatry of the surrogate. BMJ 2011;343:d7995. This article features in the 19 January 2012 edition of PHC RIS eBulletin, available at http://www.phcris.org.au/publications/ebulletin/index.php.

The eBulletin is designed to inform readers of recently published articles and reports, news items, media releases, upcoming conferences and courses, research grants, scholarships and fellowships, PHC RIS products and services and relevant websites in the primary health care field. Those interested in receiving the weekly eBulletin are invited to subscribe to the free service at http://www.phcris.org.au/mailinglists/index.php

***

Previous Croakey posts from the PHC RIS

Are Australians willing to pay more for better oral health?

What helps encourage shared care for those with chronic illness?

More efforts needed to strengthen shared care for those with serious mental illness

 

 

 

Comments 2

  1. Jenny Haines says:

    That’s easy to answer – surrogate markers are considered more important because they allow non clinical managers to sit in their offices engaging in so called monitoring of clinical care using the markers while actual clinical care goes down the toilet because of the lack of experienced and skilled staff.

  2. Jimmy says:

    Strange article. I understand (though don’t agree with) the premise, however the background reasoning is faulty to say the least.

    Diabetes is a silent disease – ie the irreversable damage is done over a typically long period of time with typically minimal symptoms, and those that are suffered early are easy to ignore. Good blood sugar level management = delayed onset of debilitating eye, sensory, cardiac, and kidney symptoms. Good sugar management level requires regular testing to ensure sugar levels are neither too high OR too low. Waiting until the patient has ‘end points’ which are ‘central to the patient experience’ such as amputation, renal, or retinal problems kind of misses the point doesn’t it? Perhaps we should recommend patients taste their own urine for presence of sugar to give them someting ‘central to the patient experience’!

    Jenny – to equate use of surrogate markers with ‘non-clinical managers’ is disingenous. In this example, surrogate markers are of critical importance to pick up and manage diseases with long term sequele but minimal to no observable symptoms. Perhaps a more appropriate argument is that too much money is wasted on health care which would be better spent on subsidies for lifestyle interventions – exercise / improved diet / harm minimisation.

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Australian Palliative Care Conference
2018 conferences
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2019 Conferences
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