What’s your blood count? Blood pressure? Bone density? PSA?
If it is abnormal, odds are that you will want it to be normal. In doing so, you
are making the same leap of faith that your doctor is making when he commences
treatment: that treating the numbers will improve your health. Like much of
what we do, treating the numbers is often naïve, and sometimes harmful, no
matter how well intentioned. Read these short examples and tell me if you still
want your numbers normalised.
- Tight control of blood glucose levels in a medical intensive care unit does not improve outcomes, and it has been shown to be harmful in another study.
- Attempts to prop up the haemoglobin level of patients with chronic kidney disease raised the haemoglobin level, but caused overall harm.
- Attempts to prop up the blood pressure in trauma patients caused more bleeding, leading to the current policy of ‘permissive hypotension’ (low blood pressure).
- Propping up the haemoglobin in critically ill people makes them slightly more likely to die.
- This study showed that giving patients beta-blockers to control their heart rate and blood pressure around surgery lowered their chance of dying from a heart attack, but increased their chance of dying (from anything).
- Giving oxygen to newborn babies who can’t breath properly (and have low oxygen levels) increases their chances of dying.
Surrogate outcomes
The problem here is the use of “surrogate outcomes”. This is
where we control a surrogate value, as a short cut for fixing the real thing.
In theory, this sounds fine but it is only valid when the connection between
the surrogate and the real thing is pretty tight. Sometimes, using a surrogate
is valid, but there are many reasons why control of your surrogate measure
might not change the clinically important outcome. For example:
- The two may not be causally related
- Treatment of extreme values may be helpful, but generalisation to milder cases doesn’t work
- The connection may be valid but the treatment might not alter the surrogate value
- The treatment might alter the surrogate, but have unintended harmful consequences via another pathway.
Sometimes it works, for example if you control the blood
glucose levels of diabetics, they are less likely to have diabetic-related
complications in the future. But so many of the surrogate outcomes we use have
either not been validated, or have been shown to be invalid measures of the
real, clinically important outcome.
The famous case
A famous case of the failure of surrogate outcomes is that
of flecainide (and related antiarrhythmic drugs). In the period after a heart
attack, some patients die suddenly of an arrhythmia (abnormal heart rhythm). In
order to prevent these sudden deaths, doctors gave antiarrhythmics. This sounds
completely logical, but as many of you know, biological explanations don’t
carry much weight with me. The effectiveness of these drugs was proven in
clinical trials where they gave some patients antiarrhythmics and some patients
placebo and then followed them around with continuous heart monitors: the
patients who took the antiarrhythmics definitely had less arrythmias.
Based on these trials, the drug was approved by the FDA
(thanks to the flawed
accelerated approval process) and used all across the USA on hundreds of
thousands of patients in the 1980s. Although an association with lower
mortality was not established, doctors felt that a randomised trial to test
this would be unethical, as the drugs clearly worked (by now, regular readers
will understand why I flinch whenever I hear that claim).
My argument is that instead of reading reams of printouts
from heart monitors and counting the regular and irregular beats (the surrogate
outcome), why didn’t they measure the mortality (the relevant outcome)? It
would have been easier. Well that’s what some doctors did, in a large trail
called CAST (Cardiac
Arrhythmic Suppression Trial), which showed that you were much more likely
to die if you were given the antiarrhythmic drug. I guess the only
consolation was that you definitely had less arrhythmias before you died. The
rate of death with the drugs was so high that they had to stop the trial early.
Overall, the introduction of those drugs (based on the surrogate outcome tests)
was responsible for ten of thousands of deaths in the US alone.
The normalisation heuristic
Nowhere in medicine is the ‘strive for normal’ greater than
in the intensive care unit. The basis for most treatment decisions in intensive
care is to make a number normal. It might be the pulse, oxygen, temperature,
blood clotting, blood glucose, haemoglobin, salts (Na, K, Ca, Mg, etc.), urine
output, blood urea and creatinine, or the blood pressure, pulmonary artery
pressure, respiratory pressure, intra-cranial pressure, abdominal pressure, or
compartment pressure (once the pressure transducer was invented, it got used,
everywhere). Prescribing the drugs gets tricky though, particularly when each
drug raises one number but lowers another, and other drugs need to be given to
counter the effects of the previous drug. Intensive care patients often end up
on a finely balanced regimen of multiple drugs, and have tests done repeatedly
each day just to get the fine-tuning right.
This obsession with the ‘normal’ has been termed the “Normalization Heuristic” and is
explained extremely well by the authors (follow the link).
Outside of the intensive care setting, you will regularly see
doctors treating numbers and test results, always hoping that by doing so, some
measure of health improvement may result. In my field, this is referred to as
“treating the X-ray”. But even effective surrogate treatments like cholesterol
lowering drugs and blood
pressure lowering drugs only reduce the absolute chance of death by 1.5%, and
sometimes only when treatment is pursued aggressively, as many studies barely
even control the surrogate, let alone the main outcome. The effectiveness of
blood pressure and cholesterol control are particularly called into question
when we aim to treat milder and milder cases.
The bottom line
Be skeptical next time a doctor wants to treat a number
(PSA, hormone level, cholesterol, blood pressure, arterial stenosis, or even an
X-ray or MRI finding) instead of your health. Ask about the evidence of the
treatment making a difference to the outcome that is important to you (whether
that be function, quality of life, survival or something else).
It's interesting that i've completed ATLS and similar courses in the not to distant past and never heard about "permissive hypotension". I guess it makes sense to question all of the things we are taught!
ReplyDeleteThanks,
DeleteYes, it appears that pumping trauma patients full of fluid in order to "normalise" their blood pressure only bursts the clots that the body has formed in order to stop the bleeding. As is so often the case, the body knows best and our attempts to help only make things worse. And yes, question everything, it so often pays off.
Ooh nice, the normalization heuristic! Source of so many pages from the ward for potassiums of 3.3 and heart rates of 108. Never knew I needed a word for that until now.
ReplyDeleteI remember reading somewhere that the great American academic hospitals had a tradition that patients would be given a proper "Harvard death" whereby all electrolytes and other lab tests would be maintained within normal limits even up to the moment of death.
Ah, the medicalization of dying. Along with grief, pain, giving birth, and mating, it appears that our ability to manage and cope with these characteristics of life requires medical input. Otherwise, left to our own devices, we might find that we don't need doctors to face life's predicaments.
DeleteI like the idea of the Harvard Death as a sign of medicalizing death; I might use that in a future post.
I went to the doctor in 2004 after complaining of dizziness. The cause was never found, but he did find that I had high blood pressure 140/90. I had had this for years and it was always considered "borderline". Now it was high. He insisted that I need medication: Diovan. Here's the thing - at times my BP is high, but most of the time it is normal and even below normal. I told him this and said I didn't think I needed the medication. He disagreed because I had these surges of high BP and that had to be treated. So here I am, 10 years later taking BP medicine with Metoprolol (which also lowers BP) for since discovered afibs. This is too much medication in my opinion. One time I passed out. The cardiologist told me to cut the dosage of the metoprolol - thank goodness. I know you can't advise, but what are your thoughts on off and on high BP? Just wondering if you agree or not---
ReplyDelete