One in ten medical treatments are supported by high-quality evidence – study
sciencealert.com
sciencealert.com
Often, the method was asessed by asking patients to score their situation before and after the surgery (e.g one year later).
For sure, many people try to be positive and give too optimistic scores. At least I felt it hard to admit that the costly procedure had failed and saying it to my surgeon didn't feel easy.
What I fear is, there are many research papers done using patient questionaire and giving us biased results
There is basically no risk of harm from such a thing. If all you are doing is using it verify whether a surgery worked or not, then it's not actually a treatment is it? Surgeons make their own tools, jigs and tests all the time.
And if for some reason you had to, there are different grades of hard with a medical regulating body. For instance, it is super easy to develop medical tools. Harder again to do implants, harder again to do medicines.
So I want to reiterate. Not hard at all.
- source. Worked for a medical device company that did implants, wound care and medical tools. Surgeons would often ask for custom tooling or jigs through us that we would get made up for them.
Unfortunately questionnaires might be only thing sometimes. My message is that, we should be more sceptical about them
Some are subjective like pain (VAS or visual analog pain scale, “rate your pain 1-10”), ability to do daily activities, “would you have this procedure again?”, return to pre-injury activity level, etc.
Others are objective like range of motion, strength, bone healing noted on Xray or ct, tendon / ligament healing observed on mri, histiologic healing observed from follow up biopsy, rehospitilzation rates, revision surgery rates, infection rates, or mortality rates (the ultimate objective outcome measure).
There is hardly a shortage of outcome measures out there, and researchers propose new ones all the time, but they need to be validated as relevant and accurate by other studies before they are widely adopted.
That's one thing I have noticed. A few years ago my girlfriend had a failed surgery. She complained constantly during the weeks before the followup meeting. In the followup meeting the surgeon talked about how well the surgery had gone. My girlfriend basically agreed and they bantered around for almost half an hour. Ten minutes before the appointment ended I lost patience and said "Hold on, guys. This thing hasn't worked at all. The pain is worse than before and she talks at home about killing herself. How do we get out of this?". The surgeon gave me the evil eye, my girlfriend said nothing and we basically got kicked out soon.
It was a really weird dynamic. I wonder how many surgeries are scored as success because patients are afraid of telling the surgeon that it wasn't. I think it may be a substantial percentage where the hospital/surgeon never hears about problems and there is no independent follow up either.
https://www.cms.gov/Medicare/Quality-Initiatives-Patient-Ass...
Beware of unintended consequences though, hospitals are less inclined to permit riskier surgeries on unhealthy patients if they think the risk of readmissions is too high. Good luck getting your knee replacement if you are a 300lb diabetic smoker.
When I was considering a Bankhart repair for my shoulder the number I looked at was return to sport. Sure, people can be biased about this, but this seems about as objective as you can get: “Are you able to participate in the activities you were able to before your injury?”
If you are getting a surgery without measurable outcomes, why are you getting this surgery at all?
I think it would be worrying if every medical review had high-quality evidence. Just because it's in the Cochrane database doesn't (to my understanding) mean that it is a frequently used treatment.
Yes please change the link to the original source as per the HN Guidelines.
The only way to know whether a person has the version of the disorder that responds to a particular drug is to administer that drug and see. Psychiatrists try prescribing different drugs until they hit one that works, or give up. Imagine designing a randomized-controlled-trial for that.
If you need help: first, select a group already using the drug. Split them up and give half a placebo. See which get worse. But first, find someone unethical enough to run it, and admits it.
https://www.psychiatrictimes.com/view/debunking-two-chemical...
In the general public, there's a logical fallacy that people seem to fall for when thinking about psychopharmacology. It seems that when it is learned that serotonin re-uptake inhibitors (SSRIs)are used to treat patients with depression it is followed with some mechanistic explanation of a "chemical imbalance" resulting from "not enough serotonin."
Yet people don't make this mistake when talking about opiods or pain killers. If you break your arm and the doctor prescribes Codeine we don't come to the conclusion that "you broke your arm and all your endogenous opoids came spilling out so we had to replace it with Codeine." Although Tylenol/paracetamol are useful for treating pain, we don't hear a lot of talk about Tylenol deficiencies.
As to your claim about antidepressants, psychiatry and psychopharmacology is abound in RCTs, many on treating depression with antidepressants. You are perhaps mistaking a common clinical approach (outside of clinical studies) for finding the best medical management for single patient with how clinical evidence is procured in the first place. There are more Cochrane reviews under "mental health" at 679 than there are under "orthopedics" at 478.
Also, when RCTs are proposed, no matter if they placebo controlled or not, they are reviewed by IRBs and ethics committees.
Those RCTs are administered by real people who are each either unaware that there is no way to get meaningful results from such a trial, or are motivated to produce meaningless results that can nonetheless be published to mislead.
So to answer your question they do test for that.
On top of that, I find it 100% believable that doctors use understudied treatments. The reverse makes a lot more sense. Treatments get studied after people have tried them, and believe they warrant further study and more frequent usage.
Consider coronavirus treatments, at first we had very little idea what to do, beyond inferring based on past virus with a similar symptom profile and reasoning from first principles. Later on, we slowly but surely identified effective treatments (corticosteroids/prone position/...) after people tried them. Even later, we had descriptive studies of past effectiveness. I assume most treatments go through a similar progression (covid treatments go through this progression on fast forward).
Medical studies are slow and retrospective. Fundamentally that gets you this 1/10 figure.
>> An exercise trial cannot be "blinded": anyone doing exercise will know they are in the exercise group...
How exactly can knowing which group you're in cause a placebo effect or any other relevant effect in that case?
https://www.theatlantic.com/magazine/archive/2020/04/why-flu...
https://onlinelibrary.wiley.com/doi/full/10.1111/jcpe.12363
Characterizing this as 'absence of evidence' is incorrect; the specific issue has been investigated by several independent investigators and consistently fails to find evidence of efficacy. Even with much higher sampling and statistical power, if any effect was observed, it would likely be well below anything that could justify flossing as a health recommendation, especially over IDBs.
Another way to put this: EBM is only good for about 1 in 10 treatments.
Great for writing papers, though.
Experimenting on humans is unethical and (mostly) illegal.