Dave,
In my opinion this could be done easily in the present context. All the pieces are there. This information is already there in the computers that scrutinize, bill and reimburse every doctor's visit, medication and procedure. It's just not available to the public. I think I can guess why.
Nearly all procedures in the US are covered by private insurance and/or government insurance. These insurance entities could create a database available to the public that would anonymously present summaries of all patient conditions, treatments and outcomes for every illness and treatment and hospital and doctor. A summary of just a fraction of a single year's treatments for every patient would give a stastically valid snapshot of every treatment plan for every possible patient profile (age, sex, pre-existing conditions), treatment, etc., given by every docotor and every hospital in the country.
And easily added is the patient satisfaction rating which could also be required as a condition of coverage, which could be reported by the patient quarterly for the first year and annually for the next 5 years, along with the initial doctor summaries of the outcome of the patient's treatment. The surveys could be taken by phone or email the way customer satisfaction surveys are solicited by Sears or the Cable Company after a service call.
Consider if every physician had 500 patient reviews, and if every procedure and medication had 5,000 or 50,000 patient reviews, and if the true outcomes of each treatment by each physician and for each hospital were recorded over time.
I don't buy a thing without first checking the customer reviews on Amazon. I only buy from ebay sellers with good customer feedback. With such a public database, very few people would eventually take a medication or go to a doctor or choose a procedure without doing the same. I could imagine a big change in the way people would consume medical treatments and medications.
In my opinion, medecine today lives on it's mythology, and exists primarily as a business. The mythology is that doctors know what they are doing all of the time, and have the patient's best interests at heart, and only advise patients with the best treatment and medication choices. That procedures are nearly all successful. And if something goes wrong, it's an isolated case. A database of tens of thousands of true outcomes would explode that myth. And maybe that's why we don't have one.
I can't be the first person in the world to have thought this was a good idea. But I've never heard anyone else, much less anyone in the medical profession, popose it.
Bob
Chicago Dave said...
ClapTheHammer said...
However, peer verified statistics are simply not available.
I see. This looks like an issue with terminology. If Clap means that Gat's study has not been corroborated independently, then he is
absolutely right. To date, all the data is from the clinic itself.
Considering the issues and expense involved in conducting clinical trials on humans, this isn't surprising. It might be sad; it might be unfortunate; it might be tragic even. But
surprising, it is not.
Maybe some day there will be a multi-center clinical trial of BPH treatments with active comparison groups (TURP, laser, GG, PAE, etc.) with deep-pockets $$$ funding. That would be nice. But I just don't see it happening in my lifetime.
Post Edited (Bob_NJ) : 12/5/2014 7:37:58 PM (GMT-7)