While researching this "medical care" mess, I discovered "the Committee" that is in charge of reviewing everyone's medical files and care has been given unbridled liberties to medically experiment on patients.
Which committee would that be?
It's called "The Federal Coordinating Council". They were handpicked by Obama. We were told this "death panel" as Sarah Palin calls them, was shut down. It wasn't.
Oh good lord. CER is what you've been railing about in all these threads? And you think the coordinating council is "reviewing everyone's medical files" instead of, you know, their legislatively mandated responsibility?
(a) ESTABLISHMENT— There is hereby established a Federal Coordinating Council for Comparative Effectiveness Research (in this section referred to as the 'Council').
(b) PURPOSE— The Council shall foster optimum coordination of comparative effectiveness and related health services research conducted or supported by relevant Federal departments and agencies, with the goal of reducing duplicative efforts and encouraging coordinated and complementary use of resources.
(c) DUTIES— The Council shall—
(1) assist the offices and agencies of the Federal Government, including the Departments of Health and Human Services, Veterans Affairs, and Defense, and other Federal departments or agencies, to coordinate the conduct or support of comparative effectiveness and related health services research; and
(2) advise the President and Congress on—
(A) strategies with respect to the infrastructure needs of comparative effectiveness research within the Federal Government; and
(B) organizational expenditures for comparative effectiveness research by relevant Federal departments and agencies.
Contrary to what appears to be popular belief in some corners, this isn't what Palin's "death panels" were supposed to be. First of all, Palin explicitly identified the section of the original House bill, H.R. 3200, she was referring to with that nonsense and it had nothing to do with CER. It was about Medicare reimbursing for voluntary consultations on end-of-life or palliative care.
Aside from the fact that CER is explicitly not what she was referring to, it isn't even conceptually what she was referring to. Palin's death panel fantasy was about denying care based on individual attributes ("level of productivity in society"), which is why she shamelessly brought in her handicapped child as an example. CER, of course, isn't even close to that. It's an attempt to systematically identify the most effective treatment for a given condition. Or
for a bit more depth:
The health reform legislation (1), the IOM priority-setting committee (2), and the Federal Coordinating Council for CER (3) define “CER” similarly. The IOM report states that CER is “the generation and synthesis of evidence that compares the benefits and harms of alternative methods to prevent, diagnose, treat, and monitor a clinical condition or to improve the delivery of care. The purpose of CER is to assist consumers, clinicians, purchasers, and policy makers to make informed decisions that will improve health care at both the individual and population levels” (2).
According to this definition, the purpose of CER is to help stakeholders, including patients and their physicians, to make informed choices among alternatives. This statement of purpose embraces the concept of individualized decision-making, in which the clinical characteristics and preferences of the patient help to determine the choice among alternatives. Consequently, comparative studies will search for evidence that the response to treatment varies within the study population, a phenomenon called “treatment response heterogeneity.” How often it occurs is not known, but 2 randomized trials show that it can occur. In each trial, the treatment that was the most effective overall caused worse outcomes in one or more large subgroups (4, 5).
Worth studying treatment outcomes scientifically, don't you think?
The "Center for Medicare Services" also has a PDF you can download (if it too hasn't been removed) titled "National Coverage Determinations with Data Collections as a Condition of Coverage: Coverage with Evidence Development".
If you think there's any payer in the world (and that includes the individual) who doesn't re-assess and update some definition of medical necessity for treatments and services it purchases, you're out of your mind. This process, unsurprisingly, is usually aided by data collection.
As I recall (because I don't have the document in front of me right now), the term "Evidence" replaced the word "Experiments" in the 50s or 60s after some Congressional hearings.
I can see you're straining very hard to connect voluntary clinical trials with something Josef Mengele would do. And I think that tells me just about all I need to know about you.