Readers know that I am obsessed with semantics. I know that words are powerful. Oft times words are labels. Too often people use words to obfuscate meaning. My hypothesis is that quality improvement is an obfuscating phrase.
The key here is the definition of quality. How does one measure quality? Opinion leaders have made the leap from performance measurement to quality. We should work through the logic.
Researchers and "quality" gurus take guidelines and transform them into performance measures. For example, the percentage of post myocardial infarction patients who are taking beta blockers or the percentage of type II diabetics with a HgbA1c < 7. We have all read many performance measures.
These "quality experts" take well documented research findings and make the logical assumption that providing this "evidence based" care defines quality care. For example, we know that lower HgbA1c correlates with better outcomes. Therefore they assume that striving to lower the HgbA1c (and succeeding) defines higher quality care.
I submit that they need to study the philosophy of logic. They are missing an important step.
The problem comes from the studies themselves. Patients in studies are often much different from other patients. As patients suffer more diseases, interpreting a performance measure on one disease must become more complex.
"Quality improvement" implies that patients will have better outcomes. Yet, few studies exist that show that improving performance measures really improves outcomes.
This model makes the unsubstantiated assumption that improving performance measures equates with improved outcomes, and thus we can label our efforts as quality improvement.
We should be precise with our semantics. We should call these programs performance measure improvement. If we call them by the proper term, we would have much higher level discussions of this entire movement. The movement, while well meaning, is increasing resource use without proving that we also are improving outcomes. Perhaps we are; perhaps we are not. We should not call these efforts quality improvement until and unless we have clear outcome data in standard patients.
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{ 5 comments… read them below or add one }
I agree. In epidemiology it’s referred to as the ecological fallacy, the mistaken approach of taking measures from a population based level and applying them to individual practice without confirming them with individual level studies.
I wish there were more real world studies. Medicare is planning some medical home pilot studies, but these won’t start until 2010. North Carolina has some data with its Medicaid reform efforts: http://www.annfammed.org/cgi/reprint/6/4/361
Bravo, now can you try to get the medical profession to abandon “reimbursement” to describe a fee or payment!
I agree. There are a great many studies providing “evidence” regarding how to optimize outcomes. Because they do not address a standardized population, they are sometimes conflicting. Even worse, they are occasionally oriented toward promotion of a particular product.
However, I do think that “evidence based care” is beneficial, albeit just one of many elements that are essential for the provision of high quality outcome-oriented care. Many in our industry have observed that fragmentation of care can impede the achievement of high quality care and superior outcomes. I believe that evidence based care guidelines, when developed by a multi-disciplinary team of physicians and clinicians, play an important role in helping the many different caregivers to anticipate and coordinate the care that is provided, and stay focused on defined outcome goals.
There’s more than a bit of a straw-man argument here. I have yet to meet a serious “quality improvement” researcher who doesn’t readily acknowledge the limitations you outline.
Most of us are exceedingly well-versed in logical argument. I would submit that what we need is agreement on terminology and an acknowledgment that we already agree on most of the issues you discuss. I once had a debate teacher who required me to state my opponent’s position–to my opponent’s satisfaction–before launching my argument. This is good advice.
You define “quality” as “better outcomes.” Fine. That is one definition, but there are others. I’m sure you’ve read Donobedian’s work, so I don’t need to review his structure-process-outcome framework for you. Donobedian doesn’t demand that improvement on a process measure always leads to better outcomes. His argument is population-level: process measure performance must be positively correlated with better health (i.e., on average produce better outcomes, however you define these). We all like outcome measures, but these are rarely available…especially in the world of chronic disease, where processes may produce measurable outcomes for decades.
When a researcher in QI studies “quality measures,” these can be anywhere in the structure-process-outcome chain. It is incumbent on the researcher to specify the level of measurement and to acknowledge that all measures (even measures of outcomes) suffer from serious limitations. There is no way around this. The best we can do is to continually test the relationships between “quality measures” at all levels and the final results we desire. Waiting for perfect measures is unrealistic.
I have to ask: if you don’t think guidelines should be followed in the populations for whom they are designed (which is how we identify the denominator populations for Bernoulli-distributed process measures), with whom are you really arguing?
I suppose the alternative is to reject empiricism entirely and adopt the framework of Cartesian doubt. After all, even outcomes-based studies don’t measure every possible outcome, and no outcomes measure is without flaws (Death? Death over what time period? Before death, are you absolutely sure you’ve measured quality of life correctly? How do you know you haven’t missed a death or two? In light of the “engage with grace” campaign, how do you know what percentage of the deaths are actually bad outcomes?)
So let’s not throw out the entire body of empirical work on QI. Trying to deduce from first principles of logic whether, say, lowering average A1c will improve “ultimate quality” will not be a productive use of time. I don’t think anybody wants to live in a world where all physicians are assumed (based on first principles, or maybe a one-time licensing exam) to deliver care of perfect quality.
An emotional reluctance to accept quality measurement is understandable. Nobody likes being measured, and the initial response of a prideful professional is to attack the measures by holding them to impossible standards…or to overinterpret them, suggesting that the measures imply an expectation of perfect care. We see the same thing every time we measure a new aspect of care, or a new subspecialty has its care examined. First, it’s “No information is better than imperfect information.” Then there’s anger, bargaining, …and I think you know the rest.
Semantics are one of those often overlooked aspects regarding Medicare.