In the second installment
I reviewed a paper published by the Center for Health Care Strategies
(CHCS) to document my statement that we have no useful information on
ACOs and to illustrate the quandary the hope-based “definition” of “ACO”
creates for researchers. I criticized the CHCS paper as well for its
cavalier attitude about evidence. The paper relied heavily on press
releases and anonymous sources, and ignored the costs providers and
insurers incur to set up and maintain ACOs.
In this last installment, I explore the
role that culture – the culture of the managed care movement and the
larger health policy community – played in elevating the ACO to the
status of national health policy and, at the same time, thwarting the
production of useful research on what it is ACOs do for patients.