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Health Affairs, 26, no. 5 (2007): 1280
doi: 10.1377/hlthaff.26.5.1280
© 2007 by Project HOPE
 
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* Minority Health

Data & Measurement

PROLOGUE

Vulnerable Populations: Data And Measurement Issues


As the twenty-first century dawned, hopes swelled that decades of data collection on health disparities would catalyze previously elusive reductions. The data, budget surpluses, and other factors had brought the nation and its policymakers to a tipping point. Federal health disparity reduction initiatives rolled out in rapid succession. Healthy People 2010, released in 2000, didn’t just call for disparity reduction; it also made elimination of specific disparities one of the nation’s two highest health priorities and provided minority-specific baseline data. The 2002 Institute of Medicine report, Unequal Treatment, galvanized the growing sense of purpose to level the health playing field for minorities; a surge in health disparities research ensued.

Subsequent fiscal reversals and strains on the health care system dampened hopes of realizing major reductions in health disparities by mid-decade. Even so, trends recently revealed in the 2006 National Healthcare Disparities Report and the Midcourse Review of Healthy People 2010 were jarring. Both documents reported no major reductions in the majority of racial and ethnic health disparities tracked, with some gaps growing. And the bad news couldn’t be written off to difficult times: Simultaneous health improvements were reported for the overall population, even in some spheres where disparities went undiminished.

In this section, Kenneth Keppel and colleagues identify one likely reason for those outcomes: decisionmakers’ preferentially investing limited local health resources in overall health improvement, thereby underpowering programs to help the most burdened minorities catch up. The Midcourse Review reveals that such an approach, although tempting when resources are strained, typically leaves the minorities hardest hit by disparities trailing behind; the authors elucidate why. Racial and ethnic health disparities will persist, they conclude, unless policymakers specifically commit to reduction. To facilitate locally appropriate resource allocation decisions, policymakers should also arm themselves with current, local data.

Indeed, a firm commitment to reducing racial and ethnic health disparities is the driving force behind two unprecedented initiatives to obtain highly detailed, local disparity data. In 2006 the Commonwealth of Massachusetts and the City of Boston issued overlapping mandates to collect race and ethnicity data for all acute care hospital patients. The interventions that will follow have yet to be solidified—in part, Robin Weinick and colleagues explain, because data will inform design. Crafting a flexible system to collect the data needed to support programmatic and resource allocation decisions involved everyone from patients to legislators. The lessons learned along the way, recounted by the authors, should prove illuminating for leaders in other jurisdictions contemplating similar undertakings.


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