April 15, 2009 Printable Version Newsletter Archive
REGULATORY AND PAYER
  • CMS Releases Mortality, Readmission Rates to Hospitals
  • CMS Chooses Communities for Readmission Program
  • FDA to Review Older Devices
  • QUALITY
  • Patient Empowerment, Prevention Necessary, ACC CEO Writes
  • REGULATORY

    CMS Releases Mortality, Readmission Rates to Hospitals

    The Centers for Medicare and Medicaid Services (CMS) on April 10 released performance on six key measures to all U.S. hospitals, in preparation for public announcement of these measures this summer. The measures are 30-day mortality and 30-day readmissions for heart failure, acute myocardial infarction (AMI) and community-acquired pneumonia. Members are encouraged to find the report for their hospital and to check their specific rates for each of the measures.

    The ACC will assist members in reducing their readmission rates though its Hospital to Home (H2H) program, which will officially launch when the CMS measures are publicly released this summer. H2H aims to reduce 30 day all-cause readmissions for heart failure and AMI by 20 percent nationally by December 2012. To learn more or enroll, log in to www.acc.org/h2h/enrollment, send a question to hospital2home@acc.org, or view a CVN segment on the issue.

    CMS Chooses Communities for Readmission Program

    The Centers for Medicare and Medicaid Services (CMS) on April 13 announced the 14 communities chosen for the Care Transitions Project, a program designed to reduce unnecessary hospital readmissions. The program will focus on methods of preventing readmissions on a local level, said Barry Staube, M.D., chief medical office for CMS. Each of the 14 communities will be led by a state Quality Improvement Organization to implement: hospital and community system-wide interventions; interventions that target specific diseases or conditions; and interventions that target specific reasons for admission. The Care Transitions Project will continue through summer 2011. More information, including the 14 communities chosen, is available online.

    FDA to Review Older Devices
    The Food and Drug Administration (FDA) said on April 8 that it will require some device manufacturers to prove that their “legacy devices” – devices approved before 1976 – are safe and effective, the New York Times reports. Twenty seven device types, including some external defibrillators and pacemaker parts, will be reviewed by the agency. FDA has requested additional information within the next 120 days from the device makers, and has begun a review of two of the device types. It is unclear how long the process will take, an FDA spokesperson said.

    QUALITY

    Patient Empowerment, Prevention Necessary, ACC CEO Writes
    ACC CEO Jack Lewin, M.D., was featured as a guest commenter at the Denver Post discussing the importance of prevention and patient empowerment. He writes, “As physicians we need to empower our patients, and our patients need to take responsibility for their health through preventative measures. Preventative health care can and should be part of health care reform because it not only leads to an overall better quality of life, but it reduces individual and taxpayer costs.” He adds, “In the current economic instability, we certainly need cost reduction.” Learn more about ACC’s health care reform efforts at: qualityfirst.acc.org.

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