NGC Update Service: September 12, 2011

Monday, September 12, 2011

NGC Update Service: September 12, 2011


National Guideline Clearinghouse (NGC)

September 12, 2011


New This Week


Guideline Summaries

American Academy of Sleep Medicine

American College of Radiology

Centers for Disease Control and Prevention

Emergency Nurses Association

U.S. Preventive Services Task Force


Announcements

NGC Spotlight

Visit the Preventing Hospital-Acquired Conditions page for evidence-based resources available on the NGC Web site to assist users in the prevention of the CMS-identified hospital-acquired conditions.

Conference News

  • The 2011 AHRQ Annual Conference, "AHRQ: Leading Through Innovation & Collaboration," will be held September 18-21, 2011 in Bethesda Maryland. In keeping with this year's theme, the event will emphasize how AHRQ is leading change in addressing today's challenges in improving access to care and its quality and cost, as well as partnering with others at the forefront of these issues. Visit the conference home page for more information. Registration is now open.

U.S. Food and Drug Administration (FDA) Advisories

  • September 7, 2011: Tumor Necrosis Factor-alpha (TNFα) Blockers): FDA notified healthcare professionals that the Boxed Warning for the entire class of Tumor Necrosis Factor-alpha (TNFα) blockers has been updated to include the risk of infection from two bacterial pathogens, Legionella and Listeria. In addition, the Boxed Warning and Warnings and Precautions sections of the labels have been revised so that they contain consistent information about the risk for serious infections and the associated disease-causing pathogens.
  • September 1, 2011: Saphris (asenapine maleate): FDA notified healthcare professionals and patients that serious allergic reactions have been reported with the use of Saphris (asenapine maleate). The Contraindications, Warnings and Precautions, Adverse Reactions, and Patient Counseling Information sections have been revised.
  • September 1, 2011: Reclast (zoledronic acid): FDA notified healthcare professionals and patients of an update to the drug label for Reclast (zoledronic acid) regarding the risk of kidney failure. Cases of acute renal failure requiring dialysis or having a fatal outcome following Reclast use have been reported to FDA.

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