Device advisory letters: Readability and comprehension, patient-centered outcomes not to be “misunderstood”
Author:
Publisher
Elsevier BV
Subject
Physiology (medical),Cardiology and Cardiovascular Medicine
Reference7 articles.
1. Pacemaker and ICD generator malfunctions: analysis of Food and Drug Administration annual reports;Maisel;JAMA,2006
2. Recommendations from the Heart Rhythm Society Task Force on Device Performance Policies and GuidelinesEndorsed by the American College of Cardiology Foundation (ACCF) and the American Heart Association (AHA) and the International Coalition of Pacing and Electrophysiology Organizations (COPE)
3. Mueller LA, Sharma A, Ottenberg AL, Mueller PS. Readability of “Dear Patient” device advisory notification letters created by a device manufacturer. Heart Rhythm 2013;10:501–507.
4. The prevalence of limited health literacy;Paasche-Orlow;J Gen Intern Med,2005
5. Implantable cardioverter-defibrillator FDA safety advisories: impact on patient mortality and morbidity;Sengupta;Heart Rhythm,2012
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