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Journal Articles

in Device/Product Safety
 21-40 of 78 Articles
JAMA | 
Medical News and Perspectives |  May 16, 2012
IOM Report Lays Out a Blueprint for Improving Regulatory Systems Worldwide
Mike Mitka
JAMA. 2012;307(19):2014-2016. doi:10.1001/jama.2012.4485.
JAMA | 
Capitol Health Call |  May 09, 2012
Safer Devices Bill
Mike Mitka
JAMA. 2012;307(18):1904. doi:10.1001/jama.2012.3896.
JAMA | 
Viewpoint |  March 21, 2012
Evaluating Sex Differences in Medical Device Clinical Trials:  Time for Action
Sanket S. Dhruva, MD; Rita F. Redberg, MD, MSc
JAMA. 2012;307(11):1145-1146. doi:10.1001/jama.2012.254.
JAMA | 
Capitol Health Call |  January 11, 2012
Speeding Device Approval
Mike Mitka
JAMA. 2012;307(2):134. doi:10.1001/jama.2011.1931.
JAMA | 
Commentary |  September 21, 2011
The FDA—A Misunderstood Agency
Joshua M. Sharfstein, MD
JAMA. 2011;306(11):1250-1251. doi:10.1001/jama.2011.1345.
JAMA Internal Medicine | 
Editorial |  July 25, 2011
The Archives of Internal Medicine: Making a Difference in 2010 and Beyond
Rita F. Redberg, MD, MSc, Editor
Arch Intern Med. 2011;171(14):1228-1229. doi:10.1001/archinternmed.2011.154.
JAMA Internal Medicine | 
Invited Commentary |  June 13, 2011
Medical Device Recalls: Get It Right the First Time:  Comment on “Medical Device Recalls and the FDA Approval Process”
Rita F. Redberg, MD, MSc; Sanket S. Dhruva, MD
Arch Intern Med. 2011;171(11):1011-1012. doi:10.1001/archinternmed.2011.27.
JAMA Internal Medicine | 
Original Investigation |  June 13, 2011 FREE
Medical Device Recalls and the FDA Approval Process
Diana M. Zuckerman, PhD; Paul Brown, BS; Steven E. Nissen, MD
Arch Intern Med. 2011;171(11):1006-1011. doi:10.1001/archinternmed.2011.30.
INCLUDES: CME
JAMA Internal Medicine | 
Editor's Correspondence |  June 13, 2011
FDA Recalls Not as Alarming as They Seem—Reply
Diana M. Zuckerman, PhD; Paul Brown, BS; Steven E. Nissen, MD
Arch Intern Med. 2011;171(11):1044-1046. doi:10.1001/archinternmed.2011.243.
JAMA | 
Capitol Health Call |  June 08, 2011
Device Approval
Mike Mitka
JAMA. 2011;305(22):2280. doi:10.1001/jama.2011.776.
JAMA Internal Medicine | 
Original Investigation |  March 28, 2011 FREE
Inclusion of Training Patients in US Food and Drug Administration Premarket Approval Cardiovascular Device Studies
Connie E. Chen, BA; Sanket S. Dhruva, MD; Lisa A. Bero, PhD; et al.
Arch Intern Med. 2011;171(6):534-539. doi:10.1001/archinternmed.2010.445.
JAMA | 
Editorial |  December 15, 2010
Ensuring Safe and Effective Use of Medication and Health Care:  Perfecting the Dismount
Darren A. DeWalt, MD, MPH
JAMA. 2010;304(23):2641-2642. doi:10.1001/jama.2010.1844.
JAMA | 
Commentary |  November 17, 2010
Accelerated Approval and Possible Withdrawal of Midodrine
Sanket S. Dhruva, MD; Rita F. Redberg, MD, MSc
JAMA. 2010;304(19):2172-2173. doi:10.1001/jama.2010.1695.
JAMA | 
Editorial |  November 10, 2010
Achieving Meaningful Device Surveillance:  From Reaction to Proaction
John S. Rumsfeld, MD, PhD; Eric D. Peterson, MD, MPH
JAMA. 2010;304(18):2065-2066. doi:10.1001/jama.2010.1648.
JAMA | 
Original Contribution |  November 10, 2010 FREE
Automated Surveillance to Detect Postprocedure Safety Signals of Approved Cardiovascular Devices
Frederic S. Resnic, MD, MSc; Thomas P. Gross, MD, MPH; Danica Marinac-Dabic, MD, PhD; et al.
JAMA. 2010;304(18):2019-2027. doi:10.1001/jama.2010.1633.
INCLUDES: , Supplemental Content
JAMA | 
Original Contribution |  May 26, 2010 FREE
Reporting and Interpretation of Randomized Controlled Trials With Statistically Nonsignificant Results for Primary Outcomes
Isabelle Boutron, MD, PhD; Susan Dutton, MSc; Philippe Ravaud, MD, PhD; et al.
JAMA. 2010;303(20):2058-2064. doi:10.1001/jama.2010.651.
INCLUDES: , Supplemental Content
JAMA | 
Commentary |  April 14, 2010
Reducing Distracted Driving:  Regulation and Education to Avert Traffic Injuries and Fatalities
Peter D. Jacobson, JD, MPH; Lawrence O. Gostin, JD
JAMA. 2010;303(14):1419-1420. doi:10.1001/jama.2010.414.
JAMA | 
Review |  December 23, 2009 FREE
Strength of Study Evidence Examined by the FDA in Premarket Approval of Cardiovascular Devices
Sanket S. Dhruva, MD; Lisa A. Bero, PhD; Rita F. Redberg, MD, MSc
JAMA. 2009;302(24):2679-2685. doi:10.1001/jama.2009.1899.
INCLUDES: , Supplemental Content
JAMA | 
Medical News & Perspectives |  September 16, 2009
Studies Probe US Traffic Injuries, Deaths
Mike Mitka
JAMA. 2009;302(11):1159-1160. doi:10.1001/jama.2009.1314.
JAMA | 
Commentary |  August 19, 2009
Registries for Robust Evidence
Nancy A. Dreyer, PhD; Sarah Garner, PhD
JAMA. 2009;302(7):790-791. doi:10.1001/jama.2009.1092.

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From The JAMA Network
JAMA
Medical News and Perspectives  |  June 12, 2013
Joint Commission Warns of Alarm Fatigue:  Multitude of Alarms From Monitoring Devices Problematic
Mike Mitka, MSJ
JAMA Dermatology
Viewpoint  |  June 01, 2013
Medical Application Use and the Need for Further Research and Assessment for Clinical Practice:  Creation and Integration of Standards for Best Practice to Alleviate Poor Application Design
Satish Misra, MD; Thomas Lorchan Lewis, BSc; Timothy Dy Aungst, PharmD
JAMA Internal Medicine
Original Investigation  |  March 25, 2013
Barriers to Reducing Urinary Catheter Use:  A Qualitative Assessment of a Statewide Initiative
Sarah L. Krein, PhD, RN; Christine P. Kowalski, MPH; Molly Harrod, PhD; et al.
JAMA Internal Medicine
Invited Commentary  |  March 25, 2013
Our Lights Are on for Safety:  Comment on “Preventing Catheter-Associated Uniary Tract Infection in the United States”
Paul S. Pottinger, MD
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