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NPSF Current Awareness Literature Alert
National Patient Safety Foundation Patient Safety Literature Current Awareness Alert. Updated twice monthly on the NPSF website.
This twice-monthly publication from the National Patient Safety Foundation (NPSF) Information Center identifies articles of interest to the patient safety community. The publication pinpoints items of interest from a wide array of publications.
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Adverse drug events in ambulatory care
Gandhi TK, Weingart SN, Borus J, Seger AC, Peterson J, Burdick E, Seger DL, Shu K, Federico F, Leape LL, Bates DW. Adverse drug events in ambulatory care. New England Journal of Medicine. 2003 Apr;17 348(16):1587-1589.
Adverse events related to drugs occur frequently among inpatients, and many of these events are preventable. However, few data are available on adverse drug events among outpatients. We conducted a study to determine the rates, types, severity, and preventability of such events among outpatients and to identify preventive strategies.
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The incident reporting system does not detect adverse drug events: A problem for quality improvement
Cullen DJ, Bates DW, Small SD, Cooper JB, Nemeskal AR, Leape LL. The incident reporting system does not detect adverse drug events: A problem for quality improvement. Joint Commission Journal on Quality Improvement. 1995 Oct;21(10):541-548.
The objectives of this study were 1) to determine the frequency with which adverse drug events result in an incident report (IR) in hospitalized patients; and 2) to determine if there were differences between quality assurance administrators, nurse leaders in quality assurance, and staff nurses as to whether an incident report should or would be filed for each adverse drug event.
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A computer-assisted management program for antibiotics and other antiinfective agents
Evans RS, Pestotnik SL, Classen DC, Clemmer TP, Weaver LK, Orme JF Jr, Lloyd JF, Burke JP. A computer-assisted management program for antibiotics and other antiinfective agents. New England Journal of Medicine. Jan 22;338(4):232-238.
Optimal decisions about the use of antibiotics and other antiinfective agents in critically ill patients require access to a large amount of complex information. We have developed a computerized decision-support program linked to computer-based patient records that can assist physicians in the use of antiinfective agents and improve the quality of care.
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The reliability of medical record review for estimating adverse event rates
Thomas EJ, Lipsitz SR, Studdert DM, Brennan TA. The reliability of medical record review for estimating adverse event rates. Annals of Internal Medicine. 2002 June 4;136(11):I40.
The data used by the U.S. Institute of Medicine to estimate deaths from medical errors come from a study that relied on nurse and physician reviews of medical records to detect the errors.
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Potential role of pharmacogenomics in reducing adverse drug reactions: a systematic review
Phillips KA, Veenstra DL, Oren E, Lee JK, Sadee W. Potential role of pharmacogenomics in reducing adverse drug reactions: a systematic review. Journal of the American Medical Association. 2001 Nov 14;286(18):2270-2279.
Adverse drug reactions are a significant cause of morbidity and mortality. Although many adverse drug reactions are considered nonpreventable, recent developments suggest these reactions may be avoided through individualization of drug therapies based on genetic information, an application known as pharmacogenomics.
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Detecting adverse events using information technology
Bates DW, Evans RS, Murff H, Stetson PD, Pizziferri L, Hripcsak G. Detecting adverse events using information technology. Journal of the American Medical Informatics Association. 2003 Mar-Apr;10(2):115-128.
Although patient safety is a major problem, most health care organizations rely on spontaneous reporting, which detects only a small minority of adverse events. As a result, problems with safety have remained hidden. Chart review can detect adverse events in research settings, but it is too expensive for routine use. Information technology techniques can detect some adverse events in a timely and cost-effective way, in some cases early enough to prevent patient harm.
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