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The Collection
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General Hospitals
PATIENT SAFETY PRIMERS
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STUDY
Automated medication error studies with audit supplementation were effectively designed and analyzed by time series.
Shuster JJ, Winterstein AG. J Clin Epidemiol. 2006;59:957-963.
STUDY
Improving self-reporting of adverse drug events in a West Virginia hospital.
Schade CP, Hannah K, Ruddick P, Starling C, Brehm J. Am J Med Qual. 2006;21:335-341.
STUDY
The effect of a rapid response team on major clinical outcome measures in a community hospital.
Dacey MJ, Mirza ER, Wilcox V, et al. Crit Care Med. 2007;35:2076-2082.
STUDY
Adverse drug event reporting in intensive care units: a survey of current practices.
Kane-Gill SL, Devlin JW. Ann Pharmacother. 2006;40:1267-73.
STUDY
An examination of technical efficiency, quality, and patient safety in acute care nursing units.
Mark B, Jones C, Lindley L, Ozcan Y. Policy Polit Nurs Pract. 2009;10:180-186.
STUDY
Comparison of methods for identifying patients at risk of medication-related harm.
van Doormaal JE, Rommers MK, Kosterink JGW, Teepe-Twiss IM, Haaijer-Ruskamp FM, Mol PGM. Qual Saf Health Care. 2010;19:e26.
COMMENTARY
Passing the "Yo' Mama" test.
Blair R. Health Manage Tech. June 2006;27:16.
STUDY
Assessment of adverse drug events among patients in a tertiary care medical center.
Johnston PE, France DJ, Byrne DW, et al. Am J Health Syst Pharm. 2006;63:2218-2227.
STUDY
Patient risk factors for medical injury: a case–control study.
Marbella AM, Laud PW, Brasel KJ, Layde PM. BMJ Qual Saf. 2011;20:187-193.
STUDY
Evaluating clinical decision support systems: monitoring CPOE order check override rates in the Department of Veterans Affairs' computerized patient record system.
Lin C-P, Payne TH, Nichol WP, et al. J Am Med Inform Assoc. 2008;15:620-626.
STUDY
Tiering drug–drug interaction alerts by severity increases compliance rates.
Paterno MD, Maviglia SM, Gorman PN, et al. J Am Med Inform Assoc. 2009;16:40-46.
STUDY
Incidence and nature of adverse events during pediatric sedation/anesthesia for procedures outside the operating room: report from the Pediatric Sedation Research Consortium.
Cravero JP, Blike GT, Beach M, et al. Pediatrics. 2006;118:1087-1096.
STUDY
A randomised controlled trial of the effect of continuous electronic physiological monitoring on the adverse event rate in high risk medical and surgical patients.
Watkinson PJ, Barber VS, Price JD, et al. Anaesthesia. 2006;61:1031-1039.
STUDY
Can surveillance systems identify and avert adverse drug events? A prospective evaluation of a commercial application.
Jha AK, Laguette J, Seger A, Bates DW. J Am Med Inform Assoc. 2008;15:647-653.
STUDY
Iatrogenic events resulting in intensive care admission: frequency, cause, and disclosure to patients and institutions.
Lehmann LS, Puopolo AL, Shaykevich S, Brennan TA. Am J Med. 2005;118:409-413.
STUDY
Drug-related hospitalizations in a tertiary care internal medicine service of a Canadian hospital: a prospective study.
Samoy LJ, Zed PJ, Wilbur K, Balen RM, Abu-Laban RB, Roberts M. Pharmacotherapy. 2006;26:1578-1586.
STUDY
Reducing medication errors and improving systems reliability using an electronic medication reconciliation system.
Agrawal A, Wu WY. Jt Comm J Qual Patient Saf. 2009;35:106-114.
STUDY
Medication errors resulting from computer entry by nonprescribers.
Santell JP, Kowiatek JG, Weber RJ, Hicks RW, Sirio CA. Am J Health Syst Pharm. 2009;66:843-853.
STUDY
Evaluation of causes and frequency of medication errors during information technology downtime.
Hanuscak TL, Szeinbach SL, Seoane-Vazquez E, Reichert BJ, McCluskey CF. Am J Health Syst Pharm. 2009;66:1119-1124.
STUDY
Adverse drug event rates in six community hospitals and the potential impact of computerized physician order entry for prevention.
Hug BL, Witkowski DJ, Sox CM, et al. J Gen Intern Med. 2010;25:31-38.
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