Objective To understand how the source of information affects different adverse event (AE) surveillance methods. Design Retrospective analysis of inpatient adverse drug events (ADEs) and hospital-associated infections (HAIs) detected by either a computerized surveillance system (CSS) or manual chart review (MCR). Measurement Descriptive analysis of events detected using the two methods by type of AE, type of information about the AE, and sources of the information. Results CSS detected more HAIs than MCR (92 % vs 34%); however, a similar number of ADEs was detected by both systems (52 % vs 51%). The agreement between systems was greater for HAIs than ADEs (26 % vs 3%). The CSS missed events that did not have information i
Hospitals monitor for ADRs by retrospective reviews (RR) of computerized discharge diagnosis, loo...
Abstract Background Adverse events are associated wit...
Adverse events in health care entail substantial burdens to health care systems, institutions, and p...
Objective To understand how the source of information affects different adverse event (AE) surveilla...
Background: To improve patient safety, organisations must systematically measure avoidable harms. Cl...
The occurrence of adverse drug reactions (ADRs) in the hospital has been cause for significant morbi...
Objective: This study aimed to compare the use of trigger tools and non-targeted chart review as met...
BACKGROUND: Drug safety monitoring relies primarily on spontaneous reporting, but electronic health ...
Background: Drug safety monitoring relies primarily on spontaneous reporting, but electronic health ...
BACKGROUND: Drug safety monitoring relies primarily on spontaneous reporting, but electronic health ...
CONTEXT: Current methods for tracking harm either require costly full manual chart review (FMCR) or ...
BACKGROUND: Drug safety monitoring relies primarily on spontaneous reporting, but electronic heal...
dissertationManual chart review is used as the gold standard in many adverse drug event (ADE) detect...
Background: A variety of methods are available for identifying and measuring adverse events and medi...
PURPOSE: Active surveillance of population-based health networks may improve the timeliness of detec...
Hospitals monitor for ADRs by retrospective reviews (RR) of computerized discharge diagnosis, loo...
Abstract Background Adverse events are associated wit...
Adverse events in health care entail substantial burdens to health care systems, institutions, and p...
Objective To understand how the source of information affects different adverse event (AE) surveilla...
Background: To improve patient safety, organisations must systematically measure avoidable harms. Cl...
The occurrence of adverse drug reactions (ADRs) in the hospital has been cause for significant morbi...
Objective: This study aimed to compare the use of trigger tools and non-targeted chart review as met...
BACKGROUND: Drug safety monitoring relies primarily on spontaneous reporting, but electronic health ...
Background: Drug safety monitoring relies primarily on spontaneous reporting, but electronic health ...
BACKGROUND: Drug safety monitoring relies primarily on spontaneous reporting, but electronic health ...
CONTEXT: Current methods for tracking harm either require costly full manual chart review (FMCR) or ...
BACKGROUND: Drug safety monitoring relies primarily on spontaneous reporting, but electronic heal...
dissertationManual chart review is used as the gold standard in many adverse drug event (ADE) detect...
Background: A variety of methods are available for identifying and measuring adverse events and medi...
PURPOSE: Active surveillance of population-based health networks may improve the timeliness of detec...
Hospitals monitor for ADRs by retrospective reviews (RR) of computerized discharge diagnosis, loo...
Abstract Background Adverse events are associated wit...
Adverse events in health care entail substantial burdens to health care systems, institutions, and p...