Morriss Frank H, Abramowitz Paul W, Nelson Steven P, Milavetz Gary, Michael Stacy L, Gordon Sara N, Pendergast Jane F, Cook E Francis
Department of Pediatrics, Roy J. and Lucille A. Carver College of Medicine, University of Iowa, Iowa City, IA 52242, USA.
J Pediatr. 2009 Mar;154(3):363-8, 368.e1. doi: 10.1016/j.jpeds.2008.08.025. Epub 2008 Sep 27.
Patients are at risk of harm from medication errors. Barcode medication administration (BCMA) systems are recommended to mitigate preventable adverse drug events (ADEs). Our hypothesis was that a BCMA system would reduce preventable ADEs by 45% in a neonatal intensive care unit.
We conducted a prospective, observational, cohort study of a BCMA system intervention in a neonatal intensive care unit. Participants were admitted neonates during 50 weeks. Medication errors and potential or preventable ADEs were detected by a daily structured audit of each subject's medical record, with assignment of an event as a preventable ADE made by blinded assessors. The generalized estimating equation method was used in modeling the targeted, preventable ADE rate with covariates.
A total of 92,398 medication doses were administered to 958 subjects. The generalized estimating equation method yielded a relative risk of preventable ADE when the system was implemented of 0.53 (95% confidence limits 0.29 to 0.91, P = .04), adjusted for log(10)doses of medication/subject/day, a significant predictive covariate (P < .001), as well as for birth weight, sex, Caucasian race, birth cohort number, and nursing hours/subject/day.
The BCMA system reduced the risk of targeted, preventable ADEs by 47%, controlling for the number of medication doses/subject/day, an important risk exposure.
患者面临因用药错误而受到伤害的风险。推荐使用条形码给药系统(BCMA)来减少可预防的药物不良事件(ADEs)。我们的假设是,在新生儿重症监护病房中,BCMA系统可将可预防的ADEs减少45%。
我们在新生儿重症监护病房对BCMA系统干预措施进行了一项前瞻性观察队列研究。研究对象为50周内入院的新生儿。通过每日对每位受试者的病历进行结构化审核来检测用药错误以及潜在的或可预防的ADEs,由不知情的评估人员将事件判定为可预防的ADE。采用广义估计方程法对带有协变量的目标可预防ADE发生率进行建模。
共对958名受试者给予了92398剂药物。广义估计方程法得出,在实施该系统时,经对数(10)剂量的药物/受试者/天(一个显著的预测协变量,P < 0.001)以及出生体重、性别、白种人种族、出生队列编号和护理小时数/受试者/天调整后,可预防ADE的相对风险为0.53(95%置信区间为0.29至0.91,P = 0.04)。
BCMA系统将目标可预防ADE的风险降低了47%,同时控制了药物剂量/受试者/天这一重要风险暴露因素。