Jones Aubrey N, Miller Jamie L, Neely Stephen, Ibach Bethany W, Hagemann Tracy M, Golding Charles L, Lewis Teresa V, Peek Leigh A, Johnson Peter N
J Pediatr Pharmacol Ther. 2017 Jul-Aug;22(4):286-292. doi: 10.5863/1551-6776-22.4.286.
This study aims to determine the prevalence and factors associated with unrounded doses ordered via a computerized prescriber order entry (CPOE) system among children during a 1-week reference period.
This retrospective, cross-sectional study included children younger than 18 years admitted during a 7-day period. An unrounded dose was defined as an unrounded actual dose (eg, dose calculated to the tenths place for non-neonatal intensive care (non-NICU) patients and dose calculated to the hundredth place for NICU patients) or unrounded volume per dose [eg, <0.1 mL for non-NICU patients and <0.01 mL for NICU patients]. A multilevel logistic regression model was used to determine the prevalence and factors associated with unrounded doses via a CPOE system with adjustment for clustering effects.
A total of 395 patients were admitted with 391 receiving medications. The overall prevalence of unrounded doses was 30% among the 2426 doses administered. Patients on the NICU team had the highest prevalence of unrounded doses. The odds of an unrounded dose were 4% (adjusted odds ratio, 0.96; 95% confidence interval, 0.94-0.98) lower with each additional kilogram increase in weight after controlling for age, route, scheduled versus as-needed administration, and cluster effects.
The prevalence of unrounded doses was higher than in previous studies. It was higher in smaller children after controlling for age, medication-related variables, and clustering. Future studies should focus on the role of CPOE in preventing unrounded and unmeasurable doses and if these strategies affect clinical outcomes (eg, adverse drug events).
本研究旨在确定在为期1周的参考期内,通过计算机医嘱录入(CPOE)系统为儿童开具的非整数剂量医嘱的发生率及相关因素。
这项回顾性横断面研究纳入了7天内入院的18岁以下儿童。非整数剂量定义为非整数实际剂量(例如,非新生儿重症监护病房(非NICU)患者剂量计算到十分位,NICU患者剂量计算到百分位)或每剂非整数体积[例如,非NICU患者<0.1 mL,NICU患者<0.01 mL]。采用多水平逻辑回归模型确定通过CPOE系统开具的非整数剂量的发生率及相关因素,并对聚类效应进行校正。
共收治395例患者,其中391例接受了药物治疗。在2426剂给药中,非整数剂量的总体发生率为30%。NICU团队的患者非整数剂量发生率最高。在控制年龄、给药途径、定时给药与按需给药以及聚类效应后,体重每增加1千克,非整数剂量的几率降低4%(校正优势比,0.96;95%置信区间,0.94 - 0.98)。
非整数剂量的发生率高于以往研究。在控制年龄、药物相关变量和聚类后,年幼儿童中的发生率更高。未来的研究应关注CPOE在预防非整数和不可测量剂量方面的作用,以及这些策略是否会影响临床结局(如药物不良事件)。