Department of Anaesthesiology, Faculty of Medical and Health Sciences, University of Auckland, Private Bag 92019, Auckland, 1142, New Zealand.
Can J Anaesth. 2013 Oct;60(10):990-7. doi: 10.1007/s12630-013-0003-y. Epub 2013 Aug 9.
Anesthesia information management system (AIMS) technology is designed to facilitate high-quality anesthetic recordkeeping. We examined the hypothesis that no difference exists between AIMS and handwritten anesthetic records in regard to the completeness of important information contained as text data. We also investigated the effect of observational research on the completeness of anesthesiologists' recordkeeping.
As part of a larger randomized controlled trial, participants were randomized to produce 400 anesthetic records, either handwritten (n = 200) or using an AIMS (n = 200). Records were assessed against a 32-item checklist modified from a clinical guideline. Intravenous agent and bolus recordings were quantified, and data were compared between handwritten and AIMS records. Records produced with intensive research observation during the initial phase of the study (n = 200) were compared with records produced with reduced intensity observation during the final phase of the study (n = 200).
The AIMS records were more complete than the handwritten records (mean difference 7.1%; 95% confidence interval [CI] 5.6 to 8.6%; P < 0.0001), with higher completion rates for six individual items on the checklist (P < 0.0001). Drug annotation data were equal between arms. The records completed early in the study, during a period of more intense observation, were more thorough than subsequent records (87.3% vs 81.6%, respectively; mean difference 5.7%; 95% CI 4.2 to 7.3%; P < 0.0001).
The AIMS records were more complete than the handwritten records for 32 predefined items. The potential of observational research to influence professional behaviour in an anesthetic context was confirmed. This trial was registered at the Australian New Zealand Clinical Trials Registry No 12608000068369.
麻醉信息管理系统(AIMS)技术旨在促进高质量的麻醉记录保存。我们假设,在包含文本数据的重要信息的完整性方面,AIMS 与手写麻醉记录之间没有差异。我们还研究了观察性研究对麻醉医生记录完整性的影响。
作为一项更大的随机对照试验的一部分,参与者被随机分配生成 400 份麻醉记录,手写(n=200)或使用 AIMS(n=200)。记录根据从临床指南修改的 32 项检查表进行评估。静脉内药物和推注记录进行了量化,并在手写和 AIMS 记录之间进行了比较。在研究的初始阶段进行强化研究观察(n=200)生成的记录与在研究的最后阶段进行降低强度观察(n=200)生成的记录进行了比较。
AIMS 记录比手写记录更完整(平均差异 7.1%;95%置信区间 [CI] 5.6 至 8.6%;P<0.0001),检查表上六个单独项目的完成率更高(P<0.0001)。药物注释数据在两组之间相等。在研究早期进行的、观察强度更高的记录比后续记录更全面(分别为 87.3%和 81.6%;平均差异 5.7%;95%CI 4.2 至 7.3%;P<0.0001)。
在 32 个预定义项目中,AIMS 记录比手写记录更完整。观察性研究在麻醉环境中影响专业行为的潜力得到了证实。该试验在澳大利亚新西兰临床试验注册中心注册,编号为 12608000068369。