Usability of a perioperative medication-related clinical decision support software application: a randomized controlled trial

被引:8
|
作者
Nanji, Karen C. [1 ,2 ,3 ]
Garabedian, Pamela M. [3 ]
Langlieb, Marin E. [1 ]
Rui, Angela [3 ]
Tabayoyong, Leo L. [4 ]
Sampson, Michael [5 ]
Deng, Hao [1 ]
Boxwala, Aziz [6 ]
Minehart, Rebecca D. [1 ,2 ,3 ,5 ]
Bates, David W. [2 ,3 ,7 ,8 ]
机构
[1] Massachusetts Gen Hosp, Dept Anesthesia Crit Care & Pain Med, 55 Fruit St, Boston, MA 02114 USA
[2] Harvard Med Sch, Boston, MA 02115 USA
[3] Mass Gen Brigham Inc, Somerville, MA USA
[4] Massachusetts Gen Hosp, Dept Pharm, Boston, MA 02114 USA
[5] Massachusetts Gen Hosp, Learning Lab, Boston, MA 02114 USA
[6] Elimu Informat Inc, La Jolla, CA USA
[7] Brigham & Womens Hosp, Dept Med, Div Gen Internal Med, 75 Francis St, Boston, MA 02115 USA
[8] Harvard Sch Publ Hlth, Dept Hlth Policy & Management, Boston, MA USA
基金
美国医疗保健研究与质量局;
关键词
clinical decision support systems; drug safety; anesthesia; usability testing; randomized controlled trial; ADVERSE DRUG EVENTS; PHYSICIAN ORDER ENTRY; HOSPITALIZED-PATIENTS; ERRORS; ANESTHESIA; IMPACT; IMPLEMENTATION; PRESSURE; OUTCOMES; SURGERY;
D O I
10.1093/jamia/ocac035
中图分类号
TP [自动化技术、计算机技术];
学科分类号
0812 ;
摘要
Objective We developed a comprehensive, medication-related clinical decision support (CDS) software prototype for use in the operating room. The purpose of this study was to compare the usability of the CDS software to the current standard electronic health record (EHR) medication administration and documentation workflow. Materials and Methods The primary outcome was the time taken to complete all simulation tasks. Secondary outcomes were the total number of mouse clicks and the total distance traveled on the screen in pixels. Forty participants were randomized and assigned to complete 7 simulation tasks in 1 of 2 groups: (1) the CDS group (n = 20), who completed tasks using the CDS and (2) the Control group (n = 20), who completed tasks using the standard medication workflow with retrospective manual documentation in our anesthesia information management system. Blinding was not possible. We video- and audio-recorded the participants to capture quantitative data (time on task, mouse clicks, and pixels traveled on the screen) and qualitative data (think-aloud verbalization). Results The CDS group mean total task time (402.2 +/- 85.9 s) was less than the Control group (509.8 +/- 103.6 s), with a mean difference of 107.6 s (95% confidence interval [CI], 60.5-179.5 s, P < .001). The CDS group used fewer mouse clicks (26.4 +/- 4.5 clicks) than the Control group (56.0 +/- 15.0 clicks) with a mean difference of 29.6 clicks (95% CI, 23.2-37.6, P < .001). The CDS group had fewer pixels traveled on the computer monitor (59.5 +/- 20.0 thousand pixels) than the Control group (109.3 +/- 40.8 thousand pixels) with a mean difference of 49.8 thousand pixels (95% CI, 33.0-73.7, P < .001). Conclusions The perioperative medication-related CDS software prototype substantially outperformed standard EHR workflow by decreasing task time and improving efficiency and quality of care in a simulation setting.
引用
收藏
页码:1416 / 1424
页数:9
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