A smartphone version of the Faces Pain Scale-Revised and the Color Analog Scale for postoperative pain assessment in children

被引:36
|
作者
Sun, Terri [1 ,2 ]
West, Nicholas [1 ,2 ]
Ansermino, J. Mark [1 ,2 ]
Montgomery, Carolyne J. [1 ,2 ]
Myers, Dorothy [1 ,2 ]
Dunsmuir, Dustin [1 ,2 ]
Lauder, Gillian R. [1 ,2 ]
von Baeyer, Carl L. [3 ,4 ,5 ]
机构
[1] BC Childrens Hosp, Dept Pediat Anesthesia, Vancouver, BC V5Z 4H4, Canada
[2] Univ British Columbia, Dept Anesthesiol Pharmacol & Therapeut, Vancouver, BC V5Z 1M9, Canada
[3] Univ Saskatchewan, Dept Psychol, Saskatoon, SK S7N 0W0, Canada
[4] Univ Saskatchewan, Dept Pediat, Saskatoon, SK, Canada
[5] Univ Manitoba, Fac Med, Winnipeg, MB, Canada
关键词
adolescent; child; pain measurement; methods; standards; self-report; CLINICALLY SIGNIFICANT CHANGES; SELF-REPORT; INITIAL VALIDATION; PEDIATRIC PAIN; INTENSITY; AGREEMENT; VALIDITY; DIARIES;
D O I
10.1111/pan.12790
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
BackgroundEffective pain assessment is essential during postoperative recovery. Extensive validation data are published supporting the Faces Pain Scale-Revised (FPS-R) and the Color Analog Scale (CAS) in children. Panda is a smartphone-based application containing electronic versions of these scales. ObjectivesTo evaluate agreement between Panda and original paper/plastic versions of the FPS-R and CAS and to determine children's preference for either Panda or original versions of these scales. MethodsASA I-III children, 4-18years, undergoing surgery were assessed using both Panda and original versions of either the FPS-R or CAS. Pain assessments were conducted within 10min of waking from anesthesia and 30min later. ResultsSixty-two participants, median (range) age 7.5 (4-12) years, participated in the FPS-R trial; Panda scores correlated strongly with the original scores at both time points (Pearson's r>0.93) with limits of agreement within clinical significance (80% CI). Sixty-six participants, age 13 (5-18) years, participated in the CAS trial. Panda scores correlated strongly with the original scores at both time points (Pearson's r>0.87); mean pain scores were higher (up to +0.47 out of 10) with Panda than with the original tool, representing a small systematic bias, but limits of agreement were within clinical significance. Most participants who expressed a preference preferred Panda over the original tool (81% of FPS-R, 76% of CAS participants). ConclusionThe Panda smartphone application can be used in lieu of the original FPS-R and CAS for assessment of pain in children. Children's preference for Panda may translate to improved cooperation with self-report of pain.
引用
收藏
页码:1264 / 1273
页数:10
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