AdventHealth Whole-Person Research, Orlando, Florida.
AdventHealth for Children, Orlando, Florida.
Pain Manag Nurs. 2020 Apr;21(2):172-178. doi: 10.1016/j.pmn.2019.07.012. Epub 2019 Sep 7.
The Pediatric Critical-Care Observation Tool (P-CPOT) is an adaption of the Critical-Care Pain Observation Tool (CPOT) originally designed to assess pain in nonverbal critically-ill adults.
The study validated the P-CPOT in assessing nociceptive procedure pain in pediatric intensive care unit (PICU) children who are unable to verbalize pain.
Content validity was tested using a two-round expert panel review with 8 experts. With a sample of 78 PICU patients, prospective repeated measures were designed to detect the change over time at pre- (T1), during (T2), and post- (T3) for routinely scheduled nociceptive procedures. Each measure was independently completed by two raters using two scales, the P-CPOT and the FLACC (Faces, Legs, Activity, Cry and Consolability).
All categories had Item-level content validity indices of 0.88 to 1.00. A one-factor structure containing 5 items was established and accounted for 85% variance in P-CPOT scores. Inter-rater reliability was substantial with correlation coefficient of 0.996 and Kappa value of 0.90. A threshold value of 4 resulted in excellent balance between sensitivity (98.6%) and specificity (97.6%). Both tools detected the score changes over time (p = .025). P-CPOT had a larger effect size (Cohen's d = 4.1) as well as a higher score than FLACC at T2 (p = .039). Linear regression revealed that patients being ventilated tended to have a P-CPOT score of 1.1 higher than the FLACC score while controlling for heart rates (p < .001), meaning that P-CPOT is more sensitive than FLACC for detecting pain increase during nociceptive procedures in ventilated patients.
The P-CPOT is a valid scale for assessing pain in PICU patients with very good psychometric performance. It is especially adept in detecting pain in ventilated patients.
儿科重症监护观察工具(P-CPOT)是最初设计用于评估非语言重症成人疼痛的重症监护疼痛观察工具(CPOT)的改编版。
本研究旨在验证 P-CPOT 在评估无法表达疼痛的儿科重症监护病房(PICU)患儿的伤害性程序疼痛中的有效性。
采用两轮专家小组评估进行内容效度测试,共有 8 名专家参与。对 78 名 PICU 患者进行了前瞻性重复测量设计,以检测常规安排的伤害性程序在术前(T1)、术时(T2)和术后(T3)的时间变化。两位评估者使用两种量表(P-CPOT 和 FLACC(面部、腿部、活动、哭泣和安慰))独立完成每项测量。
所有类别均具有 0.88 至 1.00 的项目水平内容效度指数。建立了一个包含 5 个项目的单因素结构,占 P-CPOT 评分的 85%。评分者间信度较高,相关系数为 0.996,Kappa 值为 0.90。阈值为 4 时,灵敏度(98.6%)和特异性(97.6%)之间达到了良好的平衡。两种工具均检测到评分随时间的变化(p =.025)。P-CPOT 在 T2 时具有更大的效应量(Cohen's d = 4.1)和比 FLACC 更高的评分(p =.039)。线性回归显示,在控制心率的情况下,与 FLACC 相比,接受通气的患者的 P-CPOT 评分平均高 1.1 分(p <.001),这意味着 P-CPOT 比 FLACC 更能敏感地检测到通气患者在伤害性程序中疼痛的增加。
P-CPOT 是一种评估 PICU 患儿疼痛的有效量表,具有很好的心理测量性能。它尤其擅长检测通气患者的疼痛。