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Reliability and validity of observer ratings of pain using the visual analog scale (VAS) in infants undergoing immunization injections.

机译:使用视觉模拟量表(VAS)对接受免疫注射的婴儿进行的疼痛观察者评分的信度和效度。

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We tested the reliability and validity of observer-rated pain in infants undergoing immunization using the visual analog scale (VAS). Pain was assessed in real time and later, from videotapes, in 120 1-year-old infants participating in a double-blind randomized controlled trial of amethocaine vs. placebo. Altogether, 2 (1 physician, 1 non-physician) of 4 raters [2 physicians, 2 non-physicians (nurse and graduate student)] independently assessed baseline and vaccine injection pain using a 100mm unmarked VAS line. Intra- and inter-rater reliability, assessed using the intra-class correlation coefficient (ICC), ranged from 0.69 to 0.91 and 0.55 to 0.97, respectively. Bland-Altman plots demonstrated no evidence of bias between real time and video assessments. When scores were dichotomized into 2 groups (no pain and pain) using a cut-off of >or=30mm, intra-rater reliability ranged from 0.35 to 0.92. The percent of scores deviating by >20mm was 4.5-14.29%. Criterion validity was demonstrated by correlations between the VAS and Modified Behavioural Pain Scale, a validated observational measure; (rho: 0.81-0.94). Injection scores were lower in the amethocaine group, when comparing difference (baseline-injection) or dichotomized scores; significance (p<0.036) was achieved for non-physician scores, but not physician scores. Together, these results provide initial support for the VAS as an outcome measure for acute procedural pain in infants. However, different conclusions may be reached about the effectiveness of analgesic interventions depending on the rater. Sources of variability include use of multiple raters, rater focus (procedure vs. child) and experience level.
机译:我们使用视觉模拟量表(VAS)测试了接受免疫接种的婴儿的观察者额定疼痛的可靠性和有效性。实时评估了疼痛,后来通过录像带对参加了Amethocaine与安慰剂双盲随机对照试验的120名1岁婴儿进行了录像。总共有4位评估者中的2位(1位医师,1位非医师)[2位医师,2位非医师(护士和研究生)]使用100mm无标记VAS线独立评估了基线和疫苗注射疼痛。使用组内相关系数(ICC)评估的评定者内部和评定者之间的可靠性分别为0.69至0.91和0.55至0.97。 Bland-Altman图没有显示实时评估和视频评估之间存在偏差的证据。当使用大于或等于30mm的分界线将得分分为2组(无痛苦和无痛苦)时,评定者的信度在0.35至0.92之间。分数偏离> 20mm的百分比为4.5-14.29%。通过VAS与经修正的行为疼痛量表(一种经过验证的观察指标)之间的相关性来证明标准的有效性。 (rho:0.81-0.94)。比较差异(基线注射)或二分法得分时,氨甲卡因组的注射得分较低。非医师评分达到显着性(p <0.036),但医师评分未达到。总之,这些结果为VAS提供了初步的支持,将其作为婴儿急性程序性疼痛的结局指标。但是,根据评分者的不同,关于镇痛措施的有效性可能会得出不同的结论。变异性的来源包括使用多个评估者,评估者重点(过程与儿童)和经验水平。

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