使用儿科RSV电子严重程度和结局评分系统(PRESORS)监测婴幼儿呼吸道合胞病毒(RSV)严重程度:初步定量验证的结果

IF 1.8 Q3 HEALTH CARE SCIENCES & SERVICES
Patient Related Outcome Measures Pub Date : 2021-07-23 eCollection Date: 2021-01-01 DOI:10.2147/PROM.S298736
Christine de la Loge, Fatoumata Fofana, Paul Williams, Sarah Rusch, Marita Stevens, Jane Scott
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引用次数: 3

摘要

目的:采用临床医生完成的preors ClinRO和护理人员完成的ObsRO来描述呼吸道合胞病毒(RSV)感染的临床病程。本研究使用临床试验数据对PRESORS的测量特性进行了初步分析。患者和方法:PRESORS ClinRO和ObsRO数据收集于一项为期28天的随机、双盲、1b期试验中,在医院接受RSV感染治疗的婴儿和≤24月龄儿童中使用JNJ-53718678或安慰剂。对PRESORS数据进行评分,并对得分的关键心理测量特性进行评估,包括区分已知群体和检测随时间变化的能力。使用两种响应者定义探索RSV标志的解决时间。结果:在研究中的44名儿童中,PRESORS ClinRO和ObsRO的每日完成率很高(中位数分别为100%和93%)。在基线时观察到严重呼吸道合胞病毒感染的症状,这些症状要么不存在(发绀、发烧、呼吸暂停),要么很少报告(排尿减少/脱水、呕吐)。令人难以置信的ObsRO评分表明,一些护理人员无法准确测量心率。已知组效度得到证实:基于基线ClinRO的健康状况较差的儿童的平均基线综合评分在ObsRO (p=0.001)和ClinRO (p)中均显著差。结论:PRESORS ClinRO和ObsRO可以告知终点,并能够监测儿科试验中RSV的临床病程。改善ClinRO和ObsRO之间的一致性以及确保护理人员能够评估所有体征的修订将在修订后的PRESORS中得到解决。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Monitoring Severity of Respiratory Syncytial Virus (RSV) in Infants and Young Children Using the Pediatric RSV Electronic Severity and Outcome Rating System (PRESORS): Results of Initial Quantitative Validation.

Monitoring Severity of Respiratory Syncytial Virus (RSV) in Infants and Young Children Using the Pediatric RSV Electronic Severity and Outcome Rating System (PRESORS): Results of Initial Quantitative Validation.

Monitoring Severity of Respiratory Syncytial Virus (RSV) in Infants and Young Children Using the Pediatric RSV Electronic Severity and Outcome Rating System (PRESORS): Results of Initial Quantitative Validation.

Monitoring Severity of Respiratory Syncytial Virus (RSV) in Infants and Young Children Using the Pediatric RSV Electronic Severity and Outcome Rating System (PRESORS): Results of Initial Quantitative Validation.

Purpose: PRESORS ClinRO completed by clinicians and ObsRO completed by caregivers were developed to characterize the clinical course of respiratory syncytial virus (RSV) infection. This study describes preliminary analysis of PRESORS' measurement properties using clinical trial data.

Patients and methods: PRESORS ClinRO and ObsRO data were collected in a 28-day randomized, double-blind, Phase 1b trial of JNJ-53718678 or placebo in infants and children ≤24 months of age treated for RSV infection in hospitals. PRESORS data were scored and key psychometric properties of scores were evaluated, including ability to discriminate between known groups and to detect change over time. Time to resolution of RSV signs was explored using two responder definitions.

Results: Daily completion rates for PRESORS ClinRO and ObsRO were high for the 44 children in the study (median: 100% and 93%, respectively). Large floor effects were observed at baseline for signs of severe RSV infection that were either absent (cyanosis, fever, apnea) or rarely reported (reduced urination/dehydration, vomiting). Implausible ObsRO ratings suggested some caregivers could not accurately measure heart rate. Known-group validity was confirmed: children in poor health based on baseline ClinRO had mean baseline composite scores that were significantly worse for both ObsRO (p=0.001) and ClinRO (p<0.001) compared to those with better overall health. ObsRO (p=0.009) and ClinRO (p<0.001) composite scores were responsive to change in overall health status from baseline to Day 3. Mean scores for RSV sign dimensions decreased rapidly from baseline to Day 7 except for coughing and sleep ratings by caregivers. Time to recovery varied greatly depending on definitions used.

Conclusion: PRESORS ClinRO and ObsRO can inform endpoints and enable monitoring the clinical course of RSV in pediatric trials. Improved alignment between ClinRO and ObsRO and revisions ensuring caregivers can assess all signs will be addressed in revised PRESORS.

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Patient Related Outcome Measures
Patient Related Outcome Measures HEALTH CARE SCIENCES & SERVICES-
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4.80%
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审稿时长
16 weeks
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