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儿童癫痫不良反应问卷的编制与验证。

Development and validation of the Pediatric Epilepsy Side Effects Questionnaire.

机构信息

Division of Neurology, Cincinnati Children’s Hospital Medical Center, Cincinnati, OH,

出版信息

Neurology. 2012 Sep 18;79(12):1252-8. doi: 10.1212/WNL.0b013e3182635b87. Epub 2012 Aug 8.

Abstract

OBJECTIVE

To develop and validate a measure of antiepileptic drug (AED) side effects in children with a variety of seizure types, treatments, and therapy durations.

METHODS

Content for an initial 44-item measure was developed using the previously published Hague Scale and expert opinion from recognized pediatric epileptologists (n = 12) and caregivers of children with epilepsy (n = 21). The measure was completed by caregivers during routine clinic visits. Demographic and medical data were collected through chart reviews. Factor analysis was conducted and internal consistency, test-retest reliability, and construct validity were assessed.

RESULTS

Questionnaires were analyzed from 495 children with epilepsy (M(age) = 10.1 years; range 2-21 years; 42% female; 14% African American; 32% new onset vs 68% chronic epilepsy). The final questionnaire, the Pediatric Epilepsy Side Effects Questionnaire (PESQ), is a 19-item measure with 5 subscales (i.e., cognitive, motor, behavioral, general neurological, and weight) that accounts for 99% of the variance. Internal consistency coefficients and test-retest reliabilities ranged from 0.72 to 0.93 and 0.74 to 0.97, respectively. Construct validity was demonstrated by increasing side effects as the number of drugs increased. Participants on valproic acid had significantly higher scores on the Weight Scale compared to those on carbamazepine.

CONCLUSIONS

The PESQ is a reliable and valid measure of AED side effects in children across the epilepsy spectrum that can be used in both clinical and research settings.

摘要

目的

开发并验证一种用于评估各种发作类型、治疗方法和治疗持续时间的儿童抗癫痫药物(AED)副作用的测量工具。

方法

使用先前发表的 Hague 量表和来自知名儿科癫痫专家(n=12)和癫痫患儿照顾者(n=21)的专家意见,为最初的 44 项措施制定内容。照顾者在常规就诊期间完成该测量。通过病历回顾收集人口统计学和医疗数据。进行了因子分析,并评估了内部一致性、重测信度和结构有效性。

结果

对 495 名癫痫患儿(M(年龄)=10.1 岁;范围 2-21 岁;42%为女性;14%为非裔美国人;14%为新发病例,68%为慢性癫痫)的问卷进行了分析。最终的问卷是儿科癫痫副作用问卷(PESQ),它是一个 19 项的测量工具,有 5 个分量表(即认知、运动、行为、一般神经和体重),占总方差的 99%。内部一致性系数和重测信度范围分别为 0.72 至 0.93 和 0.74 至 0.97。结构有效性通过随着药物数量的增加而增加副作用来证明。与使用卡马西平相比,使用丙戊酸钠的患者在体重量表上的得分明显更高。

结论

PESQ 是一种可靠且有效的评估儿童癫痫谱中 AED 副作用的测量工具,可用于临床和研究环境。

相似文献

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Development and validation of the Pediatric Epilepsy Side Effects Questionnaire.儿童癫痫不良反应问卷的编制与验证。
Neurology. 2012 Sep 18;79(12):1252-8. doi: 10.1212/WNL.0b013e3182635b87. Epub 2012 Aug 8.
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Validation of the Azeri version of the Pediatric Epilepsy Side Effects Questionnaire.阿塞拜疆语版儿童癫痫副作用问卷的验证
Childs Nerv Syst. 2019 Dec;35(12):2379-2383. doi: 10.1007/s00381-019-04287-w. Epub 2019 Jul 6.

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