เปรียบเทียบวิธี

	แบบวัดคุณภาพชีวิตด้านสุขภาพเด็ก (Child Health Questionnaire - CHQ)	PAQLQ	คุณภาพชีวิตในวัยเด็กสำหรับผู้ป่วยลมชัก (QOLCE)
สาขาวิชา	กุมารเวชศาสตร์	กุมารเวชศาสตร์	กุมารเวชศาสตร์
ตระกูล	Process / pipeline	Process / pipeline	Process / pipeline
ปีกำเนิด	1996	1996	2000
ผู้ริเริ่ม	John M. Landgraf	E. F. Juniper	Mark Sabaz
ประเภท	Parent report (primary) and child self-report versions available	Child self-report; parent version available	Parent report; child self-report version available
แหล่งต้นตำรับ	Landgraf, J. M., Abetz, L., & Ware, J. E. (1996). The CHQ User's Manual. HealthAct. ISBN: 978-0965475303	Juniper, E. F., Guyatt, G. H., Feeny, D. H., Ferrie, P. J., Griffith, L. E., & Townsend, M. (1996). Measuring quality of life in children with asthma. Quality of Life Research, 5(1), 35-46.	Sabaz, M., Cairns, D. R., Lah, S., Williams, B., Gurrin, L., Connelly, A., & Berkovic, S. F. (2000). Validation of the Quality of Life in Childhood Epilepsy Questionnaire in Australian children with newly diagnosed and chronic epilepsy. Neurology, 55(9), 1646-1652.
ชื่อเรียกอื่น	CHQ-50, CHQ-28, CHQ-PF28, CHQ-CF87	PAQLQ-S	QOL in Childhood Epilepsy Questionnaire
ที่เกี่ยวข้อง	4	4	4
สรุป	The Child Health Questionnaire is a generic, parent-reported instrument developed by Landgraf et al. in 1996 to measure health-related quality of life in children aged 5–18 years. Unlike disease-specific measures, the CHQ captures broad domains of physical, emotional, social, and school functioning, making it suitable for diverse pediatric populations with or without chronic conditions. The CHQ-50 is the most widely used parent-report form; shorter (CHQ-28) and comprehensive (CHQ-CF87 child + family) versions are also available.	The PAQLQ is a 23-item self-report instrument developed by Juniper et al. in 1996 to measure quality of life in children aged 7–17 years with asthma. It assesses how asthma and its treatment affect daily functioning, emotions, and activity levels. The instrument has become the gold standard for evaluating asthma-specific health-related quality of life in pediatric populations.	The QOLCE is a comprehensive 76-item disease-specific instrument developed by Sabaz et al. in 2000 to assess quality of life in children with epilepsy aged 4–16 years. Measuring across 16 distinct domains including seizure worry, cognitive concerns, medication effects, school/peer functioning, and family impact, the QOLCE provides a nuanced profile of how epilepsy and its treatment affect daily life. It exists in parent-report (QOLCE-P) and child self-report (QOLCE-C) versions.