قارن الطرق

	استبيان جودة الحياة لربو الأطفال (PAQLQ)	وحدة PedsQL لمرض فقر الدم المنجلي
المجال	طب الأطفال	طب الأطفال
العائلة	Process / pipeline	Process / pipeline
سنة النشأة	1996	2012
صاحب الطريقة	E. F. Juniper	James W. Varni
النوع	Child self-report; parent version available	Child self-report and parent proxy
المصدر التأسيسي	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.	Varni, J. W., Limbers, C. A., Bryant, W. P., & Wilson, D. P. (2012). The PedsQL in pediatric sickle cell disease: Measurement model, factor structure, and reliability and validity of the pediatric quality of life inventory sickle cell disease module. Journal of Health Psychology, 17(7), 1012-1024.
الأسماء البديلة	PAQLQ-S	PedsQL 3.0 Sickle Cell
ذات صلة	4	4
الملخص	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 PedsQL Sickle Cell Disease Module is a disease-specific instrument developed by Varni et al. in 2012 to measure quality of life in children and adolescents with sickle cell disease aged 2–18 years. Measuring across domains including pain and symptoms, functional limitations, school impact, and disease-related worry, it captures how sickle cell disease and its complications affect daily life and well-being. Used alongside the PedsQL Generic Core Scales, it provides comprehensive assessment of sickle cell disease-specific and general health-related quality of life.