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| PedMIDAS: Skala oceny niepełnosprawności w migrenie u dzieci× | Jakość Życia w Padaczce Dziecięcej (QOLCE)× | |
|---|---|---|
| Dziedzina | Pediatria | Pediatria |
| Rodzina | Process / pipeline | Process / pipeline |
| Rok powstania≠ | 2001 | 2000 |
| Twórca≠ | Amy D. Hershey | Mark Sabaz |
| Typ≠ | Parent-report and/or child self-report of missed activities | Parent report; child self-report version available |
| Źródło pierwotne≠ | Hershey, A. D., Powers, S. W., Vockell, A. L., LeCates, S., & Ellinwood, E. H. (2001). PedMIDAS: Development of a questionnaire to assess disabilities in migrainous children. Headache, 41(6), 556-563. DOI ↗ | 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. DOI ↗ |
| Inne nazwy≠ | Pediatric Migraine Disability Assessment, MIDAS, MIDAS Pediatric | QOL in Childhood Epilepsy Questionnaire |
| Pokrewne | 4 | 4 |
| Podsumowanie≠ | The PedMIDAS is a brief 6-item parent-report (with child input for older youth) instrument developed by Hershey et al. in 2001 to quantify migraine-related functional disability in children and adolescents. Rather than measuring pain intensity or headache frequency, the PedMIDAS focuses on the ultimate impact of migraine on daily life: how many days of school, sports/play, and family activities does the child miss or participate in only with significant limitation? This outcome-focused approach makes it particularly useful for assessing the real-world burden of migraine in children and evaluating treatment effectiveness. | 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. |
| ScholarGateZbiór danych ↗ |
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