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Cuestionario de Impacto de la Fibromialgia×Cuestionario de Insuficiencia Cardíaca Crónica×
CampoResultados en saludResultados en salud
FamiliaProcess / pipelineProcess / pipeline
Año de origen19912000
Autor originalCynthia S. Burckhardt et al.Luc Guyonnet et al.
TipoSelf-report symptom and functional impairment questionnaireSelf-report quality of life questionnaire
Fuente seminalBurckhardt, C. S., Clark, S. R., & Bennett, R. M. (1991). The Fibromyalgia Impact Questionnaire: Development and validation. The Journal of Rheumatic Diseases, 18(5), 728-735. link ↗Guyonnet, S., Vellas, B., Garry, P. J., & Albarede, J. L. (2000). The Chronic Heart Failure Questionnaire: A pilot study of validity, reliability, and responsiveness. Journal of Cardiac Failure, 6(1), 21-26. link ↗
AliasFIQ, Fibromyalgia Impact, Fibromyalgia QuestionnaireCHQ, Heart Failure Quality of Life, Chronic Heart Failure QoL
Relacionados44
ResumenThe FIQ is the most widely used patient-reported outcome measure for fibromyalgia disease burden. Developed by Cynthia Burckhardt and colleagues in 1991, this 10-item questionnaire quantifies how fibromyalgia affects physical function, work capacity, depression, anxiety, sleep, pain, and fatigue. The revised version (FIQR, 21 items) offers enhanced psychometric properties and is the current standard in fibromyalgia clinical trials and practice.The CHQ is a disease-specific quality of life measure for chronic heart failure (CHF). Developed by Luc Guyonnet and colleagues in 2000, this 20-item questionnaire assesses how heart failure affects dyspnea, fatigue, emotional function, and activity limitation. It is used in heart failure clinical trials and research to quantify patient-experienced burden and treatment benefit.
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ScholarGateComparar métodos: FIQ · CHQ. Recuperado el 2026-06-19 de https://scholargate.app/es/compare