Humanistic burden of haemophilia A without inhibitors: A cross-sectional analysis of the HemoLIFE study

dc.contributor
Institut Català de la Salut
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[Álvarez-Román MT] Unidad de Trombosis y Hemostasia, Hospital Universitario la Paz, Madrid, Spain. [Nuñez Vazquez RJ] Unidad de Hematología y Hemoterapia, Hospital Universitario Virgen del Rocío, Sevilla, Spain. [Benitez Hidalgo O] Servei d’Hematologia, Vall d’Hebron Hospital Universitari, Barcelona, Spain. [Quintana Paris L] Unidad de Hematología y Hemoterapia, Hospital Universitario de Gran Canaria Doctor Negrín, Las Palmas de Gran Canaria, Spain. [Entrena Ureña L] Servicio de Hematología y Hemoterapia, Hospital Universitario Virgen de las Nieves, Granada, Spain. [Lopez Jaime FJ] Servicio de Hematología y Hemoterapia, Hospital Regional Universitario de Málaga, Málaga, Spain
dc.contributor
Vall d'Hebron Barcelona Hospital Campus
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Quintana Paris, Laura
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Entrena Ureña, Laura
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Álvarez Román, María Teresa
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Nuñez, Ramiro
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Benítez Hidalgo, Olga
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López Jaime, Francisco José
dc.date.accessioned
2025-10-24T10:25:19Z
dc.date.available
2025-10-24T10:25:19Z
dc.date.issued
2024-07-29T13:09:42Z
dc.date.issued
2024-07-29T13:09:42Z
dc.date.issued
2024-07
dc.identifier
Álvarez-Román MT, Nuñez Vazquez RJ, Benitez Hidalgo O, Quintana Paris L, Entrena Ureña L, Lopez Jaime FJ, et al. Humanistic burden of haemophilia A without inhibitors: A cross-sectional analysis of the HemoLIFE study. Haemophilia. 2024 Jul;30(4):950–8.
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1365-2516
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https://hdl.handle.net/11351/11793
dc.identifier
10.1111/hae.15057
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38825766
dc.identifier
001237588100001
dc.identifier.uri
https://hdl.handle.net/11351/11793
dc.description.abstract
Haemophilia A; Productivity; Psychological impact
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Hemofília A; Productivitat; Impacte psicològic
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Hemofilia A; Productividad; Impacto psicológico
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Aim To evaluate the impact of haemophilia A without inhibitors on humanistic outcomes in patients and caregivers. Herein, we report a cross-sectional analysis of the baseline data of persons with haemophilia (PWH) participating in the prospective study HEMOLIFE. Methods These data are part of a prospective, observational, and multicentre study currently being conducted in 20 hospitals in Spain by haematologists. We included subjects 12 years or older diagnosed with haemophilia. The evaluations included the Maladjustment Scale, Haemophilia–Specific Quality of Life Questionnaire for Adults (HaemoQol)/HaemoQol Short Form (Children), haemophilia-specific version of the Work Productivity and Impairment Questionnaire plus the Classroom Impairment Questionnaire (WPAI+CIQ:HS), Haemophilia Activity List (HAL)/Paediatric Haemophilia Activities List (pedHAL), visual analogue scale (VAS) for evaluating pain, Coping Pain Questionnaire–Reduced (CAD-R), and Hospital Anxiety and Depression Scale (HADS). Results A total of 81 PWH were recruited at 18 centres; 66 PWH were ≥18 years (i.e., adults), and PWH 15 were <18 years (i.e., paediatric patients). Out of the 79 evaluable subjects, 16 (20%) showed an impact of haemophilia on daily life, and the areas most affected were “leisure time” (58% showed maladjustment) and “work/studies” (47% showed maladjustment). Patients reported a higher impact of haemophilia on quality of life (mean [SD] of the transformed score) in the dimensions of “sport” (49.4 [28.6]), “physical health” (40.5 [25.8]) and “future” (37.7 [28.9]). In adults, according to HAL scores, greater impairment of function was observed in “lying/sitting/kneeling/standing,” “function of legs” and “leisure activities and sports,” with mean normalized scores of 64.7, 65.1 and 69.0, respectively. Productivity was mostly impacted by presenteeism. The pain was infrequent and moderate. According to the HADS scores, nine (11.5%) patients had clinical anxiety and depression. Conclusion PWH without inhibitors exhibited impairments in adjustment, quality of life and functionality, especially related to leisure and sports activities, and exhibit relevant levels of anxiety and depression.
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RocheFarmaS.A
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application/pdf
dc.language
eng
dc.publisher
Wiley
dc.relation
Haemophilia;30(4)
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https://doi.org/10.1111/hae.15057
dc.rights
Attribution-NonCommercial 4.0 International
dc.rights
http://creativecommons.org/licenses/by-nc/4.0/
dc.rights
info:eu-repo/semantics/openAccess
dc.source
Scientia
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Pacients - Satisfacció
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Qüestionaris
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Hemofília
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Ansietat
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DISEASES::Hemic and Lymphatic Diseases::Hematologic Diseases::Blood Coagulation Disorders::Blood Coagulation Disorders, Inherited::Hemophilia A
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ANALYTICAL, DIAGNOSTIC AND THERAPEUTIC TECHNIQUES, AND EQUIPMENT::Investigative Techniques::Epidemiologic Methods::Data Collection::Surveys and Questionnaires
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HEALTH CARE::Environment and Public Health::Public Health::Epidemiologic Measurements::Demography::Health Status::Quality of Life
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PSYCHIATRY AND PSYCHOLOGY::Behavior and Behavior Mechanisms::Emotions::Anxiety
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ENFERMEDADES::enfermedades hematológicas y linfáticas::enfermedades hematológicas::trastornos de la coagulación sanguínea::trastornos de la coagulación sanguínea hereditarios::hemofilia A
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TÉCNICAS Y EQUIPOS ANALÍTICOS, DIAGNÓSTICOS Y TERAPÉUTICOS::técnicas de investigación::métodos epidemiológicos::recopilación de datos::encuestas y cuestionarios
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ATENCIÓN DE SALUD::ambiente y salud pública::salud pública::medidas epidemiológicas::demografía::estado de salud::calidad de vida
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PSIQUIATRÍA Y PSICOLOGÍA::conducta y mecanismos de la conducta::emociones::ansiedad
dc.title
Humanistic burden of haemophilia A without inhibitors: A cross-sectional analysis of the HemoLIFE study
dc.type
info:eu-repo/semantics/bachelorThesis
dc.type
info:eu-repo/semantics/publishedVersion


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