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

Author:

Álvarez‐Román María Teresa1ORCID,Nuñez Vazquez Ramiro Jose2ORCID,Benitez Hidalgo Olga3,Quintana Paris Laura4,Entrena Ureña Laura5,Lopez Jaime Francisco Jose6,la De Corte‐Rodríguez Hortensia78,García Dasí María9ORCID,Bosch Pau10,Mingot Castellano María Eva11ORCID,Guerra Garaeta Itziar12,Soto‐Ortega Inmaculada13ORCID

Affiliation:

1. Unidad de Trombosis y Hemostasia Hospital Universitario la Paz Madrid Spain

2. Unidad de Hematología y Hemoterapia Hospital Universitario Virgen del Rocío Sevilla Spain

3. Servicio de Hematología Vall d'Hebron Barcelona Hospital Campus Barcelona Spain

4. Unidad de Hematología y Hemoterapia Hospital Universitario de Gran Canaria Doctor Negrín Las Palmas de Gran Canaria Spain

5. Servicio de Hematología y Hemoterapia Hospital Universitario Virgen de las Nieves Granada Spain

6. Servicio de Hematología y Hemoterapia Hospital Regional Universitario de Málaga Málaga Spain

7. Physical and Rehabilitation Medicine Department La Paz University Hospital Madrid Spain

8. IdiPAZ Institute for Health Research Madrid Spain

9. General Health Psychologist Freelance Independent Consultor Valencia Spain

10. Unidad de Trombosis y Hemostasia Hospital Universitario y Politécnico de La Fe Valencia Spain

11. Servicio de Hematología Hospital Universitario Virgen del Rocío Instituto de Biomedicina de Sevilla Sevilla Spain

12. Medical Expert Hemophilia & Rare Blood Disorders Roche Farma S.A. Madrid Spain

13. Sección de Hemostasia y Trombosis Hospital Universitario Central de Asturias Oviedo Spain

Abstract

AbstractAimTo 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.MethodsThese 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).ResultsA 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.ConclusionPWH 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.

Publisher

Wiley

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