Quality of life in haemophilia A: Hemophilia Utilization Group Study Va (HUGS-Va)
| Autor: | Cassie Ross, Joanne Wu, Ann D. Forsberg, Brenda Riske, M. Lou, J.L. Poon, Jason N. Doctor, Z.Y. Zhou, M. Ullman, Randall Curtis, Marion A. Koerper, F. Gwadry-Sridhar, Kathleen A. Johnson, K. L. Parish |
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| Rok vydání: | 2012 |
| Předmět: |
education.field_of_study
medicine.medical_specialty Pediatrics business.industry Population Haemophilia A Hematology General Medicine Haemophilia medicine.disease humanities Quality of life Joint pain Severity of illness medicine Physical therapy medicine.symptom education business Psychosocial Genetics (clinical) Cohort study |
| Zdroj: | Haemophilia. 18:699-707 |
| ISSN: | 1351-8216 |
| DOI: | 10.1111/j.1365-2516.2012.02791.x |
| Popis: | This study describes health-related quality of life (HRQoL) of persons with haemophilia A in the United States (US) and determines associations between self-reported joint pain, motion limitation and clinically evaluated joint range of motion (ROM), and between HRQoL and ROM. As part of a 2-year cohort study, we collected baseline HRQoL using the SF-12 (adults) and PedsQL (children), along with self-ratings of joint pain and motion limitation, in persons with factor VIII deficiency recruited from six Haemophilia Treatment Centres (HTCs) in geographically diverse regions of the US. Clinically measured joint ROM measurements were collected from medical charts of a subset of participants. Adults (N = 156, mean age: 33.5 ± 12.6 years) had mean physical and mental component scores of 43.4 ± 10.7 and 50.9 ± 10.1, respectively. Children (N = 164, mean age: 9.7 ± 4.5 years) had mean total PedsQL, physical functioning, and psychosocial health scores of 85.9 ± 13.8, 89.5 ± 15.2, and 84.1 ± 15.3, respectively. Persons with more severe haemophilia and higher self-reported joint pain and motion limitation had poorer scores, particularly in the physical aspects of HRQoL. In adults, significant correlations (P < 0.01) were found between ROM measures and both self-reported measures. Except among those with severe disease, children and adults with haemophilia have HRQoL scores comparable with those of the healthy US population. The physical aspects of HRQoL in both adults and children with haemophilia A in the US decrease with increasing severity of illness. However, scores for mental aspects of HRQoL do not differ between severity groups. These findings are comparable with those from studies in European and Canadian haemophilia populations. |
| Databáze: | OpenAIRE |
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