Generic and disease-specific quality of life among youth and young men with Hemophilia in Canada.

Q2 Medicine
BMC Hematology Pub Date : 2016-05-05 eCollection Date: 2016-01-01 DOI:10.1186/s12878-016-0052-x
J St-Louis, D J Urajnik, F Ménard, S Cloutier, R J Klaassen, B Ritchie, G E Rivard, M Warner, V Blanchette, N L Young
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引用次数: 20

Abstract

Background: This study was undertaken to explore the longitudinal patterns of health-related quality of life (HRQoL) among youth and young adults with Hemophilia A (HA) over a 3-year period. This report presents the baseline characteristics of the study cohort.

Methods: Males, 14 to 29 years of age, with predominantly severe HA were recruited from six treatment centres in Canada. Subjects completed a comprehensive survey. HRQoL was measured using: the CHO-KLAT2.0 (youth), Haemo-QoL-A (young adults) and the SF-36v2 (all).

Results: 13 youth (mean age = 15.7, range = 12.9-17.9 years) and 33 young adults (mean age = 23.6; range = 18.4 -28.7 years) with moderate (7 %) and severe (93 %) HA were enrolled. All were on a prophylactic regimen with antihemophilic factor (Helixate FS®) during the study. The youth had minimal joint damage (mean HJHS = 5.2) compared to young adults (mean HJHS = 13.3). The mean HRQoL scores for youth were: 79.2 (SD = 11.9) for the CHO-KLAT, and 53.0 (5.5) and 52.3 (6.8) for the SF-36 Physical Component Summary (PCS) and Mental Component Summary (MCS) scores respectively. The mean HRQoL scores for young adults were: 85.8 (9.5) for the Haemo-Qol-A, and 50.8 (6.4) and 50.9 (8.8) for PCS and MCS respectively. PCS and MCS scores were comparable to published Canadian norms, however significant differences were found for the domains of Physical Functioning and Bodily Pain. The disease-specific HRQoL scores were weakly correlated with the PCS for youth (CHO-KLAT vs. PCS r = 0.28, p = 0.35); and moderately correlated for the MCS (r = 0.39, p = 0.19). Haemo-QoL-A scores for young adults were strongly correlated with the PCS (r = 0.53, p = 0.001); and weakly correlated with the MCS (r = 0.26, p = 0.13). Joint status as assessed by HJHS was correlated with PCS scores. A history of lifelong prophylaxis resulted in better PCS but worse MCS scores.

Conclusion: Despite having hemophilia, the youth in this cohort have minimal joint disease and good HRQoL. The young adults demonstrated more joint disease and slightly worse HRQoL in the domains of physical functioning and pain. The data presented here provide new information to inform the selection of Health Related Quality of Life (HRQoL) instruments for use in future clinical trials involving persons with hemophilia.

Trial registration: ClinicalTrials.gov : NCT01034904. Study funded by CSL Behring Canada.

Abstract Image

加拿大青年和年轻男性血友病患者的一般和疾病特异性生活质量
背景:本研究旨在探讨青年和青年血友病A (HA)患者在3年期间与健康相关的生活质量(HRQoL)的纵向模式。本报告介绍了研究队列的基线特征。方法:从加拿大6个治疗中心招募年龄在14 - 29岁的男性,主要患有严重HA。受试者完成全面调查。HRQoL采用CHO-KLAT2.0(青年)、Haemo-QoL-A(青年)和SF-36v2(所有人)进行测量。结果:青少年13例(平均年龄15.7岁,范围12.9 ~ 17.9岁),青壮年33例(平均年龄23.6岁;纳入中度(7%)和重度(93%)HA患者。在研究期间,所有患者都采用了抗血友病因子(Helixate FS®)的预防性方案。与年轻人(平均HJHS = 13.3)相比,年轻人的关节损伤最小(平均HJHS = 5.2)。青少年的HRQoL平均得分:CHO-KLAT为79.2 (SD = 11.9), SF-36生理成分总结(PCS)和心理成分总结(MCS)分别为53.0(5.5)和52.3(6.8)。年轻人的HRQoL平均得分为:Haemo-Qol-A为85.8分(9.5分),PCS和MCS分别为50.8分(6.4分)和50.9分(8.8分)。PCS和MCS得分与加拿大公布的标准相当,但在身体功能和身体疼痛领域发现了显著差异。疾病特异性HRQoL评分与青年PCS呈弱相关(CHO-KLAT vs. PCS r = 0.28, p = 0.35);与MCS中度相关(r = 0.39, p = 0.19)。青壮年Haemo-QoL-A评分与PCS呈正相关(r = 0.53, p = 0.001);与MCS呈弱相关(r = 0.26, p = 0.13)。HJHS评估的关节状态与PCS评分相关。终生预防史导致更好的PCS,但更差的MCS评分。结论:尽管患有血友病,该队列中的青年关节疾病极少,HRQoL良好。年轻人表现出更多的关节疾病,在身体功能和疼痛方面的HRQoL略差。本文提供的数据为在血友病患者的临床试验中选择与健康相关的生活质量(HRQoL)仪器提供了新的信息。试验注册:ClinicalTrials.gov: NCT01034904。研究由加拿大CSL Behring公司资助。
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来源期刊
BMC Hematology
BMC Hematology Medicine-Hematology
CiteScore
4.10
自引率
0.00%
发文量
0
期刊介绍: BMC Hematology is an open access, peer-reviewed journal that considers articles on basic, experimental and clinical research related to hematology. The journal welcomes submissions on non-malignant and malignant hematological diseases, hemostasis and thrombosis, hematopoiesis, stem cells and transplantation.
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