La Paz University Hospital, Madrid, Spain.
Swedish Orphan Biovitrum AB, Stockholm, Sweden.
BMJ Open. 2024 Sep 10;14(9):e082204. doi: 10.1136/bmjopen-2023-082204.
To evaluate joint health, pain and health-related quality of life (HRQoL) in patients with moderate/severe haemophilia A in Europe.
Multinational, cross-sectional survey, with retrospective data collection. Data were taken from the Adelphi Real World Haemophilia Disease Specific Programme Wave II, using surveys completed by physicians and patients between February 2020 and May 2021.
Haematologists/haemato-oncologists and their patients in France, Germany, Italy, Spain and the UK.
Males aged ≥18 years with moderate or severe haemophilia A (baseline clotting factor level ≤5%), without existing inhibitors and currently receiving prophylaxis. Patients were grouped into those with or without haemophilia-affected joints (HAJs) based on bleeding, radiographic, surgical, mobility and joint pain data.
Characterisation of humanistic and clinical outcomes in patients with or without HAJs.
A total of 120 physicians provided data for 351 eligible patients; 209 (59.5%) patients had HAJs and 142 (40.5%) had no HAJs. Pain/discomfort was significantly different (p=0.01) and reported more frequently in the HAJ (85.7%) vs non-HAJ group (53.3%). Pain medication use was significantly higher in the HAJ versus non-HAJ group (73.2% vs 60.6%; p=0.01). Up to half of the patients with HAJs had synovitis (49.8%) or arthropathy (48.4%), and one-third had undergone joint surgery (35.4%). Overall health status was significantly worse in the HAJ versus non-HAJ group (mean (SD) EuroQol Visual Analogue Scale score: 65.5 (19.3) vs 81.1 (14.6); p=0.01).
In this multinational real-world study, nearly two-thirds of adults with moderate/severe haemophilia A without inhibitors experienced HAJs despite prophylaxis. Individuals with HAJs had higher rates of pain and pain medication use, and lower HRQoL compared with those without HAJs. These data indicate that HAJs represent a clinically relevant burden and early identification/monitoring and management of affected joints should be an important consideration to help prevent long-term joint morbidity.
评估欧洲中重度 A 型血友病患者的关节健康状况、疼痛和健康相关生活质量(HRQoL)。
跨国、横断面调查,回顾性数据收集。数据来自 Adelphi 真实世界血友病疾病专项计划第二波,使用医生和患者于 2020 年 2 月至 2021 年 5 月之间完成的调查。
法国、德国、意大利、西班牙和英国的血液科医生/血液肿瘤学家及其患者。
年龄≥18 岁、基线凝血因子水平≤5%(中重度)、无现有抑制剂且目前正在接受预防治疗的男性血友病 A 患者。根据出血、影像学、手术、活动度和关节疼痛数据,患者分为有或无血友病相关关节(HAJ)的患者。
有或无 HAJ 的患者的人文和临床结局特征。
共 120 名医生提供了 351 名合格患者的数据;209 名(59.5%)患者有 HAJ,142 名(40.5%)患者无 HAJ。疼痛/不适有显著差异(p=0.01),HAJ 组(85.7%)比非 HAJ 组(53.3%)更频繁报告。HAJ 组疼痛药物使用率显著高于非 HAJ 组(73.2% vs 60.6%;p=0.01)。有 HAJ 的患者中,有一半的患者患有滑膜炎(49.8%)或关节病(48.4%),三分之一的患者接受了关节手术(35.4%)。HAJ 组的总体健康状况明显差于非 HAJ 组(平均(SD)欧洲五维健康量表评分:65.5(19.3) vs 81.1(14.6);p=0.01)。
在这项多国家真实世界研究中,近三分之二的无抑制剂的中重度 A 型血友病成人尽管接受了预防治疗,但仍经历了 HAJ。有 HAJ 的患者疼痛发生率和疼痛药物使用率较高,HRQoL 较低,与无 HAJ 的患者相比。这些数据表明,HAJ 是一种具有临床意义的负担,早期识别/监测和管理受影响的关节应是预防长期关节疾病的重要考虑因素。