Department of Experimental Haematology and Transfusion Medicine, University Clinic Bonn, Bonn, Germany.
The Alfred Hospital, Melbourne, Vic., Australia.
Haemophilia. 2021 May;27(3):398-407. doi: 10.1111/hae.14270. Epub 2021 Feb 12.
Real-world data on health-related outcomes in persons with haemophilia A (PwHA) can provide useful information for improving patient care. The global, non-interventional study (NIS; NCT02476942) prospectively collected high-quality data in PwHA, including those without factor VIII (FVIII) inhibitors treated according to local routine clinical practice.
To report health-related quality of life (HRQoL) and health status of adult/adolescent PwHA without FVIII inhibitors.
Participants were PwHA without FVIII inhibitors age ≥12 years; they remained on existing episodic treatment or prophylaxis. HRQoL was assessed by Haemophilia Quality of Life Questionnaire for Adults (Haem-A-QoL) or Haemophilia-Specific Quality of Life Assessment for Children and Adolescents Short Form (Haemo-QoL-SF II). Health status was assessed through EuroQol 5-Dimensions 5-Levels (EQ-5D-5L) index utility score and visual analogue scale (EQ-VAS).
Ninety-four participants enrolled; median age was 34.0 years (range 12-76). Forty-five received episodic treatment and 49 received prophylaxis for a median time of 27.7 weeks and 30.4 weeks, respectively. Mean (standard deviation) baseline Haem-A-QoL total scores were 40.1 (17.0) for the episodic group and 26.6 (14.6) for the prophylaxis group, indicating impairments in HRQoL, which remained consistent over time. Mean EQ-5D-5L IUS scores were similar between treatment regimens (0.8 episodic; 0.9 prophylaxis) and consistent over time. The mean EQ-VAS scores were similar between treatment regimens, and lower on days when bleeding occurred (79.0 vs 85.0 for episodic treatment; 77.0 vs 82.0 for prophylaxis, respectively).
Adult and adolescent PwHA without FVIII inhibitors had HRQoL impairments regardless of whether they were treated with episodic or prophylactic standard care with FVIII.
真实世界数据可提供血友病 A 患者(PwHA)相关健康结局的有用信息,有助于改善患者护理。本全球性、非干预性研究(NIS;NCT02476942)前瞻性收集了 PwHA 的高质量数据,包括未接受因子 VIII(FVIII)抑制剂治疗但根据当地常规临床实践接受治疗的患者。
报告无 FVIII 抑制剂的成年/青少年 PwHA 的健康相关生活质量(HRQoL)和健康状况。
纳入无 FVIII 抑制剂且年龄≥12 岁的 PwHA;他们继续接受现有按需治疗或预防治疗。HRQoL 通过成人血友病生活质量问卷(Haem-A-QoL)或儿童和青少年血友病特异性生活质量评估量表短表(Haemo-QoL-SF II)进行评估。健康状况通过欧洲五维健康量表 5 维度 5 水平(EQ-5D-5L)指数效用评分和视觉模拟评分(EQ-VAS)进行评估。
94 名参与者入组,中位年龄为 34.0 岁(范围 12-76 岁)。45 名接受按需治疗,49 名接受预防治疗,中位治疗时间分别为 27.7 周和 30.4 周。按需治疗组的 Haem-A-QoL 总分基线平均值(标准差)为 40.1(17.0),预防治疗组为 26.6(14.6),表明 HRQoL 受损,且随时间保持一致。治疗方案之间的 EQ-5D-5L IUS 评分均值相似(按需治疗 0.8;预防治疗 0.9),且随时间保持一致。治疗方案之间的 EQ-VAS 评分均值相似,出血发生时评分较低(按需治疗分别为 79.0 和 85.0;预防治疗分别为 77.0 和 82.0)。
有无 FVIII 抑制剂的成年和青少年 PwHA 无论接受按需或预防标准 FVIII 治疗,均存在 HRQoL 受损。