探索欧洲 A 型血友病患者病情严重程度与健康相关生活质量之间的关系:对 CHESS II 研究数据的多变量分析。

IF 3.2 2区 医学 Q1 HEALTH CARE SCIENCES & SERVICES Health and Quality of Life Outcomes Pub Date : 2024-07-29 DOI:10.1186/s12955-024-02267-6
Enrico Ferri Grazzi, Charles Hawes, Charlotte Camp, David Hinds, Jamie O'Hara, Tom Burke
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引用次数: 0

摘要

背景:血友病 A(HA;因子 VIII 缺乏症)是一种先天性 X 连锁出血性疾病,其特征是与创伤相关或自发性出血事件,最明显的是关节内出血,并导致受影响关节的慢性炎症和退化。相对于正常水平的内源性凝血因子活性决定了 HA 症状的严重程度,可分为轻度(> 5-40%)、中度(1-5%)或重度(方法:将内源性凝血因子活性与正常水平进行比较):在 "欧洲血友病成本--社会经济调查 II"(CHESS II)横断面回顾性疾病负担研究中,对来自 8 个欧洲国家的 A 型或 B 型遗传性血友病成年患者进行了抽样调查,建立了广义线性回归模型(GLM),以探讨 HA 严重程度与 EQ-5D-5 L 指数得分之间的关系。研究对象包括任何严重程度的血友病患者,这些患者在数据采集前的 12 个月内没有使用过有效的抑制剂,并且对 EQ-5D-5 L 有完整的反应。建立了一个基础 GLM 模型,其中包含人口统计学和临床特征的协变量(年龄、体重指数、国家、就业、HA 严重程度、年出血率、问题关节和慢性疼痛):在381名可评估的患者中,221人(58.0%)患有重度HA,96人(25.2%)患有中度HA,64人(16.8%)患有轻度HA。在纳入 GLM 模型的协变量中,在控制了血友病相关结果后,观察到轻度 HA 与较高的 EQ-5D-5 L 指数得分之间存在显著关联(平均边际效应为 0.084;p = 0.016)。患者居住国和与HA相关的慢性疼痛程度也与指数得分的显著差异有关,后者与HRQoL结果呈负相关:结论:病情严重程度和慢性疼痛是预测 PwHA HRQoL 的重要因素。持久的出血保护和有效的慢性疼痛管理有可能满足这一人群尚未得到满足的治疗需求。
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Exploring the relationship between condition severity and health-related quality of life in people with haemophilia A across Europe: a multivariable analysis of data from the CHESS II study.

Background: Haemophilia A (HA; Factor VIII deficiency) is a congenital X-linked bleeding disorder characterized by trauma-related or spontaneous bleeding events, most notably arising within the intraarticular space and resulting in chronic inflammation and degeneration of affected joints. Endogenous clotting factor activity relative to normal levels determines the severity of HA symptoms, as mild (> 5-40%), moderate (1-5%), or severe (< 1%). Within the current environment of rapid evolution in HA management, we seek to understand the interplay of condition severity and health-related quality of life (HRQoL) to characterise and differentiate unmet needs among people with HA (PwHA).

Methods: A generalised linear regression model (GLM) was developed to explore the relationship between HA severity and EQ-5D-5 L index score from adult HA patients sampled in the "Cost of Haemophilia across Europe - a Socioeconomic Survey II" (CHESS II) cross-sectional, retrospective burden of illness study among adults with hereditary haemophilia A or B from eight European countries. HA patients of any severity with no active inhibitors during the 12 months prior to data capture and a completeEQ-5D-5 L response were included. A base GLM model was specified with covariates for demographic and clinical characteristics (age, body mass index, country, employment, HA severity, annual bleeding rate, problem joints, and chronic pain).

Results: Of 381 evaluable patients, 221 (58.0%) had severe HA, 96 (25.2%) had moderate HA, and 64 (16.8%) had mild HA. Among the covariates included in the GLM model and after controlling for haemophilia-related outcomes, a significant association was observed between mild HA and higher EQ-5D-5 L index score (average marginal effects, 0.084; p = 0.016) relative to severe HA. Patient country of residence and magnitude of HA-related chronic pain were also associated with significant differences in index scores, with the latter showing a negative relationship with HRQoL outcomes.

Conclusions: Condition severity and chronic pain are significant predictors of HRQoL in PwHA. Durable bleeding protection and effective management of chronic pain have the potential to address unmet treatment needs in this population.

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来源期刊
CiteScore
7.30
自引率
2.80%
发文量
154
审稿时长
3-8 weeks
期刊介绍: Health and Quality of Life Outcomes is an open access, peer-reviewed, journal offering high quality articles, rapid publication and wide diffusion in the public domain. Health and Quality of Life Outcomes considers original manuscripts on the Health-Related Quality of Life (HRQOL) assessment for evaluation of medical and psychosocial interventions. It also considers approaches and studies on psychometric properties of HRQOL and patient reported outcome measures, including cultural validation of instruments if they provide information about the impact of interventions. The journal publishes study protocols and reviews summarising the present state of knowledge concerning a particular aspect of HRQOL and patient reported outcome measures. Reviews should generally follow systematic review methodology. Comments on articles and letters to the editor are welcome.
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