Xu Y, Deforest M, Grabell J, Hopman W, James P
School of Medicine, Queen's University, Kingston, Canada.
NCIC Clinical Trials Group, Queen's University, Kingston, Canada.
Haemophilia. 2017 Jan;23(1):115-121. doi: 10.1111/hae.13062. Epub 2016 Sep 9.
von Willebrand disease (VWD) is the most common inherited bleeding disorder known in humans. Currently, studies investigating the health-related quality of life (HR-QoL) in VWD using standardized tools are limited, particularly among patients with mild decreases in von Willebrand factor or activity.
To determine HR-QoL and its predictors among patients with mild, moderate and severe forms of VWD.
Patients with clinical diagnosis of VWD were recruited from a tertiary Inherited Bleeding Disorder Clinic. Upon informed consent, bleeding scores were obtained via a standardized, self-administered tool. Each participant also completed a HR-QoL questionnaire (SF-36). Analyses included paired t-test, independent t-test, one-way anova and multivariate regression.
A total of 102 patients were recruited (consent rate = 95%). Participants were 38 years on average (SD 14.8), 78% were female and 80% were diagnosed with VWD Type 1. Compared to age- and sex-matched normative data, VWD patients had clinically and statistically significant reductions in seven of eight HR-QoL domains and the physical and mental component summaries. Adjusted for age, sex, socioeconomic status and rurality, there was a trend towards lower physical component summary with increasing bleeding score, and lower mental domains with iron deficiency status (P = 0.07 and P = 0.08 respectively).
This study is the first to examine the impact of VWD on HR-QoL across disease severity while incorporating socioeconomic status and rurality. Significant reductions in HR-QoL among VWD patients, especially the relationship between iron status and mental HR-QoL, strengthen the rationale for prospective studies to evaluate the efficacy of iron replacement in this setting.
血管性血友病(VWD)是人类已知的最常见的遗传性出血性疾病。目前,使用标准化工具对血管性血友病患者健康相关生活质量(HR-QoL)进行调查的研究有限,尤其是在血管性血友病因子或活性轻度降低的患者中。
确定轻度、中度和重度血管性血友病患者的健康相关生活质量及其预测因素。
从一家三级遗传性出血性疾病诊所招募临床诊断为血管性血友病的患者。在获得知情同意后,通过标准化的自我管理工具获得出血评分。每位参与者还完成了一份健康相关生活质量问卷(SF-36)。分析包括配对t检验、独立t检验、单因素方差分析和多变量回归。
共招募了102名患者(同意率=95%)。参与者的平均年龄为38岁(标准差14.8),78%为女性,80%被诊断为1型血管性血友病。与年龄和性别匹配的正常数据相比,血管性血友病患者在八个健康相关生活质量领域中的七个领域以及身体和心理成分总结方面在临床和统计学上均有显著降低。在调整了年龄、性别、社会经济地位和农村地区因素后,随着出血评分的增加,身体成分总结有降低的趋势,缺铁状态下心理领域有降低的趋势(分别为P=0.07和P=0.08)。
本研究首次在纳入社会经济地位和农村地区因素的同时,考察了不同疾病严重程度的血管性血友病对健康相关生活质量的影响。血管性血友病患者的健康相关生活质量显著降低,尤其是铁状态与心理健康相关生活质量之间的关系,加强了前瞻性研究评估在这种情况下铁替代疗法疗效的理论依据。