Jones Georgina L, Williams Kate, Edmondson-Jones Mark, Prevot Johan, Drabwell Jose, Solis Leire, Shrimpton Anna, Mahlaoui Nizar
Department of Psychology, School of Social Sciences, Leeds Beckett University, Leeds, UK.
PAREXEL International, London, UK.
Patient Prefer Adherence. 2020 Sep 3;14:1567-1584. doi: 10.2147/PPA.S234669. eCollection 2020.
To describe the development and psychometric testing of a new questionnaire to measure the burden of immunoglobulin treatment (Ig) from the perspective of patients with primary immunodeficiencies (PID).
An online, cross-sectional survey was administered to PID patients across 10 countries (nine European and Canada) who were receiving either intravenous (IVIg) or subcutaneous (SCIg) immunoglobulin therapy. The range and distribution of the responses (ie, levels of missing data, floor and ceiling effects), exploratory factor analysis (using factor loadings of 0.4 or greater) and measures of internal consistency reliability (ie, Cronbach's alpha coefficient, inter-item and item-total correlations) were used to identify the domain and item pool.
In total, 472 patients completed the questionnaire, of which 395 were included in the analysis (32% underwent IVIg and 67% underwent SCIg). The final instrument contained 34 items across eight domains of treatment burden (time, organisation and planning, leisure and social, interpersonal relationships, employment and education, travel, consequences of treatment and emotional) and an additional Ig treatment burden global question at the end of the measure. All the scales achieved good internal reliability (Cronbach's alpha coefficient ranged from 0.70 to 0.85) and, with the exception of one item exceeded the minimum threshold of 0.35 for item-total correlations. Treatment burden was lower than anticipated across the different treatment routes and countries, although overall was more burdensome for patients undergoing IVIg compared to SCIg treatment.
The IgBoT-35 appears to be a reliable, patient-generated questionnaire and may help to identify more individualised and preferred therapies for the PID patient when used in clinical practice. A new survey with a sample of US patients is currently being undertaken to further establish its validity and conceptual model. The overall Ig burden of treatment scores appeared to be low. PID patient preferences are important to guide treatment decisions and ensuring patients receive the right treatment at the right time.
描述一种新问卷的开发及心理测量学测试,该问卷用于从原发性免疫缺陷病(PID)患者的角度衡量免疫球蛋白治疗(Ig)的负担。
对来自10个国家(9个欧洲国家和加拿大)接受静脉注射免疫球蛋白(IVIg)或皮下注射免疫球蛋白(SCIg)治疗的PID患者进行了一项在线横断面调查。使用回答的范围和分布(即缺失数据水平、地板效应和天花板效应)、探索性因素分析(使用因子载荷0.4或更高)以及内部一致性信度测量(即克朗巴哈α系数、项目间相关性和项目与总分相关性)来确定领域和项目库。
共有472名患者完成了问卷,其中395名纳入分析(32%接受IVIg治疗,67%接受SCIg治疗)。最终工具包含34个项目,涵盖治疗负担的八个领域(时间、组织与规划、休闲与社交、人际关系、就业与教育、旅行、治疗后果和情绪),并在量表末尾附加了一个Ig治疗负担总体问题。所有量表均具有良好的内部信度(克朗巴哈α系数范围为0.70至0.85),除一项外,项目与总分相关性均超过了0.35的最低阈值。不同治疗途径和国家的治疗负担均低于预期,尽管总体而言,与SCIg治疗相比,接受IVIg治疗的患者负担更重。
IgBoT - 35似乎是一份可靠的、由患者生成的问卷,在临床实践中使用时,可能有助于为PID患者确定更个性化和更理想的治疗方法。目前正在对美国患者样本进行一项新的调查,以进一步确定其有效性和概念模型。治疗的总体Ig负担得分似乎较低。PID患者的偏好对于指导治疗决策以及确保患者在正确的时间接受正确的治疗非常重要。