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The Development of a New Questionnaire to Measure the Burden of Immunoglobulin Treatment in Patients with Primary Immunodeficiencies: The IgBoT-35

机译:开发新的调查问卷,以衡量原发性免疫缺失患者免疫球蛋白治疗的负担:IGBOT-35

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Purpose: 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). Patients and Methods: 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. Results: 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. Conclusion: 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.
机译:目的:描述一种新的调查问卷的发展和心理测量测试,从初级免疫缺乏患者(PID)的角度来衡量免疫球蛋白治疗(Ig)的负担。患者和方法:在线,横断面调查跨越10个国家(九个欧洲和加拿大)的PID患者,他们接受静脉内(IVIG)或皮下(突发)免疫球蛋白疗法。响应的范围和分布(即缺失数据,地板和天花板效应的水平),探索性因子分析(使用0.4或更大的因子负载)和内部一致性可靠性的测量(即Cronbach的alpha系数,项目间项目 - 总相关性)用于标识域和项目池。结果:共有472名患者完成问卷,其中395分析(32%接受IVIG和67%的突发)。最后的仪器占八个治疗负担域的34个项目(时间,组织和规划,休闲和社会,人际关系,就业和教育,旅行,治疗和情绪后果)以及结束时额外的IG治疗负担全球问题的措施。所有尺度都实现了良好的内部可靠性(Cronbach的alpha系数范围为0.70至0.85),并且除了一个项目超过0.35的项目总相关性的最小阈值。治疗负担低于各种治疗路线和国家的预期,尽管与突然处理相比,其总体而言,对于所接受IVIG的患者而言,对患者进行了更加繁重。结论:IGBOT-35似乎是可靠的患者生成的问卷,并且在临床实践中使用时可能有助于识别PID患者的更个性化和优选的治疗。目前正在进行具有美国患者样本的新调查,以进一步建立其有效性和概念模型。整体IG治疗得分似乎似乎很低。 PID患者偏好对于指导治疗决策并确保患者在合适的时间接受正确的治疗。

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