系统性硬化症患者健康评估问卷的长期过程。

IF 1.4 Q3 RHEUMATOLOGY
Sophie Ie Liem, Sytske Anne Bergstra, Jacopo Ciaffi, Coen van der Meulen, David A Ueckert, Marisca R Schriemer, Tom Wj Huizinga, Theodora Pm Vliet Vlieland, Jeska K de Vries-Bouwstra
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引用次数: 0

摘要

目的:健康评估问卷残疾指数是反映功能残疾的一项重要指标,但对系统性硬化症患者随时间变化的过程知之甚少。因此,我们调查了系统性硬化症患者健康评估问卷残疾指数的长期过程及其与基线特征的关系。方法:符合欧洲抗风湿病联盟和美国风湿病学会2013年标准的系统性硬化症患者被纳入莱顿系统性硬化综合护理队列,并进行年度评估,包括硬皮病健康评估问卷残疾指数(范围 = 0-3)。健康评估问卷残疾指数的过程是在总随访期间(从基线到最后一次可用的健康评估问卷的残疾指数)和每年访问之间进行评估的。根据0.22的最小临床重要差异,将病程分为恶化、稳定或改善。健康评估问卷残疾指数随时间的变化过程采用线性混合模型进行评估。在整个随访期内,用逻辑回归分析比较健康评估问卷残疾指数恶化或改善的患者的基线特征。结果:共纳入517名系统性硬化症患者,中位随访时间为7 年(四分位间距 = 4-9;2649次访问)和0.625的基线健康评估问卷残疾指数(四分位间距 = 0.125-1.25)。在组水平上,健康评估问卷残疾指数稳定,每年增加0.019(95%置信区间 = 0.011至0.027)。从亚组来看,65岁以上的患者 年或在随访期间死亡/身体不能来的患者的平均健康评估问卷残疾指数较差。在从基线到最后一次随访的各个疗程中,健康评估问卷残疾指数有临床意义的恶化、稳定或改善的患者比例分别为35%、42%和23%。免疫抑制剂患者(比值比 = 0.5,95%置信区间 = 0.3至0.9)或胃肠道受累(比值比 = 0.6,95%置信区间 = 0.4至0.9)显示,在整个随访期内,健康评估问卷残疾指数恶化的几率降低。结论:随着时间的推移,系统性硬化症患者的健康评估问卷残疾指数的平均病程是稳定的。然而,各个疗程各不相同,三分之一的疗程病情恶化。基线时使用免疫抑制剂或胃肠道受累的患者病情恶化的发生率较低。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

The long-term course of the Health Assessment Questionnaire in patients with systemic sclerosis.

The long-term course of the Health Assessment Questionnaire in patients with systemic sclerosis.

The long-term course of the Health Assessment Questionnaire in patients with systemic sclerosis.

The long-term course of the Health Assessment Questionnaire in patients with systemic sclerosis.

Objective: The Health Assessment Questionnaire-Disability Index is an important outcome measure reflecting functional disability, but knowledge on its course over time in patients with systemic sclerosis is scarce. Therefore, we investigated the long-term course of the Health Assessment Questionnaire-Disability Index and its association with baseline characteristics in systemic sclerosis patients.

Methods: Systemic sclerosis patients, fulfilling the European League Against Rheumatism and the American College of Rheumatology 2013 criteria, were included from the Leiden Combined Care in Systemic Sclerosis cohort with annual assessments including the Scleroderma Health Assessment Questionnaire-Disability Index (range = 0-3). The course of the Health Assessment Questionnaire-Disability Index was evaluated over the total follow-up (baseline to last available Health Assessment Questionnaire-Disability Index) and between yearly visits. Based on a minimal clinical important difference of 0.22, courses were categorized into worsening, stable or improvement. The course of the Health Assessment Questionnaire-Disability Index over time was evaluated with linear mixed models. Baseline characteristics were compared between patients with a worsening or improvement of the Health Assessment Questionnaire-Disability Index over the total follow-up period with logistic regression analyses.

Results: A total of 517 systemic sclerosis patients were included, with a median follow-up of 7 years (interquartile range = 4-9; 2649 visits) and a baseline Health Assessment Questionnaire-Disability Index of 0.625 (interquartile range = 0.125-1.25). On group level, the Health Assessment Questionnaire-Disability Index is stable with an annual increase of 0.019 (95% confidence interval = 0.011 to 0.027). Looking at subgroups, patients >65 years or who died/were physically unable to come during follow-up had a worse mean Health Assessment Questionnaire-Disability Index. In individual courses from baseline to the last follow-up, the proportions of patients with a clinically meaningful worsening, stable or improved Health Assessment Questionnaire-Disability Index were 35%, 42% and 23%, respectively. Patients with immunosuppressants (odds ratio = 0.5, 95% confidence interval = 0.3 to 0.9) or gastrointestinal involvement (odds ratio = 0.6, 95% confidence interval = 0.4 to 0.9) at baseline showed a reduced chance of worsening of the Health Assessment Questionnaire-Disability Index over the total follow-up period.

Conclusion: Over time, the average course of the Health Assessment Questionnaire-Disability Index was stable in systemic sclerosis patients. However, individual courses vary, with worsening occurring in one-third. Worsening occurred less often in individuals using immunosuppressants or with gastrointestinal involvement at baseline.

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