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成人普通变异性免疫缺陷患者的疲劳和药效减退效应。

Fatigue and the wear-off effect in adult patients with common variable immunodeficiency.

机构信息

Baylor College of Medicine, Section of Immunology, Allergy and Rheumatology, Texas Children's Hospital, Houston, TX, USA.

The Immune Deficiency Foundation, Towson, MD, USA.

出版信息

Clin Exp Immunol. 2018 Dec;194(3):327-338. doi: 10.1111/cei.13210. Epub 2018 Oct 14.

Abstract

Patients with common variable immunodeficiency (CVID) have increased fatigue compared with the general population. Fatigue is associated with lower quality of life (QoL), which is associated with higher mortality in CVID. This study aimed to determine the prevalence of self-reported fatigue for patients with CVID and to identify its possible drivers and burden on QoL. We analysed data from the 2013 Immune Deficiency Foundation (IDF) treatment survey. Answers were included from 873 CVID patients who responded (respondents). Of the 873 respondents included in the analysis, 671 (76·9%) reported fatigue, of whom 400 (83·7%) were receiving intravenous (i.v.) immunoglobulins (IVIG) and 271 (68·6%) were receiving subcutaneous (s.c.) immunoglobulins. This difference in fatigue between patients receiving IVIG and SCIG was statistically significant (P < 0·001). Dose and frequency of immunoglobulin replacement therapy (IgGRT) did not affect fatigue prevalence. Fatigued patients on IVIG reported greater infection rates and required more anti-microbials during the wear-off period. Fatigued patients reported worse health status than non-fatigued patients, and had lower rates of employment, education, household income and school attendance than their non-fatigued counterparts. Fatigue is increased in CVID, especially among patients receiving IVIG, compared to SCIG. Fatigue has a significant impact on QoL and productivity in patients with CVID. Further studies to identify the mechanisms of fatigue are warranted to help advance therapeutic measures to treat this disease and improve patients' QoL and wellbeing.

摘要

普通变异性免疫缺陷症(CVID)患者比一般人群更容易感到疲劳。疲劳与生活质量(QoL)降低有关,而 CVID 患者的死亡率与生活质量降低有关。本研究旨在确定 CVID 患者自我报告疲劳的患病率,并确定其可能的驱动因素和对 QoL 的负担。我们分析了 2013 年免疫缺陷基金会(IDF)治疗调查的数据。该分析纳入了 873 名回答问题的 CVID 患者(应答者)。在纳入分析的 873 名应答者中,有 671 名(76.9%)报告有疲劳,其中 400 名(83.7%)正在接受静脉注射(i.v.)免疫球蛋白(IVIG)治疗,271 名(68.6%)正在接受皮下(s.c.)免疫球蛋白治疗。接受 IVIG 和 SCIG 治疗的患者之间疲劳的差异具有统计学意义(P<0.001)。免疫球蛋白替代治疗(IgGRT)的剂量和频率并不影响疲劳的患病率。接受 IVIG 治疗的疲劳患者报告的感染率更高,在免疫球蛋白作用消退期间需要更多的抗生素。疲劳患者报告的健康状况比非疲劳患者差,与非疲劳患者相比,他们的就业率、受教育程度、家庭收入和出勤率较低。与 SCIG 相比,CVID 患者,尤其是接受 IVIG 治疗的患者,疲劳感更明显。疲劳对 CVID 患者的 QoL 和生产力有显著影响。需要进一步研究以确定疲劳的机制,以帮助推进治疗措施来治疗这种疾病,提高患者的 QoL 和幸福感。

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