接受免疫抑制治疗的特发性微小变化肾病综合征成人患者的感染并发症。

IF 1.9
Nephrology (Carlton, Vic.) Pub Date : 2022-12-01 Epub Date: 2022-10-19 DOI:10.1111/nep.14119
Chih-Yang Hsu, Chung Chang, Hsin-Yu Chen, Shih-Hsiang Ou, Kang-Ju Chou, Hua-Chang Fang, Chien-Liang Chen, Chien-Wei Huang, Tzung-Yo Ho, Po-Tsang Lee
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引用次数: 0

摘要

背景:接受免疫抑制治疗的特发性微小改变肾病综合征(MCNS)患者易发生感染性并发症。目前缺乏专门针对成人感染并发症的研究。方法:回顾性收集101例经活检证实的特发性MCNS成年患者,分析其感染并发症。并对已发表的文献进行综述,以评价预防性抗生素治疗的可行性。结果:101例患者中发生感染性并发症17例(16.8%),其中肺炎4例、蜂窝织炎/筋膜炎4例、尿路感染4例为优势疾病,以革兰氏阴性杆菌为主。AKI分期≥2期(风险比= 6.1;95% CI: 1.2-31.9, p = 0.031)和治疗后未缓解(风险比= 4.4;95% CI: 1.2 ~ 15.6, p = 0.023)是发生感染并发症的两个独立危险因素。回顾16篇已发表的文献和我们的数据显示,即使没有预防性抗生素治疗,在1787例MCNS累积病例中,只有一例发生了耶洛维奇肺囊虫肺炎。相比之下,在36例未接受抗病毒预防治疗的乙型肝炎表面抗原阳性患者中,有16例(44%)急性发作病例。结论:晚期急性肾损伤和治疗后未缓解是接受免疫抑制治疗的成人MCNS发生感染性并发症的危险因素。对于耶洛维奇肺囊虫肺炎或其他细菌性感染,预防性抗生素似乎是不必要的,而对流行地区的患者进行乙型肝炎和潜伏性结核病的筛查和预防性治疗至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Infectious complications in adult patients with idiopathic minimal change nephrotic syndrome undergoing immunosuppressive therapy.

Background: Patients with idiopathic minimal change nephrotic syndrome (MCNS) undergoing immunosuppressive therapy are susceptible to infectious complications. Study specifically focusing on adult population's infectious complications is lacking.

Methods: We retrospectively collected 101 adult patients with biopsy-proven idiopathic MCNS and analysed for the infectious complications. Published literatures were also reviewed aiming to evaluate the feasibility of prophylactic antibiotic treatment.

Results: Infectious complications developed in 17 of 101 (16.8%) patients, with pneumonia (n = 4), cellulitis/fasciitis (n = 4) and urinary tract infection (UTI) (n = 4) being the dominant diseases, and Gram-negative bacilli the main cause. AKI stage ≥2 (Hazard ratio = 6.1; 95% CI: 1.2-31.9, p = 0.031) and non-remission by treatment (Hazard ratio = 4.4; 95% CI: 1.2-15.6, p = .023) were the two independent risk factors relevant to developing infectious complications. Review of 16 published literatures and our data showed that even no prophylactic antibiotic therapy, only one case of Pneumocystis jirovecii pneumonia developed among the 1787 accumulative cases of MCNS. In contrast, 16 (44%) of acute flare cases were reported among the 36 patients with positive hepatitis B surface antigen that did not receive antiviral prophylactic therapy.

Conclusions: Advanced acute kidney injury and non-remission by treatment are the risk factors toward developing infectious complications in adult MCNS undergoing immunosuppressive therapy. It appears unnecessary to use prophylactic antibiotic for Pneumocystis jirovecii pneumonia or other bacterial infections, while screening and prophylactic therapy for hepatitis B and latent tuberculosis are critical for patients in prevalent area.

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