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法国HIV相关隐球菌病并发免疫重建炎症综合征的发病率及危险因素

Incidence and risk factors of immune reconstitution inflammatory syndrome complicating HIV-associated cryptococcosis in France.

作者信息

Lortholary Olivier, Fontanet Arnaud, Mémain Nathalie, Martin Antoine, Sitbon Karine, Dromer Françoise

机构信息

National Reference Centre for Mycoses and Antifungals, Molecular Mycology Unit bEmerging Diseases Epidemiology Unit, Institut Pasteur, Paris, France.

出版信息

AIDS. 2005 Jul 1;19(10):1043-9. doi: 10.1097/01.aids.0000174450.70874.30.

DOI:10.1097/01.aids.0000174450.70874.30
PMID:15958835
Abstract

BACKGROUND

Immune reconstitution inflammatory syndrome (IRIS) in association with cryptococcosis has been anecdotically reported following administration of highly active antiretroviral therapy (HAART).

OBJECTIVE

To analyse the incidence and risk factors for IRIS-associated cryptococcosis among HIV-infected patients.

DESIGN

Retrospective multicentre study between 1996 and 2000 through the French Cryptococcosis Database.

METHODS

Subsequent occurrence of IRIS examined in 120 HIV-infected adult patients treated with HAART and experiencing a first episode of culture-confirmed cryptococcosis.

RESULTS

Ten patients developed IRIS during the study period, giving an incidence of 10/239, or 4.2/100 person-years [95% confidence interval (CI), 2.2-7.8]. IRIS consisted of acute symptoms consistent with inflammation occurring within a median of 8 months (range, 2-37) after the diagnosis of cryptococcosis in the context of negative cultures and immunological and/or virological response to HAART. Radiology and histopathology detected features compatible with inflammation. Symptom severity required transfer into intensive care units for three patients and use of anti-inflammatory drugs for four. Three patients with evolutive IRIS died. Compared with patients without IRIS for whom complete clinical and microbiological information were available at baseline, previously unknown HIV infection [odds ratio (OR), 4.8; 95% CI, 1.0-21.7], CD4 cell count < 7 x 10 cells/l (OR, 4.0; 95% CI, 0.9-17.2), fungaemia (OR, 6.1; 95% CI, 1.1-35.2) and HAART initiation within 2 months of cryptococcosis diagnosis (OR, 5.50; 95% CI, 1.0-29.6) were independently associated with the risk of subsequent IRIS.

CONCLUSIONS

IRIS-related cryptococcosis was observed more frequently in severely immunocompromised patients with disseminated infection and HAART initiation soon after the diagnosis.

摘要

背景

有零星报道称,在接受高效抗逆转录病毒治疗(HAART)后,免疫重建炎症综合征(IRIS)与隐球菌病有关。

目的

分析HIV感染患者中与IRIS相关的隐球菌病的发病率及危险因素。

设计

通过法国隐球菌病数据库进行的1996年至2000年的回顾性多中心研究。

方法

在120例接受HAART治疗且首次发生培养确诊隐球菌病的HIV感染成年患者中,对随后发生的IRIS进行检查。

结果

在研究期间,有10例患者发生了IRIS,发病率为10/239,即4.2/100人年[95%置信区间(CI),2.2 - 7.8]。IRIS表现为急性症状,与在隐球菌病诊断后中位8个月(范围2 - 37个月)内出现的炎症一致,此时培养结果为阴性,且对HAART有免疫和/或病毒学反应。放射学和组织病理学检测到与炎症相符的特征。症状严重程度导致3例患者转入重症监护病房,4例患者使用了抗炎药物。3例病情进展的IRIS患者死亡。与在基线时可获得完整临床和微生物学信息的无IRIS患者相比,既往未知的HIV感染[比值比(OR),4.8;95%CI,1.0 - 21.7]、CD4细胞计数<7×10⁹细胞/L(OR,4.0;95%CI,0.9 - 17.2)、真菌血症(OR,6.1;95%CI,1.1 - 35.2)以及在隐球菌病诊断后2个月内开始HAART(OR,5.50;95%CI,1.0 - 29.6)均与随后发生IRIS的风险独立相关。

结论

在免疫严重受损且有播散性感染并在诊断后不久开始HAART的患者中,更频繁地观察到与IRIS相关的隐球菌病。

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