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高效抗逆转录病毒治疗时代获得性免疫缺陷综合征患者进行性多灶性白质脑病的临床特征及预后研究——一项观察性研究

Study of clinical profile and outcomes in progressive multifocal leukoencephalopathy in acquired immunodeficiency syndrome patients in the highly active antiretroviral therapy era - An observational study.

作者信息

Arora Sumit, Ahmad Faiz M H, Deshwal Rajesh, Behal Pradeep

机构信息

Assoc Prof Department of Medicine, Apex Immunodeficiency Centre, Base Hospital Delhi Cantt, Army College of Medical Sciences, Pataudi, Gurugram, Haryana, India.

Prof Department of Medicine, Base Hospital Delhi Cantt, Army College of Medical Sciences, Pataudi, Gurugram, Haryana, India.

出版信息

Indian J Sex Transm Dis AIDS. 2022 Jul-Dec;43(2):156-160. doi: 10.4103/ijstd.IJSTD_29_18. Epub 2022 Nov 17.

DOI:10.4103/ijstd.IJSTD_29_18
PMID:36743095
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9891026/
Abstract

BACKGROUND AND OBJECTIVES

Progressive multifocal leukoencephalopathy (PML) is a viral infection affecting the central nervous system (CNS) seen mostly in advanced human immunodeficiency virus (HIV) infection. There is limited data on the epidemiology and disease course of these patients from India. This study was aimed to determine the frequency of PML in patients with HIV/acquired immunodeficiency syndrome (AIDS) and the clinical presentation and prognosis of these patients.

MATERIALS AND METHODS

The study was conducted at a tertiary care HIV center in New Delhi. Data of 765 patients from our anti-retroviral therapy (ART) clinic during a span of 4 years were retrospectively analyzed and reviewed. The diagnosis was based on the clinical and radiological picture and exclusion of other differential diagnosis by cerebrospinal fluid and serological studies.

RESULTS

Of 765 patients with HIV/AIDS, 12 (1.56%) were diagnosed with PML on the basis of consistent clinical and radiological features after ruling out other differential diagnosis. PML was the initial presentation of HIV infection in 8 (55.5%) patients. 11 (89%) patients had CD4 count <200/μl. Insidious onset focal limb weakness (50%) and dysarthria (50%) were common symptoms. Magnetic resonance imaging of the brain revealed characteristic white matter lesions in all the patients. The estimated median survival was 40 months (95% confidence interval, 23.88-53.19 months).

INTERPRETATION AND CONCLUSIONS

Our results show that PML is associated with high morbidity despite the institution of highly active ART (HAART), but mortality has significantly declined if ART is started early. Key to good response is early diagnosis and HAART.

摘要

背景与目的

进行性多灶性白质脑病(PML)是一种影响中枢神经系统(CNS)的病毒感染,多见于晚期人类免疫缺陷病毒(HIV)感染。来自印度的关于这些患者的流行病学和病程的数据有限。本研究旨在确定HIV/获得性免疫缺陷综合征(AIDS)患者中PML的发生率以及这些患者的临床表现和预后。

材料与方法

本研究在新德里的一家三级护理HIV中心进行。回顾性分析和审查了我们抗逆转录病毒治疗(ART)诊所4年内765例患者的数据。诊断基于临床和影像学表现,并通过脑脊液和血清学研究排除其他鉴别诊断。

结果

在765例HIV/AIDS患者中,排除其他鉴别诊断后,12例(1.56%)根据一致的临床和影像学特征被诊断为PML。8例(55.5%)患者PML为HIV感染的首发表现。11例(89%)患者的CD4细胞计数<200/μl。隐匿性起病的肢体局部无力(50%)和构音障碍(50%)是常见症状。所有患者的脑部磁共振成像均显示特征性的白质病变。估计中位生存期为40个月(95%置信区间,23.88 - 53.19个月)。

解读与结论

我们的结果表明,尽管采用了高效抗逆转录病毒治疗(HAART),PML仍与高发病率相关,但如果早期开始ART,死亡率已显著下降。良好反应的关键是早期诊断和HAART。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/375b/9891026/67ccece7772a/IJSTD-43-156-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/375b/9891026/a195ce382dc4/IJSTD-43-156-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/375b/9891026/605a935510c5/IJSTD-43-156-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/375b/9891026/67ccece7772a/IJSTD-43-156-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/375b/9891026/a195ce382dc4/IJSTD-43-156-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/375b/9891026/605a935510c5/IJSTD-43-156-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/375b/9891026/67ccece7772a/IJSTD-43-156-g003.jpg

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