Unmasking the hidden tuberculosis mortality burden in a large post mortem study in Maputo Central Hospital, Mozambique

A. García-Basteiro, J. Hurtado, P. Castillo, Fabiola Fernandes, M. Navarro, Lucilia Lovane, Isaac Casas, L. Quintó, Dércio Jordão, Mamudo R Ismail, C. Lorenzoni, C. Carrilho, Ariadna Sanz, N. Rakislova, Á. Mira, M. Álvarez-Martínez, A. Cossa, F. Cobelens, I. Mandomando, J. Vila, Q. Bassat, C. Menéndez, J. Ordi, M. Martínez
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引用次数: 31

Abstract

Sensitive tools are needed to accurately establish the diagnosis of tuberculosis (TB) at death, especially in low-income countries. The objective of this study was to evaluate the burden of TB in a series of patients who died in a tertiary referral hospital in sub-Saharan Africa using an in-house real time PCR (TB-PCR) and the Xpert MTB/RIF Ultra (Xpert Ultra) assay. Complete diagnostic autopsies were performed in a series of 223 deaths (56.5% being HIV-positive), including 54 children, 57 maternal deaths and 112 other adults occurring at the Maputo Central Hospital, Mozambique. TB-PCR was performed in all lung, cerebrospinal fluid and central nervous system samples in HIV-positive patients. All samples positive for TB-PCR or showing histological findings suggestive of TB were analysed with the Xpert Ultra assay. TB was identified as the cause of death in 31 patients: three out of 54 (6%) children, five out of 57 (9%)maternal deaths and 23 out of 112 (21%) other adults. The sensitivity of the main clinical diagnosis to detect TB as the cause of death was 19.4% (95% CI 7.5–37.5) and the specificity was 97.4% (94.0–99.1) compared to autopsy findings. Concomitant TB (TB disease in a patient dying of other causes) was found in 31 additional cases. Xpert Ultra helped to identify 15 cases of concomitant TB. In 18 patients, Mycobacterium tuberculosis DNA was identified by TB-PCR and Xpert Ultra in the absence of histological TB lesions. Overall, 62 (27.8%) cases had TB disease at death and 80 (35.9%) had TB findings. The use of highly sensitive, easy to perform molecular tests in complete diagnostic autopsies may contribute to identifying TB cases at death that would have otherwise been missed. Routine use of these tools in certain diagnostic algorithms for hospitalised patients needs to be considered. Clinical diagnosis showed poor sensitivity for the diagnosis of TB at death. This study shows the usefulness of molecular assays in ascertaining TB diagnosis at death. It questions the information of clinical diagnoses obtained from hospital registries as a reliable tool for TB mortality estimation. http://bit.ly/2KrzTBJ
在莫桑比克马普托中心医院进行的一项大型尸检研究揭示了隐藏的结核病死亡率负担
特别是在低收入国家,需要敏感的工具来准确确定死亡时的结核病诊断。本研究的目的是利用内部实时PCR (TB-PCR)和Xpert MTB/RIF Ultra (Xpert Ultra)检测,评估撒哈拉以南非洲一家三级转诊医院死亡的一系列患者的结核病负担。对发生在莫桑比克马普托中心医院的223例死亡(56.5%为艾滋病毒阳性)进行了全面诊断尸检,其中包括54名儿童、57名产妇和112名其他成年人。对所有hiv阳性患者的肺、脑脊液和中枢神经系统样本进行TB-PCR检测。所有结核- pcr阳性或显示结核组织学结果的样品均用Xpert Ultra法进行分析。结核病被确定为31名患者死亡的原因:54名儿童中有3名(6%),57名产妇中有5名(9%),112名其他成年人中有23名(21%)。与尸检结果相比,主要临床诊断检测结核病为死亡原因的敏感性为19.4% (95% CI为7.5-37.5),特异性为97.4%(94.0-99.1)。在另外31例病例中发现了合并结核病(因其他原因死亡的患者的结核病)。Xpert Ultra帮助确定了15例合并结核病例。在18例患者中,在没有结核组织学病变的情况下,通过TB- pcr和Xpert Ultra鉴定结核分枝杆菌DNA。总体而言,62例(27.8%)死亡时患有结核病,80例(35.9%)有结核病发现。在完全诊断性尸检中使用高度敏感、易于执行的分子检测,可能有助于在死亡时发现本来可能被遗漏的结核病病例。需要考虑在住院患者的某些诊断算法中常规使用这些工具。临床诊断对死亡时结核病的诊断敏感性较差。本研究显示分子测定在确定死亡时结核病诊断的有用性。它质疑从医院登记处获得的临床诊断信息作为估计结核病死亡率的可靠工具。http://bit.ly/2KrzTBJ
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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