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用于诊断胸膜结核的实时聚合酶链反应检测

Real-time PCR assay for the diagnosis of pleural tuberculosis.

作者信息

Casallas-Rivera Martha Alejandra, Cárdenas Bernal Ana María, Giraldo-Cadavid Luis Fernando, Prieto Diago Enrique, Santander Sandra Paola

机构信息

Universidad de la Sabana. Chía, Colombia.

Internal Medicine, Hospital Universitario de la Samaritana. Bogotá, Colombia.

出版信息

Colomb Med (Cali). 2017 Jun 30;48(2):47-52.

Abstract

INTRODUCTION

The diagnosis of pleural tuberculosis requires an invasive and time-consuming reference method. Polymerase chain reaction (PCR) is rapid, but validation in pleural tuberculosis is still weak.

OBJECTIVE

To establish the operating characteristics of real-time polymerase chain reaction (RT-PCR) hybridization probes for the diagnosis of pleural tuberculosis.

METHODS

The validity of the RT-PCR hybridization probes was evaluated compared to a composite reference method by a cross-sectional study at the Hospital Universitario de la Samaritana. 40 adults with lymphocytic pleural effusion were included. Pleural tuberculosis was confirmed (in 9 patients) if the patient had at least one of three tests using the positive reference method: Ziehl-Neelsen or tuberculosis culture in fluid or pleural tissue, or pleural biopsy with granulomas. Pleural tuberculosis was ruled out (in 31 patients) if all three tests were negative. The operating characteristics of the RT-PCR, using the Mid-P Exact Test, were determined using the OpenEpi 2.3 Software (2009).

RESULTS

The RT-PCR hybridization probes showed a sensitivity of 66.7% (95% CI: 33.2%-90.7%) and a specificity of 93.5% (95% CI: 80.3%-98.9%). The PPV was 75.0% (95% CI: 38.8%-95.6%) and a NPV of 90.6% (95% CI: 76.6%-97.6%). Two false positives were found for the test, one with pleural mesothelioma and the other with chronic pleuritis with mesothelial hyperplasia.

CONCLUSIONS

The RT-PCR hybridization probes had good specificity and acceptable sensitivity, but a negative value cannot rule out pleural tuberculosis.

摘要

引言

胸膜结核的诊断需要一种具有侵入性且耗时的参考方法。聚合酶链反应(PCR)速度快,但在胸膜结核中的验证仍然不足。

目的

建立用于诊断胸膜结核的实时聚合酶链反应(RT-PCR)杂交探针的操作特征。

方法

在萨马利塔纳大学医院通过横断面研究,将RT-PCR杂交探针的有效性与复合参考方法进行比较。纳入40例淋巴细胞性胸腔积液的成年人。如果患者使用阳性参考方法进行的三项检测中至少有一项呈阳性,则确诊为胸膜结核(9例患者):齐-尼氏染色或胸腔积液或胸膜组织中的结核培养,或胸膜活检发现肉芽肿。如果三项检测均为阴性,则排除胸膜结核(31例患者)。使用OpenEpi 2.3软件(2009),采用Mid-P精确检验确定RT-PCR的操作特征。

结果

RT-PCR杂交探针的敏感性为66.7%(95%置信区间:33.2%-90.7%),特异性为93.5%(95%置信区间:80.3%-98.9%)。阳性预测值为75.0%(95%置信区间:38.8%-95.6%),阴性预测值为90.6%(95%-置信区间:76.6%-97.6%)。该检测发现两例假阳性,一例为胸膜间皮瘤,另一例为伴有间皮增生的慢性胸膜炎。

结论

RT-PCR杂交探针具有良好特异性和可接受的敏感性,但阴性结果不能排除胸膜结核。

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