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Real-time PCR assay for the diagnosis of pleural tuberculosis

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 (...

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Autores principales: Casallas-Rivera, Martha Alejandra, Cárdenas Bernal, Ana María, Giraldo-Cadavid, Luis Fernando, Prieto Diago, Enrique, Santander, Sandra Paola
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Universidad del Valle 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5625560/
https://www.ncbi.nlm.nih.gov/pubmed/29021638
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author Casallas-Rivera, Martha Alejandra
Cárdenas Bernal, Ana María
Giraldo-Cadavid, Luis Fernando
Prieto Diago, Enrique
Santander, Sandra Paola
author_facet Casallas-Rivera, Martha Alejandra
Cárdenas Bernal, Ana María
Giraldo-Cadavid, Luis Fernando
Prieto Diago, Enrique
Santander, Sandra Paola
author_sort Casallas-Rivera, Martha Alejandra
collection PubMed
description 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 Mycobacterium 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.
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spelling pubmed-56255602017-10-11 Real-time PCR assay for the diagnosis of pleural tuberculosis Casallas-Rivera, Martha Alejandra Cárdenas Bernal, Ana María Giraldo-Cadavid, Luis Fernando Prieto Diago, Enrique Santander, Sandra Paola Colomb Med (Cali) Original Article 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 Mycobacterium 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. Universidad del Valle 2017-06-30 /pmc/articles/PMC5625560/ /pubmed/29021638 Text en Copyright © 2017 Universidad del Valle This article is distributed under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Original Article
Casallas-Rivera, Martha Alejandra
Cárdenas Bernal, Ana María
Giraldo-Cadavid, Luis Fernando
Prieto Diago, Enrique
Santander, Sandra Paola
Real-time PCR assay for the diagnosis of pleural tuberculosis
title Real-time PCR assay for the diagnosis of pleural tuberculosis
title_full Real-time PCR assay for the diagnosis of pleural tuberculosis
title_fullStr Real-time PCR assay for the diagnosis of pleural tuberculosis
title_full_unstemmed Real-time PCR assay for the diagnosis of pleural tuberculosis
title_short Real-time PCR assay for the diagnosis of pleural tuberculosis
title_sort real-time pcr assay for the diagnosis of pleural tuberculosis
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5625560/
https://www.ncbi.nlm.nih.gov/pubmed/29021638
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