Utility of nucleic acid amplification techniques for the diagnosis of pulmonary tuberculosis in sub-Saharan Africa
SETTING: Lusaka, Zambia.OBJECTIVES: To investigate the utility of nucleic amplification tests for the diagnosis of pulmonary tuberculosis in a resource-poor setting with a high incidence of human immunodeficiency virus (HIV).DESIGN: Sputum specimens from suspects attending a referral chest clinic we...
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creator | KAMBASHI, B MBULO, G MCNERNEY, R TEMBWE, R KAMBASHI, A TIHON, V GODFREY-FAUSSETT, P |
description | SETTING: Lusaka, Zambia.OBJECTIVES: To investigate the utility of nucleic amplification tests for the diagnosis of pulmonary tuberculosis in a resource-poor setting with a high incidence of human immunodeficiency virus (HIV).DESIGN: Sputum specimens from suspects attending a referral chest clinic were examined by low-cost 'in-house' one-tube nested polymerase chain reaction (PCR), the enhanced Gen-Probe Amplified Mycobacterium Direct Test (AMTD), auramine smear and Löwenstein-Jensen culture.RESULTS: PCR and AMTD detected respectively 80% and 92% of smear-positive specimens and 40% and 60% of smear-negative, culture-positive specimens. AMTD was positive for 18 culture-negative suspects; subsequent investigation indicated these to be six confirmed tuberculosis patients, nine judged from radiological data and clinical follow-up studies to have pulmonary tuberculosis, and three non-tuberculosis patients. Sensitivity for smear, culture, PCR and AMTD, when compared to a gold standard incorporating both microbiological and clinical data, was respectively 29%, 69%, 55% and 81%.CONCLUSION: In this setting, the sensitivity of the low-cost PCR proved insufficient for its effective use as a tool for diagnosing pulmonary tuberculosis, while AMTD performed considerably better than the current laboratory methods for diagnosis of pulmonary tuberculosis. However, the high cost of this technology may limit its application in the public sector of low-income countries. |
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AMTD was positive for 18 culture-negative suspects; subsequent investigation indicated these to be six confirmed tuberculosis patients, nine judged from radiological data and clinical follow-up studies to have pulmonary tuberculosis, and three non-tuberculosis patients. Sensitivity for smear, culture, PCR and AMTD, when compared to a gold standard incorporating both microbiological and clinical data, was respectively 29%, 69%, 55% and 81%.CONCLUSION: In this setting, the sensitivity of the low-cost PCR proved insufficient for its effective use as a tool for diagnosing pulmonary tuberculosis, while AMTD performed considerably better than the current laboratory methods for diagnosis of pulmonary tuberculosis. However, the high cost of this technology may limit its application in the public sector of low-income countries.</description><identifier>ISSN: 1027-3719</identifier><identifier>EISSN: 1815-7920</identifier><identifier>PMID: 11334256</identifier><language>eng</language><publisher>Paris: The International Union Against Tuberculosis & Lung Disease</publisher><subject>Adult ; AIDS-Related Opportunistic Infections - diagnosis ; AIDS-Related Opportunistic Infections - epidemiology ; Amtd ; Bacterial diseases ; Bacterial diseases of the respiratory system ; Base Sequence ; Biological and medical sciences ; Developing Countries ; Diagnosis ; Female ; Human bacterial diseases ; Humans ; Infectious diseases ; Male ; Medical sciences ; Molecular Sequence Data ; Mycobacterium tuberculosis - isolation & purification ; Nucleic Acid Amplification Techniques - methods ; Nucleic Acid Amplification Techniques - utilization ; PCR ; Polymerase Chain Reaction - methods ; Sampling Studies ; Sensitivity and Specificity ; Tuberculosis ; Tuberculosis, Pulmonary - diagnosis ; Tuberculosis, Pulmonary - epidemiology ; Zambia - epidemiology</subject><ispartof>The international journal of tuberculosis and lung disease, 2001-04, Vol.5 (4), p.364-369</ispartof><rights>2001 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=991709$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11334256$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>KAMBASHI, B</creatorcontrib><creatorcontrib>MBULO, G</creatorcontrib><creatorcontrib>MCNERNEY, R</creatorcontrib><creatorcontrib>TEMBWE, R</creatorcontrib><creatorcontrib>KAMBASHI, A</creatorcontrib><creatorcontrib>TIHON, V</creatorcontrib><creatorcontrib>GODFREY-FAUSSETT, P</creatorcontrib><title>Utility of nucleic acid amplification techniques for the diagnosis of pulmonary tuberculosis in sub-Saharan Africa</title><title>The international journal of tuberculosis and lung disease</title><addtitle>Int J Tuberc Lung Dis</addtitle><description>SETTING: Lusaka, Zambia.OBJECTIVES: To investigate the utility of nucleic amplification tests for the diagnosis of pulmonary tuberculosis in a resource-poor setting with a high incidence of human immunodeficiency virus (HIV).DESIGN: Sputum specimens from suspects attending a referral chest clinic were examined by low-cost 'in-house' one-tube nested polymerase chain reaction (PCR), the enhanced Gen-Probe Amplified Mycobacterium Direct Test (AMTD), auramine smear and Löwenstein-Jensen culture.RESULTS: PCR and AMTD detected respectively 80% and 92% of smear-positive specimens and 40% and 60% of smear-negative, culture-positive specimens. AMTD was positive for 18 culture-negative suspects; subsequent investigation indicated these to be six confirmed tuberculosis patients, nine judged from radiological data and clinical follow-up studies to have pulmonary tuberculosis, and three non-tuberculosis patients. Sensitivity for smear, culture, PCR and AMTD, when compared to a gold standard incorporating both microbiological and clinical data, was respectively 29%, 69%, 55% and 81%.CONCLUSION: In this setting, the sensitivity of the low-cost PCR proved insufficient for its effective use as a tool for diagnosing pulmonary tuberculosis, while AMTD performed considerably better than the current laboratory methods for diagnosis of pulmonary tuberculosis. However, the high cost of this technology may limit its application in the public sector of low-income countries.</description><subject>Adult</subject><subject>AIDS-Related Opportunistic Infections - diagnosis</subject><subject>AIDS-Related Opportunistic Infections - epidemiology</subject><subject>Amtd</subject><subject>Bacterial diseases</subject><subject>Bacterial diseases of the respiratory system</subject><subject>Base Sequence</subject><subject>Biological and medical sciences</subject><subject>Developing Countries</subject><subject>Diagnosis</subject><subject>Female</subject><subject>Human bacterial diseases</subject><subject>Humans</subject><subject>Infectious diseases</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Molecular Sequence Data</subject><subject>Mycobacterium tuberculosis - isolation & purification</subject><subject>Nucleic Acid Amplification Techniques - methods</subject><subject>Nucleic Acid Amplification Techniques - utilization</subject><subject>PCR</subject><subject>Polymerase Chain Reaction - methods</subject><subject>Sampling Studies</subject><subject>Sensitivity and Specificity</subject><subject>Tuberculosis</subject><subject>Tuberculosis, Pulmonary - diagnosis</subject><subject>Tuberculosis, Pulmonary - epidemiology</subject><subject>Zambia - epidemiology</subject><issn>1027-3719</issn><issn>1815-7920</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kctqHDEQRZuQEDtOfiEIAtk1SOrWqLU0zhMMNiReixo9ZmpQqyd6BJyvj9ozzi61UBXo6FJX90V3ySYmeqk4fdlmymU_SKYuujc5HyjljDH5urtgbBhGLjaXXXooGLA8ksWTWE1waAgYtATmY0CPBgoukRRn9hF_VZeJXxIpe0cswi4uGfP69FjDvERIj6TUrUumhqcbjCTXbf8D9pAgkmufmuDb7pWHkN27c7_qHr58_nnzrb-9-_r95vq2x2GjSm-Y2ngwVtoJJj45ykQrs2USKFXeSTHAZMUomZPeeSVBDcwJS83YcMaHq-7jSfeYlnXzomfMxoUA0S01a0knKgYhGvj-DNbt7Kw-JpybFf38Sw34cAYgGwi-eTGY_3FKMUlVo-5PFMadiwX0YakpNocajcYKJVi9JrIGon-LOGreAqETF5oJNmrrPNRQdIGkd390frLw6X-SJz08rCenlGl6KvE8jBpSab3J_AWfE6Nj</recordid><startdate>20010401</startdate><enddate>20010401</enddate><creator>KAMBASHI, B</creator><creator>MBULO, G</creator><creator>MCNERNEY, R</creator><creator>TEMBWE, R</creator><creator>KAMBASHI, A</creator><creator>TIHON, V</creator><creator>GODFREY-FAUSSETT, P</creator><general>The International Union Against Tuberculosis & Lung Disease</general><general>Union internationale contre la tuberculose et les maladies respiratoires</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>20010401</creationdate><title>Utility of nucleic acid amplification techniques for the diagnosis of pulmonary tuberculosis in sub-Saharan Africa</title><author>KAMBASHI, B ; MBULO, G ; MCNERNEY, R ; TEMBWE, R ; KAMBASHI, A ; TIHON, V ; GODFREY-FAUSSETT, P</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-i369t-c196facd7d8a828e015555cb17a009fe753a8d5471e7fef97a931e5d0c4828123</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>Adult</topic><topic>AIDS-Related Opportunistic Infections - diagnosis</topic><topic>AIDS-Related Opportunistic Infections - epidemiology</topic><topic>Amtd</topic><topic>Bacterial diseases</topic><topic>Bacterial diseases of the respiratory system</topic><topic>Base Sequence</topic><topic>Biological and medical sciences</topic><topic>Developing Countries</topic><topic>Diagnosis</topic><topic>Female</topic><topic>Human bacterial diseases</topic><topic>Humans</topic><topic>Infectious diseases</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Molecular Sequence Data</topic><topic>Mycobacterium tuberculosis - isolation & purification</topic><topic>Nucleic Acid Amplification Techniques - methods</topic><topic>Nucleic Acid Amplification Techniques - utilization</topic><topic>PCR</topic><topic>Polymerase Chain Reaction - methods</topic><topic>Sampling Studies</topic><topic>Sensitivity and Specificity</topic><topic>Tuberculosis</topic><topic>Tuberculosis, Pulmonary - diagnosis</topic><topic>Tuberculosis, Pulmonary - epidemiology</topic><topic>Zambia - epidemiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>KAMBASHI, B</creatorcontrib><creatorcontrib>MBULO, G</creatorcontrib><creatorcontrib>MCNERNEY, R</creatorcontrib><creatorcontrib>TEMBWE, R</creatorcontrib><creatorcontrib>KAMBASHI, A</creatorcontrib><creatorcontrib>TIHON, V</creatorcontrib><creatorcontrib>GODFREY-FAUSSETT, P</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>The international journal of tuberculosis and lung disease</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>KAMBASHI, B</au><au>MBULO, G</au><au>MCNERNEY, R</au><au>TEMBWE, R</au><au>KAMBASHI, A</au><au>TIHON, V</au><au>GODFREY-FAUSSETT, P</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Utility of nucleic acid amplification techniques for the diagnosis of pulmonary tuberculosis in sub-Saharan Africa</atitle><jtitle>The international journal of tuberculosis and lung disease</jtitle><addtitle>Int J Tuberc Lung Dis</addtitle><date>2001-04-01</date><risdate>2001</risdate><volume>5</volume><issue>4</issue><spage>364</spage><epage>369</epage><pages>364-369</pages><issn>1027-3719</issn><eissn>1815-7920</eissn><abstract>SETTING: Lusaka, Zambia.OBJECTIVES: To investigate the utility of nucleic amplification tests for the diagnosis of pulmonary tuberculosis in a resource-poor setting with a high incidence of human immunodeficiency virus (HIV).DESIGN: Sputum specimens from suspects attending a referral chest clinic were examined by low-cost 'in-house' one-tube nested polymerase chain reaction (PCR), the enhanced Gen-Probe Amplified Mycobacterium Direct Test (AMTD), auramine smear and Löwenstein-Jensen culture.RESULTS: PCR and AMTD detected respectively 80% and 92% of smear-positive specimens and 40% and 60% of smear-negative, culture-positive specimens. AMTD was positive for 18 culture-negative suspects; subsequent investigation indicated these to be six confirmed tuberculosis patients, nine judged from radiological data and clinical follow-up studies to have pulmonary tuberculosis, and three non-tuberculosis patients. Sensitivity for smear, culture, PCR and AMTD, when compared to a gold standard incorporating both microbiological and clinical data, was respectively 29%, 69%, 55% and 81%.CONCLUSION: In this setting, the sensitivity of the low-cost PCR proved insufficient for its effective use as a tool for diagnosing pulmonary tuberculosis, while AMTD performed considerably better than the current laboratory methods for diagnosis of pulmonary tuberculosis. However, the high cost of this technology may limit its application in the public sector of low-income countries.</abstract><cop>Paris</cop><pub>The International Union Against Tuberculosis & Lung Disease</pub><pmid>11334256</pmid><tpages>6</tpages></addata></record> |
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subjects | Adult AIDS-Related Opportunistic Infections - diagnosis AIDS-Related Opportunistic Infections - epidemiology Amtd Bacterial diseases Bacterial diseases of the respiratory system Base Sequence Biological and medical sciences Developing Countries Diagnosis Female Human bacterial diseases Humans Infectious diseases Male Medical sciences Molecular Sequence Data Mycobacterium tuberculosis - isolation & purification Nucleic Acid Amplification Techniques - methods Nucleic Acid Amplification Techniques - utilization PCR Polymerase Chain Reaction - methods Sampling Studies Sensitivity and Specificity Tuberculosis Tuberculosis, Pulmonary - diagnosis Tuberculosis, Pulmonary - epidemiology Zambia - epidemiology |
title | Utility of nucleic acid amplification techniques for the diagnosis of pulmonary tuberculosis in sub-Saharan Africa |
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