Dynamics of the laboratory results in patients with pulmonary tuberculosis
Abstract The process of infection and disease development is difficult to follow-up before tuberculosis (TB) confirmation. The laboratory analysis mirrors the infection with the possible subsequent breakdown to clinical TB. To better define the dynamics of the laboratory results in suspected and alr...
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Veröffentlicht in: | Diagnostic microbiology and infectious disease 2010-08, Vol.67 (4), p.327-332 |
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description | Abstract The process of infection and disease development is difficult to follow-up before tuberculosis (TB) confirmation. The laboratory analysis mirrors the infection with the possible subsequent breakdown to clinical TB. To better define the dynamics of the laboratory results in suspected and already confirmed patients with pulmonary TB, we studied the analysis of 1467 pathologic samples collected during the hospitalization of 841 patients. The samples were analyzed by 3 laboratory methods—direct microscopy, culture, and polymerase chain reaction (PCR). It was found that compared to cultures, the PCR method is more sensitive. For few cases, we demonstrate that the PCR result is positive about 2 weeks before the first positive culture. During the treatment follow-up, the PCR result remains positive for a long time, up to 4 to 5 months after the last positive culture. For better definition of the period during which microscopy and culture results remain positive, we studied the laboratory results of 100 casually selected patients with pulmonary TB positive on culture. The median periods during which these patients were found to be microscopy and culture positive were 10 and 25 days, respectively. Second to the dynamics of the laboratory results, we demonstrate that TB development is very rapid, whereas the period of recovery is long. The PCR results have to be reproducibly negative to accept that the process of active therapy is completed and the patient can remain under surveillance. On the basis of the laboratory data obtained, we propose empiric models for the dynamics of the laboratory results for patients with pulmonary tuberculosis. |
doi_str_mv | 10.1016/j.diagmicrobio.2010.03.002 |
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The laboratory analysis mirrors the infection with the possible subsequent breakdown to clinical TB. To better define the dynamics of the laboratory results in suspected and already confirmed patients with pulmonary TB, we studied the analysis of 1467 pathologic samples collected during the hospitalization of 841 patients. The samples were analyzed by 3 laboratory methods—direct microscopy, culture, and polymerase chain reaction (PCR). It was found that compared to cultures, the PCR method is more sensitive. For few cases, we demonstrate that the PCR result is positive about 2 weeks before the first positive culture. During the treatment follow-up, the PCR result remains positive for a long time, up to 4 to 5 months after the last positive culture. For better definition of the period during which microscopy and culture results remain positive, we studied the laboratory results of 100 casually selected patients with pulmonary TB positive on culture. The median periods during which these patients were found to be microscopy and culture positive were 10 and 25 days, respectively. Second to the dynamics of the laboratory results, we demonstrate that TB development is very rapid, whereas the period of recovery is long. The PCR results have to be reproducibly negative to accept that the process of active therapy is completed and the patient can remain under surveillance. On the basis of the laboratory data obtained, we propose empiric models for the dynamics of the laboratory results for patients with pulmonary tuberculosis.</description><identifier>ISSN: 0732-8893</identifier><identifier>EISSN: 1879-0070</identifier><identifier>DOI: 10.1016/j.diagmicrobio.2010.03.002</identifier><identifier>PMID: 20638599</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Bacteriological Techniques - methods ; Diagnosis ; Drug Monitoring ; Follow-Up Studies ; Humans ; Infectious Disease ; Internal Medicine ; Microscopy - methods ; Mycobacterium ; Mycobacterium tuberculosis ; Mycobacterium tuberculosis - cytology ; Mycobacterium tuberculosis - genetics ; Mycobacterium tuberculosis - growth & development ; Mycobacterium tuberculosis - isolation & purification ; PCR ; Polymerase Chain Reaction - methods ; Tuberculosis, Pulmonary - diagnosis ; Tuberculosis, Pulmonary - drug therapy ; Tuberculosis, Pulmonary - microbiology</subject><ispartof>Diagnostic microbiology and infectious disease, 2010-08, Vol.67 (4), p.327-332</ispartof><rights>Elsevier Inc.</rights><rights>2010 Elsevier Inc.</rights><rights>Copyright 2010 Elsevier Inc. 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The laboratory analysis mirrors the infection with the possible subsequent breakdown to clinical TB. To better define the dynamics of the laboratory results in suspected and already confirmed patients with pulmonary TB, we studied the analysis of 1467 pathologic samples collected during the hospitalization of 841 patients. The samples were analyzed by 3 laboratory methods—direct microscopy, culture, and polymerase chain reaction (PCR). It was found that compared to cultures, the PCR method is more sensitive. For few cases, we demonstrate that the PCR result is positive about 2 weeks before the first positive culture. During the treatment follow-up, the PCR result remains positive for a long time, up to 4 to 5 months after the last positive culture. For better definition of the period during which microscopy and culture results remain positive, we studied the laboratory results of 100 casually selected patients with pulmonary TB positive on culture. The median periods during which these patients were found to be microscopy and culture positive were 10 and 25 days, respectively. Second to the dynamics of the laboratory results, we demonstrate that TB development is very rapid, whereas the period of recovery is long. The PCR results have to be reproducibly negative to accept that the process of active therapy is completed and the patient can remain under surveillance. On the basis of the laboratory data obtained, we propose empiric models for the dynamics of the laboratory results for patients with pulmonary tuberculosis.</description><subject>Bacteriological Techniques - methods</subject><subject>Diagnosis</subject><subject>Drug Monitoring</subject><subject>Follow-Up Studies</subject><subject>Humans</subject><subject>Infectious Disease</subject><subject>Internal Medicine</subject><subject>Microscopy - methods</subject><subject>Mycobacterium</subject><subject>Mycobacterium tuberculosis</subject><subject>Mycobacterium tuberculosis - cytology</subject><subject>Mycobacterium tuberculosis - genetics</subject><subject>Mycobacterium tuberculosis - growth & development</subject><subject>Mycobacterium tuberculosis - isolation & purification</subject><subject>PCR</subject><subject>Polymerase Chain Reaction - methods</subject><subject>Tuberculosis, Pulmonary - diagnosis</subject><subject>Tuberculosis, Pulmonary - drug therapy</subject><subject>Tuberculosis, Pulmonary - microbiology</subject><issn>0732-8893</issn><issn>1879-0070</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkU9v1DAQxS0EotvCV0ARF05ZxnbiPxyQUAulqFIPwNlynAn14sSLnYD22-NoC0K9UF9syW_ezPsNIS8pbClQ8Xq37b39NnqXYufjlkH5AL4FYI_IhiqpawAJj8kGJGe1UpqfkNOcdwCU6QaekhMGgqtW6w35dHGYbLHKVRyq-RarYLuY7BzToUqYlzDnyk_V3s4ep_L-5efbar-EMU62SOalw-SWELPPz8iTwYaMz-_uM_L1w_sv5x_r65vLq_N317VrhJjrDrEdlF2TtGg514x1DIahbVrBqRgkSIe2oVQ1nEkuGuy14Chb3tAerOZn5NXRd5_ijwXzbEafHYZgJ4xLNgoka1Vbwv9PKTlvtWBSFeWbo7IwzTnhYPbJjyWhoWDWUc3O_AvdrNANcFOgl-IXd22WbsT-b-kfykVwcRRgwfLTYzLZFZwOe5_QzaaP_mF93t6zccFP3tnwHQ-Yd3FJUwFvqMnMgPm8rn_dPoVylBD8N6qkrls</recordid><startdate>20100801</startdate><enddate>20100801</enddate><creator>Panaiotov, Stefan</creator><creator>Amicosante, Massimo</creator><general>Elsevier Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>7QL</scope><scope>C1K</scope></search><sort><creationdate>20100801</creationdate><title>Dynamics of the laboratory results in patients with pulmonary tuberculosis</title><author>Panaiotov, Stefan ; Amicosante, Massimo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c466t-bee5f8a10165ea33922b20ff5456316f707cea41184327364ed963e75341d0a93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Bacteriological Techniques - methods</topic><topic>Diagnosis</topic><topic>Drug Monitoring</topic><topic>Follow-Up Studies</topic><topic>Humans</topic><topic>Infectious Disease</topic><topic>Internal Medicine</topic><topic>Microscopy - methods</topic><topic>Mycobacterium</topic><topic>Mycobacterium tuberculosis</topic><topic>Mycobacterium tuberculosis - cytology</topic><topic>Mycobacterium tuberculosis - genetics</topic><topic>Mycobacterium tuberculosis - growth & development</topic><topic>Mycobacterium tuberculosis - isolation & purification</topic><topic>PCR</topic><topic>Polymerase Chain Reaction - methods</topic><topic>Tuberculosis, Pulmonary - diagnosis</topic><topic>Tuberculosis, Pulmonary - drug therapy</topic><topic>Tuberculosis, Pulmonary - microbiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Panaiotov, Stefan</creatorcontrib><creatorcontrib>Amicosante, Massimo</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Environmental Sciences and Pollution Management</collection><jtitle>Diagnostic microbiology and infectious disease</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Panaiotov, Stefan</au><au>Amicosante, Massimo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Dynamics of the laboratory results in patients with pulmonary tuberculosis</atitle><jtitle>Diagnostic microbiology and infectious disease</jtitle><addtitle>Diagn Microbiol Infect Dis</addtitle><date>2010-08-01</date><risdate>2010</risdate><volume>67</volume><issue>4</issue><spage>327</spage><epage>332</epage><pages>327-332</pages><issn>0732-8893</issn><eissn>1879-0070</eissn><abstract>Abstract The process of infection and disease development is difficult to follow-up before tuberculosis (TB) confirmation. 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subjects | Bacteriological Techniques - methods Diagnosis Drug Monitoring Follow-Up Studies Humans Infectious Disease Internal Medicine Microscopy - methods Mycobacterium Mycobacterium tuberculosis Mycobacterium tuberculosis - cytology Mycobacterium tuberculosis - genetics Mycobacterium tuberculosis - growth & development Mycobacterium tuberculosis - isolation & purification PCR Polymerase Chain Reaction - methods Tuberculosis, Pulmonary - diagnosis Tuberculosis, Pulmonary - drug therapy Tuberculosis, Pulmonary - microbiology |
title | Dynamics of the laboratory results in patients with pulmonary tuberculosis |
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