Detecting Drug-Resistant Tuberculosis: The Importance of Rapid Testing
Despite numerous intervention strategies, including the direct observed short-course treatment strategy and improved diagnostic methods, the incidence of multidrug-resistant and extensively drug-resistant tuberculosis (TB) continues to rise globally. Many treatment policies are based on the model th...
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Veröffentlicht in: | Molecular diagnosis & therapy 2011-07, Vol.15 (4), p.189-194 |
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description | Despite numerous intervention strategies, including the direct observed short-course treatment strategy and improved diagnostic methods, the incidence of multidrug-resistant and extensively drug-resistant tuberculosis (TB) continues to rise globally.
Many treatment policies are based on the model that acquisition of drug resistance in already infected individuals drives the drug-resistant TB epidemic, hence the focus on drug-resistance testing of retreatment cases. However, molecular epidemiology and mathematical modeling suggest that the majority of multidrug-resistant TB cases are due to ongoing transmission of multidrug-resistant strains. This is most likely the result of diagnostic delay, thereby emphasizing the need for rapid diagnostics and comprehensive contact tracing, as well as active case finding.
Current diagnosis of TB in low-income, high-burden regions relies on smear microscopy and clinical signs and symptoms. However, this smear-centered approach has many pitfalls, including low sensitivity in HIV patients and children, the inability of smear to reveal drug-resistance patterns, and the need for sampling on consecutive days.
In order to address these limitations, efforts have been made to expand access to
Mycobacterium tuberculosis
culture and drug susceptibility testing. However, the slow growth rate of the causative agent,
M. tuberculosis
, contributes to significant diagnostic delay.
Molecular-based diagnostic methods, targeting mutations that are known to confirm drug resistance, are capable of significantly reducing diagnostic delay. Two such methods, the line-probe assay and the real-time PCR-based Xpert® MTB/RIF assay, have been described. The latter test shows particular promise for smear-negative and extrapulmonary specimens. This may prove especially useful in settings where co-infection rates with HIV are high. However, since most research focuses on the performance of both of these assays, further investigations need to be done regarding the impact of the routine implementation of these assays on TB control programs and the cost effectiveness thereof. |
doi_str_mv | 10.1007/BF03256410 |
format | Article |
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Many treatment policies are based on the model that acquisition of drug resistance in already infected individuals drives the drug-resistant TB epidemic, hence the focus on drug-resistance testing of retreatment cases. However, molecular epidemiology and mathematical modeling suggest that the majority of multidrug-resistant TB cases are due to ongoing transmission of multidrug-resistant strains. This is most likely the result of diagnostic delay, thereby emphasizing the need for rapid diagnostics and comprehensive contact tracing, as well as active case finding.
Current diagnosis of TB in low-income, high-burden regions relies on smear microscopy and clinical signs and symptoms. However, this smear-centered approach has many pitfalls, including low sensitivity in HIV patients and children, the inability of smear to reveal drug-resistance patterns, and the need for sampling on consecutive days.
In order to address these limitations, efforts have been made to expand access to
Mycobacterium tuberculosis
culture and drug susceptibility testing. However, the slow growth rate of the causative agent,
M. tuberculosis
, contributes to significant diagnostic delay.
Molecular-based diagnostic methods, targeting mutations that are known to confirm drug resistance, are capable of significantly reducing diagnostic delay. Two such methods, the line-probe assay and the real-time PCR-based Xpert® MTB/RIF assay, have been described. The latter test shows particular promise for smear-negative and extrapulmonary specimens. This may prove especially useful in settings where co-infection rates with HIV are high. However, since most research focuses on the performance of both of these assays, further investigations need to be done regarding the impact of the routine implementation of these assays on TB control programs and the cost effectiveness thereof.</description><identifier>ISSN: 1177-1062</identifier><identifier>EISSN: 1179-2000</identifier><identifier>DOI: 10.1007/BF03256410</identifier><language>eng</language><publisher>Cham: Springer International Publishing</publisher><subject>Biomedical and Life Sciences ; Biomedicine ; Cancer Research ; Current Opinion ; Diagnosis ; Extensively drug-resistant tuberculosis ; Human Genetics ; Laboratory Medicine ; Medical tests ; Methods ; Molecular Medicine ; Pharmacotherapy</subject><ispartof>Molecular diagnosis & therapy, 2011-07, Vol.15 (4), p.189-194</ispartof><rights>Adis Data Information BV 2011</rights><rights>COPYRIGHT 2011 Wolters Kluwer Health, Inc.</rights><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c223t-45aef716dbf7404ede16962c40243e0309a74476a4b4216586a188e15a5773533</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/BF03256410$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/BF03256410$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids></links><search><creatorcontrib>Hoek, Kim G. P.</creatorcontrib><creatorcontrib>Van Rie, Annelies</creatorcontrib><creatorcontrib>van Helden, Paul D.</creatorcontrib><creatorcontrib>Warren, Robin M.</creatorcontrib><creatorcontrib>Victor, Thomas C.</creatorcontrib><title>Detecting Drug-Resistant Tuberculosis: The Importance of Rapid Testing</title><title>Molecular diagnosis & therapy</title><addtitle>Mol Diag Ther</addtitle><description>Despite numerous intervention strategies, including the direct observed short-course treatment strategy and improved diagnostic methods, the incidence of multidrug-resistant and extensively drug-resistant tuberculosis (TB) continues to rise globally.
Many treatment policies are based on the model that acquisition of drug resistance in already infected individuals drives the drug-resistant TB epidemic, hence the focus on drug-resistance testing of retreatment cases. However, molecular epidemiology and mathematical modeling suggest that the majority of multidrug-resistant TB cases are due to ongoing transmission of multidrug-resistant strains. This is most likely the result of diagnostic delay, thereby emphasizing the need for rapid diagnostics and comprehensive contact tracing, as well as active case finding.
Current diagnosis of TB in low-income, high-burden regions relies on smear microscopy and clinical signs and symptoms. However, this smear-centered approach has many pitfalls, including low sensitivity in HIV patients and children, the inability of smear to reveal drug-resistance patterns, and the need for sampling on consecutive days.
In order to address these limitations, efforts have been made to expand access to
Mycobacterium tuberculosis
culture and drug susceptibility testing. However, the slow growth rate of the causative agent,
M. tuberculosis
, contributes to significant diagnostic delay.
Molecular-based diagnostic methods, targeting mutations that are known to confirm drug resistance, are capable of significantly reducing diagnostic delay. Two such methods, the line-probe assay and the real-time PCR-based Xpert® MTB/RIF assay, have been described. The latter test shows particular promise for smear-negative and extrapulmonary specimens. This may prove especially useful in settings where co-infection rates with HIV are high. However, since most research focuses on the performance of both of these assays, further investigations need to be done regarding the impact of the routine implementation of these assays on TB control programs and the cost effectiveness thereof.</description><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Cancer Research</subject><subject>Current Opinion</subject><subject>Diagnosis</subject><subject>Extensively drug-resistant tuberculosis</subject><subject>Human Genetics</subject><subject>Laboratory Medicine</subject><subject>Medical tests</subject><subject>Methods</subject><subject>Molecular Medicine</subject><subject>Pharmacotherapy</subject><issn>1177-1062</issn><issn>1179-2000</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><recordid>eNptkE9Lw0AQxRdRsFYvfoKCeFFSZ_8nx9paFQqC1POy3UzCljSR3eTgt-9qBRHKHGZ4_N6DeYRcU5hSAP3wuATOpBIUTsiIUl1kDABOf26dUVDsnFzEuAUQUhVsRG4X2KPrfVtPFmGos3eMPva27SfrYYPBDU2XhEtyVtkm4tXvHpOP5dN6_pKt3p5f57NV5hjjfSakxUpTVW4qLUBgiVQVijkBTHAEDoXVQmhlxUYwqmSuLM1zpNJKrbnkfExuDrm1bdD4tur6YN3OR2dmTOUpk6kiUdMjVJoSd951LVY-6f8MdweDC12MASvzGfzOhi9DwXz3Zv56S_D9AY4JamsMZtsNoU1vH6P3651pBQ</recordid><startdate>20110701</startdate><enddate>20110701</enddate><creator>Hoek, Kim G. P.</creator><creator>Van Rie, Annelies</creator><creator>van Helden, Paul D.</creator><creator>Warren, Robin M.</creator><creator>Victor, Thomas C.</creator><general>Springer International Publishing</general><general>Wolters Kluwer Health, Inc</general><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20110701</creationdate><title>Detecting Drug-Resistant Tuberculosis</title><author>Hoek, Kim G. P. ; Van Rie, Annelies ; van Helden, Paul D. ; Warren, Robin M. ; Victor, Thomas C.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c223t-45aef716dbf7404ede16962c40243e0309a74476a4b4216586a188e15a5773533</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Cancer Research</topic><topic>Current Opinion</topic><topic>Diagnosis</topic><topic>Extensively drug-resistant tuberculosis</topic><topic>Human Genetics</topic><topic>Laboratory Medicine</topic><topic>Medical tests</topic><topic>Methods</topic><topic>Molecular Medicine</topic><topic>Pharmacotherapy</topic><toplevel>online_resources</toplevel><creatorcontrib>Hoek, Kim G. P.</creatorcontrib><creatorcontrib>Van Rie, Annelies</creatorcontrib><creatorcontrib>van Helden, Paul D.</creatorcontrib><creatorcontrib>Warren, Robin M.</creatorcontrib><creatorcontrib>Victor, Thomas C.</creatorcontrib><collection>CrossRef</collection><jtitle>Molecular diagnosis & therapy</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hoek, Kim G. P.</au><au>Van Rie, Annelies</au><au>van Helden, Paul D.</au><au>Warren, Robin M.</au><au>Victor, Thomas C.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Detecting Drug-Resistant Tuberculosis: The Importance of Rapid Testing</atitle><jtitle>Molecular diagnosis & therapy</jtitle><stitle>Mol Diag Ther</stitle><date>2011-07-01</date><risdate>2011</risdate><volume>15</volume><issue>4</issue><spage>189</spage><epage>194</epage><pages>189-194</pages><issn>1177-1062</issn><eissn>1179-2000</eissn><abstract>Despite numerous intervention strategies, including the direct observed short-course treatment strategy and improved diagnostic methods, the incidence of multidrug-resistant and extensively drug-resistant tuberculosis (TB) continues to rise globally.
Many treatment policies are based on the model that acquisition of drug resistance in already infected individuals drives the drug-resistant TB epidemic, hence the focus on drug-resistance testing of retreatment cases. However, molecular epidemiology and mathematical modeling suggest that the majority of multidrug-resistant TB cases are due to ongoing transmission of multidrug-resistant strains. This is most likely the result of diagnostic delay, thereby emphasizing the need for rapid diagnostics and comprehensive contact tracing, as well as active case finding.
Current diagnosis of TB in low-income, high-burden regions relies on smear microscopy and clinical signs and symptoms. However, this smear-centered approach has many pitfalls, including low sensitivity in HIV patients and children, the inability of smear to reveal drug-resistance patterns, and the need for sampling on consecutive days.
In order to address these limitations, efforts have been made to expand access to
Mycobacterium tuberculosis
culture and drug susceptibility testing. However, the slow growth rate of the causative agent,
M. tuberculosis
, contributes to significant diagnostic delay.
Molecular-based diagnostic methods, targeting mutations that are known to confirm drug resistance, are capable of significantly reducing diagnostic delay. Two such methods, the line-probe assay and the real-time PCR-based Xpert® MTB/RIF assay, have been described. The latter test shows particular promise for smear-negative and extrapulmonary specimens. This may prove especially useful in settings where co-infection rates with HIV are high. However, since most research focuses on the performance of both of these assays, further investigations need to be done regarding the impact of the routine implementation of these assays on TB control programs and the cost effectiveness thereof.</abstract><cop>Cham</cop><pub>Springer International Publishing</pub><doi>10.1007/BF03256410</doi><tpages>6</tpages></addata></record> |
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subjects | Biomedical and Life Sciences Biomedicine Cancer Research Current Opinion Diagnosis Extensively drug-resistant tuberculosis Human Genetics Laboratory Medicine Medical tests Methods Molecular Medicine Pharmacotherapy |
title | Detecting Drug-Resistant Tuberculosis: The Importance of Rapid Testing |
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