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Treatment decisions and mortality in HIV-positive presumptive smear-negative TB in the Xpert (TM) MTB/RIF era: a cohort study

Treatment decisions and mortality in HIV-positive presumptive smear-negative TB in the Xpert (TM) MTB/RIF era: a cohort study

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dc.contributor.author Hermans, Sabine M.
dc.contributor.author Babirye, Juliet A.
dc.contributor.author Mbabazi, Olive
dc.contributor.author Kakooza, Francis
dc.contributor.author Colebunders, Robert
dc.contributor.author Castelnuovo, Barbara
dc.contributor.author Sekaggya-Wiltshire, Christine
dc.contributor.author Parkes-Ratanshi, Rosalind
dc.contributor.author Manabe, Yukari C.
dc.date.accessioned 2021-01-01T21:58:20Z
dc.date.available 2021-01-01T21:58:20Z
dc.date.issued 2017
dc.identifier.issn 1471-2334
dc.identifier.uri http://combine.alvar.ug/handle/1/48266
dc.description.abstract Background: The Xpert (TM) MTB/RIF (XP) has a higher sensitivity than sputum smear microscopy (70% versus 35%) for TB diagnosis and has been endorsed by the WHO for TB high burden countries to increase case finding among HIV co-infected presumptive TB patients. Its impact on the diagnosis of smear-negative TB in a routine care setting is unclear. We determined the change in diagnosis, treatment and mortality of smear-negative presumptive TB with routine use of Xpert MTB/RIF (XP). Methods: Prospective cohort study of HIV-positive smear-negative presumptive TB patients during a 12-month period after XP implementation in a well-staffed and trained integrated TB/HIV clinic in Kampala, Uganda. Prior to testing clinicians were asked to decide whether they would treat empirically prior to Xpert result; actual treatment was decided upon receipt of the XP result. We compared empirical and XP-informed treatment decisions and all-cause mortality in the first year. Results: Of 411 smear-negative presumptive TB patients, 175 (43%) received an XP; their baseline characteristics did not differ. XP positivity was similar in patients with a pre-XP empirical diagnosis and those without (9/29 [17%] versus 14/142 [10%], P = 0.23). Despite XP testing high levels of empirical treatment prevailed (18%), although XP results did change who ultimately was treated for TB. When adjusted for CD4 count, empirical treatment was not associated with higher mortality compared to no or microbiologically confirmed treatment. Conclusions: XP usage was lower than expected. The lower sensitivity of XP in smear-negative HIV-positive patients led experienced clinicians to use XP as a "rule-in" rather than "rule-out" test, with the majority of patients still treated empirically.
dc.description.sponsorship Infectious Diseases Network for Treatment and Research in Africa (INTERACT) programme
dc.description.sponsorship Netherlands Organization for Scientific Research - WOTRO Science for Global Development: NACCAP [W07.05.20100]
dc.description.sponsorship European UnionEuropean Union (EU) [SANTE/2006/105-316]
dc.description.sponsorship European Union Marie Curie International Outgoing Fellowship for Career Development [PIOF-GA-2012-332,311]
dc.description.sponsorship National Institutes of Health (DMID under the Tuberculosis Clinical Diagnostics Research Consortium [NIH/NIAID] [HHSN272200900050C]
dc.description.sponsorship Office of the Global AIDS Coordinator [RFA-TW-10-008]
dc.description.sponsorship FOGARTY INTERNATIONAL CENTERUnited States Department of Health & Human ServicesNational Institutes of Health (NIH) - USANIH Fogarty International Center (FIC) [D43TW009771, D43TW009771, D43TW009771, D43TW009771, D43TW009771, D43TW009771] Funding Source: NIH RePORTER
dc.language English
dc.publisher BMC
dc.relation.ispartof BMC Infectious Diseases
dc.subject Empirical Treatment
dc.subject Molecular Diagnostic Techniques/Methods
dc.subject Tuberculosis
dc.subject Pulmonary/Diagnosis
dc.subject Tuberculosis
dc.subject Pulmonary/Epidemiology
dc.subject Hiv Infections/Complications
dc.title Treatment decisions and mortality in HIV-positive presumptive smear-negative TB in the Xpert (TM) MTB/RIF era: a cohort study
dc.type Article
dc.identifier.isi 000403621700001
dc.identifier.doi 10.1186/s12879-017-2534-2
dc.identifier.pmid 28622763
dc.publisher.city LONDON
dc.publisher.address CAMPUS, 4 CRINAN ST, LONDON N1 9XW, ENGLAND
dc.identifier.volume 17
dc.subject.wc Infectious Diseases
dc.subject.sc Infectious Diseases
dc.description.oa DOAJ Gold
dc.description.oa Green Published
dc.description.pages 8
dc.subject.kwp Roll-Out
dc.subject.kwp Tuberculosis
dc.subject.kwp Implementation
dc.subject.kwp Feasibility
dc.subject.kwp Multicenter
dc.subject.kwp Diagnosis
dc.subject.kwp Accuracy
dc.subject.kwp Impact
dc.identifier.articleno 433
dc.description.affiliation Makerere Univ, Coll Hlth Sci, Infect Dis Inst, POB 22418, Kampala, Uganda
dc.description.affiliation Makerere Univ, Coll Hlth Sci, Sch Med, Dept Internal Med, Kampala, Uganda
dc.description.affiliation Univ Amsterdam, Acad Med Ctr, Amsterdam Inst Global Hlth & Dev, Dept Global Hlth, Amsterdam, Netherlands
dc.description.affiliation Univ Antwerp, Inst Trop Med, Antwerp, Belgium
dc.description.affiliation Univ Antwerp, Global Hlth Inst, Antwerp, Belgium
dc.description.affiliation Univ Cambridge, Inst Publ Hlth, Cambridge, England
dc.description.affiliation Johns Hopkins Univ, Sch Med, Dept Med, Div Infect Dis, Baltimore, MD 21205 USA
dc.description.email s.hermans@aighd.org
dc.description.corr Hermans, SM (corresponding author), Makerere Univ, Coll Hlth Sci, Infect Dis Inst, POB 22418, Kampala, Uganda.; Hermans, SM (corresponding author), Makerere Univ, Coll Hlth Sci, Sch Med, Dept Internal Med, Kampala, Uganda.; Hermans, SM (corresponding author), Univ Amsterdam, Acad Med Ctr, Amsterdam Inst Global Hlth & Dev, Dept Global Hlth, Amsterdam, Netherlands.
dc.description.orcid Parkes-Ratanshi, Rosalind/0000-0001-9297-1311
dc.description.orcid Hermans, Sabine/0000-0001-5146-2932
dc.description.orcid Sekaggya-Wiltshire, Christine/0000-0001-9247-2950


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