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Cohort profile of a study on outcomes related to tuberculosis and antiretroviral drug concentrations in Uganda: design, methods and patient characteristics of the SOUTH study

Cohort profile of a study on outcomes related to tuberculosis and antiretroviral drug concentrations in Uganda: design, methods and patient characteristics of the SOUTH study

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dc.contributor.author Sekaggya-Wiltshire, Christine
dc.contributor.author Castelnuovo, Barbara
dc.contributor.author von Braun, Amrei
dc.contributor.author Musaazi, Joseph
dc.contributor.author Muller, Daniel
dc.contributor.author Buzibye, Allan
dc.contributor.author Gutteck, Ursula
dc.contributor.author Henning, Lars
dc.contributor.author Ledergerber, Bruno
dc.contributor.author Corti, Natascia
dc.contributor.author Lamorde, Mohammed
dc.contributor.author Fehr, Jan
dc.contributor.author Kambugu, Andrew
dc.date.accessioned 2021-01-01T21:57:58Z
dc.date.available 2021-01-01T21:57:58Z
dc.date.issued 2017
dc.identifier.issn 2044-6055
dc.identifier.uri http://combine.alvar.ug/handle/1/48096
dc.description.abstract Purpose Tuberculosis (TB) is a leading cause of death among people living with HIV in sub-Saharan Africa. Several factors influence the efficacy of TB treatment by leading to suboptimal drug concentrations and subsequently affecting treatment outcome. The aim of this cohort is to determine the association between anti-TB drug concentrations and TB treatment outcomes. Participants Patients diagnosed with new pulmonary TB at the integrated TB-HIV outpatient clinic in Kampala, Uganda, were enrolled into the study and started on first-line anti-TB treatment. Findings to date Between April 2013 and April 2015, the cohort enrolled 268 patients coinfected with TB/HIV; 57.8% are male with a median age of 34 years (IQR 29-40). The median time between the diagnosis of HIV and the diagnosis of TB is 2 months (IQR 0-22.5). The majority of the patients are antiretroviral therapy naive (75.4%). Our population is severely immunosuppressed with a median CD4 cell count at enrolment of 163 cells/mu L (IQR 46-298). Ninety-nine per cent of the patients had a diagnosis of pulmonary TB confirmed by sputum microscopy, Xpert/RIF or culture and 203 (75.7%) have completed TB treatment with 5099 aliquots of blood collected for pharmacokinetic analysis. Future plans This cohort provides a large database of well-characterised patients coinfected with TB/HIV which will facilitate the description of the association between serum drug concentrations and TB treatment outcomes as well as provide a research platform for future substudies including evaluation of virological outcomes.
dc.description.sponsorship Infectious Diseases Institute Makerere University
dc.description.sponsorship University of Zurich - Abbvie
dc.description.sponsorship Bristol Myers SquibbBristol-Myers Squibb
dc.description.sponsorship Gilead SciencesGilead Sciences
dc.description.sponsorship JanssenJohnson & Johnson USAJanssen Biotech Inc
dc.description.sponsorship Lunge Zurich
dc.description.sponsorship MerckMerck & Company
dc.description.sponsorship Shimadzu
dc.description.sponsorship Swiss HIV Cohort Study
dc.description.sponsorship ViiV Healthcare
dc.language English
dc.publisher BMJ PUBLISHING GROUP
dc.relation.ispartof BMJ Open
dc.title Cohort profile of a study on outcomes related to tuberculosis and antiretroviral drug concentrations in Uganda: design, methods and patient characteristics of the SOUTH study
dc.type Article
dc.identifier.isi 000412650700023
dc.identifier.doi 10.1136/bmjopen-2016-014679
dc.identifier.pmid 28928173
dc.publisher.city LONDON
dc.publisher.address BRITISH MED ASSOC HOUSE, TAVISTOCK SQUARE, LONDON WC1H 9JR, ENGLAND
dc.identifier.volume 7
dc.identifier.issue 9
dc.subject.wc Medicine, General & Internal
dc.subject.sc General & Internal Medicine
dc.description.oa DOAJ Gold
dc.description.oa Green Accepted
dc.description.oa Green Published
dc.description.pages 9
dc.subject.kwp Hiv-Infected Patients
dc.subject.kwp Pulmonary Tuberculosis
dc.subject.kwp Antituberculosis Drugs
dc.subject.kwp Plasma-Concentrations
dc.subject.kwp Rifampin
dc.subject.kwp Pharmacokinetics
dc.subject.kwp Services
dc.subject.kwp Tb
dc.identifier.articleno e014679
dc.description.affiliation Makerere Univ, Coll Hlth Sci, Infect Dis Inst, Kampala, Uganda
dc.description.affiliation Univ Zurich, Univ Hosp Zurich, Div Infect Dis & Infect Control, Zurich, Switzerland
dc.description.affiliation Univ Zurich, Univ Hosp Zurich, Dept Clin Chem, Zurich, Switzerland
dc.description.affiliation Univ Zurich, Univ Hosp Zurich, Div Clin Pharmacol & Toxicol, Zurich, Switzerland
dc.description.email csekaggya@idi.co.ug
dc.description.corr Sekaggya-Wiltshire, C (corresponding author), Makerere Univ, Coll Hlth Sci, Infect Dis Inst, Kampala, Uganda.
dc.description.orcid Ledergerber, Bruno/0000-0002-6881-4401
dc.description.orcid Henning, Lars/0000-0003-3533-1515
dc.description.orcid Sekaggya-Wiltshire, Christine/0000-0001-9247-2950
dc.description.orcid BUZIBYE, ALLAN/0000-0001-5874-3219
dc.description.orcid Mueller, Daniel/0000-0002-4674-4019


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