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 |
|