Test and Treat TB: a pilot trial of GeneXpert MTB/RIF screening on a mobile HIV testing unit in South Africa.


Journal

BMC infectious diseases
ISSN: 1471-2334
Titre abrégé: BMC Infect Dis
Pays: England
ID NLM: 100968551

Informations de publication

Date de publication:
04 Feb 2019
Historique:
received: 18 01 2018
accepted: 23 01 2019
entrez: 6 2 2019
pubmed: 6 2 2019
medline: 14 3 2019
Statut: epublish

Résumé

Community-based GeneXpert MTB/RIF testing may increase detection of prevalent TB in the community and improve rates of TB treatment completion. We conducted a pilot randomized trial to evaluate the impact of GeneXpert screening on a mobile HIV testing unit. Adults (≥18y) underwent rapid HIV testing and TB symptom screening and were randomized to usual mobile unit care (providing sputum on the mobile unit sent out for GeneXpert testing) or the "Test & Treat TB" intervention with immediate GeneXpert testing. Symptomatic participants in usual care produced sputum that was sent for hospital-based GeneXpert testing; participants were contacted ~ 7 days later with results. In the "Test & Treat TB" intervention, HIV-infected or HIV-uninfected/TB symptomatic participants underwent GeneXpert testing on the mobile unit. GeneXpert+ participants received expedited TB treatment initiation, monthly SMS reminders and non-cash incentives. We assessed 6-month TB treatment outcomes. 4815 were eligible and enrolled; median age was 27 years (IQR 22 to 35). TB symptoms included cough (5%), weight loss (4%), night sweats (4%), and fever (3%). 42% of eligible participants produced sputum (intervention: 56%; usual care: 26%). Seven participants tested GeneXpert+, six in the intervention (3%, 95% CI 1%, 5%) and one in usual care (1%, 95% CI 0%, 6%). 5 of 6 intervention participants completed TB treatment; the GeneXpert+ participant in usual care did not. GeneXpert MTB/RIF screening on a mobile HIV testing unit is feasible. Yield for GeneXpert+ TB was low, however, the "Test & Treat TB" strategy led to high rates of TB treatment completion. This study was registered on November 21, 2014 at ClinicalTrials.gov ( NCT02298309 ).

Sections du résumé

BACKGROUND BACKGROUND
Community-based GeneXpert MTB/RIF testing may increase detection of prevalent TB in the community and improve rates of TB treatment completion.
METHODS METHODS
We conducted a pilot randomized trial to evaluate the impact of GeneXpert screening on a mobile HIV testing unit. Adults (≥18y) underwent rapid HIV testing and TB symptom screening and were randomized to usual mobile unit care (providing sputum on the mobile unit sent out for GeneXpert testing) or the "Test & Treat TB" intervention with immediate GeneXpert testing. Symptomatic participants in usual care produced sputum that was sent for hospital-based GeneXpert testing; participants were contacted ~ 7 days later with results. In the "Test & Treat TB" intervention, HIV-infected or HIV-uninfected/TB symptomatic participants underwent GeneXpert testing on the mobile unit. GeneXpert+ participants received expedited TB treatment initiation, monthly SMS reminders and non-cash incentives. We assessed 6-month TB treatment outcomes.
RESULTS RESULTS
4815 were eligible and enrolled; median age was 27 years (IQR 22 to 35). TB symptoms included cough (5%), weight loss (4%), night sweats (4%), and fever (3%). 42% of eligible participants produced sputum (intervention: 56%; usual care: 26%). Seven participants tested GeneXpert+, six in the intervention (3%, 95% CI 1%, 5%) and one in usual care (1%, 95% CI 0%, 6%). 5 of 6 intervention participants completed TB treatment; the GeneXpert+ participant in usual care did not.
CONCLUSION CONCLUSIONS
GeneXpert MTB/RIF screening on a mobile HIV testing unit is feasible. Yield for GeneXpert+ TB was low, however, the "Test & Treat TB" strategy led to high rates of TB treatment completion.
TRIAL REGISTRATION BACKGROUND
This study was registered on November 21, 2014 at ClinicalTrials.gov ( NCT02298309 ).

Identifiants

pubmed: 30717693
doi: 10.1186/s12879-019-3738-4
pii: 10.1186/s12879-019-3738-4
pmc: PMC6360783
doi:

Banques de données

ClinicalTrials.gov
['NCT02298309']

Types de publication

Journal Article Randomized Controlled Trial

Langues

eng

Sous-ensembles de citation

IM

Pagination

110

Subventions

Organisme : NIAID NIH HHS
ID : R21 AI110264
Pays : United States
Organisme : National Institute of Allergy and Infectious Diseases
ID : R21 AI110264-01A1

Références

AIDS. 2005 Dec 2;19(18):2141-8
pubmed: 16284464
Trans R Soc Trop Med Hyg. 2009 Jun;103(6):588-93
pubmed: 19012940
Clin Infect Dis. 2010 May 15;50 Suppl 3:S208-14
pubmed: 20397950
Arch Intern Med. 2010 Aug 9;170(15):1347-54
pubmed: 20696960
Lancet. 2011 Apr 30;377(9776):1495-505
pubmed: 21507477
J Acquir Immune Defic Syndr. 2011 Nov 1;58(3):344-52
pubmed: 21836524
Int J Tuberc Lung Dis. 2012 May;16(5):701; author reply 702
pubmed: 22507934
PLoS Med. 2012;9(8):e1001281
pubmed: 22879816
PLoS One. 2012;7(8):e43400
pubmed: 22916256
Clin Infect Dis. 2012 Dec;55(12):1690-7
pubmed: 22955429
J Acquir Immune Defic Syndr. 2013 Aug 1;63(4):498-505
pubmed: 23572010
HIV Med. 2014 Jul;15(6):367-72
pubmed: 24251725
PLoS One. 2014 Mar 04;9(3):e90754
pubmed: 24595317
Int J Tuberc Lung Dis. 2016 Feb;20(2):235-9
pubmed: 26792477
Trans R Soc Trop Med Hyg. 2016 May;110(5):305-11
pubmed: 27198215
N Engl J Med. 2016 Sep 1;375(9):830-9
pubmed: 27424812
S Afr Med J. 2016 Sep 05;106(10):1002-1009
pubmed: 27725021
Open Forum Infect Dis. 2017 May 04;4(3):ofx092
pubmed: 28695145
Am J Respir Crit Care Med. 2017 Oct 1;196(7):901-910
pubmed: 28727491
J Int AIDS Soc. 2018 Jan;21(1):null
pubmed: 29381257

Auteurs

Ingrid V Bassett (IV)

Division of Infectious Disease, Massachusetts General Hospital, Boston, MA, USA. ibassett@partners.org.
Medical Practice Evaluation Center, Department of Medicine, Massachusetts General Hospital, 100 Cambridge Street, 16th Floor, Boston, MA, 02114, USA. ibassett@partners.org.
Harvard University Center for AIDS Research (CFAR), Boston, MA, USA. ibassett@partners.org.
Harvard Medical School, Boston, MA, USA. ibassett@partners.org.

Leah S Forman (LS)

Data Coordinating Center, Boston University School of Public Health, Boston, MA, USA.

Sabina Govere (S)

AIDS Healthcare Foundation, Durban, South Africa.

Hilary Thulare (H)

AIDS Healthcare Foundation, Durban, South Africa.

Simone C Frank (SC)

Medical Practice Evaluation Center, Department of Medicine, Massachusetts General Hospital, 100 Cambridge Street, 16th Floor, Boston, MA, 02114, USA.
Division of General Internal Medicine, Massachusetts General Hospital, Boston, MA, USA.

Bright Mhlongo (B)

AIDS Healthcare Foundation, Durban, South Africa.

Elena Losina (E)

Medical Practice Evaluation Center, Department of Medicine, Massachusetts General Hospital, 100 Cambridge Street, 16th Floor, Boston, MA, 02114, USA.
Harvard University Center for AIDS Research (CFAR), Boston, MA, USA.
Harvard Medical School, Boston, MA, USA.
Department of Biostatistics, Boston University School of Public Health, Boston, MA, USA.
Division of Rheumatology, Department of Medicine, and Department of Orthopedic Surgery, Brigham and Women's Hospital, Boston, MA, USA.

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Classifications MeSH