Risk-benefit analysis of tuberculosis infection testing for household contact management in high-burden countries: a mathematical modelling study.


Journal

The Lancet. Global health
ISSN: 2214-109X
Titre abrégé: Lancet Glob Health
Pays: England
ID NLM: 101613665

Informations de publication

Date de publication:
05 2020
Historique:
received: 18 11 2019
revised: 15 02 2020
accepted: 20 02 2020
entrez: 1 5 2020
pubmed: 1 5 2020
medline: 28 8 2020
Statut: ppublish

Résumé

Preventive therapy for tuberculosis reduces the risk of disease in people who have been infected but who are not sick. Countries with a high burden of tuberculosis that are expanding preventive therapy use must decide how tuberculosis infection testing should be used for risk stratification among household contacts of patients with tuberculosis. We modelled the risks of tuberculosis disease and severe adverse events, comparing the following two preventive therapy strategies: preventive therapy for all household contacts, or preventive therapy for only household contacts with a positive tuberculin skin test (TST) result. We used data from clinical trials and literature on tuberculosis natural history to model outcomes, assuming different preventive therapy regimens, ages, and TST positivity prevalence. Assuming 25% prevalence of TST positivity among 1000 household contacts aged 0-17 years, a treat-all approach with isoniazid and rifapentine compared with a treat-TST-only approach led to 13 fewer incident tuberculosis cases (IQR -5 to -18) and four additional severe adverse events (2 to 6). With rifampicin, the difference was 11 fewer incident tuberculosis cases (-3 to -17) and two additional severe adverse events (1 to 3). For adults, a treat-all approach led to fewer incident tuberculosis cases, and additional adverse events increased with age. Assuming 25% prevalence of TST positivity among adult contacts, a treat-all approach would lead to around two fewer tuberculosis cases per 1000 contacts for all regimens; the number of additional severe adverse events ranged from seven (IQR 5 to 8) for 18 to 34-year-olds treated with rifampicin to 63 (50 to 74) for people older than 64 years treated with isoniazid and rifapentine. A rifampicin-only regimen was associated with the fewest additional severe adverse events (seven [IQR 5 to 8] per 1000 adults aged 18-34 years and 35-64 years, and 17 [9 to 23] per 1000 adults older than 64 years). Based on the available data, giving preventive therapy to all household contacts would probably reduce the incidence of tuberculosis cases in high-burden settings. Adverse events could be minimised by using non-isoniazid regimens and, in adults older than 18 years, focusing treatment on individuals with a positive infection test. Bill & Melinda Gates Foundation, UK Medical Research Council, and UK Department for International Development.

Sections du résumé

BACKGROUND
Preventive therapy for tuberculosis reduces the risk of disease in people who have been infected but who are not sick. Countries with a high burden of tuberculosis that are expanding preventive therapy use must decide how tuberculosis infection testing should be used for risk stratification among household contacts of patients with tuberculosis.
METHODS
We modelled the risks of tuberculosis disease and severe adverse events, comparing the following two preventive therapy strategies: preventive therapy for all household contacts, or preventive therapy for only household contacts with a positive tuberculin skin test (TST) result. We used data from clinical trials and literature on tuberculosis natural history to model outcomes, assuming different preventive therapy regimens, ages, and TST positivity prevalence.
FINDINGS
Assuming 25% prevalence of TST positivity among 1000 household contacts aged 0-17 years, a treat-all approach with isoniazid and rifapentine compared with a treat-TST-only approach led to 13 fewer incident tuberculosis cases (IQR -5 to -18) and four additional severe adverse events (2 to 6). With rifampicin, the difference was 11 fewer incident tuberculosis cases (-3 to -17) and two additional severe adverse events (1 to 3). For adults, a treat-all approach led to fewer incident tuberculosis cases, and additional adverse events increased with age. Assuming 25% prevalence of TST positivity among adult contacts, a treat-all approach would lead to around two fewer tuberculosis cases per 1000 contacts for all regimens; the number of additional severe adverse events ranged from seven (IQR 5 to 8) for 18 to 34-year-olds treated with rifampicin to 63 (50 to 74) for people older than 64 years treated with isoniazid and rifapentine. A rifampicin-only regimen was associated with the fewest additional severe adverse events (seven [IQR 5 to 8] per 1000 adults aged 18-34 years and 35-64 years, and 17 [9 to 23] per 1000 adults older than 64 years).
INTERPRETATION
Based on the available data, giving preventive therapy to all household contacts would probably reduce the incidence of tuberculosis cases in high-burden settings. Adverse events could be minimised by using non-isoniazid regimens and, in adults older than 18 years, focusing treatment on individuals with a positive infection test.
FUNDING
Bill & Melinda Gates Foundation, UK Medical Research Council, and UK Department for International Development.

Identifiants

pubmed: 32353315
pii: S2214-109X(20)30075-9
doi: 10.1016/S2214-109X(20)30075-9
pmc: PMC7196883
pii:
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e672-e680

Subventions

Organisme : Medical Research Council
ID : MR/R007942/1
Pays : United Kingdom

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2020 The Author(s). Published by Elsevier Ltd. This is an Open Access article under the CC BY 4.0 license. Published by Elsevier Ltd.. All rights reserved.

Références

Clin Infect Dis. 2016 Jun 1;62(11):1390-1400
pubmed: 26951571
N Engl J Med. 2018 Aug 2;379(5):454-463
pubmed: 30067928
Lancet Infect Dis. 2018 Oct;18(10):1077-1087
pubmed: 30174209
Respirology. 2018 Jun;23(6):567-575
pubmed: 29607596
Am J Respir Crit Care Med. 2019 Mar 1;199(5):564-571
pubmed: 30335466
Lancet Glob Health. 2018 Dec;6(12):e1329-e1338
pubmed: 30266570
Chest. 2016 Feb;149(2):516-525
pubmed: 26867835
Lancet Glob Health. 2016 Nov;4(11):e806-e815
pubmed: 27720688
PLoS One. 2016 Mar 09;11(3):e0150849
pubmed: 26959366
Lancet Infect Dis. 2017 Nov;17(11):1190-1199
pubmed: 28827142
N Engl J Med. 2018 Aug 2;379(5):440-453
pubmed: 30067931
Ann Intern Med. 2017 Aug 15;167(4):248-255
pubmed: 28761946
Eur Respir J. 2013 Jan;41(1):140-56
pubmed: 22936710
Int J Tuberc Lung Dis. 2008 May;12(5):498-505
pubmed: 18419884
Lancet. 2015 Dec 5;386(10010):2344-53
pubmed: 26515679
CMAJ. 2011 Feb 22;183(3):E173-9
pubmed: 21220436
Clin Infect Dis. 2020 Feb 3;70(4):698-703
pubmed: 31414121
Lancet Infect Dis. 2012 Jan;12(1):45-55
pubmed: 21846592
PLoS One. 2017 Jan 6;12(1):e0169539
pubmed: 28060926
Ann Intern Med. 2007 Mar 6;146(5):340-54
pubmed: 17339619
Annu Rev Public Health. 2013;34:271-86
pubmed: 23244049
Eur Respir J. 2014 Sep;44(3):714-24
pubmed: 25063246
JAMA Pediatr. 2015 Mar;169(3):247-55
pubmed: 25580725
N Engl J Med. 2011 Dec 8;365(23):2155-66
pubmed: 22150035
Int J Tuberc Lung Dis. 2017 Aug 1;21(8):935-940
pubmed: 28786803

Auteurs

Courtney M Yuen (CM)

Division of Global Health Equity, Brigham and Women's Hospital, Boston, MA, USA; Department of Global Health and Social Medicine, Harvard Medical School, Boston, MA, USA. Electronic address: courtney_yuen@hms.harvard.edu.

James A Seddon (JA)

Department of Infectious Diseases, Imperial College London, London, UK; Desmond Tutu TB Centre, Department of Paediatrics and Child Health, Stellenbosch University, Cape Town, South Africa.

Salmaan Keshavjee (S)

Division of Global Health Equity, Brigham and Women's Hospital, Boston, MA, USA; Department of Global Health and Social Medicine, Harvard Medical School, Boston, MA, USA.

Peter J Dodd (PJ)

School of Health and Related Research, University of Sheffield, Sheffield, UK.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH