Treatment of Latent Tuberculosis Infection An Updated Network Meta-analysis

被引:146
|
作者
Zenner, Dominik [5 ]
Beer, Netta [4 ]
Harris, Ross J. [6 ]
Lipman, Marc C. [2 ,3 ]
Stagg, Helen R. [1 ]
van der Werf, Marieke J. [4 ]
机构
[1] UCL, Inst Global Hlth, 3rd Floor,30 Guilford St, London WC1N 1EH, England
[2] Royal Free London Natl Hlth Serv Fdn Trust, Ctr Resp Med, London NW3 2QG, England
[3] Royal Free London Natl Hlth Serv Fdn Trust, Dept Med, London NW3 2QG, England
[4] European Ctr Dis Prevent & Control, Granitsvag 8, S-17165 Stockholm, Sweden
[5] Publ Hlth England, Resp Dis Dept, TB Sect, 61 Colindale Ave, London NW9 5EQ, England
[6] Publ Hlth England, Stat Modelling & Bioinformat Dept, 61 Colindale Ave, London NW9 5EQ, England
关键词
ISONIAZID PREVENTIVE THERAPY; ANTIRETROVIRAL THERAPY; DOUBLE-BLIND; RIFAPENTINE; CHILDREN; REGIMENS; EFFICACY; ADULTS; TRIAL; RATES;
D O I
10.7326/M17-0609
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Treatment of latent tuberculosis infection (LTBI) is an important component of tuberculosis (TB) control, and this study updates a previous network meta-analysis of the best LTBI treatment options to inform public health action and programmatic management of LTBI. Purpose: To evaluate the comparative efficacy and harms of LTBI treatment regimens aimed at preventing active TB among adults and children. Data Sources: PubMed, Embase, and Web of Science from indexing to 8 May 2017; clinical trial registries; and conference abstracts. No language restrictions were applied. Study Selection: Randomized controlled trials that evaluated human LTBI treatments and recorded at least 1 of 2 prespecified end points (hepatotoxicity and prevention of active TB). Data Extraction: 2 investigators independently extracted data from eligible studies and assessed study quality according to a standard protocol. Data Synthesis: The network meta-analysis of 8 new and 53 previously included studies showed that isoniazid regimens of 6 months (odds ratio [OR], 0.65 [95% credible interval {CrI}, 0.50 to 0.83]) or 12 to 72 months (OR, 0.50 [CrI, 0.41 to 0.62]), rifampicin-only regimens (OR, 0.41 [CrI, 0.19 to 0.85]), rifampicinisoniazid regimens of 3 to 4 months (OR, 0.53 [CrI, 0.36 to 0.78]), rifampicin-isoniazid-pyrazinamide regimens (OR, 0.35 [CrI, 0.19 to 0.61]), and rifampicin-pyrazinamide regimens (OR, 0.53 [CrI, 0.33 to 0.84]) were efficacious compared with placebo. Evidence existed for efficacy of weekly rifapentine-isoniazid regimens compared with no treatment (OR, 0.36 [CrI, 0.18 to 0.73]). No conclusive evidence showed that HIV status altered treatment efficacy. Limitation: Evidence was sparse for many comparisons and hepatotoxicity outcomes, and risk of bias was high or unknown for many studies. Conclusion: Evidence exists for the efficacy and safety of 6-month isoniazid monotherapy, rifampicin monotherapy, and combination therapies with 3 to 4 months of isoniazid and rifampicin.
引用
收藏
页码:248 / +
页数:9
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