Initial drug resistance and tuberculosis treatment outcomes: systematic review and meta-analysis
- PMID: 18626051
- DOI: 10.7326/0003-4819-149-2-200807150-00008
Initial drug resistance and tuberculosis treatment outcomes: systematic review and meta-analysis
Abstract
Background: Despite the increasing prevalence of drug-resistant tuberculosis, most low- and middle-income countries use standardized regimens, without assessment of drug susceptibility.
Purpose: To perform a systematic review and meta-analysis of the effect of initial drug resistance and treatment regimen on tuberculosis treatment outcomes.
Data sources: PubMed, the Cochrane Central Database of Clinical Trials, and EMBASE were searched for studies published in English from 1965 to June 2007. Additional studies were identified from cited references.
Study selection: Randomized, controlled trials and cohort studies of standardized treatment of previously untreated patients with culture-confirmed pulmonary tuberculosis. Drug-susceptibility testing was done on pretreatment isolates from all patients and from patients with treatment failure or relapse.
Data extraction: Two authors reviewed the studies for methods, initial drug resistance, treatment regimens, and outcomes.
Data synthesis: Pooled cumulative incidences were computed with random-effects meta-analyses. Association between risk factors and outcomes were determined by using stratified analyses. The cumulative incidence of acquired drug resistance with initially pan-sensitive strains was 0.8% (95% CI, 0.5% to 1.0%) compared with 6% (CI, 4% to 8%) with initially single drug-resistant strains and 14% (CI, 9% to 20%) with initially polydrug-resistant strains. Failure and relapse were most strongly associated with initial drug resistance. Failure was also associated with shorter duration of rifampin therapy and nonuse of streptomycin, whereas the rate of relapse was higher with shorter duration of rifampin therapy and nonuse of pyrazinamide.
Limitations: Few studies included HIV-infected persons, and treatment outcomes were pooled despite considerable heterogeneity.
Conclusion: Treatment outcomes were substantially worse in the presence of initial drug resistance, which has important implications in resource-limited settings in which drug resistance is prevalent.
Similar articles
-
Effect of duration and intermittency of rifampin on tuberculosis treatment outcomes: a systematic review and meta-analysis.PLoS Med. 2009 Sep;6(9):e1000146. doi: 10.1371/journal.pmed.1000146. Epub 2009 Sep 15. PLoS Med. 2009. PMID: 19753109 Free PMC article.
-
Xpert® MTB/RIF assay for extrapulmonary tuberculosis and rifampicin resistance.Cochrane Database Syst Rev. 2018 Aug 27;8(8):CD012768. doi: 10.1002/14651858.CD012768.pub2. Cochrane Database Syst Rev. 2018. Update in: Cochrane Database Syst Rev. 2021 Jan 15;1:CD012768. doi: 10.1002/14651858.CD012768.pub3. PMID: 30148542 Free PMC article. Updated.
-
Xpert MTB/RIF Ultra assay for tuberculosis disease and rifampicin resistance in children.Cochrane Database Syst Rev. 2022 Sep 6;9(9):CD013359. doi: 10.1002/14651858.CD013359.pub3. Cochrane Database Syst Rev. 2022. PMID: 36065889 Free PMC article.
-
Systemic pharmacological treatments for chronic plaque psoriasis: a network meta-analysis.Cochrane Database Syst Rev. 2021 Apr 19;4(4):CD011535. doi: 10.1002/14651858.CD011535.pub4. Cochrane Database Syst Rev. 2021. Update in: Cochrane Database Syst Rev. 2022 May 23;5:CD011535. doi: 10.1002/14651858.CD011535.pub5. PMID: 33871055 Free PMC article. Updated.
-
Xpert MTB/XDR for detection of pulmonary tuberculosis and resistance to isoniazid, fluoroquinolones, ethionamide, and amikacin.Cochrane Database Syst Rev. 2022 May 18;5(5):CD014841. doi: 10.1002/14651858.CD014841.pub2. Cochrane Database Syst Rev. 2022. PMID: 35583175 Free PMC article.
Cited by
-
A guide to the management of tuberculosis in patients with chronic liver disease.J Clin Exp Hepatol. 2012 Sep;2(3):260-70. doi: 10.1016/j.jceh.2012.07.007. Epub 2012 Sep 21. J Clin Exp Hepatol. 2012. PMID: 25755442 Free PMC article. Review.
-
A systems approach using OSMAC, Log P and NMR fingerprinting: An approach to novelty.Synth Syst Biotechnol. 2017 Oct 21;2(4):276-286. doi: 10.1016/j.synbio.2017.10.001. eCollection 2017 Dec. Synth Syst Biotechnol. 2017. PMID: 29552652 Free PMC article.
-
Rates and risk factors for drug resistance tuberculosis in Northeastern China.BMC Public Health. 2013 Dec 13;13:1171. doi: 10.1186/1471-2458-13-1171. BMC Public Health. 2013. PMID: 24330553 Free PMC article.
-
Addressing the Challenges of Tuberculosis: A Brief Historical Account.Front Pharmacol. 2017 Sep 26;8:689. doi: 10.3389/fphar.2017.00689. eCollection 2017. Front Pharmacol. 2017. PMID: 29033842 Free PMC article. Review.
-
Estimating the future burden of multidrug-resistant and extensively drug-resistant tuberculosis in India, the Philippines, Russia, and South Africa: a mathematical modelling study.Lancet Infect Dis. 2017 Jul;17(7):707-715. doi: 10.1016/S1473-3099(17)30247-5. Epub 2017 May 9. Lancet Infect Dis. 2017. PMID: 28499828 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources