Improving outcomes for multidrug-resistant tuberculosis: aggressive regimens prevent treatment failure and death
- PMID: 24729493
- PMCID: PMC4305127
- DOI: 10.1093/cid/ciu209
Improving outcomes for multidrug-resistant tuberculosis: aggressive regimens prevent treatment failure and death
Abstract
Background: Evidence is sparse regarding the optimal construction of regimens to treat multidrug-resistant (MDR) tuberculosis disease due to strains of Mycobacterium tuberculosis resistant to at least both isoniazid and rifampin. Given the low potency of many second-line antituberculous drugs, we hypothesized that an aggressive regimen of at least 5 likely effective drugs during the intensive phase, including a fluoroquinolone and a parenteral agent, would be associated with a reduced risk of death or treatment failure.
Methods: We conducted a retrospective cohort study of patients initiating MDR tuberculosis treatment between 2000 and 2004 in Tomsk, Russian Federation. We used a multivariate Cox proportional hazards model to assess whether monthly exposure to an aggressive regimen was associated with the risk of death or treatment failure.
Results: Six hundred fourteen individuals with confirmed MDR tuberculosis were eligible for analysis. On multivariable analysis that adjusted for extensively drug-resistant (XDR) tuberculosis-MDR tuberculosis isolates resistant to fluoroquinolones and parenteral agents-we found that monthly exposure to an aggressive regimen was significantly associated with a lower risk of death or treatment failure (hazard ratio, 0.52 [95% confidence interval, .29-.94]; P = .030).
Conclusions: Receipt of an aggressive treatment regimen was a robust predictor of decreased risk of death or failure during MDR tuberculosis treatment. These findings further support the use of this regimen definition as the benchmark for the standard of care of MDR tuberculosis patients and should be used as the basis for evaluating novel therapies.
Keywords: MDR-TB; clinical outcomes; drug resistance; optimized background regimen; treatment.
© The Author 2014. Published by Oxford University Press on behalf of the Infectious Diseases Society of America. All rights reserved. For Permissions, please e-mail: journals.permissions@oup.com.
Figures
Similar articles
-
Aggressive Regimens Reduce Risk of Recurrence After Successful Treatment of MDR-TB.Clin Infect Dis. 2016 Jul 15;63(2):214-20. doi: 10.1093/cid/ciw276. Epub 2016 May 8. Clin Infect Dis. 2016. PMID: 27161772
-
Aggressive regimens for multidrug-resistant tuberculosis decrease all-cause mortality.PLoS One. 2013;8(3):e58664. doi: 10.1371/journal.pone.0058664. Epub 2013 Mar 13. PLoS One. 2013. PMID: 23516529 Free PMC article.
-
Treatment efficacy of drug-resistant tuberculosis in Bashkortostan, Russia: A retrospective cohort study.Int J Infect Dis. 2019 Apr;81:203-209. doi: 10.1016/j.ijid.2019.02.010. Epub 2019 Feb 19. Int J Infect Dis. 2019. PMID: 30794942
-
Delamanid: From discovery to its use for pulmonary multidrug-resistant tuberculosis (MDR-TB).Tuberculosis (Edinb). 2018 Jul;111:20-30. doi: 10.1016/j.tube.2018.04.008. Epub 2018 May 3. Tuberculosis (Edinb). 2018. PMID: 30029909 Review.
-
Trends in the discovery of new drugs for Mycobacterium tuberculosis therapy with a glance at resistance.Tuberculosis (Edinb). 2018 Mar;109:17-27. doi: 10.1016/j.tube.2017.12.002. Epub 2017 Dec 9. Tuberculosis (Edinb). 2018. PMID: 29559117 Review.
Cited by
-
The Race Is On To Shorten the Turnaround Time for Diagnosis of Multidrug-Resistant Tuberculosis.J Clin Microbiol. 2015 Dec;53(12):3715-8. doi: 10.1128/JCM.02398-15. Epub 2015 Sep 16. J Clin Microbiol. 2015. PMID: 26378276 Free PMC article.
-
New Antituberculosis Drugs: From Clinical Trial to Programmatic Use.Infect Dis Rep. 2016 Jun 24;8(2):6569. doi: 10.4081/idr.2016.6569. eCollection 2016 Jun 24. Infect Dis Rep. 2016. PMID: 27403268 Free PMC article. Review.
-
Time to Multidrug-Resistant Tuberculosis Treatment Initiation in Association with Treatment Outcomes in Shanghai, China.Antimicrob Agents Chemother. 2018 Mar 27;62(4):e02259-17. doi: 10.1128/AAC.02259-17. Print 2018 Apr. Antimicrob Agents Chemother. 2018. PMID: 29437632 Free PMC article.
-
Risk factors for poor multidrug-resistant tuberculosis treatment outcomes in Kyiv Oblast, Ukraine.BMC Infect Dis. 2017 Feb 7;17(1):129. doi: 10.1186/s12879-017-2230-2. BMC Infect Dis. 2017. PMID: 28173763 Free PMC article.
-
Multidrug-Resistant Tuberculosis Treatment Outcomes in Relation to Treatment and Initial Versus Acquired Second-Line Drug Resistance.Clin Infect Dis. 2016 Feb 15;62(4):418-430. doi: 10.1093/cid/civ910. Epub 2015 Oct 27. Clin Infect Dis. 2016. PMID: 26508515 Free PMC article.
References
-
- World Health Organization. Geneva, Switzerland: WHO; 2010. Multidrug and extensively drug-resistant TB (M/XDR-TB): 2010 global report on surveillance and response. Available at: http://www.who.int/tb/publications/2010/en/index.html . Accessed 20 March 2014.
-
- Keshavjee S, Farmer PE. Picking up the pace—scale-up of MDR tuberculosis treatment programs. N Engl J Med. 2010;363:1781–4. - PubMed
-
- World Health Organization. Geneva, Switzerland: WHO; 2012. Global tuberculosis report 2012. Available at: http://www.who.int/tb/publications/global_report/en/ . Accessed 4 September 2013.
-
- Mitnick CD, Bayona JJ, Palacios EE, et al. Community-based therapy for multidrug-resistant tuberculosis in Lima, Peru. N Engl J Med. 2003;348:119–28. - PubMed
-
- Shin SS, Pasechnikov AD, Gelmanova IY, et al. Treatment outcomes in an integrated civilian and prison MDR-TB treatment program in Russia. Int J Tuberc Lung Dis. 2006;10:402–8. - PubMed
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources