Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Observational Study
. 2016 Feb 15;62(4):418-430.
doi: 10.1093/cid/civ910. Epub 2015 Oct 27.

Multidrug-Resistant Tuberculosis Treatment Outcomes in Relation to Treatment and Initial Versus Acquired Second-Line Drug Resistance

J Peter Cegielski  1 Ekaterina Kurbatova  1 Martie van der Walt  2 Jeannette Brand  2 Julia Ershova  1 Thelma Tupasi  3 Janice Campos Caoili  3 Tracy Dalton  1 Carmen Contreras  4 Martin Yagui  5 Jaime Bayona  4 Charlotte Kvasnovsky  1 Vaira Leimane  6 Liga Kuksa  6 Michael P Chen  1 Laura E Via  7 Soo Hee Hwang  8 Melanie Wolfgang  1 Grigory V Volchenkov  9 Tatiana Somova  9 Sarah E Smith  1 Somsak Akksilp  10 Wanpen Wattanaamornkiet  11 Hee Jin Kim  12 Chang-Ki Kim  12 Boris Y Kazennyy  13 Tatiana Khorosheva  13 Kai Kliiman  14 Piret Viiklepp  15 Ruwen Jou  16 Angela Song-En Huang  16 Irina A Vasilyeva  17 Olga V Demikhova  17 Global PETTS InvestigatorsJoey LancasterRonel OdendaalLois DiemTherese C PerezTarcela GlerKathrine TanCesar BonillaOswaldo JaveLuis AsenciosGloria YaleCarmen SuarezAllison Taylor WalkerInga NorvaishaGirts SkendersIngrida StureVija RiekstinaAndra CiruleErika SigmanSang-Nae ChoYing CaiSeokyong EumJongseok LeeSeungkyu ParkDoosoo JeonIsdore C ShamputaBeverly MetchockTatiana KuznetsovaRattanawadee AkksilpWanlaya SittiJirapan InyapongElena V KiryanovaIrina DegtyarevaEvgenia S NemtsovaKlavdia LevinaManfred DanilovitsTiina KummikYung-Chao LeiWei-Lun HuangVladislav V ErokhinLarisa N ChernousovaSofia N AndreevskayaElena E LarionovaTatyana G Smirnova
Affiliations
Observational Study

Multidrug-Resistant Tuberculosis Treatment Outcomes in Relation to Treatment and Initial Versus Acquired Second-Line Drug Resistance

J Peter Cegielski et al. Clin Infect Dis. .

Abstract

Background: Resistance to second-line drugs develops during treatment of multidrug-resistant (MDR) tuberculosis, but the impact on treatment outcome has not been determined.

Methods: Patients with MDR tuberculosis starting second-line drug treatment were enrolled in a prospective cohort study. Sputum cultures were analyzed at a central reference laboratory. We compared subjects with successful and poor treatment outcomes in terms of (1) initial and acquired resistance to fluoroquinolones and second-line injectable drugs (SLIs) and (2) treatment regimens.

Results: Of 1244 patients with MDR tuberculosis, 973 (78.2%) had known outcomes and 232 (18.6%) were lost to follow-up. Among those with known outcomes, treatment succeeded in 85.8% with plain MDR tuberculosis, 69.7% with initial resistance to either a fluoroquinolone or an SLI, 37.5% with acquired resistance to a fluoroquinolone or SLI, 29.3% with initial and 13.0% with acquired extensively drug-resistant tuberculosis (P < .001 for trend). In contrast, among those with known outcomes, treatment success increased stepwise from 41.6% to 92.3% as the number of drugs proven effective increased from ≤1 to ≥5 (P < .001 for trend), while acquired drug resistance decreased from 12% to 16% range, depending on the drug, down to 0%-2% (P < .001 for trend). In multivariable analysis, the adjusted odds of treatment success decreased 0.62-fold (95% confidence interval, .56-.69) for each increment in drug resistance and increased 2.1-fold (1.40-3.18) for each additional effective drug, controlling for differences between programs and patients. Specific treatment, patient, and program variables were also associated with treatment outcome.

Conclusions: Increasing drug resistance was associated in a logical stepwise manner with poor treatment outcomes. Acquired resistance was worse than initial resistance to the same drugs. Increasing numbers of effective drugs, specific drugs, and specific program characteristics were associated with better outcomes and less acquired resistance.

Keywords: acquired drug resistance; extensively drug-resistant tuberculosis; multidrug-resistant tuberculosis; second-line drugs; treatment outcome.

PubMed Disclaimer

Figures

Figure 1.
Figure 1.
Preserving Effective Tuberculosis Treatment Study population and derivation of the sample of subjects included in the analysis cohort. Abbreviations: CDC, Centers for Disease Control and Prevention; DST, drug susceptibility testing; MDR, multidrug-resistant; SLD, second-line drug.

References

    1. World Health Organization. Global tuberculosis report 2014. Geneva, Switzerland: World Health Organization, 2014.
    1. Centers for Disease Control and Prevention. Emergence of Mycobacterium tuberculosis with extensive resistance to second-line drugs—worldwide, 2000–2004. MMWR 2006; 55:301–5. - PubMed
    1. Shah NS, Wright A, Bai G-H et al. . Worldwide emergence of extensively drug-resistant tuberculosis. Emerg Infect Dis 2007; 13:380–7. - PMC - PubMed
    1. Dalton T, Cegielski P, Akksilp S et al. . Prevalence of and risk factors for resistance to second-line drugs in people with multidrug-resistant tuberculosis in eight countries: a prospective cohort study. Lancet 2012; 380:1406–17. - PMC - PubMed
    1. David HL. Probability distribution of drug-resistant mutants in unselected populations of Mycobacterium tuberculosis. Appl Microbiol 1970; 20:810–4. - PMC - PubMed

Publication types

Substances