Risk factors for MDR and XDR-TB in a tertiary referral hospital in India

India has a high burden of drug resistant TB, although there are few data on XDR-TB. Although XDR-TB has existed previously in India, the definition has not been widely applied, and surveillance using second line drug susceptibility testing has not been performed. Our objective was to analyze clinic...

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Published inPloS one Vol. 5; no. 3; p. e9527
Main Authors Balaji, V, Daley, Peter, Anand, Alok Azad, Sudarsanam, Thambu, Michael, Joy Sarojini, Sahni, Rani Diana, Chordia, Poorvi, George, Ige Abraham, Thomas, Kurien, Ganesh, Alka, John, K R, Mathai, Dilip
Format Journal Article
LanguageEnglish
Published United States Public Library of Science 04.03.2010
Public Library of Science (PLoS)
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Summary:India has a high burden of drug resistant TB, although there are few data on XDR-TB. Although XDR-TB has existed previously in India, the definition has not been widely applied, and surveillance using second line drug susceptibility testing has not been performed. Our objective was to analyze clinical and demographic risk factors associated with isolation of MDR and XDR TB as compared to susceptible controls, at a tertiary center. Retrospective chart review based on positive cultures isolated in a high volume mycobacteriology laboratory between 2002 and 2007. 47 XDR, 30 MDR and 117 susceptible controls were examined. Drug resistant cases were less likely to be extrapulmonary, and had received more previous treatment regimens. Significant risk factors for XDR-TB included residence outside the local state (OR 7.43, 3.07-18.0) and care costs subsidized (OR 0.23, 0.097-0.54) in bivariate analysis and previous use of a fluoroquinolone and injectable agent (other than streptomycin) (OR 7.00, 95% C.I. 1.14-43.03) and an initial treatment regimen which did not follow national guidelines (OR 5.68, 1.24-25.96) in multivariate analysis. Cavitation and HIV did not influence drug resistance. There is significant selection bias in the sample available. Selection pressure from previous treatment and an inadequate initial regimen increases risk of drug resistance. Local patients and those requiring financial subsidies may be at lower risk of XDR-TB.
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Conceived and designed the experiments: PD. Performed the experiments: VB AAA TS JSM RDS PC IAG. Analyzed the data: PD AAA. Contributed reagents/materials/analysis tools: KT AG KRJ DM. Wrote the paper: PD AAA.
ISSN:1932-6203
1932-6203
DOI:10.1371/journal.pone.0009527