Risk Factors for MDR and XDR-TB in a Tertiary Referral Hospital in India

被引:36
作者
Balaji, V. [1 ]
Daley, Peter [2 ]
Anand, Alok Azad [3 ]
Sudarsanam, Thambu [2 ]
Michael, Joy Sarojini [1 ]
Sahni, Rani Diana [1 ]
Chordia, Poorvi [2 ]
George, Ige Abraham [2 ]
Thomas, Kurien [2 ]
Ganesh, Alka [2 ]
John, K. R. [4 ]
Mathai, Dilip [2 ]
机构
[1] Christian Med Coll Vellore, Dept Microbiol, Vellore, Tamil Nadu, India
[2] Christian Med Coll Vellore, Dept Med, Vellore, Tamil Nadu, India
[3] Tufts Univ, Sch Med, Boston, MA 02111 USA
[4] Christian Med Coll Vellore, Dept Community Med, Vellore, Tamil Nadu, India
来源
PLOS ONE | 2010年 / 5卷 / 03期
关键词
DRUG-RESISTANT TUBERCULOSIS; MULTIDRUG-RESISTANT; TREATMENT OUTCOMES;
D O I
10.1371/journal.pone.0009527
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background: 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. Methodology/Findings: 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. Conclusions/Significance: 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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页数:6
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