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Treatment Outcomes and Survival Based on Drug Resistance Patterns in Multidrug-resistant Tuberculosis

Authors
Kim, Doh HyungKim, Hee JinPark, Seung-KyuKong, Suck-JunKim, Young SamKim, Tae-HyungKim, Eun KyungLee, Ki ManLee, Sung-SoonPark, Jae SeukKoh, Won-JungLee, Chang-HoonShim, Tae Sun
Issue Date
Jul-2010
Publisher
AMER THORACIC SOC
Keywords
tuberculosis; multidrug-resistant; survival rate; treatment outcome; drug susceptibility
Citation
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, v.182, no.1, pp.113 - 119
Indexed
SCIE
SCOPUS
Journal Title
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE
Volume
182
Number
1
Start Page
113
End Page
119
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/174526
DOI
10.1164/rccm.200911-1656OC
ISSN
1073-449X
Abstract
Rationale: Few large-scale studies have investigated multidrug-resistant tuberculosis (MDR-TB) treatment outcomes relative to drug-resistance patterns. Objectives: To assess the impact of additional drug resistances on treatment outcomes and long-term survival in a large HIV-negative MDR-TB cohort. Methods: Treatment outcomes and long-term survival of patients with MDR-TB newly diagnosed or retreated in 2000 to 2002 were retrospectively analyzed based on drug-resistance patterns after 5-8 years of follow-up. Measurements and Main Results: Of 1,407 patients with MDR-TB, 75 (5.3%) had extensively drug-resistant TB (XDR-TB,) by the revised definition; 159 (11.3%) had ofloxacin-resistant pre-XDR-TB (pre-XDR-TB.); and 117 (8.3%) had second-line injectable drug (SLID)-resistant pre-XDR-TB (pre-XDR-TB(s)). Patients with XDR-TB, showed the lowest treatment success rate (29.3%) and the poorest long-term survival, and XDR-TB(re) was more strongly associated with long-term mortality than XDR-TB as originally defined (hazards ratio [HR], 3.15; 95% confidence interval [Cl], 2.06-4.83; P < 0.001 vs. HR, 2.15; 95% Cl, 1.49-3.09; P < 0.001). Patients with either form of pre-XDR-TB showed poorer cumulative survival than those with ofloxacin-susceptible/SLID-susceptible MDR-TB (P < 0.05 for each comparison). Although streptomycin susceptibility did not affect the treatment outcomes of patients with pre-XDR-TB, streptomycin-resistant pre-XDR-TB was more strongly associated with long-term mortality than ofloxacin-susceptible/SLID-susceptible MDR-TB (HR, 2.17; 95% Cl, 1.22-3.84; P < 0.008 for preXDR-TB.; and HR, 2.69; 95% Cl, 1.40-5.16; P= 0.003 for pre-XDR-TBs). Conclusions: The revised XDR-TB definition is appropriate for defining patients with MDR-TB with the poorest outcomes. Both pre-XDR-TB(o) and pre-XDR-TBs were independently associated with poor long-term survival in patients with MDR-TB. SM susceptibility was linked to better survival in patients with pre-XDR-TB.
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