Risk factors for unfavourable treatment outcomes among rifampicin-resistant tuberculosis patients in Tajikistan

被引:12
作者
Makhmudova, M. [1 ]
Maxsumova, Z. [2 ]
Rajabzoda, A. [3 ]
Makhmadov, A. [1 ]
van den Hof, S. [4 ]
Mirtskhulava, V. [4 ,5 ]
机构
[1] KNCV TB Fdn, Country Off, Dushanbe, Tajikistan
[2] USAID TB Control Project, Dushanbe, Tajikistan
[3] Natl Ctr Populat Protect TB, Dushanbe, Tajikistan
[4] KNCV TB Fdn, Team Evidence, Tech Div, The Hague, Netherlands
[5] David Tvildiani Med Univ, Dept Publ Hlth Epidemiol & Biostat, Tbilisi, Georgia
关键词
second-line anti-tuberculosis drug; treatment failure; loss to follow-up; adverse event; retrospective cohort study; MDR-TB; DRUG-RESISTANCE; IMPACT; PREDICTORS; MORTALITY; DEFAULT; PROGRAM; ASSAY;
D O I
10.5588/ijtld.18.0311
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
SETTING: Tajikistan is among the 30 countries with the highest multidrug-resistant tuberculosis (MDR-TB) burden. OBJECTIVE : To investigate the risk factors for unfavourable treatment outcomes among rifampicin-resistant (RR)/MDR-TB patients. DESIGN: Retrospective medical chart review of RR/MDR-TB patients enrolled for treatment in 2012-2013. RESULTS : Of 601 RR/MDR-TB patients, 58 (9.7%) had pre-extensively drug-resistant TB (pre-XDR-TB; i.e., MDR-TB with additional resistance to a fluoroquinolone or second-line injectable agent) and 45 (8%) had XDR-TB (MDR-TB with additional resistance to both). Treatment failure and death were reported in respectively 40 (7%) and 89 (15%) cases; 60 (10%) patients were lost to follow-up (LTFU). Inmultivariable analysis, treatment failure was associated with pre-XDR-TB (adjusted odds ratio [aOR] 3.67, 95% CI 1.47-9.18) or XDR-TB (aOR 8.61, 95% CI 3.48-21.34). Death was associated with age >45 years vs. <25 years (aOR 3.47, 95% CI 1.68-7.19) and no record of any adverse event during treatment (aOR 2.55, 95% CI 1.48-4.39). Changing place of residence during treatment was an independent predictor of LTFU (aOR 4.61, 95% CI 2.41-8.8). CONCLUSIONS : Our findings highlight the need for 1) the use of regimens with new anti-tuberculosis drugs; 2) good handover of TB patients and 3) effective tracing mechanisms if patients change a place of residence to prevent LTFU.
引用
收藏
页码:331 / +
页数:7
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