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台湾实施直接观察治疗短程化疗(DOTS)和 DOTS-Plus 方案后,获得性耐多药结核病发病率下降。

Decline in rates of acquired multidrug-resistant tuberculosis after implementation of the directly observed therapy, short course (DOTS) and DOTS-Plus programmes in Taiwan.

机构信息

Chest Hospital, Department of Health, Executive Yuan, Tainan, Taiwan.

出版信息

J Antimicrob Chemother. 2013 Aug;68(8):1910-6. doi: 10.1093/jac/dkt103. Epub 2013 Apr 10.

DOI:10.1093/jac/dkt103
PMID:23580558
Abstract

OBJECTIVES

To investigate the impact of the directly observed therapy, short course (DOTS) and DOTS-Plus strategies on changes in resistance profiles among Mycobacterium tuberculosis (MTB).

METHODS

We performed a retrospective analysis of resistance profiles among isolates of MTB obtained from 2160 consecutive patients with culture-confirmed pulmonary tuberculosis (TB) between 2005 and 2011 at a referral centre in southern Taiwan.

RESULTS

Of the 2160 patients, 70 (3.2%) had primary multidrug-resistant (MDR)-TB, 178 (8.2%) had acquired MDR-TB, 10 (0.5%) had primary extensively drug-resistant (XDR)-TB, 23 (1.1%) had acquired XDR-TB and 5 (0.2%) had totally drug-resistant (TDR)-TB. Trend analysis revealed that the rates of acquired MDR-TB were significantly lower after implementation of the DOTS and DOTS-Plus programmes (P < 0.01). There was a significant negative correlation between the coverage rates of the DOTS and DOTS-Plus programmes and the rates of acquired MDR-TB (r = -0.84, P = 0.02 and r = -0.92, P = 0.03, respectively). The rates of resistance to rifampicin, isoniazid, ofloxacin, moxifloxacin, levofloxacin and para-aminosalicylic acid also decreased significantly during the study period. However, the rates of primary MDR-TB remained stable (P = 0.11). Multivariate logistic regression analysis showed that age ranging from 45 to 64 years, positive acid-fast stain results at the initiation of treatment and treatment without DOTS were independent risk factors associated with acquired MDR-TB. In addition, previous treatment for TB (100% versus 19% for TDR-TB and non-TDR-TB, P < 0.01) and treatment without DOTS (80% versus 44% for TDR-TB and non-TDR-TB, P = 0.18) were risk factors for TDR-TB.

CONCLUSIONS

DOTS and DOTS-Plus are both effective at preventing the acquisition of MDR-TB in Taiwan.

摘要

目的

调查直接观察治疗短程方案(DOTS)和 DOTS-Plus 策略对结核分枝杆菌(MTB)耐药谱变化的影响。

方法

我们对 2005 年至 2011 年间在台湾南部一家转诊中心经培养证实的 2160 例肺结核(TB)连续患者的 MTB 分离株耐药谱进行了回顾性分析。

结果

2160 例患者中,70 例(3.2%)为原发性耐多药(MDR)-TB,178 例(8.2%)为获得性 MDR-TB,10 例(0.5%)为原发性广泛耐药(XDR)-TB,23 例(1.1%)为获得性 XDR-TB,5 例(0.2%)为完全耐药(TDR)-TB。趋势分析显示,实施 DOTS 和 DOTS-Plus 方案后,获得性 MDR-TB 的发生率显著降低(P<0.01)。DOTS 和 DOTS-Plus 方案的覆盖率与获得性 MDR-TB 的发生率呈显著负相关(r=-0.84,P=0.02 和 r=-0.92,P=0.03)。研究期间,利福平、异烟肼、氧氟沙星、莫西沙星、左氧氟沙星和对氨基水杨酸的耐药率也显著下降。然而,原发性 MDR-TB 的发生率保持稳定(P=0.11)。多变量 logistic 回归分析显示,年龄在 45 至 64 岁之间、治疗开始时抗酸染色阳性结果和无 DOTS 治疗是与获得性 MDR-TB 相关的独立危险因素。此外,既往 TB 治疗(100%比 TDR-TB 和非 TDR-TB 的 19%,P<0.01)和无 DOTS 治疗(80%比 TDR-TB 和非 TDR-TB 的 44%,P=0.18)是 TDR-TB 的危险因素。

结论

DOTS 和 DOTS-Plus 均可有效预防台湾获得性 MDR-TB。

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