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6 个月的贝达喹啉是否足够?亚美尼亚和格鲁吉亚贝达喹啉同情用药的结果。

Is 6 months of bedaquiline enough? Results from the compassionate use of bedaquiline in Armenia and Georgia.

机构信息

Médecins Sans Frontières (MSF), Paris.

Epicentre, Paris, France.

出版信息

Int J Tuberc Lung Dis. 2018 Jul 1;22(7):766-772. doi: 10.5588/ijtld.17.0840.

Abstract

BACKGROUND AND SETTING

Bedaquiline (BDQ) was initially only available through compassionate use programmes.

OBJECTIVE

To assess the effectiveness and safety of multidrug-resistant tuberculosis (MDR-TB) treatment containing BDQ.

METHOD

Retrospective analysis of data from patients receiving BDQ through compassionate use in Armenia and Georgia from April 2013 to April 2015. Logistic regression was used to assess the risk factors associated with unsuccessful treatment outcomes.

RESULTS

Of 82 patients included, 84.2% (69/82) had fluoroquinolone-resistant MDR-TB and 43.4% (23/53) were seropositive for the hepatitis C virus (HCV). The culture conversion rate was 84.4% (54/64), and 18.5% (10/54) reverted back to positive. In total, 79.3% (65/82) of the patients reported at least one adverse event. Serious adverse events were reported in 14 patients, with 10/14 patients experiencing fatal outcomes-6/10 related to advanced TB and 2/10 assessed as possibly related to BDQ. Treatment outcomes were as follows: 58.5% treatment success, 12.2% deaths, 7.3% failures and 21.9% lost to follow-up. HCV coinfection was associated with unsuccessful outcomes (adjusted OR 4.45, 95%CI 1.23-16.13).

CONCLUSION

BDQ through compassionate use showed relatively good success rates and safety profiles in a cohort with difficult-to-treat MDR-TB. High rates of reversion may indicate that >24 weeks of BDQ is necessary in some cases. HCV coinfection should be diagnosed and treatment considered in MDR-TB patients.

摘要

背景和设置

贝达喹啉(BDQ)最初仅通过同情用药计划获得。

目的

评估含有 BDQ 的耐多药结核病(MDR-TB)治疗的有效性和安全性。

方法

对 2013 年 4 月至 2015 年 4 月期间通过亚美尼亚和格鲁吉亚同情用药接受 BDQ 的患者数据进行回顾性分析。采用逻辑回归评估与治疗结局失败相关的风险因素。

结果

在 82 例患者中,84.2%(69/82)患有氟喹诺酮耐药 MDR-TB,43.4%(23/53)丙型肝炎病毒(HCV)血清阳性。培养转化率为 84.4%(54/64),18.5%(10/54)转为阳性。共有 79.3%(65/82)的患者报告至少发生了一次不良事件。14 例患者报告了严重不良事件,其中 10 例死亡,6/10 例与晚期结核病相关,2/10 例评估为可能与 BDQ 相关。治疗结局如下:58.5%治疗成功,12.2%死亡,7.3%失败,21.9%失访。HCV 合并感染与治疗结局失败相关(调整 OR 4.45,95%CI 1.23-16.13)。

结论

在一组治疗难度较大的 MDR-TB 患者中,通过同情用药使用 BDQ 显示出相对较高的成功率和安全性。较高的逆转率可能表明在某些情况下需要使用 BDQ 超过 24 周。在 MDR-TB 患者中应诊断 HCV 合并感染并考虑进行治疗。

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