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儿童耐多药结核病治疗结局的基线预测因素:一项回顾性队列研究。

Baseline Predictors of Treatment Outcomes in Children With Multidrug-Resistant Tuberculosis: A Retrospective Cohort Study.

机构信息

Department of Pediatrics, Section of Infectious Diseases, Baylor College of Medicine, Houston, Texas Department of Global Health and Social Medicine, Harvard Medical School, Boston, Massachusetts.

Department of Pediatrics, Section of Infectious Diseases, Baylor College of Medicine, Houston, Texas.

出版信息

Clin Infect Dis. 2016 Oct 15;63(8):1063-71. doi: 10.1093/cid/ciw489. Epub 2016 Jul 25.

Abstract

BACKGROUND

Globally, >30 000 children fall sick with multidrug-resistant (MDR) tuberculosis every year. Without robust pediatric data, clinical management follows international guidelines that are based on studies in adults and expert opinion. We aimed to identify baseline predictors of death, treatment failure, and loss to follow-up among children with MDR tuberculosis disease treated with regimens tailored to their drug susceptibility test (DST) result or to the DST result of a source case.

METHODS

This retrospective cohort study included all children ≤15 years old with confirmed and probable MDR tuberculosis disease who began tailored regimens in Lima, Peru, between 2005 and 2009. Using logistic regression, we examined associations between baseline patient and treatment characteristics and (1) death or treatment failure and (2) loss to follow-up.

RESULTS

Two hundred eleven of 232 (90.9%) children had known treatment outcomes, of whom 163 (77.2%) achieved cure or probable cure, 29 (13.7%) were lost to follow-up, 10 (4.7%) experienced treatment failure, and 9 (4.3%) died. Independent baseline predictors of death or treatment failure were the presence of severe disease (adjusted odds ratio [aOR], 4.96; 95% confidence interval [CI], 1.61-15.26) and z score ≤-1 (aOR, 3.39; 95% CI, 1.20-9.54). We did not identify any independent predictors of loss to follow-up.

CONCLUSIONS

High cure rates can be achieved in children with MDR tuberculosis using tailored regimens containing second-line drugs. However, children faced significantly higher risk of death or treatment failure if they had severe disease or were underweight. These findings highlight the need for early interventions that can improve treatment outcomes for children with MDR tuberculosis.

摘要

背景

全球每年有超过 30000 名儿童感染耐多药(MDR)结核病。由于缺乏针对儿科的可靠数据,临床管理沿用的是基于成人研究和专家意见制定的国际指南。我们旨在确定根据药敏试验(DST)结果或源病例 DST 结果量身定制方案治疗的耐多药结核病患儿死亡、治疗失败和失访的基线预测因素。

方法

本回顾性队列研究纳入了 2005 年至 2009 年期间在秘鲁利马开始使用量身定制方案治疗的所有确诊和疑似耐多药结核病的≤15 岁儿童。使用逻辑回归分析,我们检查了基线患者和治疗特征与(1)死亡或治疗失败和(2)失访之间的关联。

结果

232 名儿童中有 211 名(90.9%)有已知的治疗结局,其中 163 名(77.2%)治愈或可能治愈,29 名(13.7%)失访,10 名(4.7%)治疗失败,9 名(4.3%)死亡。死亡或治疗失败的独立基线预测因素是存在严重疾病(调整比值比[aOR],4.96;95%置信区间[CI],1.61-15.26)和 z 评分≤-1(aOR,3.39;95% CI,1.20-9.54)。我们未发现失访的任何独立预测因素。

结论

使用含有二线药物的量身定制方案可以使耐多药结核病患儿获得较高的治愈率。然而,如果儿童患有严重疾病或体重不足,他们死亡或治疗失败的风险显著增加。这些发现强调需要早期干预,以改善耐多药结核病患儿的治疗结局。

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