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Clinical Characteristics, Treatment Outcomes, and Resistance Mutations Associated with Macrolide-Resistant Mycobacterium avium Complex Lung Disease

机译:耐大环内酯类鸟分枝杆菌复杂肺疾病的临床特征,治疗结果和耐药突变

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Macrolide antibiotics are key components of the multidrug treatment regimen for treating lung disease (LD) due to Mycobacterium avium complex ( MAC). Despite the emergence of macrolide resistance, limited data are available on macrolide-resistant MAC-LD. This study evaluated the clinical features and treatment outcomes of patients with macrolide-resistant MAC-LD and the molecular characteristics of the macrolide-resistant isolates. A retrospective review of the medical records of 34 patients with macrolide-resistant MAC-LD who were diagnosed between January 2002 and December 2014 was performed, along with genetic analysis of 28 clinical isolates. Nineteen ( 56%)patientshad the fibrocavitary form of MAC-LD, and 15 (44%) had the nodular bronchiectatic form. M. intracellulare was the etiologic organism in 21 ( 62%) patients. Approximately two-thirds ( 22/34 [ 65%]) of the patients had been treated with currently recommended multidrug regimens that included macrolide, ethambutol, and rifamycin prior to the emergence of macrolide resistance, and none had been treated with macrolide monotherapy. The median duration of treatment after the detection of macrolide resistance was 23.0 months ( interquartile range, 16.8 to 45.3 months). Treatment outcomes were poor after the development of macrolide resistance, with favorable treatment outcomes achieved in only five ( 15%) patients, including two patients who underwent surgical resection. One-, 3-, and 5-year mortality rates were 9, 24, and 47%, respectively. Molecular analysis of 28 clinical isolates revealed that 96% ( 27/ 28) had point mutations at position 2058 or 2059 of the 23S rRNA gene. Our analyses indicate that more effective therapy is needed to treat macrolide-resistant MAC- LD and prevent its development.
机译:大环内酯类抗生素是治疗因鸟分枝杆菌复合物(MAC)引起的肺部疾病(LD)的多药治疗方案的关键成分。尽管出现了大环内酯耐药性,但有关大环内酯耐药MAC-LD的数据仍然有限。这项研究评估了大环内酯耐药MAC-LD患者的临床特征和治疗结果以及大环内酯耐药菌株的分子特征。回顾性分析了2002年1月至2014年12月期间确诊的34例大环内酯耐药MAC-LD患者的病历,并对28株临床分离株进行了基因分析。 19例(56%)的患者为MAC-LD的纤维腔形式,而15例(44%)的为结节性支气管扩张形式。细胞内分枝杆菌是21例(62%)患者的病原体。大约三分之二(22/34 [65%])的患者在出现大环内酯耐药之前已经接受了目前推荐的多药治疗方案,包括大环内酯,乙胺丁醇和利福霉素,并且均未接受大环内酯单药治疗。在检测到大环内酯耐药性后,中位治疗时间为23.0个月(四分位间距为16.8至45.3个月)。大环内酯类药物耐药后,治疗结果较差,仅5例(15%)患者获得了良好的治疗效果,其中包括2例接受了手术切除的患者。一年,三年和五年死亡率分别为9%,24%和47%。对28种临床分离株的分子分析表明,有96%(27/28)在23S rRNA基因的2058或2059位置具有点突变。我们的分析表明,需要更有效的疗法来治疗大环内酯类耐药MAC-LD并阻止其发展。

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