Moon Seong Mi, Park Hye Yun, Kim Su-Young, Jhun Byung Woo, Lee Hyun, Jeon Kyeongman, Kim Dae Hun, Huh Hee Jae, Ki Chang-Seok, Lee Nam Yong, Kim Hong Kwan, Choi Yong Soo, Kim Jhingook, Lee Seung-Heon, Kim Chang Ki, Shin Sung Jae, Daley Charles L, Koh Won-Jung
Division of Pulmonary and Critical Care Medicine, Department of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, South Korea.
Department of Laboratory Medicine and Genetics, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, South Korea.
Antimicrob Agents Chemother. 2016 Oct 21;60(11):6758-6765. doi: 10.1128/AAC.01240-16. Print 2016 Nov.
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%) patients had 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.
大环内酯类抗生素是治疗鸟分枝杆菌复合群(MAC)所致肺部疾病(LD)的多药治疗方案的关键组成部分。尽管出现了大环内酯耐药性,但关于大环内酯耐药MAC-LD的数据有限。本研究评估了大环内酯耐药MAC-LD患者的临床特征和治疗结局以及大环内酯耐药菌株的分子特征。对2002年1月至2014年12月期间诊断的34例大环内酯耐药MAC-LD患者的病历进行了回顾性分析,并对28株临床分离株进行了基因分析。19例(56%)患者为纤维空洞型MAC-LD,15例(44%)为结节性支气管扩张型。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接受了目前推荐的包括大环内酯、乙胺丁醇和利福霉素的多药治疗方案,且无人接受过大环内酯单药治疗。检测到大环内酯耐药后的中位治疗持续时间为23.0个月(四分位间距,16.8至45.3个月)。大环内酯耐药出现后的治疗结局较差,只有5例(15%)患者获得了良好的治疗结局,包括2例接受手术切除的患者。1年、3年和5年死亡率分别为9%、24%和47%。对28株临床分离株的分子分析显示,96%(27/28)在23S rRNA基因的2058或2059位点存在点突变。我们的分析表明,需要更有效的治疗方法来治疗大环内酯耐药MAC-LD并预防其发生。