Division of Infectious Diseases, Department of Medicine, Taipei Veterans General Hospital, Taipei, Taiwan.
Institute of Emergency and Critical Care Medicine, National Yang Ming Chiao Tung University, Taipei, Taiwan.
Int J Antimicrob Agents. 2021 Jun;57(6):106342. doi: 10.1016/j.ijantimicag.2021.106342. Epub 2021 Apr 14.
Colistin is one of the last-resort antibiotics for treating carbapenem-resistant Klebsiella pneumoniae (CRKP). However, colistin resistance in CRKP poses a global antimicrobial crisis, as therapeutic options are limited. We investigated risk factors for in vivo emergence of colistin resistance in CRKP and explored the underlying resistance mechanisms. We conducted this matched case-control study of patients with sequential CRKP clinical strains at a medical centre in Taiwan between October 2016 and June 2019. The case group included patients with an index colistin-resistant CRKP (ColR-CRKP) strain and a previous colistin-susceptible CRKP (ColS-CRKP) counterpart. The control group encompassed patients with both an index and previous ColS-CRKP strains. Cases and controls were matched according to the time at risk, and conditional logistic regression was used to evaluate potential risk factors. Alterations in genes associated with resistance were compared between ColR-CRKP and ColS-CRKP strains. We identified 24 CRKP cases with in vivo-emergent colistin resistance, matched in a 1:2 ratio with controls. Multivariate analysis showed that colistin exposure is the only independent risk factor predisposing to colistin resistance (adjusted odds ratio = 19.09, 95% confidence interval 1.26-290.45; P = 0.034). Alteration in the mgrB gene was the predominant mechanism for emergent colistin resistance (17/24; 71%). In conclusion, colistin use is a risk factor for in vivo emergence of colistin resistance in CRKP. Given the lack of a rapid and reliable method to detect colistin resistance in daily practice, physicians should be vigilant for the emergence of resistance during colistin treatment.
黏菌素是治疗碳青霉烯类耐药肺炎克雷伯菌(CRKP)的最后手段之一。然而,CRKP 中的黏菌素耐药性构成了全球抗菌药物危机,因为治疗选择有限。我们研究了 CRKP 中体内出现黏菌素耐药性的危险因素,并探讨了潜在的耐药机制。我们在台湾的一家医疗中心进行了这项病例对照研究,纳入了 2016 年 10 月至 2019 年 6 月期间连续出现 CRKP 临床分离株的患者。病例组包括具有指数性黏菌素耐药 CRKP(ColR-CRKP)菌株和之前的黏菌素敏感 CRKP(ColS-CRKP)对应菌株的患者。对照组包括具有指数和之前 ColS-CRKP 菌株的患者。病例和对照根据风险时间进行匹配,使用条件逻辑回归评估潜在的危险因素。比较了 ColR-CRKP 和 ColS-CRKP 菌株中与耐药相关的基因的变化。我们确定了 24 例具有体内出现的黏菌素耐药性的 CRKP 病例,按照 1:2 的比例与对照匹配。多变量分析表明,黏菌素暴露是导致黏菌素耐药的唯一独立危险因素(调整后的优势比=19.09,95%置信区间 1.26-290.45;P=0.034)。mgrB 基因突变是体内出现黏菌素耐药的主要机制(17/24;71%)。总之,黏菌素的使用是 CRKP 中体内出现黏菌素耐药的危险因素。鉴于目前缺乏一种快速可靠的方法在日常实践中检测黏菌素耐药性,医生在黏菌素治疗期间应警惕耐药性的出现。