Infectious Diseases Research Department, King Abdullah International Medical Research Center, Riyadh, Saudi Arabia.
King Saud Bin Abdulaziz University for Health Sciences, Riyadh, Saudi Arabia.
Sci Rep. 2021 May 6;11(1):9684. doi: 10.1038/s41598-021-89255-8.
Pandrug-resistant (PDR) K. pneumoniae refractory to conventional treatment has been reported worldwide, causing a huge burden on the healthcare system, patient safety and the economy. K. pneumoniae is a prominent opportunistic pathogen causing hospital-acquired and community-acquired infections, but is rarely associated with infective endocarditis. Currently, there are sparse data guiding the optimal regimen when commonly used antibiotics fail, notably for the treatment of endocarditis infections. Here we report our experience in treating a 40-year-old female with PDR K. pneumoniae infection of cardiovascular implantable electronic device (CIED) and right-sided infective endocarditis. Initial susceptibility testing of the incriminated pathogen showed an apparent susceptibility to colistin but the prolonged course of colistin, gentamicin and meropenem did not resolve the infection. However, the synergistic combinations of aztreonam with ceftazidime-avibactam was able to overcome resistance and clear the infection rapidly. Genome sequencing showed that the PDR K. pneumoniae isolate belongs to the international high-risk clone ST14. The isolate harbored genes encoding NDM-1, OXA-48, CTX-M-14b, SHV-28 and OXA-1, explaining resistance to all β-lactams, including carbapenems. It carried the armA gene conferring resistance to all clinically important aminoglycosides and had alterations in GyrA, ParC and MgrB, explaining resistance to ciprofloxacin and colistin.
已在全球范围内报道了对常规治疗具有抗药性的泛耐药(PDR)肺炎克雷伯菌(K. pneumoniae),这给医疗保健系统、患者安全和经济带来了巨大负担。肺炎克雷伯菌是一种引起医院获得性和社区获得性感染的重要机会性病原体,但很少与感染性心内膜炎相关。目前,当常用抗生素治疗无效时,指导最佳治疗方案的相关数据很少,特别是在治疗心内膜炎感染方面。在此,我们报告了我们治疗一名 40 岁女性心血管植入式电子设备(CIED)和右侧感染性心内膜炎伴 PDR 肺炎克雷伯菌感染的经验。最初对可疑病原体的药敏试验显示对黏菌素明显敏感,但黏菌素、庆大霉素和美罗培南的长期疗程并未解决感染问题。然而,氨曲南与头孢他啶-阿维巴坦的协同组合能够克服耐药性并迅速清除感染。基因组测序表明,该 PDR 肺炎克雷伯菌分离株属于国际高风险克隆 ST14。该分离株携带编码 NDM-1、OXA-48、CTX-M-14b、SHV-28 和 OXA-1 的基因,解释了对所有β-内酰胺类药物(包括碳青霉烯类)的耐药性。它携带 armA 基因,对所有临床重要的氨基糖苷类药物具有耐药性,并且在 GyrA、ParC 和 MgrB 中发生了改变,解释了对环丙沙星和黏菌素的耐药性。