Gugliandolo Agnese, Caio Carla, Mezzatesta Maria Lina, Rifici Carmela, Bramanti Placido, Stefani Stefania, Mazzon Emanuela
IRCCS Centro Neurolesi "Bonino-Pulejo", Via Provinciale Palermo, Messina Section of Microbiology, Department of Biomedical and Biotechnological Sciences, University of Catania, Catania, Italy.
Medicine (Baltimore). 2017 Aug;96(31):e7664. doi: 10.1097/MD.0000000000007664.
Carbapenem-resistant Enterobacteriaceae infections are a serious health care problem, because of the high mortality. Carbapenem resistance is mainly caused by carbapenemases production, including Klebsiella pneumoniae carbapenemase (KPC). Ceftazidime-avibactam is a new cephalosporin/β-lactamase inhibitor combination for the treatment of complicated urinary, intra-abdominal infections, and nosocomial pneumonia caused by gram negative, or other serious gram-negative infections.
We showed the case of a 27-year-old patient, hospitalized for traumatic brain injury and chest trauma, with KPC-producing Klebsiella pneumoniae infection.
Blood and bronchial aspirate culture analysis detected an infection caused by MDR Klebsiella pneumoniae, resistant to meropenem, ertapenem, piperacillin/tazobactam, amoxicillin/clavulanic acid, aztreonam, ceftazidime, cefotaxime, cefepime, amikacin, ciprofloxacin, trimethoprim/sulfamethoxazole, colistin while it showed an intermediate sensitivity to gentamicin and was sensitive to ceftazidime-avibactam. Molecular analyses revealed that the isolate belonged to the epidemic clone sequence type 258 (ST258) carrying blaKPC-3, blaTEM-1, and blaSHV-11genes.
After various combined antibiotic therapies without improvements, he was treated with ceftazidime-avibactam, on a compassionate-use basis.
With ceftazidime-avibactam monotherapy clinical and microbiological clearance was obtained. A week after the end of the therapy microbiological analysis was repeated and a positive rectal swab for KPC-Klebsiella pneumoniae was found, becoming negative after 1 month. Moreover, the patient did not show any relapses for up to 18 weeks.
This case indicates that ceftazidime-avibactam monotherapy could be efficacious against KPC positive Klebsiella pneumoniae infections.
耐碳青霉烯类肠杆菌科细菌感染是一个严重的医疗保健问题,因为死亡率很高。碳青霉烯类耐药主要是由碳青霉烯酶的产生引起的,包括肺炎克雷伯菌碳青霉烯酶(KPC)。头孢他啶-阿维巴坦是一种新型头孢菌素/β-内酰胺酶抑制剂组合,用于治疗由革兰氏阴性菌引起的复杂性尿路感染、腹腔内感染和医院获得性肺炎,或其他严重的革兰氏阴性菌感染。
我们展示了一名27岁患者的病例,该患者因创伤性脑损伤和胸部创伤住院,感染了产KPC的肺炎克雷伯菌。
血液和支气管吸出物培养分析检测到由多重耐药肺炎克雷伯菌引起的感染,该菌对美罗培南、厄他培南、哌拉西林/他唑巴坦、阿莫西林/克拉维酸、氨曲南、头孢他啶、头孢噻肟、头孢吡肟、阿米卡星、环丙沙星、甲氧苄啶/磺胺甲恶唑、黏菌素耐药,对庆大霉素表现出中度敏感性,对头孢他啶-阿维巴坦敏感。分子分析显示,分离株属于携带blaKPC-3、blaTEM-1和blaSHV-11基因的流行克隆序列类型258(ST258)。
在多种联合抗生素治疗均无改善后,在同情用药的基础上,他接受了头孢他啶-阿维巴坦治疗。
采用头孢他啶-阿维巴坦单药治疗后,实现了临床和微生物学清除。治疗结束一周后重复进行微生物学分析,发现直肠拭子肺炎克雷伯菌产KPC呈阳性,1个月后转阴。此外,该患者长达18周未出现任何复发。
该病例表明,头孢他啶-阿维巴坦单药治疗可能对产KPC的肺炎克雷伯菌感染有效。