Evaluation of ceftazidime/avibactam for treatment of carbapenemase-producing carbapenem-resistant Enterobacterales with OXA-48 and/or NDM genes with or without combination therapy

被引:9
作者
Alqahtani, Hajar [1 ]
Alghamdi, Ahlam [2 ,3 ]
Alobaidallah, Nouf [4 ]
Alfayez, Amal [4 ]
Almousa, Rawan [4 ]
Albagli, Rawan [4 ]
Shamas, Nour [5 ]
Farahat, Fayssal [5 ,6 ]
Mahmoud, Ebrahim [7 ,8 ]
Bosaeed, Mohammad [7 ,8 ,9 ]
Abanamy, Reem [7 ]
机构
[1] Minist Natl Guard Hlth Affairs, Dept Pharmaceut Care, Riyadh, Saudi Arabia
[2] Princess Nourah Bint Abdulrahman Univ, Coll Pharm, Dept Pharm Practice, Riyadh, Saudi Arabia
[3] King Abdullah Bin Abdulaziz Univ Hosp, Dept Pharmaceut Care, Riyadh, Saudi Arabia
[4] Princess Nourah Bint Abdulrahman Univ, Coll Pharm, Riyadh, Saudi Arabia
[5] Minist Natl Guard, Hlth Affairs, Dept Infect Prevent & Control, Riyadh, Saudi Arabia
[6] King Saud Bin Abdulaziz Univ Hlth Sci, Coll Publ Hlth & Hlth Informat, Riyadh, Saudi Arabia
[7] Minist Natl Guard Hlth Affairs, Dept Med, Riyadh, Saudi Arabia
[8] King Saud Bin Abdulaziz Univ Hlth Sci, Coll Med, Riyadh, Saudi Arabia
[9] King Abdullah Int Med Res Ctr, Dept Clin Trial Serv, Riyadh, Saudi Arabia
来源
JAC-ANTIMICROBIAL RESISTANCE | 2022年 / 4卷 / 05期
关键词
KLEBSIELLA-PNEUMONIAE; INFECTIONS; AVIBACTAM; COLISTIN;
D O I
10.1093/jacamr/dlac104
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Background Carbapenem-resistant Enterobacterales (CRE) is an urgent public health threat of significant global concern. Few observational studies have evaluated the clinical outcomes for treatment of CRE harbouring OXA-48 or NDM genes with ceftazidime/avibactam. Previous findings showed lower 30 day mortality with ceftazidime/avibactam ranges between 8.3% and 22%. Method This single-centre retrospective cohort study included adult patients aged >= 18 years admitted to King Abdulaziz Medical City (KAMC) who had received ceftazidime/avibactam for at least 72 h for infections caused by CRE with genes encoding for carbapenemase production (CP-CRE). Results A total of 211 patients, mostly male (57%), having CP-CRE infections treated with ceftazidime/avibactam were included, with an average age of 62 years. More than 50% of patients were critically ill, for which 46% received invasive ventilation and 36% were on inotropes. The most frequent infectious disease was hospital/ventilator-acquired pneumonia with Klebsiella pneumoniae being the most frequent causative pathogen. The majority of isolates harboured OXA-48 (81%), followed by NDM +/- OXA-48 (19%). The overall clinical cure and 30 day mortality was 78% and 21% respectively (stratified per gene: 79% and 21.6% for OXA-48 and 75% and 17.5% for NDM +/- OXA-48). Conclusions This was the largest study that evaluated clinical outcomes associate with CP-CRE harbouring OXA-48 gene infections treated with ceftazidime/avibactam. Clinical cure and 30 day mortality were consistent with those of previous studies. Findings suggested that combination therapy with ceftazidime/avibactam had no direct impact on clinical outcomes for CP-CRE with OXA-48.
引用
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页数:9
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