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Chinese Journal of Clinical Pharmacology and Therapeutics ›› 2023, Vol. 28 ›› Issue (9): 1008-1017.doi: 10.12092/j.issn.1009-2501.2023.09.006

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Real-world study of ceftazidime-avibactam in the treatment of multidrug-resistant gram-negative bacterial infections

JIANG Daoli1, CHOU Xiaohua1, LIU Zhidong1, LI Wei1, ZHANG Bo1, XU Sang2, TAN Defei3, FANG Yi4, LV Dongmei1, WANG Tao1   

  1. 1Department of Pharmacy, the Affiliated Hospital of Xuzhou Medical University, Xuzhou 221004, Jiangsu, China; 2Department of Pharmacy, Yixing People's Hospital, Yixing 214200, Jiangsu, China; 3Department of Pharmacy, the First People's Hospital of Zhenjiang, Zhenjiang 212000, Jiangsu, China; 4Phase I clinical trial center, Peking University People's Hospital, Beijing 100044, China
  • Received:2023-03-14 Revised:2023-07-27 Online:2023-09-26 Published:2023-09-25

Abstract:

AIM: To describe and evaluate the clinical characteristics, treatment management and clinical outcomes of ceftazidime-avibactam (CZA) in the treatment of patients with multidrug-resistant gram-negative bacterial (MDR-GNB) infections. METHODS: A retrospective cohort study was performed on patients hospitalized in the Affiliated Hospital of Xuzhou Medical University from September 2019 to December 2021. Adult patients who received CZA for ≥ 72 hours consecutively were eligible for inclusion. The primary outcome was clinical failure, defined as a composite of 30-day all-cause mortality, microbiological failure and/or failure to resolve or improve signs and symptoms of infection during treatment with CZA. RESULTS: A total of 198 patients with MDR-GNB infections were described and evaluated, including 132 in the carbapenem-resistant Enterobatceriaceae (CRE) cohort and 66 in the Pseudomonas spp. cohort. The main infection sites were lung infection (92.42%), abdominal infection (10.61%), and intracranial infection (10.61%), among which 63 patients (31.82%) were positive for blood culture. Clinical failure, 30-day all-cause mortality and microbiological failure occurred in 61(30.81%), 33(16.67%) and 11(5.56%) patients, respectively. Body mass index (BMI), acute physiology and chronic health evaluation scoring system (APACHE Ⅱ) and polymicrobial infections were positively associated with clinical outcome failure [adjusted OR 1.109, 95%CI 1.017,1.209; adjusted OR 1.071, 95%CI 1.015,1.129; adjusted OR 2.844, 95%CI 1.391,5.814], however, initiation of CZA within 48 hours of admission was protective (adjusted OR 0.424, 95%CI 0.205, 0.879). A total of 15 patients had adverse reactions possibly related to CZA, including 2 cases of rash, 6 cases of nausea and vomiting, and 7 cases of antibiotic-related diarrhea. CONCLUSION: CZA can be used to treat infections caused by a range of MDR-GNB, including Pseudomonas spp. and CRE.

Key words: ceftazidime-avibactam, multidrug-resistant gram-negative bacterial, carbapenem-resistant enterobatceriaceae, Pseudomonas spp

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