{"title":"In vitro susceptibility of Burkholderia cepacia to ceftazidime-avibactam: A systematic review","authors":"Abolfazl Rafati Zomorodi , Leila Ghanbari_Afra , Hossein Faridafshar , Seyed Nooreddin Faraji , Fatemeh Zarepour , Maryamosadat Mavaei , Mohammad Rahmanian","doi":"10.1016/j.nmni.2025.101601","DOIUrl":null,"url":null,"abstract":"<div><h3>Background</h3><div><em>Burkholderia cepacia</em> complex (BCC) is a group of multi-drug resistant (MDR) pathogens that are challenging to treat, especially in cystic fibrosis (CF) patients. Ceftazidime-avibactam is a promising antibiotic combination for treating BCC infections, but its efficacy requires further in vitro evaluation.</div></div><div><h3>Methods</h3><div>This systematic review was conducted following the PRISMA guidelines to assess the in vitro susceptibility of BCC strains to ceftazidime-avibactam. We systematically searched PubMed, Web of Science, Scopus, and Embase databases. Inclusion criteria required original articles reporting on BCC susceptibility to ceftazidime-avibactam using standard antimicrobial susceptibility testing methods.</div></div><div><h3>Results</h3><div>A total of 9 studies met the inclusion criteria. These studies were conducted between 2010 and 2024, with data from the USA, France, Germany, Belgium, and other countries. The studies used various methods, including agar dilution, broth microdilution, and disc diffusion. The minimum inhibitory concentration (MIC) range for ceftazidime-avibactam was found to vary, with the combination showing significantly improved susceptibility compared to ceftazidime alone.</div></div><div><h3>Conclusion</h3><div>This systematic review demonstrates that ceftazidime-avibactam significantly enhances the susceptibility of BCC strains, supporting its potential as an effective therapeutic option for BCC infections in CF patients. Further clinical studies are needed to confirm these findings and guide treatment strategies.</div></div>","PeriodicalId":38074,"journal":{"name":"New Microbes and New Infections","volume":"66 ","pages":"Article 101601"},"PeriodicalIF":2.9000,"publicationDate":"2025-05-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"New Microbes and New Infections","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S205229752500040X","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"INFECTIOUS DISEASES","Score":null,"Total":0}
引用次数: 0
Abstract
Background
Burkholderia cepacia complex (BCC) is a group of multi-drug resistant (MDR) pathogens that are challenging to treat, especially in cystic fibrosis (CF) patients. Ceftazidime-avibactam is a promising antibiotic combination for treating BCC infections, but its efficacy requires further in vitro evaluation.
Methods
This systematic review was conducted following the PRISMA guidelines to assess the in vitro susceptibility of BCC strains to ceftazidime-avibactam. We systematically searched PubMed, Web of Science, Scopus, and Embase databases. Inclusion criteria required original articles reporting on BCC susceptibility to ceftazidime-avibactam using standard antimicrobial susceptibility testing methods.
Results
A total of 9 studies met the inclusion criteria. These studies were conducted between 2010 and 2024, with data from the USA, France, Germany, Belgium, and other countries. The studies used various methods, including agar dilution, broth microdilution, and disc diffusion. The minimum inhibitory concentration (MIC) range for ceftazidime-avibactam was found to vary, with the combination showing significantly improved susceptibility compared to ceftazidime alone.
Conclusion
This systematic review demonstrates that ceftazidime-avibactam significantly enhances the susceptibility of BCC strains, supporting its potential as an effective therapeutic option for BCC infections in CF patients. Further clinical studies are needed to confirm these findings and guide treatment strategies.
洋葱伯克霍尔德菌复合物(BCC)是一组具有多重耐药(MDR)的病原体,具有挑战性,特别是在囊性纤维化(CF)患者中。头孢他啶-阿维巴坦是一种很有前景的治疗BCC感染的抗生素组合,但其疗效需要进一步的体外评估。方法按照PRISMA指南进行系统评价,评价BCC菌株对头孢他啶-阿维巴坦的体外敏感性。我们系统地检索了PubMed、Web of Science、Scopus和Embase数据库。纳入标准要求使用标准抗菌药敏试验方法报告BCC对头孢他啶-阿维巴坦敏感性的原始文章。结果9项研究符合纳入标准。这些研究是在2010年至2024年间进行的,数据来自美国、法国、德国、比利时和其他国家。研究使用了各种方法,包括琼脂稀释,肉汤微量稀释和光盘扩散。发现头孢他啶-阿维巴坦的最小抑制浓度(MIC)范围不同,与头孢他啶单独使用相比,联合用药的敏感性明显提高。结论本系统综述表明,头孢他啶-阿维巴坦可显著提高BCC菌株的敏感性,支持其作为CF患者BCC感染的有效治疗选择的潜力。需要进一步的临床研究来证实这些发现并指导治疗策略。