Distribution and Antimicrobial Resistance of Complicated Intraabdominal Infection Pathogens in Two Tertiary Hospitals in Egypt.

IF 1.4 4区 医学 Q4 INFECTIOUS DISEASES Surgical infections Pub Date : 2024-08-22 DOI:10.1089/sur.2023.375
Ihab Saad Hussein, Arwa R El-Manakhly, Ahmed Saeed Salama, Adel Alaa El-Din Habib, Tarek Marei, Jehan Ali Elkholy, May S Soliman, Amani A El-Kholy
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Abstract

Background: Management of complicated intraabdominal infections (cIAIs) requires containment of the source and appropriate initial antimicrobial therapy. Identifying the local data is important to guide the empirical selection of antimicrobial therapy. In this study, we aimed to describe the pathogen distribution and antimicrobial resistance of cIAI. Methods: In two major tertiary care hospitals in Egypt, we enrolled patients who met the case definition of cIAI from October 2022 to September 2023. Blood cultures were performed using the BACTAlert system (BioMerieux, Marcy l'Etoile, France). A culture of aspirated fluid, resected material, or debridement of the infection site was performed. Identification of pathogens and antimicrobial susceptibility testing were conducted by the VITEK-2 system (BioMerieux, Marcy l'Etoile, France). Gram-negative resistance genes were identified by PCR and confirmed by whole bacterial genome sequencing using the Nextera XT DNA Library Preparation Kit and sequencing with the MiSeq Reagent Kit 600 v3 (Illumina, USA) on the Illumina MiSeq. Results: We enrolled 423 patients, 275 (65.01%) males. The median age was 61.35 (range 25-72 years). We studied 452 recovered bacterial isolates. Gram-negative bacteria were the vast majority, dominated by E. coli, followed by Klebsiella pneumoniae, Pseudomonas aeruginosa, Acinetobacter baumannii, and Proteus mirabilis (33.6%, 30.5%, 13.7%, 13%, and 5.4%, respectively). High rates of resistance were detected to third- and fourth-generation cephalosporins and fluoroquinolones. No resistance was detected to colistin. Resistance to amikacin and tigecycline was low among all isolates. Resistance to meropenem and ceftazidime/avibactam was moderate. ESBL genes were common in E. coli and K. pneumoniae. CTX-M15 gene was the most frequent. Among Enterobacterales, blaOXA-48 and blaNDM were the most prevalent carbapenemase genes. Pseudomonas aeruginosa isolates harbored a wide variety of carbapenemase genes (OXA, NDM, VIM, SIM, GIM, SPM, IMP, AIM), dominated by metallo-beta-lactamases. In 20.6% of isolates, we identified two or more resistance genes. Conclusion: High resistance rates were detected to third- and fourth-generation cephalosporins and fluoroquinolones. Amikacin and tigecyclines were the most active antimicrobials. Our data call for urgent implementation of antimicrobial stewardship programs and reinforcement of infection control.

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埃及两家三级医院并发腹腔感染病原体的分布和抗菌药耐药性。
背景:处理复杂腹腔内感染 (cIAI) 需要控制感染源和适当的初始抗菌治疗。确定当地数据对于指导抗菌治疗的经验性选择非常重要。本研究旨在描述腹腔感染的病原体分布和抗菌药物耐药性。方法:2022 年 10 月至 2023 年 9 月期间,我们在埃及的两家大型三级医院招募了符合 cIAI 病例定义的患者。使用 BACTAlert 系统(BioMerieux,法国 Marcy l'Etoile)进行血液培养。对抽出的液体、切除物或感染部位的清创物进行培养。病原体鉴定和抗菌药敏感性测试由 VITEK-2 系统(法国马西埃托尔生物梅里埃公司)进行。通过 PCR 鉴定革兰氏阴性菌耐药基因,并使用 Nextera XT DNA 文库制备试剂盒进行细菌全基因组测序和使用 MiSeq Reagent Kit 600 v3(Illumina,美国)在 Illumina MiSeq 上进行测序。结果:我们共招募了 423 名患者,其中男性 275 名(65.01%)。中位年龄为 61.35 岁(25-72 岁)。我们研究了 452 个回收的细菌分离物。革兰氏阴性菌占绝大多数,以大肠杆菌为主,其次是肺炎克雷伯菌、铜绿假单胞菌、鲍曼不动杆菌和奇异变形杆菌(分别占 33.6%、30.5%、13.7%、13% 和 5.4%)。第三代和第四代头孢菌素以及氟喹诺酮类药物的耐药率较高。没有发现对可乐定的耐药性。所有分离菌株对阿米卡星和替加环素的耐药性较低。对美罗培南和头孢他啶/阿维巴坦的耐药性为中等。ESBL基因在大肠杆菌和肺炎双球菌中很常见。CTX-M15基因最为常见。在肠杆菌中,blaOXA-48 和 blaNDM 是最常见的碳青霉烯酶基因。铜绿假单胞菌分离物携带多种碳青霉烯酶基因(OXA、NDM、VIM、SIM、GIM、SPM、IMP、AIM),以金属-β-内酰胺酶为主。在 20.6% 的分离株中,我们发现了两种或两种以上的耐药基因。结论第三代和第四代头孢菌素及氟喹诺酮类药物的耐药率较高。阿米卡星和替加环素是最活跃的抗菌药物。我们的数据要求紧急实施抗菌药物管理计划并加强感染控制。
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来源期刊
Surgical infections
Surgical infections INFECTIOUS DISEASES-SURGERY
CiteScore
3.80
自引率
5.00%
发文量
127
审稿时长
6-12 weeks
期刊介绍: Surgical Infections provides comprehensive and authoritative information on the biology, prevention, and management of post-operative infections. Original articles cover the latest advancements, new therapeutic management strategies, and translational research that is being applied to improve clinical outcomes and successfully treat post-operative infections. Surgical Infections coverage includes: -Peritonitis and intra-abdominal infections- Surgical site infections- Pneumonia and other nosocomial infections- Cellular and humoral immunity- Biology of the host response- Organ dysfunction syndromes- Antibiotic use- Resistant and opportunistic pathogens- Epidemiology and prevention- The operating room environment- Diagnostic studies
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