Saeed Muhammad, Rasheed Farhan, Rasool Muhammad Hidayat, Hayat Sumreen, Khurshid Mohsin
Institute of Microbiology Government College University Faisalabad, Faisalabad, Pakistan.
Allama Iqbal Medical College and Jinnah Hospital, Lahore, Pakistan.
Transbound Emerg Dis. 2024 Aug 30;2024:3352135. doi: 10.1155/2024/3352135. eCollection 2024.
Ventilator-associated pneumonia (VAP) represents an important nosocomial infection, frequently encountered in intensive care unit (ICU) settings which results in prolonged hospitals stays. The nosocomial infections caused by complex (BCC) bacteria pose a significant challenge in healthcare settings owing to their intrinsic resistance to many antibiotics. This study investigates the antimicrobial susceptibility patterns and mechanisms of carbapenem resistance among BCC bacteria from VAP patients and the ventilator tubing. The blood and respiratory specimens from patients diagnosed with VAP were collected. In addition, the ventilators were also screened for the presence of BCC bacteria. The susceptibility profiling of BCC isolates was performed against the various antimicrobial agents, and screening for acquired beta-lactamase enzymes was conducted by polymerase chain reaction. Out of the total 134 patients with BCC-associated VAP, , , and was 68.7% ( = 92), 18.7% ( = 25), and 12.7% ( = 17). Overall, the BCC isolates showed varying susceptibility to different antibiotics: 76.9% were susceptible to chloramphenicol, 76.1% to minocycline, 69.4% to meropenem, 60.4% to ceftazidime, 51.5% to trimethoprim-sulfamethoxazole, and 50% to levofloxacin. Resistance to ceftazidime (51/92, 55.4%) and meropenem (36/92, 39.1%) was exclusively observed in isolates, and all isolates of and were found to be susceptible to both beta-lactam drugs. Among the 134 clinical isolates, 15 were found to harbor the variants, that is, and . All carbapenem-resistant isolates from the ventilator tubing were identified as and were found to harbor either the or the variants. The observed increase in resistance and the emergence of acquired beta-lactamases among BCC isolates highlight a concerning trend that could potentially lead to serious outbreaks.
呼吸机相关性肺炎(VAP)是一种重要的医院感染,在重症监护病房(ICU)环境中经常出现,会导致住院时间延长。由复杂(BCC)细菌引起的医院感染因其对多种抗生素的固有耐药性,在医疗环境中构成了重大挑战。本研究调查了VAP患者和呼吸机管道中BCC细菌的抗菌药敏模式及碳青霉烯耐药机制。收集了诊断为VAP患者的血液和呼吸道标本。此外,还对呼吸机进行了BCC细菌检测。对BCC分离株进行了针对各种抗菌药物的药敏分析,并通过聚合酶链反应进行了获得性β-内酰胺酶的检测。在总共134例与BCC相关的VAP患者中,[具体数据缺失]分别为68.7%(n = 92)、18.7%(n = 25)和12.7%(n = 17)。总体而言,BCC分离株对不同抗生素表现出不同的敏感性:76.9%对氯霉素敏感,76.1%对米诺环素敏感,69.4%对美罗培南敏感,60.4%对头孢他啶敏感,51.5%对甲氧苄啶-磺胺甲恶唑敏感,50%对左氧氟沙星敏感。仅在[具体细菌种类缺失]分离株中观察到对头孢他啶(51/92,55.4%)和美罗培南(36/92,39.1%)的耐药性,并且发现所有[具体细菌种类缺失]和[具体细菌种类缺失]分离株对两种β-内酰胺类药物均敏感。在134株临床分离株中,发现15株携带[具体变体缺失]变体,即[具体变体缺失]和[具体变体缺失]。从呼吸机管道中分离出的所有耐碳青霉烯分离株均被鉴定为[具体细菌种类缺失],并发现携带[具体变体缺失]或[具体变体缺失]变体。观察到的BCC分离株耐药性增加和获得性β-内酰胺酶的出现凸显了一个令人担忧的趋势,这可能会导致严重的疫情爆发。