头孢他啶/阿维巴坦在泰国三级医院的应用经验

Alper Tahmaz, Ayşegül Şeremet Keskin
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摘要

目的:头孢他啶/阿维巴坦治疗耐多药肺炎克雷伯菌的实际经验仍然有限。本回顾性研究旨在评价头孢他啶/阿维巴坦治疗碳青霉烯耐药病原菌感染的危重患者的疗效。方法:回顾性分析2022年1月1日至2022年12月31日期间在我院icu住院3天以上、仅头孢他啶/阿维巴坦敏感性增长并开始头孢他啶/阿维巴坦治疗的患者。38名年龄大于18岁的患者被纳入研究。结果:肺炎是ICU最常见的住院原因,脑血管事件次之,内科疾病次之。从采集培养样品到获得实验室结果的平均时间为4.6±1.46天。培养结果经实验室确认后,患者就诊于感染性疾病专科医师至开始治疗的平均时间为1.7±1.3天。患者接受CAZ-AVI单药治疗(57.9%)或联合治疗(42.1%)的平均时间为10.6±4.63天。52.6%的患者获得临床反应,63.2%的患者获得微生物反应。CAZ-AVI患者90天全因死亡率为60.5% (n=23), 14天感染死亡率为52.17%。18.4%的患者出现了副作用。未出现任何需要停止治疗的副作用。联合治疗和单药治疗患者的临床反应和微生物反应无统计学差异。接受CAZ-AVI单药治疗的患者死亡率显著降低(p<0.05)。结论:我们将低临床成功率归因于药物报销标准导致的治疗开始较晚。因此,我们认为应尽快开始经验性治疗CAZ-AVI。我们认为我们的研究在表明CAZ-AVI治疗应该在经验治疗方面是有价值的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Ceftazidime/avibactam experience in tertiary hospital in Türkiye
Aims: Real-life experience with ceftazidime/avibactam in the treatment of multidrug-resistant Klebsiella pneumoniae is still limited. This retrospective study aims to evaluate the efficacy of ceftazidime/avibactam in the treatment of critically ill patients with infections due to carbapenem-resistant pathogens. Methods: In our study, patients who were hospitalized in the ICUs of our hospital for more than three days between 01-01-2022 and 31-12-2022, who had only ceftazidime/avibactam susceptibility growth and were started on ceftazidime/avibactam treatment were retrospectively analyzed. 38 patients older than 18 years of age were included in the study. Results: Pneumonia was the most common cause of hospitalization in the ICU, followed by cerebrovascular events and internal diseases, respectively. The mean time from taking the culture samples to obtaining the laboratory results was 4.6 ±1.46 days. After the culture result was confirmed by the laboratory, the mean time between the patient's consultation by infection diseases specialist and initiation of treatment was 1.7±1.3 days. Patients received a mean of 10.6 ±4.63 days of CAZ-AVI treatment as monotherapy (57.9%) or combined therapy (42.1). Clinical response was obtained in 52.6% of the patients, and microbiological response was obtained in 63.2% of the patients. The 90-day all-cause mortality rate of patients receiving CAZ-AVI was 60.5% (n=23), and the mortality rate attributed to 14-day infection was 52.17%. Side effects developed in 18.4% of the patients. None of the developed side effects were such as to require discontinuation of treatment. There was no statistical difference in clinical response and microbiological response in patients receiving combination therapy and monotherapy. Mortality was significantly lower in patients receiving CAZ-AVI monotherapy (p<0.05). Conclusion: We attribute our low clinical success to the late initiation of treatment due to drug reimbursement criteria. Therefore, we think that CAZ-AVI treatment should be started empirically and as soon as possible. We think that our study is valuable in terms of showing that CAZ-AVI treatment should be given in empirical treatment.
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