治疗尿路外耐药头孢曲松肠杆菌的非碳青霉烯类疗法的疗效

Ethan Rausch, K. Alby, William Wilson
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摘要

摘要 目的:确定非碳青霉烯类抗生素与碳青霉烯类抗生素在治疗由头孢曲松耐药的泌尿道外感染引起的成人感染中的安全性。设计:对2018年1月至2021年10月期间分离到的有记录的由产扩展谱β-内酰胺酶(ESBL)生物引起感染的成人患者进行回顾性队列研究。地点一家学术性三级医疗中心。患者:有记录的由泌尿道外产 ESBL 菌引起感染的成人患者。治疗方法主要结果是治疗失败的复合结果,定义为 30 天死亡率、30 天再入院率、微生物复发和/或需要更换抗生素的临床恶化。次要结果包括主要复合成分的区分和抗生素治疗后艰难梭菌感染(CDI)。研究结果本研究共纳入 130 名患者。感染的主要来源是血流(67.7%)和大肠埃希菌(81.5%)。总体而言,101 名患者接受了碳青霉烯类疗法,29 名患者接受了非碳青霉烯类疗法 (NCT)。NCT 主要包括氟喹诺酮类药物(29 例中有 18 例),其次是头孢吡肟类(29 例中有 7 例)。接受 NCT 治疗的患者住院时间较短(中位数为 7 天 vs 9 天),出院时更多使用抗生素(79.3% vs 50.5%)。我们没有发现碳青霉烯类疗法(23.8%)与非碳青霉烯类疗法(24.2%;P = .967)治疗失败这一主要综合结果有明显差异。次要结果包括:与碳青霉烯类药物组相比,非碳青霉烯类药物组的 30 天死亡率更高:29例中有4例(13.8%)死亡,101例中有4例(3.9%)死亡。我们没有发现 CDI 发病率的差异。结论非碳青霉烯类疗法可能对某些由产ESBL菌引起感染的患者有一定作用。
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Efficacy of noncarbapenem therapy for the treatment of ceftriaxone-resistant Enterobacterales outside the urinary tract
Abstract Objective: To determine the safety of noncarbapenem versus carbapenem antibiotics for treatment of adults with documented infection caused by ceftriaxone-resistant infections outside the urinary tract. Design: Retrospective cohort of adult patients with a documented infection caused by an extended-spectrum β-lactamase (ESBL)–producing organism isolated between January 2018 and October 2021. Setting: An academic tertiary-care center. Patients: Adult patients with a documented infection caused by an ESBL-producing organism outside the urinary tract. Methods: The primary outcome was a composite of treatment failure defined as 30-day mortality, 30-day readmission, microbiological recurrence, and/or clinical worsening requiring antibiotic change. Secondary outcomes included differentiation of primary composite components and postantibiotic Clostridioides difficile infection (CDI). Results: This study included 130 patients. The primary source of infections were bloodstream (67.7%) and caused by Escherichia coli (81.5%). Overall, 101 patients received carbapenem therapy and 29 received noncarbapenem therapy (NCT). NCT was comprised of mainly fluoroquinolones (18 of 29) followed by cefepime (7 of 29). Patients receiving NCT had shorter hospital stays (median, 7 days vs 9 days) and were more often discharged on antibiotics (79.3% vs 50.5%). We did not detect a significant difference in the primary composite outcome of treatment failure for carbapenem (23.8%) versus noncarbapenem treatment (24.2%; P = .967). Secondary outcomes included a numerically higher 30-day mortality rate in the noncarbapenem group compared to the carbapenem group: 4 (13.8%) of 29 versus 4 (3.9%) of 101. We did not detect a difference in rates of CDI. Conclusion: Noncarbapenem therapy may play a role for certain patients with infections caused by ESBL-producing organisms.
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