Cesar Copaja-Corzo, Susy Bazán-Ruiz, Andre Fuentes-Yufra, Marlies Pizarro-Perea, Marco Montiel-González, Giancarlo Pérez-Lazo
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Ceftazidime-avibactam (CAZ-AVI) has emerged as a therapeutic alternative against these infections; however, its efficacy in immunocompromised patients remains unclear.</p><p><strong>Objective: </strong>To determine the impact of ceftazidime-avibactam on mortality due to BSI caused by CPE in patients with acute leukemia.</p><p><strong>Design: </strong>A retrospective cohort study was conducted at the Hospital Nacional Edgardo Rebagliati Martins in Lima, Peru.</p><p><strong>Methods: </strong>We included patients diagnosed with acute leukemia who developed BSI due to CPE during their hospital stays. Mortality was assessed for up to 30 days after BSI onset.</p><p><strong>Results: </strong>We evaluated 41 patients with a median age of 51 years; 56.1% had acute myeloid leukemia and 43.9% had acute lymphoblastic leukemia. Mortality at 30 days occurred in 60.9% of patients. The most frequent type of chemotherapy administered was induction (51.2%). Empiric antibiotic therapy with meropenem was administered to 97.6% of the patients, and ceftazidime-avibactam was prescribed as a targeted therapy to 48.8%. In the multivariate Cox regression model, the prescription of ceftazidime-avibactam reduced the risk of death (adjusted hazard ratio, 0.29; 95% CI: 0.09-0.92; <i>p</i> = 0.012) compared with those who received other antibiotic therapies, such as colistin.</p><p><strong>Conclusion: </strong>In patients with acute leukemia who developed bloodstream infections due to CPE during hospitalization, the prescription of ceftazidime-avibactam reduced 30-day mortality risk.</p>","PeriodicalId":46154,"journal":{"name":"Therapeutic Advances in Infectious Disease","volume":"12 ","pages":"20499361251362955"},"PeriodicalIF":3.8000,"publicationDate":"2025-08-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12357988/pdf/","citationCount":"0","resultStr":"{\"title\":\"Impact of ceftazidime-avibactam on mortality in bloodstream infections: a cohort study in patients with acute leukemia.\",\"authors\":\"Cesar Copaja-Corzo, Susy Bazán-Ruiz, Andre Fuentes-Yufra, Marlies Pizarro-Perea, Marco Montiel-González, Giancarlo Pérez-Lazo\",\"doi\":\"10.1177/20499361251362955\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>Bloodstream infections (BSI) caused by carbapenemase-producing <i>Enterobacterales</i> (CPE) represent a significant threat to patients with acute leukemia due to their high mortality. Ceftazidime-avibactam (CAZ-AVI) has emerged as a therapeutic alternative against these infections; however, its efficacy in immunocompromised patients remains unclear.</p><p><strong>Objective: </strong>To determine the impact of ceftazidime-avibactam on mortality due to BSI caused by CPE in patients with acute leukemia.</p><p><strong>Design: </strong>A retrospective cohort study was conducted at the Hospital Nacional Edgardo Rebagliati Martins in Lima, Peru.</p><p><strong>Methods: </strong>We included patients diagnosed with acute leukemia who developed BSI due to CPE during their hospital stays. Mortality was assessed for up to 30 days after BSI onset.</p><p><strong>Results: </strong>We evaluated 41 patients with a median age of 51 years; 56.1% had acute myeloid leukemia and 43.9% had acute lymphoblastic leukemia. Mortality at 30 days occurred in 60.9% of patients. The most frequent type of chemotherapy administered was induction (51.2%). 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引用次数: 0
摘要
背景:产碳青霉烯酶肠杆菌(CPE)引起的血流感染(BSI)由于其高死亡率对急性白血病患者构成重大威胁。头孢他啶-阿维巴坦(CAZ-AVI)已成为治疗这些感染的替代方案;然而,其对免疫功能低下患者的疗效尚不清楚。目的:探讨头孢他啶-阿维巴坦对急性白血病CPE致BSI死亡率的影响。设计:在秘鲁利马的Edgardo Rebagliati Martins国立医院进行了一项回顾性队列研究。方法:我们纳入了诊断为急性白血病并在住院期间因CPE发生BSI的患者。在BSI发病后30天内评估死亡率。结果:我们评估了41例患者,中位年龄51岁;56.1%为急性髓性白血病,43.9%为急性淋巴细胞白血病。30天死亡率为60.9%。最常见的化疗类型是诱导化疗(51.2%)。97.6%的患者经经验使用美罗培南抗生素治疗,48.8%的患者使用头孢他啶-阿维巴坦作为靶向治疗。在多变量Cox回归模型中,与接受粘菌素等其他抗生素治疗的患者相比,头孢他啶-阿维巴坦处方降低了死亡风险(校正风险比为0.29;95% CI: 0.09-0.92; p = 0.012)。结论:急性白血病患者住院期间因CPE发生血流感染,头孢他啶-阿维巴坦处方可降低30天死亡风险。
Impact of ceftazidime-avibactam on mortality in bloodstream infections: a cohort study in patients with acute leukemia.
Background: Bloodstream infections (BSI) caused by carbapenemase-producing Enterobacterales (CPE) represent a significant threat to patients with acute leukemia due to their high mortality. Ceftazidime-avibactam (CAZ-AVI) has emerged as a therapeutic alternative against these infections; however, its efficacy in immunocompromised patients remains unclear.
Objective: To determine the impact of ceftazidime-avibactam on mortality due to BSI caused by CPE in patients with acute leukemia.
Design: A retrospective cohort study was conducted at the Hospital Nacional Edgardo Rebagliati Martins in Lima, Peru.
Methods: We included patients diagnosed with acute leukemia who developed BSI due to CPE during their hospital stays. Mortality was assessed for up to 30 days after BSI onset.
Results: We evaluated 41 patients with a median age of 51 years; 56.1% had acute myeloid leukemia and 43.9% had acute lymphoblastic leukemia. Mortality at 30 days occurred in 60.9% of patients. The most frequent type of chemotherapy administered was induction (51.2%). Empiric antibiotic therapy with meropenem was administered to 97.6% of the patients, and ceftazidime-avibactam was prescribed as a targeted therapy to 48.8%. In the multivariate Cox regression model, the prescription of ceftazidime-avibactam reduced the risk of death (adjusted hazard ratio, 0.29; 95% CI: 0.09-0.92; p = 0.012) compared with those who received other antibiotic therapies, such as colistin.
Conclusion: In patients with acute leukemia who developed bloodstream infections due to CPE during hospitalization, the prescription of ceftazidime-avibactam reduced 30-day mortality risk.