Hobbs Athena L V, Hemmige Vagish S, Reel Katie L, Jaso Theresa C, Rose Dusten T, Shea Katherine M
Cardinal Health Innovative Delivery Solutions, Stafford, TX, USA.
Department of Medicine, Montefiore Medical Center, Bronx, NY, USA.
Antimicrob Steward Healthc Epidemiol. 2024 Jul 26;4(1):e102. doi: 10.1017/ash.2024.70. eCollection 2024.
The aim of this study was to determine if oral beta-lactam therapy is non-inferior to alternative therapy at discharge following inpatient treatment with an IV cephalosporin for acute pyelonephritis.
Institutional Review Board (IRB)-approved, multicenter, retrospective, non-inferiority cohort (15% non-inferiority margin).
Six hospitals within two healthcare systems.
Hospitalized patients admitted to the medical floor with acute pyelonephritis without urologic abnormalities who received cefazolin or ceftriaxone followed by step-down therapy.
Patients were discharged with either an oral beta-lactam or an oral alternative agent (ie, fluoroquinolone or trimethoprim-sulfamethoxazole) to complete therapy. The primary objective was treatment failure defined as a composite of hospital readmission or an ED visit for a urinary cause within 30 days of discharge of the index hospitalization. Data were extracted manually from the electronic medical record.
A total of 211 patients were included; 122 received an oral beta-lactam and 89 received an oral alternative agent at discharge. There was no difference in 30-day treatment failure between the two groups (4.9% vs 5.6% for oral beta-lactams vs oral alternatives, respectively. Absolute difference = 0.7%; 95% CI -5.4% to 6.8%; = .82). The median length of hospital stay, number of patients treated with intravenous ceftriaxone, duration of IV therapy, and median duration of oral therapy were no different between groups.
In non-ICU patients admitted for pyelonephritis without urologic abnormalities, oral beta-lactams were non-inferior to oral alternatives for step-down therapy. In finding non-inferiority between the regimens, we show the feasibility of administering oral beta-lactams to complete therapy for acute pyelonephritis.
本研究旨在确定急性肾盂肾炎患者静脉注射头孢菌素住院治疗后出院时口服β-内酰胺类疗法是否不劣于替代疗法。
经机构审查委员会(IRB)批准的多中心回顾性非劣效性队列研究(非劣效性 margin 为 15%)。
两个医疗系统内的六家医院。
因急性肾盂肾炎入住内科病房且无泌尿系统异常、接受头孢唑林或头孢曲松治疗后进行降阶梯治疗的住院患者。
患者出院时接受口服β-内酰胺类药物或口服替代药物(即氟喹诺酮类或甲氧苄啶-磺胺甲恶唑)以完成治疗。主要目标是治疗失败,定义为在首次住院出院后 30 天内因泌尿系统原因再次住院或急诊就诊的综合情况。数据从电子病历中手动提取。
共纳入 211 例患者;122 例出院时接受口服β-内酰胺类药物,89 例接受口服替代药物。两组 30 天治疗失败率无差异(口服β-内酰胺类药物组和口服替代药物组分别为 4.9%和 5.6%。绝对差异 = 0.7%;95%CI -5.4%至 6.8%;P = 0.82)。两组之间的住院中位时长、接受静脉注射头孢曲松治疗的患者数量、静脉治疗时长和口服治疗中位时长无差异。
在因肾盂肾炎入院且无泌尿系统异常的非重症监护病房患者中,口服β-内酰胺类药物在降阶梯治疗方面不劣于口服替代药物。在发现两种治疗方案非劣效的过程中,我们证明了使用口服β-内酰胺类药物完成急性肾盂肾炎治疗的可行性。