Aldardeer Namareq F, Alshreef Maram M, Alharbi Emad A, Aljabri Ahmad K, Aljawadi Mohammad H, Almangour Thamer A, Alobaili Saad, Alarifi Mohammed I, Alomari Awad, Alhammad Abdullah M
Department of Pharmacy Services, King Faisal Specialist Hospital and Research Centre, Jeddah, Saudi Arabia.
Department of Pharmacy Services, Prince Sultan Military Medical City, Riyadh, Saudi Arabia.
Open Forum Infect Dis. 2024 Feb 1;11(3):ofae059. doi: 10.1093/ofid/ofae059. eCollection 2024 Mar.
Acute kidney injury (AKI) is a common complication of sepsis, contributing to an increased mortality rate. However, some studies have demonstrated that renal function improves in sepsis patients with AKI within 48 hours, raising questions about the necessity for early antibiotic adjustment. This study evaluates the association between the timing of antipseudomonal β-lactam dose adjustment and the outcomes of critically ill sepsis patients with AKI.
A prospective, multicenter observational study of critically ill patients aged ≥18 years admitted to the intensive care unit with sepsis and AKI and started on antipseudomonal β-lactam therapy. After the initial dose, eligible patients were grouped as early β-lactam antibiotic (E-BLA) or late β-lactam antibiotic (L-BLA) dose adjustments based on the administration of subsequent renally adjusted doses within 24 hours and after 24 hours of sepsis recognition, respectively. The main outcome of interest was in-hospital mortality.
Among 1185 patients screened, 224 (mean age, 62.7 ± 16.8 years; 62% were male) met inclusion criteria. Eighty-four and 140 patients were included in the E-BLA and L-BLA groups, respectively. Approximately half of the cohort presented with AKI stage II, and piperacillin-tazobactam was prescribed as initial empirical therapy in more than 50% of the cohort. In the multivariable Cox proportional hazards model, L-BLA was associated with a significant reduction in in-hospital mortality compared to E-BLA (hazard ratio, 0.588 [95% confidence interval, .355-.974]).
In sepsis patients with AKI, L-BLA was associated with in-hospital mortality benefits.
急性肾损伤(AKI)是脓毒症的常见并发症,会导致死亡率上升。然而,一些研究表明,脓毒症合并AKI的患者在48小时内肾功能会有所改善,这引发了关于早期调整抗生素必要性的疑问。本研究评估了抗假单胞菌β-内酰胺类药物剂量调整时机与脓毒症合并AKI的重症患者预后之间的关联。
一项前瞻性、多中心观察性研究,研究对象为年龄≥18岁、因脓毒症和AKI入住重症监护病房并开始接受抗假单胞菌β-内酰胺类治疗的重症患者。初始剂量后,符合条件的患者根据分别在脓毒症确诊后24小时内和24小时后给予经肾脏调整的后续剂量,分为早期β-内酰胺类抗生素(E-BLA)组或晚期β-内酰胺类抗生素(L-BLA)剂量调整组。主要观察指标为住院死亡率。
在1185例筛查患者中,224例(平均年龄62.7±16.8岁;62%为男性)符合纳入标准。E-BLA组和L-BLA组分别纳入84例和140例患者。大约一半的队列患者为AKI II期,超过50%的队列患者初始经验性治疗使用哌拉西林-他唑巴坦。在多变量Cox比例风险模型中,与E-BLA相比,L-BLA与住院死亡率显著降低相关(风险比,0.588[95%置信区间,0.355 - 0.974])。
在脓毒症合并AKI的患者中,L-BLA与住院死亡率降低相关。