Sherman Elly R, Ta Nha Hue, Branan Trisha N, Patimavirujh Natt, Dickinson Luren Ashton, Bland Christopher M, Smith Susan E
Department of Clinical and Administrative Pharmacy, University of Georgia College of Pharmacy, Athens, GA 30602, USA.
Department of Clinical and Administrative Pharmacy, University of Georgia College of Pharmacy, Savannah, GA 31405, USA.
Antibiotics (Basel). 2024 Sep 26;13(10):921. doi: 10.3390/antibiotics13100921.
: Intravenous fluid shortages have led to fluid-sparing measures such as intravenous push (IVP) administration of antibiotics. This study aimed to compare the safety and efficacy of IVP and intravenous piggyback (IVPB) ceftriaxone in critically ill patients. : Demographics were similar in IVP ( = 201) and IVPB ( = 200) groups. Sequential Organ Failure Assessment (SOFA) score was higher, and sepsis and septic shock were more common in the IVP group. Treatment failure occurred in 37.8% of IVP and 19.5% of IVPB groups ( < 0.001). Hospital mortality was more common with IVP (21.4% vs. 9.5%, < 0.001). Hospital LOS was longer with IVP while intensive care unit (ICU) LOS was similar between the groups. IVP ceftriaxone (OR 2.33, 95% CI 1.43-3.79) and the SOFA score (OR 1.18, 95% CI 1.1-1.27) were associated with treatment failure. : A single-center, retrospective cohort study included adults admitted to an ICU from 2016 to 2021 who received empiric ceftriaxone for ≥72 h. The primary outcome was treatment failure, defined as a composite of inpatient mortality or escalation of antibiotics. Secondary outcomes included length of stay (LOS) and mortality. Chi-squared and independent-sample -tests were used. Treatment failure was evaluated using multivariate logistic regression. : Compared to IVPB, IVP ceftriaxone was associated with higher treatment failure in critically ill patients. Both safety and efficacy should be considered before implementing novel antibiotic administration strategies in practice based primarily on convenience.
静脉输液短缺已导致采取诸如静脉推注(IVP)抗生素等节约液体的措施。本研究旨在比较IVP和静脉滴注(IVPB)头孢曲松在重症患者中的安全性和有效性。:IVP组(n = 201)和IVPB组(n = 200)的人口统计学特征相似。IVP组的序贯器官衰竭评估(SOFA)评分更高,脓毒症和感染性休克更为常见。IVP组治疗失败率为37.8%,IVPB组为19.5%(P < 0.001)。IVP组医院死亡率更高(21.4%对9.5%,P < 0.001)。IVP组住院时间更长,而两组间重症监护病房(ICU)住院时间相似。IVP头孢曲松(比值比2.33,95%置信区间1.43 - 3.79)和SOFA评分(比值比1.18,95%置信区间1.1 - 1.27)与治疗失败相关。:一项单中心回顾性队列研究纳入了2016年至2021年入住ICU且接受经验性头孢曲松治疗≥72小时的成年人。主要结局为治疗失败,定义为住院死亡率或抗生素升级的综合情况。次要结局包括住院时间(LOS)和死亡率。采用卡方检验和独立样本t检验。使用多因素逻辑回归评估治疗失败情况。:与IVPB相比,IVP头孢曲松在重症患者中与更高的治疗失败率相关。在主要基于便利性实施新的抗生素给药策略之前,应同时考虑安全性和有效性。