Bavaro Davide Fiore, Belati Alessandra, Diella Lucia, Frallonardo Luisa, Guido Giacomo, Papagni Roberta, Pellegrino Carmen, Brindicci Gaetano, De Gennaro Nicolò, Di Gennaro Francesco, Denicolò Sofia, Ronga Luigi, Mosca Adriana, Pomarico Francesco, Dell'Aera Maria, Stufano Monica, Dalfino Lidia, Grasso Salvatore, Saracino Annalisa
Clinic of Infectious Diseases, Department of Precision and Regenerative Medicine and Ionian Area, University of Bari, Policlinic of Bari, Piazza Giulio Cesare n. 11, 70124 Bari, Italy.
Section of Microbiology and Virology, University of Bari, Policlinic of Bari, Piazza Giulio Cesare n. 11, 70124 Bari, Italy.
J Antimicrob Chemother. 2023 Sep 5;78(9):2175-2184. doi: 10.1093/jac/dkad215.
Optimal β-lactam dosing for the treatment of Gram-negative bacteria bloodstream infections (GNB-BSIs) remains a debated issue. Herein, the efficacy and safety of a loading dose (LD) followed by extended/continuous infusion (EI/CI) versus intermittent bolus (IB) of these drugs for the treatment of GNB-BSIs was evaluated.
This is a retrospective observational study enrolling patients with GNB-BSIs treated with β-lactams from 1 October 2020 to 31 March 2022. The 30 day infection-related mortality rate was assessed with Cox regression, while mortality risk reduction was evaluated by an inverse probability of treatment weighting regression adjustment (IPTW-RA) model.
Overall, 224 patients were enrolled: 140 and 84 in the IB and EI/CI groups, respectively. β-Lactam regimens were chosen according to pathogen antibiogram, clinical judgement and current guidelines. Interestingly, the LD + EI/CI regimen was associated with a significant lower mortality rate (17% versus 32%, P = 0.011). Similarly, β-lactam LD + EI/CI was significantly associated with a reduced risk of mortality at multivariable Cox regression [adjusted HR (aHR) = 0.46; 95%CI = 0.22-0.98; P = 0.046]. Finally, the IPTW-RA (adjusted for multiple covariates) was performed, showing a significant risk reduction in the overall population [-14% (95% CI = -23% to -5%)]; at the subgroup restricted analysis, a significant risk reduction (>15%) was observed in the case of GNB-BSI in severely immunocompromised patients (P = 0.003), for SOFA score > 6 (P = 0.014) and in septic shock (P = 0.011).
The use of LD + EI/CI of β-lactams in patients with a GNB-BSI may be associated with reduced mortality; also in patients with severe presentation of infection or with additional risk factors, such as immunodepression.
治疗革兰氏阴性菌血流感染(GNB-BSIs)时,β-内酰胺类药物的最佳给药方案仍是一个有争议的问题。本文评估了这些药物采用负荷剂量(LD)后延长/持续输注(EI/CI)与间歇推注(IB)治疗GNB-BSIs的疗效和安全性。
这是一项回顾性观察性研究,纳入了2020年10月1日至2022年3月31日期间接受β-内酰胺类药物治疗的GNB-BSIs患者。采用Cox回归评估30天感染相关死亡率,同时通过治疗权重逆概率回归调整(IPTW-RA)模型评估死亡风险降低情况。
总体上,共纳入224例患者:IB组和EI/CI组分别为140例和84例。根据病原体药敏谱、临床判断和现行指南选择β-内酰胺类治疗方案。有趣的是,LD+EI/CI方案的死亡率显著较低(17%对32%,P=0.011)。同样,在多变量Cox回归中,β-内酰胺类LD+EI/CI与死亡风险降低显著相关[调整后风险比(aHR)=0.46;95%置信区间(CI)=0.22-0.98;P=0.046]。最后,进行了IPTW-RA(对多个协变量进行调整),结果显示总体人群的风险显著降低[-14%(95%CI=-23%至-5%)];在亚组受限分析中,在严重免疫功能低下患者的GNB-BSI病例中(P=0.003)、序贯器官衰竭评估(SOFA)评分>6时(P=0.014)以及感染性休克患者中(P=0.011)观察到显著的风险降低(>15%)。
GNB-BSI患者使用β-内酰胺类药物的LD+EI/CI方案可能与死亡率降低相关;在感染严重或有其他风险因素(如免疫抑制)的患者中也是如此。