Richter Daniel Christoph, Dietrich Maximilian, Lalev Lazar Detelinov, Schmitt Felix C F, Fiedler Mascha Onida, Bruckner Thomas, Stoerzinger Dominic, Chiriac Ute, Klein Sabrina, Hackert Thilo, Brenner Thorsten, Brinkmann Alexander, Weigand Markus A
Department of Anesthesiology, Heidelberg University Hospital, Im Neuenheimer Feld 420, 69120 Heidelberg, Germany.
Institute of Medical Biometry & Biostatistics, Im Neuenheimer Feld 130.3, 69120 Heidelberg, Germany.
Antibiotics (Basel). 2021 Jun 8;10(6):687. doi: 10.3390/antibiotics10060687.
Septic shock substantially alters the pharmacokinetic properties of β-lactams with a subsequently high risk of insufficiently low serum concentrations and treatment failure. Considering their pharmacokinetic (PK)/pharmacodynamic (PD) index, prolonged infusions (PI) of β-lactams extend the time that the unbound fraction of the drug remains above the minimal inhibitory concentration MIC (t ) and may improve patient survival. The present study is a monocentric, retrospective before-and-after analysis of septic shock patients treated with β-lactams. Patients of the years 2015-2017 received intermittent bolus application whereas patients of 2017-2020 received PI of β-lactams. The primary outcome was mortality at day 30 and 90 after diagnosis of septic shock. Mortality rates in the PI group were significantly lower on day 30 (PI: 41%, = 119/290 vs. IB: 54.8%, = 68/114; = 0.0097) and day 90 (PI: 47.9%, = 139/290 vs. IB: 62.9%, = 78/124; = 0.005). After propensity-score matching, 30- and 90-day mortality remained lower for the PI group (-10%, = 0.14). PI was further associated with a reduction in the duration of invasive ventilation and a stronger decrease in SOFA scores within a 14 day-observation period. PI of β-lactams was associated with a significant reduction of mortality in patients with septic shock and may have beneficial effects on invasive ventilation and recovery from sepsis-related organ failure.
脓毒性休克会显著改变β-内酰胺类药物的药代动力学特性,进而导致血清浓度过低和治疗失败的风险增加。考虑到其药代动力学(PK)/药效学(PD)指标,β-内酰胺类药物的延长输注(PI)可延长药物游离部分浓度保持在最低抑菌浓度(MIC)以上的时间(t),并可能提高患者生存率。本研究是一项针对接受β-内酰胺类药物治疗的脓毒性休克患者的单中心回顾性前后对照分析。2015年至2017年的患者接受间歇性推注给药,而2017年至2020年的患者接受β-内酰胺类药物的延长输注。主要结局是脓毒性休克诊断后第30天和第90天的死亡率。延长输注组在第30天(PI组:41%,n = 119/290;间歇性推注组:54.8%,n = 68/114;P = 0.0097)和第90天(PI组:47.9%,n = 139/290;间歇性推注组:62.9%,n = 78/124;P = 0.005)的死亡率显著更低。在倾向评分匹配后,延长输注组的30天和90天死亡率仍然更低(降低10%,P = 0.14)。延长输注还与有创通气时间缩短以及在14天观察期内序贯器官衰竭评估(SOFA)评分更显著降低相关。β-内酰胺类药物的延长输注与脓毒性休克患者死亡率的显著降低相关,并且可能对有创通气以及从脓毒症相关器官衰竭中恢复有有益影响。