Effect of therapeutic plasma exchange on tissue factor and tissue factor pathway inhibitor in septic shock.

IF 8.8 1区 医学 Q1 CRITICAL CARE MEDICINE Critical Care Pub Date : 2024-10-30 DOI:10.1186/s13054-024-05142-4
Klaus Stahl, Georg F Lehner, Pedro David Wendel-Garcia, Benjamin Seeliger, Thorben Pape, Bernhard M W Schmidt, Heiko Schenk, Julius Schmitt, Andrea Sauer, Lennart Wild, Konrad Peukert, Christian Putensen, Christian Bode, Michael Joannidis, Sascha David
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Abstract

Background: Coagulopathy is part of the pathological host response to infection in sepsis. Higher plasma concentrations of both tissue factor (TF) and tissue factor pathway inhibitor (TFPI) are associated with occurrence of disseminated intravascular coagulation (DIC), multi-organ dysfunction and increased mortality in patients with sepsis. Currently no treatment approaches specifically targeting this axis are available. We hypothesize that therapeutic plasma exchange (TPE) might limit this coagulopathy by restoring the balance of plasma proteins.

Methods: This was a pooled post-hoc biobank analysis including 51 patients with early (shock onset < 24 h) and severe (norepinephrine dose > 0.4 μg/kg/min) septic shock, who were either receiving standard of care treatment (SOC, n = 14) or SOC + one single TPE (n = 37). Plasma concentrations of TF and TFPI were measured both at- and 6 h after study inclusion. The effect of TPE on concentrations of TF and TFPI was investigated and compared to SOC patients. Further, baseline TF and TFPI concentrations were used to modulate and predict clinical response to adjunctive TPE, indicated by longitudinal reduction of lactate concentrations over the first 24 h following study inclusion.

Results: TPE led to a significant reduction in circulating concentrations of both TF and TFPI while no difference was observed in the SOC group. Relative change of TF within 6 h was + 14 (-0.8 to + 30.4) % (p = 0.089) in the SOC and -18.3 (-32.6 to -2.2) % (p < 0.001) in the TPE group (between group p < 0.001). Similarly, relative change of TFPI was + 14.4 (-2.3 to + 30.9) % (p = 0.076) in the SOC and -20 (-32.8 to -7.9) % (p < 0.001) in the TPE group (between group p = 0.022). The ratio of TF to TFPI remained unchanged in both SOC and TPE groups. SOC patients exhibited an increase in lactate over the initial 24 h when TF and TFPI concentrations were higher at baseline. In contrast, patients undergoing TPE experienced a sustained longitudinal reduction of lactate concentrations across all levels of baseline TF and TFPI elevations. In a multivariate mixed-effects model, higher baseline TF (p = 0.003) and TFPI (p = 0.053) levels led to greater longitudinal lactate concentration reduction effects in the TPE group.

Conclusions: Adjunctive TPE in septic shock is associated with a significant removal of both TF and TFPI, which may contribute to the early hemodynamic improvement observed in septic shock patients receiving TPE. Higher baseline TF (and TFPI) plasma concentrations were identified as a putative predictor of treatment response that could be useful for predictive enrichment strategies in future clinical trials.

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治疗性血浆置换对脓毒性休克患者组织因子和组织因子通路抑制因子的影响。
背景:凝血病是败血症中宿主对感染的病理反应的一部分。组织因子(TF)和组织因子通路抑制剂(TFPI)的血浆浓度升高与脓毒症患者发生弥散性血管内凝血(DIC)、多器官功能障碍和死亡率升高有关。目前还没有专门针对这一轴心的治疗方法。我们假设治疗性血浆置换(TPE)可通过恢复血浆蛋白的平衡来限制这种凝血病变:这是一项集中的事后生物库分析,包括 51 名早期(休克发生时为 0.4 μg/kg/min)脓毒性休克患者,他们要么接受标准护理治疗(SOC,n = 14),要么接受 SOC + 单次 TPE(n = 37)。在纳入研究时和研究结束后 6 小时分别测量血浆中 TF 和 TFPI 的浓度。研究了 TPE 对 TF 和 TFPI 浓度的影响,并与 SOC 患者进行了比较。此外,基线 TF 和 TFPI 浓度被用于调节和预测辅助 TPE 的临床反应,在纳入研究后的最初 24 小时内,乳酸浓度的纵向下降表明了这一点:结果:TPE 可显著降低 TF 和 TFPI 的循环浓度,而 SOC 组则无差异。在 6 小时内,SOC 组 TF 的相对变化为 + 14 (-0.8 to + 30.4) % (p = 0.089),而 SOC 组为 -18.3 (-32.6 to -2.2) % (p 结论:TPE 可显著降低败血症患者的血液循环中 TF 和 TFPI 的浓度:脓毒性休克患者辅助 TPE 可显著降低 TF 和 TFPI,这可能是接受 TPE 治疗的脓毒性休克患者早期血流动力学改善的原因。较高的基线 TF(和 TFPI)血浆浓度被认为是治疗反应的潜在预测因子,可用于未来临床试验中的预测性富集策略。
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来源期刊
Critical Care
Critical Care 医学-危重病医学
CiteScore
20.60
自引率
3.30%
发文量
348
审稿时长
1.5 months
期刊介绍: Critical Care is an esteemed international medical journal that undergoes a rigorous peer-review process to maintain its high quality standards. Its primary objective is to enhance the healthcare services offered to critically ill patients. To achieve this, the journal focuses on gathering, exchanging, disseminating, and endorsing evidence-based information that is highly relevant to intensivists. By doing so, Critical Care seeks to provide a thorough and inclusive examination of the intensive care field.
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