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治疗性血浆置换对感染性休克组织因子和组织因子途径抑制剂的影响。

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

机构信息

Department of Gastroenterology, Hepatology, Infectious Diseases and Endocrinology, Hannover Medical School, Hannover, Germany.

Division of Intensive Care and Emergency Medicine, Medical University Innsbruck, Innsbruck, Austria.

出版信息

Crit Care. 2024 Oct 30;28(1):351. doi: 10.1186/s13054-024-05142-4.

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.

摘要

背景

凝血障碍是脓毒症患者感染后病理性宿主反应的一部分。较高的组织因子 (TF) 和组织因子途径抑制剂 (TFPI) 血浆浓度与弥散性血管内凝血 (DIC)、多器官功能障碍和脓毒症患者死亡率增加有关。目前,尚无专门针对该轴的治疗方法。我们假设治疗性血浆置换 (TPE) 通过恢复血浆蛋白的平衡可能会限制这种凝血障碍。

方法

这是一项包括 51 例早期(休克发作<24 小时)和严重(去甲肾上腺素剂量>0.4μg/kg/min)脓毒性休克患者的队列后生物库分析,这些患者接受标准治疗(SOC,n=14)或 SOC+单次 TPE(n=37)。分别在纳入研究时和 6 小时后测量 TF 和 TFPI 的血浆浓度。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 浓度用于调节和预测辅助 TPE 的临床反应,这表现为纳入研究后 24 小时内乳酸浓度的纵向降低。

结果

TPE 导致 TF 和 TFPI 的循环浓度显著降低,而 SOC 组无差异。SOC 组中 6 小时内 TF 的相对变化为+14(-0.8 至+30.4)%(p=0.089),TPE 组为-18.3(-32.6 至-2.2)%(p<0.001)(组间 p<0.001)。同样,SOC 组中 TFPI 的相对变化为+14.4(-2.3 至+30.9)%(p=0.076),TPE 组为-20(-32.8 至-7.9)%(p<0.001)(组间 p=0.022)。SOC 和 TPE 组中 TF 与 TFPI 的比值保持不变。SOC 组患者在基线时 TF 和 TFPI 浓度较高时,最初 24 小时内乳酸增加。相比之下,接受 TPE 的患者在所有基线 TF 和 TFPI 升高水平上均经历了持续的乳酸浓度纵向降低。在多变量混合效应模型中,较高的基线 TF(p=0.003)和 TFPI(p=0.053)水平导致 TPE 组乳酸浓度纵向降低效应更大。

结论

脓毒性休克患者接受辅助 TPE 治疗与 TF 和 TFPI 的显著清除有关,这可能有助于接受 TPE 治疗的脓毒性休克患者的早期血流动力学改善。较高的基线 TF(和 TFPI)血浆浓度被确定为治疗反应的潜在预测因子,这可能对未来临床试验中的预测性富集策略有用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca30/11526504/306b50b77502/13054_2024_5142_Fig1_HTML.jpg

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