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多黏菌素 B 直接血液灌流治疗血管加压素依赖性脓毒性休克患者外周灌注的改变。

Modifications of peripheral perfusion in patients with vasopressor-dependent septic shock treated with polymyxin B-direct hemoperfusion.

机构信息

Department of Anesthesiology and Intensive Care Medicine, Nagasaki University Graduate School of Biomedical Sciences, 1-7-1 Sakamoto, Nagasaki, 852-8501, Japan.

Department of Anesthesiology, Nagasaki Harbor Medical Center, 6-39 Shinchi, Nagasaki, 850-8555, Japan.

出版信息

Sci Rep. 2023 May 5;13(1):7295. doi: 10.1038/s41598-023-34084-0.

DOI:10.1038/s41598-023-34084-0
PMID:37147345
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10163011/
Abstract

Abnormal peripheral perfusion (PP) worsens the prognosis of patients with septic shock. Polymyxin B-direct hemoperfusion (PMX-DHP) increases blood pressure and reduces vasopressor doses. However, the modification of PP following administration of PMX-DHP in patients with vasopressor-dependent septic shock have not yet been elucidated. A retrospective exploratory observational study was conducted in patients with septic shock treated with PMX-DHP. Pulse-amplitude index (PAI), vasoactive inotropic score (VIS), and cumulative fluid balance data were extracted at PMX-DHP initiation (T0) and after 24 (T24) and 48 (T48) h. Changes in these data were analyzed in all patients and two subgroups (abnormal PP [PAI < 1] and normal PP [PAI ≥ 1]) based on the PAI at PMX-DHP initiation. Overall, 122 patients (abnormal PP group, n = 67; normal PP group, n = 55) were evaluated. Overall and in the abnormal PP group, PAI increased significantly at T24 and T48 compared with that at T0, with a significant decrease in VIS. Cumulative 24-h fluid balance after PMX-DHP initiation was significantly higher in the abnormal PP group. PMX-DHP may be an effective intervention to improve PP in patients with abnormal PP; however, caution should be exercised as fluid requirements may differ from that of patients with normal PP.

摘要

异常的外周灌注 (PP) 会使脓毒性休克患者的预后恶化。多黏菌素 B 直接血液灌流 (PMX-DHP) 可升高血压并减少血管加压药剂量。然而,在依赖血管加压药的脓毒性休克患者中,PMX-DHP 给药后 PP 的变化尚未阐明。本回顾性探索性观察性研究纳入了接受 PMX-DHP 治疗的脓毒性休克患者。在 PMX-DHP 起始时 (T0) 以及 24 小时 (T24) 和 48 小时 (T48) 时提取了脉冲幅度指数 (PAI)、血管活性正性肌力评分 (VIS) 和累积液体平衡数据。根据 PMX-DHP 起始时的 PAI,分析了所有患者和两个亚组 (异常 PP [PAI<1] 和正常 PP [PAI≥1]) 中这些数据的变化。总体而言,共评估了 122 例患者 (异常 PP 组,n=67;正常 PP 组,n=55)。总体而言和在异常 PP 组中,与 T0 相比,T24 和 T48 时 PAI 显著增加,VIS 显著降低。PMX-DHP 起始后 24 小时累积液体平衡在异常 PP 组显著更高。PMX-DHP 可能是改善异常 PP 患者 PP 的有效干预措施;但是,应谨慎使用,因为液体需求可能与正常 PP 的患者不同。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f8a/10163011/5ba348bf0566/41598_2023_34084_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f8a/10163011/330604aba6c0/41598_2023_34084_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f8a/10163011/5ba348bf0566/41598_2023_34084_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f8a/10163011/330604aba6c0/41598_2023_34084_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f8a/10163011/5ba348bf0566/41598_2023_34084_Fig2_HTML.jpg

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