跳至主要内容
临床试验/NCT06318689
NCT06318689招募中不适用

In Situ Exploration of Vascular Function in Vasoplegic Shock Following Cardiac Surgery With Cardiopulmonary Bypass

University Hospital, Rouen1 个研究点 分布在 1 个国家目标入组 124 人开始时间: 2024年2月5日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
124
试验地点
1
主要终点
Association between the percentage of brachial artery variation measured by the flow-mediated vasodilation method and the presence of vasoplegic shock at incusion.

研究概览

简要总结

The goal of this observational study is to assess in situ vascular function, glycocalyx and microcirculation in postoperative vasoplegic shock following cardiac surgery with cardiopulmonary bypass.

The main question is to investigate the relationship between NO-dependent vasomotor reserve and the presence of vasoplegic shock following cardiac surgery with cardiopulmonary bypass.

Participants will have two visits, during which a number of non-invasive examinations will be carried out to study glycocalyx, microcirculation and vascular function. Biological and morphological data will be collected up to 3 months after inclusion, as well as information on treatments administered and outcome.

Researchers will compare a group of patients with vasoplegic shock against a group without vasoplegic shock in order to study possible alterations in function in the vasoplegic shock group.

详细描述

Objective : the primary objective of this study is to explore in situ the glycocalyx, the microcirculation and vascular function in postoperative vasoplegic shock following cardiac surgery with CPB. Secondary objectives are to study links between vascular function and damage to the glycocalyx and microcirculation and patient prognosis, in particular their impact on fluid balance.

Method :

Constitution of a single-centre prospective cohort study of 124 patients. Patients hospitalised in the cardiac intensive care unit after cardiac surgery with CPB will be consecutively included from 4 to 24 hours after surgery: 62 patients with vasoplegic shock (noradrenaline > 0.05µg/kg/min for at least 4 hours and after correction of any hypovolaemia), 62 patients without vasoplegic shock.

Endothelial function will be assessed using the flow-mediated dilation (FMD) method to test brachial artery vasodilation mediated by nitric oxide (NO) after induced ischemia. Microcirculation and glycocalyx will be evaluated using GlycoCheck, providing several measurements of microcirculation and glycocalyx using Sidestream Dark Field technology (mucosal illumination by a green LED and continuous x20 magnification video recording at the sublingual mucosa level). Various endothelial and inflammatory markers will also be measured (VCAM-1, syndecan, endothelin, interleukin-6).

Each patient will be assessed at inclusion and 48 hours using GlycoCheck, FMD, and endothelial measurements, then followed through their medical records for 90 days, where a follow-up call will be conducted to assess outcomes. Collected information will include routine care data (morphological data, vital signs, laboratory tests, fluid balance, scores, treatments, surgical data).

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
18 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients aged between 18 and 80 years old
  • Patient undergoing cardiac surgery with cardiopulmonary bypass
  • Hospitalised in a cardiac surgical unit, between 4 and 24 hours after the end of cardiopulmonary bypass, after volemic optimisation

排除标准

  • Sepsis at inclusion
  • Cardiac transplant
  • Circulatory assistance
  • Known alteration of the microcirculation
  • Any condition contraindicating measurement via Glycocheck or flux mediated dilatation measurement
  • New surgery within 48 hours of the operation
  • Person deprived of liberty by an administrative or judicial decision or person placed under legal protection / sub-guardianship or guardianship
  • Patient refusal

结局指标

主要结局

Association between the percentage of brachial artery variation measured by the flow-mediated vasodilation method and the presence of vasoplegic shock at incusion.

时间窗: At inclusion

Association between the percentage of brachial artery variation measured by the flow-mediated vasodilation method and the presence of vasoplegic shock.

次要结局

  • Endothelial function markers (Endothelin-1, pg/mL) with the presence of vasoplegic shock(At inclusion and at 48 hours)
  • Total density (number of 10 micron long vessel segments with diameter of 4 to 25 microns per tissue surface area /mm^2) obtained from Glycocheck with the presence of vasoplegic shock(At inclusion and at 48 hours)
  • Endothelial function markers (interleukin-6, pg/mL) with the presence of vasoplegic shock(At inclusion and at 48 hours)
  • Association between the percentage of brachial artery variation measured by the flow-mediated vasodilation method and the presence of vasoplegic shock at 48 hours.(At 48 hours)
  • Pefused boundary region (PBR, µm) obtained from Glycocheck with the presence of vasoplegic shock.(At inclusion and at 48 hours)
  • Microvascular blood flow (10^3 microns^3 / sec / mm^2) obtained from Glycocheck with the presence of vasoplegic shock(At inclusion and at 48 hours)
  • Endothelial function markers (syndecan-1, pg/mL) with the presence of vasoplegic shock(At inclusion and at 48 hours)
  • Multivariate analysis explaining the occurrence of vasoplegic shock.(At inclusion and at 48 hours)
  • Endothelial function markers (VCAM-1, pg/mL) with the presence of vasoplegic shock(At inclusion and at 48 hours)
  • Multivariate analysis explaining the occurrence of an altered perfused boundary region (µm).(At inclusion and at 48 hours)

研究者

发起方
University Hospital, Rouen
申办方类型
Other
责任方
Sponsor

研究点 (1)

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