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危重症患者的组织灌注与液体反应性评估。一项使用IKORUS膀胱上皮体积描记装置的可行性初步研究。

Tissue perfusion and fluid responsiveness assessment in critically ill patients. A feasibility pilot study using the IKORUS urothelial plethysmography device.

作者信息

Wong Adrian, McDonald Rory, Roslan Nurul Liana, Bramham Kate, Hutchings Sam

机构信息

Department of Emergency Medicine, Kuala Lumpur MALAYSIA.

School of Life Course and Population Sciences and School of Immunology and Microbial Science Faculty of Life Sciences and Medicine, King's College London.

出版信息

Shock. 2025 Jul 25. doi: 10.1097/SHK.0000000000002672.

DOI:10.1097/SHK.0000000000002672
PMID:40729501
Abstract

BACKGROUND

Accurate assessment of tissue perfusion is challenging. Commonly used markers like lactate levels and central venous oxygen saturation are indirect, intermittent, and provide a global picture of circulatory status which may not reflect perfusion at the organ level. The urethral perfusion index (UPi), measured through a specialized urinary catheter, is a novel technique that offers continuous, real-time monitoring of perfusion in a central tissue bed, potentially providing more immediate and targeted clinical information.

OBJECTIVES

  1. To assess the correlation between changes to left ventricular outflow tract velocity time integral (LVOT VTi) and UPi following a fluid challenge.2. To assess the relationship between UPi and other markers of tissue perfusion.

DESIGN

Interventional, feasibility pilot study.

SETTING

Single-centre, study conducted at a tertiary-level institution in the United Kingdom. All patients were mechanically ventilated adults, whom the primary clinical team thought would benefit from a fluid challenge.

INTERVENTION

A fluid challenge (FC) was defined as a 250 ml bolus of crystalloid solution.

MAIN OUTCOME MEASURES

Focused transthoracic echocardiogram measured LVOT VTi and UPi, measured pre- and post-FC.

RESULTS

There were no reported complications associated with device use or insertion. Mean duration of data recorded was 19 hours and the Signal Quality Index of the UPi trace was high (93%). There was a moderate positive correlation between the time matched values of UPi and LVOT VTi (Spearman r = 0.55, p < 0.0001), R2 value of 0.272. However, there was no discernible correlation seen between change in UPi and VTi following fluid (Spearman r = 0.24, p = 0.14). Patients with below-average UPi at baseline had evidence of poorer systemic tissue perfusion, as measured by lactate concentration and capillary refill time, and received more vasoactive drugs.ConclusionUPi may be a marker of tissue perfusion in a diverse group of critically ill patients. With further evaluation it may, therefore, present a future therapeutic target. Although there is some relationship between LVOT VTi and UPi, it is not precise enough to be used as a marker of fluid responsiveness.Trial registration: London Southeast Research and Ethics Committee (22/LO/0911).

摘要

背景

准确评估组织灌注具有挑战性。常用的标志物如乳酸水平和中心静脉血氧饱和度是间接的、间歇性的,只能提供循环状态的整体情况,可能无法反映器官水平的灌注。通过专用导尿管测量的尿道灌注指数(UPi)是一种新技术,可对中央组织床的灌注进行连续、实时监测,有可能提供更即时和有针对性的临床信息。

目的

  1. 评估液体冲击后左心室流出道速度时间积分(LVOT VTi)变化与UPi之间的相关性。2. 评估UPi与其他组织灌注标志物之间的关系。

设计

干预性可行性初步研究。

地点

在英国一家三级医疗机构进行的单中心研究。所有患者均为接受机械通气的成年人,其主治临床团队认为他们将从液体冲击中获益。

干预

液体冲击(FC)定义为静脉推注250ml晶体溶液。

主要观察指标

在液体冲击前后,通过经胸超声心动图测量LVOT VTi,通过专用导尿管测量UPi。

结果

未报告与设备使用或插入相关的并发症。记录数据的平均时长为19小时,UPi曲线的信号质量指数较高(93%)。UPi与LVOT VTi的时间匹配值之间存在中度正相关(Spearman秩相关系数r = 0.55,p < 0.0001),决定系数R2为0.272。然而,液体冲击后UPi的变化与VTi之间未发现明显相关性(Spearman秩相关系数r = 0.24,p =  0.14)。基线时UPi低于平均水平的患者,根据乳酸浓度和毛细血管再充盈时间测量,有全身组织灌注较差的证据,且接受了更多血管活性药物治疗。

结论

UPi可能是各类重症患者组织灌注的一个标志物。因此,经过进一步评估,它可能成为未来的治疗靶点。虽然LVOT VTi与UPi之间存在一定关系,但不够精确,不能用作液体反应性的标志物。

试验注册号

伦敦东南部研究与伦理委员会(22/LO/0911)

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