Direct assessment of microcirculation in shock: a randomized-controlled multicenter study

医学 重症监护室 临床终点 复苏 随机对照试验 重症监护 休克(循环) 心源性休克 相对风险 麻醉学 感染性休克 危险系数 毛细管再灌注 不利影响 置信区间 麻醉 内科学 急诊医学 重症监护医学 血压 心肌梗塞 败血症
作者
Raphael Romano Bruno,Jakob Wollborn,Karl Fengler,Moritz Flick,Christian Wunder,Sebastian Allgäuer,Holger Thiele,Mara Schemmelmann,Johanna Hornemann,Helene Mathilde Emilie Moecke,F. Demirtaş,Lina Palici,Marcus Franz,Bernd Saugel,Eduardo Kattan,Daniel De Backer,Jan Bakker,Glenn Hernández,Malte Kelm,Christian Jung
出处
期刊:Intensive Care Medicine [Springer Science+Business Media]
卷期号:49 (6): 645-655 被引量:24
标识
DOI:10.1007/s00134-023-07098-5
摘要

Shock is a life-threatening condition characterized by substantial alterations in the microcirculation. This study tests the hypothesis that considering sublingual microcirculatory perfusion variables in the therapeutic management reduces 30-day mortality in patients admitted to the intensive care unit (ICU) with shock. This randomized, prospective clinical multicenter trial-recruited patients with an arterial lactate value above two mmol/L, requiring vasopressors despite adequate fluid resuscitation, regardless of the cause of shock. All patients received sequential sublingual measurements using a sidestream-dark field (SDF) video microscope at admission to the intensive care unit (± 4 h) and 24 (± 4) hours later that was performed blindly to the treatment team. Patients were randomized to usual routine or to integrating sublingual microcirculatory perfusion variables in the therapy plan. The primary endpoint was 30-day mortality, secondary endpoints were length of stay on the ICU and the hospital, and 6-months mortality. Overall, we included 141 patients with cardiogenic (n = 77), post cardiac surgery (n = 27), or septic shock (n = 22). 69 patients were randomized to the intervention and 72 to routine care. No serious adverse events (SAEs) occurred. In the interventional group, significantly more patients received an adjustment (increase or decrease) in vasoactive drugs or fluids (66.7% vs. 41.8%, p = 0.009) within the next hour. Microcirculatory values 24 h after admission and 30-day mortality did not differ [crude: 32 (47.1%) patients versus 25 (34.7%), relative risk (RR) 1.39 (0.91–1.97); Cox-regression: hazard ratio (HR) 1.54 (95% confidence interval (CI) 0.90–2.66, p = 0.118)]. Integrating sublingual microcirculatory perfusion variables in the therapy plan resulted in treatment changes that do not improve survival at all.
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