Pathophysiological Markers of Acute Respiratory Distress Syndrome Severity Are Correlated With Ventilation-Perfusion Mismatch Measured by Electrical Impedance Tomography.

IF 7.7 1区 医学 Q1 CRITICAL CARE MEDICINE
Elena Spinelli, Joaquin Perez, Valentina Chiavieri, Marco Leali, Nadia Mansour, Fabiana Madotto, Lorenzo Rosso, Mauro Panigada, Giacomo Grasselli, Valentina Vaira, Tommaso Mauri
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引用次数: 0

Abstract

Objectives: Pulmonary ventilation/perfusion (V/Q) mismatch measured by electrical impedance tomography (EIT) is associated with the outcome of patients with the acute respiratory distress syndrome (ARDS), but the underlying pathophysiological mechanisms have not been fully elucidated. The present study aimed to verify the correlation between relevant pathophysiological markers of ARDS severity and V/Q mismatch.

Design: Prospective observational study.

Setting: General ICU of a university-affiliated hospital.

Patients: Deeply sedated intubated adult patients with ARDS under controlled mechanical ventilation.

Interventions: Measures of V/Q mismatch by EIT, respiratory mechanics, gas exchange, lung imaging, and plasma biomarkers.

Measurements and main results: Unmatched V/Q units were assessed by EIT as the fraction of ventilated nonperfused plus perfused nonventilated lung units. At the same time, plasma biomarkers with proven prognostic and mechanistic significance for ARDS (carbonic anhydrase 9 [CA9], hypoxia-inducible factor 1 [HIF1], receptor for advanced glycation endproducts [RAGE], angiopoietin 2 [ANG2], gas exchange, respiratory mechanics, and quantitative chest CT scans were measured. Twenty-five intubated ARDS patients were included with median unmatched V/Q units of 37.1% (29.2-49.2%). Unmatched V/Q units were correlated with plasma levels of CA9 (rho = 0.47; p = 0.01), HIF1 (rho = 0.40; p = 0.05), RAGE (rho = 0.46; p = 0.02), and ANG2 (rho = 0.42; p = 0.03). Additionally, unmatched V/Q units correlated with plateau pressure (r = 0.38; p = 0.05) and with the number of quadrants involved on chest radiograph (r = 0.73; p < 0.01). Regional unmatched V/Q units were correlated with the corresponding fraction of poorly aerated lung tissue (r = 0.62; p = 0.01) and of lung tissue weight (rho: 0.51; p = 0.04) measured by CT scan.

Conclusions: In ARDS patients, unmatched V/Q units are correlated with pathophysiological markers of lung epithelial and endothelial dysfunction, increased lung stress, and lung edema. Unmatched V/Q units could represent a comprehensive marker of ARDS severity, reflecting the complex organ pathophysiology and reinforcing their prognostic significance.

急性呼吸窘迫综合征严重程度的病理生理标志物与电阻抗断层扫描测量的通气-灌注失配相关。
目的:电阻抗断层扫描(EIT)测量的肺通气/灌注(V/Q)失配与急性呼吸窘迫综合征(ARDS)患者的预后有关,但其潜在的病理生理学机制尚未完全阐明。本研究旨在验证 ARDS 严重程度的相关病理生理指标与 V/Q 不匹配之间的相关性:设计:前瞻性观察研究:地点:一所大学附属医院的普通重症监护室:深度镇静插管、接受可控机械通气的 ARDS 成年患者:干预措施:通过EIT、呼吸力学、气体交换、肺部成像和血浆生物标志物测量V/Q不匹配:通过 EIT 评估不匹配的 V/Q 单位,即通气的非灌注肺单位和灌注的非通气肺单位的比例。与此同时,还测量了对 ARDS 有预后和机理意义的血浆生物标志物(碳酸酐酶 9 [CA9]、缺氧诱导因子 1 [HIF1]、高级糖化终产物受体 [RAGE]、血管生成素 2 [ANG2])、气体交换、呼吸力学和定量胸部 CT 扫描。25 名插管 ARDS 患者的未匹配 V/Q 单位中位数为 37.1%(29.2-49.2%)。未匹配的 V/Q 单位与血浆中 CA9(rho = 0.47;p = 0.01)、HIF1(rho = 0.40;p = 0.05)、RAGE(rho = 0.46;p = 0.02)和 ANG2(rho = 0.42;p = 0.03)的水平相关。此外,未匹配的 V/Q 单位与高原压(r = 0.38;p = 0.05)和胸片上受累象限的数量(r = 0.73;p < 0.01)相关。区域非匹配 V/Q 单位与 CT 扫描测量的相应通气不良肺组织比例(r = 0.62;p = 0.01)和肺组织重量(rho:0.51;p = 0.04)相关:结论:在 ARDS 患者中,不匹配的 V/Q 单位与肺上皮和内皮功能障碍、肺压力增加和肺水肿的病理生理指标相关。不匹配的V/Q单位可代表ARDS严重程度的综合标志物,反映复杂的器官病理生理学并加强其预后意义。
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来源期刊
Critical Care Medicine
Critical Care Medicine 医学-危重病医学
CiteScore
16.30
自引率
5.70%
发文量
728
审稿时长
2 months
期刊介绍: Critical Care Medicine is the premier peer-reviewed, scientific publication in critical care medicine. Directed to those specialists who treat patients in the ICU and CCU, including chest physicians, surgeons, pediatricians, pharmacists/pharmacologists, anesthesiologists, critical care nurses, and other healthcare professionals, Critical Care Medicine covers all aspects of acute and emergency care for the critically ill or injured patient. Each issue presents critical care practitioners with clinical breakthroughs that lead to better patient care, the latest news on promising research, and advances in equipment and techniques.
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