Àrea de Crítics, Parc Taulí Hospital Universitari, Parc Taulí, 1, 08208, Sabadell, Spain.
ICFO-Institut de Ciències Fotòniques, The Barcelona Institute of Science and Technology, Castelldefels, Barcelona, Spain.
Crit Care. 2021 Nov 8;25(1):381. doi: 10.1186/s13054-021-03803-2.
COVID-19 is primarily a respiratory disease; however, there is also evidence that it causes endothelial damage in the microvasculature of several organs. The aim of the present study is to characterize in vivo the microvascular reactivity in peripheral skeletal muscle of severe COVID-19 patients.
This is a prospective observational study carried out in Spain, Mexico and Brazil. Healthy subjects and severe COVID-19 patients admitted to the intermediate respiratory (IRCU) and intensive care units (ICU) due to hypoxemia were studied. Local tissue/blood oxygen saturation (StO) and local hemoglobin concentration (THC) were non-invasively measured on the forearm by near-infrared spectroscopy (NIRS). A vascular occlusion test (VOT), a three-minute induced ischemia, was performed in order to obtain dynamic StO parameters: deoxygenation rate (DeO), reoxygenation rate (ReO), and hyperemic response (H). In COVID-19 patients, the severity of ARDS was evaluated by the ratio between peripheral arterial oxygen saturation (SpO) and the fraction of inspired oxygen (FiO) (SF ratio).
Healthy controls (32) and COVID-19 patients (73) were studied. Baseline StO and THC did not differ between the two groups. Dynamic VOT-derived parameters were significantly impaired in COVID-19 patients showing lower metabolic rate (DeO) and diminished endothelial reactivity. At enrollment, most COVID-19 patients were receiving invasive mechanical ventilation (MV) (53%) or high-flow nasal cannula support (32%). Patients on MV were also receiving sedative agents (100%) and vasopressors (29%). Baseline StO and DeO negatively correlated with SF ratio, while ReO showed a positive correlation with SF ratio. There were significant differences in baseline StO and ReO among the different ARDS groups according to SF ratio, but not among different respiratory support therapies.
Patients with severe COVID-19 show systemic microcirculatory alterations suggestive of endothelial dysfunction, and these alterations are associated with the severity of ARDS. Further evaluation is needed to determine whether these observations have prognostic implications. These results represent interim findings of the ongoing HEMOCOVID-19 trial. Trial registration ClinicalTrials.gov NCT04689477 . Retrospectively registered 30 December 2020.
COVID-19 主要是一种呼吸道疾病;然而,也有证据表明它会导致几个器官的微血管内皮损伤。本研究的目的是描述严重 COVID-19 患者外周骨骼肌的微血管反应性。
这是在西班牙、墨西哥和巴西进行的一项前瞻性观察性研究。研究对象为因低氧血症而入住中级呼吸(IRCU)和重症监护病房(ICU)的健康受试者和严重 COVID-19 患者。通过近红外光谱(NIRS)在手前臂上无创测量局部组织/血氧饱和度(StO)和局部血红蛋白浓度(THC)。进行血管闭塞试验(VOT),即 3 分钟的诱导性缺血,以获得动态 StO 参数:脱氧率(DeO)、再氧合率(ReO)和充血反应(H)。在 COVID-19 患者中,通过外周动脉血氧饱和度(SpO)与吸入氧分数(FiO)的比值(SF 比值)评估 ARDS 的严重程度。
共研究了 32 名健康对照者和 73 名 COVID-19 患者。两组间基线 StO 和 THC 无差异。COVID-19 患者的动态 VOT 衍生参数显著受损,表现为代谢率降低(DeO)和内皮反应减弱。入组时,大多数 COVID-19 患者正在接受有创机械通气(MV)(53%)或高流量鼻导管支持(32%)。接受 MV 的患者还接受镇静剂(100%)和血管加压素(29%)。基线 StO 和 DeO 与 SF 比值呈负相关,而 ReO 与 SF 比值呈正相关。根据 SF 比值,不同 ARDS 组间的基线 StO 和 ReO 存在显著差异,但不同呼吸支持治疗组间无差异。
严重 COVID-19 患者表现出全身性微循环改变,提示内皮功能障碍,这些改变与 ARDS 的严重程度相关。需要进一步评估这些观察结果是否具有预后意义。这些结果代表正在进行的 HEMOCOVID-19 试验的中期结果。试验注册 ClinicalTrials.gov NCT04689477。2020 年 12 月 30 日回顾性注册。