Greenway Andrew, Leahy Nicole, Torrieri Lisa, An Anjile, Fink Sarah A, Witenko Corey, Shikar Morgan, Winchell Robert J, Barie Philip S, Liu Susan I
159947NewYork-Presbyterian Hospital/Weill Cornell Medical Center, New York, NY.
Weill Cornell Medicine, New York, NY.
J Intensive Care Med. 2021 Nov;36(11):1331-1339. doi: 10.1177/08850666211046532. Epub 2021 Sep 30.
To characterize skin integrity among coronavirus disease 2019 (COVID-19) patients treated in the intensive care unit (ICU), and identify risk factors for skin failure (SF) in these patients. The characteristic, profound pro-inflammatory, hypercoagulable state of COVID-19 is manifested by the high severity of illness and extensive organ dysfunction observed in these patients. SF in critically ill patients, although described previously, exhibits a uniquely complex pathogenesis in this population. Retrospective review of all COVID-19 patients (confirmed positive for severe acute respiratory syndrome coronavirus-2 [SARS-CoV-2]) admitted to a single surgical ICU for at least 48 hours between March-June 2020. Data were extracted from a COVID-19 institutional data repository that harvested data from electronic health records and other clinical data sources. Demographics; coagulation/inflammation biomarkers; number, location, and stage of SF lesions; resource utilization; and outcomes were captured. 64 patients met inclusion criteria; 51 (80%) developed SF (SF+ ). Forty-three (85%) developed stage 3 or higher SF (χ = 22.66, < .0001). Thirty-nine of 51 (76%) SF+ patients developed more than one SF lesion (χ = 13.26, = .0003). SF+ patients manifested a profound pro-inflammatory, hypercoagulable phenotype (lower serum albumin and higher ferritin, interleukin [IL]-6 and D-dimer concentrations [all, < .001]). Durations of mechanical ventilation, vasopressor therapy, and ICU length of stay were significantly longer (all, < .05) in the SF + patients. The unique characteristics of COVID-19 dermatopathology and the strong correlation between markers of inflammation and development of SF reflect COVID-19-related organ dysfunction and its deleterious effects on the microcirculation. Considering that skin is invaded directly by SARS-CoV-2 and affected by COVID-19-related immune complex deposition and microthrombosis, SF may reflect disease as opposed to pressure injuries related to processes of care. In the context of COVID-19 critical illness, SF should not be considered a "never event."
为了描述在重症监护病房(ICU)接受治疗的2019冠状病毒病(COVID-19)患者的皮肤完整性,并确定这些患者发生皮肤衰竭(SF)的危险因素。COVID-19具有特征性的、严重的促炎、高凝状态,表现为这些患者的高疾病严重程度和广泛的器官功能障碍。重症患者的SF虽然之前已有描述,但在这一人群中表现出独特而复杂的发病机制。对2020年3月至6月期间入住单一外科ICU至少48小时的所有COVID-19患者(严重急性呼吸综合征冠状病毒2 [SARS-CoV-2]确诊阳性)进行回顾性研究。数据从一个COVID-19机构数据存储库中提取,该存储库收集了来自电子健康记录和其他临床数据源的数据。记录了人口统计学资料;凝血/炎症生物标志物;SF病变的数量、位置和阶段;资源利用情况;以及结局。64例患者符合纳入标准;51例(80%)发生了SF(SF+)。43例(85%)发生了3期或更高阶段的SF(χ = 22.66,P <.0001)。51例SF+患者中有39例(76%)出现了不止一处SF病变(χ = 13.26,P =.0003)。SF+患者表现出严重的促炎、高凝表型(血清白蛋白较低,铁蛋白、白细胞介素[IL]-6和D-二聚体浓度较高[均P <.001])。SF+患者的机械通气时间、血管升压药治疗时间和ICU住院时间显著更长(均P <.05)。COVID-19皮肤病理学的独特特征以及炎症标志物与SF发生之间的强相关性反映了COVID-19相关的器官功能障碍及其对微循环的有害影响。考虑到皮肤直接受到SARS-CoV-2的侵袭,并受到COVID-19相关免疫复合物沉积和微血栓形成的影响,SF可能反映疾病情况,而非与护理过程相关的压力性损伤。在COVID-19危重症的背景下,SF不应被视为一种“绝不应该发生的事件”。