Peñuelas Oscar, Del Campo-Albendea Laura, de Aledo Amanda Lesmes González, Añón José Manuel, Rodríguez-Solís Carmen, Mancebo Jordi, Vera Paula, Ballesteros Daniel, Jiménez Jorge, Maseda Emilio, Figueira Juan Carlos, Franco Nieves, Algaba Ángela, Avilés Juan Pablo, Díaz Ricardo, Abad Beatriz, Canabal Alfonso, Abella Ana, Gordo Federico, García Javier, Suarez Jessica García, Cedeño Jamil, Martínez-Palacios Basilia, Manteiga Eva, Martínez Óscar, Blancas Rafael, Bardi Tommaso, Pestaña David, Lorente José Ángel, Muriel Alfonso, Esteban Andrés, Frutos-Vivar Fernando
Intensive Care Unit, Hospital Universitario de Getafe, Carretera de Toledo km 12,500, 28905, Madrid, Spain.
Centro de Investigación Biomédica en Red de Enfermedades Respiratorias, Instituto de Salud Carlos III, Madrid, Spain.
Ann Intensive Care. 2021 Oct 2;11(1):143. doi: 10.1186/s13613-021-00929-y.
Information is lacking regarding long-term survival and predictive factors for mortality in patients with acute hypoxemic respiratory failure due to coronavirus disease 2019 (COVID-19) and undergoing invasive mechanical ventilation. We aimed to estimate 180-day mortality of patients with COVID-19 requiring invasive ventilation, and to develop a predictive model for long-term mortality.
Retrospective, multicentre, national cohort study between March 8 and April 30, 2020 in 16 intensive care units (ICU) in Spain. Participants were consecutive adults who received invasive mechanical ventilation for COVID-19. Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection detected in positive testing of a nasopharyngeal sample and confirmed by real time reverse-transcriptase polymerase chain reaction (rt-PCR). The primary outcomes was 180-day survival after hospital admission. Secondary outcomes were length of ICU and hospital stay, and ICU and in-hospital mortality. A predictive model was developed to estimate the probability of 180-day mortality.
868 patients were included (median age, 64 years [interquartile range [IQR], 56-71 years]; 72% male). Severity at ICU admission, estimated by SAPS3, was 56 points [IQR 50-63]. Prior to intubation, 26% received some type of noninvasive respiratory support. The unadjusted overall 180-day survival rates was 59% (95% CI 56-62%). The predictive factors measured during ICU stay, and associated with 180-day mortality were: age [Odds Ratio [OR] per 1-year increase 1.051, 95% CI 1.033-1.068)), SAPS3 (OR per 1-point increase 1.027, 95% CI 1.011-1.044), diabetes (OR 1.546, 95% CI 1.085-2.204), neutrophils to lymphocytes ratio (OR per 1-unit increase 1.008, 95% CI 1.001-1.016), failed attempt of noninvasive positive pressure ventilation prior to orotracheal intubation (OR 1.878 (95% CI 1.124-3.140), use of selective digestive decontamination strategy during ICU stay (OR 0.590 (95% CI 0.358-0.972) and administration of low dosage of corticosteroids (methylprednisolone 1 mg/kg) (OR 2.042 (95% CI 1.205-3.460).
The long-term survival of mechanically ventilated patients with severe COVID-19 reaches more than 50% and may help to provide individualized risk stratification and potential treatments.
ClinicalTrials.gov Identifier: NCT04379258. Registered 10 April 2020 (retrospectively registered).
关于2019冠状病毒病(COVID-19)导致的急性低氧性呼吸衰竭且接受有创机械通气患者的长期生存情况及死亡预测因素的信息尚缺。我们旨在估算需要有创通气的COVID-19患者的180天死亡率,并建立一个长期死亡率预测模型。
2020年3月8日至4月30日在西班牙16个重症监护病房(ICU)进行的一项回顾性、多中心、全国性队列研究。参与者为因COVID-19接受有创机械通气的连续成年患者。通过鼻咽样本检测呈阳性并经实时逆转录聚合酶链反应(rt-PCR)确认感染严重急性呼吸综合征冠状病毒2(SARS-CoV-2)。主要结局为入院后180天生存情况。次要结局为ICU住院时长和住院时长,以及ICU死亡率和院内死亡率。建立一个预测模型以估算180天死亡率的概率。
纳入868例患者(中位年龄64岁[四分位间距[IQR],56 - 71岁];72%为男性)。根据序贯器官衰竭评估(SOFA)评分在ICU入院时的严重程度为56分[IQR 50 - 63]。在插管前,26%的患者接受过某种类型的无创呼吸支持。未经调整的总体180天生存率为59%(95%CI 56 - 62%)。在ICU住院期间测量的且与180天死亡率相关的预测因素为:年龄[每增加1岁的比值比[OR] 1.051, 95%CI 1.033 - 1.068]、SOFA评分(每增加1分的OR 1.027, 95%CI 1.011 - 1.044)、糖尿病(OR 1.546, 95%CI 1.085 - 2.204)、中性粒细胞与淋巴细胞比值(每增加1个单位的OR 1.008, 95%CI 1.001 - 1.016)、经口气管插管前无创正压通气尝试失败(OR 1.878 [95%CI l.124 - 3.140])、在ICU住院期间使用选择性消化道去污策略(OR 0.590 [95%CI 0.358 - 0.972])以及给予低剂量皮质类固醇(甲泼尼龙1mg/kg)(OR 2.042 [95%CI 1.205 - 3.460])。
重症COVID-19机械通气患者的长期生存率超过50%,这可能有助于进行个体化风险分层和潜在治疗。
ClinicalTrials.gov标识符:NCT04379258。于2020年4月10日注册(追溯注册)。