UFR de médecine, Université de Paris, Paris, France.
Médecine intensive - réanimation, Assistance Publique-Hôpitaux de Paris (AP-HP), Hôpital Bichat - Claude Bernard, F-75018 Paris, France.
Crit Care Med. 2022 Aug 1;50(8):e674-e682. doi: 10.1097/CCM.0000000000005500. Epub 2022 Feb 8.
To describe 3-6-month neurologic outcomes of survivors of COVID-19-associated acute respiratory distress syndrome, invasively ventilated in the ICU.
A bicentric prospective study during the two first waves of the pandemic (March to May and September to December, 2020).
Two academic hospital ICUs, Paris, France.
Adult COVID-19-associated acute respiratory distress syndrome survivors, invasively ventilated in the ICU, were eligible for a neurologic consultation between 3 and 6 months post ICU discharge.
Follow-up by face-to-face neurologic consultation.
The primary endpoint was favorable functional outcome defined by a modified Rankin scale score less than 2, indicating survival with no significant disability. Secondary endpoints included mild cognitive impairment (Montreal Cognitive Assessment score < 26), ICU-acquired weakness (Medical Research Council score < 48), anxiety and depression (Hospital Anxiety and Depression score > 7), and posttraumatic stress disorder (posttraumatic stress disorder checklist for Diagnostic and Statistical Manual of Mental Disorders 5 score > 30). Of 54 eligible survivors, four non-French-speaking patients were excluded, eight patients were lost-to-follow-up, and one died during follow-up. Forty-one patients were included. Time between ICU discharge and neurologic consultation was 3.8 months (3.6-5.9 mo). A favorable functional outcome was observed in 16 patients (39%) and mild cognitive impairment in 17 of 33 patients tested (52%). ICU-acquired weakness, depression or anxiety, and posttraumatic stress disorder were reported in six of 37 cases (16%), eight of 31 cases (26%), and two of 27 cases (7%), respectively. Twenty-nine patients (74%) required rehabilitation (motor, cognitive, or psychologic). ICU and hospital lengths of stay, tracheostomy, and corticosteroids were negatively associated with favorable outcome. By contrast, use of alpha-2 agonists during ICU stay was associated with favorable outcome.
COVID-19-associated acute respiratory distress syndrome requiring intubation led to slight-to-severe functional disability in about 60% of survivors 4 months after ICU discharge. Cognitive impairment, muscle weakness, and psychologic symptoms were frequent. A large multicenter study is warranted to allow identification of modifiable factors for improving long-term outcome.
描述 COVID-19 相关急性呼吸窘迫综合征(ARDS)患者在 ICU 接受有创通气后 3-6 个月的神经系统结局。
在大流行的两个第一波(2020 年 3 月至 5 月和 9 月至 12 月)期间进行的一项双中心前瞻性研究。
法国巴黎的两家学术医院 ICU。
符合条件的 COVID-19 相关 ARDS 幸存者,在 ICU 接受有创通气,在 ICU 出院后 3-6 个月之间有资格接受神经科会诊。
面对面的神经科会诊随访。
主要终点是通过改良 Rankin 量表评分定义的有利功能结局,评分低于 2 分,表示生存且无明显残疾。次要终点包括轻度认知障碍(蒙特利尔认知评估量表评分<26)、ICU 获得性肌无力(医学研究委员会评分<48)、焦虑和抑郁(医院焦虑和抑郁量表评分>7)和创伤后应激障碍(创伤后应激障碍检查表 5 分>30)。在 54 名符合条件的幸存者中,排除了 4 名非法语患者,8 名失访,1 名在随访期间死亡。41 名患者入组。从 ICU 出院到神经科会诊的时间为 3.8 个月(3.6-5.9 个月)。16 名患者(39%)出现有利的功能结局,33 名接受测试的患者中有 17 名(52%)出现轻度认知障碍。37 例中有 6 例(16%)、31 例中有 8 例(26%)和 27 例中有 2 例(7%)报告有 ICU 获得性肌无力、抑郁或焦虑、创伤后应激障碍。29 名患者(74%)需要康复(运动、认知或心理)。ICU 和住院时间、气管切开术和皮质类固醇与有利结局呈负相关。相比之下,在 ICU 期间使用α-2 激动剂与有利结局相关。
需要插管的 COVID-19 相关 ARDS 在 ICU 出院后 4 个月导致约 60%的幸存者出现轻微至严重的功能障碍。认知障碍、肌肉无力和心理症状很常见。需要进行大规模的多中心研究,以确定可改善长期结局的可改变因素。