Famirea Study Group, Medical Intensive Care Unit, APHP, Saint Louis University Hospital, Paris, France.
Clinical Research Unit, APHP, Saint Louis University Hospital, Paris, France.
JAMA. 2022 Mar 15;327(11):1042-1050. doi: 10.1001/jama.2022.2017.
Persistent physical and mental disorders are frequent in survivors of COVID-19-related acute respiratory distress syndrome (ARDS). However, data on these disorders among family members are scarce.
To determine the association between patient hospitalization for COVID-19 ARDS vs ARDS from other causes and the risk of posttraumatic stress disorder (PTSD)-related symptoms in family members.
DESIGN, SETTING, AND PARTICIPANTS: Prospective cohort study in 23 intensive care units (ICUs) in France (January 2020 to June 2020 with final follow-up ending in October 2020). ARDS survivors and family members (1 family member per patient) were enrolled.
Family members of patients hospitalized for ARDS due to COVID-19 vs ARDS due to other causes.
The primary outcome was family member symptoms of PTSD at 90 days after ICU discharge, measured by the Impact of Events Scale-Revised (score range, 0 [best] to 88 [worst]; presence of PTSD symptoms defined by score >22). Secondary outcomes were family member symptoms of anxiety and depression at 90 days assessed by the Hospital Anxiety and Depression Scale (score range, 0 [best] to 42 [worst]; presence of anxiety or depression symptoms defined by subscale scores ≥7). Multivariable logistic regression models were used to determine the association between COVID-19 status and outcomes.
Among 602 family members and 307 patients prospectively enrolled, 517 (86%) family members (median [IQR] age, 51 [40-63] years; 72% women; 48% spouses; 26% bereaved because of the study patient's death; 303 [50%] family members of COVID-19 patients) and 273 (89%) patients (median [IQR] age, 61 [50-69] years; 34% women; 181 [59%] with COVID-19) completed the day-90 assessment. Compared with non-COVID-19 ARDS, family members of patients with COVID-19 ARDS had a significantly higher prevalence of symptoms of PTSD (35% [103/293] vs 19% [40/211]; difference, 16% [95% CI, 8%-24%]; P < .001), symptoms of anxiety (41% [121/294] vs 34% [70/207]; difference, 8% [95% CI, 0%-16%]; P= .05), and symptoms of depression (31% [91/291] vs 18% [37/209]; difference, 13% [95% CI, 6%-21%]; P< .001). In multivariable models adjusting for age, sex, and level of social support, COVID-19 ARDS was significantly associated with increased risk of PTSD-related symptoms in family members (odds ratio, 2.05 [95% CI, 1.30 to 3.23]).
Among family members of patients hospitalized in the ICU with ARDS, COVID-19 disease, as compared with other causes of ARDS, was significantly associated with increased risk of symptoms of PTSD at 90 days after ICU discharge.
ClinicalTrials.gov Identifier: NCT04341519.
COVID-19 相关急性呼吸窘迫综合征(ARDS)幸存者常伴有持续的身心障碍。然而,关于这些障碍在家庭成员中的数据却很少。
确定 COVID-19 相关 ARDS 与其他原因导致的 ARDS 患者住院与家庭成员创伤后应激障碍(PTSD)相关症状风险之间的关系。
设计、地点和参与者:这是一项在法国 23 个重症监护病房(ICU)进行的前瞻性队列研究(2020 年 1 月至 2020 年 6 月,最终随访于 2020 年 10 月结束)。纳入 ARDS 幸存者及其家庭成员(每位患者 1 名家庭成员)。
COVID-19 导致的 ARDS 患者与其他原因导致的 ARDS 患者的家庭成员。
主要结局是 ICU 出院后 90 天家庭成员的 PTSD 症状,通过修订后的事件影响量表(评分范围:0 [最佳] 至 88 [最差];评分 >22 定义 PTSD 症状存在)进行评估。次要结局是 90 天时家庭成员的焦虑和抑郁症状,通过医院焦虑和抑郁量表(评分范围:0 [最佳] 至 42 [最差];亚量表评分≥7 定义为焦虑或抑郁症状存在)进行评估。采用多变量逻辑回归模型来确定 COVID-19 状态与结局之间的关系。
在 602 名家庭成员和 307 名患者中,有 517 名(86%)家庭成员(中位数 [IQR] 年龄,51 [40-63] 岁;72%为女性;48%为配偶;26%因研究患者死亡而失去亲人;303 [50%] 为 COVID-19 患者的家庭成员)和 273 名(89%)患者(中位数 [IQR] 年龄,61 [50-69] 岁;34%为女性;181 [59%] 为 COVID-19 患者)完成了第 90 天的评估。与非 COVID-19 ARDS 相比,COVID-19 ARDS 患者的家庭成员 PTSD 症状的患病率明显更高(35% [103/293] 比 19% [40/211];差异为 16% [95% CI,8%-24%];P < 0.001)、焦虑症状(41% [121/294] 比 34% [70/207];差异为 8% [95% CI,0%-16%];P = 0.05)和抑郁症状(31% [91/291] 比 18% [37/209];差异为 13% [95% CI,6%-21%];P < 0.001)。在调整年龄、性别和社会支持水平的多变量模型中,COVID-19 ARDS 与家庭成员 PTSD 相关症状的风险增加显著相关(比值比,2.05 [95% CI,1.30 至 3.23])。
在 ICU 中因 ARDS 住院的患者的家庭成员中,与其他原因导致的 ARDS 相比,COVID-19 疾病与 ICU 出院后 90 天 PTSD 症状的风险增加显著相关。
ClinicalTrials.gov 标识符:NCT04341519。