Department of Pulmonary Medicine, QingPu Branch of Zhongshan Hospital Affiliated to Fudan University, Shanghai, China.
Infection Division, Wuhan Jinyintan Hospital, Wuhan, China.
JAMA Intern Med. 2020 Jul 1;180(7):934-943. doi: 10.1001/jamainternmed.2020.0994.
Coronavirus disease 2019 (COVID-19) is an emerging infectious disease that was first reported in Wuhan, China, and has subsequently spread worldwide. Risk factors for the clinical outcomes of COVID-19 pneumonia have not yet been well delineated.
To describe the clinical characteristics and outcomes in patients with COVID-19 pneumonia who developed acute respiratory distress syndrome (ARDS) or died.
DESIGN, SETTING, AND PARTICIPANTS: Retrospective cohort study of 201 patients with confirmed COVID-19 pneumonia admitted to Wuhan Jinyintan Hospital in China between December 25, 2019, and January 26, 2020. The final date of follow-up was February 13, 2020.
Confirmed COVID-19 pneumonia.
The development of ARDS and death. Epidemiological, demographic, clinical, laboratory, management, treatment, and outcome data were also collected and analyzed.
Of 201 patients, the median age was 51 years (interquartile range, 43-60 years), and 128 (63.7%) patients were men. Eighty-four patients (41.8%) developed ARDS, and of those 84 patients, 44 (52.4%) died. In those who developed ARDS, compared with those who did not, more patients presented with dyspnea (50 of 84 [59.5%] patients and 30 of 117 [25.6%] patients, respectively [difference, 33.9%; 95% CI, 19.7%-48.1%]) and had comorbidities such as hypertension (23 of 84 [27.4%] patients and 16 of 117 [13.7%] patients, respectively [difference, 13.7%; 95% CI, 1.3%-26.1%]) and diabetes (16 of 84 [19.0%] patients and 6 of 117 [5.1%] patients, respectively [difference, 13.9%; 95% CI, 3.6%-24.2%]). In bivariate Cox regression analysis, risk factors associated with the development of ARDS and progression from ARDS to death included older age (hazard ratio [HR], 3.26; 95% CI 2.08-5.11; and HR, 6.17; 95% CI, 3.26-11.67, respectively), neutrophilia (HR, 1.14; 95% CI, 1.09-1.19; and HR, 1.08; 95% CI, 1.01-1.17, respectively), and organ and coagulation dysfunction (eg, higher lactate dehydrogenase [HR, 1.61; 95% CI, 1.44-1.79; and HR, 1.30; 95% CI, 1.11-1.52, respectively] and D-dimer [HR, 1.03; 95% CI, 1.01-1.04; and HR, 1.02; 95% CI, 1.01-1.04, respectively]). High fever (≥39 °C) was associated with higher likelihood of ARDS development (HR, 1.77; 95% CI, 1.11-2.84) and lower likelihood of death (HR, 0.41; 95% CI, 0.21-0.82). Among patients with ARDS, treatment with methylprednisolone decreased the risk of death (HR, 0.38; 95% CI, 0.20-0.72).
Older age was associated with greater risk of development of ARDS and death likely owing to less rigorous immune response. Although high fever was associated with the development of ARDS, it was also associated with better outcomes among patients with ARDS. Moreover, treatment with methylprednisolone may be beneficial for patients who develop ARDS.
2019 年冠状病毒病(COVID-19)是一种新发传染病,最初在中国武汉报告,随后在全球范围内传播。COVID-19 肺炎临床结局的危险因素尚未得到很好的阐明。
描述在中国武汉市金银潭医院住院的确诊为 COVID-19 肺炎并发生急性呼吸窘迫综合征(ARDS)或死亡的患者的临床特征和结局。
设计、地点和参与者:对 2019 年 12 月 25 日至 2020 年 1 月 26 日期间在中国武汉市金银潭医院住院的 201 例确诊为 COVID-19 肺炎的患者进行回顾性队列研究。随访的最终日期为 2020 年 2 月 13 日。
确诊为 COVID-19 肺炎。
ARDS 的发生和死亡。还收集和分析了流行病学、人口统计学、临床、实验室、管理、治疗和结局数据。
在 201 例患者中,中位年龄为 51 岁(四分位距,43-60 岁),128 例(63.7%)为男性。84 例(41.8%)发生 ARDS,其中 44 例(52.4%)死亡。在发生 ARDS 的患者中,与未发生 ARDS 的患者相比,更多的患者出现呼吸困难(84 例中有 50 例[59.5%]和 117 例中有 30 例[25.6%],差异为 33.9%;95%CI,19.7%-48.1%)和合并症,如高血压(84 例中有 23 例[27.4%]和 117 例中有 16 例[13.7%],差异为 13.7%;95%CI,1.3%-26.1%)和糖尿病(84 例中有 16 例[19.0%]和 117 例中有 6 例[5.1%],差异为 13.9%;95%CI,3.6%-24.2%)。在二元 Cox 回归分析中,与发生 ARDS 和从 ARDS 进展为死亡相关的危险因素包括年龄较大(风险比[HR],3.26;95%CI,2.08-5.11;和 HR,6.17;95%CI,3.26-11.67,分别)、中性粒细胞增多(HR,1.14;95%CI,1.09-1.19;和 HR,1.08;95%CI,1.01-1.17,分别)和器官和凝血功能障碍(例如,乳酸脱氢酶升高[HR,1.61;95%CI,1.44-1.79;和 HR,1.30;95%CI,1.11-1.52,分别]和 D-二聚体[HR,1.03;95%CI,1.01-1.04;和 HR,1.02;95%CI,1.01-1.04,分别)。高热(≥39°C)与发生 ARDS 的可能性更高相关(HR,1.77;95%CI,1.11-2.84),而与死亡的可能性更低相关(HR,0.41;95%CI,0.21-0.82)。在发生 ARDS 的患者中,甲泼尼龙治疗降低了死亡风险(HR,0.38;95%CI,0.20-0.72)。
年龄较大与发生 ARDS 和死亡的风险增加有关,这可能是由于免疫反应较弱所致。虽然高热与 ARDS 的发生有关,但它也与 ARDS 患者的更好结局有关。此外,甲泼尼龙治疗可能对发生 ARDS 的患者有益。