Lee Hyun Woo, Park Jimyung, Lee Jung-Kyu, Park Tae Yeon, Heo Eun Young
Division of Respiratory and Critical Care, Department of Internal Medicine, Seoul Metropolitan Government-Seoul National University Boramae Medical Center, Seoul, Republic of Korea.
Tuberc Respir Dis (Seoul). 2021 Jul;84(3):217-225. doi: 10.4046/trd.2021.0009. Epub 2021 Mar 29.
Despite the proven benefits of dexamethasone in hospitalized coronavirus disease 2019 (COVID-19) patients, the optimum time for the administration of dexamethasone is unknown. We investigated the progression of COVID-19 pneumonia based on the timing of dexamethasone administration.
A single-center, retrospective cohort study based on medical record reviews was conducted between June 10 and September 21, 2020. We compared the risk of severe COVID-19, defined as the use of a high-flow nasal cannula or a mechanical ventilator, between groups that received dexamethasone either within 24 hours of hypoxemia (early dexamethasone group) or 24 hours after hypoxemia (late dexamethasone group). Hypoxemia was defined as room-air SpO2 <90%.
Among 59 patients treated with dexamethasone for COVID-19 pneumonia, 30 were in the early dexamethasone group and 29 were in the late dexamethasone group. There was no significant difference in baseline characteristics, the time interval from symptom onset to diagnosis or hospitalization, or the use of antiviral or antibacterial agents between the two groups. The early dexamethasone group showed a significantly lower rate of severe COVID-19 compared to the control group (75.9% vs. 40.0%, p=0.012). Further, the early dexamethasone group showed a significantly shorter total duration of oxygen supplementation (10.45 days vs. 21.61 days, p=0.003) and length of stay in the hospital (19.76 days vs. 27.21 days, p=0.013). However, extracorporeal membrane oxygenation and in-hospital mortality rates were not significantly different between the two groups.
Early administration of dexamethasone may prevent the progression of COVID-19 to a severe disease, without increased mortality.
尽管地塞米松对住院的2019冠状病毒病(COVID-19)患者已证实有益,但地塞米松的最佳给药时间尚不清楚。我们基于地塞米松给药时间研究了COVID-19肺炎的进展情况。
于2020年6月10日至9月21日进行了一项基于病历回顾的单中心回顾性队列研究。我们比较了在低氧血症发生后24小时内接受地塞米松治疗的组(早期地塞米松组)和低氧血症发生24小时后接受地塞米松治疗的组(晚期地塞米松组)中发生严重COVID-19(定义为使用高流量鼻导管或机械通气)的风险。低氧血症定义为室内空气下血氧饱和度(SpO2)<90%。
在59例接受地塞米松治疗COVID-19肺炎的患者中,30例属于早期地塞米松组,29例属于晚期地塞米松组。两组在基线特征、从症状出现到诊断或住院的时间间隔,或抗病毒或抗菌药物的使用方面无显著差异。与对照组相比,早期地塞米松组发生严重COVID-19的比例显著更低(75.9%对40.0%,p=0.012)。此外,早期地塞米松组的总氧疗时间显著更短(10.45天对21.61天,p=0.003),住院时间也显著更短(19.76天对27.21天,p=0.013)。然而,两组之间体外膜肺氧合和院内死亡率无显著差异。
早期给予地塞米松可能预防COVID-19进展为重症疾病,且不会增加死亡率。