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新冠肺炎患者在开始吸氧时延迟地塞米松治疗与临床病情恶化有关。

Delayed dexamethasone treatment at initiation of oxygen supplementation for coronavirus disease 2019 is associated with the exacerbation of clinical condition.

机构信息

Department of Hospital Pharmacy, Sapporo Medical University Hospital, Sapporo, Hokkaido, Japan.

Department of Hospital Pharmacy, Sapporo Medical University Hospital, Sapporo, Hokkaido, Japan.

出版信息

J Infect Chemother. 2022 Jul;28(7):875-883. doi: 10.1016/j.jiac.2022.03.007. Epub 2022 Mar 18.

DOI:10.1016/j.jiac.2022.03.007
PMID:35339384
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8930397/
Abstract

INTRODUCTION

Coronavirus disease 2019 (COVID-19) frequently causes inflammatory lung injury as its symptoms progress. While dexamethasone reportedly reduces inflammation and prevents progression to respiratory failure, the appropriate time to administer dexamethasone in patients with COVID-19 remains unclear.

METHODS

This was a single-center, retrospective cohort study, where we consecutively enrolled patients hospitalized with COVID-19 who received oxygen and oral dexamethasone (n = 85). We assessed the association between the number of days to the initiation of dexamethasone and the cumulative rate of exacerbation defined as death or initiation of mechanical ventilation within 28 days of symptom onset.

RESULTS

The optimal cut-off value from the initiation of oxygen supplementation to that of dexamethasone administration was two days (sensitivity, 85%; specificity, 59%), whereas that from oxygen saturation (SpO) < 95% to the initiation of dexamethasone administration was five days (sensitivity, 78%; specificity, 59%). adjusting for age, sex, body mass index, Charlson comorbidity index score, time of oxygen supplementation (two or more days), and SpO < 95% (five or more days), Cox regression analysis results showed that delayed dexamethasone administration since the initiation of oxygen supplementation was significantly associated with a higher risk of death or greater need for mechanical ventilation (hazard ratio: 5.51, 95% confidence interval, 1.79-16.91).

CONCLUSIONS

In patients with COVID-19 and hypoxemia, early administration of dexamethasone, preferably less than two days from initiation of oxygen supplementation, may be required to improve clinical outcomes.

摘要

简介

随着 2019 年冠状病毒病(COVID-19)症状的发展,其经常导致炎症性肺损伤。虽然地塞米松据报道可减轻炎症并防止发展为呼吸衰竭,但 COVID-19 患者使用地塞米松的适当时间仍不清楚。

方法

这是一项单中心回顾性队列研究,我们连续纳入了接受氧疗和口服地塞米松治疗的 COVID-19 住院患者(n=85)。我们评估了从开始氧疗到开始地塞米松治疗的天数与 28 天内死亡或开始机械通气的恶化累积发生率之间的关系。

结果

从开始氧疗到开始地塞米松治疗的最佳截断值为两天(敏感性,85%;特异性,59%),而从血氧饱和度(SpO2)<95%到开始地塞米松治疗的最佳截断值为五天(敏感性,78%;特异性,59%)。调整年龄、性别、体重指数、Charlson 合并症指数评分、氧疗时间(两天或更长时间)以及 SpO2<95%(五天或更长时间)后,Cox 回归分析结果表明,从开始氧疗到开始地塞米松治疗的时间延迟与死亡风险增加或更需要机械通气显著相关(风险比:5.51,95%置信区间,1.79-16.91)。

结论

在 COVID-19 合并低氧血症的患者中,可能需要早期给予地塞米松治疗,最好在开始氧疗的两天内,以改善临床结局。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a567/8930397/c2b6f6214971/gr4_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a567/8930397/86420641d306/gr1_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a567/8930397/4c3475dda8c6/gr2_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a567/8930397/c0f3b377b64b/gr3_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a567/8930397/c2b6f6214971/gr4_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a567/8930397/86420641d306/gr1_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a567/8930397/4c3475dda8c6/gr2_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a567/8930397/c0f3b377b64b/gr3_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a567/8930397/c2b6f6214971/gr4_lrg.jpg

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