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新型冠状病毒肺炎住院患者高剂量皮质类固醇治疗的最佳剂量与时机:一项回顾性观察性多中心研究(SELECT)的研究方案

Optimal Dosing and Timing of High-Dose Corticosteroid Therapy in Hospitalized Patients With COVID-19: Study Protocol for a Retrospective Observational Multicenter Study (SELECT).

作者信息

Daenen Katrijn, Huijben Jilske A, Boyd Anders, Bos Lieuwe D J, Stoof Sara C M, van Willigen Hugo, Gommers Diederik A M P J, Moeniralam Hazra S, den Uil Corstiaan A, Juffermans Nicole P, Kant Merijn, Valkenburg Abraham J, Pillay Janesh, van Meenen David M P, Paulus Frederique, Schultz Marcus J, Dalm Virgil A S H, van Gorp Eric C M, Schinkel Janke, Endeman Henrik

机构信息

Department of Intensive Care, Erasmus University Medical Center, Rotterdam, Netherlands.

Department of Viroscience, Erasmus University Medical Center, Rotterdam, Netherlands.

出版信息

JMIR Res Protoc. 2023 Jun 2;12:e48183. doi: 10.2196/48183.

Abstract

BACKGROUND

In hospitalized patients with COVID-19, the dosing and timing of corticosteroids vary widely. Low-dose dexamethasone therapy reduces mortality in patients requiring respiratory support, but it remains unclear how to treat patients when this therapy fails. In critically ill patients, high-dose corticosteroids are often administered as salvage late in the disease course, whereas earlier administration may be more beneficial in preventing disease progression. Previous research has revealed that increased levels of various biomarkers are associated with mortality, and whole blood transcriptome sequencing has the ability to identify host factors predisposing to critical illness in patients with COVID-19.

OBJECTIVE

Our goal is to determine the most optimal dosing and timing of corticosteroid therapy and to provide a basis for personalized corticosteroid treatment regimens to reduce morbidity and mortality in hospitalized patients with COVID-19.

METHODS

This is a retrospective, observational, multicenter study that includes adult patients who were hospitalized due to COVID-19 in the Netherlands. We will use the differences in therapeutic strategies between hospitals (per protocol high-dose corticosteroids or not) over time to determine whether high-dose corticosteroids have an effect on the following outcome measures: mechanical ventilation or high-flow nasal cannula therapy, in-hospital mortality, and 28-day survival. We will also explore biomarker profiles in serum and bronchoalveolar lavage fluid and use whole blood transcriptome analysis to determine factors that influence the relationship between high-dose corticosteroids and outcome. Existing databases that contain routinely collected electronic data during ward and intensive care admissions, as well as existing biobanks, will be used. We will apply longitudinal modeling appropriate for each data structure to answer the research questions at hand.

RESULTS

As of April 2023, data have been collected for a total of 1500 patients, with data collection anticipated to be completed by December 2023. We expect the first results to be available in early 2024.

CONCLUSIONS

This study protocol presents a strategy to investigate the effect of high-dose corticosteroids throughout the entire clinical course of hospitalized patients with COVID-19, from hospital admission to the ward or intensive care unit until hospital discharge. Moreover, our exploration of biomarker and gene expression profiles for targeted corticosteroid therapy represents a first step towards personalized COVID-19 corticosteroid treatment.

TRIAL REGISTRATION

ClinicalTrials.gov NCT05403359; https://clinicaltrials.gov/ct2/show/NCT05403359.

INTERNATIONAL REGISTERED REPORT IDENTIFIER (IRRID): DERR1-10.2196/48183.

摘要

背景

在新冠肺炎住院患者中,皮质类固醇的给药剂量和时间差异很大。低剂量地塞米松治疗可降低需要呼吸支持患者的死亡率,但当这种治疗失败时如何治疗患者仍不清楚。在危重症患者中,高剂量皮质类固醇通常在病程后期作为挽救治疗使用,而早期给药可能对预防疾病进展更有益。先前的研究表明,各种生物标志物水平升高与死亡率相关,全血转录组测序能够识别新冠肺炎患者易患危重症的宿主因素。

目的

我们的目标是确定皮质类固醇治疗的最佳给药剂量和时间,并为个性化皮质类固醇治疗方案提供依据,以降低新冠肺炎住院患者的发病率和死亡率。

方法

这是一项回顾性、观察性、多中心研究,纳入了在荷兰因新冠肺炎住院的成年患者。我们将利用不同医院(根据方案是否使用高剂量皮质类固醇)随时间的治疗策略差异,来确定高剂量皮质类固醇对以下结局指标的影响:机械通气或高流量鼻导管治疗、院内死亡率和28天生存率。我们还将探索血清和支气管肺泡灌洗液中的生物标志物谱,并使用全血转录组分析来确定影响高剂量皮质类固醇与结局之间关系的因素。将使用包含病房和重症监护病房入院期间常规收集的电子数据的现有数据库以及现有的生物样本库。我们将应用适合每种数据结构的纵向模型来回答手头的研究问题。

结果

截至2023年4月,共收集了1500例患者的数据,预计数据收集将于2023年12月完成。我们预计首批结果将于2024年初公布。

结论

本研究方案提出了一种策略,用于调查高剂量皮质类固醇在新冠肺炎住院患者从入院到病房或重症监护病房直至出院的整个临床过程中的效果。此外,我们对靶向皮质类固醇治疗的生物标志物和基因表达谱的探索是迈向个性化新冠肺炎皮质类固醇治疗的第一步。

试验注册

ClinicalTrials.gov NCT05403359;https://clinicaltrials.gov/ct2/show/NCT05403359。

国际注册报告识别码(IRRID):DERR1-10.2196/48183。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c8f3/10276318/ebf5d65aa371/resprot_v12i1e48183_fig1.jpg

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