跳至主要内容
临床试验/NCT04385069
NCT04385069Unknown不适用

COVID-19 Hyperinflammation Syndrome (COV-HI): Protocol for a Rapidly Executed Cohort Study

University College, London5 个研究点 分布在 1 个国家目标入组 500 人开始时间: 2020年4月16日最近更新:
适应症

试验速览

阶段
不适用
入组人数
500
试验地点
5
主要终点
To collect retrospective demographic information on 500 people admitted to selected hospital sites across the UK with a COVID-19 diagnosis confirmed through positive laboratory PCR swab.

研究概览

简要总结

Based on emerging experience and trials from countries affected early by the COVID-19 (COV19) pandemic, there is evidence that a subgroup of severely affected people develop a hyperinflammatory (HI) syndrome (COV-HI). Trials are in progress of cytokine inhibition and other immune modulation to treat COV-HI. This proposal aims to use a rapidly executed cohort study to characterise the clinical phenotypes of COV-HI in patients in the UK through an established and nimble network of clinicians and scientists with broad experience of identifying and treating HI. The aim is to confirm the COV-HI clinical phenotype and using routine data to try to infer the inflexion point where COV-HI emerges. This would enable refinement of the proposed treatment algorithm and translates to routine clinical practice to improve the outlook for COV-HI.

详细描述

Early information from the UK ICNARC (Intensive Care National Audit and Research Centre)- COVID-19 Study Case Mix Programme Database 27 March 2020 report that critical care unit admissions with COVID-19 totaled 775 patients of whom 79 patients have died, 86 patients were discharged alive from critical care and 609 patients were last reported as still being in critical care. It is imperative to reduce this high death rate. Emerging evidence from China, Italy and the US suggests that in a small subset of patients with severe COVID-19 respiratory disease there is a hyperinflammatory syndrome (COV-HI), which may be contributing to the high mortality and morbidity.

Terminology regarding hyperinflammation is heterogenous. When caused by genetic abnormalities in children it is called primary or familial haemophagocytic lymphohistiocytosis (fHLH). Secondary HLH (sHLH) is a hyperinflammatory process driven by infection, rheumatic disorders and malignancy (usually lymphoproliferative disorders). sHLH is termed macrophage activation syndrome (MAS) when associated with rheumatic disease, macrophage activation-like syndrome (MALS) in sepsis, and cytokine release syndrome (CRS) following immune effector cell therapies (haplo-identical allogeneic stem cell transplantation or CAR-T cell therapy). It is likely that such hyperinflammatory states lie on a spectrum and collectively the clinical phenomenon has been called cytokine storm syndrome (CSS) or hyperinflammation (HI).

Current diagnostic criteria for HI are based on fHLH (HLH-2004 guidelines) and the H score (a weighted composite generating a probability). Recently published management algorithms in adults are based on consensus expert opinion and clinical experience, extrapolated from paediatric literature in fHLH.

The HLH Across-speciality Collaboration (HASC) is a 162-strong group of clinicians/scientists who specialize in the management of patients with hyperinflammation. HASC member include Rheumatologists, Haematologists, Intensivists, Infectious Disease specialists, Immunologists, Virologists, Nephrologists and Gatroenterologists from both adult and paediatric backgrounds. Members of HASC have led the set-up of multidisciplinary team meetings (MDTs) to raise awareness of and manage hyperinflammatory illness, completed national audits to demonstrate hyperinflammation is often missed and have set up HLH registries and bioresources (https://research.ncl.ac.uk/ukhr/).

COVID-19 hyperinflammation (COV-HI): rationale for treatment and summary of available evidence In COVID-19 respiratory failure from acute respiratory distress syndrome (ARDS) is the leading cause of mortality. ARDS is a late pre-terminal event in these patients but there is a reported clinical phenotype of severe COVID-19 where hyperinflammation complicates the respiratory failure, termed here COVID-19 hyperinflammation or COV-HI.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Retrospective

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Adults (18 years and over) admitted to hospital who are COVID-19 positive (PCR positive on a swab, through routine clinical laboratory testing)

排除标准

  • No exclusion criteria

结局指标

主要结局

To collect retrospective demographic information on 500 people admitted to selected hospital sites across the UK with a COVID-19 diagnosis confirmed through positive laboratory PCR swab.

时间窗: within 3 months

Confirm positive diagnosis within electronic hospital records and collate selected demographic data from eligible patients identified.

To record the results of each patient's measured medical observations, clinical investigations and outcomes during the course of their admission.

时间窗: within 3 months

Research staff will review the electronic patient record for all eligible participants and record the results of each patients routine blood tests, chest x-rays, echos and any other associated clinical investigations conducted during the course of their admission onto a database for analysis.

To conduct retrospective analysis of data collected to map each patient's clinical journey during their admission

时间窗: within 3 months of data collection

Research staff will record data collected from eligible patients' electronic medical records from routine blood tests, chest x-rays, echos and any other associated clinical investigations conducted during the course of their admission onto a database and conduct comprehensive analysis.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (5)

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