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Deprecated: Implicit conversion from float 267.2 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Infection 2020 ; 48 (4): 619-626 Nephropedia Template TP
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Studying the pathophysiology of coronavirus disease 2019: a protocol for the Berlin prospective COVID-19 patient cohort (Pa-COVID-19) #MMPMID32535877
Kurth F; Roennefarth M; Thibeault C; Corman VM; Muller-Redetzky H; Mittermaier M; Ruwwe-Glosenkamp C; Heim KM; Krannich A; Zvorc S; Schmidt S; Kretzler L; Dang-Heine C; Rose M; Hummel M; Hocke A; Hubner RH; Opitz B; Mall MA; Rohmel J; Landmesser U; Pieske B; Knauss S; Endres M; Spranger J; Mockenhaupt FP; Tacke F; Treskatsch S; Angermair S; Siegmund B; Spies C; Weber-Carstens S; Eckardt KU; Schurmann D; Uhrig A; Stegemann MS; Zoller T; Drosten C; Suttorp N; Witzenrath M; Hippenstiel S; von Kalle C; Sander LE
Infection 2020[Aug]; 48 (4): 619-626 PMID32535877show ga
PURPOSE: Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has spread worldwide causing a global health emergency. Pa-COVID-19 aims to provide comprehensive data on clinical course, pathophysiology, immunology and outcome of COVID-19, to identify prognostic biomarkers, clinical scores, and therapeutic targets for improved clinical management and preventive interventions. METHODS: Pa-COVID-19 is a prospective observational cohort study of patients with confirmed SARS-CoV-2 infection treated at Charite - Universitatsmedizin Berlin. We collect data on epidemiology, demography, medical history, symptoms, clinical course, and pathogen testing and treatment. Systematic, serial blood sampling will allow deep molecular and immunological phenotyping, transcriptomic profiling, and comprehensive biobanking. Longitudinal data and sample collection during hospitalization will be supplemented by long-term follow-up. RESULTS: Outcome measures include the WHO clinical ordinal scale on day 15 and clinical, functional, and health-related quality-of-life assessments at discharge and during follow-up. We developed a scalable dataset to (i) suit national standards of care, (ii) facilitate comprehensive data collection in medical care facilities with varying resources, and (iii) allow for rapid implementation of interventional trials based on the standardized study design and data collection. We propose this scalable protocol as blueprint for harmonized data collection and deep phenotyping in COVID-19 in Germany. CONCLUSION: We established a basic platform for harmonized, scalable data collection, pathophysiological analysis, and deep phenotyping of COVID-19, which enables rapid generation of evidence for improved medical care and identification of candidate therapeutic and preventive strategies. The electronic database accredited for interventional trials allows fast trial implementation for candidate therapeutic agents. TRIAL REGISTRATION: Registered at the German registry for clinical studies (DRKS00021688).