Reina-Couto, Marta
Roboredo-Madeira, Mariana
Pereira-Terra, Patrícia
Silva-Pereira, Carolina
Martins, Sandra
Teixeira-Santos, Luísa
Pinho, Dora
Dias, Andreia
Cordeiro, Gonçalo
Dias, Cláudia Camila
Sarmento, António
Tavares, Margarida
Guimarães, João T.
Roncon-Albuquerque, Roberto
Paiva, José-Artur
Albino-Teixeira, António
Sousa, Teresa
Funding for this research was provided by:
Fundação para a Ciência e a Tecnologia (RESEARCH 4 COVID-19 grant (project 519, reference number: 613690173), RESEARCH 4 COVID-19 grant (project 519, reference number: 613690173), RESEARCH 4 COVID-19 grant (project 519, reference number: 613690173), RESEARCH 4 COVID-19 grant (project 519, reference number: 613690173), RESEARCH 4 COVID-19 grant (project 519, reference number: 613690173), RESEARCH 4 COVID-19 grant (project 519, reference number: 613690173), RESEARCH 4 COVID-19 grant (project 519, reference number: 613690173), RESEARCH 4 COVID-19 grant (project 519, reference number: 613690173), RESEARCH 4 COVID-19 grant (project 519, reference number: 613690173), RESEARCH 4 COVID-19 grant (project 519, reference number: 613690173), RESEARCH 4 COVID-19 grant (project 519, reference number: 613690173), RESEARCH 4 COVID-19 grant (project 519, reference number: 613690173), RESEARCH 4 COVID-19 grant (project 519, reference number: 613690173))
FEDER via COMPETE, Portugal 2020 – Operational Programme for Competitiveness and Internationalization (POCI-01-0145-FEDER-032188)
Fundação para a Ciência e a Tecnologia, Portugal & MedInUP (UI/BD/150816/2020)
Universidade do Porto
Article History
Received: 17 October 2022
Revised: 5 December 2022
Accepted: 16 December 2022
First Online: 8 January 2023
Declarations
:
: The authors declare that there is no conflict of interest regarding the publication of this paper.
: The CHUSJ Health Ethics Committee approved this study [CES 75-16], with project amended specifically for inclusion of subjects with COVID-19, within the scope of a RESEARCH 4 COVID-19 grant from FCT (special support for rapid implementation projects for innovative response solutions to COVID-19 pandemic)].
: All eligible patients provided written informed consent to participate in the study. For ICU patients unable to give consent, this was solicited to their next of kin. These patients provided informed consent retrospectively, where possible. Blood donor volunteers provided oral informed consent.
: All the authors agree to publish this article.