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Cohort profile of Acutelines: a large data/biobank of acute and emergency medicine

PURPOSE: Research in acute care faces many challenges, including enrolment challenges, legal limitations in data sharing, limited funding and lack of singular ownership of the domain of acute care. To overcome these challenges, the Center of Acute Care of the University Medical Center Groningen in t...

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Autores principales: ter Avest, Ewoud, van Munster, Barbara C, van Wijk, Raymond J, Tent, Sanne, Ter Horst, Sanne, Hu, Ting Ting, van Heijst, Lisanne E, van der Veer, Felien S, van Beuningen, Fleur E, ter Maaten, Jan Cornelis, Bouma, Hjalmar R
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8286769/
https://www.ncbi.nlm.nih.gov/pubmed/34266842
http://dx.doi.org/10.1136/bmjopen-2020-047349
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author ter Avest, Ewoud
van Munster, Barbara C
van Wijk, Raymond J
Tent, Sanne
Ter Horst, Sanne
Hu, Ting Ting
van Heijst, Lisanne E
van der Veer, Felien S
van Beuningen, Fleur E
ter Maaten, Jan Cornelis
Bouma, Hjalmar R
author_facet ter Avest, Ewoud
van Munster, Barbara C
van Wijk, Raymond J
Tent, Sanne
Ter Horst, Sanne
Hu, Ting Ting
van Heijst, Lisanne E
van der Veer, Felien S
van Beuningen, Fleur E
ter Maaten, Jan Cornelis
Bouma, Hjalmar R
author_sort ter Avest, Ewoud
collection PubMed
description PURPOSE: Research in acute care faces many challenges, including enrolment challenges, legal limitations in data sharing, limited funding and lack of singular ownership of the domain of acute care. To overcome these challenges, the Center of Acute Care of the University Medical Center Groningen in the Netherlands, has established a de novo data, image and biobank named ‘Acutelines’. PARTICIPANTS: Clinical data, imaging data and biomaterials (ie, blood, urine, faeces, hair) are collected from patients presenting to the emergency department (ED) with a broad range of acute disease presentations. A deferred consent procedure (by proxy) is in place to allow collecting data and biomaterials prior to obtaining written consent. The digital infrastructure used ensures automated capturing of all bed-side monitoring data (ie, vital parameters, electrophysiological waveforms) and securely importing data from other sources, such as the electronic health records of the hospital, ambulance and general practitioner, municipal registration and pharmacy. Data are collected from all included participants during the first 72 hours of their hospitalisation, while follow-up data are collected at 3 months, 1 year, 2 years and 5 years after their ED visit. FINDINGS TO DATE: Enrolment of the first participant occurred on 1 September 2020. During the first month, 653 participants were screened for eligibility, of which 180 were approached as potential participants. In total, 151 (84%) provided consent for participation of which 89 participants fulfilled criteria for collection of biomaterials. FUTURE PLANS: The main aim of Acutelines is to facilitate research in acute medicine by providing the framework for novel studies and issuing data, images and biomaterials for future research. The protocol will be extended by connecting with central registries to obtain long-term follow-up data, for which we already request permission from the participant. TRIAL REGISTRATION NUMBER: NCT04615065.
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spelling pubmed-82867692021-07-30 Cohort profile of Acutelines: a large data/biobank of acute and emergency medicine ter Avest, Ewoud van Munster, Barbara C van Wijk, Raymond J Tent, Sanne Ter Horst, Sanne Hu, Ting Ting van Heijst, Lisanne E van der Veer, Felien S van Beuningen, Fleur E ter Maaten, Jan Cornelis Bouma, Hjalmar R BMJ Open Emergency Medicine PURPOSE: Research in acute care faces many challenges, including enrolment challenges, legal limitations in data sharing, limited funding and lack of singular ownership of the domain of acute care. To overcome these challenges, the Center of Acute Care of the University Medical Center Groningen in the Netherlands, has established a de novo data, image and biobank named ‘Acutelines’. PARTICIPANTS: Clinical data, imaging data and biomaterials (ie, blood, urine, faeces, hair) are collected from patients presenting to the emergency department (ED) with a broad range of acute disease presentations. A deferred consent procedure (by proxy) is in place to allow collecting data and biomaterials prior to obtaining written consent. The digital infrastructure used ensures automated capturing of all bed-side monitoring data (ie, vital parameters, electrophysiological waveforms) and securely importing data from other sources, such as the electronic health records of the hospital, ambulance and general practitioner, municipal registration and pharmacy. Data are collected from all included participants during the first 72 hours of their hospitalisation, while follow-up data are collected at 3 months, 1 year, 2 years and 5 years after their ED visit. FINDINGS TO DATE: Enrolment of the first participant occurred on 1 September 2020. During the first month, 653 participants were screened for eligibility, of which 180 were approached as potential participants. In total, 151 (84%) provided consent for participation of which 89 participants fulfilled criteria for collection of biomaterials. FUTURE PLANS: The main aim of Acutelines is to facilitate research in acute medicine by providing the framework for novel studies and issuing data, images and biomaterials for future research. The protocol will be extended by connecting with central registries to obtain long-term follow-up data, for which we already request permission from the participant. TRIAL REGISTRATION NUMBER: NCT04615065. BMJ Publishing Group 2021-07-15 /pmc/articles/PMC8286769/ /pubmed/34266842 http://dx.doi.org/10.1136/bmjopen-2020-047349 Text en © Author(s) (or their employer(s)) 2021. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) .
spellingShingle Emergency Medicine
ter Avest, Ewoud
van Munster, Barbara C
van Wijk, Raymond J
Tent, Sanne
Ter Horst, Sanne
Hu, Ting Ting
van Heijst, Lisanne E
van der Veer, Felien S
van Beuningen, Fleur E
ter Maaten, Jan Cornelis
Bouma, Hjalmar R
Cohort profile of Acutelines: a large data/biobank of acute and emergency medicine
title Cohort profile of Acutelines: a large data/biobank of acute and emergency medicine
title_full Cohort profile of Acutelines: a large data/biobank of acute and emergency medicine
title_fullStr Cohort profile of Acutelines: a large data/biobank of acute and emergency medicine
title_full_unstemmed Cohort profile of Acutelines: a large data/biobank of acute and emergency medicine
title_short Cohort profile of Acutelines: a large data/biobank of acute and emergency medicine
title_sort cohort profile of acutelines: a large data/biobank of acute and emergency medicine
topic Emergency Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8286769/
https://www.ncbi.nlm.nih.gov/pubmed/34266842
http://dx.doi.org/10.1136/bmjopen-2020-047349
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