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Dutch multicentre, prospective follow-up, cohort study comparing the neurological and neuropsychological sequelae of hospitalised non-ICU- and ICU-treated COVID-19 survivors: a study protocol.
Klinkhammer, Simona; Horn, Janneke; Visser-Meilij, Johanna M A; Verwijk, Esmée; Duits, Annelien; Slooter, Arjen J C; van Heugten, Caroline M.
  • Klinkhammer S; Department of Psychiatry and Neuropsychology, Maastricht University Faculty of Health Medicine and Life Sciences, Maastricht, The Netherlands.
  • Horn J; School for Mental Health and Neuroscience, Maastricht University, Maastricht, The Netherlands.
  • Visser-Meilij JMA; Department of Intensive Care, Amsterdam UMC Locatie AMC, Amsterdam, The Netherlands.
  • Verwijk E; Amsterdam Neuroscience, Amsterdam UMC Locatie AMC, Amsterdam, The Netherlands.
  • Duits A; Department of Rehabilitation, Physical Therapy Science and Sports, UMC Utrecht, Utrecht, The Netherlands.
  • Slooter AJC; UMC Utrecht Brain Center, UMC Utrecht, Utrecht, The Netherlands.
  • van Heugten CM; Department of Medical Psychology, Amsterdam UMC Locatie AMC, Amsterdam, The Netherlands.
BMJ Open ; 11(10): e054901, 2021 10 07.
Article in English | MEDLINE | ID: covidwho-1462977
ABSTRACT

INTRODUCTION:

Owing to the novelty of COVID-19, there are still large knowledge gaps concerning its effect on the brain and the resulting impact on peoples' lives. This large-scale prospective follow-up study investigates COVID-19-associated brain damage, neuropsychological dysfunction and long-term impact on the well-being of patients and their close ones. It is hypothesised that structural brain damage and cognitive dysfunction primarily occur in severely ill patients, as compared with moderately ill patients. Cognitive complaints, emotional distress and impact on well-being are hypothesised to be less dependent on illness severity. METHODS AND

ANALYSIS:

For this multicentre study, 200 patients with COVID-19 (100 intensive care unit (ICU) patients and 100 non-ICU patients) formerly hospitalised in one of the six recruiting hospitals during the first European infection wave (ie, March to June 2020) and their close ones will be recruited. At minimally 6 months posthospital discharge, patients will perform a set of neuropsychological tests and are subjected to a 3T MRI scan. Patients and close ones will fill out a set of questionnaires, also at minimally 6 months posthospital discharge and again another 6 months thereafter. Data related to COVID-19 hospitalisation will be extracted from the patients' medical records. MRI abnormalities will ultimately be related to neuropsychological test performance and questionnaire outcomes. ETHICS AND DISSEMINATION Ethics approval was granted by the medical research ethics committee of Maastricht University Medical Centre and Maastricht University (NL75102.068.20). The project is sponsored by The Brain Foundation Netherlands. Findings will be presented at national and international conferences, as well as published in peer-reviewed scientific journals. TRIAL REGISTRATION NUMBER NCT04745611.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: COVID-19 Type of study: Cohort study / Observational study / Prognostic study / Randomized controlled trials Topics: Long Covid Limits: Humans Language: English Journal: BMJ Open Year: 2021 Document Type: Article Affiliation country: Bmjopen-2021-054901

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Full text: Available Collection: International databases Database: MEDLINE Main subject: COVID-19 Type of study: Cohort study / Observational study / Prognostic study / Randomized controlled trials Topics: Long Covid Limits: Humans Language: English Journal: BMJ Open Year: 2021 Document Type: Article Affiliation country: Bmjopen-2021-054901