Neuropsychological outcome after cardiac arrest: results from a sub-study of the targeted hypothermia versus targeted normothermia after out-of-hospital cardiac arrest (TTM2) trial.


Journal

Critical care (London, England)
ISSN: 1466-609X
Titre abrégé: Crit Care
Pays: England
ID NLM: 9801902

Informations de publication

Date de publication:
26 08 2023
Historique:
received: 02 06 2023
accepted: 16 08 2023
medline: 28 8 2023
pubmed: 27 8 2023
entrez: 26 8 2023
Statut: epublish

Résumé

Cognitive impairment is common following out-of-hospital cardiac arrest (OHCA), but the nature of the impairment is poorly understood. Our objective was to describe cognitive impairment in OHCA survivors, with the hypothesis that OHCA survivors would perform significantly worse on neuropsychological tests of cognition than controls with acute myocardial infarction (MI). Another aim was to investigate the relationship between cognitive performance and the associated factors of emotional problems, fatigue, insomnia, and cardiovascular risk factors following OHCA. This was a prospective case-control sub-study of The Targeted Hypothermia versus Targeted Normothermia after Out-of-Hospital Cardiac Arrest (TTM2) trial. Eight of 61 TTM2-sites in Sweden, Denmark, and the United Kingdom included adults with OHCA of presumed cardiac or unknown cause. A matched non-arrest control group with acute MI was recruited. At approximately 7 months post-event, we administered an extensive neuropsychological test battery and questionnaires on anxiety, depression, fatigue, and insomnia, and collected information on the cardiovascular risk factors hypertension and diabetes. Of 184 eligible OHCA survivors, 108 were included, with 92 MI controls enrolled. Amongst OHCA survivors, 29% performed z-score ≤ - 1 (at least borderline-mild impairment) in ≥ 2 cognitive domains, 14% performed z-score ≤ - 2 (major impairment) in ≥ 1 cognitive domain while 54% performed without impairment in any domain. Impairment was most pronounced in episodic memory, executive functions, and processing speed. OHCA survivors performed significantly worse than MI controls in episodic memory (mean difference, MD = - 0.37, 95% confidence intervals [- 0.61, - 0.12]), verbal (MD = - 0.34 [- 0.62, - 0.07]), and visual/constructive functions (MD = - 0.26 [- 0.47, - 0.04]) on linear regressions adjusted for educational attainment and sex. When additionally adjusting for anxiety, depression, fatigue, insomnia, hypertension, and diabetes, executive functions (MD = - 0.44 [- 0.82, - 0.06]) were also worse following OHCA. Diabetes, symptoms of anxiety, depression, and fatigue were significantly associated with worse cognitive performance. In our study population, cognitive impairment was generally mild following OHCA. OHCA survivors performed worse than MI controls in 3 of 6 domains. These results support current guidelines that a post-OHCA follow-up service should screen for cognitive impairment, emotional problems, and fatigue. ClinicalTrials.gov, NCT03543371. Registered 1 June 2018.

Sections du résumé

BACKGROUND
Cognitive impairment is common following out-of-hospital cardiac arrest (OHCA), but the nature of the impairment is poorly understood. Our objective was to describe cognitive impairment in OHCA survivors, with the hypothesis that OHCA survivors would perform significantly worse on neuropsychological tests of cognition than controls with acute myocardial infarction (MI). Another aim was to investigate the relationship between cognitive performance and the associated factors of emotional problems, fatigue, insomnia, and cardiovascular risk factors following OHCA.
METHODS
This was a prospective case-control sub-study of The Targeted Hypothermia versus Targeted Normothermia after Out-of-Hospital Cardiac Arrest (TTM2) trial. Eight of 61 TTM2-sites in Sweden, Denmark, and the United Kingdom included adults with OHCA of presumed cardiac or unknown cause. A matched non-arrest control group with acute MI was recruited. At approximately 7 months post-event, we administered an extensive neuropsychological test battery and questionnaires on anxiety, depression, fatigue, and insomnia, and collected information on the cardiovascular risk factors hypertension and diabetes.
RESULTS
Of 184 eligible OHCA survivors, 108 were included, with 92 MI controls enrolled. Amongst OHCA survivors, 29% performed z-score ≤ - 1 (at least borderline-mild impairment) in ≥ 2 cognitive domains, 14% performed z-score ≤ - 2 (major impairment) in ≥ 1 cognitive domain while 54% performed without impairment in any domain. Impairment was most pronounced in episodic memory, executive functions, and processing speed. OHCA survivors performed significantly worse than MI controls in episodic memory (mean difference, MD = - 0.37, 95% confidence intervals [- 0.61, - 0.12]), verbal (MD = - 0.34 [- 0.62, - 0.07]), and visual/constructive functions (MD = - 0.26 [- 0.47, - 0.04]) on linear regressions adjusted for educational attainment and sex. When additionally adjusting for anxiety, depression, fatigue, insomnia, hypertension, and diabetes, executive functions (MD = - 0.44 [- 0.82, - 0.06]) were also worse following OHCA. Diabetes, symptoms of anxiety, depression, and fatigue were significantly associated with worse cognitive performance.
CONCLUSIONS
In our study population, cognitive impairment was generally mild following OHCA. OHCA survivors performed worse than MI controls in 3 of 6 domains. These results support current guidelines that a post-OHCA follow-up service should screen for cognitive impairment, emotional problems, and fatigue.
TRIAL REGISTRATION
ClinicalTrials.gov, NCT03543371. Registered 1 June 2018.

Identifiants

pubmed: 37633944
doi: 10.1186/s13054-023-04617-0
pii: 10.1186/s13054-023-04617-0
pmc: PMC10463667
doi:

Banques de données

ClinicalTrials.gov
['NCT03543371']

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

328

Subventions

Organisme : Skane University Hospital Foundations
ID : 2019-o000032

Informations de copyright

© 2023. BioMed Central Ltd., part of Springer Nature.

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Auteurs

Erik Blennow Nordström (E)

Neurology, Department of Clinical Sciences Lund, Skane University Hospital, Lund University, Lund, Sweden. erik.blennow_nordstrom@med.lu.se.

Susanna Vestberg (S)

Department of Psychology, Lund University, Lund, Sweden.

Lars Evald (L)

Hammel Neurorehabilitation Centre and University Research Clinic, Hammel, Denmark.

Marco Mion (M)

Essex Cardiothoracic Centre, Mid and South Essex NHS Foundation Trust, Basildon, UK.
Medical Technology Research Centre, Anglia Ruskin School of Medicine, Chelmsford, UK.

Magnus Segerström (M)

Department of Neurology and Department of Cardiology, Sahlgrenska University Hospital, Gothenburg, Sweden.

Susann Ullén (S)

Clinical Studies Sweden - Forum South, Skane University Hospital, Lund, Sweden.

John Bro-Jeppesen (J)

Department of Cardiology, Aarhus University Hospital, Aarhus, Denmark.

Hans Friberg (H)

Intensive and Perioperative Care, Department of Clinical Sciences Lund, Skane University Hospital, Lund University, Malmö, Sweden.

Katarina Heimburg (K)

Neurology, Department of Clinical Sciences Lund, Skane University Hospital, Lund University, Lund, Sweden.

Anders M Grejs (AM)

Department of Intensive Care Medicine and Department of Clinical Medicine, Aarhus University Hospital and Aarhus University, Aarhus, Denmark.

Thomas R Keeble (TR)

Essex Cardiothoracic Centre, Mid and South Essex NHS Foundation Trust, Basildon, UK.
Medical Technology Research Centre, Anglia Ruskin School of Medicine, Chelmsford, UK.

Hans Kirkegaard (H)

Research Centre for Emergency Medicine, Emergency Department and Department of Clinical Medicine, Aarhus University Hospital and Aarhus University, Aarhus, Denmark.

Hanna Ljung (H)

Neurology, Department of Clinical Sciences Lund, Skane University Hospital, Lund University, Lund, Sweden.

Sofia Rose (S)

Clinical Psychology, Cardiff and Vale University Health Board, NHS Wales, Cardiff, UK.

Matthew P Wise (MP)

Adult Critical Care, University Hospital of Wales, Cardiff, UK.

Christian Rylander (C)

Anaesthesiology and Intensive Care Medicine, Department of Surgical Sciences, Uppsala University, Uppsala, Sweden.

Johan Undén (J)

Intensive and Perioperative Care, Department of Clinical Sciences Lund, Skane University Hospital, Lund University, Malmö, Sweden.
Operation and Intensive Care, Hallands Hospital Halmstad, Halmstad, Sweden.

Niklas Nielsen (N)

Anesthesiology and Intensive Care, Department of Clinical Sciences Lund, Helsingborg Hospital, Lund University, Lund, Sweden.

Tobias Cronberg (T)

Neurology, Department of Clinical Sciences Lund, Skane University Hospital, Lund University, Lund, Sweden.

Gisela Lilja (G)

Neurology, Department of Clinical Sciences Lund, Skane University Hospital, Lund University, Lund, Sweden.

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