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Long-Term Outcomes After Cardiac Arrest: Protocol for the Extended Follow-Up Sub-Study of the STEPCARE Trial

Gisela Lilja, Dorit Töniste, Frances Bass, Janus Christian Jakobsen, Niklas Nielsen, Markus B Skrifvars, Susann Ullén, Josef Dankiewicz, Helena Levin, Johanna Hästbacka, Marion Moseby Knappe, Manoj Saxena, Matt P Wise, Paul Young, Anders Aneman, Koen Ameloot, Jade M Cole, Tobias Cronberg, Anthony Delaney, Patrick DruwéJoachim During, Tobias Graf, Matthias Haenggi, Katarina Heimburg, Manuela Itens, Caroline Kamp Barkholt, Thomas R Keeble, Christoph Leithner, Anna Lybeck, Andreas Lundin, Peter McGuigan, Annerose Mengel, Tuomas Oksanen, John Ridgway, Luis Romundstad, Claudia Schrag, Pascal Stammet, Anna Tippett, Matthew Thomas, Joonas Tirkkonen, Johan Undén, Bala Venkatesh, Marjaana Tiainen, Naomi Hammond

Abstract

BACKGROUND: The international multi-center randomized controlled STEPCARE-trial will investigate optimal management of sedation, temperature, and mean arterial pressure (MAP) during intensive care in out-of-hospital cardiac arrest (OHCA) patients due to various etiologies. The primary outcome is mortality at 6 months. This protocol describes an extended follow-up sub-study of the STEPCARE-trial with the main objective to provide detailed long-term outcomes for survivors and caregivers. It will focus on potential neuroprotection and improved recovery for different targets of sedation, temperature, and MAP management at 6 and 12 months post-OHCA.

METHODS: All survivors and one caregiver per survivor at selected STEPCARE sites will be invited to participate. Randomization is stratified by site. This sub-study extends the main STEPCARE follow-up at 6 months by undertaking detailed assessments, face-to-face meetings, inclusion of a caregiver, and repeating the assessments at 12 months. Our main outcome for survivors is cognitive function measured by the Montreal Cognitive Assessment, and for caregivers, the caregiver burden measured by the Zarit Burden Interview. Additional outcomes include symptoms of anxiety, depression, post-traumatic stress disorder, fatigue, physical function, life satisfaction, and life impact (disability), assessed by psychometrically robust measures. The estimated sample size is 600. Efforts to improve interrater reliability and decrease missing data are integral to the study design.

CONCLUSION: These detailed long-term outcomes will explore the possible benefits or risks of fever, sedation, and blood pressure management in post-OHCA survivors. Additionally, this study will explore survivorship after cardiac arrest from various perspectives, including different causes of arrest.

CLINICALTRIALS: gov: NCT0207942.

OriginalspracheEnglisch
Aufsatznummere70114
ZeitschriftActa Anaesthesiologica Scandinavica
Jahrgang69
Ausgabenummer9
Seiten (von - bis)e70114
ISSN0001-5172
PublikationsstatusVeröffentlicht - 10.2025

Fördermittel

This work was supported by The Swedish Research Council; ALF‐project funding within the Swedish Health Care; Skane University Hospital Foundations; scientific council from Region Halland; the Hans‐Gabriel and Alice Trolle‐Wachtmeisters Foundation for Medical Research; Skåne County Council's Research and Development Foundation; National Health and Medical Research Council APP2015994; The Academy of Finland, 341277; Hospital district of Helsinki and Uusimaa, 199449; Health Research Council of New Zealand. Funding:

TrägerTrägernummer
Skåne County Council's Research and Development Foundation
Hans-Gabriel och Alice Trolle-Wachtmeisters stiftelse för medicinsk forskning
Swedish Health Care
Health Research Council of New Zealand
Region Halland
Skånes universitetssjukhus
Vetenskapsrådet
National Health and Medical Research CouncilAPP2015994
Research Council of Finland341277

    UN SDGs

    Dieser Output leistet einen Beitrag zu folgendem(n) Ziel(en) für nachhaltige Entwicklung

    1. SDG 3 – Gesundheit und Wohlergehen
      SDG 3 – Gesundheit und Wohlergehen

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