Cytokine hemoadsorption with CytoSorb<sup>®</sup> in post-cardiac arrest syndrome, a pilot randomized controlled trial.

Détails

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Etat: Public
Version: Final published version
Licence: CC BY 4.0
ID Serval
serval:BIB_C87FFD6CE79A
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
Cytokine hemoadsorption with CytoSorb<sup>®</sup> in post-cardiac arrest syndrome, a pilot randomized controlled trial.
Périodique
Critical care
Auteur⸱e⸱s
Monard C., Bianchi N., Poli E., Altarelli M., Debonneville A., Oddo M., Liaudet L., Schneider A.
ISSN
1466-609X (Electronic)
ISSN-L
1364-8535
Statut éditorial
Publié
Date de publication
23/01/2023
Peer-reviewed
Oui
Volume
27
Numéro
1
Pages
36
Langue
anglais
Notes
Publication types: Randomized Controlled Trial ; Journal Article
Publication Status: epublish
Résumé
Hemoadsorption (HA) might mitigate the systemic inflammatory response associated with post-cardiac arrest syndrome (PCAS) and improve outcomes. Here, we investigated the feasibility, safety and efficacy of HA with CytoSorb <sup>®</sup> in cardiac arrest (CA) survivors at risk of PCAS.
In this pilot randomized controlled trial, we included patients admitted to our intensive care unit following CA and likely to develop PCAS: required norepinephrine (> 0.2 µg/kg/min), and/or had serum lactate > 6 mmol/l and/or a time-to-return of spontaneous circulation (ROSC) > 25 min. Those requiring ECMO or renal replacement therapy were excluded. Eligible patients were randomly allocated to either receive standard of care (SOC) or SOC plus HA. Hemoadsorption was performed as stand-alone therapy for 24 h, using CytoSorb <sup>®</sup> and regional heparin-protamine anticoagulation. We collected feasibility, safety and clinical data as well as serial plasma cytokines levels within 72 h of randomization.
We enrolled 21 patients, of whom 16 (76%) had out-of-hospital CA. Median (IQR) time-to-ROSC was 30 (20, 45) minutes. Ten were assigned to the HA group and 11 to the SOC group. Hemoadsorption was initiated in all patients allocated to the HA group within 18 (11, 23) h of ICU admission and conducted for a median duration of 21 (14, 24) h. The intervention was well tolerated except for a trend for a higher rate of aPTT elevation (5 (50%) vs 2 (18%) p = 0.18) and mild (100-150 G/L) thrombocytopenia at day 1 (5 (50%) vs 2 (18%) p = 0.18). Interleukin (IL)-6 plasma levels at randomization were low (< 100 pg/mL) in 10 (48%) patients and elevated (> 1000 pg/mL) in 6 (29%). The median relative reduction in IL-6 at 48 h was 75% (60, 94) in the HA group versus 5% (- 47, 70) in the SOC group (p = 0.06).
In CA survivors at risk of PCAS, HA was feasible, safe and was associated with a nonsignificant reduction in cytokine plasma levels. Future trials are needed to further define the role of HA after CA. Those studies should include cytokine assessment to enrich the study population.
NCT03523039, registered 14 May 2018.
Mots-clé
Humans, Cytokines, Post-Cardiac Arrest Syndrome, Pilot Projects, Interleukin-6, Out-of-Hospital Cardiac Arrest/chemically induced, Cardiac arrest, Cytokine hemoadsorption, Extracorporeal blood purification, Hemoperfusion, Inflammation, Post-cardiac arrest syndrome
Pubmed
Web of science
Open Access
Oui
Création de la notice
31/01/2023 16:29
Dernière modification de la notice
16/08/2023 7:15
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