Cardiogenic Shock in a Hemodialyzed Patient on Flecainide: Treatment with Intravenous Fat Emulsion, Extracorporeal Cardiac Life Support, and CytoSorb® Hemoadsorption.


Journal

Case reports in cardiology
ISSN: 2090-6404
Titre abrégé: Case Rep Cardiol
Pays: United States
ID NLM: 101576452

Informations de publication

Date de publication:
2019
Historique:
received: 22 02 2019
revised: 28 05 2019
accepted: 15 07 2019
entrez: 21 8 2019
pubmed: 21 8 2019
medline: 21 8 2019
Statut: epublish

Résumé

A 67-year-old woman with a history of end-stage renal disease on hemodialysis received a therapeutic dose (150 mg daily) of flecainide for three weeks. She was admitted to the Emergency Department for malaise and dizziness, and the electrocardiogram revealed ventricular tachycardia treated by amiodarone. Hemodynamic condition remained stable, and the toxicity of flecainide was initially not suspected until she developed within 8 hours a cardiogenic shock requiring vasopressors. The patient then received sodium bicarbonate (300 mmol) and dobutamine but experienced cardiac arrest two hours later. The administration of intravenous fat emulsion (IFE) was associated with return of spontaneous circulation, but there was a relapse of cardiovascular shock at the end of IFE infusion. The patient was placed on extracorporeal cardiac life support (ECLS), continuous hemofiltration, and hemoadsorption using the CytoSorb® cartridge. Serial determinations of serum flecainide concentration were obtained during the course of hemoadsorption, with a terminal half-life of 3.7 h during the first four hours and a global plasma clearance of 40.3 ml/min over the first 22 hours. The weaning of ECLS was possible on day 7. Intravenous fat emulsion infusion was followed by a significant increase in serum flecainide concentration. In addition, while conventional techniques of extrarenal epuration usually appear as poorly effective for flecainide removal, a mean plasma clearance of 40.3 ml/min was observed using the hemoadsorption technique based on CytoSorb® cartridge. However, the impact on the clinical course was probably extremely modest in comparison with ECLS.

Identifiants

pubmed: 31428479
doi: 10.1155/2019/1905871
pmc: PMC6681578
doi:

Types de publication

Case Reports

Langues

eng

Pagination

1905871

Déclaration de conflit d'intérêts

The authors report no conflict of interest.

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Auteurs

Nicolas De Schryver (N)

Department of Intensive Care, Clinique St-Pierre, 1340 Ottignies, Belgium.

Philippe Hantson (P)

Department of Intensive Care, Cliniques St-Luc, Université catholique de Louvain, 1200 Brussels, Belgium.
Louvain Centre of Toxicology and Applied Pharmacology, Université catholique de Louvain, 1200 Brussels, Belgium.

Vincent Haufroid (V)

Louvain Centre of Toxicology and Applied Pharmacology, Université catholique de Louvain, 1200 Brussels, Belgium.
Department of Clinical Chemistry, Cliniques St-Luc, Université catholique de Louvain, 1200 Brussels, Belgium.

Mélanie Dechamps (M)

Cardiovascular Intensive Care, Cliniques St-Luc, Université catholique de Louvain, 1200 Brussels, Belgium.

Classifications MeSH