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Propafenone and propranolol dual toxicity

Propranolol is a highly lipid‐soluble beta‐receptor antagonist and propafenone is a potent class 1c anti‐arrhythmic agent with strong Na‐channel blockade effect. We describe a novel case of dual overdose of propafenone and propranolol resulting in hypotension, generalized seizures, and reduced level...

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Autores principales: Farooq, Moonis, Qureshi, Faisal, Kamkoum, Wael, Abuzeyad, Feras
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7593489/
https://www.ncbi.nlm.nih.gov/pubmed/33145565
http://dx.doi.org/10.1002/emp2.12126
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author Farooq, Moonis
Qureshi, Faisal
Kamkoum, Wael
Abuzeyad, Feras
author_facet Farooq, Moonis
Qureshi, Faisal
Kamkoum, Wael
Abuzeyad, Feras
author_sort Farooq, Moonis
collection PubMed
description Propranolol is a highly lipid‐soluble beta‐receptor antagonist and propafenone is a potent class 1c anti‐arrhythmic agent with strong Na‐channel blockade effect. We describe a novel case of dual overdose of propafenone and propranolol resulting in hypotension, generalized seizures, and reduced level of consciousness that was successfully treated. A 52‐year‐old female ingested 500 mg of propranolol and 1.5 g of propafenone. The patient was brought to the emergency department (ED) and exhibited signs of systemic toxicity and reduced level of consciousness. The patient was treated as a case of combined β‐blocker and propafenone toxicity using high dose insulin, NaHCO(3), glucagon, atropine, and dopamine. She started improving and becoming more alert, with subsequent ECGs revealing normal sinus rhythm. The patient was discharged 4 days later. We believe that early administration of NaHCO(3) should be administered in patients exhibiting signs of Na‐channel blockade.
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spelling pubmed-75934892020-11-02 Propafenone and propranolol dual toxicity Farooq, Moonis Qureshi, Faisal Kamkoum, Wael Abuzeyad, Feras J Am Coll Emerg Physicians Open Toxicology Propranolol is a highly lipid‐soluble beta‐receptor antagonist and propafenone is a potent class 1c anti‐arrhythmic agent with strong Na‐channel blockade effect. We describe a novel case of dual overdose of propafenone and propranolol resulting in hypotension, generalized seizures, and reduced level of consciousness that was successfully treated. A 52‐year‐old female ingested 500 mg of propranolol and 1.5 g of propafenone. The patient was brought to the emergency department (ED) and exhibited signs of systemic toxicity and reduced level of consciousness. The patient was treated as a case of combined β‐blocker and propafenone toxicity using high dose insulin, NaHCO(3), glucagon, atropine, and dopamine. She started improving and becoming more alert, with subsequent ECGs revealing normal sinus rhythm. The patient was discharged 4 days later. We believe that early administration of NaHCO(3) should be administered in patients exhibiting signs of Na‐channel blockade. John Wiley and Sons Inc. 2020-06-11 /pmc/articles/PMC7593489/ /pubmed/33145565 http://dx.doi.org/10.1002/emp2.12126 Text en © 2020 The Authors. JACEP Open published by Wiley Periodicals LLC on behalf of the American College of Emergency Physicians. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Toxicology
Farooq, Moonis
Qureshi, Faisal
Kamkoum, Wael
Abuzeyad, Feras
Propafenone and propranolol dual toxicity
title Propafenone and propranolol dual toxicity
title_full Propafenone and propranolol dual toxicity
title_fullStr Propafenone and propranolol dual toxicity
title_full_unstemmed Propafenone and propranolol dual toxicity
title_short Propafenone and propranolol dual toxicity
title_sort propafenone and propranolol dual toxicity
topic Toxicology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7593489/
https://www.ncbi.nlm.nih.gov/pubmed/33145565
http://dx.doi.org/10.1002/emp2.12126
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