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Verapamil-associated cardiogenic shock in a 71-year-old man with myasthenia gravis: a case report

INTRODUCTION: Myasthenia gravis is a rare neuromuscular disorder associated with a reduction in the availability of acetylcholine receptors at the post-synaptic membranes of skeletal muscles. This is caused by the production of anti-acetylcholine receptor antibodies at the neuromuscular junction due...

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Autores principales: Drolet, Benoit, Gabra, Geneviève, Simard, Chantale, Noël, Bernard, Poirier, Paul
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2726557/
https://www.ncbi.nlm.nih.gov/pubmed/19830220
http://dx.doi.org/10.4076/1752-1947-3-8219
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author Drolet, Benoit
Gabra, Geneviève
Simard, Chantale
Noël, Bernard
Poirier, Paul
author_facet Drolet, Benoit
Gabra, Geneviève
Simard, Chantale
Noël, Bernard
Poirier, Paul
author_sort Drolet, Benoit
collection PubMed
description INTRODUCTION: Myasthenia gravis is a rare neuromuscular disorder associated with a reduction in the availability of acetylcholine receptors at the post-synaptic membranes of skeletal muscles. This is caused by the production of anti-acetylcholine receptor antibodies at the neuromuscular junction due to an autoimmune insult, leading to a compromised neuromuscular transmission. Verapamil can influence, in a dose-dependent fashion, the neuromuscular transmission in myasthenia gravis. CASE PRESENTATION: We report a 71-year-old Caucasian man with myasthenia gravis suffering from a cardiogenic shock following a single dose of verapamil. The patient had uncontrolled atrial fibrillation with a heart rate of 120 beats/min. Atenolol 100 mg was started. The next day, verapamil SR 240 mg was started. Two hours after the first dose of verapamil, the patient complained of weakness and dyspnea with signs of shock; his blood pressure was 70/50 mm Hg and heart rate at 101 beats/min. An echocardiogram showed diffuse hypokinesis of both ventricles with an ejection fraction of 20%. Cardiac catheterization was performed and coronary arteries appeared without significant stenosis, but there was a diffuse hypokinesis. Verapamil was stopped and the patient received intravenous glucagon and calcium chloride. Both the anti-acetylcholine receptor and anti-striated muscle antibodies tested positive. A few hours later, another echocardiogram showed an improvement in the ventricular function, which returned to normal five days later. CONCLUSION: Caution is needed when administering verapamil to patients with myasthenia gravis, especially when the anti-acetylcholine receptor and anti-striated muscle antibodies titres are positive.
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spelling pubmed-27265572009-10-14 Verapamil-associated cardiogenic shock in a 71-year-old man with myasthenia gravis: a case report Drolet, Benoit Gabra, Geneviève Simard, Chantale Noël, Bernard Poirier, Paul J Med Case Reports Case report INTRODUCTION: Myasthenia gravis is a rare neuromuscular disorder associated with a reduction in the availability of acetylcholine receptors at the post-synaptic membranes of skeletal muscles. This is caused by the production of anti-acetylcholine receptor antibodies at the neuromuscular junction due to an autoimmune insult, leading to a compromised neuromuscular transmission. Verapamil can influence, in a dose-dependent fashion, the neuromuscular transmission in myasthenia gravis. CASE PRESENTATION: We report a 71-year-old Caucasian man with myasthenia gravis suffering from a cardiogenic shock following a single dose of verapamil. The patient had uncontrolled atrial fibrillation with a heart rate of 120 beats/min. Atenolol 100 mg was started. The next day, verapamil SR 240 mg was started. Two hours after the first dose of verapamil, the patient complained of weakness and dyspnea with signs of shock; his blood pressure was 70/50 mm Hg and heart rate at 101 beats/min. An echocardiogram showed diffuse hypokinesis of both ventricles with an ejection fraction of 20%. Cardiac catheterization was performed and coronary arteries appeared without significant stenosis, but there was a diffuse hypokinesis. Verapamil was stopped and the patient received intravenous glucagon and calcium chloride. Both the anti-acetylcholine receptor and anti-striated muscle antibodies tested positive. A few hours later, another echocardiogram showed an improvement in the ventricular function, which returned to normal five days later. CONCLUSION: Caution is needed when administering verapamil to patients with myasthenia gravis, especially when the anti-acetylcholine receptor and anti-striated muscle antibodies titres are positive. BioMed Central 2009-06-16 /pmc/articles/PMC2726557/ /pubmed/19830220 http://dx.doi.org/10.4076/1752-1947-3-8219 Text en Copyright ©2009 licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case report
Drolet, Benoit
Gabra, Geneviève
Simard, Chantale
Noël, Bernard
Poirier, Paul
Verapamil-associated cardiogenic shock in a 71-year-old man with myasthenia gravis: a case report
title Verapamil-associated cardiogenic shock in a 71-year-old man with myasthenia gravis: a case report
title_full Verapamil-associated cardiogenic shock in a 71-year-old man with myasthenia gravis: a case report
title_fullStr Verapamil-associated cardiogenic shock in a 71-year-old man with myasthenia gravis: a case report
title_full_unstemmed Verapamil-associated cardiogenic shock in a 71-year-old man with myasthenia gravis: a case report
title_short Verapamil-associated cardiogenic shock in a 71-year-old man with myasthenia gravis: a case report
title_sort verapamil-associated cardiogenic shock in a 71-year-old man with myasthenia gravis: a case report
topic Case report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2726557/
https://www.ncbi.nlm.nih.gov/pubmed/19830220
http://dx.doi.org/10.4076/1752-1947-3-8219
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