Volume 19, Issue 2 pp. 214-216

Treatment of Pyridostigmine-Induced AV Block with Hyoscyamine in a Patient with Myasthenia Gravis

ANIL GEHI M.D.

ANIL GEHI M.D.

Section of Cardiac Electrophysiology, Division of Cardiology

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MICHAEL BENATAR M.D., Ph.D.

MICHAEL BENATAR M.D., Ph.D.

Department of Neurology, Emory University School of Medicine, Atlanta, Georgia, USA

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JONATHAN LANGBERG M.D.

JONATHAN LANGBERG M.D.

Section of Cardiac Electrophysiology, Division of Cardiology

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First published: 25 October 2007
Citations: 13
Address for correspondence: Anil Gehi, M.D., 1364 Clifton Rd. NE, Suite 424, Atlanta, GA 30322. Fax: 404-712-4948; E-mail: [email protected]

Manuscript received 15 May 2007; Revised manuscript received 19 June 2007; Accepted for publication 3 July 2007.

Abstract

Myasthenia gravis is an autoimmune disorder of the nervous system typically mediated by antibodies against the nicotinic acetylcholine receptor at the neuromuscular junction. Treatment of myasthenia gravis frequently involves the use of cholinesterase inhibitors such as pyridostigmine. Treatment with these agents has been associated with bradycardia and syncope requiring pacemaker implantation. We report a case of a 60-year-old man with a 1-year history of myasthenia gravis treated with pyridostigmine who presented with syncope due to high degree AV block. Before committing the patient to a permanent pacemaker, a trial of medical therapy with hyoscyamine was attempted. Hyoscyamine is a muscarinic antagonist commonly used to block cholinergic side effects associated with pyridostigmine without reducing its efficacy at the neuromuscular junction. Treatment with hyoscyamine resulted in complete resolution of AV block, thereby avoiding pacemaker implantation.

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