Abstract
Myasthenia gravis (MG) is an autoimmune disorder caused by a decrease in functional acetylcholine receptors at the neuromuscular junction resulting from their destruction or inactivation by antibodies. Patients with MG can experience marked sensitivity to nondepolarizing neuromuscular blocking agents (NMBAs), and require specialized anesthetic care because of their increased risk of postoperative weakness and respiratory failure. Since pyridostigmine, a cholinesterase inhibitor, is a mainstay of MG treatment, the conventional neostigmine antagonism is unfavorable. Sugammadex is a direct, selective antagonist of aminosteroid NMBAs. It is a cyclodextrin derivative that irreversibly encapsulates rocuronium or vecuronium to terminate its action at the nicotinic receptor. Sugammadex is not reliant on acetylcholinesterase or any receptor system and appears to be capable of antagonizing profound neuromuscular blockade (NMB).
Sigma Membership
Non-member
Lead Author Affiliation
Samford University, Birmingham, Alabama, USA
Type
DNP Capstone Project
Format Type
Text-based Document
Study Design/Type
N/A
Research Approach
N/A
Keywords:
Myasthenia Gravis, Sugammadex, Residual Neuromuscular Blockade
Advisor
Herbinger, Lisa
Second Advisor
Greenway, Mary Beth
Degree
DNP
Degree Grantor
Samford University
Degree Year
2021
Recommended Citation
Harrison, Presley, "Sugammadex in patients with Myasthenia Gravis" (2021). Group: Samford University Moffett & Sanders School of Nursing. 13.
https://www.sigmarepository.org/samford/13
Rights Holder
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Review Type
None: Degree-based Submission
Acquisition
Proxy-submission
Date of Issue
2021-03-24
Full Text of Presentation
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