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Questions and Answers
What is the gold standard for testing for malignant hyperthermia?
What is the gold standard for testing for malignant hyperthermia?
Which of the following is NOT a characteristic of the pathogenesis of malignant hyperthermia?
Which of the following is NOT a characteristic of the pathogenesis of malignant hyperthermia?
What is the primary underlying cause of the hypermetabolic state seen in malignant hyperthermia?
What is the primary underlying cause of the hypermetabolic state seen in malignant hyperthermia?
Which of the following is NOT a common clinical manifestation of malignant hyperthermia?
Which of the following is NOT a common clinical manifestation of malignant hyperthermia?
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Which of the following is a risk factor for postoperative nausea and vomiting (PONV)?
Which of the following is a risk factor for postoperative nausea and vomiting (PONV)?
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What is the leading cause of delayed discharge from the post-anesthesia care unit (PACU)?
What is the leading cause of delayed discharge from the post-anesthesia care unit (PACU)?
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Which of the following is NOT a cause of temporary pseudocholinesterase deficiency?
Which of the following is NOT a cause of temporary pseudocholinesterase deficiency?
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What is the purpose of the dibucaine number test?
What is the purpose of the dibucaine number test?
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Which of the following is NOT an example of a disease state that can cause pseudocholinesterase deficiency?
Which of the following is NOT an example of a disease state that can cause pseudocholinesterase deficiency?
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What is the significance of pseudocholinesterase deficiency in relation to the use of succinylcholine?
What is the significance of pseudocholinesterase deficiency in relation to the use of succinylcholine?
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Which of the following is responsible for the metabolism of succinylcholine?
Which of the following is responsible for the metabolism of succinylcholine?
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Study Notes
Malignant Hyperthermia (MH)
- A hypermetabolic state characterized by tachycardia, hyperthermia, hypercarbia, hypoxemia, and acidosis (metabolic)
- Muscle rigidity and DIC are common complications
- Asymptomatic until triggered, typically by exposure to succinylcholine and volatile anesthetic agents
- 3 times greater incidence in children than adults
Genetic Testing for MH
- Gold standard for testing: Caffeine-halothane contracture test
- Genetic component of the ryanodine receptor (RYR1 gene) is associated with MH
Associated Conditions
- Strabismus
- Scoliosis
- Burkitt lymphoma
- Neuroleptic malignant syndrome
- Myelomeningocele
- Congenital hip dislocations
Post-Operative Nausea and Vomiting (PONV)
- Strong association with motion sickness
- Risk factors: female, young, laparoscopic, ear, breast, colon, or eye surgery, non-smoker, use of volatile agents, and use of nitrous oxide
- 30% of all patients undergoing general anesthesia (GA) experience PONV
- 70% of at-risk patients undergoing GA experience PONV
- Leading cause of delayed PACU discharge and 2nd leading cause of hospital re-admission within 24 hours
Pseudocholinesterase Deficiency
- Succinylcholine is the only depolarizing agent used, metabolized by plasma cholinesterase (pseudocholinesterase)
- Prolonged paralysis and apnea can occur due to deficiency
- Genetic component: three distinct allele phenotypes
- Disease states: hepatic failure, malnutrition, acute infection, carcinoma
- Drug therapy: neostigmine, oral contraceptives
- Alterations in enzyme activity: 3rd trimester of pregnancy, newborns, and infants
Dibucaine Number
- Dibucaine inhibits metabolism of a choline substrate by plasma cholinesterase
- Percentage of inhibition of plasma cholinesterase by dibucaine is the dibucaine number
- Dibucaine number can help diagnose pseudocholinesterase deficiency: normal is 80%, atypical is 20%
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Description
Test your knowledge on anesthesia-specific topics like Pseudocholinesterase deficiency, Malignant hyperthermia, Post-op nausea and vomiting, and Difficult airway. Learn about Succinylcholine metabolism, prolonged paralysis, and apnea.
