reviewOrphanet Journal of Rare DiseasesAug 3, 2015GOLD OA

Malignant hyperthermia: a review

Saint Barnabas Medical Center · Palmerston North Hospital · +1 more institution

PubMed
Indexed incrossrefdoajpubmed

Abstract

Malignant hyperthermia (MH) is a pharmacogenetic disorder of skeletal muscle that presents as a hypermetabolic response to potent volatile anesthetic gases such as halothane, sevoflurane, desflurane, isoflurane and the depolarizing muscle relaxant succinylcholine, and rarely, in humans, to stressors such as vigorous exercise and heat. The incidence of MH reactions ranges from 1:10,000 to 1: 250,000 anesthetics. However, the prevalence of the genetic abnormalities may be as great as one in 400 individuals. MH affects humans, certain pig breeds, dogs and horses. The classic signs of MH include hyperthermia, tachycardia, tachypnea, increased carbon dioxide production, increased oxygen consumption, acidosis,…

Citation impact

568
total citations
FWCI
18.97
Percentile
100%
References
206
Citations per year

Authors

5

Topics & keywords

Keywords
  • Malignant hyperthermia
  • Central core disease
  • RYR1
  • Dantrolene
  • Halothane
  • Ryanodine receptor
  • Medicine
  • Desflurane
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