Malignant hyperthermia

Other names: Malignant hyperpyrexia, anesthesia related hyperthermia[1]
Abnormalities in the ryanodine receptor 1 gene are commonly detected in people who have experienced an episode of malignant hyperthermia
Specialty| Anesthesiology, critical care medicine
Symptoms| Muscle rigidity, high body temperature, fast heart rate[1]
Complications| Rhabdomyolysis, high blood potassium[1][2]
Causes| Volatile anesthetic agents or succinylcholine in those who are susceptible[1][3]
Diagnostic method| Based on symptoms and situation[2]
Differential diagnosis| Sepsis, anaphylaxis, serotonin syndrome, neuroleptic malignant syndrome[3]
Prevention| Avoiding potential triggers in those susceptible[2]
Treatment| Dantrolene, supportive care[4]
Prognosis| Risk of death: 5% (treatment), 75% (no treatment)[3]
Frequency| ~1 in 25,000 cases where anesthetic gases are used[1]

Malignant hyperthermia (MH) is a type of severe reaction that occurs in response to particular medications used during general anesthesia, among those who are susceptible.[1] Symptoms include muscle rigidity, high fever, and a fast heart rate.[1] Complications can include muscle breakdown and high blood potassium.[1][2] Most people who are susceptible are generally otherwise normal when not exposed.[3]

The cause of MH is the use of certain volatile anesthetic agents or succinylcholine in those who are susceptible.[1][3] Susceptibility can occur due to at least six genetic mutations, with the most common one being of the RYR1 gene.[1] These genetic variations are often inherited from a person's parents in an autosomal dominant manner.[1] The condition may also occur as a new mutation or be associated with a number of inherited muscle diseases, such as central core disease.[1][4]

In susceptible individuals, the medications induce the release of stored calcium ions within muscle cells.[1] The resulting increase in calcium concentrations within the cells cause the muscle fibers to contract.[1] This generates excessive heat and results in metabolic acidosis.[1] Diagnosis is based on symptoms in the appropriate situation.[2] Family members may be tested to see if they are susceptible by muscle biopsy or genetic testing.[4]

Treatment is with dantrolene and rapid cooling along with other supportive measures.[2][4] The avoidance of potential triggers is recommended in susceptible people.[2] The condition affects one in 5,000 to 50,000 cases where people are given anesthetic gases.[1] Males are more often affected than females.[3] The risk of death with proper treatment is about 5% while without it is around 75%.[3] While cases that appear similar to MH have been documented since the early 20th century, the condition was only formally recognized in 1960.[3]

## Contents

* 1 Signs and symptoms
* 2 Causes
* 2.1 Genetics
* 3 Pathophysiology
* 3.1 Disease mechanism
* 3.2 Animal model
* 4 Diagnosis
* 4.1 During an attack
* 4.2 Susceptibility testing
* 4.2.1 Muscle testing
* 4.2.2 Genetic testing
* 4.3 Criteria
* 5 Prevention
* 5.1 Anesthesia machine preparation
* 6 Treatment
* 6.1 Dantrolene
* 6.2 Training
* 7 Prognosis
* 8 Epidemiology
* 9 History
* 10 Other animals
* 11 Research
* 12 References
* 13 External links

## Signs and symptoms[edit | edit source]

The typical signs of malignant hyperthermia are due to a hypercatabolic state, which presents as a very high temperature, an increased heart rate and abnormally rapid breathing, increased carbon dioxide production, increased oxygen consumption, mixed acidosis, rigid muscles, and rhabdomyolysis.[5] These signs can develop any time during the administration of the anesthetic triggering agents. It is difficult to find confirmed cases in the postoperative period more than several minutes after discontinuation of anesthetic agents.[6]

## Causes[edit | edit source]

Malignant hyperthermia is a disorder that can be considered a gene-environment interaction. In most people with malignant hyperthermia susceptibility, they have few or no symptoms unless they are exposed to a triggering agent. The most common triggering agents are volatile anesthetic gases, such as halothane, sevoflurane, desflurane, isoflurane, enflurane or the depolarizing muscle relaxants suxamethonium and decamethonium used primarily in general anesthesia.[5] In rare cases, the biological stresses of physical exercise or heat may be the trigger.[5][7]

Other anesthetic drugs do not trigger malignant hyperthermia. These include local anesthetics (lidocaine, bupivacaine, mepivacaine), opiates (morphine, fentanyl), ketamine, barbiturates, nitrous oxide, propofol, etomidate, and benzodiazepines.

The nondepolarizing muscle relaxants pancuronium, cisatracurium, atracurium, mivacurium, vecuronium and rocuronium also do not cause MH.

There is mounting evidence that some individuals with malignant hyperthermia susceptibility may develop MH with exercise and/or on exposure to hot environments.[8]

### Genetics[edit | edit source]

Malignant hyperthermia's inheritance is autosomal dominant with variable penetrance.[5] The defect is typically located on the long arm of chromosome 19 (19q13.2[9]) involving the ryanodine receptor.[5] More than 25 different mutations in this gene are linked with malignant hyperthermia.[5] These mutations tend to cluster in one of three domains within the protein, designated MH1-3. MH1 and MH2 are located in the N-terminus of the protein, which interacts with L-type calcium channels and Ca2+
. MH3 is located in the transmembrane forming C-terminus. This region is important for allowing Ca2+
passage through the protein following opening.[citation needed]

Chromosome 7q and chromosome 17 have also been implicated. It has also been postulated that MH and central core disease may be allelic and thus can be co-inherited.

## Pathophysiology[edit | edit source]

Pathophysiologic changes during a malignant hyperthermia crisis

### Disease mechanism[edit | edit source]

In a large proportion (50–70%) of cases, the propensity for malignant hyperthermia is due to a mutation of the ryanodine receptor (type 1), located on the sarcoplasmic reticulum (SR), the organelle within skeletal muscle cells that stores calcium.[10][11] RYR1 opens in response to increases in intracellular Ca2+
level mediated by L-type calcium channels, thereby resulting in a drastic increase in intracellular calcium levels and muscle contraction. RYR1 has two sites believed to be important for reacting to changing Ca2+
concentrations: the A-site and the I-site. The A-site is a high affinity Ca2+
binding site that mediates RYR1 opening. The I-site is a lower affinity site that mediates the protein's closing. Caffeine, halothane, and other triggering agents act by drastically increasing the affinity of the A-site for Ca2+
and concomitantly decreasing the affinity of the I-site in mutant proteins. Mg2+
also affect RYR1 activity, causing the protein to close by acting at either the A- or I-sites. In MH mutant proteins, the affinity for Mg2+
at either one of these sites is greatly reduced. The end result of these alterations is greatly increased Ca2+
release due to a lowered activation and heightened deactivation threshold.[12][13] The process of sequestering this excess Ca2+
consumes large amounts of adenosine triphosphate (ATP), the main cellular energy carrier, and generates the excessive heat (hyperthermia) that is the hallmark of the disease. The muscle cell is damaged by the depletion of ATP and possibly the high temperatures, and cellular constituents "leak" into the circulation, including potassium, myoglobin, creatine, phosphate and creatine kinase.

The other known causative gene for MH is CACNA1S, which encodes an L-type voltage-gated calcium channel α-subunit. There are two known mutations in this protein, both affecting the same residue, R1086.[14][15] This residue is located in the large intracellular loop connecting domains 3 and 4, a domain possibly involved in negatively regulating RYR1 activity. When these mutant channels are expressed in human embryonic kidney (HEK 293) cells, the resulting channels are five times more sensitive to activation by caffeine (and presumably halothane) and activate at 5–10mV more hyperpolarized. Furthermore, cells expressing these channels have an increased basal cytosolic Ca2+
concentration. As these channels interact with and activate RYR1, these alterations result in a drastic increase of intracellular Ca2+
, and, thereby, muscle excitability.[16]

Other mutations causing MH have been identified, although in most cases the relevant gene remains to be identified.[17]

### Animal model[edit | edit source]

Research into malignant hyperthermia was limited until the discovery of "porcine stress syndrome" (PSS) in Danish Landrace and other pig breeds selected for muscling, a condition in which stressed pigs develop "pale, soft, exudative" flesh (a manifestation of the effects of malignant hyperthermia) rendering their meat less marketable at slaughter. This "awake triggering" was not observed in humans, and initially cast doubts on the value of the animal model, but subsequently, susceptible humans were discovered to "awake trigger" (develop malignant hyperthermia) in stressful situations. This supported the use of the pig model for research. Pig farmers use halothane cones in swine yards to expose piglets to halothane. Those that die were MH-susceptible, thus saving the farmer the expense of raising a pig whose meat he would not be able to market. This also reduced the use of breeding stock carrying the genes for PSS. The condition in swine is also due to a defect in ryanodine receptors.[18]

Gillard et al. discovered the causative mutation in humans only after similar mutations had first been described in pigs.[10]

Horses also suffer from malignant hyperthermia. A causative mutated allele, ryanodine receptor 1 gene (RyR1) at nucleotide C7360G, generating a R2454G amino acid substitution.[19] has been identified in the American Quarter Horse and breeds with Quarter Horse ancestry, inherited as an autosomal dominant.[20][21] It can be caused by overwork, anesthesia, or stress.[22] In dogs, its inheritance is autosomal recessive.[5]

An MH mouse has been constructed, bearing the R163C mutation prevalent in humans. These mice display signs similar to human MH patients, including sensitivity to halothane (increased respiration, body temperature, and death). Blockade of RYR1 by dantrolene prevents adverse reaction to halothane in these mice, as with humans. Muscle from these mice also shows increased K+
-induced depolarization and an increased caffeine sensitivity.[23]

## Diagnosis[edit | edit source]

### During an attack[edit | edit source]

The earliest signs may include: masseter muscle contracture following administration of succinylcholine, a rise in end-tidal carbon dioxide concentration (despite increased minute ventilation), unexplained tachycardia, and muscle rigidity.[5] Despite the name, elevation of body temperature is often a late sign, but may appear early in severe cases. Respiratory acidosis is universally present and many patients have developed metabolic acidosis at the time of diagnosis. A fast rate of breathing (in a spontaneously breathing patient), cyanosis, hypertension, abnormal heart rhythms, and high blood potassium may also be seen. Core body temperatures should be measured in any patient undergoing general anesthesia longer than 30 minutes.

Malignant hyperthermia is diagnosed on clinical grounds, but various laboratory investigations may prove confirmatory. These include a raised creatine kinase level, elevated potassium, increased phosphate (leading to decreased calcium) and—if determined—raised myoglobin; this is the result of damage to muscle cells. Severe rhabdomyolysis may lead to acute kidney failure, so kidney function is generally measured on a frequent basis. Patients may also get premature ventricular contractions due to the increased levels of potassium released from the muscles during episodes.[citation needed]

### Susceptibility testing[edit | edit source]

#### Muscle testing[edit | edit source]

The main candidates for testing are those with a close relative who has suffered an episode of MH or have been shown to be susceptible. The standard procedure is the "caffeine-halothane contracture test", CHCT. A muscle biopsy is carried out at an approved research center, under local anesthesia. The fresh biopsy is bathed in solutions containing caffeine or halothane and observed for contraction; under good conditions, the sensitivity is 97% and the specificity 78%.[24] Negative biopsies are not definitive, so any patient who is suspected of MH by their medical history or that of blood relatives is generally treated with non-triggering anesthetics, even if the biopsy was negative. Some researchers advocate the use of the "calcium-induced calcium release" test in addition to the CHCT to make the test more specific.[citation needed]

Less invasive diagnostic techniques have been proposed. Intramuscular injection of halothane 6 vol% has been shown to result in higher than normal increases in local pCO
2 among patients with known malignant hyperthermia susceptibility. The sensitivity was 100% and specificity was 75%. For patients at similar risk to those in this study, this leads to a positive predictive value of 80% and negative predictive value of 100%. This method may provide a suitable alternative to more invasive techniques.[25] A 2002 study examined another possible metabolic test. In this test, intramuscular injection of caffeine was followed by local measurement of the pCO
2; those with known MH susceptibility had a significantly higher pCO
2 (63 versus 44 mmHg). The authors propose larger studies to assess the test's suitability for determining MH risk.[26]

#### Genetic testing[edit | edit source]

Genetic testing is being performed in a limited fashion to determine susceptibility to MH.[5] In people with a family history of MH, analysis for RYR1 mutations may be useful.[17]

### Criteria[edit | edit source]

A 1994 consensus conference led to the formulation of a set of diagnostic criteria. The higher the score (above 6), the more likely a reaction constituted MH:[27]

* Respiratory acidosis (end-tidal CO
2 above 55 mmHg/7.32 kPa or arterial pCO
2 above 60 mmHg/7.98 kPa)
* Heart involvement (unexplained sinus tachycardia, ventricular tachycardia or ventricular fibrillation)
* Metabolic acidosis (base excess lower than -8, pH <7.25)
* Muscle rigidity (generalized rigidity including severe masseter muscle rigidity)
* Muscle breakdown (CK >20,000/L units, cola colored urine or excess myoglobin in urine or serum, potassium above 6 mmol/l)
* Temperature increase (rapidly increasing temperature, T >38.8 °C)
* Other (rapid reversal of MH signs with dantrolene, elevated resting serum CK levels)
* Family history (autosomal dominant pattern)

## Prevention[edit | edit source]

In the past, the prophylactic use of dantrolene was recommended for MH-susceptible patients undergoing general anesthesia.[28] However, multiple retrospective studies have demonstrated the safety of trigger-free general anesthesia in these patients in the absence of prophylactic dantrolene administration. The largest of these studies looked at the charts of 2214 patients who underwent general or regional anesthesia for an elective muscle biopsy. About half (1082) of the patients were muscle biopsy positive for MH. Only five of these patients exhibited signs consistent with MH, four of which were treated successfully with parenteral dantrolene, and the remaining one recovered with only symptomatic therapy.[29] After weighing its questionable benefits against its possible adverse effects (including nausea, vomiting, muscle weakness and prolonged duration of action of nondepolarizing neuromuscular blocking agents[30]), experts no longer recommend the use of prophylactic dantrolene prior to trigger-free general anesthesia in MH-susceptible patients.[28]

### Anesthesia machine preparation[edit | edit source]

Anesthesia for people with known MH susceptible requires avoidance of triggering agent concentrations above 5 parts per million (all volatile anesthetic agents and succinylcholine). Most other drugs are safe (including nitrous oxide), as are regional anesthetic techniques. Where general anesthesia is planned, it can be provided safely by either flushing the machine or using charcoal filters.

To flush the machine, first remove or disable the vaporizers and then flush the machine with 10 L/min or greater fresh gas flow rate for at least 20 minutes. While flushing the machine the ventilator should be set to periodically ventilate a new breathing circuit. The soda lime should also be replaced. After machine preparation, anesthesia should be induced and maintained with non-triggering agents.[30] The time required to flush a machine varies for different machines and volatile anesthetics. This prevention technique was optimized to prepare older generation anesthesia machines. Modern anesthetic machines have more rubber and plastic components which provide a reservoir for volatile anesthetics, and should be flushed for 60 minutes.[31]

Charcoal filters can be used to prepare an anesthesia machine in less than 60 seconds for people at risk of malignant hyperthermia. These filters prevent residual anesthetic from triggering malignant hyperthermia for up to 12 hours, even at low fresh gas flows.[32] Prior to placing the charcoal filters, the machine should be flushed with fresh gas flows greater than 10 L/min for 90 seconds.[33]

## Treatment[edit | edit source]

Dantrolene sodium, the only available medical treatment for malignant hyperthermia

The current treatment of choice is the intravenous administration of dantrolene, the only known antidote, discontinuation of triggering agents, and supportive therapy directed at correcting hyperthermia, acidosis, and organ dysfunction. Treatment must be instituted rapidly on clinical suspicion of the onset of malignant hyperthermia.[30]

### Dantrolene[edit | edit source]

Dantrolene is a muscle relaxant that appears to work directly on the ryanodine receptor to prevent the release of calcium. After the widespread introduction of treatment with dantrolene, the mortality of malignant hyperthermia fell from 80% in the 1960s to less than 5%.[5] Dantrolene remains the only drug known to be effective in the treatment of MH.[28] The recommended dose of dantrolene is 2.5 mg/kg, repeated as necessary.[5] It is recommended that each hospital keeps a minimum stock of 36 dantrolene vials (720 mg), sufficient for four doses in a 70-kg person.[34]

### Training[edit | edit source]

This is a mixed modality medical simulation of the treatment of malignant hyperthermia by anesthesia residents. The residents are managing care, mixing dantrolene and utilizing a cognitive aid at the bedside.

Fast recognition and treatment of MH utilizes skills and procedures that are utilized with a low-frequency and high-risk.[35] Conducting MH crisis training for perioperative teams can identify system failures as well as improve response to these events.[36] Simulation techniques to include the use of cognitive aids have also been shown to improve communication in clinical treatment of MH.[37][38]

## Prognosis[edit | edit source]

Prognosis is poor if this condition is not aggressively treated.[5] In the 1970s, mortality was greater than 80%; with the current management, however, mortality is now less than 5%.[5]

## Epidemiology[edit | edit source]

It occurs in between 1:5,000 and 1:100,000 in procedures involving general anaesthesia.[5] This disorder occurs worldwide and affects all racial groups.

In the Manawatu region of New Zealand, up to 1 in 200 people are at high risk of the condition.[39]

## History[edit | edit source]

The syndrome was first recognized in Royal Melbourne Hospital, Australia in an affected family by Denborough et al. in 1962.[40][41] Denborough did much of his subsequent work on the condition at the Royal Canberra Hospital.[42] Similar reactions were found in pigs.[43] The efficacy of dantrolene as a treatment was discovered by South African anesthesiologist Gaisford Harrison and reported in a 1975 article published in the British Journal of Anaesthesia.[44] After further animal studies corroborated the possible benefit from dantrolene, a 1982 study confirmed its usefulness in humans.[45]

In 1981, the Malignant Hyperthermia Association of the United States (MHAUS) hotline was established to provide telephone support to clinical teams treating patients with suspected malignant hyperthermia. The hotline became active in 1982 and since that time MHAUS has provided continuous access to board-certified anesthesiologists to assist teams in treatment.[46]

## Other animals[edit | edit source]

Other animals, including certain pig breeds, dogs, and horses, are susceptible to malignant hyperthermia.[5]

In dogs its inheritance is autosomal dominant.[47]

In pigs its inheritance is autosomal recessive.[5]

In horses its inheritance is autosomal dominant, and most associated with the American Quarter Horse although it can occur in other breeds.[48]

## Research[edit | edit source]

Azumolene is a 30-fold more water-soluble analog of dantrolene that also works to decrease the release of intracellular calcium by its action on the ryanodine receptor. In MH-susceptible swine, azumolene was as potent as dantrolene.[49] It has yet to be studied in vivo in humans, but may present a suitable alternative to dantrolene in the treatment of MH.

## References[edit | edit source]

1. ↑ 1.00 1.01 1.02 1.03 1.04 1.05 1.06 1.07 1.08 1.09 1.10 1.11 1.12 1.13 1.14 1.15 "malignant hyperthermia". Genetics Home Reference. Jan 27, 2017. Archived from the original on 27 June 2017. Retrieved 30 June 2017.
2. ↑ 2.0 2.1 2.2 2.3 2.4 2.5 2.6 "Malignant hyperthermia" (PDF). Orpha.net. March 2013. Archived (PDF) from the original on 17 June 2013. Retrieved 30 June 2017.
3. ↑ 3.0 3.1 3.2 3.3 3.4 3.5 3.6 3.7 Schneiderbanger, D; Johannsen, S; Roewer, N; Schuster, F (2014). "Management of malignant hyperthermia: diagnosis and treatment". Therapeutics and Clinical Risk Management. 10: 355–62. doi:10.2147/TCRM.S47632. PMC 4027921. PMID 24868161.
4. ↑ 4.0 4.1 4.2 4.3 "Malignant hyperthermia". GARD. 30 June 2014. Archived from the original on 4 July 2017. Retrieved 30 June 2017.
5. ↑ 5.00 5.01 5.02 5.03 5.04 5.05 5.06 5.07 5.08 5.09 5.10 5.11 5.12 5.13 5.14 5.15 Rosenberg H, Davis M, James D, Pollock N, Stowell K (April 2007). "Malignant hyperthermia". Orphanet Journal of Rare Diseases. 2: 21. doi:10.1186/1750-1172-2-21. PMC 1867813. PMID 17456235.
6. ↑ Litman, Ronald; Flood, Christopher D.; Kaplan, Richard F.; Kim, Yung Ly; Tobin, Joseph R. (November 2008). "Postoperative Malignant Hyperthermia". Anesthesiology. 109 (5): 825–9. doi:10.1097/aln.0b013e31818958e5. PMID 18946294. Archived from the original on 2019-09-30. Retrieved 2019-09-09.
7. ↑ Groom, Linda; Muldoon, Sheila M.; Tang, Zhen Zhi; Brandom, Barbara W.; Bayarsaikhan, Munkhuu; Bina, Saiid; Lee, Hee-Suk; Qiu, Xing; Sambuughin, Nyamkhishig; Dirksen, Robert T. (November 2011). "Identical de novo Mutation in the Type 1 Ryanodine Receptor Gene Associated with Fatal, Stress-induced Malignant Hyperthermia in Two Unrelated Families". Anesthesiology. 115 (5): 938–45. doi:10.1097/aln.0b013e3182320068. PMC 3203251. PMID 21918424.
8. ↑ Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJ, Stephens K, Amemiya A, Rosenberg H, Sambuughin N, Riazi S, Dirksen R (2013). "Malignant Hyperthermia Susceptibility". GeneReviews. PMID 20301325.
9. ↑ "OMIM Entry - * 180901 - RYANODINE RECEPTOR 1; RYR1". www.omim.org. Archived from the original on 2015-07-26. Retrieved 2016-01-06.
10. ↑ 10.0 10.1 Gillard EF, Otsu K, Fujii J, Khanna VK, de Leon S, Derdemezi J, Britt BA, Duff CL, Worton RG, MacLennan DH (November 1991). "A substitution of cysteine for arginine 614 in the ryanodine receptor is potentially causative of human malignant hyperthermia". Genomics. 11 (3): 751–5. doi:10.1016/0888-7543(91)90084-R. PMID 1774074.
11. ↑ Galli L, Orrico A, Lorenzini S, Censini S, Falciani M, Covacci A, Tegazzin V, Sorrentino V (August 2006). "Frequency and localization of mutations in the 106 exons of the RYR1 gene in 50 individuals with malignant hyperthermia". Human Mutation. 27 (8): 830. doi:10.1002/humu.9442. PMID 16835904.
12. ↑ Balog, E; Fruen, B; Shomer, N; Louis, C (2001). "Divergent effects of the malignant hyperthermia-susceptible Arg(615)-->Cys mutation on the Ca(2+) and Mg(2+) dependence of the RyR1". Biophys J. 81 (4): 2050–8. Bibcode:2001BpJ....81.2050B. doi:10.1016/S0006-3495(01)75854-7. PMC 1301678. PMID 11566777. Archived from the original on 2008-12-02.
13. ↑ Yang T, Ta TA, Pessah IN, Allen PD (July 2003). "Functional defects in six ryanodine receptor isoform-1 (RyR1) mutations associated with malignant hyperthermia and their impact on skeletal excitation-contraction coupling". The Journal of Biological Chemistry. 278 (28): 25722–30. doi:10.1074/jbc.M302165200. PMID 12732639.
14. ↑ Monnier N, Procaccio V, Stieglitz P, Lunardi J (June 1997). "Malignant-hyperthermia susceptibility is associated with a mutation of the alpha 1-subunit of the human dihydropyridine-sensitive L-type voltage-dependent calcium-channel receptor in skeletal muscle". American Journal of Human Genetics. 60 (6): 1316–25. doi:10.1086/515454. PMC 1716149. PMID 9199552.
15. ↑ The R1086C mutant has never been published, but has nevertheless been referenced multiple times in the literature, e.g. Jurkat-Rott K, McCarthy T, Lehmann-Horn F (January 2000). "Genetics and pathogenesis of malignant hyperthermia". Muscle & Nerve. 23 (1): 4–17. doi:10.1002/(SICI)1097-4598(200001)23:1<4::AID-MUS3>3.0.CO;2-D. PMID 10590402.
16. ↑ Weiss RG, O'Connell KM, Flucher BE, Allen PD, Grabner M, Dirksen RT (October 2004). "Functional analysis of the R1086H malignant hyperthermia mutation in the DHPR reveals an unexpected influence of the III-IV loop on skeletal muscle EC coupling". American Journal of Physiology. Cell Physiology. 287 (4): C1094–102. doi:10.1152/ajpcell.00173.2004. PMID 15201141. Archived from the original on 2021-08-28. Retrieved 2019-12-04.
17. ↑ 17.0 17.1 Litman R, Rosenberg H; Rosenberg (2005). "Malignant hyperthermia: update on susceptibility testing". JAMA. 293 (23): 2918–24. doi:10.1001/jama.293.23.2918. PMID 15956637.
18. ↑ J Fujii; K Otsu; F Zorzato; S de Leon; VK Khanna; JE Weiler; PJ O'Brien; DH MacLennan (1991). "Identification of a mutation in porcine ryanodine receptor associated with malignant hyperthermia". Science. 253 (5018): 448–451. Bibcode:1991Sci...253..448F. doi:10.1126/science.1862346. PMID 1862346.
19. ↑ Aleman M, Nieto JE, Magdesian KG (2009). "Malignant hyperthermia associated with ryanodine receptor 1 (C7360G) mutation in Quarter Horses". Journal of Veterinary Internal Medicine. 23 (2): 329–34. doi:10.1111/j.1939-1676.2009.0274.x. PMID 19220734.
20. ↑ "Archived copy" (PDF). Archived from the original (PDF) on 2014-06-09. Retrieved 2012-06-12.`{{cite web}}`: CS1 maint: archived copy as title (link)
21. ↑ ftp://ftp.aave.inv.org.ar/IVIS/aaep/Equine Malignant Hyperthermia.pdf[permanent dead link]
22. ↑ Valberg SJ, Mickelson JR, Gallant EM, MacLeay JM, Lentz L, de la Corte F (July 1999). "Exertional rhabdomyolysis in quarter horses and thoroughbreds: one syndrome, multiple aetiologies". Equine Veterinary Journal. Supplement. 31 (30): 533–8. doi:10.1111/j.2042-3306.1999.tb05279.x. PMID 10659313.
23. ↑ Yang T, Riehl J, Esteve E, Matthaei KI, Goth S, Allen PD, Pessah IN, Lopez JR (December 2006). "Pharmacologic and functional characterization of malignant hyperthermia in the R163C RyR1 knock-in mouse". Anesthesiology. 105 (6): 1164–75. doi:10.1097/00000542-200612000-00016. PMID 17122579.
24. ↑ Allen GC, Larach MG, Kunselman AR (March 1998). "The sensitivity and specificity of the caffeine-halothane contracture test: a report from the North American Malignant Hyperthermia Registry. The North American Malignant Hyperthermia Registry of MHAUS". Anesthesiology. 88 (3): 579–88. doi:10.1097/00000542-199803000-00006. PMID 9523799.
25. ↑ Schuster F, Gardill A, Metterlein T, Kranke P, Roewer N, Anetseder M (September 2007). "A minimally invasive metabolic test with intramuscular injection of halothane 5 and 6 vol% to detect probands at risk for malignant hyperthermia". Anaesthesia. 62 (9): 882–7. doi:10.1111/j.1365-2044.2007.05173.x. PMID 17697213.
26. ↑ Anetseder M, Hager M, Müller CR, Roewer N (May 2002). "Diagnosis of susceptibility to malignant hyperthermia by use of a metabolic test". Lancet. 359 (9317): 1579–80. doi:10.1016/S0140-6736(02)08506-9. PMID 12047971.
27. ↑ Larach MG; Localio AR; Allen GC; et al. (1994). "A clinical grading scale to predict malignant hyperthermia susceptibility". Anesthesiology. 80 (4): 771–9. doi:10.1097/00000542-199404000-00008. PMID 8024130.
28. ↑ 28.0 28.1 28.2 Krause T, Gerbershagen MU, Fiege M, Weisshorn R, Wappler F (April 2004). "Dantrolene--a review of its pharmacology, therapeutic use and new developments". Anaesthesia. 59 (4): 364–73. doi:10.1111/j.1365-2044.2004.03658.x. PMID 15023108.
29. ↑ Carr AS, Lerman J, Cunliffe M, McLeod ME, Britt BA (April 1995). "Incidence of malignant hyperthermia reactions in 2,214 patients undergoing muscle biopsy". Canadian Journal of Anesthesia. 42 (4): 281–6. doi:10.1007/BF03010703. PMID 7788824.
30. ↑ 30.0 30.1 30.2 Halsall PJ, Hopkins PM; Hopkins (2003). "Malignant hyperthermia". Continuing Education in Anaethesia, Critical Care and Pain. 3 (1): 5–9. doi:10.1093/bjacepd/mkg002. Archived from the original on 2006-10-03.
31. ↑ Kim TW, Nemergut ME (January 2011). "Preparation of modern anesthesia workstations for malignant hyperthermia-susceptible patients: a review of past and present practice". Anesthesiology. 114 (1): 205–12. doi:10.1097/ALN.0b013e3181ee2cb7. PMID 21169802.
32. ↑ Stoker, Robert; Romankowski, Mathew; Burk, Kyle; Orr, Joseph (October 15, 2013). "12 Hour Evaluation of Filters to Prepare an Anesthesia Machine for Malignant Hyperthermia Susceptible Patients" (Abstract# A4094). Anesthesiology 2013 Annual Meeting. Archived from the original on August 28, 2021. Retrieved October 14, 2014.
33. ↑ Malignant Hyperthermia Association of the United States. "Preparing the Anesthesia Machine for MHS Patients". www.mhaus.org. Archived from the original on 2016-10-22. Retrieved 2017-06-22.
34. ↑ EYH Yeung, Munroe J; Munroe (2015). "Development of a malignant hyperthermia protocol". BMC Proceedings. 9 (Suppl1): A32. doi:10.1186/1753-6561-9-S1-A32. PMC 4306034.
35. ↑ Cain CL, Riess ML, Gettrust L, Novalija J (2014). "Malignant hyperthermia crisis: optimizing patient outcomes through simulation and interdisciplinary collaboration". AORN Journal. 99 (2): 301–8, quiz 309–11. doi:10.1016/j.aorn.2013.06.012. PMC 4276305. PMID 24472592.
36. ↑ Hirshey Dirksen SJ, Van Wicklin SA, Mashman DL, Neiderer P, Merritt DR (2013). "Developing effective drills in preparation for a malignant hyperthermia crisis". AORN Journal. 97 (3): 329–53. doi:10.1016/j.aorn.2012.12.009. PMID 23452698.
37. ↑ Isaak RS, Stiegler MP (2015). "Review of crisis resource management (CRM) principles in the setting of intraoperative malignant hyperthermia". Journal of Anesthesia. 30 (2): 298–306. doi:10.1007/s00540-015-2115-8. PMID 26679497.
38. ↑ Holzman RS, Cooper JB, Gaba DM, Philip JH, Small SD, Feinstein D (1995). "Anesthesia crisis resource management: real-life simulation training in operating room crises". Journal of Clinical Anesthesia. 7 (8): 675–87. doi:10.1016/0952-8180(95)00146-8. PMID 8747567.
39. ↑ Rosenberg, Henry; Pollock, Neil; Schiemann, Anja; Bulger, Terasa; Stowell, Kathryn (4 August 2015). "Malignant hyperthermia: a review". Orphanet Journal of Rare Diseases. 10 (1): 93. doi:10.1186/s13023-015-0310-1. PMC 4524368. PMID 26238698.
40. ↑ "Anaesthesia | the Royal Melbourne Hospital". Archived from the original on 2013-08-26. Retrieved 2014-03-17.
41. ↑ Denborough MA, Forster JF, Lovell RR, Maplestone PA, Villiers JD (1962). "Anaesthetic deaths in a family". British Journal of Anaesthesia. 34 (6): 395–6. doi:10.1093/bja/34.6.395. PMID 13885389. Historical account in Denborough MA (2008). "Malignant hyperthermia. 1962". Anesthesiology. 108 (1): 156–7. doi:10.1097/01.anes.0000296107.23210.dd. PMID 18156894. Archived from the original on 2021-08-28. Retrieved 2008-03-27.
42. ↑ Malcolm Whyte. 'Clinical Science in Canberra Hospital' in AJ Proust (ed) History of Medicine in Canberra and Queanbeyan and their Hospitals Brolga Press, Gundaroo p123 at 127
43. ↑ Hall LW, Woolf N, Bradley JW, Jolly DW (November 1966). "Unusual reaction to suxamethonium chloride". British Medical Journal. 2 (5525): 1305. doi:10.1136/bmj.2.5525.1305. PMC 1944316. PMID 5924819.
44. ↑ Harrison GG (January 1975). "Control of the malignant hyperpyrexic syndrome in MHS swine by dantrolene sodium". British Journal of Anaesthesia. 47 (1): 62–5. doi:10.1093/bja/47.1.62. PMID 1148076. Archived from the original on 2021-08-28. Retrieved 2019-12-17. A reprint of the article, which became a "Citation Classic", is available in Harrison GG (October 1998). "Control of the malignant hyperpyrexic syndrome in MHS swine by dantrolene sodium. 1975". Br J Anaesth. 81: 626–9, discussion 625. doi:10.1093/bja/81.4.626. PMID 9924249.
45. ↑ Kolb ME, Horne ML, Martz R (April 1982). "Dantrolene in human malignant hyperthermia". Anesthesiology. 56 (4): 254–62. doi:10.1097/00000542-198204000-00005. PMID 7039419.
46. ↑ Dexter F, Rosenberg H, Epstein RH, Semo JJ, Litman RS (2015). "Implications of National Anesthesia Workload on the Staffing of a Call Center: The Malignant Hyperthermia Consultant Hotline". A&A Case Reports. 5 (3): 43–6. doi:10.1213/XAA.0000000000000147. PMID 26230307.
47. ↑ Roberts, M. C.; Mickelson, J. R.; Patterson, E. E.; Nelson, T. E.; Armstrong, P. J.; Brunson, D. B.; Hogan, K (Sep 2001). "Autosomal dominant canine malignant hyperthermia is caused by a mutation in the gene encoding the skeletal muscle calcium release channel (RYR1)". Anesthesiology. 95 (3): 716–25. doi:10.1097/00000542-200109000-00026. PMID 11575546.
48. ↑ Mickelson JR, Valberg SJ (2015). "The Genetics of Skeletal Muscle Disorders in Horses". Annu. Rev. Animal Biosci. 3: 197–217. doi:10.1146/annurev-animal-022114-110653. PMID 25387114.
49. ↑ Dershwitz M, Sréter FA; Sréter (1990). "Azumolene reverses episodes of malignant hyperthermia in susceptible swine". Anesth. Analg. 70 (3): 253–5. doi:10.1213/00000539-199003000-00004. PMID 2305975.

## External links[edit | edit source]

Classification|

* ICD-10: T88.3
* ICD-9-CM: 995.86
* OMIM: 145600
* MeSH: D008305
* DiseasesDB: 7776

|

External resources|

* MedlinePlus: 001315
* GeneReviews: Malignant Hyperthermia Susceptibility

* GeneReview/NIH/UW entry on Malignant Hyperthermia Susceptibility Archived 2017-01-18 at the Wayback Machine

* v
* t
* e

Consequences of external causes

Temperature|

| Elevated|

Hyperthermia
Heat syncope

|

Reduced|

Hypothermia
Immersion foot syndromes

Trench foot
Tropical immersion foot
Warm water immersion foot
Chilblains
Frostbite
Aerosol burn
Cold intolerance
Acrocyanosis
Erythrocyanosis crurum

Radiation|

Radiation poisoning
Radiation burn
Chronic radiation keratosis
Eosinophilic, polymorphic, and pruritic eruption associated with radiotherapy
Radiation acne
Radiation-induced cancer
Radiation recall reaction
Radiation-induced erythema multiforme
Radiation-induced hypertrophic scar
Radiation-induced keloid
Radiation-induced morphea

Air|

* Hypoxia/Asphyxia
* Barotrauma
* Aerosinusitis
* Decompression sickness
* High altitude
* Altitude sickness
* Chronic mountain sickness
* Death zone
* HAPE
* HACE

Food|

* Starvation

Maltreatment|

* Physical abuse
* Sexual abuse
* Psychological abuse

Travel|

* Motion sickness
* Seasickness
* Airsickness
* Space adaptation syndrome

Adverse effect|

* Hypersensitivity
* Anaphylaxis
* Angioedema
* Allergy
* Arthus reaction

* Adverse drug reaction

Other|

* Electrical injury
* Drowning
* Lightning injuries

Ungrouped
skin conditions
resulting from
physical factors|

* Dermatosis neglecta
* Pinch mark
* Pseudoverrucous papules and nodules
* Sclerosing lymphangitis
* Tropical anhidrotic asthenia
* UV-sensitive syndrome

environmental skin conditions
Electrical burn
frictional/traumatic/sports

Black heel and palm
Equestrian perniosis
Jogger's nipple
Pulling boat hands
Runner's rump
Surfer's knots
Tennis toe
Vibration white finger
Weathering nodule of ear
Wrestler's ear
Coral cut
Painful fat herniation
Uranium dermatosis

iv use

Skin pop scar
Skin track
Slap mark
Pseudoacanthosis nigricans
Narcotic dermopathy

* v
* t
* e

Diseases of ion channels

Calcium channel|

| Voltage-gated|

* CACNA1A
* Familial hemiplegic migraine 1
* Episodic ataxia 2
* Spinocerebellar ataxia type-6
* CACNA1C
* Timothy syndrome
* Brugada syndrome 3
* Long QT syndrome 8
* CACNA1F
* Ocular albinism 2
* CSNB2A
* CACNA1S
* Hypokalemic periodic paralysis 1
* Thyrotoxic periodic paralysis 1
* CACNB2
* Brugada syndrome 4

|

Ligand gated|

* RYR1
* Malignant hyperthermia
* Central core disease
* RYR2
* CPVT1
* ARVD2

Sodium channel|

| Voltage-gated|

* SCN1A
* Familial hemiplegic migraine 3
* GEFS+ 2
* Febrile seizure 3A
* SCN1B
* Brugada syndrome 6
* GEFS+ 1
* SCN4A
* Hypokalemic periodic paralysis 2
* Hyperkalemic periodic paralysis
* Paramyotonia congenita
* Potassium-aggravated myotonia
* SCN4B
* Long QT syndrome 10
* SCN5A
* Brugada syndrome 1
* Long QT syndrome 3
* SCN9A
* Erythromelalgia
* Febrile seizure 3B
* Paroxysmal extreme pain disorder
* Congenital insensitivity to pain

|

Constitutively active|

* SCNN1B/SCNN1G
* Liddle's syndrome
* SCNN1A/SCNN1B/SCNN1G
* Pseudohypoaldosteronism 1AR

Potassium channel|

| Voltage-gated|

* KCNA1
* Episodic ataxia 1
* KCNA5
* Familial atrial fibrillation 7
* KCNC3
* Spinocerebellar ataxia type-13
* KCNE1
* Jervell and Lange-Nielsen syndrome
* Long QT syndrome 5
* KCNE2
* Long QT syndrome 6
* KCNE3
* Brugada syndrome 5
* KCNH2
* Short QT syndrome
* KCNQ1
* Jervell and Lange-Nielsen syndrome
* Romano–Ward syndrome
* Short QT syndrome
* Long QT syndrome 1
* Familial atrial fibrillation 3
* KCNQ2
* BFNS1

|

Inward-rectifier|

* KCNJ1
* Bartter syndrome 2
* KCNJ2
* Andersen–Tawil syndrome
* Long QT syndrome 7
* Short QT syndrome
* KCNJ11
* TNDM3
* KCNJ18
* Thyrotoxic periodic paralysis 2

Chloride channel|

* CFTR
* Cystic fibrosis
* Congenital absence of the vas deferens
* CLCN1
* Thomsen disease
* Myotonia congenita
* CLCN5
* Dent's disease
* CLCN7
* Osteopetrosis A2, B4
* BEST1
* Vitelliform macular dystrophy
* CLCNKB
* Bartter syndrome 3

TRP channel|

* TRPC6
* FSGS2
* TRPML1
* Mucolipidosis type IV

Connexin|

* GJA1
* Oculodentodigital dysplasia
* Hallermann–Streiff syndrome
* Hypoplastic left heart syndrome
* GJB1
* Charcot–Marie–Tooth disease X1
* GJB2
* Keratitis–ichthyosis–deafness syndrome
* Ichthyosis hystrix
* Bart–Pumphrey syndrome
* Vohwinkel syndrome)
* GJB3/GJB4
* Erythrokeratodermia variabilis
* Progressive symmetric erythrokeratodermia
* GJB6
* Clouston's hidrotic ectodermal dysplasia

Porin|

* AQP2
* Nephrogenic diabetes insipidus 2

See also: ion channels

* v
* t
* e

Anesthesia and anesthesiology

Types|

* General
* Sedation
* Twilight anesthesia
* Local
* Topical
* Intercostal nerve block
* Neuraxial blockade
* Spinal
* Epidural
* Dental
* Inferior alveolar nerve

Techniques|

* Airway management
* Anesthesia provision in the US
* Arterial catheter
* Bronchoscopy
* Capnography
* Dogliotti's principle
* Drug-induced amnesia
* Intraoperative neurophysiological monitoring
* Nerve block
* Penthrox inhaler
* Tracheal intubation

Scientific principles|

* Blood–gas partition coefficient
* Concentration effect
* Fink effect
* Minimum alveolar concentration
* Second gas effect

Measurements|

* ASA physical status classification system
* Baricity
* Bispectral index
* Entropy monitoring
* Fick principle
* Goldman index
* Guedel's classification
* Mallampati score
* Neuromuscular monitoring
* Thyromental distance

Instruments|

* Anaesthetic machine
* Anesthesia cart
* Boyle's machine
* Gas cylinder
* Laryngeal mask airway
* Laryngeal tube
* Medical monitor
* Odom's indicator
* Relative analgesia machine
* Vaporiser
* Double-lumen endotracheal tube
* Endobronchial blocker

Complications|

* Emergence delirium
* Allergic reactions
* Anesthesia awareness
* Local anesthetic toxicity
* Malignant hyperthermia
* Perioperative mortality
* Postanesthetic shivering
* Postoperative nausea and vomiting
* Postoperative residual curarization

Subspecialties|

* Cardiothoracic
* Critical emergency medicine
* Geriatric
* Intensive care medicine
* Obstetric
* Oral sedation dentistry
* Pain medicine

Professions|

* Anesthesiologist
* Anesthesiologist assistant
* Nurse anesthetist
* Operating department practitioners
* Certified Anesthesia Technician
* Certified Anesthesia Technologist
* Anaesthetic technician
* Physicians' assistant (anaesthesia)

History|

* ACE mixture
* Helsinki Declaration for Patient Safety in Anaesthesiology
* History of general anesthesia
* History of neuraxial anesthesia
* History of tracheal intubation

Organizations|

* American Association of Nurse Anesthetists
* American Society of Anesthesia Technologists & Technicians
* American Society of Anesthesiologists
* Anaesthesia Trauma and Critical Care
* Association of Anaesthetists of Great Britain and Ireland
* Royal College of Anaesthetists
* Association of Veterinary Anaesthetists
* Australian and New Zealand College of Anaesthetists
* Australian Society of Anaesthetists
* International Anesthesia Research Society

* Category
* Outline

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