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MALIGNANT
HYPERTERMIA
PRESENTED BY
PANKAJ SINGH RANA
NURSE PRACTITIONER
INTRODUCTION
Malignant hyperthermia (MH) is a type of
severe reaction that occurs to particular
medications used during general
anesthesia, among those who are
susceptible. 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.
CAUSES
1. volatile anesthetic gases, such as halothane, sev
oflurane, desflurane, isoflurane, enflurane
2. depolarizing muscle relaxants suxamethonium
and decamethonium
3. Biological stresses of physical exercise or
heat may be the trigger.
4. exercise and/or on exposure to hot
environments
5. inheritance is autosomal dominant with variable
penetrance
SIGN AND SYMPTOMS
The typical signs of malignant hyperthermia are
due to a hypercatabolic state, which presents
as a very high temperature
•An increased heart rate
•Abnormally rapid breathing
•Increased carbon dioxide production
•Increased oxygen consumption
•Mixed acidosis
•Rigid muscles
•rhabdomyolysis
DIGNOSIS
Monitoring ETCO2
A rise in end-tidal carbon dioxide concentration
(despite increased minute ventilation).
ABG
Respiratory acidosis is universally present and
many patients have developed metabolic acidosis
at the time of diagnosis
Monitoring temperature
Elevation of body temperature is often a late
sign.
Blood Test
A raised creatine kinase level, elevated potassiu
m, increased phosphate (leading to decreased
calcium)
Serum Myoglobin
Raised myoglobin; this is the result of damage t
o muscle cells (rhabdomyolysis )
Gene Testing
Analysis for RYR1 mutations
Skeletal muscle biopsy:
Sample is taken from vastus muscle of thigh
under local anaesthesia. Muscle is subjected to is
ometric contracture testing under influence of
caffeine or halothane or both. It produces
exaggerated contracture in susceptible patients.
CRITERIA FOR MALIGNANT
HYPERTHERMIA
•A 1994 consensus conference led to the formulat
ion of a set of diagnostic criteria. The higher the
score (above 6), the more likely a reaction
constituted MH.
•Respiratory acidosis (end-tidal CO above 55 mm
Hg/7.32 kPa or arterial Pco 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)
COMPLICATIONS OF M H
DIC
Pulmonary Edema
Acute Renal Failure
CNS Damage
Blindness,
Seizures,
Coma,
Paralysis CVS Manifestations
Arrhythmias
TREATMENT
Etiologic treatment:
Dantrolene ( 2 – 3 mg/kg IV) as an initial bolus, followed
with repeat doses every 5– 10 minutes until symptoms are
controlled.
Prevent recurrence (dantrolene 1 mg / kg IV every 6 hours
for 72 hours )
Symptomatic Treatment:
Immediately terminate trigger drugs & conclude surgery a
s soon as possible Hyperventilate with 100 % oxygen
Initiate active cooling
Iced saline 15 ml / kg every 10 minutes
Gatric lavage with iced saline
Surface cooling
Use of alternative medication
local anesthetics (lidocaine, bupivacaine, mepivacaine),
opiates (morphine, fentanyl), ketamine, barbiturates, nitrou
s oxide, propofol, etomidate, and benzodiazepines
Correct metabolic acidosis
( NaHCO3 1 – 2 m Eq/kg IV based on arterial ph
Maintain urine output
Hydration
Mannitol ( 0.25 g/kg IV )
Furosemide ( 1mg/ kg )
Treatment of arrhythmia ( Xylocaine infusion)
Monitor in ICU
REFERENCES
Anaesthesia & co-existing diseases – Stoeltin
g.
Short practice of Anaesthesia – Churchill Dav
idson Problem oriented
Anaesthesia – Stoelting. American Society
of Anaesthesia ( ASA )
Annual refresher lecture notes – 1998. Textbo
ok of Anaesthesia – Ronald Miller.
THANKS TO
NANDKISHORE
SIR FOR HIS
GUIDANCE

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malignant hyperthermia (MH)

  • 2. INTRODUCTION Malignant hyperthermia (MH) is a type of severe reaction that occurs to particular medications used during general anesthesia, among those who are susceptible. 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.
  • 3. CAUSES 1. volatile anesthetic gases, such as halothane, sev oflurane, desflurane, isoflurane, enflurane 2. depolarizing muscle relaxants suxamethonium and decamethonium 3. Biological stresses of physical exercise or heat may be the trigger. 4. exercise and/or on exposure to hot environments 5. inheritance is autosomal dominant with variable penetrance
  • 4. SIGN AND SYMPTOMS The typical signs of malignant hyperthermia are due to a hypercatabolic state, which presents as a very high temperature •An increased heart rate •Abnormally rapid breathing •Increased carbon dioxide production •Increased oxygen consumption •Mixed acidosis •Rigid muscles •rhabdomyolysis
  • 5. DIGNOSIS Monitoring ETCO2 A rise in end-tidal carbon dioxide concentration (despite increased minute ventilation). ABG Respiratory acidosis is universally present and many patients have developed metabolic acidosis at the time of diagnosis
  • 6. Monitoring temperature Elevation of body temperature is often a late sign. Blood Test A raised creatine kinase level, elevated potassiu m, increased phosphate (leading to decreased calcium) Serum Myoglobin Raised myoglobin; this is the result of damage t o muscle cells (rhabdomyolysis )
  • 7. Gene Testing Analysis for RYR1 mutations Skeletal muscle biopsy: Sample is taken from vastus muscle of thigh under local anaesthesia. Muscle is subjected to is ometric contracture testing under influence of caffeine or halothane or both. It produces exaggerated contracture in susceptible patients.
  • 8. CRITERIA FOR MALIGNANT HYPERTHERMIA •A 1994 consensus conference led to the formulat ion of a set of diagnostic criteria. The higher the score (above 6), the more likely a reaction constituted MH. •Respiratory acidosis (end-tidal CO above 55 mm Hg/7.32 kPa or arterial Pco 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)
  • 9. •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)
  • 10. COMPLICATIONS OF M H DIC Pulmonary Edema Acute Renal Failure CNS Damage Blindness, Seizures, Coma, Paralysis CVS Manifestations Arrhythmias
  • 11. TREATMENT Etiologic treatment: Dantrolene ( 2 – 3 mg/kg IV) as an initial bolus, followed with repeat doses every 5– 10 minutes until symptoms are controlled. Prevent recurrence (dantrolene 1 mg / kg IV every 6 hours for 72 hours ) Symptomatic Treatment: Immediately terminate trigger drugs & conclude surgery a s soon as possible Hyperventilate with 100 % oxygen
  • 12. Initiate active cooling Iced saline 15 ml / kg every 10 minutes Gatric lavage with iced saline Surface cooling Use of alternative medication local anesthetics (lidocaine, bupivacaine, mepivacaine), opiates (morphine, fentanyl), ketamine, barbiturates, nitrou s oxide, propofol, etomidate, and benzodiazepines Correct metabolic acidosis ( NaHCO3 1 – 2 m Eq/kg IV based on arterial ph
  • 13. Maintain urine output Hydration Mannitol ( 0.25 g/kg IV ) Furosemide ( 1mg/ kg ) Treatment of arrhythmia ( Xylocaine infusion) Monitor in ICU
  • 14. REFERENCES Anaesthesia & co-existing diseases – Stoeltin g. Short practice of Anaesthesia – Churchill Dav idson Problem oriented Anaesthesia – Stoelting. American Society of Anaesthesia ( ASA ) Annual refresher lecture notes – 1998. Textbo ok of Anaesthesia – Ronald Miller.