MH Dantrolene Flashcards
Temp regulation centers
Hypothalamus-
Gain center-posterior
Loss center-anterior
1 degree change in temp will alter BMR by
7%
Most heat loss is by
Radiation (40%)
Convection (30%)
Burn pts lose most via evaporation
Hypothermia phys changes
Increase SVR, decrease CO, myocardial depression, increases blood viscosity, Left shift, impaired coags, decrease CO2 production, decrease O2 consumption
Shivering increase cardiac work, O2 consumption
Drug elimination slowed
MH signs and symptoms
Hypercarbia Tachycardia/pnea Hyperthermia (1-2c q5min) HTN Dysrhythmias Acidosis Skeletal muscle rigidity (Masseter muscle spasm after succs in children CPK >20,000 confirms) Myoglobinuria Hypoxia
MH incidence, genetics
1 in 15,000 anesthetics in children
1 in 50,000 anesthetics in adults
Dominant pattern of inheritance
Ryanodine receptor mutation found in 50% of MH families and 20% of all MH patients
Triggers
Full episodes- Halothane, Enflurane, Isoflurane, Desflurane, Sevoflurane, Succinylcholine
MIld episodes- Exercise in hot conditions, neuroleptic drugs, ETOH, infection
MH patho
Increased myoplasmic Ca+
Muscle spasms–> rhabdomyolysis
Heat production–>fever–> hypermetabolism
MH clinical features
Skeletal muscle involvement
SNS hyperactivity
Hypercapnia
Hyperthermia
Masseter muscle rigidity
May be normal sign after succs, but- if sustained immediately check a K+ and blood gas. Clinical MH occurs about 20% of the time after this.
Skeletal muscle in MH
Pain
Myoglobinuria
Cardiac arrhythmias
CPK in MH
> 20,000
What is the main concern with rapid rhabdomyolysis in MH
Rapid increase in K+
SNS hyperactivity
Tachy, acidosis, ATP depletion, hypoxemia, heat production, hyperventilation, CV instability
Labs
Get an A-line
Decreased PaO2, increased PaCO2
High lactate and low pH
CPK very high, up to 100,000
Elevation correlates best with rhabdomyolysis, less well with fever and acidosis
Resting CK mildly increased
MMR
Continue with agents that will not trigger MH or postpone elective surgery
Unless MH manifests, dantrolene is not recommended
Pts should be closely observed for 24 hours for signs of MH
Discuss muscle biopsy with MH expert
MH testing
Halothane contracture test- gold standard
Caffeine contracture test- not reliable, many false positives
MH treatment
Must be identified early
Call for Help/MH cart
Stop all volatile agents and succs, change circuit/soda lime, change to new machine if possible
Hyperventilation on 100% O2
Dantrolene 2.5mg/kg bolus followed by 2mg/kg IV q5 minutes to a total of 10mg/kg
Bicarb for acidosis
Monitor temp, aggressively cool to under 38C
Maintain 2ml/kg/hr UO with fluids, lasix
Tx for dysrhythmias and hyperkalemia in MH
No Ca channel blockers
Other standard antiarrhythmics ok (Procainamide 15mg/kg IV)
Correction of hyperkalemia and acidosis correct most problems. Hyperventilation, dantrolene, and bicarb may be sufficient.
Treat hyperkalemia with glucose, insulin, and calcium
MH care once initial episode is controlled
ICU for 36 hours (25% recrudescence rate)
Continue dantrolene for at least 24 hours, 1mg/kg q6 hrs
No K+ fluids, avoid LR
Follow coags as DIC may occur
Measure CK q6h until normal after pt has improved/stabilized
CK may remain elevated for 2 weeks
MH cart drugs
36 vials of dantrolene, 20mg each with 60ml sterile water for each vial (1000ml x 2)
8.4% bicarb 50ml x 5
Lasix 40mg/amp x 4 amps
D50 50ml vials x 2
CaCl 10% 20ml vial x 2
Regular insulin 100units/ml x 1 (must be refrigerated)
Lidocaine HCl 2% 1 box = 2 grams or 10ml/100mg preloaded vial
MH cart equipment
Syringes 60ml x 5 to dilute dantrolene
Mini-spike IV additive pins x 2 and multi-ad fluid transfer sets x2 (to reconstitute dantrolene)
Angiocaths 20g-2inch, 22g-1inch, 24g-3/4inch (4 each)
D5W 250ml x1, Microdrip IV set x 1
NG tubes
Irrigation tray with piston syringe x 1
Toomy irrigation syringes 60ml x 2
MH monitoring
Core temp probes
CVP kits
A-line/CVP transducers
Additional MH stuff
Large sterile drap Three-way irrigating foley Urinometer Rectal tubes Plastic bags for ice, large and small Bucket for ice