B43 - cardio, anaphylaxis Flashcards
Shockable rhythms (2)
VF, pulseless VT
Non-shockable rhythms
include pulseless electrical activity/asystole
Patient in VF, 3 shocks administered. What next? (3 steps)
Give 1mg adrenaline IV (every 3-5 mins) and amiodarone 300mg IV (after 3 shocks) whilst performing further CPR.
Give further adrenaline 1mg IV after alternate shocks.
Further amiodarone 150mg IV may be administered after a total of five defibrillation attempts.
How would drug choice change in CPR if rhythm was non-shockable (as opposed to adrenaline every 3-5 mins and amiodarone after 3 shocks in shockable)
Amiodarone would not be administered but adrenaline 1mg IV is given as soon as intravascular access is achieved and repeated every 3-5 minutes
What is adrenaline?
endogenous catecholamine hormone and neurotransmitter in the sympathetic nervous system.
Where and from what is adrenaline normally synthesised?
from noradrenaline in the adrenal medulla, specifically chromaffin cells.
Adrenaline MOA
α and β adrenoceptor agonist
Actions of adrenaline on α1 (4)
vasoconstriction
relaxation of smooth muscle in GI
saliva secretion
hepatic glycogenolysis
Actions of adrenaline on α2 (3)
vasoconstriction
inhibition of transmitter release
platelet aggregation
Actions of adrenaline on β2
position ionotropic and chonotropic effects
Actions of adrenaline on β2 (2)
broncodilation
vasodilation
Action of adrenaline on β3
lipolysis
Actions of adrenaline with regards to cardiac arrest scenario
increases coronary and cerebral perfusion pressure as a result of vasoconstriction
thought to increase the chance of restoring a heartbeat and of improving long-term neurological outcome.
Adrenaline cautions in non-emergency situations (11)
ischaemic heart disease, cerebrovascular disease, diabetes, hypertension, hyperthyroidism Hypokalaemia hypertension (risk of cerebral haemorrhage) hypokalemia palpitations - dysrhythmias tissue necrosis (e.g. ring blocks) metabolic acidosis
Adrenaline side effects (10)
hypersalivation, headache, hyperhidrosis, angle closure glaucoma, reduced appetite, hyperglycaemia, hypertension, mydriasis, peripheral coldness, urinary disorders
Adrenaline interactions (3)
Amitriptyline (increased effects of adrenaline) Beta blockers (severe hypertension) MAO inhibitors (hypertensive crisis - MAO is one of the routes of metabolising adrenaline, therefore inhibiting their action leads to an increase in adrenaline.)
Route and dose adrenaline administered in cardiac arrest
1mg by IV injection using 1 in 10,000 solution (100micrograms/mL) i.e. 10ml
Followed by 20ml flush of 0.9% sodium chloride
Flush is required to aid entry into central circulation.
Beta blockers can be used as antihypertensive drugs.Why is there a risk of severe hypertension when beta blockers and adrenaline interact?
In the absence of a beta-blocker, adrenaline does not have much effect on mean blood pressure because it has both alpha-adrenergic effects (producing vasoconstriction) and beta-adrenergic effects (producing vasodilation). If a patient on a nonselective beta-blocker receives adrenaline however, the beta-blocker prevents the beta-adrenergic vasodilation, leaving unopposed alpha vasoconstriction. Cardio-selective beta-blockers would not be expected to precipitate hypertensive reactions.
Amiodarone drug class
Class III anti-arrhythmic
Amiodarone MOA (3)
Multiple anti-arrhythmic actions across all four groups
Prolongs cardiac action potential and delays refractory period
Inhibits K+ channels involved in repolarisation
Challenges of amiodarone (3)
Incomplete oral absorption
Large volume of distribution
Extremely long half-life