Beta Blockers Flashcards
Beta Adrenergic Receptor Antagonists
Disallow sympathomimetics from provoking a beta response on the heart, airway, blood vessels, JG cells, and pancreas
BB on the Heart
bradycardia, decreased contractility, conduction velocity, improve O2 supply and demand balance
BB on the Airway
bronchoconstriction and can provoke bronchospasm in patients with asthma or COPD
BB on the Blood Vessels
Vasoconstriction in skeletal muscles; PVD symptoms (increase)
BB on the JG cells
Decreased renin release (indirect way of decreasing BP)
BB on the Pancreas
Decreased stimulation of insulin release by epi/NE at B2 and masks s/s of hypoglycemia beta 1
Beta Blockers MOA
selective binding to beta receptors: influence on inotropy and chronotropy
competitive and reversible inhibition: large doses of agonist (epi & glucagon) can overcome block
chronic use, upregulation of receptor (dont abruptly stop, can lead to increased HR and BP)
Nonselective BB
beta 1 & 2
propranolol, nadalol, timolol, pindolol
Cardioselective BB
beta 1 only
metoprolol, atenolol, acebutolol, betaxolol, esmolol
large doses or repeated doses can lose selectivity
Clinical Use of BB
HTN, angina, tachyarrythmias, block excessive SNS activity, pts at risk for MI, decreases mortality in tx of post MI patients
Relative Contraindications
Pre-existing AV heart block or cardiac failure
Reactive airway disease
DM (without BS monitoring)
Hypovolemia
Side Effects of BB
see other cards for specific systems
- reduction in IOP d/t decreased aqueous humor production
- N/V/D
- fatigue, lethargy
- inhibition of potassium uptake into skeletal muscles
- alter carb & fat metabolism, mask hypoglycemia increased in HR
Propranolol (prototype)
non-selective beta blocker (longer acting)
ADMIN WITH A GOAL OF 55-60 BPM
limited use in current anesthesia practice
concerns with chronic use: decreased clearance of amide L.A. & pulmonary clearance of fentanyl (both drugs are lipophilic amines)
Propranolol CV effects
decreased HR, contractility, and CO (b1)
O2 demand lowered
increased PVR, coronary vascular resistance (b2)
reduced renin release (b1)
Propranolol PK
undergoes 1st pass effect liver (90-95%)
PO dose larger than IV
PPB: 90-95%
liver metabolism: E1/2 T 2-3 hours
DECREASES CLEARANCE OF AMIDE LAs D/T DECREASE IN HEPATIC BLOOD FLOW INHIBITING LIVER METABOLISM (RISK OF SYSTEMIC TOXICITY OF AMIDE LAs)