Session 05 (Prehospital Pharmacology)
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Transcript Session 05 (Prehospital Pharmacology)
Prehospital Pharmacology
Advanced Care Paramedicine
Module: 6
Session: 5
Prehospital medicating
Prescribed by GP
Standing Orders
Protocols
Transfer orders (should be written)
EMS administered
Ace Inhibitors
Inhibits the effect of the Angiotensin
Converting Enzyme (ACE) in the lungs,
blocking the conversion of Angiotension I to
Angiotension II thus inhibits the release of
ADH and helps decrease blood pressure.
Captopril
Enalapril
Quinipril
Benazepril
Lisinopril
Antibiotics
Kills or disrupts/stops the growth and
development of bacteria
Amoxicillin
Azithromycin
Bactrim
Ceclor
Ceftin
Ciprofloxacin
Clarithromycin
Cloxicillin
Dicloxicillin
Erythromycin
Keflex
Metrodiazanole
Nitrofurantoin
Penicillin
PenVee
Rifampin
Suprax
Tetracycline
Vancomycin
Vantin
Antidysrhythmics
Vaughn-Williams Classifications
Class I
Class II
Class III
Class IV
Antidysrhythmics
Class I
Na Channel Blockers
Slow the maximum rate of Phase 0 depolarization
Slow conduction velocity
Slow rate and force of contraction refractory period effects
Mechanisms of Action
Blocks Na influx through fast Na channels
Antidysrhythmics
Differential effects:
Ia
Increase duration of AP, prolonged repolarization, prolonged refractory
period, decreased membrane responsiveness
Decreased depolarization of SA node thus decreased pacemaker
activity
Also blocks K+ channels
Ib
Decreased duration of AP, decreased membrane responsiveness in
ventricles
Blocks activated and inactivated Na+ channels, depresses damaged
or depolarized cells (eg. post MI)
Does not block K+ channels
Ic
No effect or minimal increase in duration of AP & repolarization
Decreased membrane responsiveness
Decreased conduction velocity in atrial & ventricular cells
Also blocks K+ channels
Antidysrhythmics
Class Ia
Quinidine
Procainamide
Disopyramide
Class Ib
Lidocaine
Tocainide (Mexilitine)
Phenytoin
Class Ic
Flecainide
Propanfenone
Moricizine
Antidysrhythmics
Class II
Beta Blockers
Mechanisms of Action
Blockade of ß-receptors
Inhibition of norepinephrine release (bretylium)
Propranolol
Metoprolol
Atenolol
Antidysrhythmics
Class III
K Channel blockers
Prolong action potential and affiliated refractory period
Mechanisms of Action
Do not alter normal fast Na conductance
Do not compete for ß-receptors
Bretylium
Amiodarone (Has effects of all classes)
Sotalol (no longer used – causes Torsades)
Antidysrhythmics
Class IV
Ca Channel Blockers
Mechanisms of Action
Selectively block slow Ca channels
Inhibit slow inward Ca current during phase 2
Decrease rate of phase 4 depolarization
Effect on the “pacemaker in charge”
Depress conduction velocity in purkinji system and AV node
Decrease contractility in myocardium
Vasodilatation (lower intracellular Ca in arterial muscle)
Verapamil (Isoptin)
Diltiazem
Cardizem
Nifedepine
Plendil
Antihistamines
Compete with histamine for H1 and H2
receptors thus decreasing the
histamines affect
Chlorpheniramine
Cyproheptidine
Diphenhydramine
Hydroxizine
Promethazine
Antihypoglycemics
Treat diabetes by increasing the amount of
sugar in the blood, and decreasing the
amount transported into the tissues
Diabeta
Diabinese
Glypizide
Glyburide
Metformin
Tolinase
Antifungals
Acts primarily by damaging the permeability barrier
in the membrane of the fungi. This leads to the
inability for the cell to construct an intact membrane
and leads to the death of the fungus
Diflucan (Fluconazole)
Canesten (Clotrimazol)
Griseofluvin
Ketoconazole
Lamisil
Nizoral
Monostat
Sopranox
Tinactin
Antituberculosis
Inhibits RNA synthesis in bacteria
Ethambutol
Rifampin
Isoniazid
Pyrazinamide
Streptomycin
Antivirals
Affects the reproduction of the virus.
Acyclovir
Amatadine
Rimantadine
3TC
Acyclovir
Amatadine
AZT
DDI
Quinivere
Rimatadine
Zovirax
Anxiolytics
Combat anxiety by binding with
receptors (GABA) in the cerebral
cortex and limbic regions.
Valium
Wellbutrin
Xanax
Benzodiazepines
Bind with receptors (GABA) to
decrease anxiety and prevent seizures
Valium
Versed
Halcyon
Beta 1 Specific Blockers
Compete for the ß-1 receptor sites
Blocadren
Corgard
Lopressor
Tenormin
Bronchodilators
ß-2 agonists
Albuterol
Aminophylline
Atrovent (anti-cholinergic)
Metaproterenol
Ventolin
Cardiac glycosides
Block ionic pumps in heart increasing
Ca concentrations and contraction,
decreasing rate and speed of
conduction
Digitalis
Digitoxin
Digoxin
Lanoxin
Cholesterol lowering
Prohibits the synthesis of cholesterol
Lopid
Lozol
Mevacor
Zocor
Diuretics
Causes body’s water balance to shift, excreting water and
some electrolytes
Loop Diuretics
inhibit reabsorption of sodium and chloride in the ascending Loop of
Henle, thus excreting water and potassium. Most potent of the
diuretics
Thiazide Diuretics
Affect the distal tubule blocking cotransport of Na-CL
HCTZ
Potassium-sparing Diuretics
Furosemide (Lasix)
Amiloride
Aldactone
Osmotic Diuretics
pharmacologically inert nonelectrolyte which is freely filtered by the
renal glomerulus and not reabsorbed from the nephron. Osmotically
pulls large amounts of water from the cells which it carries with it
when it is excreted
Mannitol
D50
Gastrointestinal
Chlopromazine
Dimenhydrinate
Famotidine
Loperamide
Magnesium hydroxide
Omeprazole
Prochloperazine
Scopolamine
H2 blockers
Blocks H2 receptors in the stomach
Axid
Pepcid
Ranitidine
Tagamet
Cimetidine
Migraine therapy
Typically decrease the vasodilatation
in the cranial vascualture relieving the
headache
Inderal
Ergotamine
Fiorinol
Sumatripan
Narcotics
Act on the CNS to slow down all body systems and
are used medically as cough suppressants or pain
relievers
High potential for abuse and for dependency
Narcotics can be classified into three groups:
Natural origin
Codeine, Morphine, Fentanyl
Semi-synthetic
Heroin
Synthetic
Merperidine (Demerol), Methadone, Hydromorphone
(Dilaudid)
Non-Narcotic analgesics
Relieve pain without producing unconsciousness or impairing
mental capacities.
Many of these drugs also have an antipyretic and/or an antiinflammatory effect
Aspirin (ASA)
Acetaminophen (Tylenol)
Analgesic, antipyretic, and anti-inflammatory agent used for mild to
moderate pain. It is contraindicated in peptic ulcer disease. It acts as
a gastric mucosal irritant and has an anticoagulant effect.
Similar to aspirin, but has no anti-inflammatory action.
Ibuprofen
Ibuprofen is indicated for the relief of mild to moderate pain. Has an
anti-inflammatory agent. It is not to be given to patients in the third
trimester of pregnancy or anyone with a history of gastrointestinal
bleeding
NSAIDS
Non-Steroidal Anti-inflammatory Drug
Inhibits the cyclooxygenase enzyme from
synthesizing prostaglandins
Alleve
ASA
Ibuprofen
Indomethacin
Relafen
Toradol
Voltaren
Steroids
Synthetic hormones
Possess anti-inflammatory (glucocorticoid) and/or salt-retaining
(mineralocorticoid) properties to varying degrees.
Glucocorticoids
Affect almost all body systems and cause varied metabolic effects
Decrease inflammation
Stabilization of leukocyte lysosomal membranes
Inhibition of macrophage accumulation in inflamed areas
Reduction of capillary permeability.
Suppress immune responses
Promote gluconeogenesis
Redistribution of fat from peripheral to central areas of the body
Reduce intestinal absorption and increase renal excretion of Ca
Reduction of activity and volume of the lymphatic system
Decreased immunoglobulin and complement concentrations
Decreased passage of immune complexes through basement membranes
Mineralocorticoids
Affect electrolyte and fluid balance by acting on the distal renal tubule to
promote Na reabsorption and K and H excretion.
Steroids
Glucocorticoids
Mineralocorticoids
Short Acting
Fludrocortisone
Cortisone
Hydrocortisone
Intermediate Acting
Methylprednisolone
Prednisolone
Prednisone
Triamcinolone
Long Acting
Betamethasone
Dexamethasone
Education
Previous Training was “ see this... give
this ”
Education
A&P
Pathophysiology
Drug specifics
Drug specifics
Class
Mechanism of action
Indications
Contraindications
Precautions
Side effects
Interactions
Dosage
Administration