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115 Cards in this Set

  • Front
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Oxygen class

Gas

Oxygen MOA

Enters through respiratory system and transported by hemoglobin. Used to breakdown glucose into usable energy.

Oxygen pharmacokinetics

Onset: immediate


Peak effects: <1 min


Duration: <2 mins


Half-life: N/A

Oxygen indications

Hypoxia (as determined by physical exam and SPO2)

Oxygen contraindications

Non-hypoxic patients

Oxygen precautions

Titrate to avoid hyperoxia. Prolonged high concentration O2 to neonates can damage their eyes. >6L/min should be humidified. Monitor O2 with pulse oximetry.

Oxygen side effects

Hyperoxia can cause free-radical induction and oxidative stress.


Mucous membrane irritation. Nosebleeds.

Oxygen dosage

The least concentration that will correct the patient's hypoxia.

Epinephrine class

Sympathetic agonist, catecholamine

Epinephrine MOA

Acts on alpha and beta receptors. More profound effect on beta. Causes increase in HR, contractile force, electrical activity (in the myocardium), SVR, B/P and automaticity.

Epinephrine pharmacokinetics

(IV/ET)


Onset: <2 mins


Peak effects: <5 mins


Duration: 5-10 mins


Half-life: 5 mins

Epinephrine indications

Cardiac arrest


Severe anaphylaxis


Severe reactive airway disease


Calcium channel blocker or beta blocker overdose.

Epinephrine contraindications

Patients who do not require extensive cardiopulmonary resuscitation.

Epinephrine precautions

Protect from light.


Can be deactivated by alkaline solutions so flush line well between Epi and sodium bicarbonate.

Epinephrine side effects

Palpitations.


Anxiety.


Tremulousness.


Headache.


Dizziness


N/V


Increases myocardial O2 demand so can cause myocardial ischaemia.

Epinephrine interactions

Can be deactivated by sodium bicarbonate. Effects of Epi can be intensified by antidepressants.

Epinephrine cardiac arrest dosage

1.0 mg Epinephrine 1:10,000 IV or IO q 3-5 min prn

Epinephrine anaphylaxis dosage

0.3 mg Epinephrine 1:1,000 IM q 5 min prn to total max 0.9 mg


0.1 mg Epinephrine 1:10,000 SIVP/IO q 2 min to total max 1 mg


Infusion: (Anaphylaxis refractory to normal saline 500 mL administered and transport time greater than 30 minutes)IV/IO start at 1 mcg/min, increase by 1 mcg/min prn, titrate to systolic BP 90 mmHg or greater, to a maximum of 8 mcg/min

Epinephrine bronchospasm dosage

0.3 mg Epinephrine 1:1,000 IM q 20 min to total max of 0.9 mg

Epinephrine CCB or BB OD

Mandatory OLMC – Hypotensive beta blocker or calcium channel blocker overdose refractory to fluid boluses, glucagon and calcium chlorideInfusionIV/IO start at 2 mcg/min, increase by 1 mcg/min prn, titrate to systolic BP 90 mmHg or greater, to a maximum of 10 mcg/min

Norepinephrine class

Sympathetic agonist


Catecholamine

Norepinephrine MOA

Acts on alpha and beta receptors but more profound action on alpha. Potent peripheral vasoconstriction.

Norepinephrine pharmacokinetics

Onset: immediate


Peak effects: <1 min


Duration: 1-2 mins


Half-life: 3 mins

Norepinephrine precautions

Measure B/P q 5-10 mins to prevent dangerously high B/P.


Initiate fluid replacement prior to norepi.


Give through large vein as can caused necrosis if extravasates. Increases myocardial O2 demand. Typically induces renal and mesenteric vasoconstriction.


In septic pt, improves renal blood flow and urine output.

Norepinephrine side effects

Anxiety


Tremulousness


Headache


Dizziness


N/V


Bradycardia (reflex response to peripheral vasoconstriction)


Myocardial ischaemia

Norepinephrine interactions

Deactivated by alkaline solutions (sodium bicarb)


Administration with beta blockers can result in markedly elevated B/P

Norepinephrine indications

Hypotension (<70) not related to hypovolemia (i.e. septic shock)

Norepinephrine contraindications

Pts who are hypotensive from hypovolemia

Norepinephrine dosage

(Not AHS)


0.1-0.5 mcg/min to a max of 30 mcg/min

Dopamine trade name

Intropin

Dopamine class

Sympathetic agonist


Catecholamine

Dopamine MOA

Acts on alpha, beta and dopaminergic receptors. Effects are dose dependent. Increases B/P by acting an alpha and beta. Beta effect is positive inotropic. It does not increase myocardial O2 demand as much as other catecholamines and does not have same positive chronotropic effects. Acts on alpha receptors to cause peripheral vasoconstriction.

Dopamine pharmacokinetics

Onset: <5 mins


Peak effects: 5-8 mins


Duration: <10 mins


Half-life 2 mins

Dopamine precautions

Can induce or worsen supraventricular or ventricular arrhythmias. When dose is >20 mcg/kg/min, alpha effects dominate and acts like norepi. Do not administer if tachyarrhythmias or Vfib.

Dopamine side effects

Nervousness


Headache


Arrhythmias


Palpitations


CP


Dyspnea


N/V

Dopamine interactions

Deactivated by alkaline solutions.


Reduce dose if pt is taking MAOIs.


May cause hypotension if given cocomitantly with phenytoin (Dilantin)


Dopamine indications

Beta blocker/CCB OD


Heart block/bradycardia


Pulmonary edema


Sepsis


Shock

Dopamine contraindications

Hypovolemic shock where complete fluid resuscitation has not occurred


Pheochromocytoma (adrenal gland tumour)


Uncorrected tachyarrhythmias


V-fib


Monoamine oxidase inhibitor therapy within last 14 days


Hypersensitivity to sulphites

Dopamine BB/CCB OD dose

OLMC!


IV/IO start at 5 mcg/kg/min increase by 5 mcg/kg/min prn, titrate to systolic BP 90 mmHg or greater, to a maximum of 20 mcg/kg/min

Dopamine bradycardia/heart block dose

(Refractory to atropine and TCP)


IV/IO start at 5 mcg/kg/min, increase by 5 mcg/kg/min prn to a maximum of 10 mcg/kg/min

Dopamine pulmonary edema dose

(B/P <90)


IV/IO start at 5 mcg/kg/min, increase by 5 mcg/kg/min to a maximum of 20 mcg/kg/min; titrate to systolic BP 90 mmHg or greater

Dopamine sepsis dose

(Septic shock refractory to 2 fluid boluses)


IV/IO start at 5 mcg/kg/min, increase by 5 mcg/kg/min to a maximum of 20 mcg/kg/min; titrate to systolic BP 90 mmHg or greater

Dopamine shock dose

(Refractory to 2 fluid boluses)


IV/IO start at 5 mcg/kg/min, increase by 5 mcg/kg/min to a maximum of 20 mcg/kg/min; titrate to systolic BP 90 mmHg or greater

Vasopressin MOA

acts as a non-alpha-adrenergic vasoconstrictor through direct stimulation of smooth muscle receptors

Vasopressin pharmacokinetics

Onset: variable


peak effects: variable


Duration: 30-60 mins


Half-life: 10-20 mins

Vasopressin indications

used to replace 1st or 2nd dose of Epi in cardiac arrest. Used to increase peripheral vascular resistance during CPR

Vasopressin contraindications

pts with chronic nephritis, ischemic heart disease, PVCs, or advanced arteriosclerosis. When used in CPR, no contraindications.

Vasopressin precautions

Use with caution in pts with epilepsy, migraine, asthma, heart failure and angina.

Vasopressin side effects

blanching of the skin


abd cramps


nausea


hypertension


bradycardia


minor arrythmias

Vasopressin interactions

none in ACLS setting

Vasopressin dosage

40 units IV/IO. Single dose only. Replaces 1st or 2nd Epi in cardiac arrest.

Sotalol class

Beta-blocker

Class 2 and Class 3 antiarryhthmic properties



Sotalol MOA

blocks stimulation of B1 and B2

Sotalol pharmacokinetics

Onset: variable


Peak Effects: 2-3 hours


Duration: 24 hours


Half-Life: 7-18 hours

Sotalol indications

hemodynamically stable monomorphic V-tach

Sotalol contraindications

Pts with:


bronchial asthma


allergic rhinitis


severe sinus-node dysfunction


sinus brad


2nd and 3rd degree AV blocks (unless functioning pacemaker is present)


cardiogenic shock


severe or uncontrolled heart failure


hypersensitivity


prolonged QT interval

Sotalol precautions

may cause new or worsen existing arrhythmias. Such effects range from more frequent PVCs to development of more severe V-tach, V-fib and Torsades de pointes.

Sotalol side effects

CNS: fatigue, weakness, anxiety, dizziness, drowsiness, insomnia, memory loss, mental status changes, nervousness, nightmares


Resp: bronchospasm, wheezing


Cardiovascular: arrhythmias, bradycardia, CHF, pulmonary edema, orthostatic hypotension, peripheral vasoconstriction

Sotalol interactions

+general anesthesia, IV phenytoin or verapamil = additional myocardial depression


+digitalis glycosides = additional bradycardia


+ antihypertensives, ETOH, nitrates or MAOIs within 14 days = additional hypotension


May interact with class 1A antiarrhythmics (procainamide) and class 3 medications (amiodarone).



Sotalol dosage

1-1.5 mg/kg may be given at a rate of 10 mg/minute

Metoprolol class

Selective beta-blocker


Class 2 antiarrhythmic

Metoprolol MOA

Blocks both B1 and B2 receptors but is selective for B1 receptors. Has minimal (if any) effects on B2 at doses less than 100 mg.


Reduces HR, systolic B/P and cardiac output.


Inhibits tachycardia especially after AMI. Reduces the incidence of V-fib and chest pain in AMI pts.

Metoprolol pharmacokinetics

Onset: Immediate (IV)


Peak Effects: 20 mins


Duration: 5-8 hours


Half-Life: 3-4 hours

Metoprolol indications

AHS: Mandatory OLMC - stable (BP > 80 mmHg) and symptomatic (ALOC, CP, SOB and/or CHF) atrial fibrillation or atrial flutter


Other: AMI pts who are hypertensive and don't have contraindications, certain forms of polymorphic V-tach (associated with acute ischemia, familial long QT syndrome, catecholaminergic)

Metoprolol contraindications

AHS:


Hypersensitivity


Second and third degree AV blocks


Bradycardia less than 50 bpm


Systolic BP less than 100 mmHg


Severe acute heart failure


Bronchospastic COPD,


reactive airway disease


Recent (less than 24 hrs) cocaine use



Metoprolol precautions

Monitor B/P, pulse, ECG and resp status.


Watch for signs of CHF, bradycardia, shock, heart block or bronchospasm. If seen, discontinue.

Metoprolol side effects

bradycardia


hypotension


lethargy


CHF


dyspnea


wheezing


weakness

Metoprolol interactions

Do not administer to pts who have received IV CCBs.


Administer with caution to pts taking anti-hypertensives.

Metoprolol dosage

Mandatory OLMC


5 mg SIVP q 5 minutes prn to a total maximum of 15 mg or HR < 110 bpm or BP < 100 mmHg

Salbutamol trade name

Ventolin

Salbutamol class

sympathetic agonist

Salbutamol MOA

a selective B2 agonist. Causes prompt bronchodilation with minimal side effects.

Salbutamol pharmacokinetics

Onset: 5-15 mins


Peak effects: 1-1.5 hrs


Duration: 3-6 hrs


Half life: <3 hrs

Salbutamol indications

Bronchospasm


Anaphylaxis-induced bronchospasm

Salbutamol contraindications

Hypersensitivity


Tachydysrhythmias

Salbutamol precautions

Monitor pt's V/S.


Auscultate lung sounds before and after each dose.

Salbutamol side effects

Palpitations


Anxiety


Dizziness


Headache


Nervousness


Tremor


HTN


Arrhythmias


CP


N/V

Salbutamol interactions

Unpleasant side effects are more likely if given with other sympathetic agonists. B-blockers may blunt it's effects.

Salbutamol dosage

5 mg nebulized. Repeat PRN.


10 puffs via MDI spacer. Repeat q 5min PRN.

Ipratropium bromide trade name

Atrovent


Ipratropium class


Anticholinergic


Ipratropium MOA


A parasympatholytic used in Tx of resp emergencies. Causes bronchodilation and dries respiratory tract secretions. Works by blocking acetylcholine receptors thus inhibiting parasympathetic stimulation.

Ipratropium pharmacokinetics

Onset: varies


Peak effects: 1.5-2 hours


Duration: 4-6 hrs


Half-life: 1.5-2 hrs

Ipratropium indications

Anaphylaxis


Bronchospasm

Ipratropium contraindications

hypersensitivity

Ipratropium precautions

Monitor V/S.


Auscultate lung sounds before and after each dose.


Administer during rapid transport for pts in severe distress.


Prevent it from reaching pt's eyes.

Ipratropium side effects

Palpitations, anxiety, dizziness, HA, nervousness, rash, N/V

Ipratropium interactions

none in the emergency setting

Ipratropium dosage

500 mcg nebulized. Repeat prn in anaphylaxis. Repeat x2 in bronchospasm.

Methylprednisolone trade name

Solu-medrol

Methylprednisolone class

Corticosteroid and anti-inflammatory

Methylprednisolone MOA

Potent anti-inflammatory properties. Inhibits the release of substances which cause inflammation (cytokines, interleukin, interferon). Inhibits the synthesis of pro-inflammatory enzymes.

Methylprednisolone pharmacokinetics

Onset: varies


Peak effects: 4-8 days


Duration: 1-5 weeks


Half-life: 3.5 hours

Methylprednisolone indications

NOT AHS


severe anaphylaxis, asthma or COPD, and urticaria.

Methylprednisolone contraindications

none in emergency setting

Diphenhydramine trade name

Benadryl

Diphenhydramine class

antihistamine

Diphenhydramine MOA

a H1 (histamine 1) receptor antagonist blocking histamine release. It also has anticholinergic activity.

Diphenhydramine pharmacokinetics

Onset: 10-15 mins (IV)


Peak effects: 1 hr


Duration: 6-8 hrs


Half-life: 1-4 hrs

Diphenhydramine indications

Allergic reaction, anaphylaxis, headache (prevention or relief of extrapyramidal reaction or agitation due to metoclopramide), nausea and vomiting (prevention or relief of extrapyramidal reaction or agitation due to metoclopramide).

Diphenhydramine contraindications

hypersensitivity to diphenhydramine or dimenhydrinate.

Diphenhydramine precautions

Use with caution in pts with asthma, narrow-angle glaucoma, benign prostatic hypertrophy and in nursing mothers or neonates.

Diphenhydramine side effects

Drowsiness, dizziness, headache, fatigue, palpitations, euphoria, urinary frequency

Diphenhydramine interactions

Furosemide (hypotension)

Diphenhydramine dosage

Allergic reaction: 50 mg PO or 1mg/kg IM/SIVP to a single max dose of 50mg. NO repeat.


Anaphylaxis: 1 mg/kg IM/SIVP/IO to a single max of 50 mg. NO repeat.


Headache: 25 mg SIVP or deep IM. NO repeat.


N/V: 25 mg SIVP/IM. NO repeat

Dexamethasone trade name

Decadron

Dexamethasone class

Corticosteroid and anti-inflammatory

Dexamethasone MOA

Potent anti-inflammatory properties. Inhibits the substances that cause inflammation (cyotkines, interleukin, interferon) and also inhibits the synthesis of pro-inflammatory enzymes.

Dexamethasone pharmacokinetics

Onset: Immediate.


Peak effects: 1-2 hrs


Duration: 2.75 days


Half-life: 3-4.5 hrs

Dexamethasone indications

anaphylaxis, bronchospasm

Dexamethasone contraindications

Systemic fungal infections


Hypersensitivity to dexamethasone or other steroids.


Hypersensitivity to benzyl alcohol or sodium sulfite.


Patients with penumonia and any symptoms of SIRS

Dexamethasone precautions

Only give single dose. Effects will appear 2-4 hrs after dose.

Dexamethasone interactions

none in the emergency setting

Dexamethasone side effects

fluid retention, CHF, HTN, abdominal distension, vertigo, HA, N/V, malaise and hiccups

Dexamethasone dosage

8 mg IM/SIVP/IO. NO repeat