Use LEFT and RIGHT arrow keys to navigate between flashcards;
Use UP and DOWN arrow keys to flip the card;
H to show hint;
A reads text to speech;
115 Cards in this Set
- Front
- Back
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 |