Cardiac Flashcards

1
Q

Acetylsalicylic acid trade name

A

Novasen, Aspirin, ASA, Bufferin

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2
Q

ASA class

A

salicylate, antiplatelet, antipyretic, anti-inflammatory, non-opioid analgesic (NSAID)

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3
Q

ASA MOA

A

Anticoagulant: at low doses, impedes clotting by inhibiting the enzyme COX-1 and prostaglandin synthesis, which
prevents formation of platelet-aggregating substance thromboxane A2 (this is irreversible and can prolong bleeding
time).

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4
Q

ASA Indications

A

Acute coronary syndromes suggestive of an acute myocardial infarction

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5
Q

ASA Dose

A

160-325 mg PO – Chewed and swallowed
*Note: May be given even if patient has taken a partial dose of ASA prior to incident

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6
Q

ASA Contraindications

A

 Hypersensitivity to ASA and NSAIDS or other salicylates
 Hypersensitivity to tartrazine (FDC yellow dye #5)
 Active GI Bleed
 Known bleeding disorders or thrombocytopenia (excessive low platelet levels)
 Breastfeeding - Children with viral infections, chicken pox or flu-like symptoms (can increase risk or Reye’s
syndrome)
 Pregnancy after 30 weeks gestation
 Hemorrhagic stroke
 Acute bronchospasm
 Asthma with history of induced bronchospasm by salicylates or NSAIDS

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7
Q

Adenosine trade name

A

Adenocard

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8
Q

Adenosine class

A

antiarrhythmic, (a naturally occurring nucleoside)

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9
Q

Adenosine MOA

A

Antiarrhythmic:
 Decreases automaticity in the SA node and greatly slows conduction through the AV node and inhibit reentry
pathways.
 Also useful in PSVT linked to accessory bypass tracts (Wolf-Parkinson White Syndrome)

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10
Q

Adenosine indications

A

 Stable, narrow-complex regular tachycardia (SA and AV nodal origin)
 Therapeutic and diagnostic maneuver for stable narrow complex SVT (Not AV nodal in origin)
 May be considered for: Unstable narrow-complex regular tachycardias while preparations are made for electrical
cardioversion
 Stable, regular, monomorphic, wide complex tachycardia thought or previously defined to be re-entry SVT with
aberrancy.

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11
Q

Adenosine Adult Dose

A

6 mg FIVP (over 1-3 seconds), repeat in 1-2 mins if needed once at 12 mg FIVP
*Note: Each dose of adenosine is to be followed immediately with a 20 ml flush while elevating the arm

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12
Q

Adenosine Pediatric Dose

A

0.1 mg/kg FIVP (over 1-3 secs) to a single max dose of 6 mg per repeat once in 1-2 mins if needed at 0.2mg/kg FIVP
to a max single dose of 12 mg
*Note: Each dose of adenosine is to be followed immediately with a 5-10 ml flush while elevating the arm

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13
Q

Adenosine Contraindications

A

 Hypersensitivity to drug or any component
 Poisoning / drug induced tachycardia
 2nd or 3rd degree block; symptomatic bradycardia
 Sick sinus syndrome
 Atrial fibrillation / atrial flutter; may induce ventricular arrhythmias

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14
Q

Amiodarone trade name

A

Codarone, Nexteribem Oaceribe

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15
Q

Amiodarone Class

A

benzofuran derivative, ventricular & supraventricular antiarrhythmic (class III)

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16
Q

Amiodarone MOA

A

 Inhibits alpha and beta adrenergic receptors producing vasodilation and AV nodal suppression (this slows
the conduction through the AV node and decreases peripheral vascular resistance PVR)
 Inhibits the outward potassium current so it prolongs the QT duration, prolongs the action potential and
refractory period (repolarization inhibition).
 Inhibits sodium channels, which slows conduction in the ventricles and prolongs the QRS duration.

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17
Q

Amiodarone Indications

A

 VF/pVT unresponsive to shock delivery, CPR, and a vasopressor
 Recurrent, hemodynamic unstable VT
 With expert consultation amiodarone may be used for tx of some atrial (SVT) and ventricular arrhythmias

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18
Q

Amiodarone Adult Dose

A

VF/pVT:
300 mg IVP, repeat 3-5 minutes if pt remains in VF pVT administer second dosage of 150 mg The
maximum total accumulative dosage is 450mg. Micron filter is not required in cardiac arrest

Wide Complex tachycardias with a pulse:
Rapid Infusion:
150 mg over 10 minutes, if required repeat 150 mg q 10 minutes (until suppression of arrhythmia or max
cumulative dose is reached).
Mix 150mg in 100ml bag of D5W with a micron filter (Conc

1st Maintenance Infusion (Immediately post suppression of arrhythmia):
360 mg over 6 hours (1 mg/min) (with micron filter)
2nd Maintenance Infusion:
540 mg over 18 hours (0.5 mg/min) (with micron filter)
*Note: Max cumulative dose of 2.2 G/24 hrs

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19
Q

Amiodarone pediatric dose

A

VF/pVT:
5 mg/kg IVP to a single max dose of 300 mg, q 5 mins, can repeat to a cumulative maximum of 15 mg/kg
/day or 2.2 g IV per 24 hours.

Wide complex tachycardias with a pulse:
5 mg/kg IV (over 20 to 60 mins) to a single max dose of 300 mg, q 5 mins, can repeat to a cumulative
maximum of 15 mg/kg /day or 2.2 g IV per 24 hours

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20
Q

Amiodarone contraindications

A

 AV block, pre-existing 2nd or 3rd degree block (without artificial pacemaker); Sinus node dysfunction
 Bradycardia
 Do not administer with other drugs that prolong QT interval (ie, procainamide)
 Sensitivity to amiodarone or iodine, (contains iodine)

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21
Q

Atropine trade name

A

atropine

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22
Q

Atropine MOA

A

 Antiarrhythmic: blocks the effects of acetylcholine on the SA and AV nodes, thereby increasing the SA and AV
conduction velocity resulting in increased heart rate.
 Has variable and clinically negligible effects on the His-Purkinge system. Small doses (less than 0.5 mg) may lead to
paradoxical slowing of the heart rate, which may be followed by a more rapid rate.
 Anticholinergic: decreases the action of the parasympathetic nervous system on certain glands (bronchial, salivary and
sweat), resulting in decreased secretions.

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23
Q

Atropine indications

A

 First drug for symptomatic bradycardias on adults
 May be beneficial in presence of AV nodal block
 Organophosphate poisoning (antidote)
 Bradycardia due to increased vagal tone can be considered with pediatrics patients including after intubation causing
bradycardia.

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24
Q

Atropine adult dose

A

Symptomatic Bradycardia: 1.0 mg IVP q 3-5 minutes prn to a total max dose of 0.04 mg/kg not to exceed total
accumulative dose of 3mg
Organophosphate Poisoning: 1- 4 mg IVP q 5 minutes until bronchial secretions dry

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25
Atropine pediatric dose
Dosage for Bradycardia: 0.02 mg/kg (minimum dose of 0.1 mg) to a single max of 0.5 mg IV/IO may repeat dose once in 5 minutes Organophosphate Poisoning Under 12 y/o 0.01 – 0.04 mg/kg max 1mg (minimum dose of 0.1 mg) IV/IO, then repeated and doubling the dose q 5 minutes until bronchial secretions dry
26
Atropine contraindications
 Hypersensitivity to atropine, belladonna alkaloids or sulfites  Tachycardia  Closed-angle Glaucoma  Acute MI  Myasthenia gravis  GI obstruction  Heart transplant patients
27
Clopidogrel bisulfate trade name
Plavix
28
clopidogrel class
P2Y12 Adenosine Diphosphate Receptor (ADP) antagonist
29
clopidogrel MOA
Irreversibly inhibits the binding of adenosine diphosphate (ADP) to its platelet receptor and the subsequent ADP-mediated activation of glycoprotein IIb/IIIa complex, thereby inhibiting platelet aggregation
30
clopidogrel indications
Acute STEMI/NSTEMI ACS
31
clopidogrel dose
Under age 75 years: Loading dose of 300-600 mg PO/OG Over age 75 years: Loading dose of 75 mg PO/OG
32
clopidogrel contraindications
 Hypersensitivity  Active bleeding  Significant liver impairment or cholestatic jaundice  Suspected liver impairment with history of hepatitis; long term ETOH abuse; or a presentation of jaundice  Thrombotic thrombocytopenic purpura  Suspected aortic dissection  Do not give if coronary bypass graft (CABG) surgery is planned, withhold for 5 days before CABG unless need for revascularization
33
diltiazem trade name
cardizem
34
diltiazem class
Class IV: Calcium Channel Blocker
35
diltiazem MOA
 Antiarrhythmic action: By inhibits the inward influx of calcium at the AV node, diltiazem decreases conduction velocity and increases refractory period, thereby decreasing the impulses transmitted to the ventricles in A-fib or Aflutter. The result is a decreased ventricular rate
36
diltiazem indications
 To control rate of ventricular response in patients with A-Fib or A-Flutter  Use after adenosine to treat refractory reentry SVT in patients with narrow QRS complex and adequate blood pressure
37
diltiazem dose
Only Adults – no Pediatric dose: 0.25 mg/kg SIVP q 15 mins may repeat once if needed at 0.35 mg/kg SIVP. Maintenance Infusion: For acute rate control of A-Fib or atrial flutter maintenance is initiated at a rate of 5 to 15 mg/hr titrated to the patient’s heart rate. Mix: 50 mg in 500ml NS or D5W (concentration 0.1 mg/ml)
38
diltiazem contraindications
 Hypersensitivity to drug  Wide-QRS tachycardia of uncertain origin  Poison-or drug-induced tachycardia.  Sick sinus syndrome  WPW  Bradycardia; second- or third-degree AV block  LV dysfunction; Heart Failure  Hypotension <90 systolic  Recent MI  Severe heart failure (ie: with pulmonary edema)  IV Calcium Channel Blockers, Beta Blockers or cardiac depressant drugs that can produce reduction in myocardial contractility of the AV conduction.
39
dopamine HCL trade name
intropin
40
dopamine class
adrenergic agonist (sympathomimetic), vasopressor, inotropic (dose dependent)
41
dopamine MOA
 Vasopressor: an immediate precursor to norepinepherine, dopamine stimulates the dopaminergic, beta-adrenergic and alpha-adrenergic receptors of the sympathetic nervous system.
42
dopamine indications
 Second line drug for symptomatic bradycardia (after atropine)  Use for hypotension with signs and symptoms of shock – correct hypovolemia with volume replacement before initiating dopamine
43
dopamine dose
Adult: 5 – 20 mcg/kg/min IV Infusion; titrate to patient response; initiate dose at 5 mcg/kg/min and titrate to patient response Pre-Mix bag or mix as: 400 mg/250ml N/S [1600mcg/ml]
44
dopamine contraindications
 Uncorrected tachydysrhythmias  Ventricular fibrillation/Ventricular Tachycardia  Pheochromocytoma – may precipitate hypertensive crisis  Allergies to corn or corn products
45
enoxaparin sodium trade name
lovenox
46
enoxaparin class
low-molecular-weight heparin (LMWH) / anticoagulant
47
enoxaparin MOA
Anticoagulation action: LMWH that accelerates formation of antithrombin III-thrombin complex and deactivates thrombin preventing conversion of fibrinogen to fibrin, inhibits factor Xa.
48
enoxaparin indications
Acute STEMI /NSTEMI/ACS
49
enoxaparin dose
<75 yr: Initial dose: 30mg IVP followed by a Second dose of 1mg/kg SQ Note: maximum dose of 100mg SQ (Maximum SQ dose does NOT include IV dose) >75 yr: Eliminate initial IV dose; Give 0.75 mg/kg SQ Note: maximum dose 75mg SQ
50
enoxaparin contraindications
 Hypersensitivity to Sulfite or heparin  Active major bleeding or bleeding disorders  Type II Heparin or LMWH induced thrombocytopenia  Severe thrombocytopenia (low platelets)  Peptic ulceration  Aortic aneurysm
51
epinephrine trade name
adrenalin
52
epinephrine class
adrenergic agonist (Sympathomimetic)
53
epinephrine MOA
 A catecholamine that stimulates the alpha and beta-adrenergic receptors in the sympathetic nervous system.  Alpha1 Receptors: causes vasoconstriction used to delay absorption of local anesthetics, control superficial bleeding, suppress glottal edema and elevate blood pressure by increasing peripheral vascular resistance. Alpha1 receptors on the iris produces mydriasis during ophthalmologic procedures  Beta1 Receptors: produces inotropic (strength of contraction), chronotropic (rate of contraction) and dromotropic (speed of conduction) effects, increasing cardiac output and myocardial oxygen consumption.  Beta2 Receptors: Relaxes bronchial smooth muscle increasing tidal volume and vital capacity.  Activation of these three types of adrenergic receptors can reverse the degranulation of the anaphylactic reaction caused largely by the release of leukotrienes with histamine.
54
epinephrine indications
 Cardiac Arrest – V-fib, Pulseless V-Tach, Asystole, PEA  Symptomatic bradycardia, particularly if associated with hypotension, for whom atropine may be inappropriate or after atropine fails  Used to treat severe hypotension  Maintain cardiac output during Post-Cardiac Arrest Care  Anaphylaxis  Severe status asthmaticus  Croup with stridor  Beta Blocker/Ca+ channel Blocker overdose
55
epinephrine adult dose
Cardiac Arrest: 1 mg of 1mg/10 mL (0.1 mg/ml concentration) IVP q 3-5 minutes ROSC (Hypotension): 2 - 10 mcg/min infusion Symptomatic Bradycardia with Hypotension: 2 – 10 mcg/minute IV infusion Croup / Anaphylaxis: 0.5 mg/kg of (1mg/1 mL) to max 5mg neb. Repeat every 5 minutes to a max of 10mg Anaphylactic Shock/ Asthma (refractory to initial treatment): 0.3 to 0.5 mg IM (1mg/1 mL) q 5 minutes prn to a maximum of 3 doses, then transition to a continuous infusion if needed starting at 1 mcg/min
56
epinephrine pediatric dose
Cardiac Arrest: 0.01 mg/kg to a max of 1mg/10 mL (0.1 mg/ml concentration) IVP q 3-5 minutes ROSC (Hypotension): 0.03 - 0.2 mcg/kg/min Symptomatic Bradycardia with Hypotension: 0.01 mg/kg of 1mg/10 ml (0.1 mg/ml concentration) to a max of 1 mg IVP/I.O. q 3-5 minutes followed by: Infusion of 0.1-0.3 mcg/kg/min may be followed for persistent bradycardia Croup / Anaphylaxis: 0.5 mg/kg of (1 mg/1 mL) to max 5mg neb. Repeat every 5 minutes to a max of 10 mg Anaphylactic Shock/ Asthma (refractory to initial treatment): 0.01 mg/kg IM of (1 mg/1 mL) to a single max dose of 0.5 mg q 5 minutes prn, (maximum of 3 doses) then transition to continuous infusion if needed at 0.1 – 0.3 mcg/kg/min
57
epinephrine push dose
Adult/pediatric: 1 mcg/kg to a single max dose of 50 mcg Repeat q 2 minutes PRN
58
epinephrine post rosc infusion
*Mix 4 mg of Epinephrine (1mg/1mL) in 250 ml of N/S (concentration 16 mcg/ml) Pediatric: 0.03 – 0.3 mcg/kg/min IV infusion Adult: 1 – 10 mcg/min Infusion
59
epinephrine contraindications
none in the emergent setting
60
ephedrine trade name
emerphed
60
ephedrine MOA
 Mixed acting drug because it activates adrenergic receptors by direct and indirect mechanisms. Direct activation results from binding of the drug to alpha and beta receptors. Release of norepinephrine from its storage sites is one of its indirect effects.  In therapeutic doses, ephedrine relaxes bronchial smooth muscles and produces cardiac stimulation with increased systolic and diastolic blood pressure when norepinephrine stores aren’t depleted.  Non-catecholamine as a result has a longer half life than catecholamines (i.e. norepinephrine, epinephrine)
60
ephedrine class
adrenergic, vasopressor
61
ephedrine indications
 To correct hypotensive states (i.e. sepsis, spinal trauma, head injury, anaphylaxis, shock states, etc.)  Ephedrine can be given as a “bridge drug” (due the drugs half life) until an inotropic / vasopressor infusion is started to maintain an adequate BP.
62
ephedrine dose
0.2 mg/kg IV/IO to a single dose of 10 mg q 5 minutes prn
63
ephedrine contraindications
 Hypersensitivity to drug or other sympathomimetics  Severe CAD  Patients taking MAO inhibitors
64
furosemide trade name
lasix
65
furosemide class
loop diuretic
66
furosemide MOA
 Diuretic: Inhibits sodium and chloride reabsorption in the proximal part of the ascending loop of Henle and distal renal tubule, promoting excretion of sodium, water, chloride and potassium.  Non-potassium (K+) sparing diuretic; potassium (K+) excreted from the body in the urine.
67
furosemide adult dose
Congestive Heart Failure and Pulmonary Edema: No usual prescription of Lasix: 20-40 mg SIVP/IO If patient has a usual prescription of Lasix: Dose may be increased 2 times the patient’s usual prescribed dose to a maximum of 160 mg Hyperkalemia: 40-80 SIVP/IO Hypertensive Emergencies: 40 mg SIVP/IO
67
furosemide indications
 Acute pulmonary edema (BP >100 mmHg without S&S of shock)  Hypertensive emergencies  Removal of Potassium for management of Hyperkalemia
68
furosemide pediatric dose
Congestive Heart Failure and Pulmonary Edema: 1 mg/kg slow IV/IO push. q 1-2 hours if no response has occurred. You may repeat at 2 mg/kg. Hyperkalemia (with normal renal function, non-hypovolemic) 0.5-1.0 mg/kg to max of 40 mg SIVP Hypertensive Emergencies: 1 mg/kg mg IV/IO (over 1-2 minutes)
69
furosemide contraindications
 Hypersensitivity to furosemide and sulphonamides  Complete renal shutdown (anuria except acute)  Hypokalemia  Severe hypovolemia, hypotension, dehydration, BP < 100 systolic  Electrolyte imbalance
70
hydrocortisone trade name
Cortef, Anusol HC, Caldecort, Colocort, Solu-Cortef
71
hydrocortisone class
Adrenal corticosteroid; Glucocorticoid
72
hydrocortisone MOA
 Inhibits accumulation of inflammatory cells at inflammation sites, phagocytosis, lysosomal enzyme release, synthesis and or release of mediators of inflammation.  Reverses increased capillary permeability  Prevents/suppresses cell-mediated immune reactions. Decreases/prevents tissue response to inflammatory process
73
hydrocortisone indications
 Management of adrenocortical insufficiency, anti-inflammatory, immunosuppressive  Anaphylactic shock
74
hydrocortisone adult dose
Adrenal Insufficiency emergencies: 100 mg SIVP/IO; reconstitution – as per manufactures instructions; may further dilute with NS; for IVP dilute to 50mg/ml; no repeat dose Anaphylaxis: 250 - 500 mg IV
75
hydrocortisone pediatric dose
Adrenal Insufficiency emergencies: 1 – 2 mg/kg slow IV. To a maximum dose of 100 mg; no repeat dose (Don’t use a low dose or less than 25 mg daily) Anaphylaxis: 5 - 10 mg/kg to single max dose of 500 mg IV
76
hydrocortisone contraindications
 Active untreated infections  Hypersensitivity to hydrocortisone  Systemic Fungal infections  Tuberculosis
77
labetalol hydrochloride trade name
trandate
78
labetalol class
alpha and beta-adrenergic blocker, antihypertensive
79
labetalol MOA
Antihypertensive: Inhibits catecholamine access to both beta and postsynaptic alpha-adrenergic receptor sites. Has vasodilating effect).
80
labetalol indications
 Severe hypertension and hypertensive emergencies  Hypertension in acute Ischemic stroke patients who are potential candidates for acute reperfusion therapy with a blood pressure level of Systolic >185 mmHg or diastolic >110 mmHg  Management of blood pressure during reperfusion therapy and after reperfusion therapy; blood pressure level under 180 mmHg Systolic or under 105mmHg diastolic
80
labetalol dose
Severe Hypertension / Hypertensive emergency: 10 - 20 mg SIVP over 2 minutes initially; may repeat at 40 – 80 mg SIVP q 10 min to total maximum dose of 300 mg. Hypertension in acute Ischemic stroke prior to reperfusion therapy: 10 – 20 mg SIVP, may repeat X 1 Management of blood pressure during reperfusion therapy and after reperfusion therapy for Ischemic Strokes: 10 mg SIVP followed by a continuous IV infusion of 2 -8 mg/minute: Do not exceed a total cumulation of 300 mg labetalol. Mix infusion to concentration of 1 mg/1ml may be mixed in D5W, NS or RL initiate at 2 mg/min titrate to response
80
labetalol contraindications
 Hypersensitivity to beta blockers  CHF – severe LV failure  Pulmonary Edema  2nd or 3rd degree AV blocks  Bradycardia  Hypotension  Cardiogenic shock  Sick sinus syndrome  Bronchospasm  Cocaine in past 24 hours which causes chest pain  Children
80
lidocaine HCL trade name
Xylocaine; Synera (lidocaine / tetracaine)
80
lidocaine class
anesthetic, antiarrhythmic (class IBVW)
81
lidocaine MOA
 Ventricular antiarrhythmic: Suppresses automaticity of conduction tissue; increases electrical stimulation threshold of ventricle, His Purkinje system and spontaneous depolarization of ventricles during diastole.  Local anesthetic: acts to block initiation and conduction of nerve impulses by decreasing the permeability of the nerve cell membrane to sodium ions.
82
lidocaine indications
 Alternative to amiodarone in cardiac arrest from VF / pVT  Stable VT, wide complex tachycardia of uncertain ectopy (with normal baseline QT interval and preserved LV function when ischemia is treated, and electrolyte imbalance is corrected)  Can be used for stable polymorphic VT with baseline QT-interval prolongation if torsade is suspected.  Premature ventricular beats (PVCs) of a life-threatening nature  Procedural anesthetic  IO infusion pain
83
lidocaine adult dose
Cardiac arrest from VF/VT (pulseless) (2% lidocaine preload) Initial dose: 1 - 1.5 mg/kg IVP repeat 5- 10 mins for refractory VF at 0.5 to 0.75 mg/kg IVP maximum 3 doses or total max dose of 3 mg/kg – followed by a maintenance infusion if indicated Perfusing Arrhythmia (VT/Torsade) (2% lidocaine preload) 0.5 to 0.75 mg/kg SIVP, repeat in 5 to 10 minutes; maximum total of 3 mg/kg – Followed by a maintenance infusion if indicated Maintenance Infusion: A continuous maintenance infusion MAY be initiated when indicated Mix 1 gm in 250 ml NS (concentration 4 mg/ml); Infuse at 1-4 mg/min (30-50 mcg/kg/min) IO infusion pain (2% lidocaine preload) If patient is responsive to pain or complains of pain when you flush the marrow cavity: First dose 40 mg (2ml) IO over 2 mins q 60 seconds if needed 20 mg (1ml) IO over 1 min Local Anesthetic for male urethra – urinary catheterization: 5-10 ml of the 2% lidocaine jelly – prior to catherization Injection for local infiltration: (subdermal) 0.5% - 1% - Inject small volumes SQ until the entire area is anesthetized Maximum dose is 4 mg/kg
83
lidocaine pediatric dose
Cardiac Arrest from VF/VT (pulseless) (2% lidocaine preload) 1mg/kg IV/IO, q 5 minutes prn to a total max dose of 3 mg/kg – Followed by a maintenance infusion if indicated Perfusing Arrhythmia (VT/Torsade) (2% lidocaine preload) 1mg/kg IV/IO, q 5 minutes prn to a total max dose of 3 mg/kg – Followed by a maintenance infusion if indicated Maintenance Infusion: A continuous maintenance infusion MAY be initiated when indicated 20 to 50 mcg/kg/min IV/IO IO infusion pain (2% lidocaine preload) If patient is responsive to pain or complains of pain when you flush the marrow cavity: 0.5 mg/kg IO to a total maximum of 40 mg (2ml) delivered over 2 minutes, repeat if needed with 0.25 mg/kg max 20 mg (1 ml) Injection for local infiltration: (subdermal) 0.5% - 1% - Inject small volumes SQ until the entire area is anesthetized Maximum dose is 4 mg/kg
84
lidocaine contraindications
 Hypersensitivity to lidocaine and to amide-type local anesthetics  Idioventricular rhythms  3rd degree AV blocks  Stroke Adams syndrome  Wolf Parkinson White (WPW) syndrome
85
mag adult dose
Cardiac Arrest VT polymorphic / VF due to hypomagnesaemia or Torsade’s de Pointes) Adult-1 - 2 g SIVP diluted in 10 ml of NS over 20 mins Torsades de Pointes with a pulse or cardiac arrythmias with hypomagnesemia: Loading dose: 1 - 2 g IV diluted in 50 -100 ml of NS or D5W IV given over 5 – 60 minutes; Follow with 0.5 – 1 g/hr IV (titrate rate to control torsade’s or arrythmias). Bronchospasm 2 g IV diluted in 50 ml NS infused over 20 -30 minutes TCA Overdose: 2 g IV diluted in 50 ml NS infused over 10- 20 minutes Eclampsia/Tocolytic: Loading dose: 4 g IV in 50 ml over 20-30 minutes IV/IO followed by an maintenance infusion 1-2 g/hr. for 24 hours. (Mix 2 G/250 ml NS or D5W)
85
mag sulfate trade name
MgSO4
85
mag class
mineral/electrolyte
85
mag MOA
 Replaces magnesium and maintains magnesium level  As an anticonvulsant, reduces muscle contractions by interfering with release of acetylcholine at myoneural junction  As an anti-arrhythmic magnesium inhibits calcium currents which slows the sinoatrial node activity, prolongs myocardial conduction time and stabilizes excited membranes.  Acts as a bronchodilator by inhibiting smooth muscle contractions
85
mag indications
 Refractory ventricular fibrillation/tachycardia with suspected hypomagnesemia (alcoholism, malnutrition or protracted diarrhea)  Polymorphic ventricular tachycardia / Torsades de Pointes  Life threatening ventricular arrhythmias due to digitalis toxicity  Hypomagnesemia  Adjunctive therapy in severe bronchospasm refractory to nebulized medications  Tricyclic Antidepressant (TCA) overdose  Moderate to severe eclampsia symptoms  Preterm Tocolytic – Medical Control
86
mag pediatric dose
Cardiac Arrest VT polymorphic / VF due to hypomagnesaemia, Torsade’s de Pointes with or without perfusion, or cardiac arrythmias with hypomagnesemia 20 – 50 mg/kg to a single max dose of 2 G SIVP over 10-20 mins Bronchospasm 25 – 50 mg/kg IV to a max dose of 2 G in 50 ml NS or D5W infused over 10-20 minutes TCA Overdose: 25 mg/kg IV to a max dose of 2 G in 50 ml NS infused over 15-20 minutes
86
mag contraindications
 Heart Blocks  Renal failure  Hyper-magnesia, hypocalcemia
87
metoprolol tartrate trade name
lopressor
88
metoprolol class
beta blocker, antihypertensive
89
metoprolol MOA
Selectively blocks beta 1 adrenergic receptors; slow heart rate, decreases cardiac output, decreases myocardial ischemia severity
90
metoprolol indications
 Stable, narrow-complex tachycardias if rhythm remains uncontrolled or unconverted by adenosine or vagal maneuvers or if SVT is recurrent  Control ventricular rate in patients with atrial fibrillation or atrial flutter
91
metoprolol dose
Treatment of SVT (post-adenosine) / Atrial Fibrillation / Atrial Flutter: 5 mg SIVP (over 2 minutes) doses q 5 minutes prn total max accumulative dose of 15 mg (vital signs must remain stable)
92
metoprolol contraindications
 Hypersensitivity  CHF – severe LV failure – pulmonary edema  Sick sinus syndrome – in absence of a pacemaker  Systolic blood pressure less then 100 mmHg  Cocaine used in past 24 hours with chest pain  AV Heart block  Bradycardia < 60 bpm  Cardiogenic shock
93
nitro trade name
Nitrostat, Nitro-Bid, Tridil
94
nitro class
nitrate, anti-anginal, vasodilator
95
nitro MOA
 Antianginal: relaxes vascular smooth muscle of both venous and arterial beds, resulting in a net decrease in the myocardial oxygen consumption. It also dilates coronary vessels, leading to redistribution of blood flow to ischemic tissue and improves collateral circulation.  Vasodilating: dilates peripheral vessels, decreasing venous return to the heart (preload) useful in treating pulmonary edema and heart failure. Arterial vasodilation decreases afterload, thereby decreasing left ventricular work and aiding the failing heart.
96
nitro indications
 Initial antianginal for suspected ischemic chest pain  For initial 24 – 48 hours in patient with AMI and CHF, large interior wall infarction, persistent or recurrent ischemia  Continued use (beyond 48 hours) for patients with recurrent angina or persistent pulmonary congestion  Pulmonary Edema
97
nitro adult dose
SL - 0.3 mg tab or 0.4 mg spray q 5-minute intervals (prn); max of 3 doses IV - begin infusion at 5 mcg/min; titrate to effect; increase prn by 5 – 10 mcg/min q 5 min. Max dose of 200 mcg/min; Mix: 25 mg of nitroglycerin to a 250 ml NS or D5W (100 mcg/ml) Transdermal Patch – 0.2 – 0.8 mg/hr. Topical nitrates are acceptable alternatives for antianginal therapy with hemodynamic stability in the absence of ongoing refractory ischemic symptoms.
98
nitro pediatric dose
0.25 - 0.5 mcg/kg/min IV/IO increase by 0.5- 1 mcg/kg/min prn as tolerated q 15-20 mins to a max of 5 mcg/kg/min.
99
nitro contraindications
 Hypersensitivity to nitrates  Right ventricular infarction (Sublingual Spray Administration- 0.3mg to 0.4 mg are too large a dose and will drop preload and significantly decreasing cardiac output. These increases mortality rates in these patients)  Avoid use in extreme bradycardia (<50 bpm) or extreme tachycardia (>160 bpm)  Hypotension (<90 mmHg) or a drop of >30 mmHg below baseline (systolic BP)  Uncorrected hypovolemia  sildenafil (Viagra), vardenafil (Levitra), avanafil (Stendra),) use within 24 hours or tadalafil (Cialis) within 48 hours  Severe anemia  Pericardial Tamponade and pericarditis
100
norepi trade name
levophed
101
norepi class
adrenergic agonist (sympathomimetic), vasopressor
102
norepi MOA
 Vasopressor: direct stimulation of alpha-adrenergic receptors, constricting both capacitance and resistance blood vessels. This result in increased total peripheral vascular resistance, increased systolic and diastolic blood pressure, and decreased blood flow to vital organs, skin, skeletal muscle and renal blood flow.  Produces a positive inotropic response of the heart (beta1 receptors).
103
norepi indications
 Hypotension MAP less than 65  Septic, Cardiogenic and Neurogenic shock  Treatment of shock after appropriate fluid resuscitation  Beta & Calcium Channel Blocker OD, Cholinesterase inhibitor poisoning, Cyclic Antidepressant OD, Digoxin OD, Ethanol poisoning, Head injury with MAP <70mmHg, Non-cyclic Antidepressant OD, Salicylate OD, Sedative OD  Vasopressor infusions may be administered after ROSC to support cardiac output, especially blood flow to the heart and brain.
104
norepi adult dose
0.1 – 1.0 mcg/kg/min. IV infusion (*start at low dose and titrate to desired blood pressure) Mix 4 mg in 250 mL D5W or NS (16 mcg/mL)
105
norepi pediatric dose
0.05 – 1.0 mcg/kg/min IV infusion Mix 4 mg in 250 mL D5W or NS (16 mcg/mL) The pediatric initial dose for NE range is chosen on the patient condition and problem, titrate infusion as needed/required:  ROSC dosing - 0.05 – 0.5 mcg/kg/min  Common dose initiation for a hypotensive pediatric patient after adequate fluid replacement - 0.1 - 1.0 mcg/kg/min.  *Always start at low dose and titrate to desired blood pressure
106
norepi contraindications
 Mesenteric or peripheral vascular thrombosis  Hypotension related to hypovolemia without appropriate fluid replacement
107
procainamide trade name
pronestyl
108
procainamide class
ventricular and supraventricular antiarrhythmic (Class Ia)
109
procainamide MOA
 Antiarrrhythmic: Blocks open sodium channels and prolongs the cardiac action potential (outward potassium (K+) currents maybe blocked.) Decreases myocardial excitability, conduction velocity and may depress contractility.  Prolongs PR and QT intervals.  Has peripheral vasodilatory properties which may result in hypotension.
110
procainamide indications
 Useful for treatment of a wide variety of arrhythmias, including stable monomorphic VT with normal QT interval and preserved LV function  May use for treatment of reentry SVT uncontrolled by adenosine and vagal maneuvers if BP is stable  Stable Wide complex tachycardia of unknown origin  Atrial fibrillation with rapid rate in WPW
111
procainamide adult dose
Administer IV loading dose: 20 to 50 mg/min until arrhythmia suppressed or hypotension ensues or QRS prolonged by 50% or total cumulative dose of 17 mg/kg; If conversion is successful, may use maintenance infusion (avoid if prolonged QT or CHF); Mix: 1 gm/250 ml NS (4mg/mL); Infuse at 1-4 mg/min
112
procainamide pediatric dose
15mg/kg slow IV/IO over 30 to 60 minutes
113
procainamide contraindications
 Hypersensitivity to procainamide, ester type local anesthetics, benzyl alcohol or sulphites  QT prolongation  A typical V-tach or Torsade de Pointe  Any dysrhythmia induced by digoxin toxicity  TCA antidepressant induced dysrhythmia  2nd or 3rd degree AV block
114
sodium bicarb trade name
none
115
sodium bicarb class
alkalinizing agent
116
sodium bicarb MOA
Alkalinizing agent: is a systemic alkalizer, which increases plasma bicarbonate, buffers excess hydrogen ion concentration, and raises blood pH, thereby reversing the clinical manifestations of acidosis. It also is a urine alkalizer, increasing the excretion of free bicarbonate ions in the urine, thus effectively raising the urinary pH.
117
sodium bicarb indications
 Patients with documented preexisting metabolic acidosis i.e.; diabetic ketoacidosis  Overdoses associated with QRS > 0.12 seconds or ventricular tachycardia in tricyclic antidepressant, sympathomimetic, beta / calcium channel blocker, opioid  Known preexisting Hyperkalemia  Cardiac arrest in special situations; prolonged resuscitation, excited delirium  Rhabdomyolysis  ASA overdose (urine alkalization)
118
sodium bicarb dose
Adult/Pediatric: Cardiac arrest in special situations/ Metabolic Acidosis / Overdoses (listed above) / Rhabdomyolysis / Urinary Alkalization / Hyperkalemia: 1.0 mEq/kg SIVP; repeat (prn) q 10 minutes at 0.75 mEq/kg to achieve hemodynamic stability and QRS narrowing TCA/ASA overdose: 1.0-2.0 mEq/kg SIVP; repeat (prn) q 10 minutes at 1.0 mEq/kg to achieve hemodynamic stability and QRS narrowing bolus then initiate infusion. Infusion: 150 mEq in a 1000ml D5W or NS = 0.15 mEq /ml - rate of 2-3 ml/kg/hour Adjustments of the IV are made based on blood pH and clinical response to the therapy.
119
sodium bicarb contraindications
 Respiratory acidosis  Early in cardiac arrest (unless a specific reason to administer)  Respiratory and metabolic alkalosis  Hypocalcemia  Avoid extravasation due to risk of tissue irritation / necrosis
120
tenecteplase trade name
TNKase
121
TNK class
thrombolytic enzyme
122
TNK MOA
 A modified form of human tissue plasminogen activator (tPA) that binds to fibrin and converts plasminogen to plasmin.  This fibrin specificity produces local fibrinolysis in the area of recent clot formation, with limited systemic proteolysis.  tenectaplase is administered as a single bolus with an initial half-life of 20-24 minutes, cleared through liver metabolism
123
TNK indications
 ST elevation (threshold values: J-point elevation of 2 mm (men) or 1.5 mm (women) in leads V2 and V3 and 1 mm in all other leads) or new presumably new LBBB; in context of signs and symptoms of AMI and time of onset of signs and symptoms <12 hrs
124
TNK dose
 Once diluted with 10 ml NS TNKase™ concentration is 5 mg/ml  Single bolus delivered over 5 seconds (not compatible with dextrose solutions)  *** ½ amount of dose is administered to age 76 and older. weight based chart
125
TNK contraindications
 Any prior intracranial hemorrhage  Known structural cerebrovascular lesion  Ischemic stroke within past 3 months except ischemic stroke within 4.5 h  Known intracranial neoplasm  Active internal bleeding (other than menses)  Severe uncontrolled hypertension unresponsive to emergency therapy  Suspected aortic dissection  For streptokinase, prior treatment within the previous 6 months  Intracranial or intraspinal surgery within 2 months  Significant closed head or facial trauma within 3 months  Suspected aortic dissection or pericarditis
126
ticagrelor trade name
brilinta
127
ticagrelor class
P2Y12 platelet aggregation inhibitor; Antiplatelet
128
ticagrelor MOA
 Reduces platelet aggregation – reversibly inhibits platelet P2Y12 ADP receptor to prevent signal transduction and platelet activation
129
ticagrelor indications
 Reduction of thrombolytic cardiovascular events in conjunction with aspirin in patients with acute coronary syndrome.  Treatment of STEMI patients
130
ticagrelor dose
PO – 180 mg once
131
ticagrelor contraindications
 Hypersensitivity  Active bleeding  Intercranial Bleed  5 days prior to any surgery including CABG
132
tissue plasminogen activator (tPA), alteplase trade name
activase
133
tPA class
thrombolytic enzyme
134
tPA MOA
 Binds to fibrin in a thrombus and converts entrapped plasminogen to plasmin, initiating fibrinolysis  Degrades fibrin clots, fibrinogen and other plasma proteins  Acts on the dissolution stage. Protease which activates plasmin release from endothelial cells, due to ischemic conditions, thrombin, systemic adrenaline and histamine. It acts on plasminogen converting it to plasmin, which cleaves fibrin.
135
tPA indications
 Lysis of thrombi obstructing coronary arteries in management of acute MI.  Lysis of thrombi obstructing cerebral arteries in the management of acute ischemic stroke.
136
tPA dose
STEMI 6- 12 hours of symptoms: >67 kg: 15 mg initial IV bolus; followed by 50 mg infused over the next 30 mins; then 35 mg infused over the next 60 mins < 67 kg: 15 mg initial IV bolus; followed by 0.75 mg/kg (not to exceed 50 mg) over the next 30 min; then 0.5 mg/kg (not to exceed 35 mg) over 60 min Acute Ischemic Stroke within 4.5 hours or wake-up and unknown time of onset: Ages 18 - 80 0.9 mg/kg (maximum 90 mg) IV, infused over 60 minutes; give 10% of total dose as an initial IV bolus over 1 min; give remaining 90% of total dose IV over next 60 minutes.
137
tPA contraindications
 Ensure BGL is above 3.3 mmol/l (Stroke)  Any prior intracranial hemorrhage  Known structural cerebral vascular lesion (e.g., arteriovenous malformation)  Known malignant intracranial neoplasm (primary or metastatic)  Ischemic stroke within 3 months EXCEPT acute ischemic stroke within 4.5 hours  Suspected aortic dissection  Active bleeding or bleeding diathesis (excluding menses)  Significant closed head trauma or facial trauma within 3 months  Intracranial or intraspinal surgery within 2 months  Severe uncontrolled hypertension (unresponsive to emergency therapy)
138
txa trade name
cyklokapron
139
txa class
antifibrinolytic
140
txa moa
 Inhibits the normal process of fibrin breakdown by preventing the formation of plasmin from plasminogen.  Most useful for preventing recurring bleeding; it is less useful for stopping an on-going bleed.
141
txa indications
 Bleeding within 3 hours of injury and presenting at any point with HR greater than 110 bpm or systolic BP less than 90 mmHg. Ex. TBI, Post-Partum hemorrhage, significant traumatic injury with internal bleeding.
142
txa dose
(>16 years old): 1 g IV/IO dilute in 250 mL D5W or 100ml Normal Saline bag and infuse over 10 minutes; followed by as soon as practical an infusion of 1 g over 8 hours (<16 years old): 15mg/kg IV/IO to a max of 1g over 10 minutes. Follow bolus dose with 2mg/kg/hr IV/IO to a max of 1g over 8 hours.
143
txa contraindications
 Hypersensitivity to Tranexamic Acid  Active thromboembolic disease (pulmonary embolus, DVT or stroke)  Unable to initiate bolus within 3 hrs of injury onset  GI Bleeds  Subarachnoid hemorrhage