Injection Adrenaline (Epinephrine)
Action: β1 and β2 agonist causing increased levels of cAMP, thereby producing bronchodilation, cardiac and CNS stimulation; high doses cause vasoconstriction via ∝- receptors; low dose can cause vasodilation via β2-vascular receptors.
Function class: Bronchodilator nonselective adrenergic agonist, vasopressor.
Chemical Class: Catecholamine.
Uses of Adrenaline (Epinephrine)
- Acute asthmatic attacks
- Hemostasis
- Bronchospasm
- Anaphylaxis
- Allergic reactions
- Cardiac arrest
- Adjunct in anaesthesia
- Shock
- Bradycardia
- Chloroquine overdose
- Hypersensitivity to sympathomimetics
- Closed-angle glaucoma
- Nonanaphylactic shock during general anaesthesia.
- Pregnancy
- Breastfeeding
- Cardiac disorders
- Hyperthyroidism
- Diabetes Mellitus
- Prostatic hypertrophy
- Hypertension
- Organic brain syndrome
- Local anaesthesia of certain areas
- Labor
- Cardiac dilation
- Coronary insufficiency
Dosage and Routes of Adrenaline (Epinephrine)
Anaphylaxis/severe asthma exacerbation
- Adult: IM/Subcut 0.3-0.5mg, may repeat q10-15min (anaphylaxis ) or q20min-4hr (asthma
- Adult: IV 0.1-0.25 mg q5-15 min, then 1-4 mcg/min continuous infusion if needed.
- Child: IV ≤0.1 mcg/kg/min, then 0.1 mcg/kg/min continuous infusion needed.
- Adult/child ≥30 kg: IM 0.3 mg (Epipen 2-pak)
- Child <30 Kg: IM 0.15 mg (Epipen Jr/ Epipen Jr 2-pack).
- Adult: IV 1 mg q3-5 min
- Adult: IV 2-10 mcg/min
- Child: IV 0.01 mg/kg may repeat q3-5min, may increase to 0.1-0.2 mg/kg if needed.
- Increased dose of insulin for Diabetic patients if glucose is elevated.
- Check for correct concentrations, route, dosage before administering.
- Give subcut, IM, intraosseously, IV;
- Visually inspect parenteral products for particulate matter and discolouration before use; do not use sols that are pinkish to brownish or that contain a precipitate.
- Avoid extravasation during parenteral administration; if extravasation occurs, infiltrate the affected area with phentolamine diluted NS.
- Death has occurred from drug errors; make sure the right concentration is used.
- Place in nebulizer (10 drops of a 1% base sol)
- Dilute racepinephrine 2.25% sol
- Give in the deltoid or anterior thigh (vatus lateralis); do not administer into the gluteal muscle, may give through clothing in emergency.
- Inject, taking care not to inject intradermally; massage injection site well after use to enhance absorption and to decreased local vasoconstriction; injection cause tissue irritation.
- Intracardiac route should be reversed for extreme emergencies; Intracardiac injection should only be performed by properly trained medical personal.
- Per the ACLS or PALS guidelines, the Epinephrine parenteral product is administered via endotracheal (ET) route; ET administration should only be used if access to IV or intraosseous routes is not possible.
- During CPR, the same Epinephrine dosage may be given via the intraosseous route when IV access is not available.
- Dilute dose in 5-10 mL of NS or sterile distilled water; administer via ET tube; endotracheal absorption of Epinephrine may be improved by diluting with water instead of NS.
- After dose administration, flush the ET tube with a minimum of 5 mL NS.
- 1:10,000 solution can be given directly without diluting: dilute 1:1000 ( 1mg/0.9 mL) 0.9% NaCL (1:1000 solution )
- Inject Epinephrine directly into a vein over 5-10 min for adult or 1-3 min for children; maybe given IV push in cardiac arrest.
- In neonates, may administer via the umbilical vein.
- Resuscitation drugs may be given IV by bolus injection into a peripheral vein, followed by an injection of 20 mL IV fluid; elevate the extremity for 10-20 sec to facilitate drug delivery to the central circulation.
- Dilute 1 mg Epinephrine in 250 or 500 mL of a compatible IV infusion solution to provide a concentration of 4 or 2 mcg/mL, respectively; give into a large vein, if possible; more-concentrated sols (16-32 mcg/mL) may be used in fluid-restricted patients when administered through a central line.
CNS
- Tremors, anxiety, insomnia, headache, dizziness, confusion, hallucinations, weakness, drowsiness.
- Palpitations, tachycardia, hypertension, dysrhythmias.
- Anorexia, nausea, vomiting.
- Sweating, dry eyes
- Dyspnea, paradoxical bronchospasm.
- Hypoglycemia
- Crosses placenta, metabolized in liver.
- IM: 6-10 min, duration 1-4hr.
- Subcut: Onset 5-10 min, duration 20 min-4hr.
- IV: Onset immediate, peak 20 min, duration 1-4 hr.
- INH: Onset 1-5 min, duration 1-3 hr.
- Do not use with MAOIs or tricyclics; hypertensive crisis may occur.
- Toxicity: other sympathomimetics.
- Decrease: hypertensive effects -β adrenergic blockers, stop β-blockers 3 days before starting product.
- Increase: hypotension ∝ blockers
- Increase: cardiac effects--antihistamines, thyroid replacement hormones.
- Increase: dysrhythmias--cardiac glycosides.
Assess
- Asthma: auscultate lungs, pulse B/P, respiration, monitor pulmonary function studies before and during treatment.
- Vasopressor: ECG during administration continuously; if B/P increases, decrease dose; B/P, pulse q5min after parenteral route; CVP, ISVR, PCWP during infusion if possible; inadvertent high arterial B/P can result in angina, aortic rupture, cerebral haemorrhage.
- Inj site: tissue sloughing; administrator phentolamine with NS.
- Sulfite sensitivity: may be life-threatening.
- Cardiac status, I&O, blood glucose in diabetes.
- Allergic reactions, bronchospasms (swelling of face/lips/eyelids, rash difficulty breathing): withhold dose, notify prescriber.
- Therapeutic response: increased B/P with stabilization or ease of breathing, relief of bronchospasm.
- Administer ∝-blocker and β-blocker.
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