Cardiac Glycosides

Cardiovascular Drugs 1

Name of the Cardiac Glycosides drug:

Digoxin

Mechanism of action:

  • The mechanism of action of cardiac glycosides involves inhibiting the Na+, K+ ATPase enzyme, also known as the sodium-potassium pump. This causes sodium to build up inside the heart cells, decreasing the ability of the sodium-calcium exchanger to push calcium out of the cells, consequently causing calcium to build up in the sarcoplasmic reticulum. Increased intracellular calcium results in a positive inotropic effect, which in turn has the effect of increasing the force of the heart’s contractions.
  • Indirectly slows conduction at SA node and AV node and centrally stimulates the vagus nerve, resulting in a negative chronotropic effect.

Indications:

  • Supra ventricular Arrhythmias (atrial fibrillation and atrial flutter)
  • Congestive Heart Failure

Cautions & Contraindications:

  • Complete heart block and second- degree block
  • Tachyarrhythmias associated with Wolf- Parkinson- white syndrome
  • Ventricular tachycardia/ fibrillation
  • Myocarditis/ constrictive pericarditis
  • Hypertrophic cardiomyopathy

Side- Effects:

  • GI disturbance
  • Dizziness, hallucinations.
  • Blurred or yellow vision (xanthopsia suggests toxicity)
  • Arrhythmias/ conduction defects
  • Rash
  • Abdominal pain (suggests toxicity)
  • Electrolyte Imbalance 
                                                        Digoxin
Availability: Oral Solution: (Lanoxin): 50 mcg/mL. Injection Solution: (Lanoxin): 100 mcg/mL, 250 mcg/mL. Tablets: (Lanoxin): 62.5 mcg, 125 mcg, 187.5 mcg, 250 mcg.
Administration/handling:  IM rarely used (produces severe local irritation, erratic absorption). If no other route possible, give deep into muscle followed by massage. Give no more than 2 mL at any one site
• IV may give undiluted or dilute with at least a 4-fold volume of Sterile Water for Injection or D5W (less may cause precipitate).
• Use immediately.
• Give IV slowly over at least 5 min. PO
• May give without regard to food.
• Tablets may be crushed.
Loading Dose PO: Adults, elderly: 0.75–1.5 mg. Children 10 yrs and older: 10–15 mcg/kg.  Children 5–9 yrs: 20–35 mcg/kg. Children 2–4 yrs: 30–40 mcg/kg.  Children 1–23 mos: 35–60 mcg/kg.   Neonates, full-term: 25–35 mcg/kg. Neonates, premature: 20–30 mcg/kg. IV: Adults, elderly: 0.5–1 mg. Children 10 yrs and older: 8–12 mcg/kg.  Children 5–9 yrs: 15–30 mcg/kg. Children 2–4 yrs: 25–35 mcg/kg.  Children 1–23 mos: 30–50 mcg/kg.  Neonates, full-term: 20–30 mcg/kg. Neonates, premature: 15–25 mcg/kg
Avoid doses greater than 0.125 mg/day in elderly due to decreased renal clearance
HF Loading dose not recommended in HF. PO: Adults, elderly: 0.125–0.25 mg once daily
Atrial Fibrillation Adults, elderly: Digitalizing dose (IV): Initially, 0.25–0.5 mg over several minutes. May repeat doses of 0.25 mg q6 hrs up to a maximum of 1.5 mg over 24 hrs.  Maintenance dose (PO): 0.125–0.25 mg once daily.

Metabolism and Half- Life:

Readily absorbed from GI tract. Par_x005F_x0002_tially metabolized in liver. Primarily excreted in urine. Minimally removed by haemodialysis. Half-life: 36–48 hrs (increased in renal impairment, elderly)

Monitoring:

  • Check U&Es prior to initiation of treatment
  • Digoxin levels should be taken 6hrs post – dose.

Drug Interactions:

  • Increased risk of AV block and symptomatic bradycardia with beta blockers.
  • Risk of cardiac toxicity secondary to hypokalemia with diuretics
  • Plasma concentrations increased by verapamil and diltiazem.
  • Plasma concentration increased by amiodarone and reduced by St. John’s wort

Nursing Considerations:

Baseline assessment:

  • Assess apical pulse. If pulse is 60 or less/min (70 or less/min for children), withhold drug, contact physician.
  • Blood samples are best taken 6-8 hrs after dose or just before next dose.

Intervention/evaluation:

  • Monitor pulse for bradycardia, ECG for arrhythmias for 1–2 hrs after administration (excessive slowing of pulse may be first clinical sign of toxicity).
  • Assess for GI disturbances, neurological abnormalities (signs of toxicity) q2–4h during loading dose (daily during maintenance).
  • Monitor serum potassium, magnesium, calcium, renal function.
  • Therapeutic serum level: 0.8–2 ng/mL; toxic serum level: greater than 2 ng/mL

Patient/family teaching

  • Follow-up visits, blood tests are an important part of therapy.
  • Follow guidelines to take apical pulse and report pulse of 60 or less/min (or as indicated by physician).
  • Wear/carry identification of digoxin therapy and inform dentist, other physician of taking digoxin.
  • Do not increase or skip doses.
  • Do not take OTC medications without consulting physician.
  • Report decreased appetite, nausea/vomiting, diarrhea, visual changes.

Important Points:

  • Hypokalemia and hypercalcemia predispose to digoxin toxicity
  • Narrow therapeutic index, hence, risks of toxicity
  • Requires loading dose at initiation of treatment

REFERENCES

  1. Robert Kizior, Keith Hodgson, Saunders Nursing Drug handbook,1st edition 2024, Elsevier Publications. ISBN-9780443116070
  2. McGraw Hill- Drug Handbook, Seventh Edition, 2013, McGraw Hill Education Publications,9780071799430.
  3. April Hazard, Cynthia Sanoski, Davi’s Drug Guide for Nurses -Sixteenth Edition 2019, FA Davis Company Publications,9780803669451.
  4. Jones and Bartlet, Pharmacology for Nurses, Second Edition, 2020, Jones and Bartlet Learning Publications, ISBN 9781284141986.
  5. Nursebro.com, Search – Nursebro

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