Dofetilide (Tikosyn®)
| Class: | 
						Class III Antiarrhythmic agent
					 | 
| Actions: | 
						Blocks potassium channels
					
						Prolongs action potential duration (prolonged QT interval), but not PR interval or QRS duration
					 | 
| Indications: | 
						Symptomatic atrial flutter
					
						Symptomatic atrial fibrillation
					 | 
| Pharmacokinetics: | 
						Peak: 2 – 3 hours
					
						Half-Life: 10 hours
					 | 
| Adverse Effects: | 
						Prolonged QT interval, toursades de points (especially with hypkalemia), AV blocks
					
						Headache, chest pain, dizziness
					
						Nausea, diarrhea, abdominal pain
					 | 
| Signs of Toxicity: | 
						prolonged QT interval > 0.44 seconds
					
						life-threatening dysrhythmias (toursades do pointes)
					 | 
| Contraindications: | 
						QT interval > 0.42 seconds [Risk of toursades de pointes]
					
						Ventricular dysrhythmias (PVC's, runs of V-tach)
					
						Hypersensitivity to dofetilide
					
						Concurrent administration of verapamil, cimetidine, trimethoprim, or ketoconazole
					
						Hypokalemia, hypomagnesemia
					
						Safety during pregnancy, lactation or with children not established (Category C).
					 | 
| Dosages & Routes: | Oral: 
					 
				 
						[Creatinine Clearance > 60 ml/min]  500 mcg PO BID
					
						[Creatinine Clearance  40 – 60 ml/min] 250 mcg PO BID
					
						[Creatinine Clearance < 40 ml/min] 125 mcg PO BID
					 | 
| Nursing Implications: | 
						Drug Interactions:  1) Cimetidine, verapamil, trimethoprim, ketoconazole, prochlorperazine, and megestrol compete with renal excretion of dofetilide causing toxic levels of defetilide; 2) Concurrent use with class I antidysrhythmics, class III antidysrhythmics, phenothiazines, tricyclic antidepressants, and macrolide antibiotics can result in prolonged QT interval and enhance risk of toursades de pointes.
					
						Assess renal function, especially creatinine clearance prior to dofetilide therapy.
					
						Monitor cardiac rhythm continuously during therapy with dofetilide.
					
						Defibrillator and resuscitation cart should be at bedside during first 24 hours of dofetilide therapy.
					
						Establish baseline serum electrolyte levels for potassium and magnesium prior to dofetilide therapy.
					
						Report to physician and GI alterations like vomiting or diarrhea that might alter serum electrolyte levels.
					
						Intervention of choice for stable atrial flutter or atrial fibrillation is elective synchronized cardioversion.
					 | 
	 
	References:
	Lehne, R.A. (2010). Pharmacology for nursing care (7th ed., p. 547).  St. Louis: Saunders Elsevier.
	Wilson, B.A., Shannon, M.T., Shields, K.M., & Stang, C.L. (2007).   Prentice Hall Nurse's Drug Guide 2007 (pp. 544-546).  Upper Saddle River, NJ: Pearson Prentice Hall.
	 
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