51. Frequency of Adverse Event Monitoring in Ambulatory Patients on Amiodarone or Dofetilide.
- Author
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Rickard JP, Negrelli J, Olson JL, and Dick T
- Subjects
- Aged, Aged, 80 and over, Amiodarone therapeutic use, Anti-Arrhythmia Agents therapeutic use, Cohort Studies, Drug Monitoring standards, Female, Follow-Up Studies, Humans, Male, Middle Aged, Phenethylamines therapeutic use, Retrospective Studies, Sulfonamides therapeutic use, Amiodarone adverse effects, Anti-Arrhythmia Agents adverse effects, Drug Monitoring methods, Drug-Related Side Effects and Adverse Reactions diagnosis, Drug-Related Side Effects and Adverse Reactions epidemiology, Phenethylamines adverse effects, Sulfonamides adverse effects
- Abstract
Background: Published studies state that adherence to regular laboratory assessments for anti-arrhythmic drugs is as low as 20%. Monitoring adherence is important as other studies have shown that up to 93% of patients on amiodarone experience an adverse drug event leading to a potentially lethal event., Objective: To determine whether patients prescribed amiodarone or dofetilide are being monitored according to package labeling and guideline recommendations for adverse events., Methods: Patients prescribed amiodarone or dofetilide from a 2-year period were eligible for inclusion. Patients with ventricular arrhythmias, prescribed more than 1 anti-arrhythmic agent, or received anti-arrhythmic monitoring outside the health-care system were excluded. Adherence to monitoring parameters was assessed according to labeled recommendations and published guidelines. The primary objective was to determine the frequency of baseline and follow-up monitoring recommendations for patients receiving amiodarone or dofetilide. The secondary objective was to determine rates of adverse drug events., Results: One hundred patients were evaluated (amiodarone n = 50, dofetilide n = 50). Average rates of baseline and follow-up amiodarone monitoring parameters were 55% and 57%, respectively. Average rates of baseline and follow-up dofetilide monitoring were 99.6% and 85%, respectively. There was a statistically significant difference in abnormally elevated thyroid-stimulating hormone levels (8%-30%, P ≤ .005) after patients were prescribed amiodarone. Twelve percent of patients taking dofetilide had an increase in QTc interval by >15%., Conclusions: Amiodarone adverse event monitoring was lower than dofetilide in this cohort. Improving the monitoring of these agents may decrease morbidity risk in this population.
- Published
- 2018
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