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Evaluation of a Therapeutic Conversion from Amlodipine to Felodipine
Author(s) -
Manzo Bruce A.,
Matalka Mazen S.,
Ravnan Susan L.
Publication year - 2003
Publication title -
pharmacotherapy: the journal of human pharmacology and drug therapy
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.227
H-Index - 109
eISSN - 1875-9114
pISSN - 0277-0008
DOI - 10.1592/phco.23.14.1508.31943
Subject(s) - felodipine , amlodipine , tolerability , blood pressure , medicine , heart rate , population , calcium channel blocker , diastole , cardiology , anesthesia , adverse effect , environmental health
Study Objectives. To determine patient satisfaction with and tolerability of a conversion from a long‐acting calcium channel blocker, amlodipine, to felodipine. Secondary objectives were to compare the effect of the change on blood pressure and heart rate and the economic impact of the change. Design. Retrospective study. Setting. Veterans Affairs health care system. Patients. Two hundred eighty‐three men who were taking amlodipine to manage hypertension. Intervention. Patients who were converted to felodipine were mailed a survey quantifying subjective symptoms; the survey also included questions specific to the change program. Transitory blood pressure and heart rate measurements retrieved by electronic chart review were evaluated during therapy with both amlodipine and felodipine. Measurements and Main Results. Ninety‐five percent of patients were satisfied with the conversion process and tolerated the switch from amlodipine to felodipine. Mean systolic and diastolic blood pressures were reduced by 4.4 and 2.6 mm Hg, respectively (p=0.166 and 0.187, respectively). Heart rate was reduced significantly by 4.2 beats/minute (p=0.008). The conversion realized a net annual drug cost savings of approximately $16,000. Conclusion. Our patient population was satisfied with the conversion from amlodipine to felodipine, and the new drug was found to be effective, well tolerated, and associated with a modest cost reduction.