Why the study?
Does oral maintenance digoxin therapy improve systolic time intervals in patients with compensated atherosclerotic and/or hypertensive heart disease?
Does oral maintenance digoxin therapy improve systolic time intervals in patients with compensated atherosclerotic and/or hypertensive heart disease?
Maintenance oral digoxin therapy produces a dose-dependent positive inotropic effect, as evidenced by the shortening of systolic time intervals.
Supports dose-dependent inotropy on systolic time intervals; hypothesis-generating and should not change practice in compensated heart disease.
Systolic time intervals (STI) and serum digoxin concentrations (SDC) were measured in eight patients with compensated atherosclerotic and/or hypertensive heart disease who received oral digoxin 0.25 mg/day or 0.5 mg/day for alternate two-week periods without a loading dose. Control data were obtained both before and after the four weeks of treatment. After 13 days treatment with digoxin, 0.5 mg/day, there was a significant decrease in total electromechanical systole corrected for heart rate (QS 2 i), pre-ejection period (PEP), pre-ejection period corrected for heart rate (PEP 1 ) and PEP/left ventricular ejection time (LVET). After the thirteenth dose of 0.25 mg/day there was significant shortening of PEP 1 and PEP/LVET. Shortening of QS 2 i correlated significantly with SDC 24 hours after the thirteenth dose of 0.5 mg. These data suggest that after 13 days of treatment with 0.25 and 0.5 mg/day of digoxin, a positive inotropic effect occurs as reflected by STI shortening. A greater effect was recorded with the 0.5 mg dose.
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Carliner et al. (1974) studied this question.
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