The positive inotropic effects of milrinone but not of digoxin are attenuated at short cycle lengths

Christopher J. Zeitz, Rebecca H. Ritchie, Richard G. Jarrett, John T.Y. Hii, Ronald D. Wuttke, John D. Horowitz

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The effects of inotropically active agents on the left ventricular force-interval relation are a potential determinant of their clinical utility and safety. However, little information is available concerning the effects of noncatecholamine positive inotropic agents on this relation. Therefore this study compared the short-term effects of digoxin and milrinone on resting hemodynamics, frequency potentiation (FP), and mechanical restitution (MR) in patients undergoing nonemergency cardiac catheterization. Both digoxin and milrinone produced similar increases in LV + dP/dt at rest (12.2 ± 1.3%, p < 0.000001 and 11.4 ± 3.2%, p < 0.01, respectively). The positive inotropic effects of digoxin were marginally attenuated during FP (by 8.5 ± 4.2% and 4.6 ± 2.9% at 10 and 60 s, respectively, both p = NS compared with baseline). Similarly, on MRC analysis, the parameter c (a measure of sensitivity of contractile performance to reductions in cycle length) increased by 3.6 ± 3.7% (p = NS). Whereas the positive inotropic effects of milrinone were not significantly attenuated during FP, they were abolished and possibly reversed at short cycle lengths on MR curve construction (6.8 ± 5.9% negative inotropic effect at 60% of resting cycle length; p = NS; p < 0.05 vs. resting cycle length). In conclusion, in patients with well- preserved left ventricular systolic function, the positive inotropic effects of milrinone but not of digoxin are markedly dependent on heart rate. These properties may influence both relative safety and efficacy of both agents.

Original languageEnglish
Pages (from-to)427-433
Number of pages7
JournalJournal of Cardiovascular Pharmacology
Issue number3
Publication statusPublished - 13 Mar 2000
Externally publishedYes


  • Digoxin
  • Force-interval
  • Frequency potentiation
  • Mechanical restitution
  • Milrinone
  • Rate-dependent effects

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