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Pharmacodynamics and pharmacokinetics of higher-dose, double-bolus eptifibatide in percutaneous coronary intervention.

Publication ,  Journal Article
Gilchrist, IC; O'Shea, JC; Kosoglou, T; Jennings, LK; Lorenz, TJ; Kitt, MM; Kleiman, NS; Talley, D; Aguirre, F; Davidson, C; Runyon, J; Tcheng, JE
Published in: Circulation
July 24, 2001

BACKGROUND: Pharmacodynamics of eptifibatide, a cyclic heptapeptide antagonist of platelet glycoprotein IIb/IIIa, are substantially altered by anticoagulants that chelate calcium, resulting in overestimation ex vivo of the in vivo effects of this agent. We conducted a dose-ranging study to characterize the pharmacodynamics and pharmacokinetics of eptifibatide under physiological conditions. METHODS AND RESULTS: Patients (n=39) undergoing elective percutaneous coronary intervention were randomly assigned to an eptifibatide bolus followed by an infusion (180-microgram/kg bolus followed by 2 microgram/kg per minute or 250-microgram/kg bolus followed by 3 microgram/kg per minute) for 18 to 24 hours. In a 2:1 ratio, these patients received either a second bolus of eptifibatide (90 microgram/kg or 125 microgram/kg for the initial 180-microgram/kg or 250-microgram/kg groups, respectively) or placebo 30 minutes after the initial bolus. Bleeding times, ex vivo platelet aggregation, receptor occupancy, and plasma eptifibatide levels at baseline and at 1, 2, 3, 4, 6, and 8 hours were evaluated. Platelet inhibition was dose dependent and >80% in all groups by steady state. The single-bolus regimens had a transient loss of inhibition at 1 hour, consistent with rapid distribution and drug elimination. Pharmacokinetic modeling suggested that optimal dosing of eptifibatide would be obtained with a 180-microgram/kg bolus and a 2-microgram/kg per minute infusion followed by a second 180-microgram/kg bolus 10 minutes later. CONCLUSIONS: A novel higher-dose, double-bolus regimen of eptifibatide in coronary intervention attains and maintains >90% inhibition of platelet aggregation in >90% of patients, providing the pharmacodynamic construct for the design of the Enhanced Suppression of the Platelet IIb/IIIa Receptor with Integrilin Therapy (ESPRIT) trial of adjunctive eptifibatide in coronary stent implantation.

Duke Scholars

Published In

Circulation

DOI

EISSN

1524-4539

Publication Date

July 24, 2001

Volume

104

Issue

4

Start / End Page

406 / 411

Location

United States

Related Subject Headings

  • Time Factors
  • Platelet Glycoprotein GPIIb-IIIa Complex
  • Platelet Aggregation Inhibitors
  • Platelet Aggregation
  • Peptides
  • Middle Aged
  • Metabolic Clearance Rate
  • Male
  • Humans
  • Female
 

Citation

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Gilchrist, I. C., O’Shea, J. C., Kosoglou, T., Jennings, L. K., Lorenz, T. J., Kitt, M. M., … Tcheng, J. E. (2001). Pharmacodynamics and pharmacokinetics of higher-dose, double-bolus eptifibatide in percutaneous coronary intervention. Circulation, 104(4), 406–411. https://doi.org/10.1161/hc2901.093504
Gilchrist, I. C., J. C. O’Shea, T. Kosoglou, L. K. Jennings, T. J. Lorenz, M. M. Kitt, N. S. Kleiman, et al. “Pharmacodynamics and pharmacokinetics of higher-dose, double-bolus eptifibatide in percutaneous coronary intervention.Circulation 104, no. 4 (July 24, 2001): 406–11. https://doi.org/10.1161/hc2901.093504.
Gilchrist IC, O’Shea JC, Kosoglou T, Jennings LK, Lorenz TJ, Kitt MM, et al. Pharmacodynamics and pharmacokinetics of higher-dose, double-bolus eptifibatide in percutaneous coronary intervention. Circulation. 2001 Jul 24;104(4):406–11.
Gilchrist, I. C., et al. “Pharmacodynamics and pharmacokinetics of higher-dose, double-bolus eptifibatide in percutaneous coronary intervention.Circulation, vol. 104, no. 4, July 2001, pp. 406–11. Pubmed, doi:10.1161/hc2901.093504.
Gilchrist IC, O’Shea JC, Kosoglou T, Jennings LK, Lorenz TJ, Kitt MM, Kleiman NS, Talley D, Aguirre F, Davidson C, Runyon J, Tcheng JE. Pharmacodynamics and pharmacokinetics of higher-dose, double-bolus eptifibatide in percutaneous coronary intervention. Circulation. 2001 Jul 24;104(4):406–411.

Published In

Circulation

DOI

EISSN

1524-4539

Publication Date

July 24, 2001

Volume

104

Issue

4

Start / End Page

406 / 411

Location

United States

Related Subject Headings

  • Time Factors
  • Platelet Glycoprotein GPIIb-IIIa Complex
  • Platelet Aggregation Inhibitors
  • Platelet Aggregation
  • Peptides
  • Middle Aged
  • Metabolic Clearance Rate
  • Male
  • Humans
  • Female