Acute cardiovascular effects of OPC-18790 in patients with congestive heart failure - Time- and dose-dependence analysis based on pressure-volume relations
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Feldman, MD
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机构:JOHNS HOPKINS MED INST,DIV CARDIOL,BALTIMORE,MD 21205
Feldman, MD
Pak, PH
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机构:JOHNS HOPKINS MED INST,DIV CARDIOL,BALTIMORE,MD 21205
Pak, PH
Wu, CC
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机构:JOHNS HOPKINS MED INST,DIV CARDIOL,BALTIMORE,MD 21205
Wu, CC
Haber, HL
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机构:JOHNS HOPKINS MED INST,DIV CARDIOL,BALTIMORE,MD 21205
Haber, HL
Heesch, CM
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机构:JOHNS HOPKINS MED INST,DIV CARDIOL,BALTIMORE,MD 21205
Heesch, CM
Bergin, JD
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机构:JOHNS HOPKINS MED INST,DIV CARDIOL,BALTIMORE,MD 21205
Bergin, JD
Powers, ER
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机构:JOHNS HOPKINS MED INST,DIV CARDIOL,BALTIMORE,MD 21205
Powers, ER
Cowart, TD
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机构:JOHNS HOPKINS MED INST,DIV CARDIOL,BALTIMORE,MD 21205
Cowart, TD
Johnson, W
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机构:JOHNS HOPKINS MED INST,DIV CARDIOL,BALTIMORE,MD 21205
Johnson, W
Feldman, AM
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机构:JOHNS HOPKINS MED INST,DIV CARDIOL,BALTIMORE,MD 21205
Feldman, AM
Kass, DA
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机构:JOHNS HOPKINS MED INST,DIV CARDIOL,BALTIMORE,MD 21205
Kass, DA
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[1] JOHNS HOPKINS MED INST,DIV CARDIOL,BALTIMORE,MD 21205
[2] JOHNS HOPKINS MED INST,DEPT INTERNAL MED,BALTIMORE,MD 21205
Background OPC-18790 is a water-soluble quinolinone derivative that shares the pharmacological properties of vesnarinone and that may be useful for treating heart failure. We studied the contribution and relative dose sensitivities of the inotropic, lusitropic, and vascular effects of OPC-18790 in patients with dilated cardiomyopathy. Methods and Results Pressure-volume (PV) analysis was per formed in 17 patients who received either 5 mu g . kg(-1). min(-1)(low dose, n=10) or 10 mu g . kg(-1). min(-1)(high dose, n=7) OPC-18790 by 1-hour IV infusion. Right heart pressures and flow and left heart PV relations (conductance catheter) were measured at baseline and every 15 minutes during infusion. Transient inferior vena caval obstruction was used to determine IV relations. Both doses produced venodilation reflected by a 10% decline in left ventricular end-diastolic volume and a 30% fall in atrial and pulmonary artery pressures. Arterial dilation was four times greater at the high dose, with an approximate to 40% fall in effective arterial elastance and systemic resistance. Contractility rose by 25% to 100% (depending on PV index) with both doses. Ventricular-arterial coupling (ratio of ventricular end-systolic to arterial elastances) was approximate to 0.25 at baseline and doubled (or tripled) at low (or high) dose, correlating with improved efficiency. Isovolumetric relaxation shortened, whereas the diastolic PV relation was generally unchanged. Heart rate was unaltered. Conclusions OPC-18790 has potent venous and arterial vasodilator effects and moderate inotropic and lusitropic effects without a change in heart rate. These combined actions suggest a unique potential of OPC-18790 for heart failure treatment.
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页码:474 / 483
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LEIDEN STATE UNIV HOSP,DEPT CARDIOL,CATHERIZAT LAB,2333 AA LEIDEN,NETHERLANDSLEIDEN STATE UNIV HOSP,DEPT CARDIOL,CATHERIZAT LAB,2333 AA LEIDEN,NETHERLANDS
BAAN, J
VANDERVELDE, ET
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VANDERVELDE, ET
DEBRUIN, HG
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LEIDEN STATE UNIV HOSP,DEPT CARDIOL,CATHERIZAT LAB,2333 AA LEIDEN,NETHERLANDSLEIDEN STATE UNIV HOSP,DEPT CARDIOL,CATHERIZAT LAB,2333 AA LEIDEN,NETHERLANDS
DEBRUIN, HG
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LEIDEN STATE UNIV HOSP,DEPT CARDIOL,CATHERIZAT LAB,2333 AA LEIDEN,NETHERLANDSLEIDEN STATE UNIV HOSP,DEPT CARDIOL,CATHERIZAT LAB,2333 AA LEIDEN,NETHERLANDS
SMEENK, GJ
KOOPS, J
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LEIDEN STATE UNIV HOSP,DEPT CARDIOL,CATHERIZAT LAB,2333 AA LEIDEN,NETHERLANDSLEIDEN STATE UNIV HOSP,DEPT CARDIOL,CATHERIZAT LAB,2333 AA LEIDEN,NETHERLANDS
KOOPS, J
VANDIJK, AD
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LEIDEN STATE UNIV HOSP,DEPT CARDIOL,CATHERIZAT LAB,2333 AA LEIDEN,NETHERLANDSLEIDEN STATE UNIV HOSP,DEPT CARDIOL,CATHERIZAT LAB,2333 AA LEIDEN,NETHERLANDS
VANDIJK, AD
TEMMERMAN, D
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LEIDEN STATE UNIV HOSP,DEPT CARDIOL,CATHERIZAT LAB,2333 AA LEIDEN,NETHERLANDSLEIDEN STATE UNIV HOSP,DEPT CARDIOL,CATHERIZAT LAB,2333 AA LEIDEN,NETHERLANDS
TEMMERMAN, D
SENDEN, J
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LEIDEN STATE UNIV HOSP,DEPT CARDIOL,CATHERIZAT LAB,2333 AA LEIDEN,NETHERLANDSLEIDEN STATE UNIV HOSP,DEPT CARDIOL,CATHERIZAT LAB,2333 AA LEIDEN,NETHERLANDS
SENDEN, J
BUIS, B
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LEIDEN STATE UNIV HOSP,DEPT CARDIOL,CATHERIZAT LAB,2333 AA LEIDEN,NETHERLANDSLEIDEN STATE UNIV HOSP,DEPT CARDIOL,CATHERIZAT LAB,2333 AA LEIDEN,NETHERLANDS
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LEIDEN STATE UNIV HOSP,DEPT CARDIOL,CATHERIZAT LAB,2333 AA LEIDEN,NETHERLANDSLEIDEN STATE UNIV HOSP,DEPT CARDIOL,CATHERIZAT LAB,2333 AA LEIDEN,NETHERLANDS
BAAN, J
VANDERVELDE, ET
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LEIDEN STATE UNIV HOSP,DEPT CARDIOL,CATHERIZAT LAB,2333 AA LEIDEN,NETHERLANDSLEIDEN STATE UNIV HOSP,DEPT CARDIOL,CATHERIZAT LAB,2333 AA LEIDEN,NETHERLANDS
VANDERVELDE, ET
DEBRUIN, HG
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LEIDEN STATE UNIV HOSP,DEPT CARDIOL,CATHERIZAT LAB,2333 AA LEIDEN,NETHERLANDSLEIDEN STATE UNIV HOSP,DEPT CARDIOL,CATHERIZAT LAB,2333 AA LEIDEN,NETHERLANDS
DEBRUIN, HG
SMEENK, GJ
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LEIDEN STATE UNIV HOSP,DEPT CARDIOL,CATHERIZAT LAB,2333 AA LEIDEN,NETHERLANDSLEIDEN STATE UNIV HOSP,DEPT CARDIOL,CATHERIZAT LAB,2333 AA LEIDEN,NETHERLANDS
SMEENK, GJ
KOOPS, J
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LEIDEN STATE UNIV HOSP,DEPT CARDIOL,CATHERIZAT LAB,2333 AA LEIDEN,NETHERLANDSLEIDEN STATE UNIV HOSP,DEPT CARDIOL,CATHERIZAT LAB,2333 AA LEIDEN,NETHERLANDS
KOOPS, J
VANDIJK, AD
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LEIDEN STATE UNIV HOSP,DEPT CARDIOL,CATHERIZAT LAB,2333 AA LEIDEN,NETHERLANDSLEIDEN STATE UNIV HOSP,DEPT CARDIOL,CATHERIZAT LAB,2333 AA LEIDEN,NETHERLANDS
VANDIJK, AD
TEMMERMAN, D
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LEIDEN STATE UNIV HOSP,DEPT CARDIOL,CATHERIZAT LAB,2333 AA LEIDEN,NETHERLANDSLEIDEN STATE UNIV HOSP,DEPT CARDIOL,CATHERIZAT LAB,2333 AA LEIDEN,NETHERLANDS
TEMMERMAN, D
SENDEN, J
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LEIDEN STATE UNIV HOSP,DEPT CARDIOL,CATHERIZAT LAB,2333 AA LEIDEN,NETHERLANDSLEIDEN STATE UNIV HOSP,DEPT CARDIOL,CATHERIZAT LAB,2333 AA LEIDEN,NETHERLANDS
SENDEN, J
BUIS, B
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LEIDEN STATE UNIV HOSP,DEPT CARDIOL,CATHERIZAT LAB,2333 AA LEIDEN,NETHERLANDSLEIDEN STATE UNIV HOSP,DEPT CARDIOL,CATHERIZAT LAB,2333 AA LEIDEN,NETHERLANDS