TY - JOUR
T1 - Coronary Circulation Responses to Binodenoson, a Selective Adenosine A2A Receptor Agonist
AU - Hodgson, John Mc B.
AU - Dib, Nabil
AU - Kern, Morton J.
AU - Bach, Richard G.
AU - Barrett, Richard J.
PY - 2007/6/1
Y1 - 2007/6/1
N2 - The purpose of this study was to define binodenoson dosing regimens that produce coronary hyperemia comparable to those of adenosine and that are tolerated well by patients. An open-label, randomized, parallel-group, multicenter study enrolled adult patients who had completed diagnostic cardiac catheterization. Coronary blood flow velocity (CBFV) was measured with a Doppler flow wire, and CBFV reserve was determined before binodenoson administration. Patients (n = 133) received a 3-minute infusion of 0.3, 0.5, or 1 μg/kg/min or a bolus intravenous injection of 1.5 or 3 μg/kg. Coronary hyperemic responses were evident within seconds of administering binodenoson, and the magnitudes and durations of coronary hyperemic responses were dose related. The 1.5- and 3-μg/kg doses, by infusion or bolus, produced maximal coronary hyperemia equivalent to CBFV reserve. All doses transiently decrease blood pressure and increased heart rate and rate-pressure product. In conclusion, the 1.5-μg/kg binodenoson bolus dose produced nearly maximal coronary hyperemia by 4.5 ± 3.7 minutes that was sustained for 7.4 ± 6.86 minutes, was accompanied by modest changes in blood pressure, heart rate, and rate-pressure product, and produced no adverse changes on electrocardiogram, including no second- or third-degree atrioventricular block.
AB - The purpose of this study was to define binodenoson dosing regimens that produce coronary hyperemia comparable to those of adenosine and that are tolerated well by patients. An open-label, randomized, parallel-group, multicenter study enrolled adult patients who had completed diagnostic cardiac catheterization. Coronary blood flow velocity (CBFV) was measured with a Doppler flow wire, and CBFV reserve was determined before binodenoson administration. Patients (n = 133) received a 3-minute infusion of 0.3, 0.5, or 1 μg/kg/min or a bolus intravenous injection of 1.5 or 3 μg/kg. Coronary hyperemic responses were evident within seconds of administering binodenoson, and the magnitudes and durations of coronary hyperemic responses were dose related. The 1.5- and 3-μg/kg doses, by infusion or bolus, produced maximal coronary hyperemia equivalent to CBFV reserve. All doses transiently decrease blood pressure and increased heart rate and rate-pressure product. In conclusion, the 1.5-μg/kg binodenoson bolus dose produced nearly maximal coronary hyperemia by 4.5 ± 3.7 minutes that was sustained for 7.4 ± 6.86 minutes, was accompanied by modest changes in blood pressure, heart rate, and rate-pressure product, and produced no adverse changes on electrocardiogram, including no second- or third-degree atrioventricular block.
UR - http://www.scopus.com/inward/record.url?scp=34248655923&partnerID=8YFLogxK
U2 - 10.1016/j.amjcard.2006.12.086
DO - 10.1016/j.amjcard.2006.12.086
M3 - Article
C2 - 17531571
AN - SCOPUS:34248655923
SN - 0002-9149
VL - 99
SP - 1507
EP - 1512
JO - American Journal of Cardiology
JF - American Journal of Cardiology
IS - 11
ER -