Nl. Mcintoshyellin et al., SAFETY AND EFFICACY OF CENTRAL INTRAVENOUS BOLUS ADMINISTRATION OF ADENOSINE FOR TERMINATION OF SUPRAVENTRICULAR TACHYCARDIA, Journal of the American College of Cardiology, 22(3), 1993, pp. 741-745
Objectives. This study was done to quantify the dosing differences bet
ween central and peripheral adenosine administration for treatment of
supraventricular tachycardia. Background. Earlier studies that evaluat
ed the safety and efficacy of adenosine primarily utilized a periphera
l site of administration. Although it has been recommended that lower
doses should be given centrally, dosing recommendations have not been
provided. Methods. Thirty adults with supraventricular tachycardia und
erwent invasive electrophysiologic study and were treated with central
and peripheral intravenous administration of adenosine. Peripheral in
jections were administered through a venous catheter in an upper extre
mity and central infusions were accomplished by means of a catheter po
sitioned in or near the right atrium. The site of administration was r
andomized and each subject received adenosine by both routes. Adenosin
e was administered every minute in increasing increments of 3, 6, 9 an
d 12 mg until the tachycardia terminated. Peripheral responses were co
mpared with those obtained centrally. Results. The minimal effective p
eripheral dose was distributed among the four doses: Tachycardia was t
erminated in 11 patients with 3 mg (37%), in 10 (33%) with 6 mg, in 4
(13%) with 9 mg and in 5 (17%) with 12 mg. In contrast, after central
administration, 23 episodes of tachycardia (77%) were terminated with
3 mg, 6 (20%) with 6 mg and 1 (3%) with 9 mg; none required 12 mg. Low
er doses of adenosine were more effective after central than after per
ipheral administration, with 63% of the subjects requiring a lesser do
se. There was no difference between the two routes of drug administrat
ion in the incidence of side effects or transient arrhythmias at the t
ime of tachycardia termination. Conclusions. Adenosine can be safely g
iven centrally for termination of supraventricular tachycardia. The in
itial dose should be 3 mg.