TY - JOUR
T1 - Acute conversion of paroxysmal supraventricular tachycardia with intravenous diltiazem
AU - Dougherty, Anne Hamilton
AU - Jackman, Warren M.
AU - Naccarelli, Gerald V.
AU - Friday, Karen J.
AU - Dias, Virgil C.
N1 - Funding Information:
From the Electrophysiology Laboratory, Division of Cardiology, University of Texas Medical School at Houston, Houston, Texas, and the University of Oklahoma Health Sciences Center, Oklahoma City, Oklahoma. This study was supported by a grant from Marion Merrell Dow, Inc., Kansas City, Mimi. Manuscript received February 21, 1992; revised manuscript received and accepted May 4,1992.
PY - 1992/9/1
Y1 - 1992/9/1
N2 - Diltiazem has electrophysiologic effects similar to those of verapamil. Its efficacy and safety in 4 doses for treatment of induced supraventricular tachycardia (SVT) were examined and compared with those of placebo in 87 patients (25 with atrioventricular [AV] nodal reentry tachycardia, 60 with AV reentry associated with an accessory AV connection, and 2 with atrial tachycardia). Conversion to sinus rhythm occurred in 4 of 14 patients (29%) with 0.05 mg/kg of diltiazem, 16 of 19 (84%) with 0.15 mg/kg, 13 of 13 (100%) with 0.25 mg/kg, and 14 of 17 (82%) with 0.45 mg/kg compared with 6 of 24 (25%) treated with placebo. Conversion rates in groups receiving doses of 0.15 to 0.45 mg/kg of diltiazem were superior to that in the placebo group (p < 0.001). Time to conversion was 3.0 ± 2.6 minutes in responding diltiazem patients compared with 5.9 ± 6.1 minutes in responding control patients. Diltiazem administration resulted in significant lengthening of SVT cycle length, AH interval, and AV nodal effective refractory period and block cycle length. The most frequent adverse response to diltiazem was hypotension (7 of 63 patients); however, only 4 patients had symptoms related to hypotension. Thus, intravenous diltiazem in doses of 0.15, 0.25 and 0.45 mg/kg is an effective and safe treatment for the acute management of SVT.
AB - Diltiazem has electrophysiologic effects similar to those of verapamil. Its efficacy and safety in 4 doses for treatment of induced supraventricular tachycardia (SVT) were examined and compared with those of placebo in 87 patients (25 with atrioventricular [AV] nodal reentry tachycardia, 60 with AV reentry associated with an accessory AV connection, and 2 with atrial tachycardia). Conversion to sinus rhythm occurred in 4 of 14 patients (29%) with 0.05 mg/kg of diltiazem, 16 of 19 (84%) with 0.15 mg/kg, 13 of 13 (100%) with 0.25 mg/kg, and 14 of 17 (82%) with 0.45 mg/kg compared with 6 of 24 (25%) treated with placebo. Conversion rates in groups receiving doses of 0.15 to 0.45 mg/kg of diltiazem were superior to that in the placebo group (p < 0.001). Time to conversion was 3.0 ± 2.6 minutes in responding diltiazem patients compared with 5.9 ± 6.1 minutes in responding control patients. Diltiazem administration resulted in significant lengthening of SVT cycle length, AH interval, and AV nodal effective refractory period and block cycle length. The most frequent adverse response to diltiazem was hypotension (7 of 63 patients); however, only 4 patients had symptoms related to hypotension. Thus, intravenous diltiazem in doses of 0.15, 0.25 and 0.45 mg/kg is an effective and safe treatment for the acute management of SVT.
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U2 - 10.1016/0002-9149(92)90196-6
DO - 10.1016/0002-9149(92)90196-6
M3 - Article
C2 - 1510006
AN - SCOPUS:0026756734
SN - 0002-9149
VL - 70
SP - 587
EP - 592
JO - American Journal of Cardiology
JF - American Journal of Cardiology
IS - 6
ER -