International Journal of Travel Medicine and Global Health

International Journal of Travel Medicine and Global Health

The Effects of Verapamil and Adenosine in the Treatment of Paroxysmal Supraventricular Tachycardia

Document Type : Original Article

Authors
Trauma Research Center, Clinical Sciences Institute, Baqiyatallah University of Medical Sciences, Tehran, Iran.
10.30491/ijtmgh.2025.502598.1455
Abstract
Introduction: There are several drug medicines in the treatment of Paroxysmal Supra-ventricular Tachycardia (PST) after the inefficacious vagal stimulus. This study aimed to compare two treatments: Verapamil versus adenosine triphosphate (ATP) for treating Paroxysmal Supraventricular Tachycardia.
Methods: Sixty-six patients with PST were treated with either Verapamil (5 to 10 mg) or ATP (5 to 20 mg). The basal features of each group and the efficacy and safety of the two drugs were compared. Verapamil failures were treated with ATP and vice versa.
Results: The mean heart rate after treatment in all patients was 79.46 ± 10.67, compared to baseline in both groups, showed a decrease significantly (P <0.001)) The mean heart rate after treatment in adenosine was 87.27 + 8.39 and 71.66 ± 5.95 in the verapamil group. Between groups in heart rate, significant differences were observed after treat-ment of the screw (P<0.001). Of the total, 12 (18.2%) had a recurrence of adenosine in 6 patients (9.1%), and Verapamil in 6 patients (9.1%) had a recurrence. The Average time converted to sinus rhythm in all patients was 32.04+12.79 minutes. Average time con-verted to sinus rhythm verapamil group and 36.06 ± 12.97 minutes in the adenosine group and 28.03+ 11.45 minutes (P = 0.01).
Conclusions: The more effective the drug verapamil over adenosine is in treating PSVT, the longer it proves its effectiveness. Except for headache, side effects were higher in patients treated with adenosine. In other cases, there was no difference between the two drugs.
Keywords


Articles in Press, Accepted Manuscript
Available Online from 20 August 2025

  • Receive Date 27 January 2025
  • Revise Date 01 March 2025
  • Accept Date 05 March 2025