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ARTICLE

Adenosine-Induced Atrial Arrhythmia: A Prospective Analysis

right arrow S. Adam Strickberger, MD; K. Ching Man, DO; Emile G. Daoud, MD; Rajiva Goyal, MD; Karin Brinkman, BS; Bradley P. Knight, MD; Raul Weiss, MD; Marwan Bahu, MD; and Fred Morady, MD

15 September 1997 | Volume 127 Issue 6 | Pages 417-422

Background: Adenosine is considered safe and effective for paroxysmal supraventricular tachycardia (PSVT), but anecdotal experience suggests that adenosine can precipitate atrial arrhythmias.

Objectives: To determine the frequency and mechanisms of adenosine-induced atrial arrhythmias.

Setting: Clinical electrophysiology laboratory at a university medical center.

Design: Prospective observational study.

Patients: 200 consecutive patients with PSVT undergoing an electrophysiology procedure.

Intervention: During PSVT, 12 mg of adenosine was administered centrally through the femoral vein.

Measurements: Frequency of adenosine-induced atrial fibrillation.

Results: Paroxysmal supraventricular tachycardia terminated after adenosine administration in 198 patients (99% [95% CI, 96% to 100%]). Adenosine led to atrial fibrillation (n = 22) or atrial fibrillation and atrial flutter (n = 2) in 24 patients (12% [CI, 7.5% to 16.5%]). An atrial premature complex occurred in all 24 patients who developed atrial fibrillation, atrial flutter, or both and in 102 of the 176 patients (58%) who did not (P < 0.001). The mean (±SD) time from the preceding atrial complex to the atrial premature complex was shorter when an atrial arrhythmia occurred, and the mean ratio of this interval to the preceding atrial cycle length was also lower when atrial fibrillation developed (0.37 ± 0.16 compared with 0.49 ± 0.16; P = 0.002).

Conclusions: The incidence of atrial fibrillation induced by 12 mg of adenosine administered through the femoral vein was 12%. Fibrillation seems to be associated with a "long-short" atrial sequence. If the mechanism of PSVT is unknown and the Wolff-Parkinson-White syndrome is possible, administration of adenosine should be limited to medical facilities that have emergency resuscitation equipment.

Author and Article Information
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From University of Michigan Medical Center, Ann Arbor, Michigan.
Acknowledgments: The authors thank Allyson Navyac for secretarial support and Seema Sonnad, PhD, from the Consortium for Health Outcomes, Innovations and Cost Effectiveness Studies at the University of Michigan Medical Center.
Requests for Reprints: S. Adam Strickberger, MD, University of Michigan Medical Center, 1500 East Medical Center Drive, Box 0022, Ann Arbor, MI 48109-0022.
Current Author Addresses: Drs. Strickberger, Man, Daoud, Goyal, Knight, Weiss, Bahu, and Morady and Ms. Brinkman: University of Michigan Medical Center, 1500 East Medical Center Drive, Box 0022, Ann Arbor, MI 48109-0022.
Current Author Addresses: Drs. Strickberger, Man, Daoud, Goyal, Knight, Weiss, Bahu, and Morady and Ms. Brinkman: University of Michigan Medical Center, 1500 East Medical Center Drive, Box 0022, Ann Arbor, MI 48109-0022.




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