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Annals of Internal Medicine 1997-Sep

Adenosine-induced atrial arrhythmia: a prospective analysis.

Watumiaji waliosajiliwa tu ndio wanaweza kutafsiri nakala
Ingia / Ingia
Kiungo kimehifadhiwa kwenye clipboard
S A Strickberger
K C Man
E G Daoud
R Goyal
K Brinkman
B P Knight
R Weiss
M Bahu
F Morady

Maneno muhimu

Kikemikali

BACKGROUND

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

OBJECTIVE

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

METHODS

Clinical electrophysiology laboratory at a university medical center.

METHODS

Prospective observational study.

METHODS

200 consecutive patients with PSVT undergoing an electrophysiology procedure.

METHODS

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

METHODS

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.

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