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Adenosine-induced atrial fibrillation during fractional flow reserve measurement

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CASE REPORT

Cardiology Journal 2012, Vol. 19, No. 6, pp. 650–651 10.5603/CJ.2012.0121 Copyright © 2012 Via Medica ISSN 1897–5593

650 www.cardiologyjournal.org

Address for correspondence: Mladen I. Vidovich, MD, Department of Medicine, Division of Cardiology, University of Illinois at Chicago, 840 South Wood Street, MC 715, Suite 935, Chicago, IL 60612-7323, USA, tel: 312 413 4951, fax: 312 413 2948, e-mail: miv@uic.edu

Received: 02.11.2011 Accepted: 07.11.2011

Adenosine-induced atrial fibrillation during fractional flow reserve measurement

Eugene Park, Adam Price, Mladen I. Vidovich

Department of Medicine, Division of Cardiology, University of Illinois at Chicago, Chicago, Illinois, USA

Abstract

We present the case of a 44 year-old man referred for coronary angiography with a history of coronary artery disease. Following administration of intra-coronary adenosine for fractional flow reserve (FFR) assessment, the patient developed atrial fibrillation (AF). While well de- scribed during non-invasive stress testing, this is the first description in the literature of AF following adenosine administration for FFR. The growing usage of FFR during diagnostic coronary angiography makes this an important side effect to consider. Our subsequent mana- gement and follow-up is presented. (Cardiol J 2012; 19, 6: 650–651)

Key words: atrial fibrillation, adenosine, fractional flow reserve

Introduction

A 44 year-old-man was referred for cardiac catheterization because of symptoms of worsening exertional chest pain. The patient had required multiple percutaneous interventions in the past.

Aside from his coronary history, the patient had been treated for diabetes mellitus, hypertension and hyperlipidemia. His medications included aspirin 81 mg daily, clopidogrel 75 mg daily, gemfibrozil 600 mg twice daily, simvastatin 80 mg daily, amlo- dipine 5 mg daily, carvedilol 25 mg twice daily, lisi- nopril 40 mg daily, isosorbide mononitrate 30 mg daily, and insulin. He denied any prior history of arrhythmia, dizziness, palpitations or syncope. His pre-catheterization electrocardiogram revealed normal sinus rhythm (SR) with a normal QT inter- val, and echocardiography demonstrated normal ejection fraction with apical septal hypokinesis.

Prior to coronary angiography, blood pressure (BP) was 126/61 mm Hg and heart rate was 81 bpm.

Telemetry demonstrated normal SR. Angiography revealed progression of his underlying coronary disease, with multiple non-obstructive lesions. The most severe lesion was seen in the proximal pos-

terior descending coronary artery (PDA), visually estimated at 60–70% stenosis. Given his clinical presentation of exertional angina, and the interme- diate nature of the stenosis, the decision was made to pursue additional functional testing with fraction- al flow reserve (FFR).

FFR measurement was performed with a Vol- cano 0.014” pressure wire (PrimeWire™, Volcano Corporation, Rancho Cordova, CA, USA). During his FFR assessment, 70 µg of intra-coronary ade- nosine was administered. The patient initially de- veloped transient third degree atrioventricular (AV) block during adenosine administration, and follow- ing resolution of the AV block, spontaneously de- veloped atrial fibrillation (AF) with rapid ventricu- lar response following a series of premature atrial contractions (PACs) (Fig. 1) The FFR measurement was 0.73, a clinically significant value, and the pa- tient subsequently received a drug eluting stent to his PDA. The patient remained asymptomatic and hemodynamically stable with a BP of 113/69 and a pulse of 112 bpm. He did, however, remain in AF, and the decision was made to admit the patient to the telemetry floor for further monitoring and mana- gement of his arrhythmia. Intravenous amiodarone,

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651 Eugene Park et al., FFR and atrial fibrillation

www.cardiologyjournal.org

150 mg bolus was administered, followed by a conti- nuous infusion, with a plan to perform electrical car- dioversion the following morning should he remain in AF. Aspirin, 325 mg orally, clopidogrel 75 mg oral- ly, as well as his home dose of carvedilol 25 mg twice daily were administered. The patient successfully converted to SR by the following morning, and was discharged home on full dose aspirin, clopidogrel, and the remainder of his home medications.

Discussion

To the best of our knowledge, this is the first reported case of AF associated with adenosine in- fusion during FFR assessment. There is already a vast body of literature supporting the usefulness of FFR in the assessment of intermediate lesions, as well as the improved clinical outcomes associated with its usage [1]. The expectation is that FFR and adenosine administration during coronary angio- graphy will become more widespread as a result of this evidence. To date, there is already a well-es- tablished link between adenosine and its ability to stimulate cardiac arrhythmias [2]. Adenosine infu- sion used for the diagnosis of coronary disease has confirmed this association, with AF induction fol- lowing adenosine myocardial perfusion stress test- ing having been described previously [3]. The mechanism of this association has been attributed to adenosine’s ability both to decrease atrial refrac- tory periods as well as to shorten the action poten- tial duration, making the atrial myocardium more susceptible to arrhythmia induction [2, 4]. In addi- tion, evidence also links adenosine administration to the induction of PACs, which has been clearly linked to the induction of AF [2].

Currently, there is no reported incidence of this complication related to FFR assessment; however,

the morbidity associated with AF makes this an im- portant side effect to consider during functional assessment of intermediate coronary lesions. It is uncertain whether this complication may be more frequently encountered with intracoronary or intra- venous adenosine administration. Additionally, the impact of the dose of intracoronary adenosine, ad- ministration to the left or right coronary system, coronary dominance or amount of ischemic myocar- dium on the induction of AF is unknown.

Conclusions

This case represents a well-described side effect related to adenosine infusion, albeit in a unique set- ting of FFR assessment. With the growing frequency of FFR assessment during coronary angiography, al- though rare, the initiation of AF with intracoronary adenosine may be increasingly encountered.

Conflict of interest: none declared

References

1. Tonino PA, De Bruyne B, Pijls NH et al. Fractional flow reserve versus angiography for guiding percutaneous coronary interven- tion. N Engl J Med, 2009; 360: 213–224.

2. Belhassen B, Glick A, Laniado S. Comparative clinical and elec- trophysiologic effects of adenosine triphosphate and verapamil on paroxysmal reciprocating junctional tachycardia. Circulation, 1988; 77: 795–805.

3. Kanei Y, Hanon S, Van-Tosh A, Schweitzer P. Adenosine- -induced atrial fibrillation during pharmacologic stress testing:

Report of eight cases and review of the literature. Int J Cardiol, 2008; 129: e15–e17.

4. Kabell G, Buchanan LV, Gibson JK, Belardinelli L. Effects of adenosine on atrial refractoriness and arrhythmias. Cardiovasc Res, 1994; 28: 1385–1389.

Figure 1. Continuous telemetry recording performed during coronary angiography and adenosine administration.

Telemetry reveals initial normal sinus rhythm, followed by transient third degree atrioventricular (AV) block. Following resolution of AV block, a premature atrial contraction (PAC) occurs, which triggers the development of atrial fibrillation.

Initial infusion AV block PAC Atrial fibrillation I

II III aR aL aF VI V2 V3 V4 V5 V6

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