Indian Pacing Electrophysiol. J.
Indian Pacing Electrophysiol. J. 2003 ;
Role of Atrial Fibrillation Threshold Evaluation on Guiding Treatment
Download PDF 248 KB
Takeshi Shirayama, MD, PhD
Kyoto Prefectural University of Medicine, Department of Medicine, Division of Cardiology, Kawaramachi Hirokoji, Kamigyo-ku, Kyoto, 602-8566, Japan.
Address for correspondence: Dr. Takeshi Shirayama, MD, PhD, Kyoto Prefectural University of Medicine, Department of Medicine, Division of Cardiology, Kawaramachi Hirokoji, Kamigyo-ku, Kyoto, 602-8566, Japan. E-mail: firstname.lastname@example.org
Keywords: atrial fibrillation, electrophysiological test, therapy, prognosis
Atrial fibrillation could be induced reproducibly by 50Hz rapid stimulation which was given through systolic and early diastolic phase of atrial excitation. Duration of atrial fibrillation induced in this way was roughly dependent on the current amplitude of the stimulation. The minimum current that could induce long-lasting atrial fibrillation (30sec in the clinical setting, 2sec in the rabbit or rat model) was defined as atrial fibrillation threshold (AFT). AFT was larger in patients who had history of atrial fibrillation than those who did not. Anti-arrhythmic drugs raised AFT by various degrees both in experimental and clinical cases. Long-term efficacy of a drug could be predicted in a patient, measuring how much the drug increased AFT (cut-off point = 5mA increase). AFT is a useful marker to evaluate atrial vulnerability and to guide pharmacological treatment of atrial fibrillation.
Atrial fibrillation is a target of intensive research because fibrillation is the final frontier in the arrhythmology1 ,2 ,3 . Now we have several therapeutic modalities for this common arrhythmia, including pharmacological and non-pharmacological approach. However, long-term success rate of these treatments would be 50% to 60 % at the best 4 . There are several reasons for its difficulty: 1)this arrhythmia is essentially due to aging in clinical cases, 2)the mechanism of this arrhythmia is not fully understood5 , 3)there is no appropriate animal model6 . We have been working on these problems for several years, and become to use atrial fibrillation threshold as a tool to evaluate the easiness to induce atrial fibrillation (atrial vulnerability) both in the experimental7 ,8 ,9 ,10 and the clinical11 ,12 ,13 settings. This is the unique parameter to evaluate atrial vulnerability quantitatively12 ,13 . Because very few researches have been done in this field, I will summarize the data from our laboratory, comparing with the ventricular counterpart in this review article.
What is fibrillation threshold ?
Fibrillation threshold has been studied mostly in the ventricle 14 ,15 ,16 since Wiggers et al17 ,18 . A single stimulus was given to induce ventricular fibrillation in the diseased and the normal hearts. For this purpose, the stimulus should be given at a critical time point with sufficient current amplitude. The time point is usually located at around the peak of T wave of ECG. The minimum current amplitude to induce fibrillation is defined as fibrillation threshold. This concept is based on a fact that fibrillation can be induced by larger current than a critical (threshold) amplitude. Recently, it is recognized that the second critical amplitude exists when current amplitude is increased incrementally. Larger current than the second critical point can not induce fibrillation, but rather terminate fibrillation 19 ,20 . This point is called defibrillation threshold, which is now widely studied because of implantable cardioverter defibrillators in clinical use. In the combination with vulnerable period (the zone of the critical time points to induce fibrillation), there is an area in the strength-interval curve where fibrillation can be induced by a single stimulus 17 ,18 . This area is shifted rightwards along the axis of coupling interval, for example, when myocardial ischemia or anti-arrhythmic drugs are introduced 21 (Figure 1). The same argument could be applied to the atrium. However, atrial vulnerable period was less defined than that of the ventricle 22 ,23 . Atrial T wave is barely discernable in a standard ECG.
Figure 1: Strength-interval relations in provoking fibrillation
Figure shows an example of strength-interval relations. Triangles are pacing threshold at each coupling interval after an initial deflection of atrial/ventricular activity. Circles indicate induction of repetitive responses, and squares show induction of fibrillation. Closed symbols are control data and open symbols are data obtained in the presence of ischemia or procainamide.
There have been several methods to induce ventricular fibrillation 14 ,17 . Among them, a continuous high frequency pacing at 50-100Hz which covers a whole “vulnerable period” can induce fibrillation consistently 14 . Thus we applied this type of stimulation to the atrium and the minimum current to induce long-lasting atrial fibrillation (>30sec in clinical settings, >2sec in experiments) was defined as fibrillation threshold (Figure 2). Duration of “long-lasting” atrial fibrillation was selected rather arbitrarily as the definition but it was based on the relationship between the current intensity and the duration (see Matsuo et al9 ). The duration was positively correlated with the current intensity until the current reached the threshold. This definition is different from conventional usage in terms of the stimulating pattern.
Figure 2: Measurement of atrial fibrillation threshold
Three leads of a standard ECG record and 3 intra-cardiac records are shown. HRA, RAA and CS are high right atrium, right atrial appendage and coronary sinus, respectively. In the middle of the figure, a rapid pacing at 50Hz was applied to HRA for 1sec, which was induced atrial fibrillation. A constant pacing at a rate of 120/min preceded a rapid pacing. Duration of atrial fibrillation was measured, and then current amplitude of the rapid pacing was increased for the next trial. The minimum current that could induce “sustained” fibrillation was defined as atrial fibrillation threshold.
Mechanism of induction of fibrillation
The precise mechanism of induction of fibrillation by a single pulse or train pulses is not clear. However, there are some observational studies in the ventricle14 ,15 ,17 ,19 : 1)localized repetitive activities were induced at the stimulating site, 2)excitations were propagated, 3)repetitive excitations were observed at many sites of the myocardium 4)excitations resulted in disorganized activity (fibrillation) because of inhomogeneity of conduction and repolarization. When high frequency stimulation is given to the ventricle at an intensity of diastolic threshold, ventricular response mimicking ventricular tachycardia could be observed. As the intensity is raised incrementally, the intervals of ventricular excitation become shorter. At and beyond a critical intensity of the stimulating current, ventricular excitations become fibrillation. Although these results are based on the ventricular study, it is probable that the same phenomenon could be observed in the atrium.
Experimental methodology of induction of atrial fibrillation
Most popular method to induce atrial fibrillation would be an extra-stimulus method, that is, an extra-stimulus is given to the atrium at a critical time point after basic conditioning stimulations at a fixed rate 23 . Because reproducibility of this method is relatively low, statistical evaluation is often necessary after many trials 24 to evaluate drug efficacy or atrial vulnerability. On the other hand, continuous rapid pacing could easily induce fibrillation. Thus this method was introduced for the quantitative evaluation of atrial vulnerability (easiness to induce atrial fibrillation). We chose 50Hz for 1sec stimulation for this purpose. The increment of the current intensity is 1mA for the clinical setting, and 0.1 to 0.5mA for the experimental use.
Atrial fibrillation threshold has been measured in the isolated hearts of guinea pig or rabbit. Sodium channel blockers7 ,8 ,11 (disopyramide, pilsicainide, flecainide, aprindine, lidocaine), potassium channel blockers7 ,10 (E-4031), amiodarone, and SD-32129 raised atrial fibrillation threshold by various degrees. Although the increase of atrial fibrillation threshold induced by anti-arrhythmic drugs was positively related to the increase of effective refractory period, E-4031 had the least potency 7 . This results could be explained by the fact that sodium channel blockers made refractory period longer than E-4031 did because of longer post-excitation refractoriness after a high frequency stimulation 25 . Note that the blocking effect of potassium channels by Ikr blockers (such as E-4031) is less prominent when the excitation frequency becomes higher (reverse use-dependent block26 , but see Ohler et al27 ). In the presence of anti-arrhythmic drugs in the perfusing solution, it was more difficult to induce repetitive atrial firing or atrial fibrillation by electrical stimulation. At the same time, atrial fibrillation threshold was increased.
Effective refractory period becomes shorter when a rapid pacing is continuously applied to the atrium. This phenomenon is called “atrial electrical remodeling” 28 , which is accompanied by the reduction of L-type calcium current and transient outward current2 ,29 . Expression of novel channels was also reported 30 . Large numbers of experimental studies have been performed regarding atrial remodeling. In these studies, single extra-stimulus or burst pacing similar to ours has been used to induce atrial fibrillation. However, atrial vulnerability was compared in terms of the duration of atrial fibrillation that was induced, but not the intensity of the stimulation. These studies did not evaluate how easy to induce atrial fibrillation, but how difficult to recover from the arrhythmia. The evaluation of the duration of the arrhythmia disclose its stability after the physiological and the biochemical changes of the atrium were implemented, but it could not be suitable to evaluate the propensity of the patients to paroxysmal attack of atrial fibrillation. In our experience, a stronger current to the atrium could induce longer atrial fibrillation until the current reached the fibrillation threshold12 .
Experimental data suggested that the measurement of the threshold could predict the easiness to induce atrial fibrillation. Indeed atrial fibrillation threshold was lower in the patients who had a history of atrial fibrillation (median 11mA) than normal control (median 5mA)12 . When cut-off point was set at 10mA, the sensitivity and the specificity were 94%, and 60%, respectively. Effective refractory period, conduction time, or other indicators of atrial vulnerability were not different between two groups. The secondary indicators to distinguish the patients with atrial fibrillation from normal subjects were %maximum atrial fragmentation (%MAF) and fragmented activity zone (FAZ)31 . Their sensitivity and specificity were 78%, 52% (%MAF), and 47%, 84% (FAZ), respectively. %MAF is the relative increase of the width of local atrial electrogram by the extra-stimulation. FAZ is the zone of coupling intervals that made local atrial electrogram longer by 50% or more.
Atrial fibrillation threshold (AFT) could be affected by the autonomic tone because isoproterenol infusion decreased AFT (unpublished data). The data obtained on the day when the catheters were inserted were lower than those obtained on the following days. Thus the results of the measurement should be interpreted cautiously. However, reproducibility of AFT was excellent (±1mA, r=0.95 on the regression line) during a short term examination (<3 hours), or if it was measured on the next day or later after the catheters were inserted.
Evaluation of drug efficacy in the clinical setting
The benefit of the AFT measurement would be quantitative evaluation of the drug efficacy. Anti-arrhythmic drugs raised AFT in general, but the increase of AFT by a drug was different in the individual patient. For example, procainamide raised AFT by 5mA in a patient, but propafenone did not change AFT at all in the same patient. In this way, we could categorize anti-arrhythmic drugs into 2 groups in the individual patient, i.e. drugs that raise AFT significantly, and drugs that does not increase AFT in the patient. The effective drugs in a patient were not necessarily the same in another patient. When the cut-off point of effectiveness was set to 5mA increase, “effective” drug could prevent 88% of the patients from the recurrence of atrial fibrillation at least for 1 year whereas only 13% were free from atrial fibrillation with “ineffective” drugs13 . Thus this method could be used to select effective drugs in an individual patient.
However, the prediction of the effectiveness did not mean the high efficacy of the drug in a large population. As previously reported1,4, efficacy of each drug against atrial fibrillation was around 40 to 50% in our study. AFT is a method to select beneficial drugs to the specific patient.
Serial electrophysiological test has been less recommended in case of ventricular tachycardia, because “effective drug” determined in terms of inducibility did not improve the prognosis of the patients 32 . On the other hand, AFT does not depend on all-or-none type determination of inducibility, but it determines how strong is the drug effect against the arrhythmia. As a matter of fact, atrial fibrillation was always induced in this method because of the definition of AFT.
Rate control and rhythm control
Clearly, AFT measurement determines a drug suitable to maintain sinus rhythm. Recently, the results of the Atrial Fibrillation Follow-up Investigation of Rhythm Management (AFFIRM) study were published33 . This study did not show the advantage of maintaining sinus rhythm over heart rate control in terms of prognosis. This result may argue against the usefulness of AFT measurement. However, mortality of the patients who suffered from paroxysmal atrial fibrillation is relatively low. The biggest concern of the patients is often its symptom. Thus, when mortality is not different, it would be desirable to select less symptomatic life. In this sense, pharmacological treatment with class I anti-arrhythmic drugs could still be a first line therapy for “lone” atrial fibrillation.
AFT in the future
AFT is a quantitative marker to select effective drugs against atrial fibrillation. The concept of this method is “custom-made” medicine. Large-scale population study would reveal overall efficacy of the drug, but a negative side is negligence of individuality or specificity of each patient. Because the efficacy of pharmacological and non-pharmacological treatment is still not high, it is important to know which method should be applied first. It is possible to measure AFT first, and if “effective” drug could be found, the patient should be treated with the regimen. If “effective” drug is not found, catheter ablation or some other non-pharmacological approach should be considered.
1. Khairy P, Nattel S. New insights into the mechanisms and management of atrial fibrillation. CMAJ 2002;167(9):1012-1020.
2. Bosch RF, Nattel S. Cellular electrophysiology of atrial fibrillation. Cardiovasc Res 2002;54(2):259-269.
3. Nattel S, Li D, Yue L. Basic mechanisms of atrial fibrillation--very new insights into very old ideas. Annu Rev Physiol 2000;62:51-77.
4. Wijffels MC, Crijns HJ. Non-invasive characteristics of atrial fibrillation: the value of Holter recordings for the treatment of AF. Card Electrophysiol Rev 2002;6(3):233-238.
5. Brundel BJ, Henning RH, Kampinga HH, Van Gelder IC, Crijns HJ. Molecular mechanisms of remodeling in human atrial fibrillation. Cardiovasc Res 2002;54(2):315-324.
Gaspo R. The tachycardia-induced dog model of atrial fibrillation. Clinical relevance and comparison with other models. J Pharmacol Toxicol Methods 1999;42(1):11-20.
7. Inoue M, Inoue D, Ishibashi K, Sakai R, Shirayama T, Asayama J, Nakagawa M. Effects of E-4031 on atrial fibrillation threshold in guinea pig atria: comparative study with class I antiarrhythmic drugs. J Cardiovasc Pharmacol 1994;24(4):534-541.
8. Inoue M, Inoue D, Ishibashi K, Sakai R, Omori I, Yamahara Y, Asayama J, Nakagawa M. Effects of pilsicainide on the atrial fibrillation threshold in guinea pig atria. A comparative study with disopyramide, lidocaine and flecainide. Jpn Heart J 1993;34(3):301-312.
Matsuo R, Shirayama T, Inoue K, Matoba Y, Imai H, Shiraishi H, Tatsumi T, Nakagawa M. SD3212, a new antiarrhythmic drug, raises atrial fibrillation threshold in isolated rabbit hearts. Heart Vessels 1999;14(3):127-136.
Shirayama T, Sakamoto T, Yamamura M, Yoshida A, Mani H, Sakatani T, Matoba Y, Imai H, Nakagawa M. Mechanism of shortening of atrial refractory period after short term rapid pacing. Clinical Cardiac Pacing and Electrophysiology. edited by H-F Tse, KL Lee and CP Lau. Bologna:Monduzzi Editore. 2003:467-470.
11. Ishibashi K, Inoue D, Sakai R, Inoue M, Shirayama T, Asayama J, Nakagawa M. Effects of disopyramide on the atrial fibrillation threshold in the human atrium. Int J Cardiol 1995;52(2):177-184.
Inoue K, Shirayama T, Shiraishi H, Matoba Y, Imai H, Inoue D, Nakagawa M. Clinical significance of the atrial fibrillation threshold in patients with paroxysmal atrial fibrillation. Pacing Clin Electrophysiol 2001;24(5):796-805.
Shirayama T, Shiraishi H, Yoshida S, Matoba Y, Imai H, Nakagawa M. Atrial fibrillation threshold predicted long-term efficacy of pharmacological treatment of patients without structural heart disease. Europace. 2002 ;4(4):383-389.
Sugimoto T, Schaal SF, Wallace AG. Factors determining vulnerability to ventricular fibrillation induced by 60cps alternating current. Circ Res 1967;21:601-608.
15. Toda I, Murakami Y, Nozaki A, Kawakubo K, Sugimoto T. Ventricular fibrillation threshold measured by continuous 50cps stimulation for the evaluation of the antifibrillatory effect of the drugs. Jpn Circ J 1988;52:249-253.
Kostis JB, Goodking MJ, Gotzoyannis S, et al. Effect of lidocaine on the atrial fibrillation threshold. Am Heart J 1977;94:764-768.
17. Wiggers CJ, Wégria R: Ventricular fibrillation due to single, localized induction and condensor shocks applied during the vulnerable phase of ventricular systole. Am J Physiol 1940;128: 500-505
18. Wiggers CJ, Wégria R: Quantitative measurement of fibrillation threshold of mammalian ventricles with observations on the effect of procaine. Am J Physiol 1940;131: 296-308.
19. Karagueuzian HS, Chen PS. Cellular mechanism of reentry induced by a strong electrical stimulus: implications for fibrillation and defibrillation. Cardiovasc Res 2001;50(2):251-262.
20. Chen PS, Feld GK, Kriett JM, Mower MM, Tarazi RY, Fleck RP, Swerdlow CD, Gang ES, Kass RM. Relation between upper limit of vulnerability and defibrillation threshold in humans. Circulation 1993;88(1):186-192.
21. Michelson EL, Spear JF, Neil Moore E. Effects of procainamide on strength-interval relations in normal and chronically infarcted canine myocardium. Am J Cardiol 1981:47(6),1223-1232.
Orias O, Gilbert JL, Siebens AA, Suckling EE, McC Brooks C. Effectiveness of single rectangular electrical pulses of known duration and strength in evoking auricular fibrillation. Am J Physiol 1950; 162: 219-225.
23. McC Brooks C, Orias O, Gilbert JL, Siebens AA, Hoffman BF, Suckling EE. Auricular fibrillation: relationship of ‘vulnerable period’ to ‘dip’ phenomenon of auricular excitability curve. Am J Physiol 1951;164: 301-306.
Shinagawa K, Shiroshita-Takeshita A, Schram G, Nattel S. Effects of antiarrhythmic drugs on fibrillation in the remodeled atrium: insights into the mechanism of the superior efficacy of amiodarone. Circulation 2003;107(10):1440-1446.
25. Kanki H, Mitamura H, Takatsuki S, Sueyoshi K, Shinagawa K, Sato T, Ogawa S. Postrepolarization refractoriness as a potential anti-atrial fibrillation mechanism of pilsicainide, a pure sodium channel blocker with slow recovery kinetics. Cardiovasc Drugs Ther 1998;12(5):475-482.
Wettwer E, Scholtysik G, Schaad A, Himmel H, Ravens U. Effects of the new class III antiarrhythmic drug E-4031 on myocardial contractility and electrophysiological parameters. J Cardiovasc Pharmacol 1991;17(3):480-487.
Ohler A, Amos GJ, Wettwer E, Ravens U. Frequency-dependent effects of E-4031, almokalant, dofetilide and tedisamil on action potential duration: no evidence for "reverse use dependent" block. Naunyn Schmiedebergs Arch Pharmacol 1994;349(6):602-610.
Wijffels MCEF, Kirchhof CJHJ, Dorland R, Allessie MA. Atrial fibrillation begets atrial fibrillation: a study in awake chronically instrumented goats. Circulation 1995;92(7):1954-1968.
Allessie M, Ausma J, Schotten U. Electrical, contractile and structural remodeling during atrial fibrillation. Cardiovasc Res 2002;54(2):230-246.
Yamashita T, Murakawa Y, Hayami N, Fukui E, Kasaoka Y, Inoue M, Omata M. Short-term effects of rapid pacing on mRNA level of voltage-dependent K(+) channels in rat atrium: electrical remodeling in paroxysmal atrial tachycardia. Circulation 2000;101(16):2007-2014.
Ohe T, Matsuhisa M, Kamakura S, Yamada J, Sato I, Nakajima K, Shimomura K. Relation between the widening of the fragmented atrial activity zone and atrial fibrillation. Am J Cardiol 1983;52(10):1219-1222.
Mason JW. A comparison of seven antiarrhythmic drugs in patients with ventricular tachyarrhythmias. Electrophysiologic Study versus Electrocardiographic Monitoring Investigators. N Engl J Med 1993;329(7):452-458.
Wyse DG, Waldo AL, DiMarco JP, Domanski MJ, Rosenberg Y, Schron EB, Kellen JC, Greene HL, Mickel MC, Dalquist JE, Corley SD. A comparison of rate control and rhythm control in patients with atrial fibrillation. N Engl J Med 2002;347(23):1825-1833.