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EDITORIAL
Hans Larsen |
LETTERS TO THE EDITOR
I am a 51-year-old woman who began having afib problems a long time ago (probably in my 20s). Your
comments and writings are the first that make sense to me. Recently, I have experienced 2 episodes of
persistent afib and have periodic short episodes. I am on flecainide that seems to be working to some degree.
My doctors tell me not to worry - the afib won't kill me. Nonetheless, I find this disorder devastating. It has
consumed my life and is destroying my marriage and friendships. I am afraid to do anything, go anywhere, etc.
Every time my heart blips I become more depressed. Your writing gives me a little hope and I'm grateful for that.
BD, USA
Editor: Thank you for sharing your experience with afib. Your doctors are absolutely right, atrial
fibrillation is not life-threatening, but as you say, it certainly can mess up your life. I have been suffering from it
myself for 13 years. It surely is no picnic, but I try not to let it control my life and am grateful that it is not cancer
or serious heart disease that I am dealing with. If depression is a big factor you may want to try a low-dose
antidepressant. I don't believe it would interact with the flecainide, but this you should check with your doctor.
You may also want to visit the Bulletin Board at www.afibbers.org for
additional help and advice.
I started out taking 150 mg of Rythmol 3 times a day. I can't say that it helped because I was only going into afib about once every 3 months for less than a day and I could always sleep them off. I quit for a couple of years and then went back on it after my afib got worse (more often and longer duration). Probably an age thing. I was given 125 mg 3 times a day. My hands started going numb every night and I would have to wake up and shake them two are three times a night. My oxygen level in my blood test was also low and the doctors thought it had something to do with my lungs. After reading on your website about the problems people were having with Rythmol I stopped taking it altogether. My oxygen level now checks OK and the numbness has left my hands thanks to you. Over the years my afib has gotten worse. I now go into afib about once every 14 days for about 24 hrs. I take one 225 mg Rythmol on demand now only during an afib period which I think helps bring me out. I also take a 300 mg Diltiazem to slow my heart down. I take one aspirin every day. I don't think Rythmol helped at all when I was taking it daily and probably made things worse.... Thanks for your help (I read your book). MHO, USA Editor: Thank you very much for sharing your experience with Rythmol (propafenone). I have also found the on demand approach to be quite effective (I have the adrenergic type). I take 225 mg crushed propafenone plus 12.5 mg atenolol (Tenormin) with warm water within 5-10 minutes of the onset and usually convert in a couple of hours. If I don't convert I take 150 mg of propafenone every 8 hours until I do.
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Evaluation of Survey Results
Initiation of episodes
LAF episodes among adrenergic afibbers were all initiated by events that tend to increase adrenergic tone such as exercise or emotional or work-related stress. Vagal episodes were initiated by events that increase vagal tone such as rest, sleep, digestion or winding down after exercise. Mixed episodes were initiated by either an increase in adrenergic or mixed tone with no special preference for either one. About 26% of all vagal afibbers noted that they were more likely to have an episode during the evening or night if they had experienced a stressful day. Prof. Coumel has described this phenomenon as "vagal rebound" and suggests that it may be possible to avoid it by taking a small amount of beta-blocker (atenolol) first thing in the morning if a stressful day or event is anticipated. Almost two thirds (64%) of all paroxysmal afibbers reported frequent urination at the onset of an episode. This phenomenon was most pronounced among vagal afibbers where 72% experienced it versus 50% in the adrenergic group and 59% in the mixed group. The frequent urination is caused by the release of the diuretic hormone atrial natriuretic peptide (ANP) for the walls of the atria during chaotic beating.
Termination of episodes
Twenty per cent of all respondents felt that they had more than normal difficulty in sleeping during the nights following an episode. This problem was most pronounced among mixed (22%) and vagal afibbers (20%), but not of major concern among adrenergic afibbers (6%). Repeated sneezing after the termination of an episode was reported by 5% of paroxysmal afibbers with 11% of adrenergic, 7% of vagal afibbers and none in the mixed group reporting this problem. Sneezing could be an indication of heightened vagal tone.
Pattern to episodes There was also a strong negative correlation (not too surprisingly) between the number of days between episodes and the frequency of episodes; i.e. afibbers with a short interval between episodes tended to have more frequent episodes over a 6-month period. There was, however, no correlation between the duration of episodes and the interval between episodes neither for all paroxysmal afibbers nor for drug-free paroxysmal afibbers.
Heart rate during episode
The average maximum heart rate did not differ between afibbers continuously on antiarrhythmics or beta- blockers and those not on drugs nor was there any statistically significant effect in maximum heart rate between those taking beta-blockers or calcium channel blockers on demand and those that did not. This latter finding is counter-intuitive and needs further investigation. There was no statistically significant difference in maximum episode heart rate between men and women; however, there was a slight, statistically significant trend for the maximum heart rate to decrease with age. No correlation was observed between maximum heart rate and length of time since first diagnosis of afib; nor was there any correlation between resting heart rate and maximum heart rate during an episode.
Main symptoms during episode
I. Cardiovascular Health
Blood pressure and pulse rate
Beta-blockers, calcium channel blockers and some antiarrhythmics may influence pulse rate and blood pressure. A table showing pulse rate and blood pressure for afibbers not on any drugs is presented below (83 respondents for pulse rate, 72 for blood pressure).
There were no significant differences between pulse rates or blood pressure of adrenergic, mixed, and vagal afibbers, nor was there any significant differences in these parameters between afibbers taking drugs and those not. However, there was a statistically significant correlation between resting pulse rate and gender with women tending to have higher pulse rates than men. There was also a highly significant inverse correlation (not too surprisingly) between resting pulse rate and level of physical activity with highly active afibbers having lower resting pulse rate than sedentary ones. There was no correlation between resting pulse rate and frequency or duration of episodes. Systolic blood pressure correlated moderately with the presence of diagnosed hypertension (this correlation is no doubt weakened by the use of antihypertensive drugs) and also with the perceived exposure to emotional or work-related stress. Afibbers who felt stressed had higher systolic blood pressures than those who did not feel stressed. Diastolic blood pressure correlated weakly with the presence of diagnosed hypertension (this correlation is no doubt weakened by the use of antihypertensive drugs) and also with the perceived exposure to emotional or work-related stress with stressed afibbers having higher diastolic pressures.
Hypertension
The prevalence of hypertension was significantly higher among permanent than among paroxysmal afibbers (29% versus 20%). The prevalence of hypertension in the general population varies with age, sex and race. Overall estimates are as follows[1]:
Considering that the average age of all paroxysmal afibbers is 54 years a prevalence of 20% is clearly well below the norm. This is probably a result of the generally high health level and fitness of afibbers. A more speculative reason could perhaps be that the diuretic action of the periodic release of atrial natriuretic peptide (ANP) during afib episodes prevents hypertension from taking hold. Sixty-five per cent of paroxysmal afibbers used drugs to control their hypertension (60% among adrenergic, 60% among mixed, and 68% among vagal). The most popular drugs were atenolol (Tenormin), diltiazem (Cardizem), quinapril (Accupril), followed by metoprolol (Toprol XL), hydrochlorothiazide, and amlodipine (Norvasc). There was a strong correlation between age and the presence of hypertension with hypertensive afibbers tending to be significantly older.
Congestive heart failure Our survey of 66 lone afibbers showed that not a single one had been diagnosed with CHF and only one (a 12- year veteran of permanent afib) had been diagnosed with a left ventricular ejection fraction below 0.35. An LVEF below 0.35 is considered a precursor to CHF. Thus it would seem that lone afibbers are at a particular low risk of developing CHF. This is perhaps not too surprising in view of the fact that lone afibbers are generally healthy and fit and have a low incidence of hypertension and diabetes.
Stroke The risk of a stroke increases with age; it is estimated that 5% of the population over 65 years of age will suffer a stroke. A prior stroke, heart disease, diabetes, hypertension, atrial fibrillation, high homocysteine levels, and a bacterial infection of the lining of the heart cavity (endocarditis) are significant risk factors. Major surgery accounts for a large number of ischemic strokes. It is estimated that as many as 25,000 people suffer a stroke every year as a sequel to coronary bypass surgery[4-8]. Atrial fibrillation is a risk factor for ischemic stroke because of the inefficient pumping action of the atria during fibrillation. The fibrillating atrium basically sits and quivers like a bowl of jelly. This can cause blood to stagnate and if the fibrillation goes on long enough to coagulate and form blood clots (thrombi). If one of these blood clots finds its way to a small artery in the brain a stroke may result. The danger of this happening is actually highest when the fibrillation ceases. The increased pumping action, once the atria gets back to normal, flushes out the heart chamber and with it any newly formed blood clots. This is why anticoagulation with warfarin (Coumadin) and/or heparin is essential prior to cardioversion and for about 3 weeks after. Lone atrial fibrillation, by definition, means that there are no underlying heart problems present. So unless you have hypertension, diabetes, are over 75 years of age or have suffered a previous stroke or TIA you are at no greater risk for stroke than the general population[9]. Medical experts are pretty unanimous on this point. Dr. Rodney Falk, MD of Boston University, a world-renowned expert on atrial fibrillation, says that the stroke risk in patients with lone atrial fibrillation is minimal[8]. Professor Michael D. Ezekowitz, MD of the Veterans Administration says, "patients with lone atrial fibrillation are not at higher risk for thromboembolism than the general population and can be managed without anticoagulation or anti-platelet therapy"[10]. Dr. Stephen L. Kopecky of the Mayo Clinic did the first study regarding stroke risk in patients with lone atrial fibrillation. He found that lone afibbers under the age of 60 years had an exceptionally low stroke risk (0.55%) and that this risk varied little whether the fibrillation was paroxysmal or permanent[11]. More recently Canadian researchers evaluated the stroke risk among 2500 atrial fibrillation (non-valvular AF) patients who were treated with a daily aspirin. Twenty-four per cent of the group was considered at low risk for stroke because of the absence of hypertension (systolic blood pressure below 140 mm Hg), no history of stroke or TIA, no symptomatic coronary artery disease, and no diabetes. In this low-risk group the incidence of stroke was 1.0 per 100 person years as compared to 1.2 per 100 person years in an age- and sex-matched group of people with no atrial fibrillation. Low risk patients who were randomized to oral anticoagulation (warfarin) experienced 1.5 strokes per 100 person years. Strokes included both ischemic and hemorrhagic. The researchers conclude, "Irrespective of age, patients with AF and none of the above four clinical features and who take aspirin have stroke rates comparable to those of age-matched community cohorts and would not benefit substantially from anticoagulation."[12] Our survey included 159 lone afibbers. Not one had suffered a stroke of any kind. Interpretation of this finding must, of course, be approached with extreme caution. Clearly afibbers having suffered a fatal or severely disabling stroke would be unlikely to have participated in the survey. However, there is no reason why afibbers who have suffered a mild stroke or a transient ischemic attack (TIA) should not have participated. A TIA involves a temporary deficiency of blood to the brain. Effects are usually reversible within 24 hours. A TIA is followed by a stroke in about 1 out of 3 cases[13]. A total of 5 TIAs (3 among permanent afibbers) were reported in the survey. These were in a sample covering 1145 person years of exposure (years of afib). So the incidence is 0.4 per 100 person years. Is this normal or abnormal? Dr. Jerome FX Naradzay of the Samaritan Medical Center estimates a TIA incidence rate of 0.4 to 0.8 cases per 100 person years in the general population aged 50-59 years and a recent study carried out at the Ottawa Heart Institute found a combined stroke rate of 1.0 per 100 person years in afibbers treated with aspirin[12,14]. So overall the TIA rate found in our survey would appear to be fairly normal except in the case of permanent afibbers where the rate was 2.6 per 100 person years. The sample was, however, quite small (15 people) so the results must be taken with a grain of salt. The ages of the 3 permanent afibbers who had suffered a TIA were 59, 63 and 65 years respectively. One was on aspirin or warfarin at the time of the TIA while one was not on stroke prevention medicine. The medication status of the third one is unknown.
Electrolyte levels Thirty-seven out of 159 respondents had had their intracellular electrolyte levels checked and 23 (62%) had abnormal levels. Low magnesium levels were found in 6, low potassium in 4, high calcium in 3, and one each of low and high phosphorous levels.
Conclusion Our finding that lone afibbers have excellent cardiovascular health supports those made in 1998 by researchers at the University of Helsinki[15]. Their study concluded that men who engaged in long-term vigorous exercise (as many afibbers do) have a 5 times greater risk of developing LAF, but a 3 times lower risk of developing coronary heart disease and 5 times lower overall mortality than less active men.
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AFIB NewsAt home drug-induced termination of AF is safe
CLEVELAND, OHIO. A team of American and German cardiologists has evaluated the safety and efficacy of
using large oral doses of propafenone (Rythmol) or flecainide (Tambocor) for converting atrial fibrillation to
normal sinus rhythm. A total of 107 atrial fibrillation patients were randomized to receive the drugs in a hospital
setting (56 patients) or to take the drugs at home without medical supervision (61 patients). The drugs used
were 600 mg of propafenone or 300 mg of flecainide both taken with 25-50 mg of metoprolol or 240 mg of slow-
release diltiazem. Conversion was achieved in 61% of the in-hospital patients and in 73% of the "do-it-yourself"
at-home patients. The most common side effect was a metallic taste in the mouth, but no serious side effects
were observed in either of the two groups. The researchers conclude that at-home administration of large doses
of propafenone (600 mg) or flecainide (300 mg) together with metoprolol or diltiazem for rate control is just as
safe as administration in a hospital setting. Editor's comment: I have experienced good results with 225 mg of propafenone plus 12.5 mg of atenolol (Tenormin). I swallow the tablets in crushed form with a little warm water as soon as possible after the onset of an episode. Nevertheless, both propafenone and flecainide are powerful drugs and should not be used for at-home termination without the approval of a cardiologist.
Metoprolol most effective in maintaining sinus rhythm
LUDWIGSHAFEN, GERMANY. German cardiologists have evaluated the relative effectiveness of time-release
metoprolol (Toprol XL), sotalol (Betapace), and amiodarone (Cordarone) in maintaining sinus rhythm after
cardioversion of the first recurrence (second episode) of atrial fibrillation. Their study involved 571 patients of
which 161 were treated with metoprolol (47-190 mg/day), 228 with sotalol (160-320 mg/day), and 182 with
amiodarone (200 mg/day). About 60% of the patients had some form of organic heart disease, so this was
definitely not an experiment involving just lone afibbers. About 70% of the participants were male and the
average age of all participants was 62 years. During a follow-up period of 3 years after successful cardioversion
58% of the patients treated with metoprolol experienced another AF episode as compared to 71% in the sotalol
group and 70% in the amiodarone group. The researchers conclude that metoprolol XL is more effective than
sotalol or amiodarone in maintaining sinus rhythm after successful electrical cardioversion. Editor's comment: The high percentage of organic heart disease in the group means that most of the participants probably had the adrenergic type of AF. The results obtained are unlikely to apply to vagal afibbers.
New aspirin derivative prevents blood clots
BRISTOL, UNITED KINGDOM. NO-ASA or nitric oxide donating aspirin (nitroxy-butyl-acetylsalicylate) is a new
class of drugs that shows great promise in reducing the risk of thrombosis (formation of blood clots) after surgical
procedures such as coronary artery bypass grafting (CABG). Researchers at the University of Bristol recently
concluded that NO-ASA might be useful in preventing thrombosis, vasospasm and vascular smooth muscle cell
proliferation after CABG. Editor's comment: It is possible, but not yet proven, that NO-ASA may also turn out to be an excellent anticoagulant choice for afibbers.
Atrial fibrillation and blood clots
SANTIAGO, CHILE. Atrial fibrillation is associated with an increased stroke risk, particularly among older
patients. The stroke risk is associated with the formation of blood clots in the left atrial appendage during
fibrillation. Researchers at the Catholic University of Chile have recently completed a study to determine if AF
patients have different blood levels of the coagulation activation factor thrombin-antithrombin (TAT) complex.
Having an increased level of this factor would aggravate the tendency to form blood clots. Their study involved
53 patients with atrial fibrillation and matched healthy controls. The researchers found that the TAT values for
afib patients averaged 40.1 mg/L (median 8.34 mg/L) as compared to 2.7 mg/L in healthy controls. Permanent
(chronic) afibbers had higher mean values than did paroxysmal (intermittent) afibbers (49.4 mg/dL versus 29.5
mg/dL). The researchers also noted that patients who had taken antiplatelet agents had a significantly lower
TAT value than did those who had not (17.3 m/dL versus 66.8 mg/dL). They conclude that previous antiplatelet
treatment prevents a higher activation of the coagulation cascade during afib. Editor's comment: These findings support the idea that antiplatelet agents such as aspirin, fish oils, vitamin E, vitamin C, vitamin B6, and magnesium are beneficial supplements for afibbers.
Stroke risk in ablation
RICHMOND, VIRGINIA. The risk of having a stroke during radiofrequency ablation is generally 1-2%, but
increases with age. Cardiologists at the McGuire Veterans Affairs Medical Center now warn that having
experienced a prior transient ischemic attack (TIA) may significantly increase stroke risk during ablation. Their
study involved 56 patients who underwent ablation for paroxysmal atrial fibrillation. The mean procedure time
was 4 hours (227 minutes) and 86% of the patients had trigger points in the pulmonary veins. Three of the
patients (5%) experienced a cerebrovascular event (stroke) during the procedure; all were over 60 years of age
and 2 had experienced a previous TIA.
Cryoablation for atrial fibrillation
MAASTRICT, THE NETHERLANDS. A team of Dutch cardiologists reports that cryoablation is safe and
effective for the treatment of atrial fibrillation. Their clinical trial involved 43 patients who underwent segmental
ablation of the pulmonary veins. The immediate success rate was 98%; however, after 8 months of follow-up
only 78% showed improvement and only 52% were completely afib-free. Three patients experienced serious
adverse events, but there was no evidence of stenosis as measured with a spiral CT scan 3 months after the
procedure. Editor's comment: It is not clear if all patients had lone afib or not. It is conceivable that the procedure may be more successful in lone afibbers, but, as always, the surgeon's skill is the number one factor in determining success rate.
Verapamil helps maintain sinus rhythm
MADDALONI, ITALY. Electrical remodeling of the atria is an important sequel to atrial fibrillation and increases
the risk of future episodes. It is believed that an overload of intracellular calcium is at least partly responsible for
the remodeling. Italian researchers now report that AF patients pretreated with verapamil prior to electrical
cardioversion tend to remain in sinus rhythm longer than do non-treated patients. Their study involved 88
afibbers who had experienced an early recurrence (within 7 days) after a successful cardioversion. The patients
were treated with warfarin for 3 weeks prior to attempting a second cardioversion and continued on their
antiarrhythmic drugs (mostly flecainide and amiodarone). Half the group received no other drugs, but the other
half received 240 mg of verapamil daily for the 3 days preceding and the 3 days following the electrical
cardioversion procedure. The researchers found that 21% of the patients in the verapamil group (21%)
spontaneously reverted to normal sinus rhythm (NSR) prior to the scheduled cardioversion; only two patients
(4%) in the non-verapamil group experienced spontaneous conversion. During 3 months of follow-up 26
patients (30%) experienced another AF episode, but the incidence was lower in the verapamil group (19%
versus 40%). It is also worth noting that the average number of ectopic beats experienced by the verapamil
group was significantly lower than in the non-verapamil group (145 versus 177 ectopic beats per hour). Editor's comment: There would seem to be little to lose and much to gain by asking your cardiologist to put you on 240 mg/day of verapamil for 3 days prior to and 3 days following a scheduled electrical cardioversion. Antiarrhythmics in ICD patients
BALTIMORE, MARYLAND. Implantable cardioverter-defibrillators (ICDs) are increasingly used for arrhythmia
control, especially in patients with life-threatening arrhythmias. There is no clear consensus as to whether
antiarrhythmic drugs, beta-blockers, or no drugs should be used in conjunction with the ICD. Researchers at the
Johns Hopkins University recently discovered that patients discharged from hospital on amiodarone or sotalol
(Class III antiarrhythmics) had a 47% higher risk of dying within an average 5.5-year follow-up than did patients
discharged on Class I drugs (propafenone, flecainide, etc.) or on no drugs at all. Those discharged on beta-
blockers did best with a 56% reduction in mortality when compared to patients on no drugs. The results were
obtained after adjusting for other variables that could affect mortality. The researchers conclude that the use of
beta-blockers may be associated with a significant survival advantage while the use of Class III antiarrhythmics
may be detrimental in patients with ICDs.
Renin-angiotensin system and atrial fibrillation
TAIPEI, TAIWAN. It is known that the local renin-angiotensin system (RAS) in the heart plays an important role
in atrial fibrillation. Taiwanese researchers now report that afib patients have significantly different RAS genes
than do people without AF. The study involved 110 AF patients and 110 matched controls. The researchers
found that the frequencies of M235T, G-6, and G217 allele were significantly higher in afib patients and that
these higher frequencies were associated with an increased risk of AF. They conclude that angiotensin
converting enzyme (ACE) inhibitors or angiotensin II antagonists may be useful in the treatment of AF.
Statins may help control AF
FUKUOKA, JAPAN. There is considerable evidence that atrial fibrillation is associated with an inflammation of
the heart tissue and accompanying elevation of the level of the inflammation marker, C-reactive protein (CRP).
Japanese researchers have found that atorvastatin (Lipitor), a cholesterol-lowering drug, shortens the duration of
afib episodes induced in dogs. They suggest that atorvastatin may be a novel therapeutic agent for afib. Editor's comment: Of course, these findings, discovered with dogs, cannot automatically be applied to human afibbers. There are several effective, natural ways of inhibiting inflammation and reducing CRP. |
The AFIB Report is published 10 times a year by Hans R. Larsen MSc ChE 1320 Point Street, Victoria, BC, Canada V8S 1A5 Phone: (250) 384-2524 E-mail: [email protected] URL: http://www.afibbers.org Copyright © 2003 by Hans R. Larsen The AFIB Report does not provide medical advice. Do not attempt self- diagnosis or self-medication based on our reports. Please consult your health-care provider if you wish to follow up on the information presented. |