(Circulation. 2001;103:2365.)
© 2001 American Heart Association, Inc.
Clinical Investigation and Reports |
From the Centre for Health Evaluation and Outcome Sciences (K.H.H.), Vancouver, BC; the Division of Cardiology (C.R.K., J.A.B.), University of British Columbia, Vancouver; the Division of Cardiology (S.J.C.), McMaster University, Hamilton, Ontario; the Division of Cardiology (G.K.), University of Western Ontario, London; the Ottawa Heart Institute (M.G.), Ottawa, Ontario; the Division of Cardiology (R.S.), University of Calgary, Calgary, Alberta; the Montreal Heart Institute (M.T.), Montreal, Quebec; and the Division of Cardiology (P.D., D.N.), St Michaels Hospital, Toronto, Ontario, Canada.
Correspondence to Karin H. Humphries, DSc, CHEOS-St Pauls Hospital, 620B1081 Burrard St, Vancouver, BC, Canada V6Z 1Y6. E-mail karinh{at}cheos.ubc.ca
| Abstract |
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Methods and ResultsThe Canadian Registry of Atrial Fibrillation (CARAF) enrolled subjects at the time of first ECG-confirmed diagnosis of AF. Participants were followed at 3 months, at 1 year, and annually thereafter. Treatment was at the discretion of the patients physicians and was not directed by CARAF investigators. Baseline and follow-up data collection included a detailed medical history, clinical, ECG, and echocardiographic measures, medication history, and therapeutic interventions. Three hundred thirty-nine women and 560 men were followed for 4.14±1.39 years. Compared with men, women were older at the time of presentation, more likely to seek medical advice because of symptoms, and experienced significantly higher heart rates during AF. Compared with older men, older women were half as likely to receive warfarin and twice as likely to receive acetylsalicylic acid. Compared with men on warfarin, women on warfarin were 3.35 times more likely to experience a major bleed.
ConclusionsAnticoagulants are underused in older women with AF relative to older men with AF, despite comparable risk profiles. Women receiving warfarin have a significantly higher risk of major bleeding, suggesting the need for careful monitoring of anticoagulant intensity in women.
Key Words: fibrillation sex anticoagulants
| Introduction |
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Sex differences in coronary artery disease have
received considerable
attention,1 2 3
but few studies have dealt with sex differences in
arrhythmias.4 AF is
the most common sustained cardiac arrhythmia in the general
population, and its incidence increases with
age.5 Compared with women,
men have a higher incidence of AF at all age
groups.6 However, because
there are almost twice as many women as men in the group with the
highest percentage of AF, those aged
75 years, the absolute number of
men and women with AF is
equal.7 8
Little is known about sex differences in AF presentation, treatment, or outcome. Higher heart rates during AF have been reported in women compared with men,9 as well as more frequent recurrence of paroxysmal AF after successful cardioversion.10 Some studies have identified female sex as a risk factor for stroke in the presence of AF,11 12 but this has not been shown in all studies.13
Sex differences in presentation and clinical course may dictate different approaches to detection and management. Given the limited information available, we examined sex-related differences in AF by using data from CARAF. CARAF is a prospective observational study of subjects enrolled at the time of their first ECG-confirmed diagnosis of AF.
| Methods |
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CARAF Study Eligibility
Inclusion Criteria
Patients with a first diagnosis of AF or atrial
flutter, confirmed by ECG, who presented because of symptoms or
who were diagnosed during a routine physical examination were included
in the study.
Exclusion Criteria
Patients were excluded for the following reasons: a
previous history of AF; AF or flutter as a result of electrophysiology
testing, angiography, or Swan Ganz or pacemaker insertion or removal;
<1 year of expected survival because of a major life-threatening
illness; inability to give informed consent; and inability to report
for follow-up.
Data Collection
At the time of enrollment, a detailed baseline data
form was completed that recorded symptoms (dizziness, fatigue,
nausea, anxiety, chest pain, palpitations, dyspnea, presyncope, and
syncope), clinical and laboratory data (thyroxine and
thyroid-stimulating hormone levels, blood pressure, and heart rate),
medical history (cerebrovascular, cardiovascular,
endocrine, smoking, and alcohol history), ECG and
echocardiographic data (atrial and
ventricular dimensions and valve status), medication
history, and therapeutic interventions (pharmacological intervention
and electrical cardioversion). Follow-up visits were conducted at 3
months, 1 year, and then annually. Detailed information regarding AF
recurrence, medication usage, therapeutic interventions, and
clinical history was collected at each follow-up visit. Treatment was
at the discretion of each patients caregiver and was not directed by
CARAF investigators.
Definitions
Recurrence of AF at each follow-up visit was
classified into paroxysmal and chronic forms. Chronic AF was defined as
suspected continuous AF, with ECG evidence, at 2 separate visits >7
days apart. Paroxysmal AF was defined as episodes of AF lasting <7
days that subsequently reverted to sinus rhythm. Reversion to normal
sinus rhythm was predominantly induced (93%).
A major bleed was defined as one that required transfusion or surgical intervention or that resulted in a >20-g/L decrease in hemoglobin.
To facilitate analyses of medication usage, the following categories were defined: ß-blockers, because these were the most frequently used medications for rate control, and the antiarrhythmic drugs sotalol, propafenone, and amiodarone, because these were the most frequently used antiarrhythmics.
Outcome events included progression to chronic AF, recurrence of paroxysmal AF, myocardial infarction, stroke, major bleed, and death. Treatment and recurrence of AF analyses were limited to 3 years of follow-up.
Statistical Analysis
Means of continuous variables were examined by the
Student t test, and categorical
variables were examined by the
2
test; for small sample sizes, the Fisher exact test was used. Risk of
bleed was analyzed by using the Cox proportional hazards
method. All significance tests were 2-sided, and a value of
P<0.05 was chosen as the
cutoff for statistical significance.
| Results |
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Baseline Characteristics
Women constituted 38% (n=339) of the study
cohort. Several differences in presentation and baseline
medical history were noted between men and women. Women were, on
average, 5 years older (65.4±0.7 [women] versus 60.5±0.6 [men]
years, P<0.001), more likely
to seek medical advice because of symptoms (85.2% [women] versus
73.8% [men], P<0.001), and
experienced higher heart rates during AF (126.2±1.9 [women] versus
119.1±1.4 [men] bpm,
P=0.003)
(Table 1
). Heart rates during AF were determined from ECG
recordings. The burden of ischemic disease was higher
in men, but the prevalence of hypertension and history of thyroid
dysfunction were significantly greater in women.
|
Treatment
Use of cardiac medications did not vary by sex.
Medication usage at the time of diagnosis and again after baseline
assessment and intervention is presented in
Table 2
. Digoxin was the most commonly prescribed
medication for initial management in this cohort. Warfarin use at time
of diagnosis was extremely low (2.8%) but increased over 10-fold by
the conclusion of the baseline visit (31.6%).
|
Although the overall prevalence of antithrombotic use did
not vary by sex (63.8%), the choice of therapy did. Women aged
75
years (n=67) were 54% less likely to receive warfarin but twice as
likely to receive acetylsalicylic acid than were
men aged
75 years (n=81). We modeled age and sex as predictors of
antithrombotic use and demonstrated a significant interaction between
sex and age
75 years
(P=0.025).
To determine whether the lower usage in older women was due
to a lower perceived risk of stroke, we examined warfarin use in the
cohort aged
75 years with
1 stroke risk factor. Stroke risk factors
included history of stroke or transient ischemic attack,
hypertension, diabetes, or congestive heart failure. Among the elderly
with
1 stroke risk factor, men (44.9%) were significantly more
likely to be on warfarin than were women (24.5%)
(P=0.034).
At the baseline visit, 69.9% of the cohort underwent acute pharmacological or electrical interventions to restore normal sinus rhythm, 52.8% underwent pharmacological therapy only, 15.2% underwent both pharmacological therapy and electrical cardioversion, and 2% underwent electrical cardioversion only. Men (19.6%) were more likely to undergo electrical cardioversion than were women (13.3%) (P=0.039). Conversion to normal sinus rhythm was equally successful in women (75.9%) and men (79.3%).
Over 3 years of follow-up, subsequent rates of therapeutic interventions (electric cardioversion 17.1%, radiofrequency ablation 2.7%, and pacemaker implantation 8.6%) did not vary by sex.
Outcomes
Recurrence of paroxysmal AF, determined either
by ECG (documented) or by history of symptoms consistent with
episodes of AF (undocumented), was recorded at each follow-up
visit. The proportion of women with recurrences of AF
(documented and undocumented) at each follow-up visit was significantly
greater than the proportion of men with such recurrences
(Figure 1
).
|
Despite the greater burden of paroxysmal AF, cumulative progression to chronic AF by the 3-year visit was identical in men and women (18.9%), and the mean time to progression was similar in women (1092 days) and men (1138 days) (P=0.35).
Total strokes (n=63), myocardial infarctions (n=32), and
major bleeds (n=36) did not vary by sex
(Figure 2
). However, there was a significant interaction
between sex and warfarin use for the risk of a major bleed
(P=0.006). Women on warfarin
were 3.35 times more likely to experience a major bleed than were men
on warfarin. Nine of the 10 women who experienced a major bleed were
aged <75 years. CARAF did not collect international normalized
ratio (INR) data at study visits; these data were reported only if the
patient experienced a bleed. The mean INR for the 10 women on warfarin
who had a bleed was 4.02±2.96, whereas INR in the men was 4.37±3.64
(P=0.787). The age-adjusted
relative risk for a major bleed in women on warfarin compared with
women not on warfarin was 5.49. Warfarin use was not a predictor
of age-adjusted risk for a major bleed in men
(Table 3
).
|
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There were 149 deaths in this cohort; 57.7% were due to
cardiovascular causes. The major
cardiovascular cause of death was arrhythmia
(45%). Although women were as likely to die of
cardiovascular causes as men, there were sex
differences with respect to the types of cardiovascular
death
(Figure 3
). Of the men who died, 17.5% died from congestive
heart failure, compared with 5.8% of the women
(P=0.045). The incidence of
myocardial infarction did not vary by sex, but of the 5 fatal
myocardial infarctions, 4 were in women (7.7%) (Fisher exact test,
P=0.05). Adjustment for age did
not alter the association. The "other" category included
complications arising from peripheral vascular disease and
perioperative death after cardiac
surgery.
|
| Discussion |
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75 years were half as likely to receive warfarin than were older men.
However, women on warfarin, predominantly those aged <75 years, were
3.35 times more likely to experience a major bleed than were men on
warfarin. Women were also significantly more likely to report
undocumented episodes of paroxysmal AF at follow-up visits than were
men, but the incidence of ECG-documented AF did not vary significantly
by sex, nor did progression to chronic AF. The finding that women are older at the time of first presentation with AF is consistent with the incidence of ischemic heart disease, a condition for which women are, on average, 10 years older than men at the time of presentation.14 The observation that women had faster heart rates during AF is consistent with the results of the Controlled Randomized Atrial Fibrillation Trial (CRAFT) studies in patients with symptomatic paroxysmal AF requiring drug therapy.9 One might speculate that given the older age of the women in this cohort, the increased heart rate might be due to lower vagal tone. However, adjustment for age did not alter the association. The greater prevalence of thyroid dysfunction in this cohort mirrors the female predominance of this disorder in the general population.15 The greater burden of ischemic disease among men may be a reflection of the relatively young age distribution of this population, in which the earlier manifestation of ischemic disease in men will contribute to a relatively greater burden. In an older cohort, this difference may not persist. The lower incidence of asymptomatic presentation at baseline among women is an interesting, though not unexpected, finding. In health surveys and studies of physical symptom reporting, women reported symptoms more frequently than did men.16 17
Most of the trials demonstrating the benefit of warfarin for
stroke prophylaxis in patients with AF were published in the early
1990s, around the time that CARAF recruited its first patients.
Baseline visits for the CARAF cohort occurred between April 1990 and
early 1996, with >90% completed before the end of 1994. This may
explain the low usage of warfarin in this cohort. Although a delay in
adopting evidence-based findings may explain the low overall use of
warfarin, it does not explain why elderly women are less likely to
receive warfarin than are elderly men. Recently published Stroke
Prevention in Atrial Fibrillation III (SPAF-III) data specifically
identify women aged >75 years as a high-risk
group.18 The sex difference
also does not appear to be related to differences in stroke risk. In
the subgroup of subjects aged
75 years with
1 stroke risk factor,
anticoagulant use was still significantly lower in women. Our results
are consistent with those reported in a recent study that
examined anticoagulant use in a community-based cohort in
Northumberland, UK.19 In
that study, anticoagulants were also found to be underused in elderly
women. Our results are in contrast to the findings of Perez et
al,20 who reported
significant underuse of warfarin among patients aged
75 years (8.1%)
compared with younger patients (42.2%), regardless of sex. In CARAF,
warfarin usage, although low, did not significantly differ between
those aged
75 years (29.1%) and those aged <75 years
(32.4%).
Use of cardiac medications for the initial management of AF did not differ between the sexes. Digoxin was the most commonly prescribed medication at the baseline visit, after acute intervention to control ventricular rate. Antiarrhythmic agents were the second most commonly prescribed medications: sotalol (21.7%), propafenone (8.3%), and amiodarone (2.1%).
The greater incidence of recurrence of paroxysmal AF in women was due to a greater proportion of reported, but undocumented, AF. Although there was a trend to higher incidence of ECG-documented episodes of paroxysmal AF in women, this was not significant. Progression to chronic AF was also independent of sex. The greater incidence of reported, but not documented, AF may be a reflection of a female tendency to report symptoms more frequently than men. What is not clear is whether the undocumented episodes are truly AF or whether women are just more likely to feel any rhythmic disturbance. More frequent recurrence of paroxysmal AF in women was also reported by Suttorp et al,10 who used a definition of paroxysmal AF that is equivalent to our aggregate of ECG-documented and undocumented AF.
The overall incidence of stroke, myocardial infarction, and major bleed did not vary by sex, but women on warfarin were 3.35 times more likely to experience a major bleed, with 9 of 10 bleeds occurring in women aged <75 years. As expected, INRs at the time of bleeding were elevated, but the levels were similar in men and women. This finding has not been previously reported in any of the major AF trials.21 The results of the present study may be a reflection of the difference in the intensity of monitoring in a clinical trial setting versus real-life practice. It is interesting to note that a recent study of oral anticoagulant use and risk of bleeding in a population after hospitalization for deep-vein thrombosis also reported an increased risk of bleeding associated with female sex (relative hazard 1.7, 95% CI 1.3 to 2.2).22 Clinical trials of thrombolytic regimens have also shown an increased the risk of bleeding among women.3 23 24
CARAF is subject to many of the limitations inherent in observational studies. Selection and referral biases are 2 important considerations in the present study. The majority of patients were recruited from emergency departments (41%) or hospital admissions for other diagnoses (30%), which were predominantly cardiovascular in origin. Although potentially limiting the generalizability of our findings, CARAF nevertheless provides insights into current patterns of practice in this population. Women (64.9%) were as likely to be recruited from hospital admissions or emergency departments as were men (64.9%). Selection and referral biases, if present, appear to be independent of sex, which is the focus of the comparisons in the present study.
Misclassification of baseline comorbidities and recurrence of AF is also possible. We relied on patient interviewers, by trained nurses, to obtain medical history. Thus, the accuracy of comorbidity information is largely dependent on patient recall, although the presence of some comorbidities (such as hypertension and diabetes) could be corroborated by medication usage. Nevertheless, misclassification is likely to be nondifferential with respect to sex. Recurrence of AF was monitored at annual visits and thus was subject to patient recall regarding events in the previous year. Research suggests that women are more likely to report symptoms than are men, and this may explain the higher incidence of undocumented paroxysmal AF among women.16 17 Because of the limitations of the study design, it is also possible that some of the associations we report are due to unmeasured confounders.
In a prospective cohort study of subjects with new-onset AF, compared with men, women were older, were more symptomatic, and experienced higher heart rates during AF. Warfarin use in this cohort was low. In particular, elderly women were significantly less likely to receive warfarin therapy than were elderly men, even after adjustment for stroke risk factors. When anticoagulant therapy was used in women, predominantly in those aged <75 years, the age-adjusted relative risk of a major bleed increased by >5 times. This finding requires further investigation and implies a need for careful monitoring of anticoagulant intensity in women.
| Acknowledgments |
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Received November 13, 2000; revision received February 14, 2001; accepted March 1, 2001.
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