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(Stroke. 2007;38:2935.)
© 2007 American Heart Association, Inc.
Original Contributions |
From McMaster University (J.L., Z.K., C.M., M.O.), Hamilton, Ontario, Canada; and McGill University (C.S.), Montreal, Quebec, Canada.
Correspondence to Martin ODonnell, MB, McMaster Clinic, Hamilton General Hospital, Room 715, 237 Barton St East, Hamilton, Ontario, L8L 2X2, Canada. E-mail odonnm{at}mcmaster.ca
| Abstract |
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Methods— Studies were identified from comprehensive searches of PubMed, EMBASE, Science Citation Index, and bibliographies of relevant articles. Only English language articles were included. Randomized controlled trials and prospective cohort studies of consecutive patients with acute ischemic stroke that fulfilled predefined criteria were eligible. Two authors conducted searches and abstracted data from eligible studies independently.
Results— Sixty studies were deemed potentially eligible. After application of eligibility criteria, 5 studies (736 participants) were included in the analysis. All studies evaluated Holter monitoring; 2 also evaluated event loop recording. In studies that evaluated Holter monitoring (588 participants), new atrial fibrillation/flutter was detected in 4.6% (95% CI: 0% to 12.7%) of consecutive patients with ischemic stroke. Duration of monitoring ranged from 24 to 72 hours. Two studies (140 participants) evaluated event loop recorders after Holter monitoring. New atrial fibrillation/flutter was detected in 5.7% and 7.7% of consecutive patients in these 2 studies.
Conclusions— Screening consecutive patients with ischemic stroke with routine Holter monitoring will identify new atrial fibrillation/flutter in approximately one in 20 patients. Although based on limited data, extended duration of monitoring may improve the detection rate. Further research is required before definitive recommendations can be made.
Key Words: ambulatory electrocardiography atrial fibrillation ischemic stroke systematic review transient ischemic attack
| Introduction |
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In addition to baseline electrocardiogram and clinical examination, noninvasive cardiac monitoring is used to detect AF.16–19 A previous review on this topic reported that 24- to 48-hour Holter monitoring identified AF in 1% to 5% of patients undetected by initial electrocardiogram.20 Currently, there is no clear recommendation on whether routine Holter monitoring is indicated in unselected patients with acute ischemic stroke or transient ischemic attack.20 Furthermore, many of the studies included in that review were conducted at a time when the clinical significance of paroxysmal AF was underappreciated.21–25 It is now acknowledged that paroxysmal AF is associated with a comparable increase in risk of ischemic stroke as continuous AF.6 Moreover, since the previous review of this topic, a number of studies evaluating the use of Holter monitoring, and newer methods that allow more prolonged periods of monitoring, have been published. We performed a systematic review to determine the frequency of occult AF detected by noninvasive methods of continuous cardiac rhythm monitoring in consecutive patients with ischemic stroke.
| Methods |
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Study Selection
Two investigators independently reviewed all studies identified on the search. For inclusion, studies were required to fulfill the following inclusion criteria: (1) study design: (a) randomized, controlled trials in which patients are randomized to receive noninvasive cardiac monitoring compared with control or (b) prospective cohort studies; (2) population: consecutive patients with a diagnosis of acute ischemic stroke or transient ischemic stroke; (3) intervention: participants underwent noninvasive rhythm monitoring to detect AF for a minimum duration of 12 hours; and (4) outcome: frequency of AF detected by noninvasive monitoring was reported.
Data Abstraction
Data abstraction was conducted independently by two investigators (J.L., Z.K.) using standardized data abstraction forms developed before searches were conducted.
Statistical Analysis
The study-specific effect estimates were combined using a precision-weighted (ie, reciprocal of the variance), random-effects model and 95% CIs were calculated. Zelens exact test was used to determine whether there was statistical heterogeneity between individual studies. A 95% CI that did not include one was considered to be statistically significant. Minitab 14.3 statistical software was used for the analyses. The following factors were hypothesized, a priori, to influence the detection rate of AF: duration and timing of monitoring, stroke subtype and severity, and setting.
| Results |
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Frequency of Atrial Fibrillation and Atrial Flutter Detected by Routine Cardiac Monitoring
Five studies (588 participants) evaluated Holter monitoring in the inpatient setting.24,26–29 In these studies, rates of detection of new AF ranged from 3.8% to 6.1% (Table 3). When the results of these studies were combined in a random-effects model, new AF was detected in 4.6% (95% CI: 0% to 12.7%) of consecutive patients with ischemic stroke independent of baseline electrocardiogram and clinical examination (test for heterogeneity P=0.9). Two studies (140 participants) evaluated event loop recorders after Holter monitoring.26,28 New AF was detected in 5.7% and 7.7% of consecutive patients in these 2 studies. One study (159 participants) evaluated continuous cardiac monitoring using inpatient telemetry (48 hours) and detected new AF in 2.5% of participants24 (Table 3).
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Stroke Subtype, Stroke Severity, and Setting
Two studies reported the frequency of AF within ischemic stroke subtypes.26,28 In the largest of these studies (n=149), most cases of AF were detected in patients with total and partial anterior circulation ischemic strokes (68%), whereas no cases of AF were identified in patients with lacunar stroke.28 In the other study, no significant association between AF and stroke subtype was reported.26
Two studies reported stroke severity in participants with and without AF.27,28 Jabaudon et al28 reported more severe neurological deficit (National Institutes of Health Stroke Scale
10) in patients with AF (22.7%) compared with patients without AF (3.1%). (P=0.003)27 Hornig et al25 did not report an association between stroke severity and AF. No eligible studies included nonhospitalized patients with ischemic stroke only.24,26–29
Duration and Timing of Monitoring
All studies reported the duration of monitoring.24,26–28 Duration of monitoring ranged from 21 to 159 hours. Studies evaluating event loop recorder monitors reported a detection rate of 5.7% after 70 hours and 7.7% after 159 hours of monitoring.
Three studies reported on the timing of initiating of monitoring from the diagnosis of stroke.26,28,29 One study initiated monitoring 55 days (median delay) postevent.28 Two studies reported that monitoring began on admission to the ward; however, the timing from onset of stroke was unclear.26,28 Two studies did not report the timing of initiating of monitoring.24,27
Detection of Atrial Fibrillation Resulting in a Change in Management
One study reported the proportion of patients in which the results of noninvasive monitoring resulted in a change in antithrombotic therapy.28 In that study, oral anticoagulation was started in 28.6% (2 of 7) of patients with new-onset AF detected by Holter monitoring and in all 5 patients with AF detected by event loop recorder.
| Discussion |
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Very limited data suggest that confining Holter monitoring to patients with nonlacunar stroke may improve its diagnostic use. In the study by Jabaudon et al,28 no cases of AF were reported in patients with lacunar stroke. A potential limitation of the Jabaudon study28 is the unblinded evaluation of stroke subtype, which may have been biased by knowledge of the results of cardiac monitoring. One retrospective study, not included in this review, reported that Holter monitoring identified the greatest yield of AF in patients with unexplained embolic stroke.30 This is further supported by the results by Schuchert et al,29 which found a relatively higher detection rate of 6.1% in patients with suspected cardioembolic ischemic stroke. Furthermore, there are 2 observational studies that suggest that oral anticoagulation may not be associated with the same benefit for prevention of recurrent stroke in patients with AF presenting with lacunar stroke compared with those presenting with other ischemic stroke subtypes.11,31 Although based on very limited data, these observations suggest that limiting Holter monitoring to patients with nonlacunar ischemic stroke might be reasonable, but further research is required before definitive recommendations can be made.
Increased duration of monitoring appears to be associated with increased rates of detection of AF (Table 3). In the 2 studies that evaluated event loop recorders (140 participants), new AF was detected in 5.7% and 7.7% of consecutive patients in these 2 studies.26,29 Our review is unable to determine the optimal duration of monitoring. Similarly, the best time to initiate cardiac monitoring after a stroke is uncertain. No study explicitly evaluated and reported on early monitoring (within 48 hours) from onset of stroke symptoms.
Our review has several limitations. Eligible articles were restricted to published studies in English language journals, and conference abstracts were not accessed. Thus, unpublished studies may have been overlooked. Furthermore, because only hospitalized patients were included in eligible studies, we are unable to comment on the use of Holter monitoring in the outpatient stroke population. Our strict inclusion criteria resulted in fewer numbers of eligible articles compared with a previous review. Furthermore, sample sizes of studies included were relatively small. As a result, the confidence interval about the summary estimate is wide (95% CI: 0% to 12.7%), a clear limitation of this review. However, we believe that restricting eligibility to prospective studies is an overall strength of our review.
Do the results of this review have implications for clinical practice? Should all patients with ischemic stroke be screened with Holter monitoring? If we apply the general Principles of Good Screening, we observe that Holter monitoring fulfills most criteria (Table 4).32–36 However, in unselected patients, it remains open to argument whether AF is insufficiently prevalent to justify routine screening.
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In conclusion, screening consecutive patients with ischemic stroke with routine Holter monitoring will identify new AF in approximately one in 20 patients. Extended duration of monitoring and confining its use to patients with nonlacunar stroke may improve detection rates. However, further research is needed to evaluate extended monitoring, using newer techniques, in patients with ischemic stroke.
| Acknowledgments |
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Sources of Funding
M.O. is supported by a grant from the Canadian Institutes of Health Research and holds the William Walsh Endowed Chair in Internal Medicine, McMaster University.
Disclosures
None.
Received January 6, 2007; revision received April 23, 2007; accepted April 26, 2007.
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This article has been cited by other articles:
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D. J. Gladstone, J. Blakely, P. Dorian, M. Spring, J. Fang, F. L. Silver, M. K. Kapral, and for the EMBRACE Pilot Study Group Detecting Paroxysmal Atrial Fibrillation After Ischemic Stroke and Transient Ischemic Attack: If You Don't Look, You Won't Find Stroke, May 1, 2008; 39(5): e78 - e79. [Full Text] [PDF] |
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