(Stroke. 2007;38:259.)
© 2007 American Heart Association, Inc.
Original Contributions |
From the Department of Informatics and Mathematical Modelling (K.K.A.), Section for Statistics, Technical University of Denmark, Lyngby, and the Stroke Unit (T.S.O.), Hvidovre University Hospital, Hvidovre, Denmark.
Correspondence to Tom Skyhøj Olsen, MD, PhD, Stroke Unit, Department of Neurorehabilitation, Hvidovre University Hospital, Kettegaard Allé 30, DK-2650 Hvidovre, Denmark. E-mail Tom.Skyhoej.Olsen{at}hh.hosp.dk
| Abstract |
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Methods A nationwide registry that was started in 2001 with the aim of registering all hospitalized stroke patients in Denmark now includes 24 791 patients. We studied the survival of patients with ischemic stroke and AF with respect to anticoagulation treatment. All underwent an evaluation for stroke severity (according to the Scandinavian Stroke Scale), computed tomography scan, and an evaluation for cardiovascular risk factors. Follow-up duration was 4 years (mean, 1.2 years).
Results Of all patients, 22 179 (89.4%) experienced an ischemic stroke. In total, 3670 (16.5%) had AF, and 1909 had no contraindication to anticoagulation treatment. Anticoagulation treatment was initiated in 1149 of these patients (60.2%) but omitted in 760 (39.8%) despite no contraindication to such treatment. Of the patients so treated, 18.9% died during follow-up versus 45.2% without treatment. Patients who received treatment were younger (76.7±9.5 versus 80.7±9.0 years, P<0.0001) and had less severe strokes (Scandinavian Stroke Scale score, 42.0±15.0 versus 33.6±18.2, P<0.0001). A Cox proportional-hazards model was built to study the effect of anticoagulation on survival in patients without contraindications to treatment while controlling for stroke severity, sex, and cardiovascular risk factors. Patients without anticoagulation treatment were at greater risk of dying (hazard ratio=1.91, 95% CI=1.44 to 2.52) compared with patients who received anticoagulation treatment.
Conclusions Our data suggest that anticoagulation treatment reduces poststroke mortality in patients with ischemic stroke and AF.
Key Words: anticoagulation atrial fibrillation prevention prognosis stroke
| Introduction |
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The frequency of AF increases almost exponentially with age and is highest in patients with the most severe strokes.4 Evidence for the effect of anticoagulation in patients with stroke and AF is, however, based on data from patients with minor strokes and those at the younger end of the AF spectrum.13 With reference to this evidence, however, it is widely accepted in clinical practice to also use anticoagulation in elderly patients and in patients with moderate to severe strokes associated with AF. There are no secondary prevention studies under way on the effect of anticoagulation in elderly patients and in patients with moderate to severe strokes, and there are no indications that these studies will appear in the near future.
The present study was undertaken to investigate whether anticoagulation in elderly patients and/or in patients with moderate to severe strokes associated with AF affects survival. An ongoing, nationwide Danish stroke registry was established on March 1, 2001, with the aim of registering all patients hospitalized for stroke. By August 1, 2005, the registry included 24 791 patients hospitalized for acute stroke, among whom we identified 3670 patients who had experienced an ischemic stroke and AF. Among these patients, 1909 did not have any contraindication to anticoagulation treatment. On the basis of this sizeable number of patients included without regard to age or stroke severity, we studied the effect of anticoagulation treatment on survival up to 4 years after stroke in patients without contraindication to anticoagulation treatment, while controlling for age, stroke severity, sex, and relevant cardiovascular risk factors.
| Patients and Methods |
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75% of all stroke admissions. All Danish hospitals have committed to report a predefined set of data on all patients admitted to hospital with acute stroke, including age, sex, admission stroke severity as measured by the Scandinavian Stroke Scale (SSS),5,6 and a predefined cardiovascular profile. The SSS is a validated and widely used neurological stroke scale in Scandinavia that evaluates level of consciousness; eye movement; power in the arm, hand, and leg; orientation; aphasia; facial paresis; and gait on a total score that ranges from 0 to 58. The cardiovascular profile included information on alcohol consumption (
14 and 21 drinks per week for women and men, respectively, or >14 and 21 drinks per week for women and men, respectively), smoking (current daily smoking, former smoking, never smoking), diabetes (diabetes known before admission or diagnosed during admission, with no distinction made between type 1 and type 2 diabetes), AF (chronic or paroxysmal) known before admission or diagnosed during admission), myocardial infarction (known before admission or diagnosed during admission), hypertension (known before or diagnosed during admission), previous stroke, and intermittent claudication (known before admission or diagnosed during admission). Distinction between ischemic stroke and primary intracerebral hematomas was determined after administration of a computed tomography/magnetic resonance imaging scan. Primary intracerebral hematoma was evaluated as a single entity, without distinction between lobar and nonlobar hemorrhage. Stroke was defined according to World Health Organization criteria.7 For patients with multiple records (events), only the first event was included in the analysis. Patients with transient ischemic attacks or subarachnoid hemorrhages were not included in the study. Patients <40 years of age were not included in the study. Patients for whom a computed tomography/magnetic resonance imaging scan was either not performed (0.4%) or unavailable (0.7%) were excluded from the study. Initiation or continuation of secondary preventive measures such as antiplatelet treatment or anticoagulation treatment (coumarin) was recorded. Patients in whom anticoagulation treatment was considered contraindicated (eg, risk of gastrointestinal bleeding, malignancy, critical clinical condition, risk of falls, dementia, insufficient compliance, etc) were recorded. According to the prespecified data definitions, it was left to the treating physician to decide whether or not contraindications to anticoagulation treatment were present. Patients recorded as having contraindications to treatment were subsequently excluded from the analyses. Thus, our study included only patients with stroke and AF in whom there was no contraindication to treatment. Prestroke prevention (eg, antiplatelet treatment or anticoagulation treatment) was not recorded.
Survival of patients included in the NIP database was registered and followed up through the Danish Registry of Persons. We studied all-cause mortality only. Inclusion of patients in the NIP started on March 1, 2001, and the end of the study follow-up (censoring date) was November 15, 2005. Less than 0.2% of patients were lost to follow-up, mainly attributable to emigration, and these patients data were censored in the analysis. The study was approved by the board of the NIP and the Danish Data Protection Agency.
Statistical Analyses
First, a risk profile with respect to receiving anticoagulation treatment was obtained by a multiple logistic-regression analysis according to a generalized additive model.8 Age and stroke severity score were modeled with a smooth nonlinear function, because the effect of both covariates cannot be assumed a priori to be linear. Significance of sex and cardiovascular risk factors was tested on the basis of a likelihood ratio test.
Second, independent predictors of death were identified with a Cox proportional-hazards model. Age was modeled as a delayed entry, because the patients entered the study at random ages. This implies that survival time was chosen to be the patients age at death (by any cause). Any patient entering at a later age than a given event time (death) was not included in the risk set. To assess whether the baseline hazard functions were proportional, log-log plots were performed for each variable, as well as tests and diagnostics based on weighted residuals.9 In all statistical analyses, a significance level of 5% was adopted.
In identifying the final model, only complete cases were included in the analysis. Approximately 15% of the cases were excluded owing to 1 or more missing covariates. Our analysis led us to believe that the nature of the missing data were not informative. The statistical software R10 was used for the statistical analyses.
| Results |
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In the multiple-regression model, with the objective of determining which factors were independently associated with initiation of anticoagulation treatment, only age, stroke severity, and intermittent claudication were found significant in the model. The effect of age could not be assumed to be linear. The prevalence of receiving anticoagulation treatment as a function of age is shown in Figure 1. Anticoagulation was initiated in
75% to 80% of patients <60 years of age but in <65% of patients >80 years of age, with a sharp decrease in the prevalence of receiving treatment in older patients. The prevalence of receiving anticoagulation as a function of stroke severity expressed by the SSS score is shown in Figure 1. Here, prevalence is increasing almost linearly with increasing SSS score, ie, decreasing stroke severity. The slope indicates a linear relation, corresponding to a relative risk of 1.28 per 10SSS point decrease (CI=1.18 to 1.39, P<0.0001). Patients without intermittent claudication had a 2 times higher probability of receiving anticoagulation treatment (CI=1.12 to 3.63, P=0.019).
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Independent predictors of death after stroke in patients without contraindications to anticoagulation treatment were identified by the Cox proportional-hazards model, wherein age was modeled as a delayed entry. The hazard ratios of risk factors are given in the Table. Age and stroke severity score were clearly the strongest predictors of survival. Age was accounted for by delayed entry, and hence, no hazard ratio is given. Similarly, no hazard ratio is given for the influence of SSS score, because this was modeled with a restricted cubic spline because the effect on survival was nonlinear.
Most important, survival was almost doubled in patients treated with anticoagulation compared with patients who did not have this treatment (hazard ratio=1.91, 95% CI=1.44 to 2.52). It should be noted that in our analysis, patients who died in hospital were included. If these patients (8% in total) were excluded from the analyses, the effect of anticoagulation treatment would be slightly smaller (hazard ratio=1.74, 95% CI=1.26 to 2.39). Survival curves stratified by anticoagulation treatment are given in Figure 2. The better survival probability for patients receiving anticoagulation is evident.
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| Discussion |
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Weaknesses and Strengths
The study was not randomized, and our conclusions should be considered a supportive supplement to current evidence from available randomized trials.1,2 The patients who received anticoagulation were selected and differed from patients who were not given anticoagulants, despite no contraindications to such treatment, as they were younger and had less severe strokes. In our Cox proportional-hazards model, however, we were able to adjust for these 2 important factors as well as for relevant cardiovascular risk factors.
Although the Danish NIP was designed as a nationwide registration of all patients admitted for acute stroke, coverage is not yet complete (presently
75%), and because of the large number of persons involved in a nationwide registration, missing data are unavoidable. As we registered whether anticoagulation therapy was instituted, we did not register compliance or adherence to treatment, nor did we register treatment of comorbidities, such as hypertension, hypercholesterolemia, etc. The presence of AF on acute admission does not necessarily imply causality, as AF may develop as a consequence of the acute illness, eg, stroke.11
Our studys strength lies in its large sample size, allowing for sufficient statistical power. It is the first nationwide study on secondary prevention of stroke with AF, with the largest number of patients in a study on this issue to date.12 In contrast to the 2 available randomized studies on secondary stroke prevention in patients with AF,1,2 our study included patients without limitations on age or stroke severity. Stroke severity was measured in all patients with a well-validated, neurological scale, and all patients underwent a standardized risk factor evaluation. Furthermore, we had survival data on nearly all patients, with <0.2% lost to follow-up.
We acknowledge the advantages of the randomized, controlled design. However, we consider large observational studies like ours indispensable supplementary information. Although meta-analyses of available randomized, controlled studies demonstrate the effectiveness of anticoagulation in preventing strokes in patients with AF, this evidence relates to relatively young patients with minor strokes and transient ischemic attacks.3 Furthermore, there is still no established evidence for reducing mortality, and it is questionable whether it is at all possible to establish randomized, controlled studies with enough statistical power to provide the evidence for this design.
Survival
Our study suggests that anticoagulation in patients with stroke and AF reduces poststroke mortality, if there are no contraindications to treatment. Evidence for the effect of anticoagulation in patients with stroke and AF originates from randomized studies on patients who had minor strokes and transient ischemic attacks.1,2 Our study provides evidence of a preventive effect of anticoagulation also in patients with severe strokes. The mean age of patients participating in the randomized studies was 71 to 72 years, whereas the mean age of patients receiving anticoagulation in our study population was 76.7 years. Our study thus provides evidence of a preventive effect regardless of age.
Use of Anticoagulation
Only 60.2% of the patients with stroke and AF had anticoagulation, despite the lack of contraindications. Initiation of treatment was strongly associated with age and stroke severity, whereas the presence of cardiovascular risk factors had no influence. Our results are in line with other studies.1316 There has been no clear contraindication to warfarin in
2 to 3 times the number of patients actually receiving it, and most estimates of the underuse of warfarin in patients with AF exceed 40%. Even in the mildest end of the stroke spectrum, the use of anticoagulation did not exceed 70% in our study population, whereas in patients with severe strokes, such usage was <50%. Anticoagulation was initiated in
75% to 80% of patients below the age of 60 years, but after that age, usage fell; especially after the age of 75 to 80 years, it fell abruptly.
The main reason for omitting anticoagulation treatment in patients with AF is fear of bleeding complications.17 The advantage of avoiding the risk of bleeding events, however, should be weighed not only against the risk of recurrent stroke but, as indicated is this study, also against a substantial risk of premature death, which is present regardless of age and stroke severity. We are aware of a natural relation between stroke severity, age, and compliance, but we excluded those patients who had contraindications to anticoagulation treatment. Hence, our study indicates an exaggerated caution in regard to the elderly with severe strokes, which seems to be out of balance with the obvious benefit of treatment shown in our study.
Conclusions
Our study suggests that anticoagulation reduces poststroke mortality in patients with ischemic stroke and AF, regardless of age and stroke severity. The risk of serious bleeding complications should be substantial before omission of preventive anticoagulation treatment is decided.
| Acknowledgments |
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None.
Received September 19, 2006; revision received September 26, 2006; accepted September 29, 2006.
| References |
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