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(Stroke. 2003;34:1593.)
© 2003 American Heart Association, Inc.
Original Contributions |
From the Department of Neurology, Pierre-Zobda-Quitman Hospital, Fort-de-France, Martinique, French West Indies.
Correspondence to Stéphane Olindo, MD, Department of Neurology, Pierre-Zobda-Quitman Hospital, BP 632, Fort-de-France 97261, Martinique, French West Indies. E-mail olindo.stephane{at}wanadoo.fr
| Abstract |
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Methods All Martinican patients suffering from their first-ever stroke during 1 calendar year between June 1, 1998, and May 31, 1999, were included. Epidemiological, clinical, neuroimaging, management, and outcome data during the first month were collected and compared between very old patients (
85 years) and patients aged <85 years.
Results One hundred patients aged
85 years and 480 patients aged <85 years were included (sex ratio, women/men, 2.84 and 0.85, respectively; mean±SD age, 88.8±3.6 and 65.8±13.3 years, respectively). The incidence of first-ever stroke was 1.64/1000 per year in the Martinique population and 18.2/1000 per year in patients aged
85 years. Elderly patients showed a significantly lower proportion of diabetes (19.1% versus 32.2%; P=0.012) and smoking (0% versus 8.4%; P=0.004) and a higher proportion of peripheral artery disease (23.4% versus 11.4%; P=0.002). Prevalence of hypertension was identical in the 2 groups (70%). There were no significant differences in stroke types or ischemic stroke subtypes between the 2 groups. Active medical care was poorer in older than in younger patients (hospitalization rate, 89% versus 94.4%; admission to neurological ward, 8% versus 23.8%; rate of performance of a CT scan, 82% versus 94%). The 30-day case fatality rate was approximately twice as high in elderly patients (31% versus 16.7%; P=0.0009), and disability (Rankin Scale score
3) in survivors was markedly higher (78% versus 48%; P<0.0001).
Conclusions In Martinique, the incidence of first-ever stroke in very old black Caribbean patients seems similar to that in white patients. They have the same pathological type and subtype of stroke as do young patients. The poorer stroke outcome found in the elderly during the first month may be related in large part to less active management than in younger patients.
Key Words: blacks elderly epidemiology stroke stroke management
| Introduction |
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To provide a better outcome for old stroke patients, we need to assess stroke and management features in the elderly. Few studies have reported data on very old subjects aged
85 years, and only 1 study has focused on white stroke patients in this age group.4 In very old black stroke patients, no study is yet available. On the basis of our findings in ERMANCIA (Etude Réalisée en Martinique et Centrée sur lIncidence des Accidents Vasculaires Cérébraux),6 our recent study of stroke incidence and outcome in a black Caribbean population in Martinique, French West Indies, we compared incidence, risk factors, stroke features, medical management, and outcome at 30 days in patients aged
85 years and patients aged <85 years.
| Subjects and Methods |
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The registration of patients began on June 1, 1998, and continued until May 31, 1999. The population in Martinique at the 1999 census was 381 427, including approximately 360 000 French Afro-Caribbean persons. All incident cases of stroke ("first-ever-in-a-lifetime" and recurrent stroke) occurring during the study period were registered. Any patient who might have had a cerebrovascular event was visited as soon as possible by one of us, whether or not he was hospitalized. All clinical and laboratory data were reported on a special form, including personal data, vascular risk factors, and Barthel Index between days 5 and 9 after stroke. Our cases were classified as follows: definite and probable cerebral infarction, intracerebral hemorrhage (ICH), subarachnoid hemorrhage (SAH), and undetermined stroke. Definite and probable infarctions were further subdivided according to the Oxfordshire Community Stroke Project classification8 into 4 subtypes: total anterior circulation infarction (TACI), partial anterior circulation infarction (PACI), lacunar infarction (LACI), and posterior circulation infarction (POCI). This classification had a clinical basis, but a reallocation by CT scan was done every time that it was needed. All included cases were followed up prospectively. The date of eventual death and the suspected cause of death were recorded. Death due to direct neurological damage was defined when no other evident cause was found. Investigators interviewed survivors with a structured telephone questionnaire designed to detect recurrent cerebrovascular and cardiovascular events and to determine the modified Rankin Scale9 score at 1 month.
We registered every stroke, but only first-ever-in-a-lifetime strokes were included in the study.7 A total of 973 patients with suspected stroke or transient ischemic attack (TIA) were notified to the study. After clinical assessment by a study investigator, 580 of 973 subjects (295 women and 285 men) were considered as having a first-ever stroke during the study period. Patients were divided into 2 groups on the basis of age (
BORDER="0">85 and <85 years). Incidence, clinical and neuroimaging features, and management and outcome data during the first month were compared between the 2 age groups.
Statistical Analysis
The incidence of stroke is expressed as the number of first-ever strokes per 1000 persons per year with corresponding 95% CI. Sex- and age-specific incidence rates were adjusted to the French population in 1999 by the direct method, and the comparison with different studies was performed by direct standardization to the European population.10
The 2 age groups were compared. Univariate analyses were performed, and significance was judged on the basis of the
2 test for categorical variables and the Mann-Whitney test for continuous variables. A value of P<0.05 was considered significant.
| Results |
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85 years, and 480 (82.76%) were aged <85 years. Mean ages and sex ratios (women/men) were 88.8±3.6 and 65.8±13.3 years and 2.84 and 0.85 for the older and younger groups, respectively (P<0.0001). The traditional risk factors in the 2 age groups are summarized in Table 1. The crude annual incidence of first-ever stroke in the whole population was 1.64/1000 per year (95% CI, 1.51 to 1.77). World- and Europe-standardized incidence values were 1 (95% CI, 0.91 to 1.09) and 1.51 (95% CI, 1.39 to 1.64), respectively. The crude annual incidence of first-ever stroke in very old people (
85 years) was 18.2/1000 per year (95% CI, 14.63 to 21.77). We found a high prevalence of arterial hypertension in both groups. Older patients more frequently had peripheral artery disease and TIA and less frequently had diabetes mellitus and smoking habits.
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The proportions of pathological types and subtypes of first-ever stroke were similar in the 2 groups and are shown in Table 2. We found a higher frequency of coexisting asymptomatic lesions on CT scan in the oldest patients (47% versus 25.3%; P<0.0001). Types and proportions of coexisting asymptomatic lesions were similar in the 2 groups (lacunar infarcts, 63% versus 61%; leukoaraiosis, 55% versus 59%; lacunar infarcts plus leukoaraiosis, 17% versus 15%; silent infarcts, 5% versus 8%, for patients aged <85 and
85 years, respectively).
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Management and outcome features were markedly different between the 2 age groups and are detailed in Tables 3 and 4
, respectively.
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| Discussion |
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85 years.6 The incidence rate of first-ever stroke in very old subjects was 18.2/1000 per year. Previous studies showed important variations in first-ever stroke incidence for the most elderly (Table 5).1116 This variation may be real because of differences in the detection and management of risk factors. Generally, the older group studied in black patients with stroke is aged
75 years.17 We found only 1 study on stroke incidence in a black population aged
85 years, which reported a high stroke incidence (64.1/1000) in South London, but the statistical analysis was performed on a very small sample (5 patients).15 As in many studies, we report a higher incidence in men than in women in all age groups except the elderly.
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Arterial hypertension had a high prevalence, similar to that found in US black patients,18 and was equally common in both age groups. Diabetes mellitus and smoking were statistically more frequent in younger patients than in older ones; this finding strongly suggests the recent westernization of lifestyle in Martinique. Emergence of these 2 vascular risk factors in young patients could contribute in the future to increase stroke incidence in the old population. Coronary disease and atrial fibrillation showed a trend toward being higher in old patients, but this was without statistical significance. The low frequencies of such cardiac stroke risk factors found in our black population are in accordance with the study of Sacco and al.18 Preceding TIAs in patients with cerebral infarcts were more frequent in the elderly but were rare in comparison to those in white patients.19 The reason may be related to the higher rate of intracranial artery disease in blacks,20 which seems to be associated with fewer TIAs than extracranial occlusive disease.21
The 2 age groups did not differ significantly in regard to distribution of stroke types and ischemic stroke subtypes. In accordance with the study of Arboix et al,22 rates of ICH were very close in the 2 age groups (12% and 14.8%, respectively, in patients aged
85 years and patients aged <85 years). Previous studies have found a higher prevalence of TACI subtype in elderly than in younger patients, which has been assigned to a higher rate of atrial fibrillation.23,24 However, as in our study, some authors have also shown that the black stroke population suffered significantly less atrial fibrillation than did whites.25 These data may explain the relatively low rate of TACI found in our older ischemic stroke group. We found a lower rate of undetermined stroke than in many previous studies.1214 This is likely related to the high proportion of CT scans obtained within 30 days in our study, even in very old patients. We did not find SAH in the elderly group. These results are consistent with those of the studies of Bamford et al12 and Ellekjaer et al,14 in which only 1 SAH was noted in 89 and 91 stroke patients aged
85 years, respectively. The very low rate of SAH in the elderly raises the question of the difficulty of collecting data on such patients, who often die rapidly at home and therefore are not included in death certificate searches. Subtypes of ischemic stroke were very similar in the 2 groups. Lacunar infarcts accounted for 19% of all stroke in the older group, which is slightly higher than in the hospital-based study of Arboix et al (15%).26 Thus, age does not seem to influence stroke type and ischemic stroke subtype distribution except for SAH.
Substantial differences in the management of stroke between older and younger patients were found in our study. Very old patients were less frequently hospitalized than those aged <85 years (89% versus 94.4%). However, we have shown that a great proportion of stroke patients were admitted to the hospital, including the elderly. This is consistent with the French medical practice in regard to stroke27 and is dramatically different from the practice in many countries such as the Netherlands, where a rate of hospitalization of <50% in stroke patients aged >85 years has been reported by Bots and colleagues.28 Approximately two thirds of hospitalized patients in each group were admitted in the university hospital of Fort-de-France. However, older patients were admitted to neurological wards 3 times less often than younger patients. In addition, the rate of CT scan performance within 30 days in the older group was significantly lower and the median delay in CT scan performance was higher than in the younger group. The rate of performance of a second CT scan in the first month was much lower in the oldest stroke patients (8% versus 22%). These management data suggest that elderly stroke patients are at risk of receiving suboptimal care since studies have shown that functional outcome was better in old patients treated in the Department of Neurology than those treated in the Department of Medicine.5
Outcome features were poorer in the oldest patients. The 30-day case fatality rate was twice as high in patients aged
85 years (31% versus 16.7%). These rates are similar to those reported in the hospital-based study of Arboix et al4 (27% versus 13.5%) and in the population-based study of Vemmos et al16 (38% versus 23%). Among survivors, patients aged
85 years were more dependent at 30 days than patients aged <85 years (78% versus 48%). The severity of stroke in this older age group is also illustrated by the very low proportion of independent subjects among all stroke patients at 30 days, which reached only 14%. Severe stroke type and subtype, such as ICH and TACI, were similar in the 2 groups and cannot explain the outcome differences found in our study. Several factors may lead to poorer outcome at 1 month in the elderly. The proportion of deaths due to direct neurological damage was high in both groups and may be overestimated in our study. However, the presumed cause of death was less often related to direct neurological damage in older patients; this suggests that complications such as cardiac and respiratory events occurred more frequently after stroke. This is consistent with the likely poorer health and functional status before stroke in the older group. No data were obtained in our study on prestroke functional status; this constitutes a bias for poststroke disability analysis. However, we believe that a poorer functional status before stroke in very old patients is not sufficient to explain the strong difference found between the 2 groups in regard to poststroke disability. Moreover, only first-ever-in-a-lifetime strokes have been included, and thus a high proportion of patients who were independent before stroke have been selected. Finally, in addition to poorer health and prestroke disability, the less intensive management of stroke in the elderly, as shown in our study, may contribute to the poorer outcome in this age group. This constitutes a paradox because studies have shown that older stroke patients, who generally have a poor clinical prognosis, benefit more from active medical care than younger patients.29 Stroke management appears to be one of the most important modifiable prognostic factors in older patients, and we believe that a special effort must be made to improve medical care in this older age group.
| Conclusions |
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| Acknowledgments |
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Received September 12, 2002; revision received January 27, 2003; accepted February 13, 2003.
| References |
|---|
|
|
|---|
2. Wolf PA, DAgostino RB, ONeal MA, Sytkowski P, Kase CS, Belanger AJ, Kannel WB. Secular trends in stroke incidence and mortality: the Framingham Study. Stroke. 1992; 23: 15511555.
3. Pohjasvaara T, Erkinjuntti T, Vataja R, Kaste M. Comparison of stroke features and disability in daily life in patients with ischemic stroke aged 55 to 70 and 71 to 85 years. Stroke. 1997; 28: 729735.
4. Arboix A, Garcia-Eroles L, Massons J, Oliveres M, Targa C. Acute stroke in very old people: clinical features and predictors of in-hospital mortality. J Am Geriatr Soc. 2000; 48: 3641.[Medline] [Order article via Infotrieve]
5. Kaste M, Palomäki H, Sarna S. Where and how should elderly stroke patients be treated? Stroke. 1995; 26: 249253.
6. Smadja D, Cabre P, May F, Fanon JL, René-Corail P, Riocreux C, Charpentier JC, Fournerie P, Sant-Vil M, Ketterle J. ERMANCIA: Epidemiology of stroke in Martinique, French West Indies, part I: methodology, incidence, and 30-day case fatality rate. Stroke. 2001; 32: 27412747.
7. Sudlow CLM, Warlow CP. Comparing stroke incidence worldwide: what makes studies comparable? Stroke. 1996; 27: 550558.
8. Bamford J, Sandercock P, Dennis M, Burn J, Warlow C. Classification and natural history of clinically identifiable subtypes of cerebral infarction. Lancet. 1991; 337: 15211526.[CrossRef][Medline] [Order article via Infotrieve]
9. Van Swieten JC, Koudstaal PJ, Visser MC, Schouten HJA, van Gijn J. Interobserver agreement for the assessment of handicap in stroke patients. Stroke. 1988; 19: 604607.
10. Waterhouse J, Correa P, Muir C, Powell J, eds. Cancer Incidence in Five Continents.Vol 3. Lyon, France: IARC; 1976: 476.
11. Terent A. A prospective epidemiological survey of cerebrovascular disease in Swedish community. Ups J Med Sci. 1979; 84: 235246.[Medline] [Order article via Infotrieve]
12. Bamford J, Sanderocock P, Dennis M, Warlow C, Jones L, McPherson K, Vessey M, Fowler G, Molyneux A, Hugues T, et al. A prospective study of acute cerebrovascular disease in the community: the Oxfordshire Community Stroke Project 19811986, 1: methodology, demography and incident cases of first-ever stroke. J Neurol Neurosurg Psychiatry. 1988; 51: 13731380.
13. Ricci S, Celani MG, La Rosa F, Vitali R, Duca E, Ferraguzzi R, Paolotti M, Seppoloni D, Caputo N, Chiurulla C, et al. SEPIVAC: a community-based study of stroke incidence in Umbria, Italy. J Neurol Neurosurg Psychiatry. 1991; 54: 695698.
14. Ellekjaer H, Holmen J, Indredavik B, Terent A. Epidemiology of stroke in Innherred, Norway, 1994 to 1996: incidence and 30-day case fatality rate. Stroke. 1997; 28: 21802184.
15. Stewart JA, Dundas R, Howard RS, Rudd AG, Wolfe CDA. Ethnic differences in incidence of stroke: prospective study with stroke register. BMJ. 1999; 318: 967971.
16. Vemmos KN, Bots ML, Tsibouris PK, Zis VP, Grobbee DE, Stranjalis GS, Stamatelopoulos S. Stroke incidence and case fatality in Southern Greece: the Arcadia Stroke Registry. Stroke. 1999; 30: 363370.
17. Broderick J, Brott T, Kothari R, Miller R, Khoury J, Pancioli A, Gebel J, Mills D, Minneci L, Shukla R. The Greater Cincinnati/Northern Kentucky Stroke Study: preliminary first-ever and total incidence rates of stroke among blacks. Stroke. 1998; 29: 415421.
18. Sacco RL, Kargman DE, Zamanillo MC. Race-ethnic differences in stroke risk factors among hospitalized patients with cerebral infarction: the Northern Manhattan Stroke Study. Neurology. 1995; 45: 659663.
19. Oddone EZ, Horner RD, Sloane R, McIntyre L, Ward A, Whittle J, Passman LJ, Kroupa L, Heaney R, Diem S, Matchar D. Race, presenting signs and symptoms, use of carotid artery imaging, and appropriateness of endarterectomy. Stroke. 1999; 30: 13501356.
20. Gorelick PB, Caplan LR, Hier DB, Parker SL, Patel D. Racial differences in the distribution of anterior circulation occlusive disease. Neurology. 1984; 34: 5459.
21. Caplan LR. Cerebral ischemia and infarction in blacks: clinical, autopsy, and angiographic studies. In: Gillum RF, Gorelick PB, Cooper ES, eds. Stroke in Blacks. Basel, Switzerland: Karger; 1999: 718.
22. Arboix A, Vall-Llosera A, Garcia-Eroles L, Massons J, Oliveres M, Targa C. Clinical features and functional outcome of intracerebral hemorrhage in patients aged 85 and older. J Am Geriatr Soc. 2002; 50: 449454.[CrossRef][Medline] [Order article via Infotrieve]
23. Hornig CR, Dorndorf W. Early outcome and recurrences after cardiogenic brain embolism. Acta Neurol Scand. 1993; 88: 2631.[Medline] [Order article via Infotrieve]
24. Yamanouchi H, Tomonaga M, Shimada H, Matsushita S, Kuramoto K, Toyokura Y. Nonvalvular atrial fibrillation as a cause of fatal massive cerebral infarcts in the elderly. Stroke. 1989; 20: 16531656.
25. Hajat C, Dundas R, Stewart JA, Lawrence E, Rudd AG, Howard R, Wolfe CDA. Cerebrovascular risk factors and stroke subtypes: differences between ethnic groups. Stroke. 2001; 32: 3742.
26. Arboix A, Garcia-Eroles L, Massons J, Oliveres M, Targa C. Lacunar infarcts in patients aged 85 years and older. Acta Neurol Scand. 2000; 101: 2529.[CrossRef][Medline] [Order article via Infotrieve]
27. Giroud M, Beuriat P, Vion P, DAthis PH, Dusserre L, Dumas R. Stroke in a French prospective population study. Neuroepidemiology. 1989; 8: 97104.[Medline] [Order article via Infotrieve]
28. Bots ML, Looman SJ, Koudstaal PJ, Hofman A, Hoes A, Grobbee DE. Prevalence of stroke in the general population: the Rotterdam Study. Stroke. 1996; 27: 14991501.
29. Strand T, Asplund K, Eriksson S, et al. Stroke unit care: who benefits? Comparison with general medical care in relation to prognostic indicators on admission. Stroke. 1986; 17: 377381.
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