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(Stroke. 2005;36:2421.)
© 2005 American Heart Association, Inc.
Original Contributions |
80 Years) Stroke Patients
From the Neurologische Klinik (J.B.), Kreiskrankenhaus Altenburg, Altenburg, Germany; Neurologische Klinik (J.R., J.G.), Klinikum Minden, University Hannover, Minden, Germany; Neuroradiologische Abteilung (T.K., J.F.), Klinik und Poliklinik für Radiologie, Universitätsklinikum Hamburg-Eppendorf, Hamburg, Germany; and Klinik und Poliklinik für Neurologie (G.T.), Universitätsklinikum Hamburg-Eppendorf, Hamburg, Germany.
Correspondence to Götz Thomalla, MD, Klinik und Poliklinik für Neurologie, Neurozentrum, Universitätsklinikum Hamburg-Eppendorf, Martinistr. 52, D-20246 Hamburg, Germany. E-mail thomalla{at}uke.uni-hamburg.de
| Abstract |
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Methods We analyzed data of AIS patients, treated with IV-tPA, in 3 German stroke centers. Neurologic deficit on admission was assessed using the National Institutes of Health Stroke Scale (NIHSS). Outcome was assessed after 90 days using the Modified Rankin Scale (MRS), and favorable outcome was defined as a MRS score of 0 to 1. Severe intracerebral bleeding complications were assessed on follow-up magnetic resonance imaging or cranial computed tomography. Data were compared between patients <80 years of age and patients aged
80 years.
Results A total of 228 patients were treated with IV-tPA; 38 (16%) were 80 years or older. There was no difference in NIHSS on admission or onset to treatment time between younger and older patients. Less patients
80 years of age achieved a favorable outcome (26.3 versus 46.8%, P=0.021), and mortality was higher in older patients (21.1 versus 5.3%, P=0.004). There was no difference in the rate of parenchymal hemorrhage (6.3%<80 years versus 5.3%
80 years, P=1.000) and symptomatic intracerebral hemorrhage (2.6%<80 years versus 2.6%
80 years, P=1.000) between both groups.
Conclusion There is no increase in severe intracerebral hemorrhage after IV-tPA in very old patients, but outcome is worse as compared with younger patients. There is no evidence to exclude ischemic stroke patients from thrombolysis based on a predefined age threshold.
Key Words: stroke thrombolytic therapy treatment outcome
| Introduction |
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On the other hand, stroke incidence is clearly associated with age. Although incidence of a first-ever stroke is approximately 200 to 300 per 100 000 in the 55 to 64 years old, it is approximately 10-fold higher (2000 to 2500 per 100 000) in those over 85 years.7 At the same time, outcome is worse and mortality is higher in older patients. In large epidemiologic studies, short- and long-term mortality are approximately twice as high in patients over 85 years compared with those below 85 years.8,9
In the centers participating in this study, IV-tPA was administered according to the NINDS criteria.1 As a consequence of this, also patients aged 80 and older were treated with IV-tPA. We studied outcome and severe hemorrhagic complications after thrombolysis IV-tPA in AIS patients below and 80 years and above.
| Patients and Methods |
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Treatment
IV-thrombolysis with tPA was performed within 3 hours according to the NINDS criteria.1 In the 3- to 6-hour time period, IV-thrombolysis was performed as an individual decision of the treating neurologist and neuroradiologist based on multimodal CCT or MRI findings10 after informed consent according to the Declaration of Helsinki. The study was approved by the local Institutional Review Boards in all participating centers.
Clinical Assessment
Severity of neurologic deficit at admission was assessed using the National Institutes of Health Stroke Scale (NIHSS).11 Outcome was assessed 90 days after stroke using the Modified Rankin Scale (MRS).11,12 According to the primary end points of the NINDS and ECASS II trials, favorable outcome was defined as a score of zero to one on the MRS.4,5
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Assessment of Hemorrhagic Transformation
Hemorrhagic transformation was assessed by neuroradiologists, blinded to clinical data, on follow-up CCT or MRI. Parenchymal hemorrhage (PH) and symptomatic intracerebral hemorrhage (SICH) was rated according to the definitions used in the ECASS trials,4,5 which means that SICH was defined as any signs of hemorrhage on follow-up imaging associated with clinical deterioration of 4 or more points on the NIHSS.5 As a result of the small numbers of hemorrhages in our sample, we summarized PH1 and PH2 for further analysis as PH.
Statistical Analysis
Patients were stratified into 2 age groups: <80 and
80 years. All values are presented as median (interquartile ranges [IQR]) for continuous variables and counts (percentage) for categorical variables. Group comparisons were made using the MannWhitney U test for continuous variables and Fisher exact test for categorical variables; for correlations, Spearman rank correlations were used. To identify independent predictors of favorable outcome and death, logistic regression analysis was performed. After univariate analysis, covariates with P<0.15 were entered into a multiple regression model (SPSS 9.0.1; SPSS Inc).
| Results |
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The number of patients with a favorable outcome, defined by a MRS score of zero to one, was smaller in older patients (10 of 38=26.3% versus 89 of 190=46.8%, P=0.021; see figure). At 90 days after stroke, 8 of 38 (21.1%) patients
80 years had died. The cause of death was noncerebral in 5 patients (pneumonia, cardiac arrest) and cerebral (space-occupying middle cerebral artery infarction) in 3 patients. The mortality at day 90 was higher in the very old patients compared with patients below 80 years (10 of 190=5.3%, P=0.004). One third of the patients aged 80 or older was functionally independent (as defined by an MRS score
2) after 3 months. The frequency of severe hemorrhagic complications was comparable between both groups. PH was found in 2 of 38 (5.3%) patients 80 years or older compared with 12 of 190 (6.3%) in patients <80 years (P=1.000), and the rate of SICH was 2.6% for both groups (5 of 190<80 years versus one of 38
80 years, P=1.000).
There were strong positive correlations between age and NIHSS score on admission (r=0.191, P=0.004), age, and MRS score at day 90 (r=0.303, P<0.001), and also between NIHSS score on admission and MRS score at day 90 (r=0.559, P<0.001). Age (P=0.001) and NIHSS on admission (P<0.001) were predictors of outcome in univariate analysis, whereas onset to treatment time (OTT) (P=0.581) and sex (P=0.204) were not. Both NIHSS on admission and age were identified as independent predictors by multiple regression analysis (see Table 2). In other words, the likelihood of reaching a favorable outcome decreases by 25% for every 10 year of increase in age and by approximately 91% for an increase of 5 points on the NIHSS on admission. Age (P=0.004) and NIHSS on admission (P=0.002) were also predictors of death at day 90 in univariate analysis, whereas OTT (P=0.576) and sex (P=0.313) were not. Both age and NIHSS were retained in the model after multiple regression analysis. Odds ratios (see Table 2) translate into an increased risk of death at day 90 of 72% for every 10-year increase in age and of 69% for an increase of 5 points on the NIHSS on admission.
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| Discussion |
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Only few patients aged 80 or older have been included into the large clinical trials of tPA in stroke. Until now, there exists no evidence whether very old patients benefit from treatment with IV-tPA comparable to younger patients and whether the risk of severe intracerebral bleeding complications is higher in the very old patients. In our analysis, mortality was higher and the proportion of patients with favorable outcome was smaller 90 days after stroke in patients age 80 or older, whereas the rate of severe intracerebral bleeding complications did not differ between very old and younger patients.
A small number of case series report on the use of IV-tPA in old patients. A retrospective survey of patients treated at 13 U.S. hospitals included 30 patients aged 80 or older and compared patients
80 or older and <80 years.13 They found no significant differences in the number of patients with favorable outcome at hospital discharge (37 versus 30%), symptomatic intracerebral hemorrhage (3 versus 6%), and only a tendency toward a higher inhospital mortality in older patients (20 versus 8%). These results are contrary to our data with significant differences between patients
80 and <80 years regarding favorable outcome and mortality. This may partially be explained by the different time points for the assessment of outcome, being 90 days in our study and a rather short-term outcome (hospital discharge) in the U.S. tPA Stroke Survey Experience.13 Moreover, outcome of the patients below 80 years in our study appears remarkably good with 46.8% patients reaching a favorable outcome after 90 days, which leads to a stronger contrast to the outcome in the older people.
Another study, including 16 patients aged 80 years or older, reported no significant difference in favorable outcome between very old and younger patients (29 versus 41%) nor in the number of symptomatic hemorrhages, but the small sample size may be responsible for the failure to detect significant differences between the groups.14 Recently Simon et al15 reported a series of 62 patients aged 80 and over treated by IV-tPA and found 20% patients with favorable outcome at 3 months, a mortality at 3 months of 33%, and a 9.7% rate of symptomatic intracerebral hemorrhage.
Considering the results from all reports of thrombolysis in very old patients together with our analysis, the proportion of IV-tPA patients 80 years or older with a favorable outcome is approximately 20% to 30% and by this appears smaller than in younger patients or in the pooled treatment group from the large tPA trials, in which favorable outcome was found in approximately 35% to 40% of patients.16 This is not surprising because outcome after stroke in general is related to age.79
It is remarkable that with a median NIHSS on admission of 16, the old patients in our study represent a group of very severely affected AIS patients, a trend that was also found in previous reports of thrombolysis in the very old, in which 50% of patients presented with a NIHSS score of
15.15 In line with this, age, severity of neurologic deficit on admission, and outcome were strongly correlated in our study. Age was also identified as a strong independent predictor of outcome after IV-thrombolysis with tPA in our sample, with a 72% increased risk of death and a 25% decrease in the likelihood of reaching a favorable outcome for every 10-year increase in age.
Mortality of thrombolysis in patients 80 years or older (most commonly being rated at 3 months after stroke) ranges between 15% and 30% and is approximately twice as high as in patients below 80 years. It is well documented that mortality after stroke increases with age79 relating to general age-related factors and increased comorbidity in older patients.17 In the European BIOMED study, 3-month mortality without thrombolysis was as high as 45% in patients aged 80 and older.18 Obviously, there is no excess in mortality in old patients receiving thrombolysis.
A presumed increased risk of intracerebral hemorrhage is often cited as the reason to exclude very old patients from thrombolysis. Amyloid angiopathy, a decreased renal tPA clearance, and frail vasculature in the elderly are asserted as explanations for a possibly increased risk of intracerebral hemorrhage.19 In the pooled analysis of the ATLANTIS, NINDS, and ECASS trials, multivariate analysis identified age as an independent predictor of intracerebral hemorrhage.20 In the NINDS study, however, now association between age and severe hemorrhagic complications was found.21 These results were approved in a large survey of 1205 patients treated with IV-tPA in the clinical setting, in which age also was not found to be a predictor of secondary intracerebral hemorrhage.22 In line with our data and previous reports of thrombolysis in patients aged 80 or over, the rate of severe intracerebral hemorrhages was not increased in the groups of very old patients.
There are limitations to our study and results have to be interpreted cautiously. Our data do not result from a randomized, controlled trial of IV-tPA in the very old. The decision whether to treat was left to the treating neurologist, and we cannot exclude that some bias may be introduced by this. It is well conceivable that, especially in the population of the very old, patient selection was performed very carefully. Symptomatic intracranial hemorrhage occurred in only one patient aged 80 or older, therefore any conclusions regarding the risk of SICH are limited. Moreover, part of our study population was treated beyond the 3-hour time window using multimodal computed tomography or magnetic resonance imaging as a selection tool, and we cannot exclude a bias introduced thereby. Additionally, it appears worthwhile remarking that the majority of patients in the very old group was aged 80 to 85 years (n=30), whereas only 8 patients were >85 years. Furthermore, our analysis is restricted to a selected set of covariates (age, sex, onset to treatment time, NIHSS on admission), but there are numerous other parameters that are known to be correlated with outcome after stroke such as blood pressure, blood glucose level, and body temperature on admission, or the presence of arterial hypertension and diabetes mellitus. We cannot exclude that imbalances in these parameters in our patients confound our results.
It is a matter of fact that the Western world faces demographic changes with a continuous increase of the proportion of old and very old people. In Europe, the number of people aged 80 or above is expected to grow by 180% by 2050.23 Therefore, the number of very old acute stroke patients will increase dramatically, and it appears unjustifiable to exclude this increasing patient population a priori from the only approved and effective treatment of acute ischemic stroke. Moreover, there are clear indications that older stroke patients are not resistant to therapy but may well benefit from state-of-the-art acute stroke therapy. In a post hoc subgroup analysis of the NINDS study, the number of patients with a favorable outcome in the treatment group was approximately twice as high (n=117) in the subgroup of patients >75 years than in the placebo group (n=57). This result even exceeds the treatment effect for the younger patients.16
| Conclusion |
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In the future, demographic changes will force stroke physicians to rethink current treatment concepts and to adjust acute stroke treatment to the increasing population of old and very old stroke patients.
| Acknowledgments |
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Received June 27, 2005; revision received August 19, 2005; accepted August 23, 2005.
| References |
|---|
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2. Clark WM, Albers GW, Madden KP, Hamilton S. The rtPA (alteplase) 0- to 6-hour acute stroke trial, part A (A0276g): results of a double-blind, placebo-controlled, multicenter study. Thrombolytic therapy in acute ischemic stroke study investigators. Stroke. 2000; 31: 811816.
3. Clark WM, Wissman S, Albers GW, Jhamandas JH, Madden KP, Hamilton S. Recombinant tissue-type plasminogen activator (Alteplase) for ischemic stroke 3 to 5 hours after symptom onset. The ATLANTIS Study: a randomized controlled trial. Alteplase Thrombolysis for Acute Noninterventional Therapy in Ischemic Stroke. J Am Med Assoc. 1999; 282: 20192026.
4. Hacke W, Kaste M, Fieschi C, Toni D, Lesaffre E, von Kummer R, Boysen G, Bluhmki E, Hoxter G, Mahagne MH. Intravenous thrombolysis with recombinant tissue plasminogen activator for acute hemispheric stroke. The European Cooperative Acute Stroke Study (ECASS). J Am Med Assoc. 1995; 274: 10171025.
5. Hacke W, Kaste M, Fieschi C, von Kummer R, Davalos A, Meier D, Larrue V, Bluhmki E, Davis S, Donnan G, Schneider D, Diez-Tejedor E, Trouillas P. Randomised double-blind placebo-controlled trial of thrombolytic therapy with intravenous alteplase in acute ischaemic stroke (ECASS II). Second EuropeanAustralasian Acute Stroke Study Investigators. Lancet. 1998; 352: 12451251.[CrossRef][Medline] [Order article via Infotrieve]
6. Barber PA, Zhang J, Demchuk AM, Hill MD, Buchan AM. Why are stroke patients excluded from TPA therapy? An analysis of patient eligibility. Neurology. 2001; 56: 10151020.
7. Kolominsky-Rabas PL, Sarti C, Heuschmann PU, Graf C, Siemonsen S, Neundörfer B, Katalinic A, Lang E, Gassmann KG, von Stockert TR. A prospective community-based study of stroke in Germanythe Erlangen Stroke Project (ESPro): incidence and case fatality at 1, 3, and 12 months. Stroke. 1998; 29: 25012506.
8. Bamford J, Sandercock P, Dennis M, Burn J, Warlow C. A prospective study of acute cerebrovascular disease in the community: the Oxfordshire Community Stroke Project198186. 2. Incidence, case fatality rates and overall outcome at one year of cerebral infarction, primary intracerebral and subarachnoid haemorrhage. J Neurol Neurosurg Psychiatry. 1990; 53: 1622.
9. Kammersgaard LP, Jorgensen HS, Reith J, Nakayama H, Pedersen PM, Olsen TS. Copenhagen Stroke Study. Short- and long-term prognosis for very old stroke patients. The Copenhagen Stroke Study. Age Ageing. 2004; 33: 149154.
10. Rother J, Schellinger PD, Gass A, Siebler M, Villringer A, Fiebach JB, Fiehler J, Jansen O, Kucinski T, Schoder V, Szabo K, Junge-Hulsing GJ, Hennerici M, Zeumer H, Sartor K, Weiller C, Hacke W. Kompetenznetzwerk Schlaganfall Study Group. Effect of intravenous thrombolysis on MRI parameters and functional outcome in acute stroke <6 hours. Stroke. 2002; 33: 24382445.
11. Brott T, Adams HP Jr, Olinger CP, Marler JR, Barsan WG, Biller J, Spilker J, Holleran R, Eberle R, Hertzberg V. Measurements of acute cerebral infarction: a clinical examination scale. Stroke. 1989; 20: 864870.
12. van Swieten JC, Koudstaal PJ, Visser MC, Schouten HJ, van Gijn J. Interobserver agreement for the assessment of handicap in stroke patients. Stroke. 1988; 19: 604607.
13. Tanne D, Gorman MJ, Bates VE, Kasner SE, Scott P, Verro P, Binder JR, Dayno JM, Schultz LR, Levine SR; The tPA Stroke Survey Group. Intravenous tissue plasminogen activator for acute ischemic stroke in patients aged 80 years and older. The tPA Stroke Survey experience. Stroke. 2000; 31: 370375.
14. Demaerschalk B, Merino JG, Tamayo A, Wong EH, Devasenapathy A, OCallaghan C, Kertesz A, Young GB, Spence JD, Hachinsky V. Intravenous tissue plasminogen activator for acute ischemic stroke in patients
80 years old: The London, Canada experience. Stroke. 2001; 32: I368369. (Abstract).
15. Simon JS, Sandler DL, Warwick Pexman JH, Hill MD, Buchan AM; for the Calgary Stroke Programme. Is intravenous recombinant tissue plasminogen activator (rt-PA) safe for use in patients over 80 years old with acute ischmaemic stroke?The Calgary experience. Age Ageing. 2004; 33: 143149.
16. The NINDS t-PA Stroke Study Group. Generalized efficacy of t-PA for acute stroke. Subgroup analysis of the NINDS t-PA Stroke trial. Stroke. 1997; 28: 21192125.
17. Sharma JC, Fletcher S, Vassallo M. Strokes in the elderlyhigher acute and 3-month mortalityan explanation. Cerebrovasc Dis. 1999; 9: 29.[Medline] [Order article via Infotrieve]
18. Di Carlo A, Lamassa M, Pracucci G, Basile AM, Trefoloni G, Vanni P, Wolfe CD, Tilling K, Ebrahim S, Inzitari D. Stroke in the very old: clinical presentation and determinants of 3-month functional outcome: A European perspective. European BIOMED Study of Stroke Care Group. Stroke. 1999; 30: 23132319.
19. Sloan MA, Price TA, Petito CK, Randall AMY, Solomon RE, Terrin ML, Gore J, Collen D, Kleiman N, Feit F, Babb J, Herman M, Roberts WC, Sopko G, Bovill E, Forman S, Knatterud GL; for the TIMI Investigators. Clinical features and pathogenesis of intracerebral hemorrhage after rt-PA and heparin therapy for acute myocardial infarction: the Thrombolysis in Myocardial Infarction (TIMI) II Pilot and Randomized Clinical Trial combined experience. Neurology. 1995; 45: 649658.
20. Hacke W, Donnan G, Fieschi C, Kaste M, von Kummer R, Broderick JP, Brott T, Frankel M, Grotta JC, Haley EC Jr, Kwiatkowski T, Levine SR, Lewandowski C, Lu M, Lyden P, Marler JR, Patel S, Tilley BC, Albers G, Bluhmki E, Wilhelm M, Hamilton S; ATLANTIS Trials Investigators; ECASS Trials Investigators; NINDS rt-PA Study Group Investigators. Association of outcome with early stroke treatment: pooled analysis of ATLANTIS, ECASS, and NINDS rt-PA stroke trials. Lancet. 2004; 363: 768774.[CrossRef][Medline] [Order article via Infotrieve]
21. The NINDS t-PA Stroke Study Group. Intracerebral hemorrhage after intravenous t-PA therapy for ischemic stroke. Stroke. 1997; 28: 21092118.
22. Tanne D, Kasner SE, Demchuk AM, Koren-Morag N, Hanson S, Grond M, Levine SR. Markers of increased risk of intracerebral hemorrhage after intravenous recombinant tissue plasminogen activator therapy for acute ischemic stroke in clinical practice: the Multicenter rt-PA Stroke Survey. Circulation. 2002; 9: 16791685.
23. Green PaperFaced with demographic change, a new solidarity between the generations. Communication from the European Commission, COM. 2005;94. Available at: http://europa.eu.int/comm/employment_social/news/2005/mar/demog_gp_en.html. Accessed October 4, 2005.
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