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The Outcome of Patients with Mild Stroke Improves after Treatment with Systemic Thrombolysis

  • Xabier Urra,

    Affiliations Functional Unit of Cerebrovascular Diseases, Hospital Clínic, Barcelona, Spain, Institut d’Investigacions Biomediques August Pi i Sunyer, Barcelona, Spain

  • Helena Ariño,

    Affiliation Functional Unit of Cerebrovascular Diseases, Hospital Clínic, Barcelona, Spain

  • Laura Llull,

    Affiliation Functional Unit of Cerebrovascular Diseases, Hospital Clínic, Barcelona, Spain

  • Sergio Amaro,

    Affiliations Functional Unit of Cerebrovascular Diseases, Hospital Clínic, Barcelona, Spain, Institut d’Investigacions Biomediques August Pi i Sunyer, Barcelona, Spain

  • Víctor Obach,

    Affiliation Functional Unit of Cerebrovascular Diseases, Hospital Clínic, Barcelona, Spain

  • Álvaro Cervera,

    Affiliations Functional Unit of Cerebrovascular Diseases, Hospital Clínic, Barcelona, Spain, Institut d’Investigacions Biomediques August Pi i Sunyer, Barcelona, Spain

  • Ángel Chamorro

    achamorro@clinic.ub.es

    Affiliations Functional Unit of Cerebrovascular Diseases, Hospital Clínic, Barcelona, Spain, Institut d’Investigacions Biomediques August Pi i Sunyer, Barcelona, Spain, Medicine Department, School of Medicine, Universitat de Barcelona, Barcelona, Spain

Abstract

Introduction

In up to one third of patients with mild stroke suitable to receive systemic thrombolysis the treatment is not administered because the treating physicians estimate a good spontaneous recovery. However, it is not settled whether the fate of these patients is equivalent to those who are thrombolysed.

Methods

We analyzed 203 consecutive patients (134 men and 69 women, mean age 69±14 years) without premorbid disability and a NIHSS score ≤5 at admission [median 3 (IQR 2–4)]. Intravenous thrombolysis was administered within 4.5 hours from stroke onset (n = 119), or it was withheld (n = 84) whenever the treating physician predicted a spontaneous recovery. The baseline risk factors, clinical course, infarction volume, bleeding complications, and functional outcome at 3 months were analyzed and declared to a Web-based registry which was accessible to the local Health Authorities.

Results

Expectedly, not thrombolysed patients had the mildest strokes at admission [median 2 (IQR 1–3.75)]. At day 2 to 5, the infarct volume on DWI-MRI was similar in both groups. There were no symptomatic cerebral bleedings in the study. An ordinal regression model adjusted for baseline stroke severity showed that thrombolysis was associated with a greater proportion of patients who shifted down on the modified Rankin Scale score at 3 months (OR 2.66; 95% CI 1.49–4.74, p = 0.001).

Conclusions

Intravenous thrombolysis seems to be safe in patients with mild stroke and may be associated with improved outcome compared with untreated patients. These results support the evaluation of the efficacy of intravenous thrombolysis in mild stroke patients in randomized clinical trials.

Introduction

Current guidelines offer no specific recommendations on the need of thrombolysis in stroke patients with mild or rapidly improving symptoms [1], [2]. However, this issue is of great clinical interest as up to half of ischemic stroke patients manifest mild or rapidly improving symptoms at clinical onset [3], [4], and around 30% of these patients are not treated with thrombolytic agents on the assumption that they may achieve an excellent recovery spontaneously [5][7]. However, according to some reports [5], [6], [8][11], up to one third of these patients fail to recover as much as it was anticipated by the responsible physician, and persist having symptoms as the result from a delayed growth of the infarction.

The criteria used to define mild or rapidly improving symptoms are also weak and may encounter rather loose terms such as isolated sensory loss, ataxia, facial weakness, or dysarthria [12]. In most research studies, clinical deficits measured on the National Institutes of Health Stroke Scale (NIHSS) score of up to 3 or 5 were the most common definitions of mild stroke [13].

We analyzed the clinical and radiological course of patients with mild or rapidly improving stroke on admission in which the decision to administer intravenous recombinant tissue plasminogen activator (IV rt-PA) within 4.5 h of stroke onset was judged by the responsible physician according to his prediction of spontaneous recovery.

Methods

Ethics Statement

The study protocol was approved by the Clinical Research Ethics Committee of the Hospital Clínic de Barcelona (CEIC Hospital Clínic) and the patients or their legal representatives signed a written informed consent if age was over 80 years, or treatment was to be initiated >3 h of stroke onset.

Patients

All consecutive patients with ischemic stroke admitted at our institution from January 2009 to May 2012 which fulfilled all the following criteria: 1/delay from the onset of symptoms to treatment less than 4.5 h; 2/admission or post-imaging NIHSS score ≤5; 3/premorbid modified Rankin Scale (mRS) ≤1; and 4/no absolute contraindications to IV rt-PA.

At our center, the decision to administer IV rt-PA in patients with mild strokes depends on the estimated probability of achieving a full recovery spontaneously. Accordingly, patients with very low NIHSS scores on admission are less likely to receive IV rt-PA than patients with higher NIHSS scores.

All the study participants were admitted at an intermediate care Stroke Unit and managed by certified stroke neurologists following the European Stroke Organization Guidelines [2]. The NIHSS score was assessed at hospital arrival and after baseline brain imaging (pretreatment score), at day 1, at day 7 or discharge, and at day 90. The functional outcome was assessed with the mRS at day 90 in patients that pertained to the geographical area of coverage of the institution (450.000 inhabitants). In the remainder, the mRS at hospital discharge was carried forward and used in the primary efficacy analysis. Descriptive statistics were performed to evaluate the similarities between the patients assessed at discharge and/or at 3 months. The qualifying symptoms were classified according to the Oxfordshire Stroke Project Classification (OCSP) and the stroke etiology was classified according to the Trial of Org 10172 in Acute Stroke Treatment (TOAST) criteria after a complete diagnostic workup [14]. In addition to a baseline CT scan all patients had a head CT scan within 24 h of admission in which hemorrhagic conversion was graded according to ECASS criteria as hemorrhagic infarction (HI) 1 and 2, parenchymal hemorrhage (PH) 1 and 2, and remote PH (PHr) 1 and 2 [15]. Symptomatic intracranial hemorrhage (sICH) was defined as any bleeding associated with an increment of at least 4 points in the NIHSS score. The volume of infarction was assessed on DWI-MRI between day 2 and 5 of stroke onset using AMIRA software (Visage Imaging, Inc., San Diego, CA). The brain infarctions were further categorized as lacunar, territorial or watershed [16].

Data were prospectively collected in a local database that included demographics, risk factors, main laboratory results, neuroimaging, concomitant therapies, clinical course, and functional outcome. In addition, data were declared to a Web-based registry that satisfied all legal requirements for protection of personal data and was monitored by the Catalan Health Department [17].

Statistics

Normal distribution of all studied variables was assessed, and continuous variables were compared with Student’s t-test, ANOVA, Mann-Whitney or Kruskal-Wallis tests as appropriate. Correlations were assessed with Spearman coefficients, and categorical variables were compared with the Fisher’s exact tests. Ordinal regression analysis was used to increase the statistical power of the study [18], and analyze the independent effect of thrombolytic therapy on functional outcome at 3 months. As it was anticipated that patients not treated with thrombolysis would have the mildest strokes, the pretreatment NIHSS score was forced a priori into the model. In addition, exploratory analyses were also performed and which included the variables associated to outcome (p<0.2) on the univariate analysis and the variables with significant differences between treatment groups at baseline. The level of significance was established at a two-tailed value of p<0.05. All tests were performed using SPSS version 20.0.

Results

During the 40 months of the study, 2560 acute stroke patients were assessed including 875 patients admitted within 4.5 h of clinical onset. Of those, 313 patients had a NIHSS score <5 on admission but 110 patients were not included in the study as they had a pre-morbid mRS >1 (n = 91), absolute contraindications for IV rt-PA (n = 13) or received endovascular therapy (n = 6). Therefore, the study included 203 patients (8% of the total population) that received IV rt-PA (119 patients), or standard care only (n = 84). As previously anticipated, the thrombolysed patients had a greater NIHSS score than the untreated patients at baseline (Table 1).

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Table 1. General characteristics of the study population according to the treatment group.

https://doi.org/10.1371/journal.pone.0059420.t001

The patients treated with IV rt-PA showed higher NIHSS scores at day 1, and at day 7 or discharge, but these differences did not persist at day 90 (Table 1). In 149 patients in whom a DWI-MRI was performed between day 2 and 5, the volume of infarction did not differ between patients allocated to IV rt-PA or to standard care (Table 1). The pattern of infarctions observed in order of occurrence on these patients included territorial infarcts (50%), normal brain MRIs (30%), lacunar infarctions (18%), and watershed infarctions (1%). As shown in Table 1 there were more patients with a normal MRI in patients receiving standard care only, but the differences were not significant. The overall rate of hemorrhagic complications in the study population was very low, including 5.2% of asymptomatic ICH, and 0% sICHs (95% CI 0–3.13% for treated patients and 0–4.37% for not treated patients). There were two cases of HI1 in non-thrombolysed patients and two cases of PH1, one rPHr1, one HI2 and four HI1 cases in thrombolysed patients.

Outcome

In the study, 53 of 203 patients referred from other centers were assessed only at hospital discharge (27 treated with thrombolysis and 26 not treated, p = 0.247). The baseline traits of these patients did not differ from the patients with 3 months follow up (data not shown). At 3 months, 167 (82%) patients had excellent outcome (mRS 0 to 1). As shown in Figure 1, there were no significant differences in the proportion of patients that reached excellent outcome (83% in patients that received IV rt-PA versus 81% in patients that received standard care).

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Figure 1. Distribution of modified Rankin Scales scores at 3 months in patients with mild stroke and treated or not with intravenous thrombolytic therapy.

https://doi.org/10.1371/journal.pone.0059420.g001

In the ordinal regression analysis, we found a greater proportion of patients who shifted down on the modified Rankin Scale score at 3 months in the thrombolysed group than in patients receiving standard care (OR 2.66; 95% CI 1.49–4.74, p = 0.001). The association also was significant (OR 2.02; 95% CI 1.02–3.98; p = 0.042) in models adjusted for the effect of all variables associated to mRS score at 3 months on univariate comparison and for variables with differences at baseline: pretreatment NIHSS (OR 0.77; 95% CI 0.67–0.89; p<0.001), age (OR 0.97; 95% CI 0.95–1.00; p = 0.023), prior mRS (OR 0.35; 95% CI 0.17–0.70; p = 0.003), dyslipidemia (OR 0.62; 95% CI 0.33–1.20; p = 0.157), coronary artery disease (OR 0.50; 95% CI 0.24–1.05; p = 0.068), hypertension (OR 0.78; 95% CI 0.40–1.52; p = 0.468), diabetes (OR 0.64; 95% CI 0.30–1.36; p = 0.243), systolic blood pressure (OR 0.99; 95% CI 0.98–1.00; p = 0.128) and glucose levels (OR 1.00; 95% CI 0.99–1.01; p = 0.625). In exploratory analysis, there was also a trend in the same direction for thrombolysis (OR 1.85; 95% CI 0.90–3.86; p = 0.100) after excluding patients without day 90 visit.

Discussion

The value of systemic thrombolysis in patients with mild or rapidly improving stroke is not settled. A post-hoc analysis of very few patients with mild stroke assessed in the NINDS trial suggested some benefit [19], and a subgroup analysis of the IST-3 trial did not show a significant effect of rt-PA in patients with mild stroke [20]. This study confirmed that in regular practice a significant proportion of patients with mild stroke are not deemed suitable to be thrombolysed. However, the major new finding of the study was that the administration of IV rt-PA was independently associated with a greater proportion of patients shifting down on the modified Rankin Scale score at 3 months compared with patients receiving standard care. Importantly, the association was obtained regardless that the patients who did not receive IV rt-PA had greater chances of recovery as they were in better neurological condition at baseline [21], [22]. Indeed, this benign clinical course influenced the treating physician who withheld the therapy to avoid unnecessary risks in patients likable to make a full recovery spontaneously. Therefore, it is very likely that the true beneficial effects of IV rt-PA in patients with mild stroke might be even stronger.

The rate of excellent outcome was higher in this study than in previous reports of patients with minor stroke where the functional outcome was evaluated only at hospital discharge [8], [10], [11]. Most likely, the good results of the current study obeyed to the longer duration of follow up, the admission and management of all patients into a stroke dedicated unit, and the exclusion of patients with any degree of premorbid disability.

The study also highlighted the safety profile of IV rt-PA in patients with mild or rapidly improving stroke as none of the actively treated patients suffered symptomatic bleeding complications. Therefore, any future clinical trial designed to compare the value of rt-PA versus standard care in patients with mild stroke must calculate the inclusion of a very large database.

While the patients included in this study represented only 8% of all the stroke admissions at our Stroke Unit, they also represented 24% of all the ischemic stroke patients which are candidates to receive IV rt-PA within 4.5 h. Therefore, these results may have important clinical implications for many of these patients are currently not thrombolysed in regular practice on the assumption of their benign natural course. As the study showed, 19% of these patients failed to achieve a full recovery. Yet, while the study confirmed a high rate of excellent recovery in many of these patients, it also suggested that the benefits were enhanced after thrombolysis.

The main limitation of the study was its non-randomized design although several of its traits minimized the risk of bias. Thus, the effect of the lower stroke severity on the untreated group was minimized by the appropriate adjustment of the NIHSS score in multivariate analysis. The validity of the study was also supported by the prospective collection of the data and its storage into a Web-based registry owned and monitored by the Catalan Health authorities [17]. Therefore, our results represented all the admissions at our institution that fulfilled the preestablished entry criteria. Alternatively, most of previous cohorts described the outcome of either treated [23][25] or not treated patients [6][10], or used historical controls [26].

Currently, a randomized controlled clinical trial is being planned to evaluate the role of thrombolysis in patients with mild stroke [27]. In the meantime, our findings may be very informative for the treating physicians as they support a favorable benefit/risk ratio of thrombolysis in patients with minor stroke.

Conclusions

Patients with mild or rapidly improving stroke seem to benefit from a timely administration of IV rt-PA. More patients receiving IV rt-PA shift down on the mRS at 3 months compared to patients receiving standard care. The risk of serious bleeding complications is very low in these patients while the probability of incomplete recovery is not negligible in untreated patients. While awaiting a definitive answer from a randomized clinical trial our results support the use of IV rt-PA in patients with mild or rapidly improving stroke when there are no contraindications.

Acknowledgments

We thank Dr Martha Vargas for all her work in collecting and introducing the information in the Web based registry of stroke patients.

Author Contributions

Collected data: XU HA LL SA VO A. Cervera. Reviewed the manuscript: LL SA VO A. Cervera. Conceived and designed the experiments: XU HA VO A. Cervera. Analyzed the data: XU HA SA A. Chamorro. Contributed reagents/materials/analysis tools: XU HA LL SA VO A. Cervera A. Chamorro. Wrote the paper: XU HA A. Chamorro.

References

  1. 1. Adams HP Jr, del Zoppo G, Alberts MJ, Bhatt DL, Brass L, et al. (2007) Guidelines for the early management of adults with ischemic stroke: a guideline from the American Heart Association/American Stroke Association Stroke Council, Clinical Cardiology Council, Cardiovascular Radiology and Intervention Council, and the Atherosclerotic Peripheral Vascular Disease and Quality of Care Outcomes in Research Interdisciplinary Working Groups: the American Academy of Neurology affirms the value of this guideline as an educational tool for neurologists. Stroke 38: 1655–1711.
  2. 2. European Stroke Organisation (ESO) Executive Committee; ESO Writing Committee (2008) Guidelines for management of ischaemic stroke and transient ischaemic attack 2008. Cerebrovasc Dis 25: 457–507.
  3. 3. Fonarow GC, Saver JL, Smith EE, Broderick JP, Kleindorfer DO, et al. (2012) Relationship of National Institutes of Health Stroke Scale to 30-day mortality in medicare beneficiaries with acute ischemic stroke. J Am Heart Assoc 1: 42–50.
  4. 4. Dhamoon MS, Moon YP, Paik MC, Boden-Albala B, Rundek T, et al. (2009) Long-term functional recovery after first ischemic stroke: the Northern Manhattan Study. Stroke 40: 2805–2811.
  5. 5. Barber PA, Zhang J, Demchuk AM, Hill MD, Buchan AM (2001) Why are stroke patients excluded from rtPA therapy? An analysis of patient eligibility. Neurology 56: 1015–1020.
  6. 6. Khatri P, Conaway MR, Johnston KC, Acute Stroke Accurate Prediction Study (ASAP) Investigators (2012) Ninety-day outcome rates of a prospective cohort of consecutive patients with mild ischemic stroke. Stroke 43: 560–562.
  7. 7. Leira EC, Ludwig BR, Gurol ME, Torner JC, Adams HP Jr (2012) The types of neurological deficits might not justify withholding treatment in patients with low total National Institutes of Health Stroke Scale scores. Stroke 43: 782–786.
  8. 8. Smith EE, Abdullah AR, Petkovska I, Rosenthal E, Koroshetz WJ, et al. (2005) Poor outcomes in patients who do not receive intravenous tissue plasminogen activator because of mild or improving ischemic stroke. Stroke 36: 2497–2499.
  9. 9. Nedeltchev K, Schwegler B, Haefeli T, Brekenfeld C, Gralla J, et al. (2007) Outcome of stroke with mild or rapidly improving symptoms. Stroke 38: 2531–2535.
  10. 10. Smith EE, Fonarow GC, Reeves MJ, Cox M, Olson DM, et al. (2011) Outcomes in mild or rapidly improving stroke not treated with intravenous recombinant tissue-type plasminogen activator: findings from get with the guidelines-stroke. Stroke 42: 3110–3115.
  11. 11. Rajajee V, Kidwell C, Starkman S, Ovbiagele B, Alger JR, et al. (2006) Early MRI and outcomes of untreated patients with mild or improving ischemic stroke. Neurology 67: 980–984.
  12. 12. National Institute of Neurological Disorders Stroke rt-PA Stroke Study Group (2005) Recombinant tissue plasminogen activator for minor strokes: the National Institute of Neurological Disorders and Stroke rt-PA Stroke Study experience. Ann Emerg Med 46: 243–252.
  13. 13. Willey JZ, Khatri P, Khoury JC, Merino JG, Ford AL, et al.. (2011) Variability in the use of intravenous thrombolysis for mild stroke: experience across the SPOTRIAS network. J Stroke Cerebrovasc Dis. doi: 10.1016/j.jstrokecerebrovasdis.2011.09.005.
  14. 14. Adams HP, Bendixen BH, Kappelle LJ, Biller J, Love BB, et al. (1993) Classification of subtype of acute ischemic stroke. Definitions for use in a multicenter clinical trial. TOAST. Trial of Org 10172 in Acute Stroke Treatment. Stroke 24: 35–41.
  15. 15. Hacke W, Kaste M, Fieschi C, von Kummer R, Davalos A, et al. (1998) Randomised double-blind placebo-controlled trial of thrombolytic therapy with intravenous alteplase in acute ischaemic stroke (ECASS II). Second European-Australasian Acute Stroke Study Investigators. Lancet 352: 1245–1251.
  16. 16. Wityk RJ, Goldsborough MA, Hillis A, Beauchamp N, Barker PB, et al. (2001) Diffusion- and perfusion-weighted brain magnetic resonance imaging in patients with neurologic complications after cardiac surgery. Arch Neurol 58: 571–576.
  17. 17. Abilleira S, Davalos A, Chamorro A, Alvarez-Sabín J, Ribera A, et al. (2011) Outcomes of intravenous thrombolysis after dissemination of the stroke code and designation of new referral hospitals in Catalonia: the Catalan Stroke Code and Thrombolysis (Cat-SCT) Monitored Study. Stroke 42: 2001–2006.
  18. 18. Bath PM, Lees KR, Schellinger PD, Altman H, Bland M, et al. (2012) Statistical analysis of the primary outcome in acute stroke trials. Stroke 43: 1171–1178.
  19. 19. Khatri P, Kleindorfer DO, Yeatts SD, Saver JL, Levine SR, et al. (2010) Strokes with minor symptoms: an exploratory analysis of the National Institute of Neurological Disorders and Stroke recombinant tissue plasminogen activator trials. Stroke 41: 2581–2586.
  20. 20. IST-3 collaborative group, Sandercock P, Wardlaw JM, Lindley RI, Dennis M, et al (2012) The benefits and harms of intravenous thrombolysis with recombinant tissueplasminogen activator within 6 h of acute ischaemic stroke (the third international stroke trial [IST-3]): a randomised controlled trial. Lancet 379: 2352–2363.
  21. 21. Sun MC, Lai TB (2011) Initial stroke severity is the major outcome predictor for patients who do not receive intravenous thrombolysis due to mild or rapidly improving symptoms. ISRN Neurol: 947476.
  22. 22. Kasner SE (2006) Clinical interpretation and use of stroke scales. Lancet Neurol 5: 603–612.
  23. 23. Helsinki Stroke Thrombolysis Registry Group (2012) Intravenous thrombolysis for acute ischemic stroke patients presenting with mild symptoms. Int J Stroke. doi: 10.1111/j.1747–4949.2012.00808.x.
  24. 24. Kohrmann M, Nowe T, Huttner HB, Engelhorn T, Struffert T, et al. (2009) Safety and outcome after thrombolysis in stroke patients with mild symptoms. Cerebrovasc Dis 27: 160–166.
  25. 25. Baumann CR, Baumgartner RW, Gandjour J, Budingen HC, Siegel AM, et al. (2006) Good outcomes in ischemic stroke patients treated with intravenous thrombolysis despite regressing neurological symptoms. Stroke 37: 1332–1333.
  26. 26. Hassan AE, Hassanzadeh B, Tohidi V, Kirmani JF (2010) Very mild stroke patients benefit from intravenous tissue plasminogen activator without increase of intracranial hemorrhage. South Med J 103: 398–402.
  27. 27. Khatri P, Khoury JC, Alwell K, Moomaw CJ, Kissela BM, et al. (2011) The public health impact of an effective acute treatment for mild ischemic strokes. Stroke 42: e66.