194 research outputs found

    Topographic and Clinical Analysis of Anterior Circulation Strokes - A Study of 82 Cases.

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    Stroke is the most common life threatening neurological disease and the third leading cause of death after heart disease and cancer, accounting for 1 of every 15 deaths. In the elderly, the segment of the population in which stroke occurs most frequently, it is the leading cause of disability requiring long term institutionalization. Faced with an acute stroke, the physician must determine the cause, estimate the severity, consider the possibility of progression or recurrence and seek ways of stabilizing or reversing it. Investigations should be designed to assist clinicians in subcategorizing patients at three specific levels (1) separating strokes from non strokes such as cerebral tumours and subdrual hematoma (2) distinguishing hemorrhage from infarction and (3) identifying specific pathophysiological sub types of cerebral infarction. Because the possibility of worsening or recurrence is paramount, speedy efforts should be made to arrive at a diagnosis of stroke mechanism using this approach. The ideal test should be inexpensive, noninvasive, accessible, accurate and informative. 82 patients, both male and female were included in the study satisfying the defined inclusion and exclusion criteria. Analysis of their CT brains resulted in the following conclusions. 1. Infarcts in the anterior circulation fit into 6 different patterns namely a. Large territorial or cortical infarcts, b. Large / discrete subcortical infarcts involving he striatocapsular and corona radiata region. c. Large fragmentary infarcts in the MCA/ACA territory, d. Small fragmentary infarcts in the MCA/ACA territory,e. Cortical borderzone infarcts and subcortical borderzone i.e linear corona radiata and linear centrum semiovale infarcts, f. Discrete corona-radiata and discrete centrum semiovale infarcts, Among the 6, pattern 5 or border zone infarcts are most common. 2. Two or more of these patterns can co-exist, though there are no definite combinations. Combinations vary depending on the proposed pathophysiology of stroke. 3. Cortical borderzone infarcts usually thought to be due to haemodynamic failure can be embolic in origin too. 4. Heart disease can result in infarcts in any pattern or their combinations thereof. 5. Pattern1 cortical infarcts and pattern 2 large striatocapsular infarcts show sudden peak clinically with a subsequent static or regressive course. 6. Progressive strokes are usually associated with combinations of different patterns in CT Brain 7. Sensorium at onset is associated more with the size of the infarct than with a pattern of infarct. It is difficult to correctly guess the artery involved in anterior circulation strokes from the pattern of CT Brain involvement and the clinical course, though certain patterns do indicate possible aetiologies

    Leptomeningeal collaterals are associated with modifiable metabolic risk factors

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    We seek to identify potentially modifiable determinants associated with variability in leptomeningeal collateral status in patients with acute ischemic stroke

    Rapid alteplase administration improves functional outcomes in patients with stroke due to large vessel occlusions

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    Background and Purpose: We report the relation of onset-to-treatment time and door-to-needle time with functional outcomes and mortality among patients with ischemic stroke with imaging-proven large vessel occlusion treated with intravenous alteplase. Methods: Individual patient-level data from the HERMES (Highly Effective Reperfusion Evaluated in Multiple Endovascular Stroke Trials) collaboration were pooled from 7 trials that randomized patients to mechanical thrombectomy added to best medical therapy versus best medical therapy alone. Analysis was restricted to patients who received alteplase directly at the endovascular hospital. The primary outcome was disability defined on the modified Rankin Scale at 3 months. Results: Among 601 patients, mean age was 66.0 years (SD, 13.9), 50% were women, and median National Institutes of Health Stroke Scale score was 17. Onset-to-treatment time was median 125 minutes (interquartile range, 90–170). Door-to-treatment time was median 38 minutes (interquartile range, 26–55). Each 60-minute onset-to-treatment time delay was associated with greater disability at 90 days; the odds of functional independence (modified Rankin Scale, 0–2) at 90 days was 0.82 (95% CI, 0.66–1.03). With each 60-minute delay in door-to-needle time; the odds of functional independence was 0.55 (95% CI, 0.37–0.81) at 90 days. The absolute decline in the rate of excellent outcome (modified Rankin Scale, 0–1 at 90 days) was 20.3 per 1000 patients treated per 15-minute delay in door-to-needle time. The adjusted absolute risk difference for a door-to-needle time <30 minutes versus 30 to 60 minutes was 19.3% for independent outcome (number-needed-to-treat ≈5 to gain 1 additional good outcome). Symptomatic intracranial hemorrhage occurred in 3.4% of patients, without a significant time dependency: odds ratio, 0.74 (95% CI, 0.43–1.28). Conclusions: Faster intravenous thrombolysis delivery is associated with less disability at 3 months among patients with large vessel occlusion

    Efficacy of endovascular thrombectomy in patients with M2 segment middle cerebral artery occlusions: meta-analysis of data from the HERMES Collaboration

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    Background: The Society of Neurointerventional Surgery revised its operational definition of emergent large vessel occlusion (ELVO) recently to include proximal M2 segment middle cerebral artery (MCA) occlusions. We sought to assess the benefit of endovascular thrombectomy (EVT) over best medical care for M2 segment MCA occlusion. Methods: Patient level data from trials in the HERMES Collaboration were included. The HERMES core laboratory identified patients with M2 segment MCA occlusions and further classified them as proximal versus distal, anterior versus posterior division, and dominant versus co-dominant versus non-dominant. Primary outcome was modified Rankin Scale (mRS) score 0–2 at 90 days. Secondary outcomes were modified Thrombolysis in Cerebral Infarction (mTICI) rates at end of procedure, 90-day mRS shift, 90-day mRS 0–1, 24 hours National Institute of Health Stroke Scale (NIHSS) score 0–2, symptomatic intracerebral hemorrhage (ICH), and death. Results: 130 patients with M2 MCA (proximal location n=116 vs distal n=14, anterior division n=72 vs posterior n=58, dominant n=73 vs co-dominant n=50 vs non-dominant n=7) were included. Successful reperfusion (mTICI 2b or 3) among those undergoing EVT was seen in 59.2% of patients. Treatment effect favored EVT (adjusted OR 2.39, 95% CI 1.08 to 5.28, p=0.03) for 90-day mRS 0–2 (58.2% EVT vs 39.7% control). Direction of benefit favored EVT for other outcomes. Treatment effect favoring EVT was maximal in patients with proximal M2 segment MCA occlusions (n=116, adjusted OR 2.68, 95% CI 1.13 to 6.37) and in dominant M2 segment MCA occlusions (n=73, adjusted OR 4.08, 95% CI 1.08 to 15.48). No sICH (0%) was observed in patients treated with EVT compared with five (7.9%) in the control arm. Conclusion: Patients with proximal M2 segment MCA occlusions eligible for EVT trial protocols benefited from EVT

    Confirmatory study of time-dependent computed tomographic perfusion thresholds for use in acute ischemic stroke

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    Background and Purpose: Computed tomographic perfusion (CTP) thresholds associated with follow-up brain infarction may differ by time from symptom onset to imaging and reperfusion. We confirm CTP thresholds over time to imaging and reperfusion in patients with acute ischemic stroke from the HERMES collaboration (Highly Effective Reperfusion Evaluated in Multiple Endovascular Stroke Trials) data. Methods: Patients with occlusion on CT angiography were acutely imaged with CTP. Noncontrast CT and magnetic resonance-diffusion weighted imaging at 24 to 48 hours defined follow-up infarction. Reperfusion was assessed on conventional angiogram. Tmax, cerebral blood flow (CBF), and cerebral blood volume maps were derived from delay-insensitive CTP postprocessing. These parameters were analyzed using receiver operator characteristics to derive optimal thresholds based on time from stroke onset-to-CTP or to reperfusion. ANOVA and linear regression were used to test whether the derived CTP thresholds were different by time. Results: One hundred thirty-seven patients were included. Tmax thresholds of >15.7 s and >15.8 s and absolute CBF thresholds of <8.9 and <7.5 mL·min−1·100 g−1 for gray matter and white matter respectively were associated with infarct if reperfusion was achieved <90 minutes from CTP with stroke onset-to-CTP <180 minutes. The discriminative ability of cerebral blood volume was modest. There were no statistically significant relationships between stroke onset-to-CTP time and Tmax, CBF, and cerebral blood volume thresholds (all P>0.05). A statistically significant relationship was observed between CTP-to-reperfusion time and the optimal thresholds for Tmax (P<0.001) and CBF (P<0.001). Similar but more modest relationship was noted for onset-to-reperfusion time and optimal thresholds for CBF (P≤0.01). Conclusions: CTP thresholds based on stroke onset and imaging time and taking into account time needed for reperfusion may improve infarct prediction in patients with acute ischemic stroke

    Advance consent in acute stroke trials: survey of Canadian Research Ethics Board chairs

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    dvance consent could allow individuals at high risk of stroke to provide consent before they might become eligible for enrollment in acute stroke trials. This survey explores the acceptability of this novel technique to Canadian Research Ethics Board (REB) chairs that review acute stroke trials. Responses from 15 REB chairs showed that majority of respondents expressed comfort approving studies that adopt advance consent. There was no clear preference for advance consent over deferral of consent, although respondents expressed significant concern with broad rather than trial-specific advance consent. These findings shed light on the acceptability of advance consent to Canadian ethics regulators
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