Changing stroke rehab and research worldwide now.Time is Brain! trillions and trillions of neurons that DIE each day because there are NO effective hyperacute therapies besides tPA(only 12% effective). I have 523 posts on hyperacute therapy, enough for researchers to spend decades proving them out. These are my personal ideas and blog on stroke rehabilitation and stroke research. Do not attempt any of these without checking with your medical provider. Unless you join me in agitating, when you need these therapies they won't be there.

What this blog is for:

My blog is not to help survivors recover, it is to have the 10 million yearly stroke survivors light fires underneath their doctors, stroke hospitals and stroke researchers to get stroke solved. 100% recovery. The stroke medical world is completely failing at that goal, they don't even have it as a goal. Shortly after getting out of the hospital and getting NO information on the process or protocols of stroke rehabilitation and recovery I started searching on the internet and found that no other survivor received useful information. This is an attempt to cover all stroke rehabilitation information that should be readily available to survivors so they can talk with informed knowledge to their medical staff. It lays out what needs to be done to get stroke survivors closer to 100% recovery. It's quite disgusting that this information is not available from every stroke association and doctors group.

Monday, December 5, 2022

Endovascular treatment for anterior circulation large-vessel occlusion ischemic stroke with low ASPECTS: a systematic review and meta-analysis

Solve the damn problem, don't just tell us it exists. Useless. The whole point of stroke research is to get survivors recovered. This did nothing to that goal.

Endovascular treatment for anterior circulation large-vessel occlusion ischemic stroke with low ASPECTS: a systematic review and meta-analysis


Abstract

Background:

Endovascular treatment (EVT) for acute ischemic stroke (AIS) patients presenting with Alberta Stroke Program Early CT Score (ASPECTS) 0–5 has not yet proven safe and effective by clinical trials.

Objectives:

The aim of the study was to assess whether EVT in AIS patients presenting with low ASPECTS is beneficial.

Design:

Systematic review and meta-analysis of available studies in accordance with the PRISMA statement.

Data sources and Methods:

We have searched MEDLINE, the Cochrane Central Register of Controlled Trials, and reference lists of articles published until 28 May 2022 with the aim to calculate (1) modified Rankin scale (mRS) score 0–3 at 3 months, (2) mRS score 0–2 at 3 months, (3) symptomatic intracranial hemorrhage (sICH), and (3) mortality at 3 months.

Results:

Overall, 24 eligible studies were included in the meta-analysis, comprising a total of 2539 AIS patients with ASPECTS 0–5 treated with EVT. The pooled proportion of EVT-treated patients achieving mRS 0–3 at 3 months was calculated at 38.4%. The pooled proportion of EVT-treated patients achieving mRS 0–2 at 3 months was 25.7%. Regarding safety outcomes, sICH occurred in 12.8% of patients. The 3-month pooled mortality was 30%. In pairwise meta-analysis, patients treated with EVT had a higher likelihood of achieving mRS 0–3 at 3 months compared with patients treated with best medical therapy (BMT, OR: 2.41). sICH occurred more frequently in EVT-treated patients compared with the BMT-treated patients (OR: 2.30). Mortality at 3 months was not different between the two treatment groups (OR: 0.71).

Conclusion:

EVT may be beneficial(NOT GOOD ENOUGH! Solve the problem, don't give us weasel words!) for AIS patients with low baseline ASPECTS despite an increased risk for sICH. Further data from randomized-controlled clinical trials are needed to elucidate the role of EVT in this subgroup of AIS patients.

Registration:

The protocol has been registered in the International Prospective Register of Ongoing Systematic Reviews PROSPERO; Registration Number: CRD42022334417.

Introduction

Acute ischemic stroke (AIS) treatment aims at rapid reperfusion of oligemic brain tissue, using two established recanalization therapies: intravenous thrombolysis (IVT) and endovascular treatment (EVT).1 IVT has been shown to reduce disability in eligible AIS patients up to 4.5 h from symptom onset using standard neuroimaging and up to 9 h using advanced neuroimaging.2 A main predictor of AIS outcome3 and treatment efficacy4 is infarct core volume at baseline. Baseline CT hypoattenuation of greater than one-third of the middle cerebral artery (MCA) territory has been an exclusion criterion for some – but not all – IVT clinical trials and, according to most recent American Heart Association/ American Stroke Association (AHA/ASA) guidelines, no benefit from thrombolytic treatment has been proven in this subgroup of AIS patients.5 The European Medicine Agency advises against treatment with alteplase in ‘Patients with severe stroke’ [as assessed clinically (NIHSS score > 2) or by appropriate imaging ] because ‘patients with very severe stroke are at higher risk for intracerebral hemorrhage and death’.6 European Stroke Organization (ESO) guidelines follow a different approach, highlighting the fact that there is no evidence that extensive ischemic changes on baseline imaging modify the treatment effect of IVT.7,8 However, they note a significant interaction between the presence of early ischemic changes on baseline CT and mortality after IVT treatment. In conclusion, they provide a weak recommendation in favor of IVT based on very low quality of evidence within 4.5 h from last seen well (LSW).9 As practically all AIS patients with large ischemic core suffer from large-vessel occlusion (LVO), EVT can be used in conjunction with IVT or as a standalone therapy in otherwise eligible large ischemic core patients. However, patients with extensive infarcts at baseline were excluded by many EVT clinical trials while international recommendations advocate against EVT in LVO patients with low (<6) Alberta Stroke Program Early Computed Tomography Score (ASPECTS).5,10
To quantify the extent of hypodensities in baseline CT, ASPECTS has been developed for anterior circulation LVO stroke [internal carotid artery (ICA) or MCA).11 Focal hypoattenuation of the cortex and in the basal ganglia, gray–white matter dedifferentiation and loss of the insular ribbon sign are assessed through a 10-point scoring system corresponding to anatomical regions that extend over the MCA arterial distribution: four subcortical [caudate (C), lentiform (L), internal capsule (IC), insular ribbon (I)] and six cortical areas spanning over the superficial MCA territory (M1–M6).12 It was developed to quantify early ischemic changes (hypoattenuation, loss of gray–white matter distinction, or focal swelling) on baseline CT of AIS patients eligible for IVT arriving within 3 h from symptom onset. For each region presenting early ischemic changes, the overall score of 10 is reduced by 1. The goal was to develop practical prediction tools of functional independence, dependence, and symptomatic intracranial hemorrhage (sICH) after thrombolytic treatment. In the seminal paper, ASPECTS < 8 almost excluded functional independence of AIS patients post IVT, and ASPECTS showed inverse correlation with mortality, reaching 50% for scores 0–2.11 ASPECTS never gained wide acceptance as a prognostic tool and failed to substitute the exclusion criterion of hypodensity in more than one-third of MCA territory for IVT. However, it gained momentum in the clinical trials of EVT; most of the five first positive EVT trials used an ASPECTS cut-off of 6 to include patients for randomization.10,13 Positive results led AHA/ASA and ESO guidelines to provide IA level evidence for EVT in patients with an ASPECTS of 6 or greater.5,10 As a consequence, low ASPECTS is considered any score below 6, corresponding to large core infarcts, for which there is currently no strong recommendation for EVT.
A previous meta-analysis of observational studies has indicated that EVT for low ASPECTS is associated with improved functional independence and lower mortality at 90 days without significant increase in sICH compared with the best medical treatment (BMT), across various definitions, thresholds of large core size, and time windows. EVT was associated with significantly higher odds of functional independence (EVT: 25% versus BMT: 7%) and lower likelihood of mortality (EVT: 20% versus BMT: 30%) at 90 days, whereas the odds of sICH were similar (EVT: 9% versus BMT: 5%).14 Better functional outcomes have been reported from another systematic review and meta-analysis (EVT: 28% versus 4% with BMT), with similar rates of mortality (EVT: 31% versus BMT: 37%) and sICH (EVT: 9% versus BMT: 6%).15 Similar results have been reported from three other meta-analyses, assessing ASPECTS, pre-treatment infarct core volume, or both1618 (Supplemental eTable 1). Since the publication of these analyses, the experience from large multi-center registries and one randomized-controlled clinical trial (RCT) has been published, providing exciting new data on this subgroup of LVO AIS patients, justifying an updated systematic review and meta-analysis. The current meta-analysis differs from previously published meta-analyses on the topic as we have excluded LVO patients presenting with ASPECTS of 6, given the fact that EVT has a strong recommendation (level 1/ grade A) for this specific LVO subgroup.
 
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