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.

Showing posts with label blithering idiots. Show all posts
Showing posts with label blithering idiots. Show all posts

Friday, August 7, 2026

TESLA Trial Turns Positive for Stroke Thrombectomy in Extended Analysis

 Only in the rose colored glasses of the tyranny of low expectations can this be considered positive! Measured against the only goal in stroke(100% RECOVERY!) This was a complete failure! You blithering idiots have the wrong goal! You'll want 100% recovery when you are the 1 in 4 per WHO that has a stroke

Better start working on that goal now.

TESLA Trial Turns Positive for Stroke Thrombectomy in Extended Analysis

Key Takeaways

  • The TESLA trial tested the concept of stroke thrombectomy on large-core infarcts with a noncontrast CT-alone selection paradigm to lower the barrier for imaging and patient selection.
  • While primary results at 90 days did not meet statistical superiority, extended follow-up to 1 year did significantly favor endovascular therapy over medical management alone for functional outcomes.
  • The investigators suggested that the between-group difference is related to the severe natural history of untreated large-core tissue decay, hence the diverging recovery or decline trajectories.

In the TESLA trial, stroke outcomes took a turn for the better following swift mechanical thrombectomy for large anterior circulation infarcts identified without advanced imaging.

In an extended analysis of the trial at 1 year, patients treated with CT-selected endovascular therapy (EVT) for large-core infarcts had improved functional outcomes compared with those treated with medical management alone, as measured by mean utility-weighted modified Rankin Scale (mRS) scores (3.65 vs 2.78, bayesian adjusted mean difference 1.18 points, 95% credible interval 0.42-1.93; posterior probability of superiority P=0.999).

Patients receiving EVT versus medical management alone also had a higher likelihood of functional independence (mRS score 0-2; 23.6% vs 6.8%, P<0.001) and independent ambulation (mRS score 0-3; 35.4% vs 18.0%, P<0.001) at 1 year, reported Albert Yoo, MD, PhD, of California Neurointerventional Surgeons in Riverside, and colleagues.

"Although functional independence in the IAT [intra-arterial thrombectomy] group numerically increased between 90 days and 1 year, it declined in the MM [medical management] group, which may reflect the severe natural history of untreated large-core tissue decay, delayed deconditioning, unmeasured rehabilitation intensity difference between groups, or baseline imbalances, such as age," they wrote in a research letter in JAMA.

"These exploratory observations complement the 12-month data reported in the SELECT2 and TENSION trials, supporting that early large-core reperfusion may facilitate prolonged neuroplastic remodeling up to 1 year post stroke," they added.

The favorable 1-year results of TESLA put the study more in line with these other trials, after its main analysis had indicated neutral results for EVT in the short term.

TESLA stands alone as the only EVT trial to extend the enrollment window to 24 hours while requiring only noncontrast CT for infarct size estimation and CT angiography for diagnosis of target vessel occlusion without more advanced imaging techniques to identify eligible patients with large-core strokes. Of note, with the more pragmatic entry criteria, there was a relatively long median of 11.5 hours from stroke onset to randomization in this study.

The open-label trial was conducted across 47 U.S. stroke centers and included adults presenting within 24 hours of last known well with an NIH Stroke Scale score of 6 or higher, internal carotid artery or middle cerebral artery occlusion, an Alberta Stroke Program Early Computed Tomography Score of 2 to 5 on baseline CT, and a premorbid mRS score of 0 to 1.

Yoo and team randomized 302 patients to medical management with or without intra-arterial thrombectomy; ultimately, 300 were included in the intention-to-treat analysis. Complete 1-year functional data were available for 277 people, among whom baseline profiles were balanced between groups, though the EVT group was slightly younger (median age 66 vs 68) and more likely to have diabetes (28.5% vs 16.8%).

As part of the exploratory analyses, the study authors also found that patient-reported quality of life was better in the EVT group at 1 year, as measured by the 100-point European Quality of Life 5 Dimensions, 5 Levels (EQ-5D-5L) health questionnaire (average score 60.3 vs 49.3, P=0.003).

All-cause mortality rates were not significantly different between groups (43.1% vs 46.6%, P=0.42).

As for potential harm, EVT had been associated with excess symptomatic intracranial hemorrhage at 24 hours, as previously reported (4.0% vs 1.3%).

Yoo and colleagues stressed that the present report covered exploratory analysis and may have been biased by unblinded postprocedural rehabilitation intensity and asymmetric 1-year attrition, as follow-up was complete for 144 patients in the EVT group and 133 controls. External validity to lower-resource regions remains unestablished, they added.

"Nevertheless, these descriptive data suggest longer-term benefit associated with thrombectomy in large-core stroke, indicating that a [noncontrast] CT-alone selection paradigm warrants further study as a lower-barrier strategy for global stroke systems," the investigators concluded.

 

Monday, July 27, 2026

Domain-specific functional outcome prediction in stroke rehabilitation: A multicenter artificial intelligence study

 Tell me PRECISELY HOW THIS GETS SURVIVORS RECOVERED!

Or just shut your fucking yaps and let some people with brains solve stroke! Somehow you are so blitheringly stupid you don't know predictions are completely fucking useless! WOW! IMPRESSIVE STUPIDITY!

Domain-specific functional outcome prediction in stroke rehabilitation: A multicenter artificial intelligence study


Author links open overlay panel

Highlights

  • AI-based models predicted domain-specific functional outcomes after stroke, including ambulation, cognition, and ADLs.
  • Alignment-based regularization improved cross-institutional generalizability across four multicenter rehabilitation cohorts.
  • Domain-specific prediction models achieved AUROCs up to 0.897 in internal and 0.924 in external validation.
  • A prototype web-based decision support tool provides patient-specific recovery trajectories at 3 and 6 months after stroke.

Abstract

Background

Stroke is a leading cause of long-term disability worldwide, yet existing clinical decision support tools rely on global disability metrics, such as the modified Rankin Scale, which do not adequately reflect patient-centered rehabilitation or recovery goals.

Objective

We aimed to develop, validate, and implement artificial intelligence (AI)–based clinical support models for predicting domain-specific functional outcomes after stroke across multiple rehabilitation institutions and timepoints.

Methods

We utilized prospective and retrospective multicenter data collected from patients with stroke across four rehabilitation institutions in South Korea (2017–2024). Prognostic models were developed for three functional domains—ambulation, cognitive function, and activities of daily living—under two temporal scenarios: acute-to-subacute and acute-to-early-chronic prediction. Alignment-based regularization was applied to improve cross-institutional generalizability.

Results

The proposed framework achieved strong predictive performance in internal validation (AUROC up to 0.897 for ambulation and 0.864 for cognition) and favorable external validation performance, with AUROCs up to 0.924 (ADLs) and 0.892 (cognition), despite institution-specific differences in cohort size and variable availability across centers. The implemented web-based clinical decision support system provides real-time prediction of individualized recovery trajectory with intuitive visualization designed to support clinician–patient communication.

Conclusions

Our findings demonstrate the predictive feasibility of AI-based modeling for domain-specific stroke prognosis and present a prototype implementation illustrating the potential clinical applicability of the proposed framework across heterogeneous institutional settings. The use of routinely collected clinical variables and the preliminary cross-institutional validation results support further investigation of real-world rehabilitation practices, pending prospective clinical evaluation.

Monday, July 13, 2026

Lifestyle Changes May Slow Brain Aging in Adults Younger Than 70

 WHAT A JOKE! Nothing specific at all, we need specifics so we can blame you blithering idiots for our lack of recovery instead of you blaming us for not recovering! You don't like that do you? Wait until you the 1 in 4 per WHO that has a stroke!

Lifestyle Changes May Slow Brain Aging in Adults Younger Than 70

A structured multidomain lifestyle intervention may help slow changes in brain white matter associated with aging, a secondary analysis of data from the randomized POINTER trial suggested.

Compared with a self-guided intervention, a structured intervention attenuated increases in white matter free water over time (β = -0.031, SE=0.012, P=0.009) in people under age 70, reported Pauline Maillard, PhD, of the University of California Davis, who presented findings from the POINTER Imaging analysis at the Alzheimer's Association International Conference.

This effect was not seen in participants 70 and older, and no comparable intervention-related interactions were detected for other cerebrovascular MRI markers studied, Maillard and colleagues noted in JAMA Network Open, where the study was published.

"This study provides evidence that a multidomain lifestyle intervention may help slow changes in brain white matter that are associated with aging and cognitive decline," Maillard said. It suggests earlier intervention, before age 70, may be especially beneficial for preserving brain health, she observed.

"White matter changes are often less emphasized than memory-related brain changes, but they are closely linked to vascular health, brain connectivity, and cognitive function," Maillard told MedPage Today. "Our findings support the idea that addressing several modifiable risk factors together, including physical activity, diet, cognitive and social engagement, and cardiovascular health, may have measurable effects on the brain."

"These results should not be interpreted as showing that lifestyle intervention can prevent dementia on its own, but they provide encouraging biological evidence that lifestyle changes may influence brain aging," she emphasized. "Longer follow-up will be important to determine whether these imaging differences translate into sustained cognitive benefits."

The POINTER trial tested two lifestyle interventions -- one structured, the other self-guided -- to see whether they would improve cognitive scores in over 2,000 older adults. Both 2-year interventions encouraged physical activity, cognitive activity, healthy diet, social engagement, and cardiovascular health monitoring, but they differed in structure, intensity, and accountability.

The primary findings, published in 2025, demonstrated greater cognitive benefits in the structured group compared with the self-guided group. The researchers estimated that the structured intervention slowed the cognitive aging clock by about 1 to 2 years.

Data from three of the trial's ancillary studies -- POINTER-NV (neurovascular), POINTER-Neuroimaging, and POINTER-zzz (sleep) -- showed that blood pressure regulation, cognitive resilience, and sleep apnea were better with the structured intervention.

In the POINTER Imaging analysis, Maillard and colleagues evaluated 959 participants with a mean age of 68 years; 61.9% were women. Participants underwent MRI at baseline and at up to two follow-up visits at 12 and 24 months.

The primary outcomes were cerebrovascular MRI markers of global white matter free water, fractional anisotropy, peak width of skeletonized mean diffusivity, analysis along the perivascular space index, white matter hyperintensity volume, and incident cerebral microbleeds. Free water was the marker most responsive to lifestyle intervention in adults 60 to 70 years of age, showing attenuated small-vessel disease-related injury, Maillard said.

Baseline free water also identified participants at higher risk for white matter hyperintensity progression and incident cerebral microbleeds, she added.

The imaging cohort was an ancillary subset with a slightly lower proportion of women and a modestly higher prevalence of vascular risk factors than the main study cohort, the researchers acknowledged. The 2-year timeline may be insufficient for tracking certain vascular outcomes.

During the meeting, the Alzheimer's Association announced a new study based on findings from POINTER and the LatAm-FINGERS study, which showed that a multidomain lifestyle intervention in Latin America led to greater cognitive improvements versus a flexible health-advice intervention.

The global PROTECT-Cog trial will test whether a lifestyle intervention combined with a GLP-1 receptor agonist or similar metabolism-targeting drug can help prevent or delay cognitive decline and dementia, the group said.

"PROTECT-Cog builds directly on what we learned from U.S. POINTER and takes the next critical step in prevention science," Maria Carrillo, PhD, chief science officer and medical affairs lead at the Alzheimer's Association, said in a news release. "By testing a combined approach that targets both lifestyle and biology, we have the opportunity to better understand how to meaningfully reduce the risk of cognitive decline before symptoms begin."

Judy George covers neurology and neuroscience news for MedPage Today, writing about brain aging, Alzheimer’s, dementia, MS, rare diseases, epilepsy, autism, headache, stroke, Parkinson’s, ALS, concussion, CTE, sleep, pain, and more. Connect:
Disclosures

This study was supported by the National Institute on Aging and by the Alzheimer's Association.

Maillard has no disclosures.

Quantitative multi-slice spiral CT perfusion parameters as predictors of collateral status and 90-day functional outcome in acute ischemic stroke

 

Predicting failure to recover IS STUPIDER THAN HELL! Deliver recovery you blithering idiots!

Send me personal hate mail on this: oc1dean@gmail.com. I'll print your complete statement with your name and title(If you can't stand by your name don't bother replying anonymously) and my response in my blog. Or are you afraid to engage with my stroke-addled mind? No excuses are allowed! You're medically trained; it should be simple to precisely state EXACTLY WHERE I'M WRONG.

Exactly what in this research gets survivors recovered? 100% recovery is the only goal in stroke; NOT PREDICTIONS, BIOMARKERS, PROGNOSTICATION, OR ASSESSMENTS! I'd fire anyone doing these!

Quantitative multi-slice spiral CT perfusion parameters as predictors of collateral status and 90-day functional outcome in acute ischemic stroke


  • D

    Dan Zhu

  • X

    Xiaozhou Ma

  • Y

    Yingzhi Jiao

  • S

    Shuai Liu

  • J

    Jinzhu Yan

  • Lixin Zhang

    Lixin Zhang *

  • Imaging Center, Qianwei Hospital of Jilin Province, Changchun, Jilin, China

Abstract

Objective: 

To evaluate the utility of quantitative computed tomography perfusion parameters for assessing collateral circulation and predicting 90-day functional outcomes in acute ischemic stroke.

Methods: 

This retrospective study included 82 patients who underwent perfusion imaging within 24 h of symptom onset. Parameters including relative cerebral blood flow, relative cerebral blood volume, mean transit time, time to maximum, and hypoperfusion intensity ratio were analyzed. Collateral status was classified using multiphase angiography, and 90-day outcomes were assessed using the modified Rankin Scale.

Results: 

Patients with robust collateral circulation showed higher relative cerebral blood flow and volume and shorter perfusion times compared with those with poor collaterals. Hypoperfusion intensity ratio demonstrated strong diagnostic performance (area under the curve 0.925). For predicting unfavorable 90-day outcome, HIR achieved an AUC of 0.912 and showed greater discrimination than mismatch ratio in the present cohort, while the combined HIR–rCBF–Tmax model achieved an AUC of 0.938. Hypoperfusion intensity ratio correlated positively with functional disability, while relative cerebral blood flow correlated negatively with infarct volume. Favorable outcomes were more frequent in patients with robust collaterals.

Conclusion: 

Quantitative CTP parameters bridge a natomical collateral assessment and downstream tissue-level perfusion. HIR may provide a particularly informative functional marker of collateral efficiency and 90-day prognosis beyond conventional mismatch assessment.