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 steroids. Show all posts
Showing posts with label steroids. Show all posts

Saturday, June 17, 2023

Steroids Provide Temporary Improvement of Refractory Pain Following Subarachnoid Hemorrhage

 FYI, in case you need to train your doctor.

Steroids Provide Temporary Improvement of Refractory Pain Following Subarachnoid Hemorrhage

Abstract

Introduction

Evidence for optimal analgesia following subarachnoid hemorrhage (SAH) is limited. Steroid therapy for pain refractory to standard regimens is common despite lack of evidence for its efficacy. We sought to determine if steroids reduced pain or utilization of other analgesics when given for refractory headache following SAH.

Methods

We performed a retrospective within-subjects cohort study of SAH patients who received steroids for refractory headache. We compared daily pain scores, total daily opioid, and acetaminophen doses before, during, and after steroids. Repeated measures were analyzed with a multivariable general linear model and generalized estimating equations.

Results

Included 52 patients treated with dexamethasone following SAH, of whom 11 received a second course, increasing total to 63 treatment epochs. Mean pain score on the first day of therapy was 7.92 (standard error of the mean [SEM] .37) and decreased to 6.68 (SEM .36) on the second day before quickly returning to baseline levels, 7.36 (SEM .33), following completion of treatment. Total daily analgesics mirrored this trend. Mean total opioid and acetaminophen doses on days one and two and two days after treatment were 47.83mg (SEM 6.22) and 1848mg (SEM 170.66), 34.24mg (SEM 5.12) and 1809mg (SEM 150.28), and 46.38mg (SEM 11.64) and 1833mg (SEM 174.23), respectively. Response to therapy was associated with older age, decreasing acetaminophen dosing, and longer duration of steroids. Hyperglycemia and sleep disturbance/delirium effected 28.6% and 55.6% of cases, respectively.

Conclusion

Steroid therapy for refractory pain in SAH patients may have modest, transient effects in select patients.

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Tuesday, June 4, 2019

Allopregnanolone as a Therapeutic to Regenerate the Degenerated Brain

We'll never know if this would be useful post stroke since there is NO STROKE LEADER to go to to update the stroke strategy and start research on these questions. You're screwed as long as we don't have stroke survivors running stroke associations. 

Allopregnanolone as a Therapeutic to Regenerate the Degenerated Brain


  • Gerson D. Hernandez
  • Roberta Diaz BrintonEmail author
  • Gerson D. Hernandez
    • 1
  • Roberta Diaz Brinton
    • 1
    Email author
  1. 1.Center for Innovation in Brain Science, College of MedicineUniversity of ArizonaTucsonUSA
Chapter

Part of the ISGE Series book series (ISGE)


Abstract

Neurosteroids regulate both regeneration and repair systems in the brain. Among this class of molecules, allopregnanolone (Allo) is the first regenerative therapeutic that has been extensively investigated in animal models and more recently in humans for its capacity to promote regeneration in the central and peripheral nervous system. In preclinical analyses, Allo induced generation and survival of new neurons in the hippocampus of aged mice and in transgenic mouse models of Alzheimer’s disease (AD), which was associated with restoration of learning and memory function. Allo is a proliferative factor for both neural stem cells and pre-progenitor oligodendrocytes, increasing both the number of newly generated cells and their survival. Safety characteristics of Allo regulation of neurogenesis indicate that the regenerative system it affects is tightly regulated with closely guarded thresholds for both activation and magnitude of proliferation. In the brain of mice with AD, Allo increased liver X receptor and pregnane X receptor expression, reduced ß-amyloid and microglial activation, and increased markers of white matter generation. Results of preclinical studies indicate that an optimal treatment regimen of Allo to promote endogenous regeneration is one that is administered once per week over the course of several months. Allo dose and frequency of exposure are determining factors regulating its therapeutic efficacy. Previous and current human safety exposure data supported by extensive preclinical efficacy data are strong foundations for the clinical development of Allo as a therapeutic to regenerate the degenerated brain.

Keywords

Neurosteroid Allopregnanolone Neurodegeneration Regeneration Aging brain 


Sunday, July 1, 2018

Neurosteroids: non-genomic pathways in neuroplasticity; involvement in neurological diseases

You'll have to have your doctor followup this to see how this promotes neuroplasticity, and what the protocols are for its use. 

Neurosteroids: non-genomic pathways in neuroplasticity; involvement in neurological diseases



Abstract


Neurosteroids are neuroactive brain-born steroids. They can act through non-genomic and/or through genomic pathways. Genomic pathways are largely described for steroid hormones: the binding to nuclear receptors leads to transcription regulation. Pregnenolone, Dehydroepiandrosterone, their respective sulfate esters and Allopregnanolone have no corresponding nuclear receptor identified so far whereas some of their non-genomic targets have been identified. Neuroplasticity is the capacity that neuronal networks have to change their structure and function in response to biological and/or environmental signals; it is regulated by several mechanisms, including those that involve neurosteroids.
In this review, after a description of their biosynthesis, the effects of Pregnenolone, Dehydroepiandrosterone, their respective sulfate esters and Allopregnanolone on their targets will be exposed. We then shall highlight that neurosteroids, by acting on these targets, can regulate neurogenesis, structural and functional plasticity. Finally, we will discuss the therapeutic potential of neurosteroids in the pathophysiology of neurological diseases in which alterations of neuroplasticity are associated with changes in neurosteroid levels.

Thursday, November 17, 2016

Severe dizziness treated with steroid injections into the eardrum

Ask your doctor about this intervention if your stroke left you with this problem. 

Severe dizziness treated with steroid injections into the eardrum 



Injections of steroid into the ear are an effective treatment for a common form of severe dizziness, suggests a new study.
In a new trial, scientists from Imperial College London compared current treatments for Meniere’s disease, which causes debilitating dizzy spells.
They found that injections of the steroid methylprednisolone, through the ear drum, are as effective as the current ‘gold standard’ treatment. The current option is an antibiotic called gentamicin, and is also injected into the ear, where it destroys inner ear cells. The treatment prevents dizziness attacks, but can leave patients with permanent hearing damage.
The new trial, published in the Lancet, found that the steroid injections are as effective as gentamicin, but without the side effects. Patients who received the steroid injections were better at hearing speech clearly, compared to those who received the gentamicin injections.
The researchers are now recommending medics offer the steroid injections to patients before trying gentamicin.
Professor Adolfo Bronstein, lead author on the paper from the Department of Medicine at Imperial, said: “Meniere’s disease causes disabling attacks of dizziness that in some cases can leave people unable to work. However at the moment the only treatment we have for severe cases is a so-called ‘destructive treatment’ that kill cells in the inner ear. Doctors, including ourselves, always assumed steroid injections were less effective than the current treatment, but we were surprised to see they work just as well as gentamicin, but do much less harm.”
Meniere’s disease affects around 30,000 people in the UK, and causes intense attacks of dizziness that last anything from a few minutes to 24 hours. During the attacks a person is usually unable to stand, and suffers from hearing loss, as well as nausea or even vomiting. The condition usually strikes people over 40, though scientists still do not know what triggers the disease. One theory is that the condition causes a build-up of salt and fluid in the inner ear.
This section of the ear, which is closest to the brain, holds equipment crucial to maintaining balance. This equipment constantly communicates with the brain, eyes and limbs to keep us on our feet.
Scientists believe the build-up of pressure can cause tiny leaks of fluid in the inner ear, which can cause the balance equipment to malfunction. The condition can also lead to permanent hearing loss.
There is no cure, although the early stages of the disease can be treated with medication and exercises. Severe cases can be treated with injections of gentamicin. After being injected into the ear, the medicine travels to the inner ear where it destroys the cells responsible for balance, and stops the dizzy spells. Usually only one ear is affected, therefore patients still have a working balance mechanism in their healthy ear, and can re-train their balance with exercises.
However, gentamicin can also destroy hearing cells, and up to one in five patients can be left with permanent hearing loss.
In the latest study, researchers at Imperial gave 60 patients with severe Meniere’s disease either injections of gentamicin or steroids. The patients were on average having more than one dizziness attack a week. They were given two injections of one of the treatments, under local anaesthetic, two weeks apart. Neither the patient nor the researcher knew whether a patient received steroid or the gentamicin.
After a two year period, all patients’ dizziness attacks had reduced by around 90 per cent. However the patients who received the steroid injections had better speech discrimination – the ability to hear words clearly - than those who received gentamicin.
Neither treatments were found to have any other side effects, although the injections of gentamicin often triggered a severe dizziness attack when first administered.
Professor Bronstein added that those who received steroid injections were more likely to need additional jabs to stop their dizzy spells.
“For a patient who lives in a remote location where accessing repeat injections would be difficult, then gentamicin would be an option. However, if a patient is able to receive repeat injections, and is concerned about future hearing loss, the steroid injections may be a better choice.”
Natasha Harrington-Benton, Director of the Meniere’s Society, who funded the research said: “We are pleased to have been able to support this research and are encouraged by the outcome. The trial has led to a better understanding of gentamicin and steroid treatments for Meniere’s disease; giving hope to those affected by this complex condition.”
The research was funded by the Meniere’s Society.

Saturday, October 6, 2012

Subacromial Corticosteroid Injection on Poststroke Hemiplegic Shoulder Pain: A Randomized, Triple-Blind, Placebo-Controlled Trial

Make sure your doctor and therapists know about this. When I had my shoulder pain no one knew what to do about it except don't use it. 

Subacromial Corticosteroid Injection on Poststroke Hemiplegic Shoulder Pain: A Randomized, Triple-Blind, Placebo-Controlled Trial



Abstract: Study evaluated the effect of subacromial corticosteroid injection on hemiplegic shoulder pain. Fifty-eight stroke survivors with evidence of rotator cuff disorder were randomly assigned to receive ultrasound-guided subacromial injection with triamcinolone 40mg (treatment group), or lidocaine (placebo group). After a single injection, participants were followed up for 8 weeks. Treatment efficacy was evaluated at pretreatment and weeks 2, 4, and 8 posttreatment with the following measures: visual analog scale (VAS) of the average shoulder pain level at day and night, Modified Barthel Index, Shoulder Disability Questionnaire (SDQ), and angles of shoulder active range of motion (flexion, abduction, external rotation, and internal rotation). There was no significant difference between the 2 groups in the main outcome measures at pretreatment. Compared with the placebo group, VAS-day/night, SDQ, flexion, external rotation, and internal rotation showed significant improvement in the treatment group. Results indicate that subacromial corticosteroid injection showed improvement in pain, disability, and active range of motion, and the duration of its efficacy continued up to 8 weeks.