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.

Saturday, April 8, 2023

Stroke Outcomes Provide Some Clarity on Kidney-Brain Connection

For your doctors to understand and implement protocols to address this risk.  If they do nothing you don't have a functioning stroke doctor or hospital. YOU NEED TO FIRE THE BOARD OF DIRECTORS FOR INCOMPETENCY!

From April 2018 is this; does your doctor know about it?

Coffee consumption and incident kidney disease: Results from the Atherosclerosis Risk in Communities (ARIC) study April 2018 

A lower risk for incident CKD was observed in participants who drank higher amounts of coffee, after adjusting for covariates.

 

Stroke Outcomes Provide Some Clarity on Kidney-Brain Connection

Kidney dysfunction, kidney damage increase risks in different ways, say researchers

A computer rendererd diseased kidney cutaway over a brain with a stroke highlighted.

Recognizing that not all chronic kidney disease (CKD) is the same, researchers are starting to separate the individual contributions of kidney dysfunction and kidney damage to stroke outcomes, opening the door to more specific interventions.

In a longitudinal cohort study of Japanese stroke patients, CKD was an independent predictor of recurrent stroke (adjusted HR 1.19, 95% CI 1.09-1.30) and death (adjusted HR 1.40, 95% CI 1.31-1.50) within approximately 4 years even after accounting for traditional cardiovascular risk factors, reported Ryu Matsuo, MD, PhD, of Kyushu University in Fukuoka, Japan, and colleagues.

Probing further into the underlying pathological conditions of CKD, they found that whereas worse estimated glomerular filtration rate (eGFR) was associated with an increased risk of recurrent stroke, only the highest level of proteinuria was associated with excess risk:

  • Mild to moderate kidney dysfunction (eGFR 45-59 mL/min/1.73 m2): adjusted HR 1.13, 95% CI 1.02-1.25
  • Moderate to severe kidney dysfunction (eGFR <45 mL/min/1.73 m2): adjusted HR 1.22, 95% CI 1.09-1.37
  • Kidney damage (proteinuria ≥2+): adjusted HR 1.25, 95% CI 1.07-1.46

However, any level of eGFR impairment and proteinuria were associated with increased mortality, the Fukuoka Stroke Registry investigators reported in Strokeopens in a new tab or window.

"These findings suggest that both kidney dysfunction and kidney damage are independent risk factors for recurrent stroke and death in patients with ischemic stroke, but increase the risks of cardiovascular outcomes in different ways," Matsuo's group said.

"Further studies are warranted to validate the impacts of kidney dysfunction and kidney damage on cardiovascular risks and to determine whether interventions for these pathological conditions are effective in improving the cardiovascular outcomes in patients with ischemic stroke," the study authors concluded.

The CDC estimatesopens in a new tab or window that about 37 million U.S. adults have CKD, with most cases undiagnosed. CKD tends to worsen without treatment and may reach end-stage renal disease requiring dialysis or kidney transplant. Diabetes and high blood pressure are the leading causes of kidney failure.

Matsuo's team said the question of whether impaired kidney function, kidney damage, individually or both, are involved in cardiovascular outcomes has been controversial. Prior studies had produced mixed results in the CKD-stroke sphere.

"Though CKD is a putative risk factor for stroke, the mechanisms by which CKD impacts stroke risk have proven difficult to elucidate, as many risk factors for CKD are also risk factors for stroke. Understanding the impact of CKD on outcomes after stroke poses similar challenges," commented vascular neurology fellow Samuel Bruce, MD, MA, and stroke specialist Neal Parikh, MD, MS, both of Weill Cornell Medicine in New York City.

In an accompanying editorialopens in a new tab or window, they stressed that based on the work from Matsuo and colleagues, "going beyond serum creatinine is necessary to more fully understand the impact of CKD on stroke outcomes."

"While the authors' findings do not have immediate, direct clinical implications, it is noteworthy that when treating conditions linked with CKD, such as hypertension and diabetes, treatment options include drugs with nephroprotective properties," Bruce and Parikh wrote. "Whether such drugs should be used preferentially to improve poststroke outcomes should be investigated."

Matsuo and colleagues cited research showing that renin-angiotensin-aldosterone system inhibitorsopens in a new tab or window and SGLT2 inhibitorsopens in a new tab or window can slow kidney dysfunction and kidney damage.

The observational cohort study prospectively followed 12,576 patients with ischemic stroke (mean age 73 years; 41.3% of whom were women) who were enrolled into the multicenter Fukuoka Stroke Registry from 2007 to 2019.

During the median follow-up of 4.3 years, 19.7% of patients had recurrent stroke (48.0 per 1,000 patient-years) and 32.1% died (67.3 per 1,000 patient-years).

The study was unable to control for long-term treatments or medications taken during follow-up, however.

The investigators also acknowledged the exclusion of stroke patients undergoing renal replacement therapy, whose anuria precluded proteinuria assessment using a urine dipstick test. Another study limitation was a population that was ethnically homogeneous due to registry enrollment limited to a small area of Japan.

"These data do not clarify whether kidney dysfunction and kidney damage, as opposed to upstream factors such as hypertension, are causally linked to poststroke outcomes," Bruce and Parikh said. "However, the findings do justify asking whether different aspects of CKD pathophysiology may be targeted to improve stroke outcomes."

  • author['full_name']

    Nicole Lou is a reporter for MedPage Today, where she covers cardiology news and other developments in medicine. Follow

Disclosures

The study was supported by grants from the Japanese Ministry of Education, Culture, Sports, Science and Technology.

Matsuo and co-authors had no disclosures.

Bruce had no disclosures; Parikh disclosed personal fees for medicolegal consulting and providing blinded end point assessment for a Medtronic trial being conducted at his institution.

Primary Source

Stroke

Source Reference: opens in a new tab or windowUeki K, et al "Decreased estimated glomerular filtration rate and proteinuria and long-term outcomes after ischemic stroke: a longitudinal observational cohort study" Stroke 2023; DOI: 10.1161/STROKEAHA.122.040958.

Secondary Source

Stroke

Source Reference: opens in a new tab or windowBruce SS, Parikh NS "Chronic kidney disease and stroke outcomes: beyond serum creatinine" Stroke 2023; DOI: 10.1161/STROKEAHA.123.042965.

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