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.

Tuesday, October 15, 2024

COVID-19 tied to increased risk of major adverse cardiac event for up to 3 years

 I had COVID one time for sure and likely two other times. All three were mild cases. Probably because I've had most of the vaccinations. And I'm O negative.

COVID-19 tied to increased risk of major adverse cardiac event for up to 3 years

An increased risk of incident major adverse cardiac event (MACE), including myocardial infarction (MI), stroke, and all-cause mortality, was observed among patients with COVID-19 for up to 3 years, particularly among those requiring hospitalisation, according to a study published in Arteriosclerosis, Thrombosis, and Vascular Biology.

In addition,James R. Hilser, University of Southern California, Los Angeles, California, and colleagues observed that hospitalisation for COVID-19 represented a coronary artery disease risk equivalent, with the risks of post-acute MI and stroke particularly heightened in individuals with non-O blood types. 

Using data from the UK Biobank, the researchers identified 10,005 patients with COVID-19 who had a positive PCR test for severe acute respiratory syndrome coronavirus 2 (SARS‑CoV‑2) infection (n = 8,062) or had received hospital-based International Classification of Diseases version-10 codes for COVID-19 (n = 1,943) between February 1, 2020, and December 31, 2020. Population controls (n = 217,730) and propensity score-matched controls (n = 38,860) identified from the UK Biobank during the same period were also included in the analysis. 

Overall, the risk of MACE was elevated in patients with COVID-19 at all levels of severity (hazard ratio [HR] = 2.09; 95% confidence interval [CI], 1.94-2.25; P < .0005) over 1,003 days of follow-up, with the risk being more pronounced among patients requiring hospitalisation (HR = 3.85; 95% CI, 3.51-4.24; P < .0005).

More specifically, the risk of MACE was increased among patients hospitalised with COVID-19 who did not have a history of cardiovascular disease (CVD) (HR = 1.21; 95% CI, 1.08-1.37; P < .005) compared with COVID-19-negative controls with CVD, indicating hospitalisation for COVID-19 as a coronary artery disease risk equivalent.

Furthermore, a significant genetic interaction was observed between the ABO blood groups and hospitalisation for COVID-19 (Pinteraction = .01), whereby hospitalisation for COVID-19 increased the risk of MI and stroke to a greater extent among individuals with non-O blood types (HR = 1.65; 95% CI, 1.29-2.09; P = 4.8x10-5) than those with blood type O (HR = 0.96; 95% CI, 0.66-1.39; P = .82).

“Taken together, our data indicate that the elevated risk of MACE in patients with COVID-19 shows no apparent signs of attenuation up to nearly 3 years after SARS-CoV-2 infection and suggest that COVID-19 continues to pose a significant public health burden with lingering adverse cardiovascular risk,” the authors remarked. “These observations suggest that more aggressive cardiovascular risk reduction efforts may be warranted as part of primary prevention in patients hospitalised for COVID-19 and provide new avenues for understanding the biological mechanisms underlying CVD-related adverse outcomes of severe SARS-CoV-2 infection.”

Source: Arteriosclerosis, Thrombosis, and Vascular Biology

No comments:

Post a Comment