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.

Sunday, July 2, 2023

Early versus Later Anticoagulation for Stroke with Atrial Fibrillation

 When the hell is all stroke research going to report on survivor goals of 100% recovery? With no measurements of that it will never improve. 

“What's measured, improves.” So said management legend and author Peter F. Drucker 

Early versus Later Anticoagulation for Stroke with Atrial Fibrillation


List of authors.
  • Urs Fischer, M.D.,
  • Masatoshi Koga, M.D., Ph.D.,
  • Daniel Strbian, Ph.D.,
  • Mattia Branca, Ph.D.,
  • Stefanie Abend, B.Sc.,
  • Sven Trelle, M.D.,
  • Maurizio Paciaroni, M.D.,
  • Götz Thomalla, M.D.,
  • Patrik Michel, M.D.,
  • Krassen Nedeltchev, M.D.,
  • Leo H. Bonati, M.D.,
  • George Ntaios, M.D.,
  • Thomas Gattringer, Ph.D.,
  • Else-Charlotte Sandset, Ph.D.,
  • Peter Kelly, M.D.,
  • Robin Lemmens, Ph.D.,
  • P.N. Sylaja, M.D.,
  • Diana Aguiar de Sousa, Ph.D.,
  • Natan M. Bornstein, M.D.,
  • Zuzana Gdovinova, M.D., Ph.D.,
  • Takeshi Yoshimoto, M.D., Ph.D.,
  • Marjaana Tiainen, M.D., Ph.D.,
  • Helen Thomas, R.N.,
  • Manju Krishnan, M.B., B.S.,
  • Gek C. Shim, M.B., B.Ch.,
  • Christoph Gumbinger, M.D.,
  • Jochen Vehoff, M.D.,
  • Liqun Zhang, M.D., Ph.D.,
  • Kosuke Matsuzono, M.D., Ph.D.,
  • Espen Kristoffersen, M.D., Ph.D.,
  • Philippe Desfontaines, M.D.,
  • Peter Vanacker, M.D., Ph.D.,
  • Angelika Alonso, M.D.,
  • Yusuke Yakushiji, M.D., Ph.D.,
  • Caterina Kulyk, M.D.,
  • Dimitri Hemelsoet, M.D.,
  • Sven Poli, M.D.,
  • Ana Paiva Nunes, M.D.,
  • Nicoletta Caracciolo, M.D.,
  • Peter Slade, M.B., B.Ch.,
  • Jelle Demeestere, M.D., Ph.D.,
  • Alexander Salerno, M.D.,
  • Markus Kneihsl, M.D., Ph.D.,
  • Timo Kahles, M.D.,
  • Daria Giudici, M.D.,
  • Kanta Tanaka, M.D., Ph.D.,
  • Silja Räty, M.D., Ph.D.,
  • Rea Hidalgo, R.N.,
  • David J. Werring, F.R.C.P., Ph.D.,
  • Martina Göldlin, M.D.,
  • Marcel Arnold, M.D.,
  • Cecilia Ferrari, M.B.A.-I.H.M.,
  • Seraina Beyeler, Ph.D.,
  • Christian Fung, M.D.,
  • Bruno J. Weder, M.D.,
  • Turgut Tatlisumak, M.D., Ph.D.,
  • Sabine Fenzl, M.D.,
  • Beata Rezny-Kasprzak, M.D.,
  • Arsany Hakim, M.D.,
  • Georgia Salanti, Ph.D.,
  • Claudio Bassetti, M.D.,
  • Jan Gralla, M.D.,
  • David J. Seiffge, M.D.,
  • Thomas Horvath, M.D.,
  • and Jesse Dawson, M.D.

  • for the ELAN Investigators*

Abstract

Background

The effect of early as compared with later initiation of direct oral anticoagulants (DOACs) in persons with atrial fibrillation who have had an acute ischemic stroke is unclear.

Methods

We performed an investigator-initiated, open-label trial at 103 sites in 15 countries. Participants were randomly assigned in a 1:1 ratio to early anticoagulation (within 48 hours after a minor or moderate stroke or on day 6 or 7 after a major stroke) or later anticoagulation (day 3 or 4 after a minor stroke, day 6 or 7 after a moderate stroke, or day 12, 13, or 14 after a major stroke). Assessors were unaware of the trial-group assignments. The primary outcome was a composite of recurrent ischemic stroke, systemic embolism, major extracranial bleeding, symptomatic intracranial hemorrhage, or vascular death within 30 days after randomization. Secondary outcomes included the components of the composite primary outcome at 30 and 90 days.

Results

Of 2013 participants (37% with minor stroke, 40% with moderate stroke, and 23% with major stroke), 1006 were assigned to early anticoagulation and 1007 to later anticoagulation. A primary-outcome event occurred in 29 participants (2.9%) in the early-treatment group and 41 participants (4.1%) in the later-treatment group (risk difference, −1.18 percentage points; 95% confidence interval [CI], −2.84 to 0.47) by 30 days. Recurrent ischemic stroke occurred in 14 participants (1.4%) in the early-treatment group and 25 participants (2.5%) in the later-treatment group (odds ratio, 0.57; 95% CI, 0.29 to 1.07) by 30 days and in 18 participants (1.9%) and 30 participants (3.1%), respectively, by 90 days (odds ratio, 0.60; 95% CI, 0.33 to 1.06). Symptomatic intracranial hemorrhage occurred in 2 participants (0.2%) in both groups by 30 days.

Conclusions

In this trial, the incidence of recurrent ischemic stroke, systemic embolism, major extracranial bleeding, symptomatic intracranial hemorrhage, or vascular death at 30 days was estimated to range from 2.8 percentage points lower to 0.5 percentage points higher (based on the 95% confidence interval) with early than with later use of DOACs. (Funded by the Swiss National Science Foundation and others; ELAN ClinicalTrials.gov number, NCT03148457. opens in new tab.)

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