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.

Wednesday, July 24, 2013

Meta-analysis: PFO Closure Better Than Medical Therapy at Reducing Future Stroke

Have your doctor compare this newest one to these previous studies;

CLOSURE I: Warts and all, first PFO/stroke study is best answer so far

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Landmark Study Finds Expensive Catheter Procedure to Close Hole in Heart No More Effective Than Medical Therapy to Prevent Strokes

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PFO closure bested medical management alone for reduction of ischemic stroke

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You do expect your doctor to actually know all this stuff before you bring it up, Don't you?
The newest one here;
 http://www.tctmd.com/show.aspx?id=119608&AspxAutoDetectCookieSupport=1
 Key Points:
  • Meta-analysis looks at 3 randomized controlled trials of PFO closure vs. best medical treatment
  • Clear benefits seen with closure for primary outcome of stroke and/or TIA
  • PFO closure patients with substantial shunt saw better outcomes

By Yael L. Maxwell
Tuesday, July 23, 2013


In patients with cryptogenic stroke, transcatheter patent foramen ovale (PFO) closure appears to reduce the risk of recurrent vascular events compared with medical treatment, according to a meta-analysis published online July 11, 2013, in the European Heart Journal. In addition, the benefit of closure may be greatest in patients with substantial shunt.
Abel Romero-Corral, MD, MSc, of Einstein Medical Center (Philadelphia, PA), and colleagues combined data from 3 trials (CLOSURE I, PC, and RESPECT) of 2,303 patients randomized to either transcatheter PFO closure (n = 1,150) or best medical therapy (n = 1,153) from 2000 to 2009. Devices used were the Amplatzer PFO Occluder (St. Jude Medical, St. Paul, MN) and STARFlex (NMT Medical, Boston, MA).
Clear Benefit over Medical Therapy
After a mean follow-up of 3.45 years, a total of 98 TIAs or strokes (primary endpoint) occurred in both the closure (3.47%) and medical therapy (5.03%) groups, reflecting an advantage with closure (HR 0.59; 95% CI 0.36-0.97; P = 0.04). However, the benefit disappeared when looking at stroke alone (HR 0.62; 95% CI 0.36-1.07; P = 0.09).
The composite outcome of death, recurrent neurological events, and peripheral embolism showed a trend toward a lower risk with closure in an intention-to-treat analysis (HR 0.67; 95% CI 0.44-1.00; P = 0.05), which was maintained in a per-protocol analysis of 2 of the studies (HR 0.62; 95% CI 0.38-1.00; P = 0.05).
Subgroup analyses showed that while the efficacy of closure was not affected by the presence of “high-risk” characteristics such as atrial septal aneurysm or older age, patients with substantial shunt at baseline (studied in 2 trials) saw a trend toward fewer vascular events after PFO closure (HR 0.35; 95% CI 0.12-1.03; P = 0.06). The trend was no longer evident when testing for interaction between type of intervention and shunt magnitude (P = 0.15).
Device implantation success was 93.8% on average; lowest with the STARFlex device in CLOSURE I (89.4%). The vascular complication rate was 1.13% on average. There were 2 cases of cardiac perforation and no deaths. Of note, new onset A-fib was higher in the closure group compared with the medical therapy group (2.7% vs. 0.5%; P < 0.001).
Larger Shunt, Higher Risk
In an e-mail communication with TCTMD, Dr. Romero-Corral and co-author Pablo A. Rengifo-Moreno, MD, also of Einstein Medical Center, acknowledged the negative individual outcomes of each of the 3 trials. “However, a big concern was that all 3 studies were underpowered for the primary outcome, an ideal scenario [in which] to perform a meta-analysis,” they said. “In our study, by having a larger population and greater number of adverse vascular events, we were able to overcome the underpowered concern and show a statistical benefit of transcatheter PFO closure.”
With regard to the subanalyses, Drs. Romero-Corral and Rengifo-Moreno said “a larger PFO facilitates a larger amount of debris to travel into the left-sided circulation, thus making it more likely to produce a significant clinical event. Furthermore, it has been hypothesized that fluid dynamics across a small and narrow PFO may be a protective factor when considering thrombus formation.”
Ziyad M. Hijazi, MD, MPH, of Rush University Medical Center (Chicago, IL), told TCTMD in a telephone interview that this finding is “intuitive.” Previous studies have focused more on the association between events and atrial septal aneurysm, but the meta-analysis likely did not find a relationship because not all of the included trials looked at this complication, he said.
Device Superiority vs. Operator Experience
New-onset A-fib is a real concern with PFO closure, Dr. Hijazi continued. “Nonetheless, it has a low event rate and some of the patients who had A-fib did not have a stroke. So the fact that you develop A-fib does not mean necessarily that you will have a stroke,” he said, adding that A-fib was more common with STARFlex vs. Amplatzer.
The authors agreed, suggesting that device type “might play a role” in this complication.
Because STARFlex was studied before Amplatzer, the question arises of how much operator experience factored into results, according to Dr. Hijazi. “The learning curve was so high [during CLOSURE I], so when the Amplatzer came [along], [the procedure] was a piece of cake,” he said. “But down deep in my heart I know it’s the device. The STARFlex is not as good a device as Amplatzer.
“I would love to see if the FDA will buy into the meta-analysis of randomized trials because [although] each trial individually is not very strong, if you look at the 3 trials combined, then we are talking about something significant,” he concluded.

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