http://www.youtube.com/watch?v=iQdkBKF8p5g&feature=youtu.be
Dominique Cadilhac and Chris Bladin speak about telemedicine - paper is coming soon to IJS.
The International Journal of Stroke is the flagship publication of the World Stroke Organization.
Monday, December 10, 2012
IJS is experimenting with coding - have you seen this ground breaking work on fatigue with Gillian Mead and martin Dennis? Keep an eye out for more stroke and fatigue papers as this topic garners more and more attention.
Thursday, November 29, 2012
Sri Lanka World Stroke Day
Monday, November 26, 2012
Changes in spleen size
International Journal of Stroke Managing Editor spoke to Drs. Sean Savitz and Farhaan Vahidy on the eve of the online publication of this very novel study. You can download this interview here.
The spleen in stroke patients undergoes dynamic changes of
contractions and re-expansion in the days following the onset of stroke
symptoms, releasing inflammatory cells and contributing to further brain injury,
according to researchers at The University of Texas Health Science Center at
Houston (UTHealth) Medical School.
“We’ve known from animal studies that the spleen contracts
after stroke, followed by the release of inflammatory white blood cells leading
to secondary brain injury, so we wanted to observe what happens to the spleen in
patients after a stroke,” said Sean I. Savitz, principal investigator and professor
of neurology at the UTHealth Medical School.
Photo credit: NIH |
“This is a completely understudied
area. The spleen is not normally an organ that neurologists or neuroscientists pay
attention to. This was our initial attempt to look at the size of the spleen in
stroke patients.”
The spleen is part of the lymphatic system, which fights infection by releasing white blood cells. It also helps control the amount of blood in the body and destroys old and damaged cells.
The study included 29 stroke patients and 20 healthy
volunteers. The research team performed daily abdominal ultrasounds to measure
the size of the spleens. In the stroke patients, spleens initially reduced in
size and then re-expanded. The spleens of the healthy volunteers showed minimal
variation in daily spleen size compared with the stroke patients.
Savitz said the study demonstrated a good correlation
between the contraction of the spleen and the amount of white blood cells in
the body. The results also suggested that some patients whose spleens
contracted for a longer period of time, releasing more inflammatory white blood
cells, had poorer clinical outcomes. Further studies will be needed to confirm
and explain these early findings, Savitz said.
Savitz and fellow researchers became interested in studying the
spleen after animal studies at UT-Health and elsewhere showed that stem cells
administered intravenously after a stroke travelled to the spleen, as well as to
the brain.
“The big question was why,” said Savitz, who is director of
the Stroke Program at UTHealth and an attending physician at Memorial
Hermann-Texas Medical Center. “Emerging work by our group and other researchers
suggest that some types of stem cells have a dampening effect on the inflammatory
response emanating from the spleen. The spleen is a possible target in the
future for treating stroke.”
Savitz’s research team at UTHealth included first authors
Preeti Sahota, M.D., and Farhaan Vahidy, M.D.
Tuesday, November 13, 2012
A little bit of art...
IJS are preparing to interview Swedish Neurologist Barbro B Johansson and I was touched by this image and historical note on her web page.
Her website 'banner' held this picture of a beautiful sculpture and I have left in tact the historical note she made about it as seen below.
Historical note: I took the picture of the sculpture on the top left when I visited the Institute of Neurosurgery and Brain Research in Santiago, Chile 1961. It is made by Marta Covin, a famous Chilean Sculptress (1905-1993), using the hands of Alfonso Asenjo as a model. Asenjo was a pioneer in neurosurgery that founded the Institute of Neurosurgery and Brain Research in Chile already in 1939. Because he was a friend of Salvador Allende the sculpture was removed and disappeared in connection with the military coop in Chile 1973. I think that the sculpture is a too beautiful illustration of what makes us human to be forgotten.
Saturday, November 10, 2012
Trade-offs between effectiveness and efficiency in stroke rehabilitation
Trade-offs between effectiveness and efficiency in stroke rehabilitation
Keywords:
- activities of daily living;
- effectiveness;
- efficiency;
- rehabilitation;
- stroke;
- trade-off
Background Most stroke research has studied rehabilitation effectiveness and rehabilitation efficiency separately and not investigated the potential trade-offs between these two indices of rehabilitation.
Aims To determine whether there is a trade-off between independent factors of rehabilitation effectiveness and rehabilitation efficiency.
Methods Using a retrospective cohort study design, we studied all stroke patients (n=2810) from two sub-acute rehabilitation hospitals from 1996 to 2005, representing 87·5% of national bed-years during the same period.
Results Independent predictors of poorer rehabilitation effectiveness and log rehabilitation efficiency were • older age • race-ethnicity • caregiver availability • ischemic stroke • longer time to admission • dementia • admission Barthel Index score, and • length of stay.
Rehabilitation effectiveness was lower in females, and the gender differences were significantly lower in those aged ≤70 years (β −4·7 (95% confidence interval −7·4 to −2·0)). There were trade-offs between effectiveness and efficiency with respect to admission Barthel Index score and length of stay. An increase of 10 in admission Barthel Index score predicted an increase of 3·6% (95% confidence interval 3·2–4·0) in effectiveness but a decrease of 0·04 (95% confidence interval −0·05 to −0·02) in log efficiency (a reduction of efficiency by 1·0 per 30 days). An increase in log length of stay by 1 (length of stay of 2·7 days) predicted an increase of 8·0% (95% confidence interval 5·7–10·3) in effectiveness but a decrease of 0·82 (95% confidence interval −0·90 to −0·74) in log efficiency (equivalent to a reduction in efficiency by 2·3 per 30 days). For optimal rehabilitation effectiveness and rehabilitation efficiency, the admission Barthel Index score was 30–62 and length of stay was 37–41 days.
Conclusions
There are trade-offs between effectiveness and efficiency during inpatient sub-acute stroke rehabilitation with respect to admission functional status and length of stay.
Monday, October 22, 2012
WSC in pictures
Marc Fisher and Geoffrey Donnan talk about journals STROKE and IJS |
INCOMING WSO PRESIDENT STEPHEN DAVIS |
GEOFFREY DONNAN AT THE IJS BOARD MEETING |
Dominique Cadhilaic, Marion Walker, Geoffrey Donnan and Julie Bernhardt |
The Canadian Stroke Network
http://www.canadianstrokenetwork.ca/index.php/about/our-partners-links-page/provincialterritorial-strategies/
The Canadian Stroke Network have a great blog. This blog is an excellent example of where content can be published, free and easily accessible for the public. The International Journal of Stroke are planning on working with SSOs to build a public stroke network here on our blog, which has as of this month had over 31,000 views! Blogs are a great way of disseminating important information at low, or no cost!
The Canadian Stroke Network have a great blog. This blog is an excellent example of where content can be published, free and easily accessible for the public. The International Journal of Stroke are planning on working with SSOs to build a public stroke network here on our blog, which has as of this month had over 31,000 views! Blogs are a great way of disseminating important information at low, or no cost!
Tuesday, September 18, 2012
Aphasia the Movie
Aphasia the movie is playing at the Other Film Festival this coming Friday and IJS will attend. I briefly caught the end of this film and a fantastic forum with Carl, the films subject; and an audience of stroke survivors with aphasia, and clinicians at the Stroke Society Australasia in Sydney last month.
In 2005 Carl McIntyre suffered a stroke resulting in aphasia - his journey is the subject of this film.
IJS will speak to Carl on Thursday morning before the screening and hopefully bring back a great video and sound recording capturing some of Carl's story and why the film was made.
In 2005 Carl McIntyre suffered a stroke resulting in aphasia - his journey is the subject of this film.
IJS will speak to Carl on Thursday morning before the screening and hopefully bring back a great video and sound recording capturing some of Carl's story and why the film was made.
Friday, August 31, 2012
Stroke Society Australasia in pictures
Joanne Murray and Coralie English |
Valerie Pomeroy |
Stephanie Ho and Brenda Booth |
Sandy Middleton and Simeon Dale |
Chris Levi and Jane Maguire |
David Howells and Milos Pekny |
Atte Meretoja |
Nadine Andrew and Monique Kilkenny |
Leonid Churilov Florey Statistician, Elise Cowley and Tina Soulis from NTA |
Bernard Yan and Bruce Campbell |
Ian Mosely |
Lisa Walker, Sue Mosely, Sandra Petrolo, and WenWen Zhang |
Tissa Wijeratne, Julie Bernhardt Director of the AVERT trial and Erin Godeke |
Mhairi Macrae, Neuroscientist University of Glasgow |
Fiona Ellery from NTA and AVERT Trial with Carmen Lahiff-Jenkins from IJS |
Mark Longworth Smartstrokes, Richard Lindley SSA organiser and Dennis Crimmins |
The WSO has a new website...
The WSO has a new website
http://www.world-stroke.org/
If you're having trouble with membership access to the journal please contact me: carmenl@unimelb.edu.au
http://www.world-stroke.org/
If you're having trouble with membership access to the journal please contact me: carmenl@unimelb.edu.au
Monday, August 27, 2012
Stroke Society Australasia 2012; it begins.
This week is the Stroke Society Australasia Meeting in Sydney incorporating Smart Strokes, IJS will be in attendance keeping you up to date. Andrei Alexandrov will be there speaking on his imaging 'helmet', Val Pomeroy on Neurorehabilitation, Rustam Al-Shahi Salman on mechanisms of intracerebral and subarachnoid haemorrhage, and Christian Stapf whose interests are brain vascular malformations and other conditions predisposing to intracranial haemorrhage. Caroline Watkins will be be talking about stoke service development. Stephanie Ho stroke survivor and Noel Hayman, Queensland Australian of the Year 2011 who works in Indigenous Health.
Last year IJS collected a fabulous series of interviews from SSA.
Werner Hacke
Argye Hillis
Elizabeth Holliday
Susan Hillier
Jocelyn Bowden
Karlea Kremer
Michelle McDonnell
Timothy Kleinig
Last year IJS collected a fabulous series of interviews from SSA.
Werner Hacke
Argye Hillis
Elizabeth Holliday
Susan Hillier
Jocelyn Bowden
Karlea Kremer
Michelle McDonnell
Timothy Kleinig
Monday, August 20, 2012
Protocol for the perfusion and angiography imaging sub- study of the Third International Stroke Trial (IST-3) of alteplase treatment within six hours of acute ischaemic stroke.
Joanna Wardlaw, Reudiger von Krummer, Trevor Carpenter, Mark Parsons, Richard Lindley, Geoff Cohen, Veronica Murray, Adam Kobayashi, Andre Peeters, Francesca Chappell and Peter Sandercock.
Abstract
Rationale: Intravenous thrombolysis with recombinant tissue plasminogen Activator (rt- PA) improves outcomes in patients treated early after stroke but at the risk of causing intracranial haemorrhage. Restricting rt-P A use to patients with evidence of still salvageable tissue, or with definite arterial occlusion, might help reduce risk, increase benefit and identify patients for treatment at late time windows.
Aims: To determine if perfusion or angiographic imaging with CT or MR help identify patients who are more likely to benefit from rt-PA in the context of a large multicentre randomised trial of rt-PA given within six hours of onset of acute ischaemic stroke, the Third International Stroke Trial (IST-3).
Design: IST-3 is a prospective multicentre randomised controlled trial testing rt-PA (0.9mg/kg, maximum dose 90mg) started up to six hours after onset of acute ischaemic stroke, in patients with no clear indication for or contraindication to rt-PA. Brain imaging (CT or MR) was mandatory pre-randomisation to exclude haemorrhage. Scans were read centrally, blinded to treatment and clinical information. In centres where perfusion and/or angiography imaging were used routinely in stroke, these images were also collected centrally, processed and assessed using validated visual scores and computational measures.
Study Outcomes: The primary outcome in IST-3 is alive and independent (Oxford Handicap Score 0-2) at 6 months; secondary outcomes are symptomatic and fatal intracranial haemorrhage, early and late death. The perfusion and angiography study additionally will examine interactions between rt-PA and clinical outcomes, infarct growth and recanalisation in the presence or absence of perfusion lesions and/or arterial occlusion at presentation. The study is registered ISRCTN25765518.
Coming to IJS.
Abstract
Rationale: Intravenous thrombolysis with recombinant tissue plasminogen Activator (rt- PA) improves outcomes in patients treated early after stroke but at the risk of causing intracranial haemorrhage. Restricting rt-P A use to patients with evidence of still salvageable tissue, or with definite arterial occlusion, might help reduce risk, increase benefit and identify patients for treatment at late time windows.
Aims: To determine if perfusion or angiographic imaging with CT or MR help identify patients who are more likely to benefit from rt-PA in the context of a large multicentre randomised trial of rt-PA given within six hours of onset of acute ischaemic stroke, the Third International Stroke Trial (IST-3).
Design: IST-3 is a prospective multicentre randomised controlled trial testing rt-PA (0.9mg/kg, maximum dose 90mg) started up to six hours after onset of acute ischaemic stroke, in patients with no clear indication for or contraindication to rt-PA. Brain imaging (CT or MR) was mandatory pre-randomisation to exclude haemorrhage. Scans were read centrally, blinded to treatment and clinical information. In centres where perfusion and/or angiography imaging were used routinely in stroke, these images were also collected centrally, processed and assessed using validated visual scores and computational measures.
Study Outcomes: The primary outcome in IST-3 is alive and independent (Oxford Handicap Score 0-2) at 6 months; secondary outcomes are symptomatic and fatal intracranial haemorrhage, early and late death. The perfusion and angiography study additionally will examine interactions between rt-PA and clinical outcomes, infarct growth and recanalisation in the presence or absence of perfusion lesions and/or arterial occlusion at presentation. The study is registered ISRCTN25765518.
Coming to IJS.
Sunday, August 19, 2012
Friday, August 10, 2012
NeuroThera® Efficacy and Safety Trial – 3 (NEST-3): a double-blind, randomized, sham-controlled, parallel group, multicenter, pivotal study to assess the safety and efficacy of transcranial laser therapy with the NeuroThera® Laser System for the treatment of acute ischemic stroke within 24 h of stroke onset
Rationale Transcranial laser therapy is undergoing clinical
trials in patients with acute ischemic stroke. The NeuroThera
® Efficacy and Safety Trial-1 was strongly positive for
90-day functional benefit with transcranial laser therapy,
and post hoc analyses of the subsequent NeuroThera® Efficacy
and Safety Trial-2 trial suggested a meaningful beneficial
effect in patients with moderate to moderately severe
ischemic stroke within 24 h of onset. These served as the
basis for the NeuroThera® Efficacy and Safety Trial-3 randomized
controlled trial.
Aim The purpose of this pivotal study was to demonstrate
safety and efficacy of transcranial laser therapy with the
NeuroThera® Laser System in the treatment of subjects diagnosed
with acute ischemic stroke.
Design NeuroThera® Efficacy and Safety Trial-1-3 is a
double-blind, randomized, sham-controlled, parallel group,
multicenter, pivotal study that will enroll 1000 subjects at up
to 50 sites. All subjects will receive standard medical management
based on the American Stroke Association and
European Stroke Organization Guidelines. In addition to
standard medical management, both groups will undergo
transcranial laser therapy procedure between 4·5 and 24 h of
stroke onset. The study population will be randomized into
two arms: the sham control group will receive a sham transcranial
laser therapy procedure and the transcranial laser
therapy group will receive an active transcranial laser
therapy procedure. The randomization ratio will be 1:1 and
will be stratified to ensure a balanced subject distribution
between study arms.
Study Outcomes The primary efficacy end point is disability
at 90 days (or the last rating), as assessed on the modified
Rankin Scale, dichotomized as a success (a score of 0–2) or a
failure (a score of 3 to 6).
Friday, June 29, 2012
Translational Research Themed Edition of the International Journal of Stroke
'The mortality and morbidity associated with stroke makes the development of new drugs a research priority. Recent unsuccessful clinical trials have reduced enthusiasm for the development of neuroprotective drugs. Here, we use empirical evidence derived from systematic reviews of stroke drug development to identify stages of drug development which might be improved. We then propose exemplar strategies which may be helpful, along with some basic economic modelling of what the impact of such strategies might be. This suggests that relatively straightforward measures might reduce the costs of drug development by $5·8 bn or 31%.'
Abstract from Improving the efficiency of the development of drugs for stroke
Authors:
David W. Howells1,2,*,
Emily S. Sena1,2,
Victoria O'Collins1,
Malcolm R. Macleod
Abstract from Improving the efficiency of the development of drugs for stroke
Authors:
Thursday, May 24, 2012
ESC IST-3 announcement
Researchers from the
International Stroke Trial 3; have released results from the worlds largest
ever trial of the clot busting drug rt-PA. Published today concurrently in the
Lancet, and presented at the European Stroke Conference in Lisbon.
The IST-3 trial found patients
receiving clot-busting drugs have a better chance of survival and avoiding
disability. In patients over 80, a previously untreated group in the European
Union, the use of rt-PA will dramatically increase their survival rates post
stroke.
Research has found patients under
80 benefit from rt-PA when treated within four and a half hours of stroke. Co
investigator Richard Lindley, Professor of Geriatric Medicine from the
University of Sydney’s Medical School is adamant ‘Please don’t ignore the over
80s – they benefit hugely’.
Richard Lindley, Joanna Wardlaw and Michael Hennerici at todays ESC announcement |
The trial found fatal bleeding
was a risk factor associated with rt-PA use within the first week of treatment,
although the researchers insist that the early hazard is greatly outweighed by the
late substantial benefit. Dr Lindley insists that in his practical experience
patients over 80 have an extremely high risk of death after stoke within the
six month period indicated and that the risk of rt-PA bleed is minimal compared
to the risk of no treatment at all.
This latest study sought to
establish rt-PA treatment as effective in patients over 80, and it has done
exactly that. As the population ages and age becomes a primary risk factor in
Australia these treatments will be able to alleviate the extreme costs of
stroke on the community and increase quality of life for stroke patients.
IST-3 Imaging Lead Professor
Joanna Wardlaw for the University of Edinburgh Centre for Clinical Brain
Sciences, is also pushing for better managed clinical windows so that patients
can access rt-PA within the required time, ‘the faster you treat the better the
outcome’ she said ‘ and faster treatment will result from better communication
(among health workers)’.
Carmen Lahiff-Jenkins
Managing Editor the International
Journal of Stroke
Attending the European Stroke
Conference, Lisbon, Portugal
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