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Major global study identifies a safer treatment of acute stroke

Study aims to improve survival rates of stroke victims

Date:
May 10, 2016
Source:
University of Leicester
Summary:
A new study has aimed to improve survival rates of stroke victims. It is hoped the findings from the trial of more than 3,000 patients in 100 hospitals worldwide could change the way the most common form of stroke is treated globally.
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The safety of a controversial clot-busting drug has been investigated by researchers, who have shown a modified dosage can reduce serious bleeding in the brain and improve survival rates.

It is hoped the findings from the trial of more than 3,000 patients in 100 hospitals worldwide could change the way the most common form of stroke is treated globally.

Intravenous rtPA (or alteplase) is given to people suffering acute ischaemic stroke and works by breaking up clots blocking the flow of blood to the brain.

However, it can cause serious bleeding in the brain in around five per cent of cases, with many of these proving fatal.

The study was conducted by teams at the George Institute for Global Health, and the University of Leicester's Department of Cardiovascular Sciences. The UK arm of the trial was funded by the Stroke Association.

National Coordinator of the study in the UK, Professor Tom Robinson of the University said: "This trial was a randomised controlled trial, which is the gold standard for determining whether a medicine actually has the desired effect.

"The results provide important information when discussing clot-busting treatment with patients and their families.

"Most patients who have a major stroke want to know they will survive but without being seriously dependent on their family. We have shown this to be the case with the lower dose of the drug.

"Stroke is the fourth leading cause of death in the UK and the leading cause of adult neurological disability. There are over 150,000 strokes each year in the UK, one in four of whom are in people of working age.

"Currently, approximately 11 per cent of stroke patients receive thrombolysis treatment for stroke in the UK."

Professor Craig Anderson, Lead Author of the study published in The New England Journal of Medicine, said: "At the moment you could have a stroke but end up dying from a bleed in the brain. It's largely unpredictable as to who will respond and who is at risk with rtPA.

"What we have shown is that if we reduce the dose level, we maintain most of the clot busting benefits of the higher dose but with significantly less major bleeds and improved survival rates. On a global scale, this approach could save the lives of many tens of thousands of people.

"There is a trade off with the lower dose in regards to recovery of functioning, but being alive is surely preferable to most patients than suffering an early death."

Dr Dale Webb, Director of Research and Information at the Stroke Association, said: "We've known for a while that giving stroke patients alteplase carries the risk of bleeding in the brain which can be fatal.

"However, an independent review in the UK concluded last year that the benefits outweigh the risks. This new study will be welcome news for clinicians and patients, because it suggests that we can reduce the risk of bleeding with a lower dose of alteplase, whilst retaining most of its benefit."

These differing effects meant that the trial was unable to show conclusively that the low dose was as effective as standard dose rtPA in terms of survivors being free of any disability.

rtPA is used to dissolve clots that block a blood vessel in a patient's brain within the first few hours after the onset of stroke symptoms.

Yet, because many people with stroke arrive at hospital after this crucial time window, only around five per cent of eligible people currently receive this therapy in most countries.

Concerns over the risks of bleeding on the brain associated with rtPA have prompted independent reviews of the research evidence in Australia and the UK.

Professor Tom Robinson is also from the NIHR Leicester Cardiovascular Biomedical Research Unit.

KEY FINDINGS

  • Compared to standard dose (0.9mg/kg body weight), the lower dose (0.6mg/kg) of rtPA reduced rates of serious bleeding in the brain, known as intracerebral haemorrhage (ICH), by two thirds.
  • After 90 days, 8.5 per cent of patients had died after receiving low dose rtPA, compared to 10.3 per cent who received the standard dose.
  • The survival benefit was offset by a slight rise in the amount of people suffering residual disability. For every 1000 patients treated, low dose rtPA, compared to the standard dose, 41 more people had physical disabilities, such as needing help dressing or walking, but 19 fewer people died.

Story Source:

Materials provided by University of Leicester. Note: Content may be edited for style and length.


Journal Reference:

  1. Martin B. Leon, Craig R. Smith, Michael J. Mack, Raj R. Makkar, Lars G. Svensson, Susheel K. Kodali, Vinod H. Thourani, E. Murat Tuzcu, D. Craig Miller, Howard C. Herrmann, Darshan Doshi, David J. Cohen, Augusto D. Pichard, Samir Kapadia, Todd Dewey, Vasilis Babaliaros, Wilson Y. Szeto, Mathew R. Williams, Dean Kereiakes, Alan Zajarias, Kevin L. Greason, Brian K. Whisenant, Robert W. Hodson, Jeffrey W. Moses, Alfredo Trento, David L. Brown, William F. Fearon, Philippe Pibarot, Rebecca T. Hahn, Wael A. Jaber, William N. Anderson, Maria C. Alu, John G. Webb. Transcatheter or Surgical Aortic-Valve Replacement in Intermediate-Risk Patients. New England Journal of Medicine, 2016; 374 (17): 1609 DOI: 10.1056/NEJMoa1514616

Cite This Page:

University of Leicester. "Major global study identifies a safer treatment of acute stroke." ScienceDaily. ScienceDaily, 10 May 2016. <www.sciencedaily.com/releases/2016/05/160510084203.htm>.
University of Leicester. (2016, May 10). Major global study identifies a safer treatment of acute stroke. ScienceDaily. Retrieved March 18, 2024 from www.sciencedaily.com/releases/2016/05/160510084203.htm
University of Leicester. "Major global study identifies a safer treatment of acute stroke." ScienceDaily. www.sciencedaily.com/releases/2016/05/160510084203.htm (accessed March 18, 2024).

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