This site is intended for healthcare professionals

Go to /sign-in page

You can view 5 more pages without signing in

ISIS-3 trial

Last reviewed dd mmm yyyy. Last edited dd mmm yyyy

Authoring team

41299 patients entering hospital up to 24 hr after the onset of symptoms of acute myocardial infarction were randomised to:

  • thrombolysis:
    • streptokinase (1.5 MU infused over 1 hr)
    • t-PA (0.60 MU/kg infused over 4 hr)
    • APSAC (30 U over 30 min)

  • anticoagulation:
    • aspirin alone (162 mg/day)
    • aspirin plus subcutaneous heparin (12500 IU starting at 4 hr, given twice daily for 7 days)

The study showed that there was no significant difference in the mortality and complication rates between the three thrombolytic groups.

There was a small, but significant, deficit in re-infarctions in the t-PA group. Streptokinase had a small but significant deficit in non-cerebral bleeds. APSAC and streptokinase were associated with a higher frequency of allergic and hypotensive episodes.

ISIS-3 suggests that the use of heparin and aspirin rather than aspirin alone resulted in a slightly lower mortality rate in the short-term (although there was no effect at 6 months).

Reference:

  • ISIS-3: a randomised comparison of streptokinase vs. tissue plasminogen activator vs. anistreplase and of aspirin plus heparin vs. aspirin alone among 41299 cases of suspected acute myocardial infarction. (1992). Lancet, 339, 753-770.

Create an account to add page annotations

Annotations allow you to add information to this page that would be handy to have on hand during a consultation. E.g. a website or number. This information will always show when you visit this page.

The content herein is provided for informational purposes and does not replace the need to apply professional clinical judgement when diagnosing or treating any medical condition. A licensed medical practitioner should be consulted for diagnosis and treatment of any and all medical conditions.

Connect

Copyright 2024 Oxbridge Solutions Limited, a subsidiary of OmniaMed Communications Limited. All rights reserved. Any distribution or duplication of the information contained herein is strictly prohibited. Oxbridge Solutions receives funding from advertising but maintains editorial independence.