Completed Heart, Stroke & Blood Cancer

RAPIDNSTEMI - Revascularisation in ACS Patients: Immediate versus Delayed Intervention A study assessing the impact of very early intervention on outcomes in NSTEMI-ACS patients

In plain English

AI plain-English summary

A large clinical trial is testing whether heart attack patients with a less severe form of the condition should receive emergency artery-opening treatment immediately, rather than waiting the standard 72 hours. Around 20% of patients with non-ST-elevation myocardial infarction (NSTEMI) suffer a major cardiac event—such as a second heart attack, heart failure, or death—within a year. Current guidelines recommend performing percutaneous coronary intervention (PCI) during the hospital stay, but the optimal timing remains uncertain. This trial, called RAPIDNSTEMI, will randomise 2,314 patients to either immediate PCI or the current standard of care (PCI within 72 hours). Using high-sensitivity troponin tests to quickly confirm the diagnosis, researchers aim to see if very early intervention reduces the 12-month composite rate of death, new heart attack, or heart failure readmission. If the immediate approach proves superior, it could change national and international guidelines, shifting how hospitals triage and treat a common cardiac emergency. That would directly affect patient outcomes and healthcare service planning—no fundamental science here, just a pragmatic test of a faster treatment pathway.

View original technical description
Clinical event rates in N-STEMI patients remain high, with one year MACE event rate approximately = 20%. Guidelines support a strategy of in-patient Percutaneous Coronary Intervention (PCI) in N-STEMI ACS patients since published data has shown that this reduces subsequent clinical events. The timing of the PCI to provide the best outcomes is however much less certain. While evidenced based guidelines provide general time parameters for PCI (140 being randomised in a 1: 1 fashion to immediate PCI or to current standard of care i.e. pharmacological passivation and PCI within 72hrs of admission. Using High-sensitivity Troponin (HsT) will allow us to determine the GS early and so instil a very early comparative intervention arm. Primary outcome will be a 12-month composite of overall mortality/new MI/readmission with heart failure. We require 2314 patients randomised to show superiority. Whatever the outcome this trial should determine whether there is a need for a change in patient management of a common condition, and so inform National/International Guidelines, to guide healthcare service provision.

View the original record at the funder ↗

Researchers

Anthony Gershlick (EPMC Awardee)

Related Research

Grants with similar aims, by meaning.

Randomized Controlled Trial Comparing Intracoronary Administration of Adenosine or Sodium Nitroprusside to Control for Attenuation of Microvascular Obstruction During Primary Percutaneous Coronary Intervention
A randomised controlled trial of very early versus delayed angiography +/-intervention on outcomes in patients with non ST-elevation myocardial infarction
High-Sensitive Troponin in the Evaluation of patients with Acute Coronary Syndrome (High-STEACS): A randomised controlled trial
A randomised parallel group double blind placebo-controlled dose ranging Trial of low dose adjunctive alTeplase during priMary PCI (T-TIME).
Benefit to patients and the NHS of cardiac magnetic resonance imaging (CMR) after Primary percutaneous coronary Intervention (PPCI) Pathway Activation

Original classification

Clinical Study

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