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| ID | Type | Description | Link |
|---|---|---|---|
| ISRCTN96585404 | Registry Identifier | ISRCTN |
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| Name | Class |
|---|---|
| King's College London | OTHER |
| London School of Hygiene and Tropical Medicine | OTHER |
| Barts & The London NHS Trust | OTHER |
| King's College Hospital NHS Trust |
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The aim of ARREST is to determine the best post-resuscitation care pathway for out of hospital cardiac arrest patients without ST-segment elevation. The investigators propose that changes to emergency management comprising expedited delivery to a specialist heart attack centre with organised post-cardiac arrest care including immediate access to reperfusion therapy will reduce mortality in patients without STE compared to the current standard of care, which comprises protracted pre-hospital management of the patient without definitive care plan and delivery to geographically closest hospital.
Out-of-hospital cardiac arrest (OHCA) is a global public health issue. There are 60,000 cardiac arrests per year in the United Kingdom (UK), of which resuscitation is attempted in just under half. Resuscitation attempts are successful in up to 30%. However, more than two thirds of patients who survive to hospital admission die before discharge. There is wide variation in both regional and inter-hospital survival rates from OHCA; this disparity is also present across London. This variation has been shown to be attributable to hospital infrastructure, resources and personnel rather than patient characteristics. Overall survival therefore remains poor, at 7%.
It is well known that the majority of OHCA are secondary to an acute cardiac ischaemic event. Coronary artery disease is responsible for more than 70% of OHCA of presumed cardiac cause, with acute occlusion demonstrated in 50% of consecutive patients taken for immediate coronary angiography (ICA). Early cardiopulmonary resuscitation (CPR) and defibrillation, with ICA and percutaneous coronary intervention (PCI) in a cardiac arrest centre (CAC), prevents re-arrest, preserves myocardial function and has been shown to improve post-arrest outcomes in ST-segment elevation (STE). The management of patients without STE however is controversial, with a delayed approach to intervention. Despite recently published data suggesting PCI in non-STE resulted in a two-fold increase in favourable outcome, randomised data are lacking. Emergent reperfusion therapies come with a weak recommendation from the International Liaison Committee on Resuscitation (ILCOR), and a Class IIa recommendation by the American Heart Association (AHA) and European Society of Cardiology (ESC), if there is a high suspicion of ongoing infarction.
The European Association of Percutaneous Cardiovascular Interventions (EAPCI) recommends a prior rule-out of non-cardiac cause in the emergency department followed by coronary angiography within 2 hours. It remains unclear if time-critical, definitive hospital based management of the post-arrest patient without STE in a specialist centre improves outcomes, and there has been variable uptake of this strategy both pre-hospital and amongst the interventional cardiology community.
There is an urgent need for a randomised controlled trial examining the benefits of early delivery of post-cardiac arrest care in specialist centres, specifically in the absence of STE. Post-arrest care is time-critical, requires a multi-disciplinary approach and may be more optimally delivered in centres with greater provider experience. ILCOR and the EAPCI state that randomised trials are essential in this population to determine if timely delivery by the ambulance services to a CAC with organised postcardiac arrest care including immediate access to reperfusion therapy improves survival. There are no randomised trials and only indirect evidence that CAC and systems of care may be effective and only two observational studies examining the role of immediate ICA±PCI in the absence of STE. This is an important and topical question as there is a drive to regionalise care for all patients into CACs.
To address this, ARREST will enroll 860 OHCA patients with ROSC to a randomised clinical trial. Each arm of the trial will include 430 patients.
The two arms are as follows:
Intervention Arm: Direct to CAC The intervention arm consists of activation of the pre-hospital triaging system currently in place for post-arrest STE patients. This involves pre-alert of the CAC and strategic delivery of the patient to the catheter laboratory (24 hours a day, 7 days a week). Patients will receive definitive post-resuscitation care: intubation and ventilation, where necessary, targeted temperature management, and goal directed therapies including evaluation and identification of underlying cause of arrest with access to immediate reperfusion if necessary. Prognostication will occur no earlier than 72 hours post-cardiac arrest to prevent premature withdrawal of life-sustaining treatment. Transfer times estimated from the 40-patient pilot are anticipated to be 100 minutes (median; IQR 75 to 113) from time of arrest to the designated centre.
Control Arm: Standard of Care The control arm comprises the current standard of pre-hospital advanced life support (ALS) care management for patients with ROSC following cardiac arrest of suspected cardiac aetiology. The patient is conveyed to the geographically closest emergency department. Management thereafter will be as per standard hospital protocols however as in the intervention arm, prognostication is to be delayed in trial patients until at least 72 hours post arrest.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Intervention Arm: Expedited transfer to a CAC | Experimental | The intervention arm consists of activation of the pre-hospital triaging system currently in place for post-arrest STE patients. This involves pre-alert of the CAC and strategic delivery of the patient to the catheter laboratory (24 hours a day, 7 days a week). Patients will receive definitive post-resuscitation care: intubation and ventilation, where necessary, targeted temperature management, and goal directed therapies including evaluation and identification of underlying cause of arrest with access to immediate reperfusion if necessary. Prognostication will occur no earlier than 72 hours post-cardiac arrest to prevent premature withdrawal of life-sustaining treatment. Transfer times estimated from the 40-patient pilot are anticipated to be 100 minutes (median; IQR 75 to 113) from time of arrest to the designated centre. |
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| Control Arm: Current standard of care | No Intervention | The control arm comprises the current standard of pre-hospital advanced life support (ALS) care management for patients with ROSC following cardiac arrest of suspected cardiac aetiology. The patient is conveyed to the geographically closest emergency department. Management thereafter will be as per standard hospital protocols however as in the intervention arm, prognostication is to be delayed in trial patients until at least 72 hours post arrest. |
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Transfer to cardiac arrest centre | Procedure | Patients in the intervention arm will be taken directly to a the catheter lab of a heart attack centre. |
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| Measure | Description | Time Frame |
|---|---|---|
| All-cause mortality | 30 days after randomisation |
| Measure | Description | Time Frame |
|---|---|---|
| Cerebral performance category score | Neurological status assessed using the cerebral performance category (ranked scale from 1 to 5 with 1 being the best outcome and 5 the worse outcome) | Discharge (capped at 30 days) |
| Modified Rankin Score |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Simon Redwood, MBBS, PhD | Guy's and St Thomas' NHS Foundation Trust | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Dartford and Gravesham NHS Trust | Dartford | United Kingdom | ||||
| Barts Health NHS Trust |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 30092413 | Background | Patterson T, Perkins A, Perkins GD, Clayton T, Evans R, Nguyen H, Wilson K, Whitbread M, Hughes J, Fothergill RT, Nevett J, Mosweu I, McCrone P, Dalby M, Rakhit R, MacCarthy P, Perera D, Nolan JP, Redwood SR. Rationale and design of: A Randomized tRial of Expedited transfer to a cardiac arrest center for non-ST elevation out-of-hospital cardiac arrest: The ARREST randomized controlled trial. Am Heart J. 2018 Oct;204:92-101. doi: 10.1016/j.ahj.2018.06.016. Epub 2018 Aug 6. | |
| 37647928 |
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| Type | Includes Protocol | Includes SAP | Includes ICF | Document Label | Document Date | Document Uploaded Date | Document File Name |
|---|---|---|---|---|---|---|---|
| Prot | Yes | No | No | Study Protocol | Jul 17, 2019 | May 23, 2024 |
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| OTHER |
| Imperial College Healthcare NHS Trust | OTHER |
| Royal Brompton & Harefield NHS Foundation Trust | OTHER |
| Royal Free Hospital NHS Foundation Trust | OTHER |
| St George's University Hospitals NHS Foundation Trust | OTHER |
| London Ambulance Service NHS Trust | OTHER |
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Neurological status assessed using the modified Ranking Score (ranked scale from 0 to 6 with 0 being the better outcome and 6 the worse outcome).
| Discharge (capped at 30 days) |
| Cerebral performance category score | Neurological assessed using the cerebral performance category (ranked scale from 1 to 5 with 1 being the best outcome and 5 the worse outcome) | 3 months after randomisation |
| Modified Rankin Score | Neurological status assessed using the modified Ranking Score (ranked scale from 0 to 6 with 0 being the better outcome and 6 the worse outcome). | 3 months after randomisation |
| All-cause mortality | 3 months after randomisation |
| All-cause mortality | 6 months after randomisation |
| All-cause mortality | 12 months after randomisation |
| Patient's quality of life | Assessed using the EuroQol-5 Dimension-5 Level (EQ-5D-5L) standardised survey | Discharge (capped at 30 days) |
| London |
| United Kingdom |
| BHR University Hospitals NHS Trust | London | United Kingdom |
| Chelsea and Westminster Hospital NHS Foundation Trust | London | United Kingdom |
| Croydon Health Services NHS Trust | London | United Kingdom |
| Epsom and St Helier University Hospitals NHS Trust | London | United Kingdom |
| Guy's and St Thomas' NHS FT | London | United Kingdom |
| Hillingdon Hospitals NHS Trust | London | United Kingdom |
| Homerton University Hospital NHS Trust | London | United Kingdom |
| Imperial College Healthcare NHS Trust | London | United Kingdom |
| King's College Hospital NHS Foundation Trust | London | United Kingdom |
| Kingston Hospital NHS FT | London | United Kingdom |
| Lewisham & Greenwich NHS Trust | London | United Kingdom |
| London Ambulance Service NHS Trust | London | United Kingdom |
| London North West University Healthcare | London | United Kingdom |
| North Middlesex University Hospital NHS Trust | London | United Kingdom |
| Royal Brompton and Harefield NHS Trust | London | United Kingdom |
| Royal Free London NHS Foundation Trust | London | United Kingdom |
| St George's University Hospitals NHS Foundation Trust | London | United Kingdom |
| Surrey and Sussex Healthcare NHS Trust | London | United Kingdom |
| University College London Hospitals NHS Foundation Trust | London | United Kingdom |
| West Hertfordshire Hospitals NHS Trust | Watford | United Kingdom |
| Result |
| Patterson T, Perkins GD, Perkins A, Clayton T, Evans R, Dodd M, Robertson S, Wilson K, Mellett-Smith A, Fothergill RT, McCrone P, Dalby M, MacCarthy P, Firoozi S, Malik I, Rakhit R, Jain A, Nolan JP, Redwood SR; ARREST trial collaborators. Expedited transfer to a cardiac arrest centre for non-ST-elevation out-of-hospital cardiac arrest (ARREST): a UK prospective, multicentre, parallel, randomised clinical trial. Lancet. 2023 Oct 14;402(10410):1329-1337. doi: 10.1016/S0140-6736(23)01351-X. Epub 2023 Aug 27. |
| Prot_000.pdf |
| ID | Term |
|---|---|
| D058687 | Out-of-Hospital Cardiac Arrest |
| D006323 | Heart Arrest |
| ID | Term |
|---|---|
| D006331 | Heart Diseases |
| D002318 | Cardiovascular Diseases |
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