Transient Ischaemic attack Emergency Referral (TIER): randomised feasibility trial results

Watkins, Alan, Jones, Jenna Katherine, Ali, Khalid, Dewar, Richard, Edwards, Adrian ORCID: https://orcid.org/0000-0002-6228-4446, Evans, Bridie Angela, Evans, Lyn, Ford, Gary A, Hampton, Chelsey, John, Roger, Jones, Charlene, Moore, Chris, Obiako, Michael, Porter, Alison, Pryce, Alan, Quinn, Tom, Seagrove, Anne C, Snooks, Helen, Whitman, Shirley and Rees, Nigel 2024. Transient Ischaemic attack Emergency Referral (TIER): randomised feasibility trial results. Emergency Medicine Journal 10.1136/emermed-2021-212230

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Abstract

Background: Early assessment of patients with suspected transient ischaemic attack (TIA) is crucial to provision of effective care, including initiation of preventive therapies and identification of stroke mimics. Many patients with TIA present to emergency medical services (EMS) but may not require hospitalisation. Paramedics could identify and refer patients with low-risk TIA, without conveyance to the ED. Safety and effectiveness of this model is unknown. Aim: To assess the feasibility of undertaking a fully powered randomised controlled trial (RCT) to evaluate clinical and cost-effectiveness of paramedic referral of patients who call EMS with low-risk TIA to TIA clinic, avoiding transfer to ED. Methods: The Transient Ischaemic attack Emergency Referral (TIER) intervention was developed through a survey of UK ambulance services, a scoping review of evidence of prehospital care of TIA and convening a specialist clinical panel to agree its final form. Paramedics in South Wales, UK, were randomly allocated to trial intervention (TIA clinic referral) or control (usual care) arms, with patients’ allocation determined by that of attending paramedics. Predetermined progression criteria considered: proportion of patients referred to TIA clinic, data retrieval, patient satisfaction and potential cost-effectiveness. Results: From December 2016 to September 2017, eighty-nine paramedics recruited 53 patients (36 intervention; 17 control); 48 patients (31 intervention; 17 control) consented to follow-up via routine data. Three intervention patients, of seven deemed eligible, were referred to TIA clinic by paramedics. Contraindications recorded for the other intervention arm patients were: Face/Arms/Speech/Time positive (n=13); ABCD2 score >3 (n=5); already anticoagulated (n=2); crescendo TIA (n=1); other (n=8). Routinely collected electronic health records, used to report further healthcare contacts, were obtained for all consenting patients. Patient-reported satisfaction with care was higher in the intervention arm (mean 4.8/5) than the control arm (mean 4.2/5). Health economic analysis suggests an intervention arm quality-adjusted life-year loss of 0.0094 (95% CI −0.0371, 0.0183), p=0.475. Conclusion: The TIER feasibility study did not meet its progression criteria, largely due to low patient identification and referral rates. A fully powered RCT in this setting is not recommended. Trial registration number: ISRCTN85516498.

Item Type:	Article
Date Type:	Published Online
Status:	In Press
Schools:	Medicine
Additional Information:	License information from Publisher: LICENSE 1: URL: http://creativecommons.org/licenses/by-nc/4.0/, Start Date: 2024-10-10, Type: open-access
Publisher:	BMJ Publishing Group
ISSN:	1472-0205
Date of First Compliant Deposit:	17 October 2024
Date of Acceptance:	12 September 2024
Last Modified:	17 Oct 2024 08:15
URI:	https://orca.cardiff.ac.uk/id/eprint/172973

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