A prospective multi-centre study assessing the safety and effectiveness following the implementation of an accelerated chest pain pathway using point-of-care troponin for use in New Zealand rural hospital and primary care settings

Author:

Miller Rory1ORCID,Nixon Garry1ORCID,Pickering John W2,Stokes Tim1,Turner Robin M3,Young Joanna4,Gutenstein Marc5,Smith Michelle1,Norman Tim6,Watson Antony4,George Peter7,Devlin Gerald8,Du Toit Stephen9,Than Martin10

Affiliation:

1. Department of General Practice and Rural Health, University of Otago, Dunedin School of Medicine , Dunedin , New Zealand

2. Emergency Department, University of Otago – Christchurch , Christchurch , New Zealand

3. Centre for Biostatistics, Division of Health Sciences, University of Otago , Dunedin , New Zealand

4. Canterbury DHB, Christchurch Hospital , Christchurch , New Zealand

5. Rural Health Academic Centre Ashburton, University of Otago – Christchurch , Christchurch , New Zealand

6. Project Office, Midlands Regional Health Network Charitable Trust , Hamilton , New Zealand

7. Chemical Pathology, PathoGene, Merivale , Christchurch , New Zealand

8. Tairawhiti DHB , Gisborne , New Zealand

9. Waikato DHB , Hamilton , New Zealand

10. Emergency Department, Canterbury DHB, Christchurch Hospital , Christchurch , New Zealand

Abstract

Abstract Aims Most rural hospitals and general practices in New Zealand (NZ) are reliant on point-of-care troponin. A rural accelerated chest pain pathway (RACPP), combining an electrocardiogram (ECG), a structured risk score (Emergency Department Assessment of Chest Pain Score), and serial point-of-care troponin, was designed for use in rural hospital and primary care settings across NZ. The aim of this study was to evaluate the safety and effectiveness of the RACPP. Methods and results A prospective multi-centre evaluation following implementation of the RACPP was undertaken from 1 July 2018 to 31 December 2020 in rural hospitals, rural and urban general practices, and urgent care clinics. The primary outcome measure was the presence of 30-day major adverse cardiac events (MACEs) in low-risk patients. The secondary outcome was the percentage of patients classified as low-risk that avoided transfer or were eligible for early discharge. There were 1205 patients enrolled in the study. 132 patients were excluded. Of the 1073 patients included in the primary analysis, 474 (44.0%) patients were identified as low-risk. There were no [95% confidence interval (CI): 0–0.3%] MACE within 30 days of the presentation among low-risk patients. Most of these patients (91.8%) were discharged without admission to hospital. Almost all patients who presented to general practice (99%) and urgent care clinics (97.6%) were discharged to home directly. Conclusion The RACPP is safe and effective at excluding MACEs in NZ rural hospital and primary care settings, where it can identify a group of low-risk patients who can be safely discharged home without transfer to hospital.

Funder

Heart Foundation of New Zealand

Abbott Point-of-Care

Publisher

Oxford University Press (OUP)

Subject

Cardiology and Cardiovascular Medicine,Critical Care and Intensive Care Medicine,General Medicine

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