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dc.contributor.authorHamilton, G.W.
dc.contributor.authorYeoh, J.
dc.contributor.authorDinh, D.
dc.contributor.authorBrennan, A.
dc.contributor.authorYudi, M.B.
dc.contributor.authorFreeman, M.
dc.contributor.authorHorrigan, M.
dc.contributor.authorMartin, L.
dc.contributor.authorReid, Christopher
dc.contributor.authorYip, T.
dc.contributor.authorPicardo, S.
dc.contributor.authorSharma, A.
dc.contributor.authorDuffy, S.J.
dc.contributor.authorFarouque, O.
dc.contributor.authorClark, D.J.
dc.contributor.authorAjani, A.E.
dc.date.accessioned2023-11-14T07:12:03Z
dc.date.available2023-11-14T07:12:03Z
dc.date.issued2022
dc.identifier.citationHamilton, G.W. and Yeoh, J. and Dinh, D. and Brennan, A. and Yudi, M.B. and Freeman, M. and Horrigan, M. et al. 2022. Reperfusion Times and Outcomes in Patients With ST-Elevation Myocardial Infarction Presenting Without Pre-Hospital Notification. Cardiovascular Revascularization Medicine. 41: pp. 136-141.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/93764
dc.identifier.doi10.1016/j.carrev.2022.01.024
dc.description.abstract

Background: Primary percutaneous coronary intervention (PCI) for patients with ST-elevation myocardial infarction (STEMI) is recommended within 90 min of first medical contact. Those without pre-hospital notification (PN) are less likely to meet reperfusion targets and are an understudied subset of the STEMI population. Methods: An observational cohort study from a multicentre PCI registry of consecutive patients undergoing primary PCI for STEMI between 2012 and 2017. Exclusion criteria included out-of-hospital cardiac arrest, prior thrombolysis, symptom onset >12 h prior, and cardiogenic shock. Results: 2519 patients were included: 1392 (55.3%) without PN (no-PN group) and 1127 (44.7%) with PN (PN group). Those without PN had longer median DTBT (78 min vs 51 min, p < 0.001) and STBT (206 min vs 161 min, p < 0.001), with only 55% meeting DTBT targets out-of-hours in the no-PN group. No-PN patients had lower rates of AHA/ACC type B2/C lesions, GP IIb/IIIa use, aspiration thrombectomy and had smaller stent diameter (all p ≤ 0.003), suggesting smaller areas of ischemic myocardium. There were no significant differences in 30-day MACE (no-PN 5.6% vs PN 6.5%, p = 0.36) or long-term National Death Index linked mortality (no-PN 6.2% vs PN 7.9%, p = 0.09). Lack of PN did not independently predict long-term mortality. Conclusion: Despite comparably excellent outcomes overall, those without PN had longer ischemic times and were less likely to meet DTBT targets, especially after hours. Ischemic times may be a better evaluation of PN networks than hard clinical outcomes, and efficient systems of care tailored to the individual health service are essential to ensure timely reperfusion of patients with STEMI.

dc.languageeng
dc.relation.sponsoredbyhttp://purl.org/au-research/grants/nhmrc/1111170
dc.relation.sponsoredbyhttp://purl.org/au-research/grants/nhmrc/1136372
dc.subjectDoor-to-balloon time
dc.subjectIschemic time
dc.subjectOutcomes
dc.subjectPre-hospital notification
dc.subjectSTEMI
dc.subjectHospitals
dc.subjectHumans
dc.subjectPercutaneous Coronary Intervention
dc.subjectReperfusion
dc.subjectST Elevation Myocardial Infarction
dc.subjectTime Factors
dc.subjectTreatment Outcome
dc.subjectMelbourne Interventional Group
dc.subjectHumans
dc.subjectTreatment Outcome
dc.subjectReperfusion
dc.subjectTime Factors
dc.subjectHospitals
dc.subjectPercutaneous Coronary Intervention
dc.subjectST Elevation Myocardial Infarction
dc.titleReperfusion Times and Outcomes in Patients With ST-Elevation Myocardial Infarction Presenting Without Pre-Hospital Notification
dc.typeJournal Article
dcterms.source.volume41
dcterms.source.startPage136
dcterms.source.endPage141
dcterms.source.issn1553-8389
dcterms.source.titleCardiovascular Revascularization Medicine
dc.date.updated2023-11-14T07:12:03Z
curtin.departmentCurtin School of Population Health
curtin.accessStatusFulltext not available
curtin.facultyFaculty of Health Sciences
curtin.contributor.orcidReid, Christopher [0000-0001-9173-3944]
dcterms.source.eissn1878-0938
curtin.repositoryagreementV3


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