COVID-19 and changes in activity and treatment of ST elevation MI from a UK cardiac centre.

COVID-19 Indirect morbidity and mortality STEMI Thrombolysis

Journal

International journal of cardiology. Heart & vasculature
ISSN: 2352-9067
Titre abrégé: Int J Cardiol Heart Vasc
Pays: Ireland
ID NLM: 101649525

Informations de publication

Date de publication:
Apr 2021
Historique:
received: 03 07 2020
revised: 29 01 2021
accepted: 03 02 2021
entrez: 1 3 2021
pubmed: 2 3 2021
medline: 2 3 2021
Statut: ppublish

Résumé

The international healthcare response to COVID-19 has been driven by epidemiological data related to case numbers and case fatality rate. Second order effects have been less well studied. This study aimed to characterise the changes in emergency activity of a high-volume cardiac catheterisation centre and to cautiously model any excess indirect morbidity and mortality. Retrospective cohort study of patients admitted with acute coronary syndrome fulfilling criteria for the heart attack centre (HAC) pathway at St. Bartholomew's hospital, UK. Electronic data were collected for the study period March 16th - May 16th 2020 inclusive and stored on a dedicated research server. Standard governance procedures were observed in line with the British Cardiovascular Intervention Society audit. There was a 28% fall in the number of primary percutaneous coronary interventions (PCIs) for ST elevation myocardial infarction (STEMI) during the study period (111 vs. 154) and 36% fewer activations of the HAC pathway (312 vs. 485), compared to the same time period averaged across three preceding years. In the context of 'missing STEMIs', the excess harm attributable to COVID-19 could result in an absolute increase of 1.3% in mortality, 1.9% in nonfatal MI and 4.5% in recurrent ischemia. The emergency activity of a high-volume PCI centre was significantly reduced for STEMI during the peak of the first wave of COVID-19. Our data can be used as an exemplar to help future modelling within cardiovascular workstreams to refine aggregate estimates of the impact of COVID-19 and inform targeted policy action.

Sections du résumé

BACKGROUND BACKGROUND
The international healthcare response to COVID-19 has been driven by epidemiological data related to case numbers and case fatality rate. Second order effects have been less well studied. This study aimed to characterise the changes in emergency activity of a high-volume cardiac catheterisation centre and to cautiously model any excess indirect morbidity and mortality.
METHOD METHODS
Retrospective cohort study of patients admitted with acute coronary syndrome fulfilling criteria for the heart attack centre (HAC) pathway at St. Bartholomew's hospital, UK. Electronic data were collected for the study period March 16th - May 16th 2020 inclusive and stored on a dedicated research server. Standard governance procedures were observed in line with the British Cardiovascular Intervention Society audit.
RESULTS RESULTS
There was a 28% fall in the number of primary percutaneous coronary interventions (PCIs) for ST elevation myocardial infarction (STEMI) during the study period (111 vs. 154) and 36% fewer activations of the HAC pathway (312 vs. 485), compared to the same time period averaged across three preceding years. In the context of 'missing STEMIs', the excess harm attributable to COVID-19 could result in an absolute increase of 1.3% in mortality, 1.9% in nonfatal MI and 4.5% in recurrent ischemia.
CONCLUSIONS CONCLUSIONS
The emergency activity of a high-volume PCI centre was significantly reduced for STEMI during the peak of the first wave of COVID-19. Our data can be used as an exemplar to help future modelling within cardiovascular workstreams to refine aggregate estimates of the impact of COVID-19 and inform targeted policy action.

Identifiants

pubmed: 33644297
doi: 10.1016/j.ijcha.2021.100736
pii: S2352-9067(21)00024-5
pmc: PMC7901371
doi:

Types de publication

Journal Article

Langues

eng

Pagination

100736

Informations de copyright

© 2021 Published by Elsevier B.V.

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Auteurs

Yang Chen (Y)

Institute of Cardiovascular Science, University College London, UK.
St Bartholomew's Hospital, Barts Health NHS Trust, London, UK.

Krishnaraj S Rathod (KS)

St Bartholomew's Hospital, Barts Health NHS Trust, London, UK.
Centre for Cardiovascular Medicines and Devices, Queen Mary University London, UK.

Stephen Hamshere (S)

St Bartholomew's Hospital, Barts Health NHS Trust, London, UK.
Centre for Cardiovascular Medicines and Devices, Queen Mary University London, UK.

Fizzah Choudry (F)

St Bartholomew's Hospital, Barts Health NHS Trust, London, UK.
Centre for Cardiovascular Medicines and Devices, Queen Mary University London, UK.

Mohammed M Akhtar (MM)

St Bartholomew's Hospital, Barts Health NHS Trust, London, UK.
Centre for Cardiovascular Medicines and Devices, Queen Mary University London, UK.

Miles Curtis (M)

St Bartholomew's Hospital, Barts Health NHS Trust, London, UK.

Rajiv Amersey (R)

St Bartholomew's Hospital, Barts Health NHS Trust, London, UK.

Oliver Guttmann (O)

St Bartholomew's Hospital, Barts Health NHS Trust, London, UK.

Constantinos O'Mahony (C)

Institute of Cardiovascular Science, University College London, UK.
St Bartholomew's Hospital, Barts Health NHS Trust, London, UK.

Ajay Jain (A)

St Bartholomew's Hospital, Barts Health NHS Trust, London, UK.
Centre for Cardiovascular Medicines and Devices, Queen Mary University London, UK.

Andrew Wragg (A)

St Bartholomew's Hospital, Barts Health NHS Trust, London, UK.
Centre for Cardiovascular Medicines and Devices, Queen Mary University London, UK.

Andreas Baumbach (A)

St Bartholomew's Hospital, Barts Health NHS Trust, London, UK.
Centre for Cardiovascular Medicines and Devices, Queen Mary University London, UK.

Anthony Mathur (A)

St Bartholomew's Hospital, Barts Health NHS Trust, London, UK.
Centre for Cardiovascular Medicines and Devices, Queen Mary University London, UK.

Daniel A Jones (DA)

St Bartholomew's Hospital, Barts Health NHS Trust, London, UK.
Centre for Cardiovascular Medicines and Devices, Queen Mary University London, UK.

Classifications MeSH