Treatment and 30-Day Mortality after Myocardial Infarction in Prostate Cancer Patients: A Population-Based Study from Norway.


Journal

Cardiology
ISSN: 1421-9751
Titre abrégé: Cardiology
Pays: Switzerland
ID NLM: 1266406

Informations de publication

Date de publication:
2023
Historique:
received: 23 08 2022
accepted: 08 10 2022
pubmed: 20 10 2022
medline: 3 3 2023
entrez: 19 10 2022
Statut: ppublish

Résumé

There is limited knowledge about the use of invasive treatment and mortality after acute myocardial infarction (AMI) in prostate cancer (PCa) patients. We therefore wanted to compare rates of invasive treatment and 30-day mortality between AMIs in patients with PCa and AMIs in the general Norwegian male population. Norwegian population-based registry data from 2013 to 2019 were used in this cohort study to identify AMIs in patients with a preceding PCa diagnosis. We compared invasive treatment rates and 30-day mortality in AMI patients with PCa to the same outcomes in all male AMI patients in Norway. Invasive treatment was defined as performed angiography with or without percutaneous coronary intervention or coronary artery bypass graft surgery. Standardized mortality (SMR) and incidence ratios, and logistic regression were used to evaluate the association between PCa risk groups and invasive treatment. In 1,018 patients with PCa of all risk groups, the total rates of invasive treatment for AMIs were similar to the rates in the general AMI population. In patients with ST-segment elevation AMIs, rates were lower in metastatic PCa compared to localized PCa (OR 0.15, 95% CI: 0.04-0.49). For non-ST-segment elevation AMIs, there were no differences between PCa risk groups. The 30-day mortality after AMI was lower in PCa patients than in the total population of similarly aged AMI patients (SMR 0.77, 95% CI: 0.61-0.97). Except for patients with metastatic PCa experiencing an ST-segment elevation AMI, PCa patients were treated as frequent with invasive treatment for their AMI as the general AMI population. 30-day all-cause mortality was lower after AMI in PCa patients compared to the general AMI population.

Identifiants

pubmed: 36260991
pii: 000527636
doi: 10.1159/000527636
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

83-92

Informations de copyright

© 2022 The Author(s). Published by S. Karger AG, Basel.

Auteurs

Rachel Bedenis Forster (RB)

Department of Health Registry Research and Development, Norwegian Institute of Public Health, Bergen, Norway.

Camilla Kjellstadli (C)

Department of Health Registry Research and Development, Norwegian Institute of Public Health, Bergen, Norway.
Department of Oncology and Medical Physics, Haukeland University Hospital, Bergen, Norway.

Tor Åge Myklebust (TÅ)

Department of Registration, Cancer Registry of Norway, Oslo, Norway.
Department of Research and Innovation, Møre and Romsdal Hospital Trust, Ålesund, Norway.

Grace Egeland (G)

Department of Health Registry Research and Development, Norwegian Institute of Public Health, Bergen, Norway.
Department of Global Public Health and Primary Care, University of Bergen, Bergen, Norway.

Gerhard Sulo (G)

Department of Disease Burden, Norwegian Institute of Public Health, Bergen, Norway.

Tone Bjørge (T)

Department of Global Public Health and Primary Care, University of Bergen, Bergen, Norway.
Section for Cervical Cancer Screening, Cancer Registry of Norway, Oslo, Norway.

Kaare Harald Bønaa (KH)

Department of Cardiology, St Olav's Hospital, Trondheim University Hospital, Trondheim, Norway.
Department of Circulation and Medical Imaging, NTNU, Trondheim, Norway.

Petur Benedikt Juliusson (PB)

Department of Health Registry Research and Development, Norwegian Institute of Public Health, Bergen, Norway.
Department of Clinical Science, University of Bergen, Bergen, Norway.

Rune Kvåle (R)

Department of Health Registry Research and Development, Norwegian Institute of Public Health, Bergen, Norway.
Department of Oncology and Medical Physics, Haukeland University Hospital, Bergen, Norway.

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