Coronary computed tomography angiography in primary care patients with chest pain or dyspnea - a cross-sectional study
- PMID: 40394490
- PMCID: PMC12090552
- DOI: 10.1186/s12875-025-02877-z
Coronary computed tomography angiography in primary care patients with chest pain or dyspnea - a cross-sectional study
Abstract
Aims: Coronary Computed Tomography Angiography (CCTA) is recommended as a first-line investigation to exclude significant coronary artery stenosis in case of low to intermediate pre-test probability (PTP). The aim was to investigate CCTA findings in relation to the PTP of patients referred directly from primary health care centres.
Methods/results: In this retrospective cohort study consecutive primary care CCTA referrals in a Swedish county 1st of June 2021 until 30th Nov. 2022 were included. CCTA reports were obtained for 483 patients ≥ 30 years old, without known CAD and stratified as no CAD, with atheromatosis or with suspected significant stenosis. For the 381 patients with eligible PTP data, the mean age was 60 years and 70% were women. While the median PTP was 11%, significant stenosis was suspected on CCTA in 18%. Among patients with PTP ≤ 15%, CCTA exposed no significant stenosis in 88%. No significant stenosis was found in patients with PTP < 5% true to patient age and gender in a sensitivity analysis (n = 25).
Conclusions: CCTA ruled out coronary stenosis as the cause of chest pain and dyspnea in 88% of patients referred from primary care with PTP 5-15%. PTP estimations by primary care physicians in CCTA referrals agreed with the occurrence of suspected significant stenosis among patients with PTP 5-15%, but underestimated it in PTP > 15%. The validity of PTP estimates < 5% was low.
© 2025. The Author(s).
Conflict of interest statement
Declarations. Ethics declarations: This study was approved by the Swedish Ethical Review Authority (registration number 2022-00739-01 and 2022-05381-02) who waived the requirement of obtaining written informed consent given the retrospective study design. In line with Swedish legislation, patients were informed about their enrolment in the Swedish Web-based system for Enhancement and Development of Evidence-based care in Heart Disease Evaluated According to Recommended Therapies (SWEDEHEART) registry at the time of the CCTA examination and were offered the possibility to opt out of registration [22]. The study was performed in accordance with the International Ethical Guidelines for Health-related Research Involving Humans (2016) [44]. Consent for publication: Not applicable. Competing interests: F.I. has received speaker fees and served on advisory boards for Novo Nordisk, Sanofi and Boehringer Ingelheim. S.S.L. has received speaker fees from Pfizer, Bayer, Astra Zeneca, Boehringer Ingelheim and Novartis and served on advisory boards for Novartis. All other authors declare no competing interests. Clinical trial number: None.
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