# Retrospective Analysis of Incidental Myocardial Perfusion Defects on Non-ECG-Gated Contrast-Enhanced CT in Emergency Settings

**Authors:** Jia-Hao Zhou, Meng-Yu Wu, Jong-Kai Hsiao

PMC · DOI: 10.3390/medicina62020277 · 2026-01-28

## TL;DR

This study explores how non-ECG-gated CT scans in emergency settings can reveal heart attack signs, potentially improving early diagnosis.

## Contribution

The study identifies incidental myocardial perfusion defects on non-ECG-gated CT as a potential indicator of acute myocardial infarction in emergency patients.

## Key findings

- 45% of patients with suspected AMI had confirmed AMI based on CT findings.
- Perfusion defects were present in all AMI patients but absent in non-AMI patients.
- Coronary artery calcification was significantly higher in the AMI group.

## Abstract

Background and Objectives: Coronary heart disease is a leading cause of death in developed countries. While ECG-gated coronary CT is commonly used to detect coronary artery stenosis, the potential of non-ECG-gated CT (NECE-CT) to reveal incidental myocardial perfusion defects indicative of acute myocardial infarction (AMI) remains underexplored, particularly in emergency settings where rapid diagnosis is crucial. Materials and Methods: We retrospectively analyzed 22 suspected AMI patients from the emergency department who underwent NECE-CT without either an initial AMI diagnosis or available cardiac enzyme or ECG data. Results: AMI was confirmed in 45% (n = 10) of patients, with 30% (n = 3/10) showing elevated troponin I levels only after the CT exam. In the AMI group, all patients had perfusion defects, with 20% (n = 2) showing transmural defects and 80% (n = 8) showing endocardial defects. In contrast, all patients in the non-AMI group exhibited endocardial defects. Coronary artery calcification was significantly higher in the AMI group (70%) compared to the non-AMI group (25%, p < 0.05). Conclusions: These findings suggest that NECE-CT may reveal myocardial perfusion defects as an ancillary sign of AMI. While not a standalone diagnostic tool, careful evaluation of the myocardium in emergency CT scans may raise suspicion of AMI in patients with atypical presentations, offering more insight than standard methods. Further prospective studies with larger cohorts are needed to validate the clinical utility of these incidental findings.

## Linked entities

- **Diseases:** acute myocardial infarction (MONDO:0004781), coronary heart disease (MONDO:0005010)

## Full-text entities

- **Genes:** TNNI3 (troponin I3, cardiac type) [NCBI Gene 7137] {aka CMD1FF, CMD2A, CMH7, RCM1, TNNC1, cTnI}, TNNT2 (troponin T2, cardiac type) [NCBI Gene 7139] {aka CMD1D, CMH2, CMPD2, LVNC6, RCM3, TnTC}, MYH14 (myosin heavy chain 14) [NCBI Gene 79784] {aka DFNA4, DFNA4A, FP17425, MHC16, MYH17, NMHC II-C}
- **Diseases:** cerebrovascular ischemia (MESH:D007511), pulmonary embolism (MESH:D011655), coronary artery stenosis (MESH:D023921), ST-elevation myocardial infarction (MESH:D000072657), myocardial defect (MESH:D009202), chest pain (MESH:D002637), motion abnormality (MESH:D009041), ischemic (MESH:D002545), left or right bundle branch block (MESH:D002037), aortic dissection (MESH:D000784), calcification (MESH:D002114), myocardium perfusion insufficiency (MESH:D000309), Cardiopulmonary diseases (MESH:D006323), abdominal disease (MESH:D015746), NSTEMI (MESH:D000072658), injury to (MESH:D014947), inflammation (MESH:D007249), defects (MESH:D000013), syncope (MESH:D013575), ACS (MESH:D054058), Sinus tach (MESH:D012852), Coronary heart disease (MESH:D003327), coronary calcification (MESH:D003323), perfusion (MESH:D001480), endocardial defects (MESH:D004694), ICT (MESH:C566123), infarct (MESH:D007238), Sinus tachycardia (MESH:D013616), Coronary artery calcification (MESH:D003324), cardiac perfusion defects (MESH:D006331), AMI (MESH:D009203), cardiovascular disease (MESH:D002318), atrial fibrillation (MESH:D001281), myocardial ischemia (MESH:D017202), Coronary Artery Occlusion (MESH:D054059), microvascular obstruction (MESH:D017566), Thrombus (MESH:D013927), occlusion of (MESH:D001157), hypertension (MESH:D006973), death (MESH:D003643), Takotsubo syndrome (MESH:D054549), atherosclerosis (MESH:D050197)
- **Chemicals:** reactive oxygen species (MESH:D017382), I (MESH:D007455), nitroglycerin (MESH:D005996), NECE (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12941749/full.md

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Source: https://tomesphere.com/paper/PMC12941749