# A nomogram for predicting intraoperative risk during primary percutaneous coronary intervention based on rapidly obtained data from ST-segment elevation myocardial infarction patients

**Authors:** Yutian Wang, Xiao Chen, Yejia Chen, Chen Yu, Yiming Tao, Xiaocong Liu, Kaile Zhao, Haoran Shou, Hua Liu, Jiancheng Xiu, Xiaobo Li

PMC · DOI: 10.3389/fcvm.2026.1691709 · Frontiers in Cardiovascular Medicine · 2026-02-12

## TL;DR

This study created a quick prediction tool to assess heart risks during a critical procedure for heart attack patients, using easily available data.

## Contribution

A novel nomogram model for rapid intraoperative risk prediction in STEMI patients undergoing primary PCI.

## Key findings

- The nomogram achieved good discrimination with an AUC of 0.785 for predicting MACE during PCI.
- Key risk factors included Killip classification, ST-segment elevation in ≥3 leads, and blood cell counts.
- The model showed good calibration and positive net benefits according to decision curve analysis.

## Abstract

Primary percutaneous coronary intervention (PCI) in patients with ST-segment elevation myocardial infarction (STEMI) can carry high stakes, as major adverse cardiac events (MACE) like no-reflow, malignant arrhythmias, and cardiogenic shock can disrupt the procedure and worsen outcomes. In light of these challenges, this study aimed to develop a nomogram prediction model to rapidly assess MACE risk during PCI in STEMI patients, aiding in timely risk stratification prior to surgery.

This study included 1050 STEMI patients who underwent primary PCI between December 30, 2016, and May 13, 2023. Clinical data were collected from emergency admissions. Multiple logistic regression models were used to analyze the independent risk factors for intraoperative MACE. A nomogram was then constructed and validated via bootstrap resampling. Model performance was assessed using an ROC curve for discrimination and a calibration curve for accuracy.

The incidence of intraoperative MACE in STEMI patients was 38.3%. Independent risk factors for intraoperative MACE included Killip classification, ST-segment elevation in ≥3 leads, white blood cell count, lymphocyte count, and heart rate. A simple and rapidly obtainable nomogram, developed to predict MACE during PCI, showed good differentiation, with an area under the ROC curve of 0.785 (95% CI: 0.755–0.814). Decision curve analysis indicated good fit, calibration, and positive net benefits.

A nomogram was developed to rapidly predict intraoperative MACE risk during PCI in STEMI patients before surgery. By enabling early identification of high-risk individuals, this model enhances clinical decision-making, potentially improving patient outcomes and procedural efficiency.

## Linked entities

- **Diseases:** ST-segment elevation myocardial infarction (MONDO:0041656), cardiogenic shock (MONDO:0800175)

## Full-text entities

- **Genes:** FGB (fibrinogen beta chain) [NCBI Gene 2244] {aka HEL-S-78p}
- **Diseases:** infarct (MESH:D007238), heart failure (MESH:D006333), myocardial reperfusion injury (MESH:D015428), postoperative (MESH:D019106), coronary atherosclerosis (MESH:D003324), cardiac (MESH:D006331), ventricular fibrillation (MESH:D014693), ventricular tachycardia (MESH:D017180), thrombosis (MESH:D013927), hypertension (MESH:D006973), death (MESH:D003643), atherosclerosis (MESH:D050197), AMI (MESH:D009203), MACE (MESH:D002318), atrioventricular block (MESH:D054537), ST-segment elevation myocardial infarction (MESH:D000072657), Malignant arrhythmias (MESH:D001145), myocardial damage (MESH:D009202), Chest Pain (MESH:D002637), Bradycardia (MESH:D001919), acute peripheral circulatory failure (MESH:D012769), HL (MESH:C538324), Inflammation (MESH:D007249), hyperlipidemia (MESH:D006949), syncope (MESH:D013575), sick sinus syndrome (MESH:D012804), myocardial remodeling (MESH:D064752), ACS (MESH:D054058), reflow (MESH:D054318), Cardiogenic Shock (MESH:D012770), ischemic (MESH:D002545), diabetes (MESH:D003920), HS (MESH:C567159), cardiac arrest (MESH:D006323)
- **Chemicals:** amiodarone (MESH:D000638), nicorandil (MESH:D020108), metoprolol (MESH:D008790), dopamine (MESH:D004298), verapamil (MESH:D014700), sodium nitroprusside (MESH:D009599), glucose (MESH:D005947), clopidogrel (MESH:D000077144), vasoactive agents (-), lidocaine (MESH:D008012), ticagrelor (MESH:D000077486), potassium (MESH:D011188), sodium (MESH:D012964), aspirin (MESH:D001241), atropine (MESH:D001285), metaraminol (MESH:D008680), adenosine (MESH:D000241)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

32 references — full list in the complete paper: https://tomesphere.com/paper/PMC12936023/full.md

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Source: https://tomesphere.com/paper/PMC12936023