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VeCAS: Vessel-Focused Contrast-Free Angiogram Synthesis for Vascular Interventions

De-Xing Huang, Chen-Yu Wang, Hao Liang, Xiao-Hu Zhou, Mei-Jiang Gui, Tian-Yu Xiang, Qin-Yi Zhang, Chen Wang, Xiao-Liang Xie, Shi-Qi Liu, Ming-Yuan Liu, Zhen-Chang Wang, Zeng-Guang Hou

arXiv:2608.22828v1cs.CV

TL;DR

Iodinated contrast agents carry risks, while existing contrast-free angiogram synthesis methods provide limited vascular localization control and inefficient background modeling. VeCAS separates localization from appearance synthesis using cross-modality distillation and vessel-focused inpainting, and it outperforms comparison methods while improving phantom navigation efficiency.

  • Problem

    Contrast-free angiogram synthesis remains limited by insufficient vascular localization control and inefficient modeling of redundant background content.

    Source: §I · p. 2
  • Method

    VeCAS uses discriminative vessel localization with cross-modality latent distillation, followed by vessel-focused inpainting that preserves non-vascular background.

    Source: §I · p. 2, A. Overview · p. 3
  • Results

    VeCAS outperforms comparison methods in vascular structural fidelity and image quality, with navigation time and operation steps reduced by 41.4% and 40.7%, respectively, versus non-contrast guidance.

    Source: §I · p. 2, D. Main Results · p. 7
  • Takeaways & Limitations

    Visual, physician, and phantom-navigation evaluations suggest VeCAS could provide vessel-enhanced guidance and serve as a potential meta contrast agent for vascular interventions.

    Source: §I · p. 2, §V · p. 9

Abstract

from arXiv · show

X-ray angiography relies on iodinated contrast agents to visualize vascular structures during image-guided interventions. However, contrast administration carries risks of adverse events, motivating the development of contrast-free alternatives. Generating X-ray angiograms directly from non-contrast X-ray images offers a potential solution, but existing approaches remain limited by (i) insufficient control over vascular localization and (ii) inefficient modeling of redundant background content. To address these challenges, we propose VeCAS, a two-stage vessel-focused contrast-free angiogram synthesis framework that separates vascular structure localization from angiographic appearance synthesis. In Stage I, a discriminative model localizes vascular structures in non-contrast X-ray images, while cross-modality latent distillation transfers vessel-sensitive knowledge from X-ray angiograms during training. In Stage II, a vessel-focused inpainting model synthesizes angiographic appearance within the localized vascular regions while preserving the non-vascular background. Experiments on an in-house lower-limb vascular intervention dataset show that VeCAS outperforms the comparison methods in terms of vascular structural fidelity and image quality. Visual Turing tests and physician assessments indicate the perceptual realism of the synthesized angiograms. In addition, robotic guidewire navigation experiments in vascular phantoms show that VeCAS guidance reduces the time to target by 41.4% and the number of operation steps by 40.7% compared with non-contrast guidance. Together, these results suggest the potential of VeCAS to serve as ``meta contrast agent'' for vascular interventions.

I. INTRODUCTION

VeCAS addresses risks and limitations of contrast-based angiography by separating vascular localization from angiographic appearance synthesis. Its evaluations report improved fidelity, realism, and phantom navigation efficiency.

  • Each additional 75 mL of iodinated contrast agent was associated with a 42% increase in acute kidney injury risk.Source: §I · p. 1
  • Existing contrast-free strategies often require intravascular imaging, alternative contrast agents, or previously acquired angiographic information.Source: §I · p. 1
  • VeCAS explicitly decouples vascular structure localization from angiographic appearance synthesis in a two-stage framework.Stage I predicts vessel masks using a discriminative model and cross-modality latent distillation; Stage II synthesizes appearance within localized vascular regions while preserving background.Source: §I · p. 2
  • Cross-modality latent distillation transfers vessel-sensitive knowledge from X-ray angiograms to non-contrast X-ray images during training.Source: §I · p. 2
  • VeCAS outperforms existing methods in vascular structural fidelity and image quality, with visual Turing tests and physician assessments indicating perceptual realism.Source: §I · p. 2
  • 41.4% lower navigation time and 40.7% fewer operation steps were achieved versus non-contrast guidance in phantom robotic guidewire experiments.Source: §I · p. 2

II. RELATED WORK

Related work includes clinical strategies for reducing contrast administration and image-translation methods that support angiogram synthesis. VeCAS is framed as a two-stage approach that preserves non-vascular background while synthesizing vascular appearance.

Low-Contrast & Contrast-Free Interventions

Angiogram Synthesis

  • VeCAS predicts vessel masks before synthesizing angiogram-like appearance within vascular regions while preserving the original non-vascular background.Source: Figure 2 · p. 3

Low-Contrast & Contrast-Free Interventions

  • These clinical strategies reduce or avoid iodinated contrast but may require intravascular imaging, alternative contrast agents, or previously acquired vascular information.Source: A. Low-Contrast & Contrast-Free… · p. 3

Medical Image Translation

  • Medical image translation methods have used GANs, deformable registration, and improved architectures to address anatomical variation and modality differences.Source: B. Medical Image Translation · p. 3

C. Angiogram Synthesis

VeCAS separates vascular structure localization from angiographic appearance synthesis. It uses cross-modality latent distillation for vessel-mask prediction and vessel-focused inpainting to synthesize angiographic appearance while preserving non-vascular content.

Stage I: Vascular Structure Localization

  • VeCAS predicts a binary vessel mask from non-contrast X-ray images using a discriminative localization model with explicit spatial supervision.The formulation targets vascular structure localization directly rather than relying on a generative model to infer vessel positions.Source: A. Overview · p. 3, B. Stage I: Vascular Structure… · p. 4
  • Cross-modality latent distillation transfers vessel-sensitive information from paired angiograms by predicting angiogram-domain latent features from non-contrast features.A frozen angiogram-domain segmentation model supplies the target representations, while a trainable non-contrast encoder and predictor estimate them at multiple scales.Source: B. Stage I: Vascular Structure… · p. 4, Figure 3 · p. 4
  • The predicted multi-scale latent features are decoded by the frozen angiogram-domain decoder to obtain the vessel mask used as Stage II’s structural condition.The predictor operates on high-level feature maps at scales i = 3, 4, 5.Source: B. Stage I: Vascular Structure… · p. 4
  • Combining latent prediction and segmentation supervision improves vascular localization over latent prediction alone.The prediction loss supervises latent features, while the segmentation loss combines binary cross-entropy and Dice loss; their trade-off is controlled by λpred.Source: B. Stage I: Vascular Structure… · p. 4

Stage II: Vessel-Focused Inpainting

  • Vessel-focused inpainting uses diffusion to synthesize angiographic appearance within vascular regions while preserving the non-vascular background.Its training objective restricts denoising to vascular regions, and inference fuses denoised vascular output with the forward-diffused non-contrast image according to the predicted mask.Source: Figure 4 · p. 5

C. Stage II: Vessel-Focused Inpainting

Stage II uses vessel-focused diffusion inpainting to synthesize angiographic appearance inside vascular regions while preserving the non-vascular background.

A. Clinical Dataset

The clinical dataset contains paired pre-contrast and contrast-enhanced lower-limb intervention frames from 102 patients, evaluated with patient-level five-fold cross-validation.

  • The dataset comprises 599 sequences from 102 patients undergoing lower-limb vascular interventions.Source: A. Clinical Dataset · p. 6
  • Each sequence contributes one manually selected pre-contrast frame and one clear contrast-enhanced frame from the same sequence.Source: A. Clinical Dataset · p. 6
  • Frame pairs without evident spatial displacement were treated as approximately aligned because lower-limb acquisitions had limited motion.Source: A. Clinical Dataset · p. 6
  • Five-fold cross-validation split patients into 80% training and 20% testing per fold, keeping all sequences from each patient together.Source: A. Clinical Dataset · p. 6
  • Final performance is reported as mean±std across the five folds.Source: A. Clinical Dataset · p. 6

B. Implementation Details

The implementation uses PyTorch and Python with 256 × 256 inputs, U-Net-based localization, diffusion inpainting, and reported structural-fidelity metrics.

  • All experiments used PyTorch 2.8.0 and Python 3.11.13 under Ubuntu 20.04.3 with 256 × 256 input images.Source: B. Implementation Details · p. 6
  • Stage I used U-Net for vascular localization and trained the angiogram-domain and non-contrast components in separate 100-epoch phases.Source: B. Implementation Details · p. 6
  • Stage II trained an image-space diffusion inpainting model for 300 epochs with batch size 8 and used 100 sampling steps at inference.Source: B. Implementation Details · p. 6
  • Stage I and Stage II reported Dice similarity coefficient and centerline Dice to assess vascular overlap and tubular topological consistency.Source: B. Implementation Details · p. 6

C. Perceptual and Physician Assessment

Visual Turing tests and physician assessments evaluated whether synthesized angiograms appeared realistic and procedurally useful.

D. Main Results

VeCAS achieves stronger vascular localization and complete-pipeline structural fidelity than comparison methods, while balancing vascular quality with preserved background appearance.

Stage I

  • VeCAS improves Stage I vascular localization over UNet++ by +1.17% DSC and +0.75% clDice through cross-modality latent distillation.Segmentation models outperform direct image-translation methods, and VeCAS achieves the best overall localization performance.Source: D. Main Results · p. 7

Stage I + II

  • 42.27% DSC and 47.70% clDice give VeCAS the best vascular structural fidelity in the complete pipeline.VeCAS improves DSC by +5.84% over ControlNet and clDice by +5.92% over RegGAN.Source: D. Main Results · p. 7
  • VeCAS achieves a better balance between image fidelity and vascular structural fidelity by preserving background while focusing synthesis on vascular regions.Whole-image metrics can be dominated by the large non-vascular background and may not reflect vascular structure adequately.Source: D. Main Results · p. 7

Qualitative results

  • VeCAS produces clearer and more continuous vessels than baseline methods while maintaining the non-vascular background.Most baselines preserve background appearance but generate weak, incomplete, or barely visible vessels.Source: D. Main Results · p. 7

E. Ablation Study

Ablation studies show that cross-modality supervision and vessel-focused Stage II design contribute complementary benefits, while final vascular fidelity remains sensitive to mask quality.

Distillation Loss

  • Combining Lseg and Lpred achieves the best Stage I localization performance, showing complementary pixel-level and cross-modality supervision.Using only Lpred performs poorly, whereas Lseg substantially improves results.Source: E. Ablation Study · pp. 7–8

Vessel-Focused Design

  • Combining vessel-focused loss and sampling yields the best overall Stage II performance.Sampling mainly improves PSNR and SSIM, while vessel-focused loss improves DSC and clDice; the two components play complementary roles.Source: E. Ablation Study · p. 8

Error Propagation from Stage I to Stage II

  • 60.22% DSC and 66.54% clDice form the oracle upper bound with ground-truth masks, versus 42.27% DSC and 47.70% clDice using predicted masks.The comparison indicates that mask quality directly affects vascular fidelity.Source: E. Ablation Study · p. 8
  • Random translation causes the largest degradation among mask perturbations, while erosion and dilation also reduce vascular structural fidelity.The inpainting model is sensitive to spatial misalignment, vessel boundaries, and vessel calibers.Source: E. Ablation Study · p. 8
  • PSNR and SSIM remain relatively stable across mask inputs, confirming their limited sensitivity to vascular structural errors.Preserved background content dominates these whole-image fidelity metrics.Source: E. Ablation Study · pp. 8–9

F. Phantom Experiment

A vascular-phantom study evaluates VeCAS as robotic guidewire guidance against non-contrast and contrast conditions using time and operation-step metrics.

Experimental Setup

  • The phantom platform combines vascular phantoms, a robotic vascular system, guidewire, overhead camera, and workstation for VeCAS-guided navigation.Each phantom was based on a real angiogram’s vessel annotation and spatially aligned with the corresponding non-contrast X-ray image.Source: F. Phantom Experiment · p. 9

Protocol

  • Three operators navigated guidewires to predefined distal targets under non-contrast, VeCAS, and contrast guidance conditions.Each operator repeated the task five times for each phantom and guidance condition.Source: F. Phantom Experiment · p. 9

Evaluation Metrics

  • Navigation performance was measured by time to target and number of operation steps, with each step defined as one discrete control command.Time was measured from the first control command until the guidewire tip reached the target region.Source: F. Phantom Experiment · p. 9

Main Results

  • 41.4% lower time to target and 40.7% fewer operation steps were achieved with VeCAS guidance than with non-contrast guidance.VeCAS guidance also achieved navigation performance comparable to contrast guidance.Source: F. Phantom Experiment · p. 9
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