AI Article Synopsis

  • Photoacoustic Doppler flowmetry provides important quantitative data on blood flow and vascular details for evaluating rectal cancer.
  • Researchers aimed to enhance this technique using an acoustic resolution photoacoustic microscopy (AR-PAM) system for detailed blood perfusion analysis.
  • Successful validation in lab studies indicates that this method can effectively assess treatment responses and differentiate between residual cancer and healthy tissue post-chemoradiation.

Article Abstract

Significance: Photoacoustic Doppler flowmetry offers quantitative blood perfusion information in addition to photoacoustic vascular contrast for rectal cancer assessment.

Aim: We aim to develop and validate a correlational Doppler flowmetry utilizing an acoustic resolution photoacoustic microscopy (AR-PAM) system for blood perfusion analysis.

Approach: To extract blood perfusion information, we implemented AR-PAM Doppler flowmetry consisting of signal filtering and conditioning, A-line correlation, and angle compensation. We developed flow phantoms and contrast agent to systemically investigate the flowmetry's efficacy in a series of phantom studies. The developed correlational Doppler flowmetry was applied to images collected during AR-PAM for post-treatment rectal cancer evaluation.

Results: The linearity and accuracy of the Doppler flow measurement system were validated in phantom studies. Imaging rectal cancer patients treated with chemoradiation demonstrated the feasibility of using correlational Doppler flowmetry to assess treatment response and distinguish residual cancer from cancer-free tumor bed tissue and normal rectal tissue.

Conclusions: A new correlational Doppler flowmetry was developed and validated through systematic phantom evaluations. The results of its application to patients suggest it could be a useful addition to photoacoustic endoscopy for post-treatment rectal cancer assessment.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10787588PMC
http://dx.doi.org/10.1117/1.JBO.29.S1.S11517DOI Listing

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