CC BY-NC-ND 4.0 · Journal of Clinical Interventional Radiology ISVIR 2022; 06(02): 090-097
DOI: 10.1055/s-0041-1740575
Original Article

Cone Beam CT with Automatic vessel Detection Software versus Conventional 2D Fluoroscopy with Overlay for Prostate Artery Embolization: A Comparison of Prostatic Artery Catheterization Time and Radiation Exposure

Vedant Acharya
1   University of Miami Miller School of Medicine, Miami, Florida, United States
,
Hamed Jalaeian
2   Department of Interventional Radiology, University of Miami Miller School of Medicine, Miami, Florida, United States
,
Srinivas Tummala
2   Department of Interventional Radiology, University of Miami Miller School of Medicine, Miami, Florida, United States
,
Kush Shah
3   Department of Interventional Radiology, Jackson Memorial Hospital, Miami, Florida, United States
,
Jessica Kumar
3   Department of Interventional Radiology, Jackson Memorial Hospital, Miami, Florida, United States
,
Issam Kably
2   Department of Interventional Radiology, University of Miami Miller School of Medicine, Miami, Florida, United States
,
Shivank Bhatia
2   Department of Interventional Radiology, University of Miami Miller School of Medicine, Miami, Florida, United States
› Author Affiliations
Funding This study was supported in part by a grant from Siemens Healthcare Diagnostics, (Grant/Award Numbers: MIAMI2016ATBHATIAC0022371)

Abstract

Purpose To evaluate the effect of cone-beam computed tomography (CT) with automatic vessel detection software on prostate artery catheterization and fluoroscopy time in prostate artery embolization (PAE).

Methods Fifty patients undergoing PAE for BPH were enrolled in this prospective study. Twenty-five PAEs were performed using automatic vessel detection software with syngo embolization guidance (study) and were compared with 25 PAEs performed using conventional two-dimensional (2D) fluoroscopy with overlay (control). PAE was performed using 300–500 μm trisacryl gelatin spherical particles. The primary outcome parameters were prostatic artery catheterization time and fluoroscopy time.

Results Bilateral PAE was achieved in 24/25 cases in both groups. The median right and left prostatic artery catheterization times were similar between the two groups, (p = 0.473 and p = 0.659, respectively). The median fluoroscopy time (28.0 and 42.0 minutes, p = 0.046) and total procedure time (70.0 and 118.0 minutes, p < 0.001) were shorter in the study group. The median total dose area product (DAP) was not significantly different. However, the median CBCT DAP (11406 vs. 6248, p < 0.001) was higher in the study group, while median fluoroscopy DAP (7371 vs. 8426, p < .049) was higher in the control group. Median digital subtraction angiography (DSA), CBCT, and fluoroscopy DAP accounted for 27%, 45%, and 29% of the total DAP in the study group and 32%, 29%, and 39% in the control group (p < 0.001), respectively. All complications were Clavien–Dindo Grade 1.

Conclusion Although CBCT with automatic vessel detection software had no significant effect on time-to-prostatic artery catheterization and total radiation exposure, it reduced the fluoroscopy time and procedure time.

Authors' Contributions

V Acharya: Acquisition/analysis, interpretation of data, drafting, and revision of submitted work.


H Jalaeian: Acquisition/analysis, interpretation of data, drafting, and revision of submitted work.


S Tummala: Acquisition/analysis, interpretation of data, drafting, and revision of submitted work.


K Shah: Acquisition/analysis, interpretation of data, drafting, and revision of submitted work.


J Kumar: Acquisition/analysis, interpretation of data, drafting, and revision of submitted work.


I Kably: Acquisition/analysis, interpretation of data, drafting, and revision of submitted work.


S Bhatia: Conception, design, acquisition, interpretation of data, drafting, revision, and final approval of submitted work.


Compliance with Ethical Standards

All procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki Declaration and its later amendments or comparable ethical standards.


Informed consent was obtained from all individual participants involved in the study


Ethical Approval

All procedures performed were in accordance with the ethical standards of the institutional and national research committee and with the 1964 Helsinki declaration and its later amendments or comparable ethical standards. IDE G130237, ClinicalTrials.gov Identifier NCT02173522.


Informed Consent

Informed consent was obtained from all individual participants included in the study.


Consent for Publication

The authors consent to the publisher's sole and exclusive license of the full copyright of the publication.


Statement of Data Access and Integrity

The authors declare that they had full access to all of the data in this study and the author take complete responsibility for the integrity of the data and the accuracy of the data analysis.




Publication History

Article published online:
02 July 2022

© 2022. Indian Society of Vascular and Interventional Radiology. This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commercial purposes, or adapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by-nc-nd/4.0/)

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