Technical and anatomical factors affecting intra-arterial chemotherapy fluoroscopy time and radiation dose for intraocular retinoblastoma.


Journal

Journal of neurointerventional surgery
ISSN: 1759-8486
Titre abrégé: J Neurointerv Surg
Pays: England
ID NLM: 101517079

Informations de publication

Date de publication:
Dec 2019
Historique:
received: 06 03 2019
revised: 24 04 2019
accepted: 26 04 2019
pubmed: 15 6 2019
medline: 6 2 2020
entrez: 15 6 2019
Statut: ppublish

Résumé

Intra-arterial chemotherapy has an increasingly prominent role in the management of retinoblastoma. One concern regarding this technique is procedural radiation exposure. To examine the effects of our institution's procedural technique on fluoroscopy parameters for patients undergoing intra-arterial chemotherapy infusions for intraocular retinoblastoma. Secondary goals included describing the effect of anatomical variations of the carotid siphon and ophthalmic artery on radiation dose. A retrospective review of pediatric patients with retinoblastoma referred to interventional neuroradiology for chemosurgery was performed. Techniques were classified as: A (1.2 Fr or 1.5 Fr microcatheter with continuous verapamil flush, advanced without guide through a 2 Fr sheath) or B (1.5 Fr or 1.7 Fr microcatheter advanced within a 4 Fr base catheter, through a 4 Fr sheath). Statistical analysis was performed to determine if there was a significant difference in fluoroscopy parameters based on technique or due to anatomical variation. 26 patients were treated with 94 intra-arterial chemotherapy infusions. 34 procedures were performed using technique A and 60 using technique B. Mean fluoroscopy time (4.75 min), fluoroscopy dose (23.3 mGy), and dose-area product (DAP; 85.2 μGy.m Microcatheter-only technique with continuous verapamil infusion resulted in decreased fluoroscopy times, DAP, and radiation doses at our institution for the treatment of intraocular retinoblastoma. Furthermore, our fluoroscopy times using this technique are the lowest reported in the current literature. Additionally, our anatomical analysis has demonstrated a positive correlation between increasing vessel tortuosity and fluoroscopy times.

Sections du résumé

BACKGROUND BACKGROUND
Intra-arterial chemotherapy has an increasingly prominent role in the management of retinoblastoma. One concern regarding this technique is procedural radiation exposure.
OBJECTIVES OBJECTIVE
To examine the effects of our institution's procedural technique on fluoroscopy parameters for patients undergoing intra-arterial chemotherapy infusions for intraocular retinoblastoma. Secondary goals included describing the effect of anatomical variations of the carotid siphon and ophthalmic artery on radiation dose.
METHODS METHODS
A retrospective review of pediatric patients with retinoblastoma referred to interventional neuroradiology for chemosurgery was performed. Techniques were classified as: A (1.2 Fr or 1.5 Fr microcatheter with continuous verapamil flush, advanced without guide through a 2 Fr sheath) or B (1.5 Fr or 1.7 Fr microcatheter advanced within a 4 Fr base catheter, through a 4 Fr sheath). Statistical analysis was performed to determine if there was a significant difference in fluoroscopy parameters based on technique or due to anatomical variation.
RESULTS RESULTS
26 patients were treated with 94 intra-arterial chemotherapy infusions. 34 procedures were performed using technique A and 60 using technique B. Mean fluoroscopy time (4.75 min), fluoroscopy dose (23.3 mGy), and dose-area product (DAP; 85.2 μGy.m
CONCLUSIONS CONCLUSIONS
Microcatheter-only technique with continuous verapamil infusion resulted in decreased fluoroscopy times, DAP, and radiation doses at our institution for the treatment of intraocular retinoblastoma. Furthermore, our fluoroscopy times using this technique are the lowest reported in the current literature. Additionally, our anatomical analysis has demonstrated a positive correlation between increasing vessel tortuosity and fluoroscopy times.

Identifiants

pubmed: 31197028
pii: neurintsurg-2019-014910
doi: 10.1136/neurintsurg-2019-014910
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1273-1276

Informations de copyright

© Author(s) (or their employer(s)) 2019. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: CH reports personal fees from Merck, outside the submitted work. DG reports non-financial support and other from Children’s Oncology Group, during the conduct of the study; grants from Houseman/Wilkins Ophthalmological Foundation, personal fees, and non-financial support from Abbvie, other from 3T Ophthalmics, other from Aura Biosciences, outside the submitted work.

Auteurs

Corey Area (C)

Diagnostic and Interventional Radiology, Baylor College of Medicine, Houston, Texas, USA.

Christopher J Yen (CJ)

Diagnostic and Interventional Radiology, Baylor College of Medicine, Houston, Texas, USA.

Patricia Chevez-Barrios (P)

Pathology, Houston Methodist Hospital, Houston, Texas, USA.

Cynthia Herzog (C)

Pediatric Hematology/Oncology, University of Texas MD Anderson Cancer Center, Houston, Texas, USA.

Peter Kan (P)

Neurosurgery, Baylor College of Medicine, Houston, Texas, USA.

Wei Zheng (W)

Statistics, Texas Children's Hospital, Houston, Texas, USA.

Frank Lin (F)

Hematology/Oncology, Texas Children's Hospital, Houston, Texas, USA.

Murali Chintagumpala (M)

Texas Children's Cancer Center, Baylor College of Medicine, Houston, Texas, USA.

Dan Gombos (D)

Section of Ophthalmology, Department of Head and Neck Surgery, University of Texas MD Anderson Cancer Center, Houston, Texas, USA.

Stephen R Chen (SR)

Diagnostic and Interventional Radiology, Baylor College of Medicine, Houston, Texas, USA.

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