Percutaneous Portal Vein Embolization Using a Simplified Sheathless 18-Gauge Trocar Needle Approach: Review of Efficacy and Safety.
Aged
Angiography, Digital Subtraction
Bile Duct Neoplasms
/ diagnostic imaging
Carcinoma, Hepatocellular
/ diagnostic imaging
Cholangiocarcinoma
/ diagnostic imaging
Colorectal Neoplasms
/ pathology
Computed Tomography Angiography
Embolization, Therapeutic
/ adverse effects
Enbucrilate
/ administration & dosage
Equipment Design
Ethiodized Oil
/ administration & dosage
Feasibility Studies
Female
Humans
Liver Neoplasms
/ diagnostic imaging
Liver Regeneration
Male
Middle Aged
Needles
Portal Vein
Portography
/ methods
Punctures
Retrospective Studies
Risk Factors
Time Factors
Treatment Outcome
Journal
Journal of vascular and interventional radiology : JVIR
ISSN: 1535-7732
Titre abrégé: J Vasc Interv Radiol
Pays: United States
ID NLM: 9203369
Informations de publication
Date de publication:
03 2019
03 2019
Historique:
received:
01
06
2018
revised:
29
08
2018
accepted:
04
09
2018
entrez:
2
3
2019
pubmed:
2
3
2019
medline:
7
5
2019
Statut:
ppublish
Résumé
Portal vein (PV) embolization (PVE) is traditionally performed via a PV sheath with selective embolization of PV branches. Here, the efficacy and safety of PVE with the use of only an 18-gauge needle is reported. Consecutive patients who underwent PVE from 2009 through 2017 were retrospectively reviewed. Forty-five patients (mean age, 60 y ± 7.6; 38 men) underwent 45 PVE procedures. Hepatocellular carcinoma, cholangiocarcinoma, and metastases accounted for 26 (58%), 13 (29%), and 6 (13%) patients, respectively. PVE was performed by puncturing a branch of right PV with an 18-gauge needle under US guidance. Via the same needle, direct portography was performed, followed by PVE with an N-butyl cyanoacrylate/Lipiodol mixture. Percentage increase of future liver remnant (FLR) volume and increase in ratio of FLR to total liver volume were estimated as measures of efficacy. Complications were reported according to Society of Interventional Radiology classification. Fluoroscopy time, procedure time, and dose-area product (DAP) were recorded. Technical success rate was 100%. The median DAP, fluoroscopy time, and procedure time were 74,387 mGy·cm PVE via a sheathless 18-gauge needle approach is feasible, with satisfactory FLR hypertrophy.
Identifiants
pubmed: 30819490
pii: S1051-0443(18)31491-X
doi: 10.1016/j.jvir.2018.09.006
pii:
doi:
Substances chimiques
Ethiodized Oil
8008-53-5
Enbucrilate
F8CEP82QNP
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
440-444Informations de copyright
Copyright © 2019. Published by Elsevier Inc.