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ID 69210
フルテキストURL
著者
Iguchi, Toshihiro Department of Radiology, Okayama University Hospital Kaken ID
Kawabata, Takahiro Department of Radiology, Okayama University Hospital
Matsui, Yusuke Department of Radiology, Faculty of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
Tomita, Koji Department of Radiology, Okayama University Hospital
Uka, Mayu Department of Radiology, Okayama University Hospital
Umakoshi, Noriyuki Department of Radiology, Okayama University Hospital
Okamoto, Soichiro Department of Radiology, Okayama University Hospital
Munetomo, Kazuaki Department of Radiology, Okayama University Hospital
Hiraki, Takao Department of Radiology, Faculty of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University Kaken ID publons researchmap
抄録
Purpose This study retrospectively evaluated the feasibility and safety of implanting a newly developed central venous access port (CV-port) that allows catheter insertion into a vein without the use of a peel-away sheath, with a focus on its potential to minimize risks associated with conventional implantation methods.
Materials and methods All procedures were performed using a new device (P-U CelSite Port™ MS; Toray Medical, Tokyo, Japan) under ultrasound guidance. The primary endpoint was the implantation success rate. The secondary endpoints were the safety and risk factors for infection in the early postprocedural period (< 30 days).
Results We assessed 523 CV-port implantations performed in a cumulative total of 523 patients (240 men and 283 women; mean age, 61.6 ± 13.1 years; range, 18–85 years). All implantations were successfully performed using an inner guide tube and over-the-wire technique through 522 internal jugular veins and one subclavian vein. The mean procedural time was 33.2 ± 10.9 min (range 15–112 min). Air embolism, rupture/perforation of the superior vena cava, or hemothorax did not occur during catheter insertion. Eleven (2.1%) intraprocedural complications occurred, including Grade I arrhythmia (n = 8) and subcutaneous bleeding (n = 1), Grade II arrhythmia (n = 1), and Grade IIIa pneumothorax (n = 1). Furthermore, 496 patients were followed up for ≥ 30 days. Six early postprocedural complications were encountered (1.1%), including Grade IIIa infection (n = 4), catheter occlusion (n = 1), and skin necrosis due to subcutaneous leakage of trabectedin (n = 1). These six CV-ports were withdrawn, and no significant risk factors for infection in the early postprocedural period were identified.
Conclusion The implantation of this CV-port device demonstrated comparable success and complication rates to conventional devices, with the added potential benefit of eliminating complications associated with the use of a peel-away sheath.
キーワード
Central venous catheters
Vascular access device
Treatment outcome
Safety
備考
The version of record of this article, first published in Japanese Journal of Radiology, is available online at Publisher’s website: http://dx.doi.org/10.1007/s11604-024-01658-5
発行日
2024-09-17
出版物タイトル
Japanese Journal of Radiology
43巻
2号
出版者
Springer Science and Business Media LLC
開始ページ
282
終了ページ
289
ISSN
1867-1071
NCID
AA12375935
資料タイプ
学術雑誌論文
言語
英語
OAI-PMH Set
岡山大学
著作権者
© The Author(s) 2024
論文のバージョン
publisher
PubMed ID
DOI
Web of Science KeyUT
関連URL
isVersionOf https://doi.org/10.1007/s11604-024-01658-5
ライセンス
http://creativecommons.org/licenses/by/4.0/
Citation
Iguchi, T., Kawabata, T., Matsui, Y. et al. Evaluation of a novel central venous access port for direct catheter insertion without a peel-away sheath. Jpn J Radiol 43, 282–289 (2025). https://doi.org/10.1007/s11604-024-01658-5
助成情報
( Toray Medical )