Kubo Takatoshi, Yasaka Koichiro, Kobayashi Hiroshi
Radiology, The University of Tokyo Hospital, Tokyo, JPN.
Orthopedic Surgery, The University of Tokyo Hospital, Tokyo, JPN.
Cureus. 2024 Apr 3;16(4):e57507. doi: 10.7759/cureus.57507. eCollection 2024 Apr.
Purpose Sterile inflammation along the tunneled catheter is a characteristic complication associated with trabectedin infusion via a central venous port (CVP). To date, no studies have evaluated the differences in sterile inflammation incidence according to the CVP system used. This study evaluated the differences in sterile inflammation incidence between two different CVP systems. Methods This study was conducted at The University of Tokyo Hospital, Bunkyo-Ku, Tokyo, Japan. Patients with trabectedin infusion using CVP via the internal jugular vein between April 2016 and February 2024 were retrospectively evaluated. Sterile inflammation was characterized as skin erythema, swelling, pain, or induration along the tunneled catheter after infusion of trabectedin from the CVP and negative for various infection tests. The incidence of sterile inflammation was compared using two different CVP systems: Anthron® polyurethane catheter with Celsite port (P-U Celsite; Toray Medical, Tokyo, Japan) and DewX Eterna (Terumo, Tokyo, Japan). Results Of the 21 patients, 12 and nine patients used P-U Celsite and DewX Eterna for trabectedin infusion, respectively. Sterile inflammation occurred in five patients; of these, four underwent CVP removal because of worsened pain, making trabectedin infusion difficult. Sterile inflammation occurred in 0 (0/12) and 56% (5/9) of patients using P-U Celsite and DewX Eterna, respectively, with a significantly lower incidence in patients using P-U Celsite (P = 0.006). Conclusion Sterile inflammation incidence was significantly lower in patients using P-U Celsite compared to those using DewX Eterna.
目的 沿隧道式导管的无菌性炎症是通过中心静脉端口(CVP)输注曲贝替定相关的一种特征性并发症。迄今为止,尚无研究评估根据所使用的CVP系统不同,无菌性炎症发生率的差异。本研究评估了两种不同CVP系统之间无菌性炎症发生率的差异。方法 本研究在日本东京文京区的东京大学医院进行。对2016年4月至2024年2月期间经颈内静脉使用CVP输注曲贝替定的患者进行回顾性评估。无菌性炎症的特征为从CVP输注曲贝替定后沿隧道式导管出现皮肤红斑、肿胀、疼痛或硬结,且各种感染检测结果为阴性。使用两种不同的CVP系统比较无菌性炎症的发生率:带有Celsite端口的Anthron®聚氨酯导管(P-U Celsite;日本东京东丽医疗株式会社)和DewX Eterna(日本东京泰尔茂株式会社)。结果 21例患者中,分别有12例和9例患者使用P-U Celsite和DewX Eterna进行曲贝替定输注。5例患者发生无菌性炎症;其中4例因疼痛加重而拔除CVP,导致曲贝替定输注困难。使用P-U Celsite和DewX Eterna的患者中,无菌性炎症发生率分别为0(0/12)和56%(5/9),使用P-U Celsite的患者发生率显著更低(P = 0.006)。结论 与使用DewX Eterna的患者相比,使用P-U Celsite的患者无菌性炎症发生率显著更低。