Department of Radiology, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
Department of Orthopedic Surgery, School of Medicine, Toho University, Tokyo, Japan; Musculoskeletal Intervention Center, Edogawa Hospital, Tokyo, Japan.
J Vasc Interv Radiol. 2021 Sep;32(9):1341-1347. doi: 10.1016/j.jvir.2021.06.024. Epub 2021 Jul 6.
To evaluate the efficacy and safety of intra-arterial infusion of temporary embolic material with/without radiographic monitoring via a needle placed into the radial artery to occlude abnormal neovessels for trapeziometacarpal osteoarthritis.
Thirty-one patients having Eaton stage II or III osteoarthritis, with a symptom duration longer than 6 months, resistant to conservative therapy for at least 3 months were prospectively enrolled. All procedures were performed by infusing imipenem/cilastatin sodium through a 24-gauge needle that was percutaneously inserted into the radial artery. Seven patients underwent the procedure with fluoroscopy, and 21 patients underwent the procedure without fluoroscopy. The mean Quick Disabilities of the Arm, Shoulder and Hand (QuickDASH) score, numerical rating scale (NRS), and Patient Global Impression of Change (PGIC) scale were evaluated before and at 2, 6, and 24 months after the first procedure.
Technical success was 100%. The mean procedure time (from the beginning of local anesthesia to the removal of needle) was 2.9 minutes ± 1.6. The QuickDASH score improved from the baseline to 2, 6, and 24 months (49.2 ± 11.2 vs 22.1 ± 11.2, 20.9 ± 16.6, and 19.5 ± 16.1, respectively, all P <.001). The NRS improved from the baseline to 2, 6, and 24 months (7.2 ± 1.1 vs 3.1 ± 1.8, 2.8 ± 2, and 2.5 ± 2.1, respectively, all P <.001). Improvement on PGIC was observed in 84%, 81%, and 77% of patients at 2, 6, and 24 months, respectively. No major adverse events were encountered.
Intra-arterial infusion of temporary embolic material is a feasible treatment option for trapeziometacarpal osteoarthritis.
评估经桡动脉穿刺置管,于异常新生血管内注入临时栓塞材料(有/无影像学监测)治疗掌指关节炎的疗效和安全性。
前瞻性纳入 31 例 Eaton Ⅱ或Ⅲ期关节炎患者,症状持续时间超过 6 个月,经至少 3 个月的保守治疗无效。所有患者均通过经皮插入的 24 号针注入亚胺培南/西司他丁钠。7 例患者在透视下进行该操作,21 例患者在透视下进行。分别于首次操作前、术后 2、6 和 24 个月评估患者的简易上肢功能评分(QuickDASH)、数字评分量表(NRS)和患者整体印象变化量表(PGIC)评分。
技术成功率为 100%。平均操作时间(从局部麻醉开始到拔出针)为 2.9 分钟±1.6 分钟。QuickDASH 评分从基线到术后 2、6 和 24 个月分别改善(49.2±11.2 分比 22.1±11.2 分、20.9±16.6 分和 19.5±16.1 分,均 P<.001)。NRS 评分从基线到术后 2、6 和 24 个月分别改善(7.2±1.1 分比 3.1±1.8 分、2.8±2 分和 2.5±2.1 分,均 P<.001)。术后 2、6 和 24 个月时,分别有 84%、81%和 77%的患者对 PGIC 评分改善表示满意。未发生重大不良事件。
经桡动脉内注入临时栓塞材料治疗掌指关节炎是一种可行的治疗选择。