同轴穿刺活检与射频消融系统在脾脏病变诊断中的应用: 一项前瞻性研究的安全性与有效性分析

Application of Coaxial Percutaneous Biopsy and Radiofrequency Ablation System in the Diagnosis of Splenic Lesions: a Prospective Study on Safety and Efficacy

  • 摘要:
    目的 初步评估同轴穿刺活检与射频消融系统在脾脏病变诊断中的安全性和有效性。
    方法 本研究为单臂前瞻性研究, 以脾脏病变行穿刺活检的患者为研究对象。所有患者均顺利在超声引导下完成穿刺活检, 并在活检后及时进行穿刺针道射频消融。记录患者基线特征, 评估技术成功率和并发症发生情况, 并观察手术即刻以及术后随访期间出血、感染和疼痛等并发症的发生情况。
    结果 共21例符合纳入和排除标准的患者入选本研究, 其中男性16例(76.2%), 女性5例(23.8%); 年龄15~82岁, 平均(59.5±15.2)岁。所有患者均成功完成穿刺和穿刺针道消融, 技术成功率为100%。3例(14.3%)发生轻度出血, 无中重度出血或其他严重并发症发生。随访期间未见针道种植转移。
    结论 同轴穿刺活检与射频消融系统在脾脏病变穿刺活检中安全、有效, 可为接受脾脏病变穿刺活检的患者提供一种安全、有效的新诊疗选择。

     

    Abstract:
    Objective To preliminarily evaluate the safety and efficacy of coaxial biopsy needle combined with radiofrequency ablation (RFA) system in patients undergoing percutaneous biopsy of splenic lesions.
    Methods This single-arm prospective study enrolled splenic lesions patients indicated for splenic lesion biopsy.All patients successfully underwent ultrasound-guided biopsy, immediately followed by RFA of the needle tract.Baseline characteristics of patients were recorded.The technical success rate and the incidence of complications were assessed.Occurrence of complications such as bleeding, infection, and pain were observed immediately after the procedure, as well as at follow-up period postoperatively.
    Results A total of 21 patients who met the inclusion and exclusion criteria were included in this study, including 16 males (76.2%) and5 females (23.8%).The patients' ages ranged from 15 to 82 years, with an average age of (59.5±15.2) years.All patients successfully completed the biopsy and needle tract ablation, with a success rate of 100%.Mild bleeding occurred in 3 patients (14.3%), and no moderate to severe bleeding or other serious complications were observed.No needle tract seeding was detected during the follow-up period.
    Conclusion The coaxial biopsy and RFA system is safe and effective in percutaneous biopsy of splenic lesions, providing a new safe and effective option for patients undergoing percutaneous biopsy of splenic lesions.

     

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