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首页> 外文期刊>International journal of hyperthermia: The official journal of European Society for Hyperthermic Oncology, North American Hyperthermia Group >Percutaneous microwave ablation with artificial ascites for symptomatic uterine adenomyosis: initial experience
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Percutaneous microwave ablation with artificial ascites for symptomatic uterine adenomyosis: initial experience

机译:人工腹水经皮微波消融治疗有症状子宫腺肌病的初步经验

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Purpose: To evaluate the feasibility, safety and technical efficacy of ultrasound-guided percutaneous microwave ablation with artificial ascites for adenomyosis. Materials and methods: Between May 2015 and May 2016, a total of 25 patients with symptomatic adenomyosis who underwent ultrasound-guided percutaneous microwave ablation with artificial ascites were included in this retrospective study. A matching cohort of 50 patients underwent ultrasound-guided percutaneous microwave ablation without artificial ascites as controls. The technical efficacy, complications and short-term treatment effectiveness were assessed and compared with the controls. Results: Artificial ascites was successfully achieved in all of the 25 patients with the administration of a median of 550?mL (range, 250–1200?mL) of solution. There was substantial improvement in achieving a better antenna path in 100% (20/20) of the cases with a poor antenna path. The complete separation was achieved in 23 of 25 patients. The mean ablation time was 26.5?±?7.3?min and the median non-perfusion volume ratio was 76% which was similar to the control group (p??.05). No serious complications were observed. Patient pain scores for dysmenorrhoea showed a statistically significant decline from the baseline of 6.71?±?0.96 to 2.92?±?0.79 and the symptom severity score declined statistically significantly from 21.8?±?5.5 to 16.4?±?4.8 at 3 months follow-up. Conclusions: Percutaneous microwave ablation with artificial ascites is feasible, safe and can be effective in improving access for treatment of adenomyosis.
机译:目的:评价超声引导经皮微波消融人工腹水治疗子宫腺肌病的可行性,安全性和技术效果。材料和方法:这项回顾性研究纳入了2015年5月至2016年5月之间共25例有症状的子宫腺肌病患者,这些患者接受了超声引导下经皮微波微波消融和人工腹水。队列匹配的50名患者接受了超声引导下的经皮微波消融术,无人工腹水作为对照。评估技术疗效,并发症和短期治疗效果,并与对照进行比较。结果:25例患者中位数为550?mL(范围250-1200?mL)的溶液均成功实现了人工腹水。在天线路径不良的情况下,有100%(20/20)的情况可以更好地实现更好的天线路径。 25例患者中有23例完全分离。平均消融时间为26.5?±?7.3?min,中值非灌注体积比为76%,与对照组相似(p?>?0.05)。没有观察到严重的并发症。痛经的患者疼痛评分从基线的6.71%±0.96下降到2.92%±0.79,具有统计学意义的下降,症状严重程度评分在随后的3个月中从21.8%±5.5下降到16.4%±4.8。向上。结论:人工腹水经皮微波消融术是可行,安全的,并可有效改善子宫腺肌病的治疗途径。

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