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使用美国重症肌无力基金会指南评估机器人胸腺切除术。

Assessment of robotic thymectomy using the Myasthenia Gravis Foundation of America Guidelines.

机构信息

Division of Thoracic Surgery, Department of Surgery, The Johns Hopkins Medical Institutions, Baltimore, Maryland 21287, USA.

出版信息

Ann Thorac Surg. 2010 Apr;89(4):1080-5; discussion 1085-6. doi: 10.1016/j.athoracsur.2010.01.038.

Abstract

BACKGROUND

Robotic thymectomy is an emerging treatment for myasthenia gravis. However, the Myasthenia Gravis Foundation of America clinical research standards have been infrequently adopted in the surgical literature.

METHODS

Twenty-six patients underwent robotic thymectomy for myasthenia gravis between 2003 and 2008, performed by a single surgeon using the da Vinci system (Intuitive Surgical; Sunnyvale, CA) through a four-port right-sided approach.

RESULTS

Mean operative times were 68+/-25 minutes of robotic system activation and 127+/-35 minutes from incision to closure. There were no intraoperative or postoperative mortalities; the most common intraoperative complication was desaturation after single-lung ventilation, for which four procedures were converted to open. On histologic examination, there were five thymomas. The average follow-up after surgery was 26 months. Median preoperative and postoperative Myasthenia Gravis Foundation of America disease classifications were 2 and 0, respectively, reflecting a statistically significant decrease in symptoms (p<0.01). Additionally, the average daily dose of cholinesterase inhibitor decreased by 63% postoperatively. Overall, 82% of patients improved and 18% were unchanged; no worsening disease was observed.

CONCLUSIONS

Robotic thymectomy is a safe and efficacious treatment option for myasthenia gravis. There were no notable differences in patient demographics compared with previously published reports of open thymectomies. Furthermore, surgical and neurologic outcomes in this series compare favorably with conventional approaches in the literature. Of those with follow-up greater than 6 months, 82% of patients undergoing robotic thymectomy demonstrated significant clinical improvement postoperatively, indicating that this approach in concert with optimized medical management is an effective treatment for myasthenia gravis.

摘要

背景

机器人胸腺切除术是重症肌无力的一种新兴治疗方法。然而,美国重症肌无力基金会的临床研究标准在外科文献中很少被采用。

方法

2003 年至 2008 年间,一位外科医生使用达芬奇系统(直觉外科公司;加利福尼亚州森尼韦尔)通过四端口右侧入路对 26 例重症肌无力患者进行了机器人胸腺切除术。

结果

机器人系统激活的平均手术时间为 68+/-25 分钟,从切口到关闭的平均手术时间为 127+/-35 分钟。无术中或术后死亡;最常见的术中并发症是单肺通气后缺氧,其中 4 例转为开放性手术。组织学检查发现 5 例胸腺瘤。术后平均随访 26 个月。术前和术后平均美国重症肌无力基金会疾病分类分别为 2 级和 0 级,表明症状有统计学显著改善(p<0.01)。此外,术后胆碱酯酶抑制剂的平均日剂量减少了 63%。总体而言,82%的患者病情改善,18%的患者病情不变;没有观察到病情恶化。

结论

机器人胸腺切除术是重症肌无力的一种安全有效的治疗选择。与先前发表的开放性胸腺切除术报告相比,患者的人口统计学特征无明显差异。此外,本系列的手术和神经学结果与文献中的传统方法相比具有优势。在随访时间大于 6 个月的患者中,82%的接受机器人胸腺切除术的患者术后表现出显著的临床改善,这表明这种方法与优化的药物治疗相结合是重症肌无力的有效治疗方法。

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