与侵袭性更强的方法相比,微创大鼠胸腺切除术在重症肌无力患者中的疗效--单个中心的十年经验

Agata Nawojowska, Samuel Mendes, Daniel Cabral, Cristina Rodrigues, Mariana Antunes, Magda Alvoeiro, Carolina Torres, Telma Calado, Francisco Felix
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引用次数: 0

摘要

简介重症肌无力(MG)是一种自身免疫性神经系统疾病,可引起多种症状。虽然经胸、经颈和胸廓切开术是公认的有效方法,但关于 VATS 方法仍存在争议:我们分析了本中心在胸腺切除术治疗重症肌无力方面的手术经验,比较了 10 年来使用 VATS 和更多侵入性方法进行手术的患者的结果。在该部门的手术数据库中搜索了2010年1月至2021年1月期间的重症肌无力病例,共发现了40个病例。24名患者被纳入最终分析,并被分为两组:VATS手术组(A组)和开放手术组(B组)。后者包括胸骨切开术、胸廓切开术、经颈部和半腔镜方法。只包括根治性胸腺切除术。既定结果为临床改善,即无症状缓解、减少或停用达到最佳症状控制所需的药物:中位随访时间为 27 个月(从 4 个月到 75 个月不等)。12名患者接受了视频胸腔镜下根治性胸腺切除术。1例患者(8.3%)在不服药的情况下症状完全缓解,2例患者(16.7%)在减少服药的情况下症状消失。8例患者(66.6%)的症状有所改善(症状减轻或用药减少)。1名患者(8.3%)的临床结果没有变化。没有一名患者报告症状恶化。12 名患者接受了开放性胸腺切除术。1例患者(8.3%)在不服药的情况下症状完全缓解,2例患者(16.7%)在减少服药后症状消失。6例患者(50%)的症状有所改善。3 名患者(25%)的临床结果没有变化,而其中 2 名患者(16.7%)的症状控制略有改善,但用药量显著增加。一名患者(8.3%)称临床结果没有任何明显变化。没有一名患者报告症状恶化:结论:视频孔镜方法治疗重症肌无力与开放式方法相比并无劣势,而且在长期随访中效果显著,同时还具有微创手术的所有额外优势。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Results Of Minimally Invasive Vats Thymectomy In Miastenia Gravis Patients Compared With More Invasive Approaches - 10-Year Experience In A Single Center.

Introduction: Myasthenia gravis (MG) is an autoimmune, neurologic disease that causes a wide range of symptoms. While the transsternal, transcervical and thoracotomy approaches are accepted as effective, there is still debate regarding the VATS approach.

Materials and methods: We analyzed our center's surgical experience with thymectomy for myasthenia gravis, comparing the results of patients operated on using VATS and more invasive approaches, over a period of 10 years. A search of the department's surgical database for myasthenia gravis cases between January 2010 and January 2021, revealed a total of 40 cases. Twenty-four patients were included in the final analysis and were distributed into two groups: the VATS procedure group (group A) and the open procedure group (group B). The latter included sternotomy, thoracotomy, transcervical and hemiclamshell approaches. Only radical thymectomies were included. The established outcomes were clinical improvement defined as asymptomatic remission, reduction, or discontinuation of the medication necessary to achieve optimal symptom control.

Results: The median follow-up time was 27 months (ranging from 4 to 75 months). Videothoracoscopy radical thymectomy was performed on 12 patients. Complete remission with no medication was achieved in 1 case (8.3%), while 2 patients (16.7%) became asymptomatic with reduced medication. An improvement (reduced symptoms or decreased medication) was observed in 8 cases (66.6%). No change in clinical outcome was noted in 1 patient (8.3%). None of the patients reported worsening symptoms. Open thymectomy was performed on 12 patients. Complete remission with no medication was achieved in 1 case (8.3%), while 2 patients (16.7%) became asymptomatic with reduced medication. An improvement was noted in 6 cases (50%). No change in clinical outcome was observed in 3 patients (25%) whereas 2 of them (16.7%) experienced slightly better symptom control but with a significant increase in medication. One patient (8.3%) described the clinical results as without any significant change. None of the patients reported worsening symptoms.

Conclusion: The videotoracoscopic approach in the treatment of myasthenia gravis is non-inferior compared to the open approach and effective in a long-term follow-up, offering all the additional benefits of less invasive surgery.

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