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DOI 10.21037/jtd.2018.02.11

Медицинская библиотека · Journal of thoracic disease · 2018

Subxiphoid and subcostal arch "Three ports" thoracoscopic extended thymectomy for myasthenia gravis.

Lu Qiang, Zhao Jinbo, Wang Juzheng, Chen Zhao, Han Yong, Huang Lijun, Li Xiaofei, Zhou Yongan

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Аннотация

BACKGROUND

The approaches to thoracoscopic thymectomy in myasthenia gravis (MG) are debatable. We developed a novel approach via subxiphoid and subcostal arch, with a significantly shorter duration of operation and hospital stay, less estimated blood loss, and lower postoperative pain.

METHODS

From December 2012 to December 2014, 77 myasthenia gravis patients with or without thymoma underwent thoracoscopic extended thymectomy at our hospital. Among them, 41 patients were operated via the subxiphoid and subcostal arch approach and the other 36 via the conventional unilateral approach. The patient outcomes were retrospectively reviewed and evaluated.

RESULTS

The thoracoscopic extended thymectomy was performed safely via the subxiphoid and subcostal arch approach. In this approach, no drainage tube was inserted after operation except in the first two patients. Two of the 41 patients were switched to trans-sternal approach due to the tight adhesion between the thymoma and the left innominate vein. No major complications occurred. Compared with the unilateral approach, the duration of the procedure via subxiphoid and subcostal arch was significantly shorter, with less estimated blood loss, shorter hospital-stay and lower postoperative pain (P<0.001). The cosmetic scores were comparable between the two groups (P=0.369).

CONCLUSIONS

The novel subxiphoid and subcostal arch approach is technically feasible and safe. It is an acceptable alternative to conventional thoracoscopic extended thymectomy.

Для цитирования: Lu Qiang, Zhao Jinbo, Wang Juzheng, Chen Zhao, Han Yong, Huang Lijun, Li Xiaofei, Zhou Yongan. Subxiphoid and subcostal arch "Three ports" thoracoscopic extended thymectomy for myasthenia gravis.. Journal of thoracic disease. 2018. DOI: 10.21037/jtd.2018.02.11.
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