Kallidonis Panagiotis, Kotsiris Dimitrios, Sanguedolce Francesco, Ntasiotis Panteleimon, Liatsikos Evangelos, Papatsoris Athanasios
Department of Urology, University of Patras, Patras, Greece.
Department of Urology, King's College London, King's College Hospital, London, UK.
Arab J Urol. 2017 Oct 16;15(4):280-288. doi: 10.1016/j.aju.2017.08.004. eCollection 2017 Dec.
To review the literature on the effectiveness, safety and long-term patency of ureteric metal mesh stents (MSs), as a variety of MSs have been used for managing malignant ureteric obstruction over the last three decades.
A systematic review using the search string; Ureter∗ AND (stent OR endoprosthesis) AND metal∗ was conducted on PubMed, Scopus, Web of science and Cochrane Library online databases in May 2016. Prospective, retrospective, and comparative studies including MSs were included. The primary endpoint was the patency rate and the secondary endpoint was complications.
In all, 324 publications were screened and 31 articles were included in the systematic review; 21 prospective and 10 retrospective studies. These studies reported the effectiveness of specific MSs in population studies, in comparative studies among different MSs, as well as among MSs and JJ stents. It should be noted that all comparative studies were retrospective.
The experiences with vascular MSs, such as the Wallstent™ (Boston Scientific/Microvasive, Natick, MA, USA), were related to high occlusion rates, due to endoluminal hyperplasia, and long-term disappointing patency. The use of covered MSs designed for the vascular system was also unfavourable. The Memokath 051™ (PNN Medical A/S, Kvistgaard, Denmark) had better patency rates, but also higher migration rates. The long-term results were acceptable and rendered the Memokath 051 as a viable option for the management of malignant ureteric obstruction. The Uventa™ (Taewoong Medical, Seoul, Korea) and Allium™ (Allium Medical Solutions Ltd, Caesarea, Israel) MSs, specifically designed for ureteric placement, provided promising results. Nevertheless, the wide acceptance of these MSs would require well-designed clinical studies and long-term follow-up.
回顾输尿管金属网状支架(MSs)有效性、安全性及长期通畅性的相关文献,因为在过去三十年里,多种MSs已被用于处理恶性输尿管梗阻。
2016年5月在PubMed、Scopus、科学网和考克兰图书馆在线数据库上,使用检索词“输尿管∗ AND(支架 OR 内置假体)AND 金属∗”进行系统综述。纳入包括MSs的前瞻性、回顾性和比较性研究。主要终点是通畅率,次要终点是并发症。
共筛选出324篇出版物,31篇文章纳入系统综述;21篇前瞻性研究和10篇回顾性研究。这些研究报告了特定MSs在人群研究中的有效性、不同MSs之间以及MSs与双J支架之间的比较研究结果。需要注意的是,所有比较性研究均为回顾性研究。
血管性MSs,如Wallstent™(美国波士顿科学公司/微创公司,马萨诸塞州纳蒂克),因腔内增生导致闭塞率高,长期通畅性令人失望。用于血管系统的覆膜MSs的使用效果也不佳。Memokath 051™(丹麦PNN Medical A/S公司,奎斯泰加德)通畅率较好,但迁移率也较高。长期结果可以接受,使Memokath 051成为处理恶性输尿管梗阻的一个可行选择。专门为输尿管放置设计的Uventa™(韩国太宇医疗公司,首尔)和Allium™(以色列凯撒利亚Allium Medical Solutions Ltd公司)MSs取得了有前景的结果。然而,这些MSs要被广泛接受还需要精心设计的临床研究和长期随访。