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戈尔-特克斯腹膜导管:一项临床评估及与Tenckhoff导管的比较

The Gore-Tex peritoneal catheter: a clinical evaluation and comparison with the Tenckhoff catheter.

作者信息

Bay W H, Vaccaro P S, Powell S L, Erlich L F

出版信息

Am J Kidney Dis. 1984 Nov;4(3):268-79. doi: 10.1016/s0272-6386(84)80104-3.

DOI:10.1016/s0272-6386(84)80104-3
PMID:6238527
Abstract

In January of 1983, the Gore-Tex (W.L. Gore & Associates, Inc, Flagstaff, Ariz) peritoneal catheter was introduced into the dialysis market. Presently, there is no other peritoneal catheter that offers this unique subcutaneous tunnel design. This catheter has an external and intra-abdominal Silastic (Dow Corning, Midland, Mich) segment and a transcutaneous segment with a flange and cuff of expanded polytetrafluoroethylene (PTFE). This catheter was designed to decrease the incidence of tunnel infections, catheter cuff extrusions, and exit site infections. The clinical experience with 57 Gore-Tex catheters and 47 Tenckhoff catheters at Ohio State University from May 1980 through April 1983 is presented. In addition, the Gore-Tex catheter's surgical insertion technique and postoperative care procedures are described. There was a significant decrease in the incidence of tunnel infections with the Gore-Tex catheter versus the Tenckhoff catheter (0.03 versus 0.21 infections per patient-year, respectively; P less than .05). There was no significant difference between the Gore-Tex catheter and the Tenckhoff catheter with regard to the patient peritonitis rate (1.12 versus 1.38 episodes of peritonitis per patient-year, respectively) or the exit site infection rate (0.65 versus 0.50 infections per patient-year, respectively). There were no cuff extrusions with the Gore-Tex catheter. The decrease in the incidence of tunnel infections with the Gore-Tex catheter suggests that the PTFE barrier inhibits longitudinal bacterial movement and avoids bacterial sequestration. Patients with repeat tunnel infections may benefit from a Gore-Tex catheter placement.

摘要

1983年1月,戈尔特斯(W.L.戈尔联合公司,亚利桑那州弗拉格斯塔夫)腹膜导管进入透析市场。目前,没有其他腹膜导管采用这种独特的皮下隧道设计。该导管有一个外部和腹腔内的硅橡胶(道康宁公司,密歇根州米德兰)部分以及一个带有膨体聚四氟乙烯(PTFE)法兰和袖套的经皮部分。该导管旨在降低隧道感染、导管袖套挤出和出口部位感染的发生率。本文介绍了1980年5月至1983年4月在俄亥俄州立大学对57根戈尔特斯导管和47根Tenckhoff导管的临床经验。此外,还描述了戈尔特斯导管的手术插入技术和术后护理程序。与Tenckhoff导管相比,戈尔特斯导管的隧道感染发生率显著降低(分别为每患者年0.03次感染和0.21次感染;P小于0.05)。在患者腹膜炎发生率(分别为每患者年1.12次和1.38次腹膜炎发作)或出口部位感染率(分别为每患者年0.65次和0.50次感染)方面,戈尔特斯导管和Tenckhoff导管之间没有显著差异。戈尔特斯导管没有出现袖套挤出情况。戈尔特斯导管隧道感染发生率的降低表明,PTFE屏障可抑制细菌纵向移动并避免细菌滞留。反复发生隧道感染的患者可能会从放置戈尔特斯导管中获益。

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