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切口疝修补术中深部假体感染:预测因素及临床结果

Deep prosthesis infection in incisional hernia repair: predictive factors and clinical outcome.

作者信息

Petersen S, Henke G, Freitag M, Faulhaber A, Ludwig K

机构信息

Department of General and Abdominal Surgery, General Hospital Dresden-Friedrichstadt, Teaching Hospital University Dresden, Germany.

出版信息

Eur J Surg. 2001 Jun;167(6):453-7. doi: 10.1080/110241501750243815.

DOI:10.1080/110241501750243815
PMID:11471671
Abstract

OBJECTIVE

To evaluate the incidence of prosthetic infection in incisional hernia repairs, to determine whether there are any factors associated with prosthetic infection and to describe the clinical outcome.

DESIGN

Retrospective clinical study.

SETTING

Teaching hospital, Germany.

SUBJECTS

121 consecutive patients who underwent incisional hernia repair in our department from December 1994 to December 1999.

INTERVENTION

Hernia repair by implantation of an alloplastic prosthesis by the Stoppa-Rives technique.

MAIN OUTCOME MEASURES

Postoperative deep prosthetic infection and associated factors.

RESULTS

All 121 patients had the mesh implanted in the subfascial plane, 77 had a polypropylene mesh (Prolene) (64%), 7 had a polyester mesh (Mersilene) (6%), and 37 patients had a expanded polytetrafluoroethylene patch (ePTFE, Gore-Tex) (31%). Postoperatively the mesh became infected in 8 patients (7%), a mean of 4.5 months (range 0.5-16) after hernia repair. All three infected ePTFE patches had to be removed whereas drainage was sufficient treatment for the infected polypropylene and polyester meshes.

CONCLUSION

Once a mesh infection is verified adequate drainage seems to be sufficient for polypropylene and polyester meshes but ePTFE patches should be removed.

摘要

目的

评估切口疝修补术中人工材料感染的发生率,确定是否存在与人工材料感染相关的因素,并描述临床结局。

设计

回顾性临床研究。

地点

德国教学医院。

研究对象

1994年12月至1999年12月在我科连续接受切口疝修补术的121例患者。

干预措施

采用Stoppa-Rives技术植入异体人工材料进行疝修补。

主要观察指标

术后深部人工材料感染及相关因素。

结果

121例患者均在筋膜下平面植入补片,77例使用聚丙烯补片(普理灵)(64%),7例使用聚酯补片(梅丝琳)(6%),37例使用膨化聚四氟乙烯补片(ePTFE,戈尔特斯)(31%)。术后8例患者(7%)补片发生感染,平均在疝修补术后4.5个月(范围0.5 - 16个月)。所有3例感染的ePTFE补片均需取出,而对于感染的聚丙烯和聚酯补片,引流是足够的治疗方法。

结论

一旦证实补片感染,对于聚丙烯和聚酯补片,充分引流似乎就足够了,但ePTFE补片应取出。

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