Colonic anastomotic strength and matrix metalloproteinase activity in an experimental model of bacterial peritonitis

被引:47
作者
de Hingh, IHJT [1 ]
de Man, BM [1 ]
Lomme, RMLM [1 ]
van Goor, H [1 ]
Hendriks, T [1 ]
机构
[1] Univ Med Ctr Nijmegen, Dept Surg, NL-6500 HB Nijmegen, Netherlands
关键词
D O I
10.1002/bjs.4146
中图分类号
R61 [外科手术学];
学科分类号
摘要
Background: Clinical studies report conflicting results on the safety of primary intestinal anastomoses in the presence of peritonitis, and comprehensive experimental data are lacking. The present study investigated whether the strength of experimental colonic anastomoses is affected if surgery is performed in the presence of pre-existing bacterial peritonitis. Methods: Colonic anastomoses were constructed in Wistar rats 24 h after caecal ligation and puncture or a sham procedure. Anastomotic strength was assessed by measuring breaking strength and bursting pressure during the first 5 days after operation. Anastomotic hydroxyproline levels were measured and matrix metalloproteinase (MMP) activity was analysed by quantitative gelatin zymography. Results: Anastomotic strength was lowered in the presence of bacterial peritonitis but in a minor and transient way. The breaking strength was lower only immediately after construction of the anastomosis (- 5 per cent, P = 0.011) and the bursting pressure only on the third postoperative day (-33 per cent, P = 0.038); no anastomotic dehiscence was observed. At 3 days after operation increased levels of MMP activity were observed but anastomotic hydroxyproline content was not affected by bacterial peritonitis. Conclusion: The influence of bacterial peritonitis on the development of anastomotic strength is limited. This experimental finding lends support to recent clinical studies that have demonstrated the feasibility of constructing a primary anastomosis under these conditions.
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页码:981 / 988
页数:8
相关论文
共 31 条
[1]   Intra-abdominal sepsis impairs colonic reparative collagen synthesis [J].
Ahrendt, GM ;
Tantry, US ;
Barbul, A .
AMERICAN JOURNAL OF SURGERY, 1996, 171 (01) :102-107
[2]  
AHRENDT GM, 1994, ARCH SURG-CHICAGO, V129, P1179
[3]   The matrix metalloproteinase inhibitor BB-94 improves the strength of intestinal anastomoses in the rat [J].
de Hingh, IHJT ;
Siemonsma, MA ;
de Man, BM ;
Lomme, RMLM ;
Hendriks, T .
INTERNATIONAL JOURNAL OF COLORECTAL DISEASE, 2002, 17 (05) :348-354
[4]   POSTOPERATIVE LEVAMISOLE MAY COMPROMISE EARLY HEALING OF EXPERIMENTAL INTESTINAL ANASTOMOSES [J].
DEWAARD, JWD ;
WOBBES, T ;
DEMAN, BM ;
VANDERLINDEN, CJ ;
HENDRIKS, T .
BRITISH JOURNAL OF CANCER, 1995, 72 (02) :456-460
[5]  
Golub R, 1997, J AM COLL SURGEONS, V184, P364
[6]  
Gooszen AW, 2001, EUR J SURG, V167, P35
[7]   Prospective study of primary anastomosis following sigmoid resection for suspected acute complicated diverticular disease [J].
Gooszen, AW ;
Tollenaar, RAEM ;
Geelkerken, RH ;
Smeets, HJ ;
Bemelman, WA ;
Van Schaardenburgh, P ;
Gooszen, HG .
BRITISH JOURNAL OF SURGERY, 2001, 88 (05) :693-697
[8]   FECAL PERITONITIS - THE EFFECT ON ANASTOMOTIC HEALING [J].
GUTMAN, M ;
KLAUSNER, JM ;
LELCUK, S .
EUROPEAN SURGICAL RESEARCH, 1993, 25 (06) :366-369
[9]   HEALING OF EXPERIMENTAL INTESTINAL ANASTOMOSES - PARAMETERS FOR REPAIR [J].
HENDRIKS, T ;
MASTBOOM, WJB .
DISEASES OF THE COLON & RECTUM, 1990, 33 (10) :891-901
[10]  
Hinchey E J, 1978, Adv Surg, V12, P85