Experimental study of diclofenac and its biliary metabolites on anastomotic healing
Autor: | Simon T.K. Yauw, P. van den Broek, Roger M. L. M. Lomme, Frans G. M. Russel, H. van Goor, Rick Greupink |
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Rok vydání: | 2018 |
Předmět: |
medicine.medical_specialty
Bile duct business.industry Vascular damage Radboud Institute for Health Sciences [Radboudumc 16] Original Articles General Medicine Plasma levels Anastomosis Bile composition digestive system Gastroenterology Reconstructive and regenerative medicine Radboud Institute for Health Sciences [Radboudumc 10] stomatognathic diseases medicine.anatomical_structure Diclofenac Reconstructive and regenerative medicine Radboud Institute for Molecular Life Sciences [Radboudumc 10] Renal disorders Radboud Institute for Molecular Life Sciences [Radboudumc 11] Anastomotic leakage Internal medicine medicine Original Article Leak rate Complication business medicine.drug |
Zdroj: | BJS Open, 2, 4, pp. 220-228 BJS Open BJS Open, 2, 220-228 |
ISSN: | 2474-9842 |
Popis: | Contains fulltext : 195656.pdf (Publisher’s version ) (Open Access) Background: Diclofenac increases the risk of anastomotic leakage, but the underlying mechanism is unknown. As diclofenac is excreted largely as biliary metabolites, the aim of this study was to determine the effect of these metabolites on intestinal anastomoses. Methods: This was a randomized controlled blinded experiment using 210 male Wistar rats to assess the effect of 'diclofenac bile' on the anastomotic complication score, leak rate and anastomotic strength following oral and parenteral administration of diclofenac. Bile duct and duodenal catheterization techniques were used for diversion and replacement of bile, and biliary diclofenac metabolites were determined. Results: Replacement of control bile with diclofenac bile resulted in higher anastomotic complication scores (P = 0.006) and leakage in five of 18 animals, compared with one of 18 controls (P = 0.089). In turn, following oral diclofenac administration, replacement of diclofenac bile with control bile reduced anastomotic complications (P = 0.016). The leak rate was seven of 15 versus 13 of 17 without replacement (P = 0.127). After intramuscular administration of diclofenac, the reduction in anastomotic complications was not significant when bile was replaced with control bile (P = 0.283), but it was significant when bile was drained without replacement (P = 0.025). Diclofenac metabolites in bile peaked within 2 h after administration. Administration of diclofenac bile resulted in nearly undetectable plasma levels of diclofenac (mean(s.d.) 0.01(0.01) mug/ml) after 120 min. Following oral diclofenac, bile replacement with control bile did not affect the plasma concentration of diclofenac (0.12(0.08) mug/ml versus 0.10(0.05) mug/ml with diclofenac bile; P = 0.869). Conclusion: Altered bile composition as a result of diclofenac administration increases the ileal anastomotic complication rate in rats. |
Databáze: | OpenAIRE |
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