Key result
Carprofen increases ileal dehiscence rates to 60% compared to buprenorphine, impairing intestinal healing.
Why the study?
The potential of COX-2 inhibitors to reproducibly induce anastomotic leakage and affect intestinal healing was examined.
Does carprofen induce anastomotic leakage in rats undergoing intestinal anastomosis?
Does carprofen induce anastomotic leakage in rats undergoing intestinal anastomosis?
Perioperative administration of carprofen in rats yields a reproducible model for anastomotic leakage in the ileum, allowing for translational research on perisuture line reinforcement.
Answers are grounded in this paper and cite their sources.
Caution with COX-2 inhibitors after intestinal anastomosis; Level 5 data leave open need for confirmatory trials.
The authors examined the potential of the cyclooxygenase 2 (COX-2) inhibitor carprofen to reproducibly induce anastomotic leakage. In experiment 1, an anastomosis was constructed in both ileum and colon of 20 rats, and they were given carprofen (5 mg/kg subcutaneously every 24 hours) or buprenorphine (0.02 mg/kg subcutaneously every 12 hours). In another 20 rats an anastomosis was constructed in either ileum or colon, and all received carprofen (experiment 2). Animals were sacrificed after 3 days. In experiment 1, the ileal dehiscence rate was 60% in the carprofen group and 0% in the buprenorphine group (P = .0108). Colonic anastomoses in both groups remained patent. In experiment 2, the anastomotic leakage rate was 80% in ileum and 0% in colon. Thus, COX-2 inhibitors can severely interfere with intestinal healing, particularly in the ileum. Perioperative administration of carprofen yields a unique model for anastomotic leakage, which allows translational research on the effectiveness of perisuture line reinforcement.
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Vijver et al. (2012) studied Anastomotic leakage (n=40). Carprofen vs. Buprenorphine (0.02 mg/kg subcutaneously every 12 hours) was evaluated on Ileal dehiscence rate (p=.0108). Carprofen administration resulted in a 60% ileal dehiscence rate compared to 0% with buprenorphine (P = .0108), demonstrating that COX-2 inhibitors severely interfere with intestinal healing.
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