COX-2 inhibitors may prevent severe acute pancreatitis

Dr Huang and his colleagues of West China Hospital and Sichuan University in Chengdu, China., based on an experimental evidence showing overexpression of COX-2 in acute pancreatitis, and that blocking COX-2 reduced pancreatitis severity, conducted a randomized trial in which 190 patients with predicted SAP received standard treatment or standard treatment plus 40 mg per day of parecoxib intravenously for 3 days, followed by 200 mg of celecoxib orally or through a feeding tube every day for 1 week.

COX-2 inhibitors, besides offering organ support,  "effectively block the inflammatory cascade during the development of severe acute pancreatitis," stated by  Drs. Libin Huang, Zhiyin Huang, and Chengwei Tang. "This regimen presented good cost-effectiveness," they added.

They came out with the following findings:

 • SAP developed in 21% of the COX-2 group compared to 40% of the conventional treatment group.

 • Organ failure was most likely to be transient in the cox-2 group.

 • The mortality rate was similar for the two groups.

 • all patients had above-normal serum levels of C-reactive protein (CRP), tumour necrosis factor-alpha (TNF-alpha) and interleukin-6 (IL-6). TNF-alpha and IL-6 were reduced in both groups at day 4 and day 8 of the study, but the reduction was greater in the COX-2 group.

 • Two-thirds of the conventional treatment group required meperidine injections, compared to about 43% of the COX-2 group.

 • Mean hospital stay and hospital costs were also lower with COX-2 inhibitors (21 days vs. 13 days)

"The lack of a placebo to attain double-blinding may affect the pain scoring system since it is a patient-reported outcome. Being open and conducted in a single centre, there might be some data bias." these were the limitations in the trial noted by the researchers.

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The American Journal of Gastroenterology: March 2020 - Volume 115 - Issue 3 - p 473-480

DOI: 10.14309/ajg.0000000000000529