3.8 Article

Etodolac and the risk of acute pancreatitis

Journal

BIOMEDICINE-TAIWAN
Volume 7, Issue 1, Pages 25-29

Publisher

CHINA MEDICAL UNIV-CMU
DOI: 10.1051/bmdcn/2017070104

Keywords

Acute pancreatitis; Etodolac

Funding

  1. Taiwan Ministry of Health and Welfare Clinical Trial and Research Center of Excellence [MOHW105-TDU-B-212-133019]
  2. China Medical University Hospital
  3. Academia Sinica Taiwan Biobank Stroke Biosignature Project [BM10501010037]
  4. National Research Program for Bio-pharmaceuticals (NRPB) Stroke Clinical Trial Consortium [MOST 105-2325-B-039 -003]
  5. Tseng-Lien Lin Foundation in Taichung in Taiwan
  6. Taiwan Brain Disease Foundation in Taipei in Taiwan
  7. Katsuzo and Kiyo Aoshima Memorial Funds in Japan

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Objective: The aim of this study was to explore the association between etodolac use and acute pancreatitis in Taiwan. Design: We designed a case-control study using the database of Taiwan's National Health Insurance. Subjects: In all, 7577 subjects aged 20 years or older with newly diagnosed acute pancreatitis were defined as cases, and 27032 sex-matched and age-matched subjects without acute pancreatitis were defined as controls. The period considered for this study was from 1998 to 2011. For the study, never having used etodolac is defined as a subject never receiving a prescription for etodolac. Active use of etodolac is defined as a subject receiving at least 1 prescription for etodolac within 7 days of the date of their being diagnosed with acute pancreatitis. Non-active use of etodolac is defined as a subject not receiving a prescription for etodolac within 7 days but receiving at least 1 prescription for etodolac >= 8 days before the date of their being diagnosed with acute pancreatitis. Main outcome measure: The association between etodolac use and acute pancreatitis was estimated by using the multivariable unconditional logistic regression model. Results: After correcting for covariates, the adjusted odds ratio of acute pancreatitis was 3.78 for subjects with active use of etodolac (95% confidence interval 1.11, 12.9), compared with subjects who never used etodolac. The adjusted odds ratio decreased to 1.18 for subjects with non-active use of etodolac (95% confidence interval 0.38, 3.67), but that was without statistical significance. Conclusion: There could be an association between active use of etodolac and acute pancreatitis. Clinicians should take into account the possibility of etodolac-associated acute pancreatitis when patients currently using etodolac present with acute pancreatitis with an unknown cause.

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