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Comparison of the risk of gastrointestinal perforation between patients with and without rheumatoid arthritis: A nationwide cohort study in Asia.
Chang, Ting-Chia; Kan, Wei-Chih; Cheng, Kuo-Chen; Ho, Chung-Han; Chen, Yi-Chen; Chu, Chin-Chen; Hsu, Chien-Chin; Kuo, Hsing-Tao; Lin, Hung-Jung; Huang, Chien-Cheng.
Affiliation
  • Chang TC; Department of Internal Medicine, Chi Mei Medical Center, Tainan, Taiwan.
  • Kan WC; Department of Intensive Care Medicine, Chi Mei Medical Center, Tainan, Taiwan.
  • Cheng KC; Department of Internal Medicine, Chi Mei Medical Center, Tainan, Taiwan.
  • Ho CH; Department of Biological Science and Technology, Chung Hwa University of Medical Technology, Tainan, Taiwan.
  • Chen YC; Department of Internal Medicine, Chi Mei Medical Center, Tainan, Taiwan.
  • Chu CC; Department of Intensive Care Medicine, Chi Mei Medical Center, Tainan, Taiwan.
  • Hsu CC; Department of Medical Research, Chi Mei Medical Center, Tainan, Taiwan.
  • Kuo HT; Department of Information Management, Southern Taiwan University of Science and Technology, Tainan, Taiwan.
  • Lin HJ; Department of Medical Research, Chi Mei Medical Center, Tainan, Taiwan.
  • Huang CC; Department of Anesthesiology, Chi Mei Medical Center, Tainan, Taiwan.
Front Med (Lausanne) ; 9: 974328, 2022.
Article in En | MEDLINE | ID: mdl-36250072
Objectives: Patients with rheumatoid arthritis (RA) may have an increased risk for gastrointestinal perforation (GIP) caused by medications or chronic inflammation. However, the risk of GIP between patients with and without RA remains unclear. Therefore, we conducted this study to clarify it. Methods: Using the Taiwan National Health Insurance Research Database, we identified patients with and without RA matched at 1:1 ratio by age, sex, and index date between 2000 and 2013 for this study. Comparison of the risk of GIP between the two cohorts was performed by following up until 2014 using Cox proportional hazard regression analyses. Results: In total, 11,666 patients with RA and an identical number of patients without RA were identified for this study. The mean age (±standard deviation) and female ratio were 55.3 (±15.2) years and 67.6% in both cohorts. Patients with RA had a trend of increased risk for GIP than patients without RA after adjusting for underlying comorbidities, medications, and monthly income [adjusted hazard ratio (AHR) 1.42; 95% confidence interval (CI) 0.99-2.04, p = 0.055]. Stratified analyses showed that the increased risk was significant in the female population (AHR 2.06; 95% CI 1.24-3.42, p = 0.005). Older age, malignancy, chronic obstructive pulmonary disease, and alcohol abuse were independent predictors of GIP; however, NSAIDs, systemic steroids, and DMARDs were not. Conclusion: RA may increase the risk of GIP, particularly in female patients. More attention should be paid in female population and those with independent predictors above for prevention of GIP.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Language: En Journal: Front Med (Lausanne) Year: 2022 Document type: Article Affiliation country: Taiwan Country of publication: Switzerland

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Language: En Journal: Front Med (Lausanne) Year: 2022 Document type: Article Affiliation country: Taiwan Country of publication: Switzerland