Incidences, temporal trends and risks of hospitalisation for gastrointestinal bleeding in new or chronic low-dose aspirin users after treatment for Helicobacter pylori: a territory-wide cohort study. Issue 3 (17th May 2019)

• Record Type: Journal Article
• Authors: Guo, Chuan-Guo; Cheung, Ka Shing; Zhang, Feifei; Chan, Esther W; Chen, Lijia; Wong, Ian CK; Leung, Wai K
• Is Part Of: Gut. Volume 69:Issue 3(2020)
• Page Start: 445
• Page End: 452
• Publication Date: 2019-05-17
• Subjects: gastrointestinal bleeding -- helicobacter pylori -- aspirin; Gastroenterology -- Periodicals; 616.33
• DOI: 10.1136/gutjnl-2019-318352
• Languages: English
• ISSNs: 0017-5749

Abstract

Abstract : Objective: The risk of GI bleeding (GIB) in aspirin users after Helicobacter pylori (HP) eradication remains poorly defined. We characterised the incidences and temporal trends of hospitalisations for all GIB in aspirin users after HP eradication therapy. Design: Based on a territory-wide health database, we identified all patients who had received the first course of clarithromycin-based triple therapy between 2003 and 2012. Patients were divided into three cohorts according to aspirin use: new users (commenced after HP eradication), chronic users (commenced before and resumed after HP eradication) and non-users. The primary outcome was to determine the risk of hospitalisation for GIB. Results: We included 6985 new aspirin users, 5545 chronic users and 48 908 non-users. The age-adjusted and sex-adjusted incidence of hospitalisation for all GIB in new, chronic and non-users was 10.4, 7.2 and 4.6 per 1000 person-years, respectively. Upper and lower GIB accounted for 34.7% and 45.3% of all bleeding, respectively. Compared with chronic users, new users had a higher risk of GIB (HR with propensity score matching: 1.89; 95% CI 1.29 to 2.70). Landmark analysis showed that the increased risk in new aspirin users was only observed in the first 6 months for all GIB (HR 2.10, 95% CI 1.41 to 3.13) and upper GIB (HR 2.52, 95% CI 1.38 to 4.60), but not for lower GIB. Conclusion: New aspirin users had a higher risk of GIB than chronic aspirin users, particularly during the initial 6 months. Lower GIB is more frequent than upper GIB in aspirin users who had HP eradicated.