Abstract

Treatment with non-steroidal anti-inflammatory drugs (NSAIDs) is hampered by gastrointestinal ulcer complications, such as ulcer bleeding and perforation. The efficacy of proton-pump inhibitors in the primary prevention of ulcer complications arising from the use of NSAIDs remains unproven. Selective cyclooxygenase-2 (COX-2) inhibitors reduce the risk for ulcer complications, but not completely in high-risk patients. This study determines which patients are especially at risk for NSAID ulcer complications and investigates the effectiveness of different preventive strategies in daily clinical practice. With the use of a nested case-control design, a large cohort of NSAID users was followed for 26 months. Cases were patients with NSAID ulcer complications necessitating hospitalisation; matched controls were selected from the remaining cohort of NSAID users who did not have NSAID ulcer complications. During the observational period, 104 incident cases were identified from a cohort of 51,903 NSAID users with 10,402 patient years of NSAID exposure (incidence 1% per year of NSAID use, age at diagnosis 70.4 ± 16.7 years (mean ± SD), 55.8% women), and 284 matched controls. Cases were characterised by serious, especially cardiovascular, co-morbidity. In-hospital mortality associated with NSAID ulcer complications was 10.6% (incidence 21.2 per 100,000 NSAID users). Concomitant proton-pump inhibitors (but not selective COX-2 inhibitors) were associated with a reduced risk for NSAID ulcer complications (the adjusted odds ratio 0.33; 95% confidence interval 0.17 to 0.67; p = 0.002). Especially at risk for NSAID ulcer complications are elderly patients with cardiovascular co-morbidity. Proton-pump inhibitors are associated with a reduced risk for NSAID ulcer complications.

Highlights

  • Treatment with non-steroidal anti-inflammatory drugs (NSAIDs) is known to be complicated by gastrointestinal toxicity

  • 104 cases were hospitalised with serious NSAID ulcer complications

  • Previous studies demonstrating the efficacy of selective COX-2 inhibitors in the primary prevention of NSAID ulcer complications largely excluded high-risk patients, whereas in high-risk patients selective COX-2 inhibitors may fail to prevent the recurrence of NSAID ulcer bleeding [12,14,15]

Read more

Summary

Introduction

Treatment with non-steroidal anti-inflammatory drugs (NSAIDs) is known to be complicated by gastrointestinal toxicity. NSAIDs impair prostaglandin-dependent gastric mucosal protective mechanisms. When these defences have been breached, a second wave of injury caused by luminal gastric acid may facilitate deeper ulceration [1]. Prevention of gastroduodenal ulcers attributable to the use of NSAIDs may target the inhibition of gastric acid secretion with histamine-2 receptor antagonists (H2RAs) or proton-pump inhibitors (PPIs). Locally depleted endogenous cytoprotective prostaglandins may be replaced by the administration of prostaglandin E1 analogues, such as misoprostol. Several studies have evaluated and compared these strategies [2]

Methods
Results
Discussion
Conclusion
Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.