Abstract

Introduction Acute upper gastrointestinal bleeding (AUGIB) is a common reason for hospital admission and is associated with significant cardiovascular (CVS) morbidity and mortality. Patients who have aspirin withheld for 8 weeks following AUGIB have significantly higher rates of CVS events. 1 We previously demonstrated that patients with AUGIB have significantly higher levels of platelet activation during the index hospital admission. 2 This study aimed to assess the level of platelet activation and reactivity 12 weeks following admission for AUGIB. Methods Patients admitted to SWBH NHS Trust with AUGIB were recruited. Dyspeptic patients attending for diagnostic OGD were used as controls. To assess platelet activation citrated whole blood was incubated at room temperature with monoclonal mouse antibodies against constitutively expressed platelet marker CD42a-PerCP, and markers of platelet activation PAC1-FITC, and CD62P-APC. Incubation was terminated after 15 minutes. Samples were analysed using a FACSCalibur flow cytometer. Platelets were identified on the basis of their forward and side scatter properties and the presence of the CD42a platelet-specific marker. CD62P and PAC1 expression were measured by the percentage of platelets expressing these markers. Data are expressed as mean±SD for normally distributed parameters and median (interquartile range) for non-normally distributed parameters. Statistical analysis was performed using SPSS 18.0 software. Results A total of 24 patients with AUGIB and 18 controls were recruited. Patients were age and gender matched. The mean age of the AUGIB group is 66.4 ± 18.2 years, and the control group 62.8 ± 6.1years. Significant differences were seen in all markers of platelet activation (table 1). Conclusion Patients presenting with AUGIB have prolonged levels of platelet activation for at least 12 weeks following the index event. This phenomenon may be further prolonged and further studies are required. This may explain the excess of CVS events in AUGIB patients. In patients with high cardiovascular risk early re-introduction of aspirin should be considered. Disclosure of Interest None Declared References Sung JJ, Lau JY, Ching JY, Wu JC, Lee YT, Chiu PW, Leung VK, Wong VW, Chan FK. Continuation of low-dose aspirin therapy in peptic ulcer bleeding: a randomised trial. Ann Intern Med. 2010 Jan 5; 152(1):1–9. Disney BR, Watson R, Blann A, Lip G, Tselepis C, Anderson M. Platelet activation in acute upper gastrointestinal bleeding. Gut 2012; 61 (Suppl 2): A361.

Highlights

  • The traditional diagnosis of celiac disease (CD) requires a small bowel biopsy to identify at histology the characteristic mucosal changes

  • In line with previous reports [3], we found that the incidence of upper gastrointestinal bleeding (UGIB) was higher in males

  • There was a trend toward better risk assessment, shorter time to endoscopy, reduced need for surgery and mortality in the GI group

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Summary

Introduction

The traditional diagnosis of celiac disease (CD) requires a small bowel biopsy to identify at histology the characteristic mucosal changes. The immunoreactivity in each of the three types of mucosa were compared to additional biopsies from the antrum and gastric body in same subjects and biopsies from ten patients with long-segment Barrett’s demonstrating foci with and without intestinal metaplasia (IM). Table The extent (%) of immunostaining with different antibodies in squamocolumnar junction, gastric body, antrum and Barrett’s Conclusion Cardia mucosa which is extended proximally in H. pylori negative healthy volunteers with central obesity, is immunohistochemically identical to non-IM Barrett’s mucosa. This is consistent with the expansion of cardia mucosa having similar aetiology to Barrett’s mucosa and being due to metaplasia of the most distal oesophageal mucosa resulting from short segments reflux. Detection and appropriate therapy improves quality of life and may prevent development of chronic Abstract OC-025 Table

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