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Dive into the research topics where Wilson J. Angerson is active.

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Featured researches published by Wilson J. Angerson.


Alimentary Pharmacology & Therapeutics | 2005

Upper gastrointestinal haemorrhage associated with low-dose aspirin and anti-thrombotic drugs - a 6-year analysis and comparison with non-steroidal anti-inflammatory drugs.

A. S. Taha; Wilson J. Angerson; R. P. Knill-Jones; O. Blatchford

Background:  Low‐dose aspirin and other anti‐thrombotic therapy has been increasingly used for vascular protection.


Alimentary Pharmacology & Therapeutics | 2008

Clinical trial: the incidence and early mortality after peptic ulcer perforation, and the use of low-dose aspirin and nonsteroidal anti-inflammatory drugs

Ali S Taha; Wilson J. Angerson; R. Prasad; Caroline McCloskey; D. Gilmour; C. G. Morran

Background  It is not clear whether the incidence or early mortality related to peptic ulcer perforation has changed.


Alimentary Pharmacology & Therapeutics | 2006

Upper gastrointestinal mucosal abnormalities and blood loss complicating low-dose aspirin and antithrombotic therapy

A. S. Taha; Wilson J. Angerson; R. P. Knill-Jones; O. Blatchford

Background  Little is known about the site and nature of bleeding lesions related to low‐dose aspirin and other antithrombotic agents.


Alimentary Pharmacology & Therapeutics | 2007

Upper gastrointestinal bleeding and the changing use of COX-2 non-steroidal anti-inflammatory drugs and low-dose aspirin

Ali S Taha; Wilson J. Angerson; R. Prasad; Caroline McCloskey; O. Blatchford

Background  Rofecoxib was withdrawn in 2004.


Gastroenterology | 1989

Autoradiographic study of the regional distribution of gastric blood flow in portal hypertensive rats

James G. Geraghty; Wilson J. Angerson; David Carter

This study measures regional gastric blood flow in portal hypertensive rats at three separate periods after portal vein ligation using quantitative autoradiography with 14C-labeled iodoantipyrine. The level of corpus mucosal blood flow was significantly reduced in 3-day portal vein-ligated animals compared with sham-operated control animals (30.4 +/- 2.3 vs. 47.1 +/- 5.6 ml/100 g.min). There was no significant difference in corpus mucosal blood flow between portal vein-ligated and sham-operated animals at 7- and 28-day periods, although the level of perfusion was higher in the 28-day portal vein-ligated group. There was no significant difference in antral mucosal or muscle blood flow between portal hypertensive and control animals at any of the study periods. We conclude that the acute period after portal vein ligation is associated with a reduced corpus mucosal microcirculation but that this effect is not sustained in portal hypertensive animals studied at later intervals after portal vein ligation.


Alimentary Pharmacology & Therapeutics | 2006

Clinical outcome in upper gastrointestinal bleeding complicating low‐dose aspirin and antithrombotic drugs

A. S. Taha; Wilson J. Angerson; R. P. Knill-Jones; O. Blatchford

The current risk stratification systems in upper gastrointestinal bleeding do not correct for the intake of low‐dose aspirin and other antithrombotic drugs.


Alimentary Pharmacology & Therapeutics | 2003

Reflux and Barrett's oesophagitis after gastric surgery: long-term follow-up and implications for the roles of gastric acid and bile in oesophagitis

Ali S Taha; Wilson J. Angerson; C. G. Morran

Background : The role of gastric acid is difficult to separate from that of bile in oesophageal reflux, and the complications of this can take many years to develop. Gastric surgery patients provide a good model for both significant bile reflux and marked gastric acid inhibition.


Frontline Gastroenterology | 2011

Mortality following blood transfusion for non-variceal upper gastrointestinal bleeding

Ali S Taha; Caroline McCloskey; Theresa Craigen; Wilson J. Angerson; Amir A. Shah; Christopher G. Morran

Objective Blood transfusion remains an integral step in the management of acute non-variceal upper gastrointestinal bleeding (NV-UGIB), but its safety is being increasingly questioned in less severe cases. The authors aimed to measure 30-day and 2-year mortalities after blood transfusion for NV-UGIB. Methods Cox proportional hazards models were used to estimate the association of blood transfusion with mortality while adjusting for age, Charlson comorbidity score, the complete Rockall score for acute UGIB, admission status and medication intake prior to bleeding. Main outcome measures Death from any cause at 30 days and 2 years after NV-UGIB. Results 1340 patients presented with NV-UGIB< (808 men (60.3%), median age 67 years) of whom 564 (42.1%) were transfused. The overall mortality was 5.3% at 30 days and 26.0% at 2 years in all patients. Comparing subjects with a haemoglobin concentration greater than 10.0 g/dl who were transfused with those who were not, 30-day mortalities (95% CIs) were 11.5% (6.7 to 18.0) versus 3.6% (2.3 to 5.3), respectively, p<0.001, and 2-year mortalities (95% CIs) were 40% (32 to 49) versus 20% (17 to 23), p<0.001. After adjusting for age, Charlson score, Rockall score and haemoglobin, the HRs (95% CIs) for death after transfusion were 1.88 (1.00 to 3.55) (p=0.051) at 30 days and 1.71 (1.28 to 2.28), (p<0.001) at 2 years. Conclusion In patients with moderately severe NV-UGIB, mortality is higher following blood transfusion. Whether this reflects selection bias, an effect of comorbidity or an effect of transfusion requires urgent prospective study.


Gut | 1992

Taurocholate induced gastric mucosal injuries in experimental portal hypertension.

Wilson J. Angerson; J G Geraghty; D C Carter

The susceptibility of the gastric mucosa to injury by topical sodium taurocholate (40 mmol/l) in hydrochloric acid (150 mmol/l) was studied in prehepatic and cirrhotic rat models of portal hypertension. Portal venous pressure was increased in rats who had undergone partial portal vein ligation compared with rats that had undergone sham operation on days 3, 7, and 28 after operation (20.6 (0.9), 14.8 (0.8), and 11.3 (0.5) mm Hg v 7.3 (0.7), 7.3 (0.6), and 8.2 (0.2) mmHg respectively (mean (SEM)). At day 3 gastric mucosal injuries were increased in rats with partial portal vein ligation compared with sham operated rats (55.3 (9.4) vs 22.3 (10.5) mm2, p = 0.006), but at the later time intervals there was no significant difference in injuries between the two groups. In rats with carbon tetrachloride induced hepatic cirrhosis, portal pressure was increased (15.6 (1.0) v 6.7 (0.6) mmHg), but again there was no significant difference in mucosal injuries relative to control animals. We conclude that gastric mucosal defence mechanisms are impaired in acute but not chronic experimental portal hypertension.


Frontline Gastroenterology | 2013

Gastro-protective policy and the incidence of upper gastrointestinal bleeding

Ali S Taha; Claire Kelly; Caroline McCloskey; Theresa Craigen; Wilson J. Angerson

Objectives In recent years, policies have been proposed in order to guide the safer use of non-steroidal anti-inflammatory drugs (NSAIDs) and antiulcer therapy. We aimed to investigate the incidence of upper gastrointestinal bleeding (UGIB) before and after the introduction of these policies, 2007–2009, in a well-defined population in southwest Scotland. Methods All patients with non-variceal upper gastrointestinal bleeding (NV-UGIB), diagnosed at a single regional unit, were included. Total drugs prescribed in our population were noted, including antiulcer drugs, antithrombotic drugs and both cyclo-oxygenase-2 enzyme-selective and non-selective inhibiting NSAIDs. Results The incidence, the number of cases per 100 000 population per annum, of NV-UGIB fell from 134.7 in 2007 to 125.1 in 2008, and to 90.3 cases in 2009 (p<0.001). There was also a significant rise in the use of non-selective NSAIDs, proton pump inhibitors and antithrombotic drugs. Conclusions Although a cause-and-effect relationship cannot be fully proven, physician education through drug-use policies is associated with a drop in the incidence of NV-UGIB. This is relevant to the prevention of this common condition.

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Caroline McCloskey

University Hospital Crosshouse

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