Should we Investigate Gastroenterology Patients for Pancreatic Exocrine Insufficiency? A Dual Centre UK Study.
Study Goal
The researchers aimed to identify the prevalence of pancreatic exocrine insufficiency in secondary care gastroenterology clinics and assess the response to treatment, including lifestyle interventions like smoking cessation.
Results Summary
The study found that pancreatic exocrine insufficiency was prevalent in 13.1% of tested patients, with smoking cessation suggested as a potential lifestyle intervention to improve outcomes, though specific effects of smoking were not detailed.
Population
Patients tested for pancreatic exocrine insufficiency in secondary care gastroenterology clinics (n=1821).
Effective Dosage
Not specified
Duration
Not specified
Interactions
None mentioned
| Intervention | Direction | Endpoint | Population | Dosage | Impact | Claim # |
|---|---|---|---|---|---|---|
pancreatic enzyme replacement therapy | decrease | symptoms | patients with low FEL-1 | 80.0% | reported symptomatic benefit | #1 |
high dose supplementation | no change | symptomatic benefit | patients with low FEL-1 | - | no difference in response | #2 |
low dose supplementation | no change | symptomatic benefit | patients with low FEL-1 | - | no difference in response | #3 |
lifestyle advice such as smoking cessation and minimising alcohol intake | increase | outcomes | - | - | could improve | #4 |
supplementation | neutral | - | patients with low faecal elastase | up to 80% | respond to | #5 |
BACKGROUND AND AIMS: Pancreatic exocrine insufficiency may be under recognised in gastroenterological practice. We aimed to identify the prevalence of pancreatic insufficiency in secondary care gastroenterology clinics and determine if co-morbidity or presenting symptoms could predict diagnosis. A secondary aim was to assess response to treatment. METHODS: A dual centre retrospective analysis was conducted in secondary care gastroenterology clinics. Patients tested for pancreatic exocrine insufficiency with faecal elastase-1 (FEL-1) between 2009 and 2013 were identified in two centres. Demographics, indication and co-morbidities were recorded in addition to dose and response to pancreatic enzyme replacement therapy. Binary logistic regression was used to assess if symptoms or co-morbidities could predict pancreatic insufficiency. RESULTS: 1821 patients were tested, 13.1% had low FEL-1 (<200µg/g). This prevalence was sub-analysed with 5.4% having FEL-1 100-200µg/g (mild insufficiency) and 7.6% having faecal elastase readings <100µg/g. Low FEL-1 was most significantly associated with weight loss or steatorrhoea. Co-morbidity analysis showed that low levels were significantly associated with excess alcohol intake, diabetes mellitus or human immunodeficiency virus; 80.0% treated with enzyme supplements reported symptomatic benefit with no difference in response between high and low dose supplementation (p=0.761). CONCLUSION: Targeting the use of FEL-1 in individuals with specific symptoms and associated conditions can lead to improved recognition of pancreatic exocrine insufficiency in a significant proportion of secondary care patients. Intervening with lifestyle advice such as smoking cessation and minimising alcohol intake could improve outcomes. In addition, up to 80% of patients with low faecal elastase respond to supplementation.