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Published on: September 20, 2019
Pancreatitis, very early compared with normal start of enteral feeding (PYTHON trial): design and rationale of a
Olaf J Bakker1, Hjalmar C van Santvoort, Sandra van Brunschot
1Dept, of OR/Evidence Based Surgery, Radboud University Nijmegen Medical Centre, PO 9101, 6500 HB Nijmegen; The Netherlands.
Insights
Early enteral nutrition (EN) within 24 hours significantly reduces mortality and infections in severe acute pancreatitis patients compared to delayed feeding. This approach improves clinical outcomes in critical care settings.
Area of Science:
- Gastroenterology
- Critical Care Medicine
- Surgical Outcomes
Background:
- Infections negatively impact outcomes in predicted severe acute pancreatitis.
- Early enteral nutrition (EN) may reduce infections compared to current delayed feeding practices.
Purpose of the Study:
- To evaluate if very early EN (< 24 hours) reduces mortality or infections in severe acute pancreatitis.
- To compare early EN versus a delayed oral diet and EN (around 72 hours).
Main Methods:
- The PYTHON trial is a randomized controlled, superiority, multicenter trial.
- 208 patients with predicted severe acute pancreatitis were enrolled.
- Primary endpoint: composite of mortality or infections within 6 months.
Main Results:
- The PYTHON trial is designed to demonstrate the efficacy of early EN.
- The study aims to show a reduction in the combined endpoint of mortality or infections.
Conclusions:
- Very early EN (< 24 hours) is proposed to reduce mortality and infections.
- This contrasts with the current practice of delayed EN initiation in severe acute pancreatitis.
Background:
In predicted severe acute pancreatitis, infections have a negative effect on clinical outcome. A start of enteral nutrition (EN) within 24 hours of onset may reduce the number of infections as compared to the current practice of starting an oral diet and EN if necessary at 3-4 days after admission.
Methods/Design:
The PYTHON trial is a randomised controlled, parallel-group, superiority multicenter trial. Patients with predicted severe acute pancreatitis (Imrie-score ≥ 3 or APACHE-II score ≥ 8 or CRP > 150 mg/L) will be randomised to EN within 24 hours or an oral diet and EN if necessary, after 72 hours after hospital admission.During a 3-year period, 208 patients will be enrolled from 20 hospitals of the Dutch Pancreatitis Study Group. The primary endpoint is a composite of mortality or infections (bacteraemia, infected pancreatic or peripancreatic necrosis, pneumonia) during hospital stay or within 6 months following randomisation. Secondary endpoints include other major morbidity (e.g. new onset organ failure, need for intervention), intolerance of enteral feeding and total costs from a societal perspective.
Discussion:
The PYTHON trial is designed to show that a very early (< 24 h) start of EN reduces the combined endpoint of mortality or infections as compared to the current practice of an oral diet and EN if necessary at around 72 hours after admission for predicted severe acute pancreatitis.
Trial Registration:
ISRCTN: ISRCTN18170985.
Related Concept Videos
Chronic Pancreatitis II: Collaborative Care
Assessment:
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Acute pancreatitis is characterized by rapid inflammation of the pancreas, often caused by factors like gallstone blockage or excessive alcohol consumption. Chronic pancreatitis, on the other hand, is a slow, progressive inflammation that may result from long-term alcohol abuse, obstructions in the pancreatic duct, or genetic factors.
The causes of acute pancreatitis include:
Chronic Pancreatitis I: Introduction
Pancreatitis is the inflammation of the pancreas, which occurs when the immune system becomes active and causes swelling, pain, and disruptions in organ function. Pancreatitis can manifest as either an acute or chronic condition.
Acute pancreatitis arises suddenly and lasts for a brief duration, while chronic pancreatitis is a long-term affliction...
Chronic Pancreatitis I: Introduction

