Volume 207, Issue 4 pp. 161-165
Guideline Summary

Diagnosis and management of pancreatic exocrine insufficiency

Mehrdad Nikfarjam

Corresponding Author

Mehrdad Nikfarjam

Austin Health, Melbourne, VIC

University of Melbourne, Melbourne, VIC

Correspondence: [email protected]Search for more papers by this author
Jeremy S Wilson

Jeremy S Wilson

South Western Sydney Clinical School, Liverpool Hospital, UNSW, Sydney, NSW

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Ross C Smith

Ross C Smith

Kolling Institute, Royal North Shore Hospital, University of Sydney, Sydney, NSW

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First published: 21 August 2017
Citations: 53

Abstract

Introduction: In 2015, the Australasian Pancreatic Club (APC) published the Australasian guidelines for the management of pancreatic exocrine insufficiency (http://pancreas.org.au/2016/01/pancreatic-exocrine-insufficiency-guidelines). Pancreatic exocrine insufficiency (PEI) occurs when normal digestion cannot be sustained due to insufficient pancreatic digestive enzyme activity. This may be related to a breakdown, at any point, in the pancreatic digestive chain: pancreatic stimulation; synthesis, release or transportation of pancreatic enzymes; or synchronisation of secretions to mix with ingested food.

Main recommendations: The guidelines provide advice on diagnosis and management of PEI, noting the following:

  • A high prevalence of PEI is seen in certain diseases and conditions, such as cystic fibrosis, acute and chronic pancreatitis, pancreatic cancer and pancreatic surgery.
  • The main symptoms of PEI are steatorrhoea or diarrhoea, abdominal pain, bloating and weight loss. These symptoms are non-specific and often go undetected and untreated.
  • PEI diagnosis is predominantly based on clinical findings and the presence of underlying disease. The likelihood of PEI in suspected patients has been categorised into three groups: definite, possible and unlikely.
  • If left untreated, PEI may lead to complications related to fat malabsorption and malnutrition, and have an impact on quality of life.
  • Pancreatic enzyme replacement therapy (PERT) remains the mainstay of PEI treatment with the recommended adult initial enzyme dose being 25 000–40 000 units of lipase per meal, titrating up to a maximum of 75 000–80 000 units of lipase per meal.
  • Adjunct acid-suppressing therapy may be useful when patients still experience symptoms of PEI on high dose PERT.
  • Nutritional management by an experienced dietitian is essential.

 

Changes in management as a result of these guidelines: These are the first guidelines to classify PEI as being definite, possible or unlikely, and provide a diagnostic algorithm to facilitate the early diagnosis of PEI and appropriate use of PERT.

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