Pancreatin and pancrelipase are manufactured mixtures of several digestive enzymes produced by the exocrine cells of the pancreas. They are enteric coated, delayed-release capsules that dissolve in the duodenum and jejunum and should not be crushed or chewed.
Patients with cystic fibrosis often have their pancreatic ducts blocked and are unable to normally digest food. Thus, exogenous pancreatic enzymes are indicated in helping aid digestion.
Those who have pancreatic inadequacy or insufficiency can also benefit from the administration of pancreatin or pancrelipase. Causes for this condition include pancreatitis, obstruction of the pancreatic duct, and patients who have had pancreatectomy, leading to impaired function.
If given in large doses, these commercial pancreatic enzyme mixtures can lead to GI distress. Patients can complain of diarrhea, nausea, and vomiting.
These enzymes are inactivated by gastric acid. Thus, some patients are given H2 blockers and PPIs to decrease stomach acid secretion. Furthermore, these oral enzyme mixture tablets are enteric coated to prevent inactivation by gastric acid.
Patients taking these enzymes should have their 24 hour fecal fat excretion measured in order to view their effectiveness. There should be a profound decrease in fat excretion, as these enzymes help fat absorption.
Patients are instructed to maximize nutrient absorption and take pancreatic enzymes with every meal and snack. Usually 1 to 5 capsules are taken with food intake, based on the patient’s body weight, and they should be taken within 30 minutes of eating.
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