Pancreatic Enzyme Replacement Therapy in Cystic Fibrosis
Peter Freswick, Elizabeth Reid, Maria R. Mascarenhas
Abstract
While typically considered a pulmonary disease, cystic fibrosis patients develop significant nutritional complications and comorbidities, especially those who are pancreatic insufficient. Clinicians must have a high suspicion for cystic fibrosis among patients with clinical symptoms of pancreatic insufficiency, and pancreatic enzymatic replacement therapy (PERT) must be urgently initiated. PERT presents a myriad of considerations for patients and their supporting dieticians and clinicians, including types of administration, therapy failures, and complications.
Topics & Concepts
Cystic fibrosisPancreatic enzymesMedicineEnzyme replacement therapyDieticiansExocrine pancreatic insufficiencyPancreatic diseaseDiseaseCystic fibrosis-related diabetesIntensive care medicineInternal medicinePancreatitisGastroenterologyDiabetes mellitusPancreasType 2 diabetesEndocrinologyImpaired glucose toleranceNursingCystic Fibrosis Research AdvancesChild Nutrition and Feeding IssuesInfant Nutrition and Health