Year in review 2020: Nutrition and gastrointestinal disease in cystic fibrosis.

Meghana Sathe, Preeti B Sharma, Adrienne P Savant

Journal: Pediatric pulmonology 2021;56(10):3120-3125

PMID: 34310872

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Abstract

The multisystemic manifestations of cystic fibrosis (CF) involve all parts of the gastrointestinal (GI) system, including the pancreas, intestine, and liver. As providers who care for people with CF, knowledge of the manifestations, treatment, and research related to nutrition and GI disease are important. This review is the last installment of the CF year in review 2020 series, focusing on nutritional, GI, and hepatobiliary articles from Pediatric Pulmonology and other journals of particular interest to clinicians.

Address: Division Gastroenterology, Hepatology, and Nutrition, Department of Pediatrics, University of Texas Southwestern and Children's Health, Dallas, Texas, USA.; Division of Pediatric Pulmonology and Sleep Medicine, Department of Pediatrics, University of Texas Southwestern and Children's Health, Dallas, Texas, USA.; Division of Pulmonary Medicine, Department of Pediatrics, Tulane University School of Medicine, Children's Hospital of New Orleans, New Orleans, Louisiana, USA.

DOI: 10.1002/ppul.25587

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MeSH Terms: Child, Cystic Fibrosis, Cystic Fibrosis Transmembrane Conductance Regulator, Gastrointestinal Diseases, Humans, Nutritional Status, Pulmonary Medicine