Pancreatic Malnutrition in Children.
Acyl-CoA Dehydrogenase, Long-Chain
/ deficiency
Anus, Imperforate
/ complications
Child
Child Nutrition Disorders
/ diagnosis
Chymotrypsin
/ metabolism
Congenital Bone Marrow Failure Syndromes
/ complications
Cystic Fibrosis
/ complications
Dietary Fats
/ metabolism
Ectodermal Dysplasia
/ complications
Enzyme Replacement Therapy
Exocrine Pancreatic Insufficiency
/ diagnosis
Feces
/ enzymology
Growth Disorders
/ complications
Hearing Loss, Sensorineural
/ complications
Humans
Hypothyroidism
/ complications
Intellectual Disability
/ complications
Lipid Metabolism, Inborn Errors
/ complications
Mitochondrial Diseases
/ complications
Muscular Diseases
/ complications
Nose
/ abnormalities
Nutrition Assessment
Pancreas
/ diagnostic imaging
Pancreatic Diseases
/ complications
Pancreatic Elastase
/ metabolism
Pancreatic Function Tests
Pancreatitis, Chronic
/ complications
Shwachman-Diamond Syndrome
/ complications
Steatorrhea
/ etiology
Trypsinogen
/ blood
Journal
Pediatric annals
ISSN: 1938-2359
Titre abrégé: Pediatr Ann
Pays: United States
ID NLM: 0356657
Informations de publication
Date de publication:
01 Nov 2019
01 Nov 2019
Historique:
entrez:
12
11
2019
pubmed:
12
11
2019
medline:
6
5
2020
Statut:
ppublish
Résumé
Exocrine pancreatic insufficiency in children can lead to lifelong complications related to malnutrition and poor growth. The clinical presentation can be subtle in the early stages of insufficiency as the large functional capacity of the pancreas is gradually lost. The pediatrician plays a crucial role in the early identification of these children to ensure a timely referral so that a diagnosis can be made and therapy initiated. Early nutritional therapy allows for prevention and correction of deficiencies, which leads to improved outcomes and survival. When insufficiency is suspected, the workup should start with an indirect test of exocrine pancreatic function, such as fecal elastase, to establish the diagnosis. Once a diagnosis is established, further testing to delineate the etiology should be pursued, with cystic fibrosis being high on the differential list and assessed for with a sweat test. Assessment of anthropometry at every visit is key, as is monitoring of laboratory parameters and physical examination findings that are suggestive of malabsorption and malnutrition. The mainstay of management is administration of exogenous pancreatic enzymes to facilitate digestion and absorption. [Pediatr Ann. 2019;48(11):e441-e447.].
Identifiants
pubmed: 31710363
doi: 10.3928/19382359-20191018-01
doi:
Substances chimiques
Dietary Fats
0
Trypsinogen
9002-08-8
Acyl-CoA Dehydrogenase, Long-Chain
EC 1.3.8.8
Chymotrypsin
EC 3.4.21.1
Pancreatic Elastase
EC 3.4.21.36
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
e441-e447Informations de copyright
Copyright 2019, SLACK Incorporated.