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Nutrition and Growth in Cystic Fibrosis.
Pediatr Clin North Am. 2016 08; 63(4):661-78.PC

Abstract

Close attention to nutrition and growth is essential in caring for children with cystic fibrosis (CF). Growth and nutritional status should be monitored as part of routine CF care. Children with CF should achieve growth and nutritional status comparable with that of well-nourished children without CF. Children with CF are at risk for nutritional deficiencies. Optimal nutritional and growth status may be difficult to attain in this population given risk of insufficient caloric intake and likelihood of increased caloric expenditure. Various methods to attain optimal nutritional status may be used, including oral supplementation, behavioral treatment, pharmacotherapy, and enteral nutrition.

Authors+Show Affiliations

Department of Pediatrics, Columbia University Medical Center, 622 West 168th Street, PH 17 East 105L, New York, NY 10032, USA.Department of Pediatrics, University of Vermont College of Medicine, 111 Colchester Avenue, Burlington, VT 05401, USA. Electronic address: jillian.sullivan@uvmhealth.org.

Pub Type(s)

Journal Article
Review

Language

eng

PubMed ID

27469181

Citation

Lusman, Sarah, and Jillian Sullivan. "Nutrition and Growth in Cystic Fibrosis." Pediatric Clinics of North America, vol. 63, no. 4, 2016, pp. 661-78.
Lusman S, Sullivan J. Nutrition and Growth in Cystic Fibrosis. Pediatr Clin North Am. 2016;63(4):661-78.
Lusman, S., & Sullivan, J. (2016). Nutrition and Growth in Cystic Fibrosis. Pediatric Clinics of North America, 63(4), 661-78. https://doi.org/10.1016/j.pcl.2016.04.005
Lusman S, Sullivan J. Nutrition and Growth in Cystic Fibrosis. Pediatr Clin North Am. 2016;63(4):661-78. PubMed PMID: 27469181.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Nutrition and Growth in Cystic Fibrosis. AU - Lusman,Sarah, AU - Sullivan,Jillian, PY - 2016/7/30/entrez PY - 2016/7/30/pubmed PY - 2017/2/6/medline KW - Anthropometrics KW - Body mass index KW - Cystic fibrosis KW - Enteral feeding KW - Fat-soluble vitamins KW - Growth KW - Nutrition SP - 661 EP - 78 JF - Pediatric clinics of North America JO - Pediatr Clin North Am VL - 63 IS - 4 N2 - Close attention to nutrition and growth is essential in caring for children with cystic fibrosis (CF). Growth and nutritional status should be monitored as part of routine CF care. Children with CF should achieve growth and nutritional status comparable with that of well-nourished children without CF. Children with CF are at risk for nutritional deficiencies. Optimal nutritional and growth status may be difficult to attain in this population given risk of insufficient caloric intake and likelihood of increased caloric expenditure. Various methods to attain optimal nutritional status may be used, including oral supplementation, behavioral treatment, pharmacotherapy, and enteral nutrition. SN - 1557-8240 UR - https://www.unboundmedicine.com/medline/citation/27469181/Nutrition_and_Growth_in_Cystic_Fibrosis_ L2 - https://linkinghub.elsevier.com/retrieve/pii/S0031-3955(16)30013-X DB - PRIME DP - Unbound Medicine ER -