PPT-Nutrition and Cystic Fibrosis
Author : olivia-moreira | Published Date : 2018-10-07
Module 2 Nutrition Assessment and Intervention in Pediatric CF Learning Objectives Determine appropriate energy macronutrient and micronutrient needs for pediatric
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Nutrition and Cystic Fibrosis: Transcript
Module 2 Nutrition Assessment and Intervention in Pediatric CF Learning Objectives Determine appropriate energy macronutrient and micronutrient needs for pediatric patients with cystic fibrosis. Treatment . of Cystic Fibrosis. Rebekah F. Brown, MD. Center Director, Cystic Fibrosis Center at Vanderbilt. Objectives. At . the end of this presentation, participants will have an understanding of the pathophysiology of cystic fibrosis and targets of treatment for children and adults with cystic fibrosis.. Sofhia. . Ytuarte. University of Arizona Pediatric Pulmonary Center. Nursing Trainee. June, 2015. About the Project. Request . from a parent to provide education during the spirit . week. CF Education given at . Broadening Your Health Care Team . Meredith Wiltsie, MN, ANP, FNP . Nurse Practitioner, adult Cystic Fibrosis program. Cystic Fibrosis Education Day. March 11. th. , 2017. No disclosures. If you are a CF Center patient, why do you need a Primary Care Physician? . Dr. Diana Naranjo, . Phd. Clinical Assistant Professor of Psychiatry & Behavioral Health sciences. Why I’m here. Dramatic improvements in prognosis, treatments and life expectancy in CF; . However, arduous . Dr. Diana Naranjo, . Phd. Clinical Assistant Professor of Psychiatry & Behavioral Health sciences. Why I’m here. Dramatic improvements in prognosis, treatments and life expectancy in CF; . However, arduous . This program will include a discussion of investigational agents not approved by the FDA for use in the US, and data that were presented in abstract form. These data should be considered preliminary until published in a peer-reviewed journal.. Module 1: Cystic Fibrosis Overview. Learning Objectives. Describe the pathophysiology of cystic fibrosis, and specifically how the disease process alters nutrient digestion, absorption, and metabolism.. by. Kathleen A. Nolan and Allen J. . Burdowski. . Biology . and Health Sciences. St. Francis College, Brooklyn, NY. NATIONAL CENTER FOR CASE STUDY TEACHING IN SCIENCE. Students, before coming to class you should have:. . for. . better. . awarness. of . cystic. . fibrosis. . related. . glucose. . abnormalities. 3-month . Progress. . Report. until. December 01, 2021. Adrienn Kéri. About. . the. . lecturer. Nursing College. Cystic Fibrosis. Inherited—. autosomal. recessive. Both parents must be carriers. Each child has a 1 in 4 chance of being affected. Affects primarily white children. Father Mother. ObjectivesUnderstand the genetic abnormality causing cystic fibrosis (CF) and the newborn screen processRecognize the multiple organ systems affected by CFIdentify common treatments /medications and m Annual Data Report 2017. Full report can be found at . cysticfibrosis.org.uk/. registryreports. 1.1 Summary of the UK Cystic Fibrosis Registry . UK Cystic Fibrosis Registry Annual Data Report 2017. 1.2 Age distribution by gender . Dr. JP Jarczyk, MD. February 11, 2023. Disclosures. I have no conflicts of interest to disclose. Objectives. Understand basic genetics of CF. Understand basic pathophysiology of CF. Understand treatments for pediatric patients with CF. de Almeida MB, Zerbinati RM, Tateno AF, Oliveira CM, Romão RM, Rodrigues JC, et al. Rhinovirus C and Respiratory Exacerbations in Children with Cystic Fibrosis. Emerg Infect Dis. 2010;16(6):996-999. https://doi.org/10.3201/eid1606.100063.
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