PPT-Nutrition and Cystic Fibrosis

Module 4 Patientcentered Behavior Interventions Learning Objectives Describe effective strategies for facilitating behavior change in patients Discuss the impact of parentalcaretaker life course on disease management and overall health of the pediatric CF patient . 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.. What You Need to Know. Jennifer Cannon, NP-C. Adult Cystic Fibrosis, Stanford Health Care. March 13, 2016. Overview. Contraception. Importance of Contraceptive Education. Current Research: Contraception in Cystic Fibrosis Patients. 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 . Module 2: . Nutrition Assessment and Intervention in Pediatric CF . Learning Objectives. Determine appropriate energy, macronutrient, and micronutrient needs for pediatric patients with cystic fibrosis.. 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.. . Single gene . Mendelian. disorder. Gene codes for the Cystic Fibrosis . Transmembrane. Conductance Regulator protein (CFTR). Daniel R. . Taub. and Joshua Page. Cystic Fibrosis: Exploration of evolutionary explanations for the high frequency of a common genetic disorder.. 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:. dion. By: Alex-. A. nn and . Noémy. Personal. information. She’s. . forty. - . eight. ( 48 ) . years. . old. .. S. he. . was. . born. in March. . the . thirty. ( 30 ), . nineteen. . sixty. Table of Contents Presentation 5 Presentation Resources 6-7 Teacher/Faculty Curriculum 8-9 Teacher/Faculty Resources 10 K-2nd Grade Activities/Materials 11 3rd-5th Grade A 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 .