Diet and Exercise in Cystic Fibrosis, a unique reference edited by distinguished and internationally recognized nutritionist and immunologist Ronald Ross Watson, fills the gap in the current dietary modalities aimed at controlling cystic fibrosis. Using expert evaluation on the latest studies of the role of food and exercise in lifelong management of cystic fibrosis, this valuable resource shows how to maintain intestinal, hepatic, and pulmonary high quality function for improving quality of life for those with cystic fibrosis. A helpful tool for researchers and clinicians alike, this reference helps refine research targets, and provides the beginning of a structured dietary management scheme for those with cystic fibrosis.
- Provides a detailed resource that reviews the health problems occurring in Cystic Fibrosis relative to dietary, complementary, and alternative therapies
- Contains expert evaluation on the role of foods and exercise for lifelong management of Cystic Fibrosis to maintain intestinal, hepatic, and pulmonary high quality function for improved quality of life
- Defines and evaluates various nutritional and dietary approaches to the unique problems of those with Cystic Fibrosis
Sprache
Verlagsort
Verlagsgruppe
Elsevier Science & Techn.
ISBN-13
978-0-12-800588-0 (9780128005880)
Schweitzer Klassifikation
Section A. OVERVIEW OF NUTRITION AND DIETS IN CYSTIC FIBROSIS1. Nutrition for pregnant cystic fibrosis patients2. Disordered eating and body image in cystic fibrosis 3. Neonatal screening and nutrition/growth in cystic fibrosis: A review 4. CF Nutrition: Outcomes, Treatment Guidelines and Risk Classification5. Clinical, nutritional and spirometry in cystic fibrosis 6. Family mealtimes and children with cystic fibrosis7. Disturbed sleep behaviors and melatonin in sleep dysfunction and treatment of cystic fibrosis8. Age at diagnosis and disease progression of cystic fibrosis9. Lactoferrin and cystic fibrosis airway infectionB. VITAMIN D DEFICIENCY AND SUPPLEMENTATION IN GROWTH AND HEALTH IN CHILDREN WITH CYSTIC FIBROSIS10. Vitamin D bioavailability in cystic fibrosis11. Cystic fibrosis and Vitamin D12. Specialty Foods for Children with Cystic Fibrosis13. The Effects of Caffeine, Alcohol, and Tobacco in Cystic Fibrosis14. Fat-Soluble Vitamin Deficiency in Cystic Fibrosis15. Can light provide a vitamin D supplement in cystic fibrosis?16. Pediatric cystic fibrosis children and fat-soluble vitaminsC. VITAMIN DEFICIENCY, ANTIOXIDANTS, AND SUPPLEMENTATION IN CYSTIC FIBROSIS PATIENTS17. Vitamin supplements: a role in cystic fibrosis patients?18. Nutrition oxidative stress and patients with cystic fibrosis19. Vitamin A Supplementation Therapy for Patients with Cystic Fibrosis20. The Emergence of Polyphenols in the Potentiation of Treatment Modality in Cystic Fibrosis21. Chronic infection with Pseudomonas aeruginosa in an animal model of oxidative stress: Lessons for patients with Cystic Fibrosis 22. Vitamin K in cystic fibrosis23. Vitamin K and cystic fibrosisD. MANAGEMENT OF DIABETES ASSOCIATED WITH CYSTIC FIBROSIS: ROLE OF NUTRITION AND FOOD24. Insulin, body mass and growth in young cystic fibrosis patients25. Low glycemic index dietary interventions in cystic fibrosis 26. Insulin resistance in cystic fibrosis: ManagementE. DIGESTIVE ENZYMES, PRO-BIOTICS AND FOOD IN TREATMENT OF INTESTINAL DYSFUNCTION27. Cystic fibrosis and celiac disease28. Probiotic supplementation, pulmonary exacerbations in patients with cystic fibrosisF. NUTRITION AND PULMONARY FUNCTION IN CYSTIC FIBROSIS PATIENTS29. CYSTIC FIBROSIS RELATED DIABETES: LUNG FUNCTION AND NUTRITIONAL STATUS30. Eating Disorders and Disturbed Eating Attitudes and Behaviors Typical in CF31. Buteyko: Better Breathing = Better HealthG. NUTRITION AND LIVER AND OTHER ORGANS OF CYTIC FIBROSIS PATIENTS32. The pancreatic duct ligated pig model for patients suffering from exocrine pancreatic insufficiency- studies on vitamin A and E statusH. EXERCISE AND BEHAVIOR IN MANAGEMENT OF CYSTIC FIBROSIS33. Exercise testing in CF, the what and how 34. Mechanism of exercise limitation in cystic fibrosis: A literature update of involved mechanisms 35. Assessing Physical Activity Levels using Questionnaires and Diaries36. Motivating physical activity: Skills and Strategies for Behavior Change 37. Diet, food and nutrition and exercise in cystic fibrosis 38. Personalizing Exercise Programs for CF patientsI. FAT AND LIPID METABOLISM IN CYSTIC FIBROSIS 39. Unsaturated fatty acids in cystic fibrosis: metabolism and therapy 40. Essential fatty acid deficiency in cystic fibrosis: malabsorption or metabolic abnormality? 41. Persistent fat malabsorption in cystic fibrosis 42. Omega-3 Fatty Acids and Cystic Fibrosis
