SYSTEMATIC REVIEWS

• Drug therapies for reducing gastric acidity in people with cystic fibrosis (Cochrane Review).
  Ng SM, Jones AP. In: The Cochrane Library, Issue 2, 2003. Oxford: Update Software. CD003424
• Enteral tube feeding for cystic fibrosis (Cochrane Review).
  Conway SP, Morton A, Wolfe S. In: The Cochrane Library, Issue 3, 2002. Oxford: Update Software.
• Newborn screening for cystic fibrosis (Cochrane Review)
  Merelle ME, Nagelkerke AF, Lees CM, Dezateux C. In: The Cochrane Library, Issue 3, 2002. Oxford: Update Software.
• Omega-3 fatty acids (from fish oils) for cystic fibrosis (Cochrane Review).
  Willson N, Elliott TM, Everard ML. In: The Cochrane Library, Issue 3, 2002. Oxford: Update Software.
• Oral calorie supplements for cystic fibrosis (Cochrane Review).
  Smyth R, Walters S. In: The Cochrane Library, Issue 3, 2002. Oxford: Update Software
• Oral protein calorie supplementation for children with chronic disease (Cochrane Review).
  Poustie VJ, Smyth RL, Watling RM. In: The Cochrane Library, Issue 2, 2003. Oxford: Update Software. CD001914
• Ursodeoxycholic acid for cystic fibrosis-related liver disease (Cochrane Review).
  Cheng K, Ashby D, Smyth R. In: The Cochrane Library, Issue 3, 2002. Oxford: Update Software.

Protocols for Cochrane Reviews:

• Antenatal screening for cystic fibrosis (Protocol for a Cochrane Review).
  Lees CM, Smyth RL. In: The Cochrane Library, Issue 3, 2002. Oxford: Update Software.

Database of Abstracts of Reviews of Effectiveness (DARE):

• Nutrition intervention for weight gain in cystic fibrosis: a meta analysis
  Jelalian E, Stark L J, Reynolds L, Seifer R. Journal of Pediatrics 1998; 132(3 Part 1): 486-492.
• Neonatal screening for cystic fibrosis
  Serra-Prat M. Barcelona: Catalan Agency for Health Technology Assessment (CAHTA), 2000:1-20.
• Screening for cystic fibrosis.
  Murray J, Cuckle H, Taylor G, Littlewood J O, Hewison J. Health Technology Assessment1999, 3(8), 1-104.

GUIDELINES:

• Clinical guidelines for cystic fibrosis care. Summary of guidelines
  prepared by a working group of the Cystic Fibrosis Trust, the British Paediatric Association and the British Thoracic Society (PubMed)
  Jackson A. J R Coll Physicians Lond. 1996 Jul-Aug;30(4):305-8.
• Consensus report on nutrition for pediatric patients with cystic fibrosis. (Abstract – PubMed)
  Borowitz D, Baker RD, Stallings V. J Pediatr Gastroenterol Nutr 2002 Sep;35(3):246-59
• Genetic testing for cystic fibrosis.
  National Guidelines Clearinghouse.
  Original electronic copies atNIH Consens Statement 1997 Apr 14-16;15(4):1-37
• Nutrition in patients with cystic fibrosis: a European Consensus
  M. Sinaasappel, M. Stern, J. Littlewood, S. Wolfe, G. Steinkamp, H.G.M. Heijerman, E. Robberecht, G. Doring. Journal of Cystic Fibrosis 1 (2) (2002) pp. 51-75.
• Pancreatic enzyme replacement therapy in cystic fibrosis: Australian guidelines. Pediatric Gastroenterological Society and the Dietitians Association of Australia. (Abstract – PubMed)
  Anthony H, Collins CE, Davidson G, Mews C, Robinson P, Shepherd R, Stapleton D.J Paediatr Child Health. 1999 Apr;35(2):125-9.
• Recommendations for management of liver and biliary tract disease in cystic fibrosis. Cystic Fibrosis Foundation Hepatobiliary Disease Consensus Group(PubMed)
  Sokol RJ, Durie PR. J Pediatr Gastroenterol Nutr. 1999;28 Suppl 1:S1-13.
• The diagnosis of cystic fibrosis: a consensus statement. Cystic Fibrosis Foundation Consensus Panel (Abstract – PubMed)
  Rosenstein BJ, Cutting GR. J Pediatr. 1998 Apr;132(4):589-95.

CRITICALLY APPRAISED TOPICS:

• Newborn Screening for Cystic Fibrosis
  Frangiskakis, Susan. CAT Appraisers: Katherine Layton

REVIEWS:

• Cystic fibrosis: nutritional status and micronutrients (Abstract - PubMed)
  Winklhofer-Roob BM. Curr Opin Clin Nutr Metab Care. 2000 Jul;3(4):293-7.
• Challenges in the dietary treatment of cystic fibrosis related diabetes mellitus (Abstract - PubMed)
  Wilson DC, Kalnins D, Stewart C, Hamilton N, Hanna AK, Durie PR, Tullis E, Pencharz PB. Clin Nutr. 2000 Apr;19(2):87-93.
• Vitamin K and the management of patients with cystic fibrosis.(Abstract – PubMed)
  Durie PR. CMAJ. 1994 Oct 1;151(7):933-6

E-TEXTBOOK:

• Cystic Fiborsis
  Chapter 267, Merck Manual