Growth assessment and risk factors of malnutrition in children with cystic fibrosis

References

1. ↵
   1. Gaskin KJ

   (2013) Nutritional care in children with cystic fibrosis: are our patients becoming better? Eur J Clin Nutr 67:558–564.
2. ↵
   1. Bournez M,
   2. Bellis G,
   3. Huet F

   (2012) Growth during puberty in cystic fibrosis: a retrospective evaluation of a French cohort. Arch Dis Child 97:714–720.
3. ↵
   1. Matel JL,
   2. Milla CE

   (2009) Nutrition in cystic fibrosis. Semin Respir Crit Care Med 30:579–586.
4. ↵
   1. Woestenenk JW,
   2. Ent CK,
   3. Houwen RH

   (2015) Pancreatic enzyme replacement therapy and coefficient of fat absorption in children and adolescents with cystic fibrosis. J Pediatr Gastroenterol Nutr 61:355–360.
5. ↵
   1. Dommelen PV,
   2. Grote FK,
   3. Oostdijk W,
   4. Keizer-Scharma S,
   5. Bouquet J,
   6. Hendrix J,
   7. et al.

   (2009) Growth monitoring to detect children with cystic fibrosis. Horm Res 72:218–224.
6. ↵
   1. Health Information Directorate Ministry of Health, Bahrain. Health Statistics 2012

   , Available from URL: http://www.moh.gov.bh/AR/aboutMOH/Information/Statistics.aspx. Updated 2012; Accessed 2015 Aug 13.
7. ↵
   1. Al-Mahroos F

   (1998) Cystic fibrosis in Bahrain: incidence, phenotype and outcome. J Trop Pediatr 44:35–39.
8. ↵
   1. Barr HL,
   2. Britton J,
   3. Smyth AR,
   4. Fogarty AW

   (2011) Association between socioeconomic status, sex, and age at death from cystic fibrosis in England and Wales (1959 to 2008): cross sectional study. BMJ 343:d4662.
9. ↵
   1. World Health Organization

   (2006) WHO child growth standards: length/height-for-age, weight-for-age, weight-for-length, weight-for-height and body mass index-for-age: methods and development (World Health Organization, Geneva (CH)).
10. ↵
    1. Tluczek A,
    2. Laxova A,
    3. Grieve A,
    4. Heun A,
    5. Brown RL,
    6. Rock MJ,
    7. et al.

    (2014) Long-term follow-up of cystic fibrosis newborn screening: Psychosocial functioning of adolescents and young adults. J Cyst Fibros 13:227–234.
11. ↵
    1. Accurso FJ,
    2. Goor FV,
    3. Zha J,
    4. Stone AJ,
    5. Dong Q,
    6. Ordonez CL,
    7. et al.

    (2014) Sweat chloride as a biomarker of CFTR activity: Proof of concept and ivacaftor clinical trial data. J Cyst Fibros 13:139–147.
12. ↵
    1. Haller W,
    2. Ledder O,
    3. Lewindon PJ,
    4. Couper R,
    5. Gaskin KJ,
    6. Oliver M

    (2014) Cystic fibrosis: an update for clinician. Part1: nutrition and gastrointestinal complications. J Gasrtoenterol Hepatol 29:1344–1355.
13. ↵
    1. Boeck K,
    2. Zolin A,
    3. Cuppens H,
    4. Olesen HV,
    5. Viviani L

    (2014) The relative frequency of CFTR mutation classes in European patients with cystic fibrosis. J Cyst Fibros 13:403–409.
14. ↵
    1. Leonard A,
    2. Davis E,
    3. Rosenstein BJ,
    4. Zeitlin PL,
    5. Paranjape SM,
    6. Peeler D,
    7. et al.

    (2010) Description of a standardized nutrition classification plan and its relation to nutritional outcomes in children with cystic fibrosis. J Pediatr Psychol 35:6–13.
15. ↵
    1. Kalnins D,
    2. Wilschanski M

    (2012) Maintenance of nutritional status in patients with cystic fibrosis: new and emerging therapies. Drug Des Devel Ther 6:151–161.
16. ↵
    1. Wiskin A,
    2. Johnson MJ,
    3. Leaf AA,
    4. Wootton SA,
    5. Beattie RM

    (2015) How to use: nutritional assessment in children. Arch Dis Child Educ Pract Ed 100:204–209.
17. ↵
    1. Stark LJ,
    2. Quittner AL,
    3. Powers SW,
    4. Opopari-Arrigan L,
    5. Bean JA,
    6. Duggan C,
    7. et al.

    (2009) Randomized clinical trial of behavioral intervention and nutrition education to improve calori intake and weight in children with cystic fibrosis. Arch Pediatr Adolesc Med 163:915–921.
18. ↵
    1. Jafari A,
    2. Mehdizadeh-Hakkak A,
    3. Kianifar H,
    4. Hebrani P,
    5. Ahanchian H,
    6. Abbasnejad E

    (2013) Effects of probiotics on quality of life in children with cystic fibrosis;a randomized control trial. Iran J Pediatr 23:669–674.