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Epidemiological evaluation regarding the role of cystic fibrosis as a risk factor for child malnutrition.
Rev Med Chir Soc Med Nat Iasi. 2014 Apr-Jun; 118(2):450-6.RM

Abstract

Cystic fibrosis (CF) is the most common monogenic autosomal recessive disorder with progressive chronic evolution which is potentially lethal. Poor growth is a characteristic of children suffering from cystic fibrosis. A poor nutritional status is an independent risk factor for inadequate survival in cystic fibrosis and is associated with disease complications. The appropriate nutritional management is an important part of the treatment so that the patient with cystic fibrosis can achieve normal growth and development and maintain the best possible health status. A balanced diet supplemented with snacks high in fat and calories is necessary to increase the caloric intake in children with cystic fibrosis. Children with cystic fibrosis have higher caloric needs than healthy children of the same age and sex. Malnutrition in CF is multifactorial. Cystic fibrosis is a complex multisystem disorder affecting mainly the gastrointestinal tract and respiratory system. In the past, malnutrition was an inevitable consequence of disease progression, leading to poor growth, impaired respiratory muscle function, decreased exercise tolerance and immunological impairment. A positive association between body weight and height and survival has been widely reported. The energy requirements of patients with CF vary widely and generally increase with age and disease severity. Cystic fibrosis remains a paediatric disorder which is often underdiagnosed but which, if therapeutically managed properly (by means of drug therapy as well as by appropriate physiotherapy techniques), can lead to improved quality of life and, thus, to a bigger life expectancy.

Authors

No affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Journal Article

Language

eng

PubMed ID

25076714

Citation

Florescu, Laura, et al. "Epidemiological Evaluation Regarding the Role of Cystic Fibrosis as a Risk Factor for Child Malnutrition." Revista Medico-chirurgicala a Societatii De Medici Si Naturalisti Din Iasi, vol. 118, no. 2, 2014, pp. 450-6.
Florescu L, Paduraru DT, Mîndru DE, et al. Epidemiological evaluation regarding the role of cystic fibrosis as a risk factor for child malnutrition. Rev Med Chir Soc Med Nat Iasi. 2014;118(2):450-6.
Florescu, L., Paduraru, D. T., Mîndru, D. E., Temneanu, O. R., Petrariu, F. D., & Matei, M. C. (2014). Epidemiological evaluation regarding the role of cystic fibrosis as a risk factor for child malnutrition. Revista Medico-chirurgicala a Societatii De Medici Si Naturalisti Din Iasi, 118(2), 450-6.
Florescu L, et al. Epidemiological Evaluation Regarding the Role of Cystic Fibrosis as a Risk Factor for Child Malnutrition. Rev Med Chir Soc Med Nat Iasi. 2014 Apr-Jun;118(2):450-6. PubMed PMID: 25076714.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Epidemiological evaluation regarding the role of cystic fibrosis as a risk factor for child malnutrition. AU - Florescu,Laura, AU - Paduraru,Dana Teodora Anton, AU - Mîndru,Dana Elena, AU - Temneanu,Oana Raluea, AU - Petrariu,F D, AU - Matei,Mioara Calipsoana, PY - 2014/8/1/entrez PY - 2014/8/1/pubmed PY - 2014/10/11/medline SP - 450 EP - 6 JF - Revista medico-chirurgicala a Societatii de Medici si Naturalisti din Iasi JO - Rev Med Chir Soc Med Nat Iasi VL - 118 IS - 2 N2 - Cystic fibrosis (CF) is the most common monogenic autosomal recessive disorder with progressive chronic evolution which is potentially lethal. Poor growth is a characteristic of children suffering from cystic fibrosis. A poor nutritional status is an independent risk factor for inadequate survival in cystic fibrosis and is associated with disease complications. The appropriate nutritional management is an important part of the treatment so that the patient with cystic fibrosis can achieve normal growth and development and maintain the best possible health status. A balanced diet supplemented with snacks high in fat and calories is necessary to increase the caloric intake in children with cystic fibrosis. Children with cystic fibrosis have higher caloric needs than healthy children of the same age and sex. Malnutrition in CF is multifactorial. Cystic fibrosis is a complex multisystem disorder affecting mainly the gastrointestinal tract and respiratory system. In the past, malnutrition was an inevitable consequence of disease progression, leading to poor growth, impaired respiratory muscle function, decreased exercise tolerance and immunological impairment. A positive association between body weight and height and survival has been widely reported. The energy requirements of patients with CF vary widely and generally increase with age and disease severity. Cystic fibrosis remains a paediatric disorder which is often underdiagnosed but which, if therapeutically managed properly (by means of drug therapy as well as by appropriate physiotherapy techniques), can lead to improved quality of life and, thus, to a bigger life expectancy. SN - 0048-7848 UR - https://www.unboundmedicine.com/medline/citation/25076714/Epidemiological_evaluation_regarding_the_role_of_cystic_fibrosis_as_a_risk_factor_for_child_malnutrition_ L2 - http://babysfirsttest.org/newborn-screening/conditions/cystic-fibrosis-cf DB - PRIME DP - Unbound Medicine ER -