Nutritional status of adolescents with cystic fibrosis treated at a reference center in the southeast region of Brazil

被引:4
作者
Lopes Del Ciampo, Ieda Regina [1 ,2 ]
Del Ciampo, Luiz Antonio [2 ]
Sawamura, Regina [2 ]
de Oliveira, Laiane Renolfi [3 ]
Machado Fernandes, Maria Inez [2 ]
机构
[1] Univ Fed Sao Carlos, Dept Med, Sao Paulo, Brazil
[2] Univ Sao Paulo, Dept Pediat, Ribeirao Preto Sch Med, Sao Paulo, Brazil
[3] Univ Sao Paulo, Ribeirao Preto Sch Med, Sao Paulo, Brazil
关键词
Cystic fibrosis; Nutritional status; Adolescent; Puberty; Pancreatic insufficiency; HEIGHT VELOCITY; GROWTH; CLASSIFICATION; MALNUTRITION; SURVIVAL; CHILDREN; WEIGHT;
D O I
10.1186/s13052-015-0159-x
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Background: Several factors can interfere with the full physical and emotional growth of adolescents, among them chronic diseases. The aim was to determine the nutritional status of adolescents and to associate it with puberty, pancreatic sufficiency, lung function and age range of Cystic Fibrosis (CF) diagnosis. Methods: An observational, cross-sectional, retrospective and analytical study was conducted using the data of medical records. Setting: Reference center in the northeastern region of the state of Sao Paulo - Brazil. Patients: All adolescents with CF attended in 2010 were included. Some variables included: pancreatic sufficiency (steatocrit >2 %), pancreatic enzymes replacement (yes/no), pubertal status-Tanner criteria (prepubertal: M1/G1, pubertal: M2/G2 to M4/G4, postpubertal: M5/G5), age at CF diagnosis (< 2 and >= 2 years of age), Lung function, measured as a predicted forced expiratory volume in 1 s (FEV1). Main outcome measures Nutritional indicators: body mass index for age (BMI/A) and height for age (H/A) with z-score calculated with Anthro Plus software. Cut-off reference points: >= z-score -3 and < z-score -2 (thinness); z-score -2 and <= z-score-z + 1 (normal weight); > z-score + 1 (overweight or obesity), and z-score <-2 (low or very low H/A). The groups were compared by the Kruskal-Wallis test. Level of significance: p < 0.05. Results: Thirty adolescents. Median (min; max) age: 14.4 (10.1; 19.8) years. BMI/A and H/A z-score, respectively: early diagnosis of CF (-0.8; -1.1) or late diagnosis of CF (-0.5;-0.8); with pancreatic insufficiency (-0.7; -0.8) or without pancreatic insufficiency (-0.8; -0.5) and prepubertal (-0.8; -0.7) pubertal (-0.2; -1.5) or postpubertal (-0.7; -0.5). No significant difference (p > 0.05) was observed. Patients with and without pancreatic insufficiency, presented H/A borderline z-score (p = 0.05). Association between H/A and FEV1 was borderline (p = 0.05). Conclusions: Adolescents presented adequate nutritional status, although with slightly lower values than those of developed countries. FEV1 lower levels occurred more frequently in adolescents with low H/A.
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页数:6
相关论文
共 25 条
[1]   Pancreatic enzyme replacement therapy in cystic fibrosis: Australian guidelines [J].
Anthony, H ;
Collins, CE ;
Davidson, G ;
Mews, C ;
Robinson, P ;
Shepherd, R ;
Stapleton, D .
JOURNAL OF PAEDIATRICS AND CHILD HEALTH, 1999, 35 (02) :125-129
[2]   Pubertal growth and development in cystic fibrosis: a retrospective review [J].
Aswani, N ;
Taylor, CJ ;
McGaw, J ;
Pickering, M ;
Rigby, AS .
ACTA PAEDIATRICA, 2003, 92 (09) :1029-1032
[3]   Stature as a prognostic factor in cystic fibrosis survival [J].
Beker, LT ;
Russek-Cohen, E ;
Fink, RJ .
JOURNAL OF THE AMERICAN DIETETIC ASSOCIATION, 2001, 101 (04) :438-442
[4]   Monitoring growth, body composition, pubertal and bone status [J].
Borowitz, D ;
Baker, RD ;
Stallings, V .
JOURNAL OF PEDIATRIC GASTROENTEROLOGY AND NUTRITION, 2002, 35 (03) :246-259
[5]   A new era in the treatment of cystic fibrosis: correction of the underlying CFTR defect [J].
Boyle, Michael P. ;
De Boeck, Kris .
LANCET RESPIRATORY MEDICINE, 2013, 1 (02) :158-163
[6]  
Brasil. Ministerio da Saude, 2008, PROT SIST VIG AL NUT
[7]  
Groeneweg Michael, 2002, J Cyst Fibros, V1, P276, DOI 10.1016/S1569-1993(02)00099-1
[8]   Improved survival among young patients with cystic fibrosis [J].
Kulich, M ;
Rosenfeld, M ;
Goss, CH ;
Wilmott, R .
JOURNAL OF PEDIATRICS, 2003, 142 (06) :631-636
[9]   Classification of malnutrition in cystic fibrosis: implications for evaluating and benchmarking clinical practice performance [J].
Lai, HuiChuan J. ;
Shoff, Suzanne M. .
AMERICAN JOURNAL OF CLINICAL NUTRITION, 2008, 88 (01) :161-166
[10]   Classification of nutritional status in cystic fibrosis [J].
Lai, HuiChuan J. .
CURRENT OPINION IN PULMONARY MEDICINE, 2006, 12 (06) :422-427