Rondón PM, Mustelier NS, Vázquez VE, Osorio CI, Montero VD

Language: Spanish
References: 12
Page: 1118-1123
PDF size: 96.67 Kb.

ABSTRACT

An observational, descriptive and cross-sectional study, of 19 patients with cystic fibrosis, assisted in the out-patient department of "Hermanos Cordové" Teaching Pediatric Hospital in Manzanillo, Granma was carried out during the semester of July- December, 2012, with the objective of identifying the nutritional state in them starting from the anthropometric evaluation -- for which the Waterlow score was calculated --, and then to relate it with the genetic mutation. Among the results of the series it was observed that 73.7% of the patients had adequate weight and size for the age, while 31.5% was evaluated as undernourished. Also, there was relation between the nutritional state and the genetic mutation, and it was concluded that most of the affected patients had an appropriate nutritional evaluation, as consequence of a correct multidisciplinary care.

REFERENCES

1. Salcedo Posada A, García Novo M. Fibrosis quística. Madrid: Ediciones Díaz de Santos; 1998. p. 1-5.

2. Razón Behar R, Rodríguez Cala F, Rojo Concepción M, González Valdés JA, Abreu Suárez G, Pérez Rodríguez T, et al. La fibrosis quística en Cuba. Rev Cubana Pediatr. 2009 [citado 9 May 2013]; 81(Sup). Disponible en: http://bvs.sld.cu/revistas/ped/ vol81_05_09/ped15509.pdf

3. Matilde Socarrás M, Bolet Astoviza M, Rodríguez Cala F. Seguimiento nutricional de los pacientes fibroquíticos en el Hospital Universitario General Calixto García. Rev Haban Cienc Méd. 2010 [citado 9 May 2013]; 9(4). Disponible en: http://scielo.sld.cu/scielo.php?script=sci_arttext&pid=S1729-519X2010000400016

4. Giannouli E, Sharma S, Maycher B, Amorosa JK, Coombs BD, Krasny RM. Cystic fibrosis imaging. En Medscape [citado 25 May 2013]. Disponible en: http://emedicine.medscape.com/article/354931-overview

5. Morton AM. Symposium 6: Young people, artificial nutrition and transitional care. The nutritional challenges of the young adult with cystic fibrosis: transition. Proc Nutr Soc. 2009; 68(4): 430-40.

6. Pinto IC, Silva CP, Britto MC. Nutritional, clinical and socioeconomic profile of patients with cystic fibrosis treated at a referral center in northeastern Brazil. Bras Pneumol. 2009; 35(2): 137-43.

7. Salvatore D, Buzzetti R, Baldo E, Forneris MP, Lucidi V, Manunza D, et al. An overview of international literature from cystic fibrosis registries. Neonatal screening and nutrition/growth. J Cyst Fibros. 2010; 9(2):75- 83.

8. Amador García M. Temas de Pediatría. T 2. La Habana: Editorial Pueblo y Educación; 1996. p. 75-86.

9. Jiménez Acosta S. Vigilancia Nutricional Materno Infantil. La Habana: [s.n.]; 1997. p. 1-6.

10. Souza dos Santos Simon MI, Drehmer M, Menna-Barreto SS. Association between nutritional status and dietary intake in patients with cystic fibrosis. J Bras Pneumol. 2009; 35(10): 966-72.

11. Matel JL. Nutrition in cystic fibrosis. Semin Respir Crit Care Med. 2009; 30(5): 579- 86.

12. Esplugas Montoya AE, Razón Behar R, Ojea Menéndez A, Servide Quiala RN, Vera Díaz M. Evaluación nutricional, antropométrica y bioquímica, de pacientes afectos de fibrosis quística. Rev Cubana Pediatr. 2008 [citado 25 May 2013]; 80(2). Disponible en: http://www.bvs.sld.cu/revistas/ped/vol80_2_08/ped06208.htm