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Malnutrition, Its Attributes, and Impact on Quality of Life: An Epidemiological Study among β-Thalassemia Major Children

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Background: India is home to a large number of thalassemic children. Despite malnutrition being an essential determinant of their therapeutic goals and quality of life (QoL), it was hardly ever explored. With this background, this study aimed to estimate the proportion of β-thalassemia major (β-TM) children experiencing malnutrition, its attributes, and impact on their QoL. Methods: This cross-sectional, hospital-based, analytical observational study was conducted among 328 β-TM children attending the thalassemia day care unit of a medical college from May 2016 to April 2017, with a structured schedule. Data were analyzed following appropriate statistical methods using SPSS statistical package ver. 16.0 (SPSS Inc., Chicago, IL, USA). Results: Among the study participants, 48.2% were malnourished with a mean body mass index of 13.9 kg/m2. In the multivariable logistic regression model, participants’ age (adjusted odds ratio [AOR], 1.15; 95% confidence interval [CI], 1.02–1.29), caste (AOR, 2.11; 95% CI, 1.23–3.60), mothers’ educational level (AOR, 2.05; 95% CI, 1.22– 3.44), blood transfusion frequency (AOR, 1.25; 95% CI, 1.16–1.31), and palpable spleen size (AOR, 1.22; 95% CI, 1.08–1.37) were significant predictors of malnutrition after adjusting for pre-transfusion hemoglobin level and hemolytic facies status. In multiple linear regression analysis, malnutrition negatively impacted total QoL (unstandardized beta [standard error], -4.4 [1.7]; P=0.009) and various domains of the study participants except the social and school domains adjusted for age, sex, caste, place of residence, parents’ educational level, and socioeconomic status. Conclusion: Almost half of the study participants had malnutrition. Malnutrition had a negative impact on their QoL.

Abstract

Background: India is home to a large number of thalassemic children. Despite malnutrition being an essential determinant of their therapeutic goals and quality of life (QoL), it was hardly ever explored. With this background, this study aimed to estimate the proportion of β-thalassemia major (β-TM) children experiencing malnutrition, its attributes, and impact on their QoL. Methods: This cross-sectional, hospital-based, analytical observational study was conducted among 328 β-TM children attending the thalassemia day care unit of a medical college from May 2016 to April 2017, with a structured schedule. Data were analyzed following appropriate statistical methods using SPSS statistical package ver. 16.0 (SPSS Inc., Chicago, IL, USA). Results: Among the study participants, 48.2% were malnourished with a mean body mass index of 13.9 kg/m2. In the multivariable logistic regression model, participants’ age (adjusted odds ratio [AOR], 1.15; 95% confidence interval [CI], 1.02–1.29), caste (AOR, 2.11; 95% CI, 1.23–3.60), mothers’ educational level (AOR, 2.05; 95% CI, 1.22– 3.44), blood transfusion frequency (AOR, 1.25; 95% CI, 1.16–1.31), and palpable spleen size (AOR, 1.22; 95% CI, 1.08–1.37) were significant predictors of malnutrition after adjusting for pre-transfusion hemoglobin level and hemolytic facies status. In multiple linear regression analysis, malnutrition negatively impacted total QoL (unstandardized beta [standard error], -4.4 [1.7]; P=0.009) and various domains of the study participants except the social and school domains adjusted for age, sex, caste, place of residence, parents’ educational level, and socioeconomic status. Conclusion: Almost half of the study participants had malnutrition. Malnutrition had a negative impact on their QoL.

참고문헌 (29)

  1. Kasper D, "Harrison’s principles of internal medicine" (2015), McGraw-Hill Medical Publishing
  2. Colah R, "Global burden, distribution and prevention of β-thalassemias and hemoglobin E disorders", Expert Rev Hematol, 3, pp.103~117 (2010)
  3. Sharma N, "Assessment of serum ferritin, vitamin b12 and folic acid level in thalassemia", J Med Sci Clin Res, 5, pp.29910~29914 (2017)
  4. Weatherall DJ, "Inherited haemoglobin disorders: an increasing global health problem", Bull World Health Organ, 79, pp.704~712 (2001)
  5. "Management of haemoglobin disorders:report of a joint WHO-TIF meeting, Nicosia, Cyprus, 16-18 November 2007" (2008)[URL]
  6. Ansari SH, "Molecular epidemiology of β-thalassemia in Pakistan: far reaching implications", Indian J Hum Genet, 18, pp.193~197 (2012)
  7. Mohanty D, "Prevalence of β-thalassemia and other haemoglobinopathies in six cities in India: a multicentre study", J Community Genet, 4, pp.33~42 (2013)
  8. Skordis N, "The multifactorial origin of growth failure in thalassaemia", Pediatr Endocrinol Rev, 8(Suppl 2), pp.271~277 (2011)
  9. Toulson Davisson Correia MI, "Addressing the hidden burden of malnutrition for hospitalized patients", J Acad Nutr Diet, 118, pp.37~39 (2018)
  10. Telfer PT, "Hepatic iron concentration combined with long-term monitoring of serum ferritin to predict complications of iron overload in thalassaemia major", Br J Haematol, 110, pp.971~977 (2000)
  11. "A simple guide to classifying body mass index in children" (2011)[URL]
  12. Elalfy MS, "Quality of life of Egyptian b-thalassemia major children and adolescents", Egypt J Haematol, 39, pp.222~226 (2014)
  13. Mangal A, "Updated BG Prasad socioeconomic classification, 2014: a commentary", Indian J Public Health, 59, pp.42~44 (2015)
  14. "Global strategy on diet physical activity and health" (2004)[URL]
  15. "National Center for Health Statistics: clinical growth charts"[URL]
  16. "Scaling and Scoring of the Pediatric Quality of Life Inventory" (2017)[URL]
  17. Trehan A, "Clinicoinvestigational and demographic profile of children with thalassemia major", Indian J Hematol Blood Transfus, 31, pp.121~126 (2015)
  18. Pemde HK, "Physical growth in children with transfusion-dependent thalassemia", Pediatr Health Med Ther, 2, pp.13~19 (2011)
  19. Kumari V, "Growth retardation and malnutrition in children with thalassemia major", Indian J Prev Soc Med, 43, pp.149~152 (2012)
  20. Sheikh MA, "The assessment of nutritional status of children with beta thalassemia major with body mass index", Pak J Med Health Sci, 11, pp.262~265 (2017)
  21. Mirhosseini NZ, "Factors affecting nutritional status among pediatric patients with transfusion-dependent beta thalassemia", Mediterr J Nutr Metab, 6, pp.45~51 (2013)
  22. Fahim FM, "Growth parameters and vitamin D status in children with thalassemia major in upper Egypt", Int J Hematol Oncol Stem Cell Res, 7, pp.10~14 (2013)
  23. Brook CG, "Growth in children with thalassaemia major and effect of two different transfusion regimens", Arch Dis Child, 44, pp.612~616 (1969)
  24. Pantelakis S, "Growth patterns in patients with thalassaemia major", Acta Paediatr Suppl, 406, pp.109~110 (1994)
  25. Fung EB, "The importance of nutrition for health in patients with transfusion-dependent thalassemia", Ann N Y Acad Sci, 1368, pp.40~48 (2016)
  26. Fuchs GJ, "Nutritional factors and thalassaemia major", Arch Dis Child, 74, pp.224~227 (1996)
  27. Saxena A, "Growth retardation in thalassemia major patients", Int J Hum Genet, 3, pp.237~246 (2003)
  28. Taher AT, "Optimal management of β thalassaemia intermedia", Br J Haematol, 152, pp.512~523 (2011)
  29. Tantawy AA, "Growth differentiation factor-15 in children and adolescents with thalassemia intermedia: relation to subclinical atherosclerosis and pulmonary vasculopathy", Blood Cells Mol Dis, 55, pp.144~150 (2015)

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