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Early diagnosis and treatment referral of children born small for gestational age without catch-up growth are critical for optimal growth outcomes

Approximately 10% of children born small for their gestational age (SGA) fail to show catch-up growth and may remain short-statured as adults. Despite treatment guidelines for children born SGA that recommend referral for growth hormone (GH) therapy evaluation and initiation by ages 2 to 4 years, th...

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Autores principales: Houk, Christopher P, Lee, Peter A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3441279/
https://www.ncbi.nlm.nih.gov/pubmed/22559301
http://dx.doi.org/10.1186/1687-9856-2012-11
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author Houk, Christopher P
Lee, Peter A
author_facet Houk, Christopher P
Lee, Peter A
author_sort Houk, Christopher P
collection PubMed
description Approximately 10% of children born small for their gestational age (SGA) fail to show catch-up growth and may remain short-statured as adults. Despite treatment guidelines for children born SGA that recommend referral for growth hormone (GH) therapy evaluation and initiation by ages 2 to 4 years, the average age of GH treatment initiation is typically much later, at ages 7 to 9 years. Delayed referral for GH treatment is problematic as studies show younger age at GH treatment initiation in children born SGA is an independent predictor for responses such as optimal growth acceleration, normalization of prepubertal height, and most importantly, adult height (AH). This review discusses the importance and associated challenges of early diagnosis of children born SGA who fail to show catch-up growth, contrasts the recommended age of referral for these patients and the average age of GH treatment initiation, and discusses studies showing the significant positive effects of early referral and treatment with GH on AHs in short-statured children born SGA. To optimize the eventual height in short-statured SGA children who fail to manifest catch-up growth, a lowering of the average age of referral for GH therapy evaluation is needed to better align with consensus recommendations for SGA management. The importance of increasing parental and physician awareness that most children born SGA will do well developmentally and will optimally benefit from early initiation of GH treatment when short-statured is addressed, as is the need to shift the age of referral to better align with consensus recommendations.
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spelling pubmed-34412792012-09-14 Early diagnosis and treatment referral of children born small for gestational age without catch-up growth are critical for optimal growth outcomes Houk, Christopher P Lee, Peter A Int J Pediatr Endocrinol Review Approximately 10% of children born small for their gestational age (SGA) fail to show catch-up growth and may remain short-statured as adults. Despite treatment guidelines for children born SGA that recommend referral for growth hormone (GH) therapy evaluation and initiation by ages 2 to 4 years, the average age of GH treatment initiation is typically much later, at ages 7 to 9 years. Delayed referral for GH treatment is problematic as studies show younger age at GH treatment initiation in children born SGA is an independent predictor for responses such as optimal growth acceleration, normalization of prepubertal height, and most importantly, adult height (AH). This review discusses the importance and associated challenges of early diagnosis of children born SGA who fail to show catch-up growth, contrasts the recommended age of referral for these patients and the average age of GH treatment initiation, and discusses studies showing the significant positive effects of early referral and treatment with GH on AHs in short-statured children born SGA. To optimize the eventual height in short-statured SGA children who fail to manifest catch-up growth, a lowering of the average age of referral for GH therapy evaluation is needed to better align with consensus recommendations for SGA management. The importance of increasing parental and physician awareness that most children born SGA will do well developmentally and will optimally benefit from early initiation of GH treatment when short-statured is addressed, as is the need to shift the age of referral to better align with consensus recommendations. BioMed Central 2012 2012-05-04 /pmc/articles/PMC3441279/ /pubmed/22559301 http://dx.doi.org/10.1186/1687-9856-2012-11 Text en Copyright ©2012 Lee and Houk; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
Houk, Christopher P
Lee, Peter A
Early diagnosis and treatment referral of children born small for gestational age without catch-up growth are critical for optimal growth outcomes
title Early diagnosis and treatment referral of children born small for gestational age without catch-up growth are critical for optimal growth outcomes
title_full Early diagnosis and treatment referral of children born small for gestational age without catch-up growth are critical for optimal growth outcomes
title_fullStr Early diagnosis and treatment referral of children born small for gestational age without catch-up growth are critical for optimal growth outcomes
title_full_unstemmed Early diagnosis and treatment referral of children born small for gestational age without catch-up growth are critical for optimal growth outcomes
title_short Early diagnosis and treatment referral of children born small for gestational age without catch-up growth are critical for optimal growth outcomes
title_sort early diagnosis and treatment referral of children born small for gestational age without catch-up growth are critical for optimal growth outcomes
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3441279/
https://www.ncbi.nlm.nih.gov/pubmed/22559301
http://dx.doi.org/10.1186/1687-9856-2012-11
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