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Published on: January 7, 2016
Use of Growth Hormone in children with short stature and normal Growth Hormone secretion: a growing problem
1Montreal Children's Hospital, McGill University, Quebec, Canada.
Insights
Growth hormone (GH) therapy for children with short stature shows minimal impact on final height. Most patients experience less than 1 cm/year gain, with many reporting no significant benefit from GH treatment.
Area of Science:
- Pediatric Endocrinology
- Growth and Development
- Medical Ethics
Background:
- Short stature in children presents complex ethical, economic, psychologic, and social considerations.
- Growth hormone (GH) therapy is a potential intervention, but its efficacy in achieving significant final height in otherwise healthy short children is debated.
Purpose of the Study:
- To evaluate the ethical, economic, psychologic, social, and growth attainment outcomes of GH therapy in normal children with short stature.
- To determine the actual benefit of GH treatment on final height in non-pathological short stature.
Main Methods:
- Review of ethical, economic, psychologic, and social issues.
- Analysis of data from an international survey of 99 normal short children treated with GH for at least 3 years.
- Assessment of growth velocity acceleration and final height attainment.
Main Results:
- GH treatment can accelerate growth velocity in some short children.
- Limited data indicate no significant benefit in final height attainment, with a mean gain of <1 cm/year.
- A significant portion (40%) of patients reported no benefit, and only one-third considered the results very good or good.
Conclusions:
- GH therapy is unlikely to dramatically increase final height in children with normal short stature.
- Current evidence does not support the use of GH for treating normal short stature outside of controlled clinical trials.
- Careful consideration of limited benefits versus potential risks is crucial for this patient group.
Abstract:
The ethical, economic, psychologic, social, and growth attainment outcome issues related to the use of GH therapy in normal children with short stature are discussed. Although some short children accelerate their growth velocity with GH treatment, the limited available data do not suggest a significant benefit in final height attainment. An international survey of 99 normal short children treated with GH for at least 3 years reported a net improvement in mean height gain of <1 cm/year. Only in one-third was the result considered very good or good; 40% stated that there was no benefit. Thus, it seems unlikely that GH will dramatically increase final height in short children. On this basis, the use of GH for the treatment of the normal child with short stature outside of carefully controlled clinical trials cannot be recommended at present.
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