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Growth Hormone Therapy in Children With Idiopathic Short Stature
Arch Pediatr Adolesc Med. 2002;156:946-947.
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| Since this article does not have an abstract, we have provided the first 150 words of the full text and any section headings. |
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We read with interest the meta-analysis of the effect of growth hormone
(GH) therapy on height in children with idiopathic short stature1
but were surprised that 3 randomized controlled trials were not included in
the review.
We recently completed a review of the clinical and cost-effectiveness
of GH in children, which was commissioned by the United Kingdom National Health
Service Health Technology Assessment Programme on behalf of the National Institute
for Clinical Excellence (London, England).2
As part of this, we considered randomized controlled trials of GH in children
with idiopathic short stature, GH deficiency, Turner syndrome, Prader-Willi
syndrome, or chronic renal failure. Fourteen databases, including the Cochrane
Library, MEDLINE, and the National Research Register, were searched (to September
2001, limited to English language studies). In addition, experts in the field
were contacted.
We identified 3 studies that were not included in the meta-analysis
reported by Finkelstein and colleagues but that . . . [Full Text of this Article]
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