Literature DB >> 8894665

Slipped capital femoral epiphysis in children treated with growth hormone. A summary of the National Cooperative Growth Study experience.

S L Blethen1, A C Rundle.   

Abstract

We examined the association between slipped capital femoral epiphysis (SCFE) and growth hormone (GH) treatment in 16,514 children who had not been treated with GH prior to their enrollment in the National Cooperative Growth Study. Fifteen children had SCFE prior to receiving GH therapy, 26 developed SCFE during GH treatment, and one had SCFE on one side prior to GH treatment and developed it on the contralateral side while receiving GH. Children with GH deficiency were significantly more likely to develop SCFE while on GH treatment than were children with idiopathic short stature (p = 0.006). There was no difference between GH-deficient girls and boys in the risk of developing SCFE during GH treatment. There were 3 cases of SCFE in girls with Turner syndrome before GH treatment and 3 during. Typically, children who developed SCFE while on GH were older, heavier, and grew more slowly during the first year of GH than those who did not. Children with GH deficiency, Turner syndrome, and other known causes of short stature are more likely to develop SCFE before or during GH treatment than children with idiopathic short stature.

Entities:  

Mesh:

Substances:

Year:  1996        PMID: 8894665     DOI: 10.1159/000185006

Source DB:  PubMed          Journal:  Horm Res        ISSN: 0301-0163


  9 in total

1.  Slipped capital femoral epiphyses associated with the withdrawal of a gonadotrophin releasing hormone.

Authors:  Eugène van Puijenbroek; Emil Verhoef; Linda de Graaf
Journal:  BMJ       Date:  2004-06-05

Review 2.  Growth hormone therapy.

Authors:  Anurag Bajpai; P Sn Menon
Journal:  Indian J Pediatr       Date:  2005-02       Impact factor: 1.967

Review 3.  A risk-benefit assessment of growth hormone use in children.

Authors:  S L Blethen; M H MacGillivray
Journal:  Drug Saf       Date:  1997-11       Impact factor: 5.606

4.  Chronic Bilateral Slipped Capital Femoral Epiphysis as an Unusual Presentation of Congenital Panhypopituitarism due to Pituitary Hypoplasia in a 17-Year-Old Female.

Authors:  Sasigarn A Bowden; Kevin E Klingele
Journal:  Int J Pediatr Endocrinol       Date:  2010-01-11

5.  Hypogonadism and pubertal development in Prader-Willi syndrome.

Authors:  A Crinò; R Schiaffini; P Ciampalini; S Spera; L Beccaria; F Benzi; L Bosio; A Corrias; L Gargantini; A Salvatoni; G Tonini; G Trifirò; C Livieri
Journal:  Eur J Pediatr       Date:  2003-02-27       Impact factor: 3.183

6.  Case report: bilateral slipped capital femoral epiphyses and hormone replacement.

Authors:  Ali Nourbakhsh; Hasan A Ahmed; Thomas B McAuliffe; Kim J Garges
Journal:  Clin Orthop Relat Res       Date:  2008-02-10       Impact factor: 4.176

Review 7.  Etiology and treatment of growth retardation in children with chronic kidney disease and end-stage renal disease: a historical perspective.

Authors:  Richard N Fine
Journal:  Pediatr Nephrol       Date:  2009-12-24       Impact factor: 3.714

8.  Long-Term Safety of Growth Hormone Treatment in Childhood: Two Large Observational Studies: NordiNet IOS and ANSWER.

Authors:  Lars Sävendahl; Michel Polak; Philippe Backeljauw; Joanne C Blair; Bradley S Miller; Tilman R Rohrer; Anita Hokken-Koelega; Alberto Pietropoli; Nicky Kelepouris; Judith Ross
Journal:  J Clin Endocrinol Metab       Date:  2021-05-13       Impact factor: 5.958

9.  Short-term growth hormone treatment in children with Hurler syndrome after hematopoietic cell transplantation.

Authors:  L E Polgreen; M Plog; J D Schwender; J Tolar; W Thomas; P J Orchard; B S Miller; A Petryk
Journal:  Bone Marrow Transplant       Date:  2009-03-02       Impact factor: 5.483

  9 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.