Literature DB >> 8741032

Growth and development in thalassaemia major patients with severe bone lesions due to desferrioxamine.

V De Sanctis1, A Pinamonti, A Di Palma, M Sprocati, G Atti, M R Gamberini, C Vullo.   

Abstract

UNLABELLED: Nine transfusion-dependent beta-thalassaemia major patients (seven males and two females), aged 4-15 years, with growth retardation and severe rickets-like radiological lesions due to continuous subcutaneous chelation therapy with desferrioxamine (45-75 mg/kg body weight, 6-7 time/week), were seen in our centre during the last 8 years. Serum ferritin levels ranged from 976 to 4115 micrograms/l. There was a progressive decline in growth velocity in these patients 2-3 years before the appearance of rickets-like radiological lesions. All patients underwent surgery to correct genu valgum and/or slipped capital epiphyses. The final height was below the 3rd percentile in six patients (SDS: from -2.9 to -5.2). The short stature was mainly due to a disproportion between upper and lower segments. Six of the patients had an associated sensorineural hearing loss.
CONCLUSION: Our data emphasize the importance of an accurate surveillance of the toxic effects of desferrioxamine treatment and warn of the risk of overtreating patients with low iron overload and also suggest a possible individual idiosyncrasy to the adverse effects of chelation therapy.

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Year:  1996        PMID: 8741032     DOI: 10.1007/bf01955263

Source DB:  PubMed          Journal:  Eur J Pediatr        ISSN: 0340-6199            Impact factor:   3.183


  18 in total

Review 1.  Treatment of Cooley's anemia.

Authors:  M T Fosburg; D G Nathan
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2.  Ocular changes in patients undergoing long-term desferrioxamine treatment.

Authors:  G B Arden; B Wonke; C Kennedy; E R Huehns
Journal:  Br J Ophthalmol       Date:  1984-12       Impact factor: 4.638

3.  Studies in desferrioxamine and ferrioxamine metabolism in normal and iron-loaded subjects.

Authors:  M R Summers; A Jacobs; D Tudway; P Perera; C Ricketts
Journal:  Br J Haematol       Date:  1979-08       Impact factor: 6.998

4.  Growth failure and bony changes induced by deferoxamine.

Authors:  N F Olivieri; G Koren; J Harris; S Khattak; M H Freedman; D M Templeton; J D Bailey; B J Reilly
Journal:  Am J Pediatr Hematol Oncol       Date:  1992

5.  Effect of different treatment regimes on linear growth and final height in beta-thalassaemia major.

Authors:  V De Sanctis; M Katz; C Vullo; B Bagni; M Ughi; B Wonke
Journal:  Clin Endocrinol (Oxf)       Date:  1994-06       Impact factor: 3.478

6.  Deferoxamine-induced growth retardation in patients with thalassemia major.

Authors:  S De Virgiliis; M Congia; F Frau; F Argiolu; G Diana; F Cucca; A Varsi; G Sanna; G Podda; M Fodde
Journal:  J Pediatr       Date:  1988-10       Impact factor: 4.406

7.  Prevention of cardiac disease by subcutaneous deferoxamine in patients with thalassemia major.

Authors:  L Wolfe; N Olivieri; D Sallan; S Colan; V Rose; R Propper; M H Freedman; D G Nathan
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8.  Deferoxamine (Desferal)-induced toxic retinal pigmentary degeneration and presumed optic neuropathy.

Authors:  V Lakhanpal; S S Schocket; R Jiji
Journal:  Ophthalmology       Date:  1984-05       Impact factor: 12.079

9.  Survival in medically treated patients with homozygous beta-thalassemia.

Authors:  N F Olivieri; D G Nathan; J H MacMillan; A S Wayne; P P Liu; A McGee; M Martin; G Koren; A R Cohen
Journal:  N Engl J Med       Date:  1994-09-01       Impact factor: 91.245

10.  Deferoxamine-induced bone dysplasia in patients with thalassemia major.

Authors:  P W Brill; P Winchester; P J Giardina; S Cunningham-Rundles
Journal:  AJR Am J Roentgenol       Date:  1991-03       Impact factor: 3.959

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3.  Circulating osteoprotegerin and receptor activator of NF-kappaB ligand system in patients with beta-thalassemia major.

Authors:  Nicholas G Angelopoulos; Anastasia Goula; Eugenia Katounda; Grigorios Rombopoulos; Victoria Kaltzidou; Dimitrios Kaltsas; Sophia Malaktari; Vassilis Athanasiou; George Tolis
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4.  Bone loss caused by iron overload in a murine model: importance of oxidative stress.

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5.  Liver volume in thalassaemia major: relationship with body weight, serum ferritin, and liver function.

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6.  Growth hormone secretion in polytransfused prepubertal patients with homozygous beta-thalassemia. Effect of long-term recombinant GH (recGH) therapy.

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Review 7.  Bisphosphonates in the treatment of thalassemia-associated osteoporosis.

Authors:  A Gaudio; N Morabito; A Xourafa; I Macrì; A Meo; S Morgante; A Trifiletti; A Lasco; N Frisina
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8.  Iron overload causes osteoporosis in thalassemia major patients through interaction with transient receptor potential vanilloid type 1 (TRPV1) channels.

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Review 9.  Benefits and risks of deferiprone in iron overload in Thalassaemia and other conditions: comparison of epidemiological and therapeutic aspects with deferoxamine.

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10.  Deferoxamine-induced dysplasia-like skeletal abnormalities at radiography and MRI.

Authors:  Hadeel M Seif El Dien; Reem I Esmail; Rania E Magdy; Hala M Lotfy
Journal:  Pediatr Radiol       Date:  2013-04-06
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