Literature DB >> 17252257

[Bisphosphonate therapy for children and adolescents with primary and secondary osteoporotic diseases].

O Semler1, C Land, E Schönau.   

Abstract

Bisphosphonates have a set place in the treatment of osteoporosis in adults. For the last 10 years they have also been used in pediatrics. Due to inhibition in differentiation and reduction in osteoclasts, both pamidronate and alendronate, the most commonly used preparations, cause an increase in bone density. Most experience comes from the i.v. treatment of forms with severe courses of osteogenesis imperfecta (OI). There is an increase in bone substance, a decrease in rate of fractures and a reduction in pain with higher mobility of those effected. In addition to the use of drugs, intramedullary nailing and physiotherapy are important therapeutic standards. Bisphosphonates are also used for other diseases involving bone remodeling, such as juvenile idiopathic osteoporosis or familial hyperphosphatemia. Acute side effects usually occur with the first infusion, involve "flu-like" symptoms and are self limiting. The question of long-term side effects cannot be answered with the currently available data.

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Year:  2007        PMID: 17252257     DOI: 10.1007/s00132-006-1037-4

Source DB:  PubMed          Journal:  Orthopade        ISSN: 0085-4530            Impact factor:   1.087


  13 in total

Review 1.  Long-term effects of bisphosphonates on the growing skeleton. Studies of young patients with severe osteoporosis.

Authors:  C Brumsen; N A Hamdy; S E Papapoulos
Journal:  Medicine (Baltimore)       Date:  1997-07       Impact factor: 1.889

Review 2.  Bisphosphonates: mechanisms of action.

Authors:  H Fleisch
Journal:  Endocr Rev       Date:  1998-02       Impact factor: 19.871

3.  Immobilization hypercalcemia in incomplete paraplegia: successful treatment with pamidronate.

Authors:  D Kedlaya; M E Brandstater; J K Lee
Journal:  Arch Phys Med Rehabil       Date:  1998-02       Impact factor: 3.966

4.  Type V osteogenesis imperfecta: a new form of brittle bone disease.

Authors:  F H Glorieux; F Rauch; H Plotkin; L Ward; R Travers; P Roughley; L Lalic; D F Glorieux; F Fassier; N J Bishop
Journal:  J Bone Miner Res       Date:  2000-09       Impact factor: 6.741

5.  Osteogenesis imperfecta type VI: a form of brittle bone disease with a mineralization defect.

Authors:  Francis H Glorieux; Leanne M Ward; Frank Rauch; Ljiljana Lalic; Peter J Roughley; Rose Travers
Journal:  J Bone Miner Res       Date:  2002-01       Impact factor: 6.741

6.  Genetic heterogeneity in osteogenesis imperfecta.

Authors:  D O Sillence; A Senn; D M Danks
Journal:  J Med Genet       Date:  1979-04       Impact factor: 6.318

Review 7.  Osteogenesis imperfecta.

Authors:  Frank Rauch; Francis H Glorieux
Journal:  Lancet       Date:  2004-04-24       Impact factor: 79.321

8.  Effect of pamidronate treatment on vertebral deformity in children with primary osteoporosis. A pilot study using radiographic morphometry.

Authors:  Zdenek Sumník; Christof Land; Gabriele Rieger-Wettengl; Frederike Körber; Angelika Stabrey; Eckhard Schoenau
Journal:  Horm Res       Date:  2003-12-15

9.  Delayed osteotomy but not fracture healing in pediatric osteogenesis imperfecta patients receiving pamidronate.

Authors:  Craig Fj Munns; Frank Rauch; Leonid Zeitlin; François Fassier; Francis H Glorieux
Journal:  J Bone Miner Res       Date:  2004-08-23       Impact factor: 6.741

10.  Osteogenesis imperfecta type VII: an autosomal recessive form of brittle bone disease.

Authors:  L M Ward; F Rauch; R Travers; G Chabot; E M Azouz; L Lalic; P J Roughley; F H Glorieux
Journal:  Bone       Date:  2002-07       Impact factor: 4.398

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  2 in total

1.  [Osteogenesis imperfecta].

Authors:  T Wirth
Journal:  Orthopade       Date:  2012-09       Impact factor: 1.087

2.  A case report: pregnancy-induced severe osteoporosis with eight vertebral fractures.

Authors:  Onder Ofluoglu; Demet Ofluoglu
Journal:  Rheumatol Int       Date:  2008-07-17       Impact factor: 3.580

  2 in total

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