2006
DOI: 10.1016/s1098-3015(10)63261-5
|View full text |Cite
|
Sign up to set email alerts
|

Par2 Zoledronic Acid in the Long-Term Management of Paget's Disease of the Bone in Germany-a Costsaving Approach?

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1

Citation Types

0
1
0

Year Published

2006
2006
2024
2024

Publication Types

Select...
4

Relationship

0
4

Authors

Journals

citations
Cited by 4 publications
(1 citation statement)
references
References 0 publications
0
1
0
Order By: Relevance
“…Despite a limited number of comparative studies with N-BPs have been performed in PDB, it is well established that zoledronate represents the most effective regimen, improving pain and allowing the long-term suppression of bone turnover for more than 5 years in most patients [ 72 78 ]. Together with its increased efficacy, zoledronate has been also considered a cost-effective approach for PDB [ 129 , 130 ]. Thus, in the absence of contraindications or unless intravenous treatment cannot be performed, this drug should be considered as a first-line treatment option in most patients with PDB, and particularly in those with polyostotic disease or carriers of mutations in SQSTM1 , ZNF687 or PFN1 genes, which generally have a more severe disease [ 53 57 ].…”
Section: Results and Recommendationsmentioning
confidence: 99%
“…Despite a limited number of comparative studies with N-BPs have been performed in PDB, it is well established that zoledronate represents the most effective regimen, improving pain and allowing the long-term suppression of bone turnover for more than 5 years in most patients [ 72 78 ]. Together with its increased efficacy, zoledronate has been also considered a cost-effective approach for PDB [ 129 , 130 ]. Thus, in the absence of contraindications or unless intravenous treatment cannot be performed, this drug should be considered as a first-line treatment option in most patients with PDB, and particularly in those with polyostotic disease or carriers of mutations in SQSTM1 , ZNF687 or PFN1 genes, which generally have a more severe disease [ 53 57 ].…”
Section: Results and Recommendationsmentioning
confidence: 99%