dc.contributor.author
Palmowski, Andriko
dc.contributor.author
Buttgereit, Frank
dc.date.accessioned
2022-08-04T12:17:36Z
dc.date.available
2022-08-04T12:17:36Z
dc.identifier.uri
https://refubium.fu-berlin.de/handle/fub188/35728
dc.identifier.uri
http://dx.doi.org/10.17169/refubium-35443
dc.description.abstract
Purpose: While glucocorticoids (GCs) are effective in large vessel vasculitis (LVV), they may cause serious adverse events (AEs), especially if taken for longer durations and at higher doses. Unfortunately, patients suffering from LVV often need long-term treatment with GCs; therefore, toxicity needs to be expected and countered.
Recent Findings: GCs remain the mainstay of therapy for both giant cell arteritis and Takayasu arteritis. In order to minimize their toxicity, the following strategies should be considered: GC tapering, administration of conventional synthetic (e.g., methotrexate) or biologic (e.g., tocilizumab) GC-sparing agents, as well as monitoring, prophylaxis, and treatment of GC-related AEs. Several drugs are currently under investigation to expand the armamentarium for the treatment of LVV.
Summary: GC treatment in LVV is effective but associated with toxicity. Strategies to minimize this toxicity should be applied when treating patients suffering from LVV.
en
dc.rights.uri
https://creativecommons.org/licenses/by/4.0/
dc.subject
Glucocorticoids
en
dc.subject
Large vessel vasculitis
en
dc.subject
Adverse events
en
dc.subject
Takayasu arteritis
en
dc.subject
Giant cell arteritis
en
dc.subject.ddc
600 Technik, Medizin, angewandte Wissenschaften::610 Medizin und Gesundheit::610 Medizin und Gesundheit
dc.title
Reducing the Toxicity of Long-Term Glucocorticoid Treatment in Large Vessel Vasculitis
dc.type
Wissenschaftlicher Artikel
dcterms.bibliographicCitation.articlenumber
85
dcterms.bibliographicCitation.doi
10.1007/s11926-020-00961-0
dcterms.bibliographicCitation.journaltitle
Current Rheumatology Reports
dcterms.bibliographicCitation.originalpublishername
Springer Nature
dcterms.bibliographicCitation.volume
22
refubium.affiliation
Charité - Universitätsmedizin Berlin
refubium.funding
Springer Nature DEAL
refubium.resourceType.isindependentpub
no
dcterms.accessRights.openaire
open access
dcterms.bibliographicCitation.pmid
33047263
dcterms.isPartOf.issn
1523-3774
dcterms.isPartOf.eissn
1534-6307