Article (Scientific journals)
Cutaneous side effects of antiosteoporosis treatments
Musette, P.; Kaufman, J.-M.; Rizzoli, R. et al.
2011In Therapeutic Advances in Musculoskeletal Disease, 3 (1), p. 31-41
Peer Reviewed verified by ORBi
 

Files


Full Text
Cutaneous side effects of antiosteoporosis treatments.pdf
Publisher postprint (279.14 kB)
Request a copy

All documents in ORBi are protected by a user license.

Send to



Details



Keywords :
Antiosteoporosis treatments; Cutaneous adverse reactions; Hypersensitivity reactions; Osteoporosis; DRESS syndrome; Stevens Johnson syndrome
Abstract :
[en] Cutaneous adverse reactions are reported for many therapeutic agents and, in general, are observed in between 0% and 8% of treated patients depending on the drug. Antiosteoporotic agents are considered to be safe in terms of cutaneous effects, however there have been a number of case reports of cutaneous adverse reactions which warrant consideration. This was the subject of a working group meeting of the European Society for Clinical and Economic Aspects of Osteoporosis and Osteoarthritis in April 2009, which focused on the impact of cutaneous adverse reactions and drug-induced hypersensitivity in the management of postmenopausal osteoporosis. This position paper was drafted following these discussions and includes a flowchart for their recognition. Cutaneous adverse reactions observed with antiosteoporotic agents were reviewed and included information from case reports, regulatory documents and pharmacovigilance. These reactions ranged from benign effects including exanthematous or maculopapular eruption (drug rash), photosensitivity and urticaria, to the severe and potentially life-threatening reactions of angioedema, drug rash with eosinophilia and systemic symptoms (DRESS), Stevens Johnson syndrome and toxic epidermal necrolysis. A review of the available evidence demonstrates that cutaneous adverse reactions occur with all commonly used antiosteoporotic treatments. Notably, there are reports of Stevens Johnson syndrome and toxic epidermal necrolysis for bisphosphonates, and of DRESS and toxic epidermal necrolysis for strontium ranelate. These severe reactions remain very rare (<1 in 10,000 cases). In general, with proper management and early recognition, including immediate and permanent withdrawal of the culprit agent, accompanied by hospitalization, rehydration and systemic corticosteroids if necessary, the prognosis is positive. © The Author(s), 2011.
Disciplines :
General & internal medicine
Author, co-author :
Musette, P.;  Department of Dermatology, Rouen University Hospital, 76038 Rouen, France
Kaufman, J.-M.;  Department of Internal Medicine, Gent University Hospital, B-9000 Gent, Belgium
Rizzoli, R.;  Department of Rehabilitation and Geriatrix - Service of Bone Diseases, Geneva University Hospital, 1211 Geneva 14, Switzerland
Cacoub, P.;  Department of Internal Medicine, AP-HP, Hôpital Pitié Salpétrière and Université Pierre et Marie Curie, 75013 Paris, France
Brandi, M. L.;  Department of Internal Medicine, University of Florence, 50139 Florence, Italy
REGINSTER, Jean-Yves  ;  Centre Hospitalier Universitaire de Liège - CHU > Médecine de l'appareil locomoteur
Language :
English
Title :
Cutaneous side effects of antiosteoporosis treatments
Publication date :
2011
Journal title :
Therapeutic Advances in Musculoskeletal Disease
ISSN :
1759-720X
eISSN :
1759-7218
Publisher :
SAGE Publications, New York, United States - New York
Volume :
3
Issue :
1
Pages :
31-41
Peer reviewed :
Peer Reviewed verified by ORBi
Available on ORBi :
since 18 October 2013

Statistics


Number of views
48 (2 by ULiège)
Number of downloads
0 (0 by ULiège)

Scopus citations®
 
13
Scopus citations®
without self-citations
9
OpenCitations
 
8

Bibliography


Similar publications



Contact ORBi