Introduction: Spondyloarthritis (SpA) are chronic inflammatory diseases with overlapping pathogenic mechanisms and clinical features. Treatment armamentarium against SpA includes non-steroidal anti-inflammatory drugs, glucocorticoids, conventional disease-modifying antirheumatic drugs (DMARDs, including sulfasalazine, methotrexate, leflunomide, cyclosporine), targeted synthetic DMARDs (apremilast) and biological DMARDs (TNF inhibitors, anti-IL 12/23 and anti-IL-17 agents). Areas covered: A narrative review of published literature on safety profile of available SpA treatment options was performed. Readers will be provided with a comprehensive overview on frequent and rare adverse events associated with each drug listed in current SpA treatment recommendations. Expert opinion: The overall safety profile of such molecules is good and serious adverse events are rare but need to be promptly recognized and treated. However, the monitoring of adverse events is a major challenge for clinicians because it is not adequately addressed by current treatment recommendations. A tailored treatment is crucial and rheumatologists must accurately select patients in order to identify those more susceptible to develop adverse events.

Safety of treatment options for spondyloarthritis: a narrative review / D'Angelo S.; Carriero A.; Gilio M.; Ursini F.; Leccese P.; Palazzi C.. - In: EXPERT OPINION ON DRUG SAFETY. - ISSN 1474-0338. - STAMPA. - 17:5(2018), pp. 475-486. [10.1080/14740338.2018.1448785]

Safety of treatment options for spondyloarthritis: a narrative review

Ursini F.;
2018

Abstract

Introduction: Spondyloarthritis (SpA) are chronic inflammatory diseases with overlapping pathogenic mechanisms and clinical features. Treatment armamentarium against SpA includes non-steroidal anti-inflammatory drugs, glucocorticoids, conventional disease-modifying antirheumatic drugs (DMARDs, including sulfasalazine, methotrexate, leflunomide, cyclosporine), targeted synthetic DMARDs (apremilast) and biological DMARDs (TNF inhibitors, anti-IL 12/23 and anti-IL-17 agents). Areas covered: A narrative review of published literature on safety profile of available SpA treatment options was performed. Readers will be provided with a comprehensive overview on frequent and rare adverse events associated with each drug listed in current SpA treatment recommendations. Expert opinion: The overall safety profile of such molecules is good and serious adverse events are rare but need to be promptly recognized and treated. However, the monitoring of adverse events is a major challenge for clinicians because it is not adequately addressed by current treatment recommendations. A tailored treatment is crucial and rheumatologists must accurately select patients in order to identify those more susceptible to develop adverse events.
2018
Safety of treatment options for spondyloarthritis: a narrative review / D'Angelo S.; Carriero A.; Gilio M.; Ursini F.; Leccese P.; Palazzi C.. - In: EXPERT OPINION ON DRUG SAFETY. - ISSN 1474-0338. - STAMPA. - 17:5(2018), pp. 475-486. [10.1080/14740338.2018.1448785]
D'Angelo S.; Carriero A.; Gilio M.; Ursini F.; Leccese P.; Palazzi C.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11585/781744
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