Prevalence of Giant Cell Arteritis Relapse in Patients Treated With Glucocorticoids: A Meta‐Analysis

Archive ouverte

Mainbourg, Sabine | Addario, Alexandra | Samson, Maxime | Puéchal, Xavier | François, Mathilde | Durupt, Stéphane | Gueyffier, François | Cucherat, Michel | Durieu, Isabelle | Reynaud, Quitterie | Lega, Jean‐christophe

Edité par CCSD ; Wiley-Blackwell -

International audience. Objective The relapse rate of patients with giant cell arteritis ( GCA ) treated with glucocorticoids ( GC s) alone varied widely in observational series and randomized controlled trials ( RCT s). The purpose of this systematic review was to evaluate the prevalence of relapse and predisposing factors in patients receiving GC s alone. Methods We searched Medline up to December 2017. The prevalence of relapse was pooled using a random‐effects model. Results A total of 34 studies (2,505 patients), comprising 8 RCT s, were included. The overall prevalence of relapse was 47.2% (95% confidence interval 40.0, 54.3) with a high heterogeneity (I 2 = 93%). Prevalence of relapse was significantly higher for patients included in an RCT compared to those included in an observational study ( P < 0.0001), but was not significantly different according to design ( P = 0.06). The relapse rate was associated with year of publication (34 studies, rate increase of 8.3% for 1 decade; P < 0.0001) and with shorter GC regimens (17 studies, rate decrease of 1.7% for 1 additional month; P < 0.001), the duration of scheduled GC therapy being shorter in RCT s (12.8 months) compared to observational studies (28.8 months). The effective duration of GC therapy ( P = 0.23), initial GC dose ( P = 0.49), duration of follow‐up ( P = 0.14), sex ( P = 0.29), and age ( P = 0.43) were not associated with the prevalence of relapse. Conclusion GCA relapses occur in half of patients and without improvement across decades in patients receiving GC alone, and the relapse rate is more related to short duration of GC administration than to the initial dose at induction. These results advocate for trial design with at least 12 months of GC therapy.

Consulter en ligne

Suggestions

Du même auteur

Indirect Comparison of Glucocorticoid-Sparing Agents for Remission Maintenance in Giant Cell Arteritis: A Network Meta-analysis

Archive ouverte | Mainbourg, Sabine | CCSD

International audience

Severe infections in patients with anti-neutrophil cytoplasmic antibody-associated vasculitides receiving rituximab: A meta-analysis

Archive ouverte | Thery-Casari, Clémence | CCSD

International audience

Iron Deficiency in Cystic Fibrosis: A Cross-Sectional Single-Centre Study in a Referral Adult Centre

Archive ouverte | Lobbes, Hervé | CCSD

International audience. Iron deficiency (ID) diagnosis in cystic fibrosis (CF) is challenging because of frequent systemic inflammation. We aimed to determine the prevalence and risk factors of ID in adult patients ...

Chargement des enrichissements...