dc.contributor.author | Besada, Emilio | |
dc.contributor.author | Koldingsnes, Wenche | |
dc.contributor.author | Nossent, Hans C | |
dc.date.accessioned | 2016-03-10T14:08:34Z | |
dc.date.available | 2016-03-10T14:08:34Z | |
dc.date.issued | 2015-06-25 | |
dc.description.abstract | Objective. Chronic nasal carriage of Staphylococcus aureus (SA) increases the risk
of relapse while Rituximab (RTX) is an effective agent for inducing and maintaining
remission in patients with Granulomatosis with polyangiitis (GPA). We investigated
whether B cell depletion and hypogammaglobulinemia that occur during RTX treatment
increase the risk of chronic SA nasal carriage and subsequent disease flares, in
GPA patients on long-term RTX maintenance therapy.
<p>Methods. Retrospective cohort study from a disease registry involving 29 GPA patients
receiving RTX maintenance (median RTX dose of 9 g) during a median period
of 49 months. Nasal swabs were collected prior and during RTX for a median of 3 and
9 swabs respectively. Persistent SA nasal carriage was defined with the presence of SA
in more than 75% of nasal swabs.
<p>Results. SA nasal carriage did not change during RTX (p = 0.297). However, the rate
of positive nasal swabs in GPA patients with transient SA nasal carriage during RTX
maintenance increased from 0 prior RTX to 0.42 during RTX (p = 0.017). Persistent
SA nasal carriage did not increase the risk of relapses (p = 0.844), of hypogammaglobulinemia
(p = 0.122) and of severe infections (p = 0.144), but reduced the risk
of chronic infections (p = 0.044). Change in SA carriage status during RTX did not
influence the risk of relapses (p = 0.756), hypogammaglobulinamia (p = 0.474) and
infections, either severe (p = 0.913) or chronic (p = 0.121).
<p>Conclusion. Long-term RTX maintenance therapy in GPA patients did not
significantly influence SA nasal carriage status. Persistent SA carriage during
long-term RTX treatment did not seem to increase the risk of relapses, but seemed to
decrease the risk of hypogammaglobulinemia associated chronic infections. | en_US |
dc.identifier.citation | PeerJ Preprints 2015 | en_US |
dc.identifier.cristinID | FRIDAID 1239521 | |
dc.identifier.doi | 10.7287/peerj.preprints.972v1 | |
dc.identifier.issn | 2167-9843 | |
dc.identifier.uri | https://hdl.handle.net/10037/8861 | |
dc.identifier.urn | URN:NBN:no-uit_munin_8400 | |
dc.language.iso | eng | en_US |
dc.publisher | PeerJ | en_US |
dc.relation.uri | https://dx.doi.org/10.7287/peerj.preprints.972v1 | en_US |
dc.rights.accessRights | openAccess | |
dc.subject | VDP::Medisinske Fag: 700::Klinisk medisinske fag: 750 | en_US |
dc.subject | VDP::Medical disciplines: 700::Clinical medical disciplines: 750 | en_US |
dc.subject | Rituximab | en_US |
dc.subject | Granulomatosis with polyangiitis | en_US |
dc.subject | Vasculitis | en_US |
dc.subject | Relapse | en_US |
dc.subject | Infections | en_US |
dc.subject | Hypogammaglobulinemia | en_US |
dc.subject | Maintenance | en_US |
dc.subject | Nasal carriage | en_US |
dc.subject | Microbiome | en_US |
dc.subject | Staphylococcus aureus | en_US |
dc.title | Staphylococcus Aureus carriage and long-term Rituximab treatment for Granulomatosis with polyangiitis | en_US |
dc.type | Journal article | en_US |
dc.type | Tidsskriftartikkel | en_US |
dc.type | Peer reviewed | en_US |