Management of severe renal disease in anti-neutrophil-cytoplasmic-antibody-associated vasculitis: the place of rituximab and plasma exchange?
Abstract Objective The optimal induction therapy for severe glomerulonephritis of ANCA-associated vasculitis (AAV) is debated. We compared the efficacy of glucocorticoid and rituximab (RTX) or CYC induction therapy for severe AAV-related glomerulonephritis and evaluated the potential benefit of plas...
Gespeichert in:
Veröffentlicht in: | Rheumatology 2022-10, Vol.61 (10), p.4056-4064 |
---|---|
Hauptverfasser: | , , , , , , , , , , , , , , , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 4064 |
---|---|
container_issue | 10 |
container_start_page | 4056 |
container_title | Rheumatology |
container_volume | 61 |
creator | Morel, Pauline Karras, Alexandre Porcher, Raphaël Belenfant, Xavier Audard, Vincent Rafat, Cédric Hanouna, Guillaume Beaudreuil, Séverine Vilain, Cédric Hummel, Aurélie Terrier, Benjamin Pillebout, Evangeline Groh, Matthieu Jouenne, Romain Dhote, Robin Fain, Olivier Ponsoye, Matthieu Noel, Nicolas Limal, Nicolas Puéchal, Xavier Le Jeunne, Claire Guillevin, Loïc Mouthon, Luc Régent, Alexis |
description | Abstract
Objective
The optimal induction therapy for severe glomerulonephritis of ANCA-associated vasculitis (AAV) is debated. We compared the efficacy of glucocorticoid and rituximab (RTX) or CYC induction therapy for severe AAV-related glomerulonephritis and evaluated the potential benefit of plasma exchange (PE) as adjunct therapy to CYC.
Methods
This retrospective, multicentre study included AAV patients with severe renal active disease (serum creatinine level ≥350 µmol/l and/or estimated glomerular filtration ratio ≤15 ml/min/1.73 m2). Propensity-score analysis was used to adjust for potential confounders.
Results
Between 2005 and 2017, 153 patients with AAV-related glomerulonephritis were studied (96 [60%] men; mean [s.d.] age 63 [13.1] years): 19 (12%) were treated with RTX and 134 (88%) with CYC. Remission rates did not differ between RTX- and CYC-treated groups. Although more patients with RTX than CYC were dialysis-free at month (M) 12 (79% vs 68%), the difference was not significant after adjustment. Among 134 patients with CYC-treated glomerulonephritis, 76 (57%) also had PE. M3 and M6 remission rates were comparable for weighted CYC groups with or without PE. For weighted groups, the dialysis-free survival rate with CYC was higher with than without PE at M6 (72% vs 64%; odds ratio 2.58) and M12 (74% vs 60%; odds ratio 2.78) reaching statistical significance at M12.
Conclusion
We could not find any difference between RTX and CYC as induction therapy for patients with severe AAV-related glomerulonephritis. In patients receiving CYC induction regimen, the addition of PE conferred short-term benefits with higher dialysis-free rate at M12. |
doi_str_mv | 10.1093/rheumatology/keac046 |
format | Article |
fullrecord | <record><control><sourceid>proquest_hal_p</sourceid><recordid>TN_cdi_hal_primary_oai_HAL_hal_04249800v1</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><oup_id>10.1093/rheumatology/keac046</oup_id><sourcerecordid>2625272952</sourcerecordid><originalsourceid>FETCH-LOGICAL-c381t-190232af5079fe802b769783054c61811abbd1d2f1ccc933ee3572b9be6a3d153</originalsourceid><addsrcrecordid>eNqNkclu2zAQhomiQbO0b1AEPDYHxVy05hIEQbMADnppz8SIGllsKVEhKSN-iLxz5do1csyJA8433wzwE_KVs0vOKrnwHU49RGfdarP4g6BZmn8gJzzNRcKkFB8PtUiPyWkIvxljGZflJ3IsM85KmZcn5PUJBlhhj0OkrqUB1-iRehzA0sYEhIDUDBSGaJIBp-jd2Bmb6E10o4XQG51se7VrNgmE4LSBiA1dQ9CTNdGEKxo7pDOrcbvAmzi9mB7qWdnQfwqg-KI7GFZ4_ZkctWADftm_Z-TX3feftw_J8sf94-3NMtGy5DHhFRNSQJuxomqxZKIu8qooJctSnfOSc6jrhjei5VrrSkpEmRWirmrMQTY8k2fkYuftwKrRz_f4jXJg1MPNUm3_WCrSqmRszWf2244dvXueMETVm6DRWhjQTUGJXGSiEFUmZjTdodq7EDy2Bzdnahuaehua2oc2j53vN0x1j81h6H9KM7DYAW4a36f8Cz33qwg</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2625272952</pqid></control><display><type>article</type><title>Management of severe renal disease in anti-neutrophil-cytoplasmic-antibody-associated vasculitis: the place of rituximab and plasma exchange?</title><source>Oxford University Press Journals All Titles (1996-Current)</source><source>Alma/SFX Local Collection</source><creator>Morel, Pauline ; Karras, Alexandre ; Porcher, Raphaël ; Belenfant, Xavier ; Audard, Vincent ; Rafat, Cédric ; Hanouna, Guillaume ; Beaudreuil, Séverine ; Vilain, Cédric ; Hummel, Aurélie ; Terrier, Benjamin ; Pillebout, Evangeline ; Groh, Matthieu ; Jouenne, Romain ; Dhote, Robin ; Fain, Olivier ; Ponsoye, Matthieu ; Noel, Nicolas ; Limal, Nicolas ; Puéchal, Xavier ; Le Jeunne, Claire ; Guillevin, Loïc ; Mouthon, Luc ; Régent, Alexis</creator><creatorcontrib>Morel, Pauline ; Karras, Alexandre ; Porcher, Raphaël ; Belenfant, Xavier ; Audard, Vincent ; Rafat, Cédric ; Hanouna, Guillaume ; Beaudreuil, Séverine ; Vilain, Cédric ; Hummel, Aurélie ; Terrier, Benjamin ; Pillebout, Evangeline ; Groh, Matthieu ; Jouenne, Romain ; Dhote, Robin ; Fain, Olivier ; Ponsoye, Matthieu ; Noel, Nicolas ; Limal, Nicolas ; Puéchal, Xavier ; Le Jeunne, Claire ; Guillevin, Loïc ; Mouthon, Luc ; Régent, Alexis ; French Vasculitis Study Group (FSVG)</creatorcontrib><description>Abstract
Objective
The optimal induction therapy for severe glomerulonephritis of ANCA-associated vasculitis (AAV) is debated. We compared the efficacy of glucocorticoid and rituximab (RTX) or CYC induction therapy for severe AAV-related glomerulonephritis and evaluated the potential benefit of plasma exchange (PE) as adjunct therapy to CYC.
Methods
This retrospective, multicentre study included AAV patients with severe renal active disease (serum creatinine level ≥350 µmol/l and/or estimated glomerular filtration ratio ≤15 ml/min/1.73 m2). Propensity-score analysis was used to adjust for potential confounders.
Results
Between 2005 and 2017, 153 patients with AAV-related glomerulonephritis were studied (96 [60%] men; mean [s.d.] age 63 [13.1] years): 19 (12%) were treated with RTX and 134 (88%) with CYC. Remission rates did not differ between RTX- and CYC-treated groups. Although more patients with RTX than CYC were dialysis-free at month (M) 12 (79% vs 68%), the difference was not significant after adjustment. Among 134 patients with CYC-treated glomerulonephritis, 76 (57%) also had PE. M3 and M6 remission rates were comparable for weighted CYC groups with or without PE. For weighted groups, the dialysis-free survival rate with CYC was higher with than without PE at M6 (72% vs 64%; odds ratio 2.58) and M12 (74% vs 60%; odds ratio 2.78) reaching statistical significance at M12.
Conclusion
We could not find any difference between RTX and CYC as induction therapy for patients with severe AAV-related glomerulonephritis. In patients receiving CYC induction regimen, the addition of PE conferred short-term benefits with higher dialysis-free rate at M12.</description><identifier>ISSN: 1462-0324</identifier><identifier>EISSN: 1462-0332</identifier><identifier>EISSN: 1460-2172</identifier><identifier>DOI: 10.1093/rheumatology/keac046</identifier><identifier>PMID: 35108368</identifier><language>eng</language><publisher>England: Oxford University Press</publisher><subject>Human health and pathology ; Life Sciences</subject><ispartof>Rheumatology, 2022-10, Vol.61 (10), p.4056-4064</ispartof><rights>The Author(s) 2022. Published by Oxford University Press on behalf of the British Society for Rheumatology. All rights reserved. For permissions, please email: journals.permissions@oup.com 2022</rights><rights>The Author(s) 2022. Published by Oxford University Press on behalf of the British Society for Rheumatology. All rights reserved. For permissions, please email: journals.permissions@oup.com.</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c381t-190232af5079fe802b769783054c61811abbd1d2f1ccc933ee3572b9be6a3d153</citedby><cites>FETCH-LOGICAL-c381t-190232af5079fe802b769783054c61811abbd1d2f1ccc933ee3572b9be6a3d153</cites><orcidid>0000-0003-3573-9203 ; 0000-0001-6463-2160 ; 0000-0002-5277-4679 ; 0000-0002-1974-3870 ; 0000-0002-9838-246X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,1583,27923,27924</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35108368$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.science/hal-04249800$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Morel, Pauline</creatorcontrib><creatorcontrib>Karras, Alexandre</creatorcontrib><creatorcontrib>Porcher, Raphaël</creatorcontrib><creatorcontrib>Belenfant, Xavier</creatorcontrib><creatorcontrib>Audard, Vincent</creatorcontrib><creatorcontrib>Rafat, Cédric</creatorcontrib><creatorcontrib>Hanouna, Guillaume</creatorcontrib><creatorcontrib>Beaudreuil, Séverine</creatorcontrib><creatorcontrib>Vilain, Cédric</creatorcontrib><creatorcontrib>Hummel, Aurélie</creatorcontrib><creatorcontrib>Terrier, Benjamin</creatorcontrib><creatorcontrib>Pillebout, Evangeline</creatorcontrib><creatorcontrib>Groh, Matthieu</creatorcontrib><creatorcontrib>Jouenne, Romain</creatorcontrib><creatorcontrib>Dhote, Robin</creatorcontrib><creatorcontrib>Fain, Olivier</creatorcontrib><creatorcontrib>Ponsoye, Matthieu</creatorcontrib><creatorcontrib>Noel, Nicolas</creatorcontrib><creatorcontrib>Limal, Nicolas</creatorcontrib><creatorcontrib>Puéchal, Xavier</creatorcontrib><creatorcontrib>Le Jeunne, Claire</creatorcontrib><creatorcontrib>Guillevin, Loïc</creatorcontrib><creatorcontrib>Mouthon, Luc</creatorcontrib><creatorcontrib>Régent, Alexis</creatorcontrib><creatorcontrib>French Vasculitis Study Group (FSVG)</creatorcontrib><title>Management of severe renal disease in anti-neutrophil-cytoplasmic-antibody-associated vasculitis: the place of rituximab and plasma exchange?</title><title>Rheumatology</title><addtitle>Rheumatology (Oxford)</addtitle><description>Abstract
Objective
The optimal induction therapy for severe glomerulonephritis of ANCA-associated vasculitis (AAV) is debated. We compared the efficacy of glucocorticoid and rituximab (RTX) or CYC induction therapy for severe AAV-related glomerulonephritis and evaluated the potential benefit of plasma exchange (PE) as adjunct therapy to CYC.
Methods
This retrospective, multicentre study included AAV patients with severe renal active disease (serum creatinine level ≥350 µmol/l and/or estimated glomerular filtration ratio ≤15 ml/min/1.73 m2). Propensity-score analysis was used to adjust for potential confounders.
Results
Between 2005 and 2017, 153 patients with AAV-related glomerulonephritis were studied (96 [60%] men; mean [s.d.] age 63 [13.1] years): 19 (12%) were treated with RTX and 134 (88%) with CYC. Remission rates did not differ between RTX- and CYC-treated groups. Although more patients with RTX than CYC were dialysis-free at month (M) 12 (79% vs 68%), the difference was not significant after adjustment. Among 134 patients with CYC-treated glomerulonephritis, 76 (57%) also had PE. M3 and M6 remission rates were comparable for weighted CYC groups with or without PE. For weighted groups, the dialysis-free survival rate with CYC was higher with than without PE at M6 (72% vs 64%; odds ratio 2.58) and M12 (74% vs 60%; odds ratio 2.78) reaching statistical significance at M12.
Conclusion
We could not find any difference between RTX and CYC as induction therapy for patients with severe AAV-related glomerulonephritis. In patients receiving CYC induction regimen, the addition of PE conferred short-term benefits with higher dialysis-free rate at M12.</description><subject>Human health and pathology</subject><subject>Life Sciences</subject><issn>1462-0324</issn><issn>1462-0332</issn><issn>1460-2172</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNqNkclu2zAQhomiQbO0b1AEPDYHxVy05hIEQbMADnppz8SIGllsKVEhKSN-iLxz5do1csyJA8433wzwE_KVs0vOKrnwHU49RGfdarP4g6BZmn8gJzzNRcKkFB8PtUiPyWkIvxljGZflJ3IsM85KmZcn5PUJBlhhj0OkrqUB1-iRehzA0sYEhIDUDBSGaJIBp-jd2Bmb6E10o4XQG51se7VrNgmE4LSBiA1dQ9CTNdGEKxo7pDOrcbvAmzi9mB7qWdnQfwqg-KI7GFZ4_ZkctWADftm_Z-TX3feftw_J8sf94-3NMtGy5DHhFRNSQJuxomqxZKIu8qooJctSnfOSc6jrhjei5VrrSkpEmRWirmrMQTY8k2fkYuftwKrRz_f4jXJg1MPNUm3_WCrSqmRszWf2244dvXueMETVm6DRWhjQTUGJXGSiEFUmZjTdodq7EDy2Bzdnahuaehua2oc2j53vN0x1j81h6H9KM7DYAW4a36f8Cz33qwg</recordid><startdate>20221006</startdate><enddate>20221006</enddate><creator>Morel, Pauline</creator><creator>Karras, Alexandre</creator><creator>Porcher, Raphaël</creator><creator>Belenfant, Xavier</creator><creator>Audard, Vincent</creator><creator>Rafat, Cédric</creator><creator>Hanouna, Guillaume</creator><creator>Beaudreuil, Séverine</creator><creator>Vilain, Cédric</creator><creator>Hummel, Aurélie</creator><creator>Terrier, Benjamin</creator><creator>Pillebout, Evangeline</creator><creator>Groh, Matthieu</creator><creator>Jouenne, Romain</creator><creator>Dhote, Robin</creator><creator>Fain, Olivier</creator><creator>Ponsoye, Matthieu</creator><creator>Noel, Nicolas</creator><creator>Limal, Nicolas</creator><creator>Puéchal, Xavier</creator><creator>Le Jeunne, Claire</creator><creator>Guillevin, Loïc</creator><creator>Mouthon, Luc</creator><creator>Régent, Alexis</creator><general>Oxford University Press</general><general>Oxford University Press (OUP)</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>1XC</scope><orcidid>https://orcid.org/0000-0003-3573-9203</orcidid><orcidid>https://orcid.org/0000-0001-6463-2160</orcidid><orcidid>https://orcid.org/0000-0002-5277-4679</orcidid><orcidid>https://orcid.org/0000-0002-1974-3870</orcidid><orcidid>https://orcid.org/0000-0002-9838-246X</orcidid></search><sort><creationdate>20221006</creationdate><title>Management of severe renal disease in anti-neutrophil-cytoplasmic-antibody-associated vasculitis: the place of rituximab and plasma exchange?</title><author>Morel, Pauline ; Karras, Alexandre ; Porcher, Raphaël ; Belenfant, Xavier ; Audard, Vincent ; Rafat, Cédric ; Hanouna, Guillaume ; Beaudreuil, Séverine ; Vilain, Cédric ; Hummel, Aurélie ; Terrier, Benjamin ; Pillebout, Evangeline ; Groh, Matthieu ; Jouenne, Romain ; Dhote, Robin ; Fain, Olivier ; Ponsoye, Matthieu ; Noel, Nicolas ; Limal, Nicolas ; Puéchal, Xavier ; Le Jeunne, Claire ; Guillevin, Loïc ; Mouthon, Luc ; Régent, Alexis</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c381t-190232af5079fe802b769783054c61811abbd1d2f1ccc933ee3572b9be6a3d153</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Human health and pathology</topic><topic>Life Sciences</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Morel, Pauline</creatorcontrib><creatorcontrib>Karras, Alexandre</creatorcontrib><creatorcontrib>Porcher, Raphaël</creatorcontrib><creatorcontrib>Belenfant, Xavier</creatorcontrib><creatorcontrib>Audard, Vincent</creatorcontrib><creatorcontrib>Rafat, Cédric</creatorcontrib><creatorcontrib>Hanouna, Guillaume</creatorcontrib><creatorcontrib>Beaudreuil, Séverine</creatorcontrib><creatorcontrib>Vilain, Cédric</creatorcontrib><creatorcontrib>Hummel, Aurélie</creatorcontrib><creatorcontrib>Terrier, Benjamin</creatorcontrib><creatorcontrib>Pillebout, Evangeline</creatorcontrib><creatorcontrib>Groh, Matthieu</creatorcontrib><creatorcontrib>Jouenne, Romain</creatorcontrib><creatorcontrib>Dhote, Robin</creatorcontrib><creatorcontrib>Fain, Olivier</creatorcontrib><creatorcontrib>Ponsoye, Matthieu</creatorcontrib><creatorcontrib>Noel, Nicolas</creatorcontrib><creatorcontrib>Limal, Nicolas</creatorcontrib><creatorcontrib>Puéchal, Xavier</creatorcontrib><creatorcontrib>Le Jeunne, Claire</creatorcontrib><creatorcontrib>Guillevin, Loïc</creatorcontrib><creatorcontrib>Mouthon, Luc</creatorcontrib><creatorcontrib>Régent, Alexis</creatorcontrib><creatorcontrib>French Vasculitis Study Group (FSVG)</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Hyper Article en Ligne (HAL)</collection><jtitle>Rheumatology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Morel, Pauline</au><au>Karras, Alexandre</au><au>Porcher, Raphaël</au><au>Belenfant, Xavier</au><au>Audard, Vincent</au><au>Rafat, Cédric</au><au>Hanouna, Guillaume</au><au>Beaudreuil, Séverine</au><au>Vilain, Cédric</au><au>Hummel, Aurélie</au><au>Terrier, Benjamin</au><au>Pillebout, Evangeline</au><au>Groh, Matthieu</au><au>Jouenne, Romain</au><au>Dhote, Robin</au><au>Fain, Olivier</au><au>Ponsoye, Matthieu</au><au>Noel, Nicolas</au><au>Limal, Nicolas</au><au>Puéchal, Xavier</au><au>Le Jeunne, Claire</au><au>Guillevin, Loïc</au><au>Mouthon, Luc</au><au>Régent, Alexis</au><aucorp>French Vasculitis Study Group (FSVG)</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Management of severe renal disease in anti-neutrophil-cytoplasmic-antibody-associated vasculitis: the place of rituximab and plasma exchange?</atitle><jtitle>Rheumatology</jtitle><addtitle>Rheumatology (Oxford)</addtitle><date>2022-10-06</date><risdate>2022</risdate><volume>61</volume><issue>10</issue><spage>4056</spage><epage>4064</epage><pages>4056-4064</pages><issn>1462-0324</issn><eissn>1462-0332</eissn><eissn>1460-2172</eissn><abstract>Abstract
Objective
The optimal induction therapy for severe glomerulonephritis of ANCA-associated vasculitis (AAV) is debated. We compared the efficacy of glucocorticoid and rituximab (RTX) or CYC induction therapy for severe AAV-related glomerulonephritis and evaluated the potential benefit of plasma exchange (PE) as adjunct therapy to CYC.
Methods
This retrospective, multicentre study included AAV patients with severe renal active disease (serum creatinine level ≥350 µmol/l and/or estimated glomerular filtration ratio ≤15 ml/min/1.73 m2). Propensity-score analysis was used to adjust for potential confounders.
Results
Between 2005 and 2017, 153 patients with AAV-related glomerulonephritis were studied (96 [60%] men; mean [s.d.] age 63 [13.1] years): 19 (12%) were treated with RTX and 134 (88%) with CYC. Remission rates did not differ between RTX- and CYC-treated groups. Although more patients with RTX than CYC were dialysis-free at month (M) 12 (79% vs 68%), the difference was not significant after adjustment. Among 134 patients with CYC-treated glomerulonephritis, 76 (57%) also had PE. M3 and M6 remission rates were comparable for weighted CYC groups with or without PE. For weighted groups, the dialysis-free survival rate with CYC was higher with than without PE at M6 (72% vs 64%; odds ratio 2.58) and M12 (74% vs 60%; odds ratio 2.78) reaching statistical significance at M12.
Conclusion
We could not find any difference between RTX and CYC as induction therapy for patients with severe AAV-related glomerulonephritis. In patients receiving CYC induction regimen, the addition of PE conferred short-term benefits with higher dialysis-free rate at M12.</abstract><cop>England</cop><pub>Oxford University Press</pub><pmid>35108368</pmid><doi>10.1093/rheumatology/keac046</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0003-3573-9203</orcidid><orcidid>https://orcid.org/0000-0001-6463-2160</orcidid><orcidid>https://orcid.org/0000-0002-5277-4679</orcidid><orcidid>https://orcid.org/0000-0002-1974-3870</orcidid><orcidid>https://orcid.org/0000-0002-9838-246X</orcidid></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1462-0324 |
ispartof | Rheumatology, 2022-10, Vol.61 (10), p.4056-4064 |
issn | 1462-0324 1462-0332 1460-2172 |
language | eng |
recordid | cdi_hal_primary_oai_HAL_hal_04249800v1 |
source | Oxford University Press Journals All Titles (1996-Current); Alma/SFX Local Collection |
subjects | Human health and pathology Life Sciences |
title | Management of severe renal disease in anti-neutrophil-cytoplasmic-antibody-associated vasculitis: the place of rituximab and plasma exchange? |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-12T03%3A30%3A22IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_hal_p&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Management%20of%20severe%20renal%20disease%20in%20anti-neutrophil-cytoplasmic-antibody-associated%20vasculitis:%20the%20place%20of%20rituximab%20and%20plasma%20exchange?&rft.jtitle=Rheumatology&rft.au=Morel,%20Pauline&rft.aucorp=French%20Vasculitis%20Study%20Group%20(FSVG)&rft.date=2022-10-06&rft.volume=61&rft.issue=10&rft.spage=4056&rft.epage=4064&rft.pages=4056-4064&rft.issn=1462-0324&rft.eissn=1462-0332&rft_id=info:doi/10.1093/rheumatology/keac046&rft_dat=%3Cproquest_hal_p%3E2625272952%3C/proquest_hal_p%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2625272952&rft_id=info:pmid/35108368&rft_oup_id=10.1093/rheumatology/keac046&rfr_iscdi=true |