TY - JOUR
T1 - Systematic review and meta-analysis for 2017 clinical practice guidelines of the Japan research committee of the ministry of health, labour, and welfare for intractable vasculitis for the management of ANCA-associated vasculitis
AU - Nagasaka, Kenji
AU - Harigai, Masayoshi
AU - Hagino, Noboru
AU - Hara, Akinori
AU - Horita, Tetsuya
AU - Hayashi, Taichi
AU - Itabashi, Mitsuyo
AU - Ito, Satoshi
AU - Katsumata, Yasuhiro
AU - Kawashima, Soko
AU - Naniwa, Taio
AU - Sada, Ken ei
AU - Nango, Eishu
AU - Nakayama, Takeo
AU - Tsutsumino, Michi
AU - Yamagata, Kunihiro
AU - Homma, Sakae
AU - Arimura, Yoshihiro
N1 - Funding Information:
Research grants of JPVAS from the Ministry of Health, Labour, and Welfare of Japan (H26-nanchi-nanchitou (nan)-ippan-044) and Department of Pharmacovigilance, Tokyo Medical and Dental University, were used for the payment for venues, traveling and correspondence expenses, and meals. No compensation was made to the members involved in the development of the CPG. JPVAS appreciate Tomoko Morimasa and Naoko Suwabe from Japan Library Association who carried out the literature search for SR.
Publisher Copyright:
© 2018, © 2018 Japan College of Rheumatology.
PY - 2019/1/2
Y1 - 2019/1/2
N2 - Objectives: To provide evidence for the revision of clinical practice guideline (CPG) for the management of antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV) by the Japan Research Committee for Intractable Vasculitis. Methods: PubMed, CENTRAL, and the Japan Medical Abstracts Society were searched for articles published between January 1994 and January 2015 to conduct systematic review (SR), and the quality of evidence was assessed with GRADE approach. Results: Nine randomized controlled trials (RCTs) and two non-RCTs were adopted for remission induction therapy, three RCTs and two non-RCTs for plasma exchange, and five RCTs and one non-RCT for remission maintenance therapy. A significant difference was found in efficacy and safety for the following comparisons. In the non-RCT adopted for remission induction therapy, glucocorticoid (GC) + cyclophosphamide (CY) was significantly superior to GC monotherapy regarding remission. GC + intravenous CY for remission induction therapy was superior to GC + oral CY regarding death at one year, serious adverse events, and serious infection. Concomitant use of plasma exchange for remission induction therapy of AAV with severe renal dysfunction reduced risk of end-stage renal disease versus non-users at month 3. Conclusion: This SR provided necessary evidence for developing CPG for the management of ANCA-associated vasculitis.
AB - Objectives: To provide evidence for the revision of clinical practice guideline (CPG) for the management of antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV) by the Japan Research Committee for Intractable Vasculitis. Methods: PubMed, CENTRAL, and the Japan Medical Abstracts Society were searched for articles published between January 1994 and January 2015 to conduct systematic review (SR), and the quality of evidence was assessed with GRADE approach. Results: Nine randomized controlled trials (RCTs) and two non-RCTs were adopted for remission induction therapy, three RCTs and two non-RCTs for plasma exchange, and five RCTs and one non-RCT for remission maintenance therapy. A significant difference was found in efficacy and safety for the following comparisons. In the non-RCT adopted for remission induction therapy, glucocorticoid (GC) + cyclophosphamide (CY) was significantly superior to GC monotherapy regarding remission. GC + intravenous CY for remission induction therapy was superior to GC + oral CY regarding death at one year, serious adverse events, and serious infection. Concomitant use of plasma exchange for remission induction therapy of AAV with severe renal dysfunction reduced risk of end-stage renal disease versus non-users at month 3. Conclusion: This SR provided necessary evidence for developing CPG for the management of ANCA-associated vasculitis.
KW - ANCA-associated vasculitis
KW - GRADE system
KW - granulomatosis with polyangiitis
KW - microscopic polyangiitis
KW - systematic review
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U2 - 10.1080/14397595.2018.1500111
DO - 10.1080/14397595.2018.1500111
M3 - Article
C2 - 29996690
AN - SCOPUS:85053923847
SN - 1439-7595
VL - 29
SP - 119
EP - 129
JO - Japanese Journal of Rheumatology
JF - Japanese Journal of Rheumatology
IS - 1
ER -