Effectiveness of intravenous methylprednisolone pulse in patients with severe microscopic polyangiitis and granulomatosis with polyangiitis
© The Author(s) 2024. Published by Oxford University Press on behalf of the British Society for Rheumatology. All rights reserved. For permissions, please email: journals.permissionsoup.com..
OBJECTIVES: To evaluate the effectiveness and safety of two different intravenous methylprednisolone (IVMP) pulse doses in patients with severe microscopic polyangiitis (MPA) and granulomatosis with polyangiitis (GPA).
METHODS: We emulated a target trial using observational data from the nationwide registry in Japan. Patients with severe glomerulonephritis or diffuse alveolar haemorrhage were selected and pseudo-randomised into three groups using propensity score-based overlap weighting as follows: non-IVMP, IVMP 0.5 g/day, and IVMP 1.0 g/day. The primary outcome was all-cause death, and the secondary outcomes were composite all-cause death and kidney failure, severe relapse, and serious infection from 2 to 48 weeks after treatment initiation. To estimate the treatment effects, the Cox proportional hazard model and Fine-Gray subdistribution hazard model were used.
RESULTS: In this emulated target trial, of 201 eligible patients (MPA, 175; GPA, 26), 6 (2.8%) died, 4 (2.0%) had kidney failure, 11 (5.3%) had severe relapse, and 40 (19.8%) had severe infections. Hazard ratios (HR) for IVMP 0.5 g/day and IVMP 1.0 g/day pulse groups compared with non-IVMP pulse were as follows: all-cause death = 0.46 (95% confidence interval [95%CI]: 0.07-2.81) and 0.07 (95%CI: 0.01-0.41); all-cause death/kidney failure = 1.18 (95%CI: 0.26-5.31) and 0.59 (95%CI: 0.08-4.52); subdistribution HRs for severe relapse = 1.26 (95%CI: 0.12-13.70) and 3.36 (95%CI: 0.49-23.29); and serious infection = 1.88 (95%CI: 0.76-4.65) and 0.94 (95%CI: 0.28-3.13).
CONCLUSIONS: IVMP 1.0 g/day pulse may improve 48-week mortality in patients with severe MPA/GPA.
Medienart: |
E-Artikel |
---|
Erscheinungsjahr: |
2024 |
---|---|
Erschienen: |
2024 |
Enthalten in: |
Zur Gesamtaufnahme - year:2024 |
---|---|
Enthalten in: |
Rheumatology (Oxford, England) - (2024) vom: 12. Apr. |
Sprache: |
Englisch |
---|
Beteiligte Personen: |
Omura, Satoshi [VerfasserIn] |
---|
Links: |
---|
Themen: |
Granulomatosis with polyangiitis |
---|
Anmerkungen: |
Date Revised 12.04.2024 published: Print-Electronic Citation Status Publisher |
---|
doi: |
10.1093/rheumatology/keae219 |
---|
funding: |
|
---|---|
Förderinstitution / Projekttitel: |
|
PPN (Katalog-ID): |
NLM370975057 |
---|
LEADER | 01000naa a22002652 4500 | ||
---|---|---|---|
001 | NLM370975057 | ||
003 | DE-627 | ||
005 | 20240413233013.0 | ||
007 | cr uuu---uuuuu | ||
008 | 240413s2024 xx |||||o 00| ||eng c | ||
024 | 7 | |a 10.1093/rheumatology/keae219 |2 doi | |
028 | 5 | 2 | |a pubmed24n1374.xml |
035 | |a (DE-627)NLM370975057 | ||
035 | |a (NLM)38608193 | ||
035 | |a (PII)keae219 | ||
040 | |a DE-627 |b ger |c DE-627 |e rakwb | ||
041 | |a eng | ||
100 | 1 | |a Omura, Satoshi |e verfasserin |4 aut | |
245 | 1 | 0 | |a Effectiveness of intravenous methylprednisolone pulse in patients with severe microscopic polyangiitis and granulomatosis with polyangiitis |
264 | 1 | |c 2024 | |
336 | |a Text |b txt |2 rdacontent | ||
337 | |a ƒaComputermedien |b c |2 rdamedia | ||
338 | |a ƒa Online-Ressource |b cr |2 rdacarrier | ||
500 | |a Date Revised 12.04.2024 | ||
500 | |a published: Print-Electronic | ||
500 | |a Citation Status Publisher | ||
520 | |a © The Author(s) 2024. Published by Oxford University Press on behalf of the British Society for Rheumatology. All rights reserved. For permissions, please email: journals.permissionsoup.com. | ||
520 | |a OBJECTIVES: To evaluate the effectiveness and safety of two different intravenous methylprednisolone (IVMP) pulse doses in patients with severe microscopic polyangiitis (MPA) and granulomatosis with polyangiitis (GPA) | ||
520 | |a METHODS: We emulated a target trial using observational data from the nationwide registry in Japan. Patients with severe glomerulonephritis or diffuse alveolar haemorrhage were selected and pseudo-randomised into three groups using propensity score-based overlap weighting as follows: non-IVMP, IVMP 0.5 g/day, and IVMP 1.0 g/day. The primary outcome was all-cause death, and the secondary outcomes were composite all-cause death and kidney failure, severe relapse, and serious infection from 2 to 48 weeks after treatment initiation. To estimate the treatment effects, the Cox proportional hazard model and Fine-Gray subdistribution hazard model were used | ||
520 | |a RESULTS: In this emulated target trial, of 201 eligible patients (MPA, 175; GPA, 26), 6 (2.8%) died, 4 (2.0%) had kidney failure, 11 (5.3%) had severe relapse, and 40 (19.8%) had severe infections. Hazard ratios (HR) for IVMP 0.5 g/day and IVMP 1.0 g/day pulse groups compared with non-IVMP pulse were as follows: all-cause death = 0.46 (95% confidence interval [95%CI]: 0.07-2.81) and 0.07 (95%CI: 0.01-0.41); all-cause death/kidney failure = 1.18 (95%CI: 0.26-5.31) and 0.59 (95%CI: 0.08-4.52); subdistribution HRs for severe relapse = 1.26 (95%CI: 0.12-13.70) and 3.36 (95%CI: 0.49-23.29); and serious infection = 1.88 (95%CI: 0.76-4.65) and 0.94 (95%CI: 0.28-3.13) | ||
520 | |a CONCLUSIONS: IVMP 1.0 g/day pulse may improve 48-week mortality in patients with severe MPA/GPA | ||
650 | 4 | |a Journal Article | |
650 | 4 | |a Granulomatosis with polyangiitis | |
650 | 4 | |a Intravenous methylprednisolone pulse | |
650 | 4 | |a Microscopic polyangiitis | |
650 | 4 | |a Observational study | |
650 | 4 | |a Target trial emulation | |
700 | 1 | |a Kida, Takashi |e verfasserin |4 aut | |
700 | 1 | |a Noma, Hisashi |e verfasserin |4 aut | |
700 | 1 | |a Inoue, Hironori |e verfasserin |4 aut | |
700 | 1 | |a Sofue, Hideaki |e verfasserin |4 aut | |
700 | 1 | |a Sakashita, Aki |e verfasserin |4 aut | |
700 | 1 | |a Kadoya, Masatoshi |e verfasserin |4 aut | |
700 | 1 | |a Nakagomi, Daiki |e verfasserin |4 aut | |
700 | 1 | |a Abe, Yoshiyuki |e verfasserin |4 aut | |
700 | 1 | |a Takizawa, Naoho |e verfasserin |4 aut | |
700 | 1 | |a Nomura, Atsushi |e verfasserin |4 aut | |
700 | 1 | |a Kukida, Yuji |e verfasserin |4 aut | |
700 | 1 | |a Kondo, Naoya |e verfasserin |4 aut | |
700 | 1 | |a Yamano, Yasuhiko |e verfasserin |4 aut | |
700 | 1 | |a Yanagida, Takuya |e verfasserin |4 aut | |
700 | 1 | |a Endo, Koji |e verfasserin |4 aut | |
700 | 1 | |a Hirata, Shintaro |e verfasserin |4 aut | |
700 | 1 | |a Matsui, Kiyoshi |e verfasserin |4 aut | |
700 | 1 | |a Takeuchi, Tohru |e verfasserin |4 aut | |
700 | 1 | |a Ichinose, Kunihiro |e verfasserin |4 aut | |
700 | 1 | |a Kato, Masaru |e verfasserin |4 aut | |
700 | 1 | |a Yanai, Ryo |e verfasserin |4 aut | |
700 | 1 | |a Matsuo, Yusuke |e verfasserin |4 aut | |
700 | 1 | |a Shimojima, Yasuhiro |e verfasserin |4 aut | |
700 | 1 | |a Nishioka, Ryo |e verfasserin |4 aut | |
700 | 1 | |a Okazaki, Ryota |e verfasserin |4 aut | |
700 | 1 | |a Takata, Tomoaki |e verfasserin |4 aut | |
700 | 1 | |a Ito, Takafumi |e verfasserin |4 aut | |
700 | 1 | |a Moriyama, Mayuko |e verfasserin |4 aut | |
700 | 1 | |a Takatani, Ayuko |e verfasserin |4 aut | |
700 | 1 | |a Miyawaki, Yoshia |e verfasserin |4 aut | |
700 | 1 | |a Ito-Ihara, Toshiko |e verfasserin |4 aut | |
700 | 1 | |a Yajima, Nobuyuki |e verfasserin |4 aut | |
700 | 1 | |a Kawaguchi, Takashi |e verfasserin |4 aut | |
700 | 1 | |a Hirano, Aiko |e verfasserin |4 aut | |
700 | 1 | |a Fujioka, Kazuki |e verfasserin |4 aut | |
700 | 1 | |a Fujii, Wataru |e verfasserin |4 aut | |
700 | 1 | |a Seno, Takahiro |e verfasserin |4 aut | |
700 | 1 | |a Wada, Makoto |e verfasserin |4 aut | |
700 | 1 | |a Kohno, Masataka |e verfasserin |4 aut | |
700 | 1 | |a Kawahito, Yutaka |e verfasserin |4 aut | |
773 | 0 | 8 | |i Enthalten in |t Rheumatology (Oxford, England) |d 1999 |g (2024) vom: 12. Apr. |w (DE-627)NLM102581908 |x 1462-0332 |7 nnns |
773 | 1 | 8 | |g year:2024 |g day:12 |g month:04 |
856 | 4 | 0 | |u http://dx.doi.org/10.1093/rheumatology/keae219 |3 Volltext |
912 | |a GBV_USEFLAG_A | ||
912 | |a GBV_NLM | ||
951 | |a AR | ||
952 | |j 2024 |b 12 |c 04 |