Plasmapheresis, immunosuppressive therapy and anti-GBM disease prognosis: a cohort study of 107 patients.


Journal

Renal failure
ISSN: 1525-6049
Titre abrégé: Ren Fail
Pays: England
ID NLM: 8701128

Informations de publication

Date de publication:
Dec 2024
Historique:
medline: 11 9 2024
pubmed: 11 9 2024
entrez: 11 9 2024
Statut: ppublish

Résumé

Anti-glomerular basement membrane (anti-GBM) disease presents with rapidly progressive glomerulonephritis and alveolar hemorrhage, requiring urgent management. In this study, we analyzed the relationship between plasmapheresis strategy, immunosuppressive therapy and the prognosis of anti-GBM disease patients. We screened newly diagnosed anti-GBM disease patients at West China Hospital of Sichuan University from 2010 to 2021. The primary outcome was a composite endpoint of in-hospital death or dialysis dependency upon discharge. This study enrolled 107 anti-GBM disease patients. The use of plasmapheresis was independently associated with a reduced risk of primary outcome (OR: 0.179, 95% Cl: 0.051-0.630, Plasmapheresis was protective for both in-hospital outcome and long-term survival in anti-GBM disease. Patients who initiated plasmapheresis early had a better prognosis and might only need 5-10 plasmapheresis sessions to achieve maximal risk reduction. Use of high-dose methylprednisolone or cyclophosphamide pulses was not related to improved short- or long-term outcomes in anti-GBM disease.

Sections du résumé

BACKGROUND UNASSIGNED
Anti-glomerular basement membrane (anti-GBM) disease presents with rapidly progressive glomerulonephritis and alveolar hemorrhage, requiring urgent management. In this study, we analyzed the relationship between plasmapheresis strategy, immunosuppressive therapy and the prognosis of anti-GBM disease patients.
METHOD UNASSIGNED
We screened newly diagnosed anti-GBM disease patients at West China Hospital of Sichuan University from 2010 to 2021. The primary outcome was a composite endpoint of in-hospital death or dialysis dependency upon discharge.
RESULTS UNASSIGNED
This study enrolled 107 anti-GBM disease patients. The use of plasmapheresis was independently associated with a reduced risk of primary outcome (OR: 0.179, 95% Cl: 0.051-0.630,
CONCLUSION UNASSIGNED
Plasmapheresis was protective for both in-hospital outcome and long-term survival in anti-GBM disease. Patients who initiated plasmapheresis early had a better prognosis and might only need 5-10 plasmapheresis sessions to achieve maximal risk reduction. Use of high-dose methylprednisolone or cyclophosphamide pulses was not related to improved short- or long-term outcomes in anti-GBM disease.

Identifiants

pubmed: 39258391
doi: 10.1080/0886022X.2024.2400539
doi:

Substances chimiques

Immunosuppressive Agents 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

2400539

Auteurs

Ying Liu (Y)

Department of Nephrology, West China Hospital, Sichuan University, Chengdu, China.
Kidney Research Institute, West China Hospital, Sichuan University, Chengdu, China.

Yiting Wu (Y)

Department of Nephrology, West China Hospital, Sichuan University, Chengdu, China.
Kidney Research Institute, West China Hospital, Sichuan University, Chengdu, China.

Wei Wei (W)

Department of Nephrology, West China Hospital, Sichuan University, Chengdu, China.
Kidney Research Institute, West China Hospital, Sichuan University, Chengdu, China.

Letian Yang (L)

Department of Nephrology, West China Hospital, Sichuan University, Chengdu, China.
Kidney Research Institute, West China Hospital, Sichuan University, Chengdu, China.

Caihong Liu (C)

Department of Nephrology, West China Hospital, Sichuan University, Chengdu, China.
Kidney Research Institute, West China Hospital, Sichuan University, Chengdu, China.

Jian Li (J)

Department of Nephrology, West China Hospital, Sichuan University, Chengdu, China.
Kidney Research Institute, West China Hospital, Sichuan University, Chengdu, China.

Yongxiu Huang (Y)

Department of Nephrology, West China Hospital, Sichuan University, Chengdu, China.
Kidney Research Institute, West China Hospital, Sichuan University, Chengdu, China.

Bo Wang (B)

Department of Nephrology, West China Hospital, Sichuan University, Chengdu, China.
Kidney Research Institute, West China Hospital, Sichuan University, Chengdu, China.

Yingying Yang (Y)

Department of Nephrology, West China Hospital, Sichuan University, Chengdu, China.
Kidney Research Institute, West China Hospital, Sichuan University, Chengdu, China.

Ling Zhang (L)

Department of Nephrology, West China Hospital, Sichuan University, Chengdu, China.
Kidney Research Institute, West China Hospital, Sichuan University, Chengdu, China.

Ping Fu (P)

Department of Nephrology, West China Hospital, Sichuan University, Chengdu, China.
Kidney Research Institute, West China Hospital, Sichuan University, Chengdu, China.

Yuliang Zhao (Y)

Department of Nephrology, West China Hospital, Sichuan University, Chengdu, China.
Kidney Research Institute, West China Hospital, Sichuan University, Chengdu, China.

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