Current treatment status of IgA nephropathy in Japan: a questionnaire survey.


Journal

Clinical and experimental nephrology
ISSN: 1437-7799
Titre abrégé: Clin Exp Nephrol
Pays: Japan
ID NLM: 9709923

Informations de publication

Date de publication:
Dec 2023
Historique:
received: 28 04 2023
accepted: 11 08 2023
medline: 17 11 2023
pubmed: 30 8 2023
entrez: 30 8 2023
Statut: ppublish

Résumé

In 2020, the Committee of Clinical Practical Guideline for IgA Nephropathy (IgAN) revised the clinical practice guidelines. Herein, we conducted a questionnaire survey to assess the potential discrepancies between clinical practice guidelines and real-world practice in Japan. A web-based survey of members of the Japanese Society of Nephrology was conducted between November 15 and December 28, 2021. A total of 217 members (internal physicians: 203, pediatricians: 14) responded to the questionnaire. Of these respondents, 94.0% answered that the clinical practice guidelines were referred to "always" or "often." Approximately 66.4% respondents answered that histological grade (H-Grade) derived from the "Clinical Guidelines for IgA nephropathy in Japan, 3rd version" and the "Oxford classification" were used for pathological classification. Moreover, 73.7% respondents answered that the risk grade (R-grade) derived from the "Clinical Guidelines for IgA nephropathy in Japan, 3rd version" was referred to for risk stratification. The prescription rate of renin-angiotensin system blockers increased based on urinary protein levels (> 1.0 g/day: 88.6%, 0.5-1.0 g/day: 71.0%, < 0.5 g/day: 25.0%). Similarly, the prescription rate of corticosteroids increased according to proteinuria levels (> 1.0 g/day: 77.8%, 0.5-1.0 g/day: 52.8%, < 0.5 g/day: 11.9%). The respondents emphasized on hematuria when using corticosteroids. In cases of hematuria, the indication rate for corticosteroids was higher than in those without hematuria, even if the urinary protein level was 1 g/gCr or less. Few severe infectious diseases or serious deterioration in glycemic control were reported during corticosteroid use. Our questionnaire survey revealed real-world aspects of IgAN treatment in Japan.

Sections du résumé

BACKGROUND BACKGROUND
In 2020, the Committee of Clinical Practical Guideline for IgA Nephropathy (IgAN) revised the clinical practice guidelines. Herein, we conducted a questionnaire survey to assess the potential discrepancies between clinical practice guidelines and real-world practice in Japan.
METHODS METHODS
A web-based survey of members of the Japanese Society of Nephrology was conducted between November 15 and December 28, 2021.
RESULTS RESULTS
A total of 217 members (internal physicians: 203, pediatricians: 14) responded to the questionnaire. Of these respondents, 94.0% answered that the clinical practice guidelines were referred to "always" or "often." Approximately 66.4% respondents answered that histological grade (H-Grade) derived from the "Clinical Guidelines for IgA nephropathy in Japan, 3rd version" and the "Oxford classification" were used for pathological classification. Moreover, 73.7% respondents answered that the risk grade (R-grade) derived from the "Clinical Guidelines for IgA nephropathy in Japan, 3rd version" was referred to for risk stratification. The prescription rate of renin-angiotensin system blockers increased based on urinary protein levels (> 1.0 g/day: 88.6%, 0.5-1.0 g/day: 71.0%, < 0.5 g/day: 25.0%). Similarly, the prescription rate of corticosteroids increased according to proteinuria levels (> 1.0 g/day: 77.8%, 0.5-1.0 g/day: 52.8%, < 0.5 g/day: 11.9%). The respondents emphasized on hematuria when using corticosteroids. In cases of hematuria, the indication rate for corticosteroids was higher than in those without hematuria, even if the urinary protein level was 1 g/gCr or less. Few severe infectious diseases or serious deterioration in glycemic control were reported during corticosteroid use.
CONCLUSION CONCLUSIONS
Our questionnaire survey revealed real-world aspects of IgAN treatment in Japan.

Identifiants

pubmed: 37646957
doi: 10.1007/s10157-023-02396-0
pii: 10.1007/s10157-023-02396-0
pmc: PMC10654181
doi:

Substances chimiques

Adrenal Cortex Hormones 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1032-1041

Subventions

Organisme : Arthritis Research UK
ID : FC001045
Pays : United Kingdom

Informations de copyright

© 2023. The Author(s).

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Auteurs

K Matsuzaki (K)

Department of Public Health, Kitasato University School of Medicine, Kanagawa, Japan.

H Suzuki (H)

Department of Nephrology, Juntendo University Urayasu Hospital, Chiba, Japan. shitoshi@juntendo.ac.jp.

M Kikuchi (M)

Department of Nephrology, Faculty of Medicine, University of Miyazaki, Miyazaki, Japan.

K Koike (K)

Division of Nephrology and Hypertension, Department of Internal Medicine, The Jikei University School of Medicine, Tokyo, Japan.

H Komatsu (H)

Center for Medical Education and Career Development, Faculty of Medicine, University of Miyazaki, Miyazaki, Japan.

K Takahashi (K)

Department of Biomedical Molecular Sciences, Fujita Health University School of Medicine, Aichi, Japan.

I Narita (I)

Division of Clinical Nephrology and Rheumatology, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan.

H Okada (H)

Department of Nephrology, Saitama Medical University, Saitama, Japan.

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