[Chinese guidelines on the treatment of hemophilia (2025)].

Hemophilia is an X-linked recessive inherited hemorrhagic disease primarily caused by reduced activity or deficiency of coagulation factor Ⅷ (FⅧ) or coagulation factor Ⅸ (FⅨ). Depending on the specific coagulation factor deficiency, it is classified into two types: hemophilia A (caused by F Ⅷ deficiency) and hemophilia B (caused by F Ⅸ deficiency), each attributed to gene mutations in their respective coagulation factors. Among these, hemophilia A is the most prevalent, accounting for approximately 80% of all hemophilia cases. In recent years, the advent of novel therapeutic strategies-including long-acting coagulation factor products, non-factor therapies, and gene therapy-has ushered hemophilia into a new era of treatment. Several of these innovative products have been approved for marketing in China, marking a significant improvement in treatment outcomes for patients with hemophilia. To standardize clinical practices amid these new treatment modalities and evolving therapeutic concepts, the Thrombosis and Hemostasis Group of the Hematology Branch of the Chinese Medical Association and the Chinese Hemophilia Collaboration Group have collaborated to develop relevant guidelines. These guidelines aim to provide guidance for domestic medical professionals engaged in hemophilia diagnosis and treatment, ensuring the delivery of standardized, high-quality care.

Publication Details

Journal
PubMed
Published
2025-08-14
DOI
https://doi.org/10.3760/cma.j.cn121090-20250729-00354
Primary Topic
Hemophilia Treatment and Research
Type
article
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

[Chinese guidelines on the treatment of hemophilia (2025)].

PubMed
Hemophilia Treatment and Research
article

[Chinese guidelines on the treatment of hemophilia (2025)].

article en

Abstract

Hemophilia is an X-linked recessive inherited hemorrhagic disease primarily caused by reduced activity or deficiency of coagulation factor Ⅷ (FⅧ) or coagulation factor Ⅸ (FⅨ). Depending on the specific coagulation factor deficiency, it is classified into two types: hemophilia A (caused by F Ⅷ deficiency) and hemophilia B (caused by F Ⅸ deficiency), each attributed to gene mutations in their respective coagulation factors. Among these, hemophilia A is the most prevalent, accounting for approximately 80% of all hemophilia cases. In recent years, the advent of novel therapeutic strategies-including long-acting coagulation factor products, non-factor therapies, and gene therapy-has ushered hemophilia into a new era of treatment. Several of these innovative products have been approved for marketing in China, marking a significant improvement in treatment outcomes for patients with hemophilia. To standardize clinical practices amid these new treatment modalities and evolving therapeutic concepts, the Thrombosis and Hemostasis Group of the Hematology Branch of the Chinese Medical Association and the Chinese Hemophilia Collaboration Group have collaborated to develop relevant guidelines. These guidelines aim to provide guidance for domestic medical professionals engaged in hemophilia diagnosis and treatment, ensuring the delivery of standardized, high-quality care.

PubMedVol. 46(8)
Hemophilia Treatment and Research
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.