Diagnosis and management of von Willebrand disease in China

Jianhui Xu1, Zhiqiang Yu, Lei Zhang

  • 1State Key Laboratory of Experimental Hematology, Institute of Hematology and Blood Diseases Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Tianjin, Peoples Republic of China.

Insights

Diagnosing von Willebrand disease (VWD) in China requires improved strategies. While von Willebrand factor (VWF) antigen levels help assess severity, new diagnostic tools need wider adoption for precise VWD diagnosis.

Area of Science:

  • Hematology
  • Medical Diagnostics
  • Genetic Research

Background:

  • Bleeding disorder care in China lacks centralized organization and national protocols.
  • Existing hematologist and patient organizations are emerging to improve care.
  • Diagnosis of von Willebrand disease (VWD) in China is in its early stages, leading to frequent misdiagnosis.

Purpose of the Study:

  • To highlight the current challenges in diagnosing and managing von Willebrand disease (VWD) in China.
  • To emphasize the need for improved diagnostic strategies and wider adoption of advanced testing methods.
  • To assess the role of von Willebrand factor (VWF) antigen levels in VWD severity classification.

Main Methods:

  • Analysis of current diagnostic practices for von Willebrand disease (VWD) in China.
  • Evaluation of the utility of von Willebrand factor (VWF) antigen levels in clinical practice.
  • Review of recently developed phenotypic assays and genetic testing for VWF.

Main Results:

  • Assessment of von Willebrand factor (VWF) antigen levels is crucial for determining clinical severity and guiding replacement therapy.
  • Current treatment options for VWD in China are limited to replacement therapy and antifibrinolytic drugs.
  • New phenotypic assays and genetic testing for VWF show promise for precise diagnosis but require broader implementation.

Conclusions:

  • Significant improvements are needed in the diagnostic strategy for von Willebrand disease (VWD) in China.
  • Wider application of advanced phenotypic assays and genetic testing is essential for accurate VWD diagnosis.
  • While most VWD patients may not require replacement therapy, precise diagnosis is key for appropriate management.

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