Dr Rahul Bhargava Haematologist

MBBS, MD, DM (Clinical Haematology)

Principal Director & Chief Hematology at Fortis Hospital

MBBS, MD, DM (Clinical Haematology)

Principal Director & Chief Hematology at Fortis Hospital

Von Willebrand Disease

Contact Us

Related Videos :

Frequently Asked Questions (FAQ) :

Von Willebrand Disease (VWD) is a genetic bleeding disorder caused by a deficiency or malfunction of von Willebrand factor, a protein that helps blood clot properly.

There is no cure for VWD, but with proper management and treatment, patients can lead normal lives without major bleeding complications.

VWD is diagnosed through a series of blood tests that measure von Willebrand factor levels, its functionality, and clotting activity.

Yes, women with VWD can have children, but they should be closely monitored by a hematologist and obstetrician, as there may be increased risks of bleeding during pregnancy and childbirth.

No, VWD and hemophilia are different bleeding disorders. VWD is caused by a deficiency or dysfunction in von Willebrand factor, while hemophilia is due to a deficiency of clotting factors VIII or IX.

Introduction to Von Willebrand Disease (VWD):

Von Willebrand Disease (VWD) is a common yet often underdiagnosed bleeding disorder. It is caused by a deficiency or dysfunction of a protein known as von Willebrand factor (VWF), which plays a crucial role in blood clotting. Unlike hemophilia, which affects mostly males, VWD impacts both men and women equally. This bleeding disorder can range from mild to severe, making it essential for timely diagnosis and appropriate management. Dr. Rahul Bhargava, one of India’s leading hematologists, provides expert care and guidance for patients with VWD, ensuring the best outcomes through personalized treatment plans.

Causes and Types of Von Willebrand Disease

Causes of VWD
The primary cause of VWD is genetic, meaning it is passed down from parents to children. The body either produces insufficient von Willebrand factor or produces a defective version of it. This protein is essential for helping platelets stick together and form clots, so its absence or malfunction leads to excessive bleeding.

While VWD is inherited, some rare forms of the disease can be acquired later in life due to other medical conditions, such as autoimmune disorders, certain cancers, or cardiovascular diseases.

Types of Von Willebrand Disease

There are three main types of VWD:

  1. Type 1: This is the most common and mild form, where the body produces less VWF than normal. About 60%-80% of people with VWD have Type 1.
  2. Type 2: In this form, the von Willebrand factor that the body produces doesn’t function properly. Type 2 VWD is further divided into subtypes (2A, 2B, 2M, 2N) based on specific defects in the VWF.
  3. Type 3: This is the most severe form, where the body produces very little or no VWF at all. Patients with Type 3 VWD often experience severe bleeding episodes.

Symptoms of Von Willebrand Disease

Symptoms of VWD vary depending on the type and severity of the condition. Some common symptoms include:

  • Frequent nosebleeds that last longer than usual.
  • Heavy or prolonged menstrual bleeding in women.
  • Easy bruising with minimal or no trauma.
  • Prolonged bleeding after cuts, dental work, or surgery.
  • Blood in urine or stools, which may indicate internal bleeding.
  • Heavy bleeding after childbirth or during dental procedures.

In some cases, patients may not experience noticeable symptoms, which can delay diagnosis.

Diagnosis of Von Willebrand Disease

Diagnosing VWD requires a detailed evaluation of the patient’s medical history, family history, and specific laboratory tests. Dr. Rahul Bhargava employs state-of-the-art diagnostic methods to ensure accurate detection.

The key tests used to diagnose VWD include:

  1. Von Willebrand factor antigen test: Measures the amount of VWF in your blood.
  2. Von Willebrand factor activity tests: Assess how well VWF works in your blood to help clotting.
  3. Factor VIII clotting activity test: Measures clotting factor levels, which are often low in VWD patients.
  4. Platelet function tests: Evaluate how well platelets work to form blood clots.

Treatment for Von Willebrand Disease

The treatment of VWD depends on the type and severity of the disease. Dr. Rahul Bhargava creates individualized treatment plans to manage symptoms effectively. Some of the key treatments include:

  1. Desmopressin (DDAVP): This synthetic hormone is often the first line of treatment for Type 1 VWD. It stimulates the release of stored von Willebrand factor, helping improve clotting temporarily.
  2. Clot-stabilizing medications: These drugs (e.g., antifibrinolytics) help prevent the breakdown of clots.
  3. Von Willebrand factor replacement therapy: For severe cases, or if desmopressin is not effective, replacement therapy with von Willebrand factor concentrates may be needed.
  4. Birth control pills: Women with heavy menstrual bleeding may benefit from hormonal birth control, which can reduce bleeding.
  5. Platelet transfusions: In rare cases, patients may need platelet transfusions during surgeries or severe bleeding episodes.

Cost of Treatment and Stay in India

Lorem ipsum dolor sit amet, consectetur adipiscing elit. Ut elit tellus, luctus nec ullamcorper mattis, pulvinar dapibus leo.

×