Hematology focuses on diseases of the blood, bone marrow, and lymphatic system. Learn about the diagnosis and treatment of anemia, leukemia, and lymphoma.
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The therapeutic strategy for Von Willebrand Disease is highly individualized, depending on the specific VWD subtype, the severity of the bleeding phenotype, and the clinical scenario (e.g., surgery vs. spontaneous bleeding). The goal is to correct the hemostatic defect to stop or prevent bleeding. Treatment modalities are broadly categorized into non-replacement therapies (which release the body’s own stores) and replacement therapies (which provide exogenous VWF). At Liv Hospital, we employ a tiered management plan, ensuring that patients have access to both home-based treatments for minor bleeds and hospital-based protocols for major procedures.
This synthetic analogue of vasopressin is the mainstay of treatment for responsive patients.
These agents are crucial adjuncts, especially for mucocutaneous bleeding.
Local control is often sufficient for minor surface wounds.
A multi-modal approach is often needed for women.
While most VWD patients are treated “on demand” (when bleeding occurs), some require prophylaxis.
A rare but serious complication in Type 3 VWD is the development of alloantibodies (inhibitors) against the infused VWF protein.
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Yes, modern plasma-derived concentrates undergo rigorous viral inactivation steps (like heat treatment and solvent-detergent cleaning) making the risk of viral transmission extremely low.
Yes, something called “tachyphylaxis” can happen. If you use it too frequently (e.g., daily), tissue stores of VWF become depleted and the drug stops working until stores replenish (usually taking 2 to 3 days).
On demand” means taking medicine only when you bleed. “Prophylaxis” means taking medicine regularly on a schedule to prevent bleeding from ever starting.
It is generally safe, but there is a theoretical risk. It is usually not given if there is blood in the urine (hematuria) as it can cause clots in the ureters.
Inherited bleeding disorders affect thousands worldwide. Hemophilia and von Willebrand disease are the most common. Hemophilia makes it hard for blood to clot, leading to
We are looking into how desmopressin changes medicine. It’s a synthetic hormone that has made a big difference in treating many health issues. Desmopressin is
Rare bleeding disorders affect millions worldwide, leaving patients and healthcare providers searching for answers. One in 10,000 people are born with a rare bleeding disorder,
Diagnosing some blood disorders is tough. Conditions like Von Willebrand disease and myelodysplastic syndromes show symptoms that look like other common health issues. This makes
Blood donation is a key act that saves many lives. But, some medical conditions, like hemophilia, make it risky for donors and recipients. Hemophilia stops
Uncontrolled bleeding is a big risk, mainly for those on anticoagulants. We’ll look at medicines to stop or prevent bleeding. This includes anticoagulants like warfarin
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