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Establish a Latin-American network of centers and professionals with the aim of:
von Willebrand disease (VWD) is the most common autosomal bleeding disorder, mostly inherited as dominant trait. VWD is due to deficiency/abnormality of von Willebrand factor (VWF). The prevalence of VWD is unknown, but estimated as 0.1% to 1% of the general population. Although the autosomal inheritance pattern would suggest an equal distribution of male and female patients, the disease is diagnosed in more females because of female-specific hemostatic challenges: menses, ovulation, pregnancy and childbirth. Diagnosis of VWD is made by assessing personal and family history of bleeding, physical examination and completed with specific laboratory tests.
There is limited information on the epidemiology of VWD in developing countries. Some countries in Latin America have registries of severe disease that, although it is the rarest form, carries the highest costs for regional health systems. So that the prevalence of clinical symptoms and laboratory features of the disease as well as the management of the disease in Latin America is unknown.
The present project aims to establish a network of centers and professionals with the objective to register and investigate all patients with VWD in Latin America, using a database available online common to all, to gain understanding about phenotype, genotype and management of VWD in the region.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Subjects with von Willbrand Disease Acquired |
| ||
| Subjects with von Willbrand Disease Congenital |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Observation | Other | No interventions planned: treatment of patients at the discretion of the treating/responsible physician |
|
| Measure | Description | Time Frame |
|---|---|---|
| Register of VWD patients in Latin America | Clinical presentation in hereditary/acquired VWD. Phenotype and genetic diagnosis. | assessed up to 33 months |
| Registration of the bleeding history | Bleeding history is an essential component in the diagnosis of von Willebrand disease (VWD). ISTH Bleeding Assessment Tool (ISTH-BAT) is used to assist the diagnosis. | From date of selection until the date registration, assessed up to 33 months. |
| Response to Treatment: Follow up of FVIII, VWF:Ag and VWF:RCo | The aim of therapy is to correct the dual hemostatic defect, due to defective platelet adhesion-aggregation and abnormal coagulation due to Factor VIII (FVIII) deficiency. The choice of treatment depends on a number of factors, including the severity of the bleed, the procedure planned, the subtype and severity of the disease and the age and morbidity of the patient. The evaluation of the response to the treatment is going to be through the measure of FVIII, vWF Antigen (VWF:Ag) and vWF ristocetin cofactor (vWF:RCo). | Until the end of the registry, an average of 33 months. |
| Adverse Events: Number of patients with bleeding events | Bleeding disorders and their treatment impact on patients, especially in women, can affect the everyday life of patients and their families. Measure of number of bleeding events, laboratory results such as Sodium. | until the end of the registry, an average of 33 months. |
| Measure | Description | Time Frame |
|---|---|---|
| Pregnancy outcome: Follow up of FVIII, VWF:Ag and VWF:RCo | For many women with VWD, pregnancy is a time of few bleeding problems. Women with Type 3 von Willebrand disease seem to have more frequent miscarriages, especially during the first trimester. The evaluation of the response to the treatment is going to be through the measure of FVIII, vWF Antigen (VWF:Ag) and vWF ristocetin cofactor (vWF:RCo). |
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Inclusion Criteria:
Exclusion Criteria:
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Patients with von Willebrand disease
| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Analia Sanchez Luceros, PhD, MD | Contact | +5491152203235 | sanchezluceros@gmail.com | |
| Analia Kinen | Contact | analiakinen@hotmail.com |
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| ID | Term |
|---|---|
| D014842 | von Willebrand Diseases |
| ID | Term |
|---|---|
| D025861 | Blood Coagulation Disorders, Inherited |
| D001778 | Blood Coagulation Disorders |
| D006402 | Hematologic Diseases |
| D006425 | Hemic and Lymphatic Diseases |
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| ID | Term |
|---|---|
| D019370 | Observation |
| ID | Term |
|---|---|
| D008722 | Methods |
| D008919 | Investigative Techniques |
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Plasma, DNA
| Observation | Other | No interventions planned: treatment of patients at the discretion of the treating/responsible physician |
|
| Through study completion, an average of 2 years |
| D020147 | Coagulation Protein Disorders |
| D001791 | Blood Platelet Disorders |
| D006474 | Hemorrhagic Disorders |
| D030342 | Genetic Diseases, Inborn |
| D009358 | Congenital, Hereditary, and Neonatal Diseases and Abnormalities |