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Z83.2 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. Short description: Family history of dis of the bld/bld-form org/immun mechnsm. The 2024 edition of ICD-10-CM Z83.2 became effective on October 1, 2023.
Jun 15, 2010 · The diagnosis of vWD requires two clinical criteria: (1) a personal history, family history, or physical evidence of mucocutaneous bleeding and (2) a qualitative or quantitative decrease in...
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What is the ICD 10 code for von Willebrand disease?
What is von Willebrand disease?
What are the different types of von Willebrand disease?
Pathophysiology. Synthesis of VWF occurs in the vascu-lar endothelium and megakaryocytes. It is released from platelets and endothelial cells when they are activated and binds to factor VIII in...
Hemophilioid disorder due to deficiency of von willebrand factor and thus of factor viii complex. Hereditary or acquired coagulation disorder characterized by a qualitative or quantitative deficiency of the von willebrand factor. The latter plays an important role in platelet adhesion.
CLINICAL QUESTIONS. 10 to 20 clinically-relevant questions. generated in PICO format (population, intervention, comparison, outcome) Example: Clinical Question. “In a patients with VWD and history of severe and frequent bleeds, should routine prophylaxis with VWF concentrate or no routine prophylaxis be used?” EVIDENCE SYNTHESIS.
Z83.2 is a billable diagnosis code used to specify a medical diagnosis of family history of diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism. The code is valid during the current fiscal year for the submission of HIPAA-covered transactions from October 01, 2023 through September 30, 2024.
Von Willebrand disease (VWD) is a common, inherited bleeding disorder. The current classification includes types 1 and 3, which are characterized by quantitative deficiencies of von Willebrand factor (VWF), as well as types 2A, 2B, 2M, and 2N, which are qualitative variants.
