CACMLE Hemostasis Courses

098-Online: Hereditary and Acquired Thrombotic Risk Factors


Contact Hours (Points): 7

This course presents a detailed discussion of the currently recognized Hereditary and acquired risk factors for thrombotic disease. A basic review of the biochemical pathway of coagulation and a brief discussion of the vascular phase of hemostasis are provided to orientate the reader to the sites of action of the various risk factors. This introductory section is followed by an in-depth discussion of each of the risk factors with emphasis on methods of diagnosis and treatment. Case histories are provided for each risk factor to illustrate the methods of diagnosis and types of treatment discussed in the test. The exam to this course is unchanged.

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Product Description

Hereditary and Acquired Thrombotic Risk Factors

Self-Study 098 – Intermediate Level

Contact Hours (Points): 7

Written by Michael J. Sanfelippo MS, MT(ASCP)

Reviewed 2015. Updated 2013 (Exam is unchanged). Published 2002.

Online – 098: Course Taken Online: $84.00 BUY NOW

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“Excellent material; I am glad to see more courses with this combination of relevant,
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Coagulation; Regulation of Coagulation; Vascular Phase of Hemostasis


Antithrombin; Biochemistry of Antithrombin; Inheritance and Occurrence; Clinical Manifestations; Diagnosis of AT Deficiency; Functional Assays of AT; Antigenic Assay of AT; Treatment of AT Deficiency; Case Histories; Case 1; Case 2; Protein C; Biochemistry of Protein C; Inheritance and Occurrence; Acquired Protein C Deficiency; Clinical Manifestations of Protein C Deficiency; Diagnostic Tests for Protein C; Treatment of Protein C Deficiency; Case History; Protein S Deficiency; Biochemistry of Protein S; Inheritance and Occurrence; Clinical Manifestations; Diagnostic Tests; Treatment of Protein S Deficiency; Case History; Plasminogen Deficiency; Biochemistry of Plasminogen; Inheritance and Occurrence; Diagnostic Tests for Plasminogen Deficiency; Treatment of Plasminogen Deficiency; Case History; Heparin Cofactor II; Biochemistry; Inheritance and Occurrence; Clinical Manifestation; Diagnostic Test; Treatment; Case History; Factor V Leiden; Biochemistry of Factor V Leiden; Inheritance and Occurrence of Factor V Leiden and Factor V Cambridge; Clinical Manifestations of Factor V Leiden; Diagnostic Tests; Clinical Manifestations of Factor V Leiden; Treatment of Factor V Leiden; Case History; Prothrombin 20210A Gene Mutation; Biochemistry of the Prothrombin 20210A Gene Mutation; Inheritance and Occurrence; Clinical Manifestations; Diagnostic Tests for Prothrombin 20210A Gene Mutation; Treatment of Prothrombin 20210A Gene Mutation; Case History; Dysfibrinogenemia; Diagnosis of Dysfibrinogenemia; Treatment of Dysfibrinogenemia; Case History; Factor XII Deficiency as a Risk Factor for Venous Thrombosis; Biochemistry of Factor XII; Inheritance and Occurrence of Hereditary Factor XII Deficiency; Clinical Manifestations of Factor XII Deficiency; Diagnostic Tests for Factor XII Deficiency; Treatment of Factor XII Deficiency; Case History; Prekallikrein Deficiency; Biochemistry of Prekallikrein; Inheritance and Occurrence; Clinical Manifestations of Prekallikrein Deficiency; Diagnostic Tests for Prekallikrein; Treatment of Prekallikrein Deficiency; Case History; Hyperhomocysteinemia and Defects in the Metabolism of Methionine; Biochemistry of Methionine Metabolism; Mechanism of Thrombosis in Hyperhomocysteinemia; Diagnosis of Hyperhomocysteinemia; Treatment of Hyperhomocysteinemia; Case History


The Antiphospholipid Syndrome / Lupus Anticoagulant; Historical Perspective; Mechanism of Thrombosis in the Antiphospholipid Syndrome and Lupus Anticoagulant; Diagnostic Criteria for the Antiphospholipid Syndrome and the Lupus Anticoagulant; The Lupus Anticoagulant; Laboratory Testing; Clinical Manifestation of the Antiphospholipid Syndrome; Treatment of the Antiphospholipid Syndrome; Case Histories for the Antiphospholipid Syndrome;

Case #1; Case #2; Case #3; Catastrophic Antiphospholipid Syndrome; Case study; Thrombosis Associated with Malignancy; Mechanisms of Thrombosis in Patients with Malignancies; Clinical Presentation of Thrombosis in Patients with Malignancy; Laboratory Testing; Treatment of Thrombosis in Patients with Malignancies; Case Histories; Case #1; Case #2; Thrombosis Associated with the Nephrotic Syndrome; Mechanisms of Thrombosis in the Nephrotic Syndrome; Laboratory Identification of Thrombotic Risk in Nephrotic Syndrome and Treatment; Case History; Heparin-Induced Thrombocytopenia (HIT); Mechanism; Clinical Manifestation; Laboratory Identification of HIT Antibody; Case History; Warfarin-Induced Tissue Necrosis; Case History; Pregnancy as a Thrombotic Risk Factor; Mechanism; Treatment; Case History; Oral Contraceptive Therapy as a Risk Factor for Thrombosis; Mechanism; Precautions; Case History

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