CACMLE Hemostasis Courses

211-Online: Hereditary Thrombotic Risk Factors – Section 1 of “Hereditary and Acquired Thrombotic Risk Factors”

$48.00

Contact Hours (Points): 4

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 Thrombotic Risk Factors – Section 1 of “Hereditary and Acquired Thrombotic Risk Factors”

Self-Study 211 – Intermediate Level

Contact Hours (Points): 4

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

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

Online – 211: Course Taken Online: $48.00 BUY NOW

IMPORTANT: This online course is accessible using the following:

Desktop or Laptop Computer – Download the latest Adobe Reader program.

Kindle Fire – No additional App download is necessary.

Apple iPad (all versions) / Nook / Kindle – Recommend purchase of a PDF Reader App, such as GoodReader, Cloudreaders, or Stanza by Amazon. Once downloaded, launch this App to access the course online site in order to logon to and view your course.

TABLE OF CONTENTS
SECTION I: MECHANISMS OF HEMOSTASIS – A REVIEW
Coagulation; Regulation of Coagulation; Vascular Phase of Hemostasis
SECTION II: Hereditary THROMBOTIC RISK FACTORS
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

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