Coagulation and bleeding disorders: review and update.

Abstract:

:Hemostasis is initiated by injury to the vascular wall, leading to the deposition of platelets adhering to components of the subendothelium. Platelet adhesion requires the presence of von Willebrand factor and platelet receptors (IIb/IIIa and Ib/IX). Additional platelets are recruited to the site of injury by release of platelet granular contents, including ADP. The "platelet plug" is stabilized by interaction with fibrinogen. In this review, I consider laboratory tests used to evaluate coagulation, including prothrombin time, activated partial thromboplastin time, thrombin time, and platelet count. I discuss hereditary disorders of platelets and/or coagulation proteins that lead to clinical bleeding as well as acquired disorders, including disseminated intravascular coagulation and acquired circulating anticoagulants.

journal_name

Clin Chem

journal_title

Clinical chemistry

authors

Triplett DA

subject

Has Abstract

pub_date

2000-08-01 00:00:00

pages

1260-9

issue

8 Pt 2

eissn

0009-9147

issn

1530-8561

journal_volume

46

pub_type

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