Author

Karen L. Hay

Abstract

Activated coagulation times (ACT's) of heparinized blood or plasma samples containing normal platelets were compared with ACT’s of heparinized samples containing non-viable or abnormally functional platelets. The non-viable platelets were prepared by freeze/thawing, and the abnormally functional platelets resulted from the addition of adenosine or adenosine 5'-diphosphate (ADP).

The ACT’s of the heparinized samples containing treated platelets were considerably longer than the ACT’s performed on samples with untreated platelets. Treated platelets had no effect on unheparinized samples, however. This would indicate that, although platelet factor 3 (PF3) is sufficient to promote clotting of unheparinized blood, viable platelets, in addition, are required for clotting of heparinized blood. A possible hypothesis which explains these findings is as follows:

In the unheparinized situation, coagulation factors are activated as clotting takes place. PF3 serves as a surface catalyst, thrombin is generated, and a fibrin clot is formed. The form in which PF3 is available is incidental to clot formation.

When heparin is present, however, thrombin is neutralized as fast as it is formed. Quantities sufficient to induce fibrin formation cannot therefore form in the free plasma, and prolonged or infinite clotting times result. In order for coagulation to go to completion, an environment favorable to thrombin generation must be provided.

It is probable that, even in heparinized samples, the foreign surface present and the thrombin formed are sufficient to promote platelet aggregation, even though the thrombin levels are too low to directly affect the coagulation system.

The interstices of the platelet aggregates provide an environment favorable to thrombin formation. As the platelets aggregate, plasma containing activated clotting factors and heparin is trapped within the platelet clump. Platelet factor 4 (PF4) is released from the platelets and, in the static environment within the clump, is able to completely neutralize the heparin trapped there. This then allows thrombin generation to proceed catalytically. Fibrin formation can now go to completion, both within the platelet aggregate and in the "plasmatic atmosphere" closely surrounding the clump. The large amounts of thrombin generated overcome the heparin effect, and visible clotting occurs.

The implications of an hypothesis such as this may be summarized as follows:

1. Viable platelets are essential to the coagulation of heparinized blood and plasma samples.

2. The varying sensitivities of different individuals to comparable heparin doses may in part reflect the platelet function of those individuals.

3. The fact that variable (and sometimes considerable) numbers of platelets remain in plasma used for activated partial thromboplastin time (APTT) testing implies that the APTT results on such heparinized samples will be correspondingly variable.

4. The APTT, because it is not dependent on the patient's own platelet level, cannot truly reflect that patient's response to heparin.

5. A test such as the activated coagulation time (ACT), which is dependent on the patient's quantitative and qualitative platelet level, reflects more accurately the actual in vivo function of heparin than does the APTT.

Department

Medical Technology

School

Graduate School

First Advisor

Brian S. Bull

Second Advisor

Richard W. Hubbard

Third Advisor

Robert E. Moncrieff

Degree Name

Master of Science (MS)

Degree Level

M.S.

Year Degree Awarded

1975

Date (Title Page)

8-1975

Language

English

Library of Congress/MESH Subject Headings

Blood Coagulation Factors; Blood Platelets.

Type

Thesis

Page Count

x; 43

Digital Format

PDF

Digital Publisher

Loma Linda University Libraries

Usage Rights

This title appears here courtesy of the author, who has granted Loma Linda University a limited, non-exclusive right to make this publication available to the public. The author retains all other copyrights.

Collection

Loma Linda University Electronic Theses and Dissertations

Collection Website

http://scholarsrepository.llu.edu/etd/

Repository

Loma Linda University. Del E. Webb Memorial Library. University Archives

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