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Coagulation
Coagulation

... used, in combination with Amicar, in mild hemophiliacs to avoid transfusions prior to surgery. An even easier rule of thumb is that there are about 15 units of FFP in an adult. To get 50% activity requires about 7.5 units of FFP. Recombinant Factor VIII: Recombinant human antihemophilic factor is no ...
Sustained hypothermia accelerates microvascular thrombus
Sustained hypothermia accelerates microvascular thrombus

... encountered systemic hypothermia on microvascular thrombosis in vivo and in vitro. Ferric chloride-induced microvascular thrombus formation was analyzed in cremaster muscle preparations from hypothermic mice. Additionally, flow cytometry and Western blot analysis was used to evaluate the effect of h ...
Understanding Blood Tests
Understanding Blood Tests

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RDCR – Blood Products Module
RDCR – Blood Products Module

... ¡  For example, if type B blood (with B antigens) were transfused into a type A recipient (with anti-B antibodies), the recipient’s anti-B antibodies would immediately bind the donor’s RBCs, causing a transfusion reaction where the binded RBCs block small vessels causing reduced bloodflow to vital o ...
Cardiovascular Physiology
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Hematology - science4warriors
Hematology - science4warriors

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Pathogenesis of Thrombocytopenia in Cyanotic Congenital Heart

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BLOOD
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Quality Analysis of blood component (PRBC and platelet concentrates)
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Hemostasis
Hemostasis

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1-14-08 Bone Marrow Stem Cell Disorder Pathology
1-14-08 Bone Marrow Stem Cell Disorder Pathology

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Safari Souvenir
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Ch 12 Blood Cells
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Production and Nucleotide Sequence of an
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Chapter 19 - Dr. Jerry Cronin
Chapter 19 - Dr. Jerry Cronin

... steps and occurs rapidly, often within seconds, once the protein “tissue factor” (TF) leaks into the blood  The intrinsic pathway is more complex and occurs more slowly in response to damage to endothelial cells or phospholipids released by activated platelets ...
Production and nucleotide sequence of an inhibitory human IgM
Production and nucleotide sequence of an inhibitory human IgM

... in Fig 3A, along with the sequence of the germline gene DP-77,I8 a member of the VHlllfamily, with a nucleotide similarity of 98.5%. In addition, within the overlapping region, DP-77 is identical to the WHG16I9 germline gene, and to two fetal liver-derived heavy chains: the hse 54 3.2 mRNAZ0and the ...
Clinical Manifestations
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... involve many organs and can be seen as infarction of large areas of skin, subcutaneous tissue, or kidneys. Anemia caused by hemolysis may develop rapidly, owing to microangiopathic hemolytic anemia. ...
HLA typing in transfusion and transplantation
HLA typing in transfusion and transplantation

... • Depends on – immune system function in recipient – lymphocytes in transfused component – degree of HLA similarity between donor and recipient • Donor lymphocytes not recognized as foreign if HLA similar • More common with related donors – Especially if donors homozygous for shared HLA haplotype wi ...
What your hematology instrument isn`t telling you
What your hematology instrument isn`t telling you

... What your blood smear can tell you. Confirm leukocyte counts + differentials Confirm the presence of nRBCs, platelet clumps, blasts, agglutination, rouleaux Assess morphology lf erythrocytes, leukocytes, and platelets Identify intra- or extracellular infectious agents Identify inclusions, e.g. Heinz ...
Thromboelastography
Thromboelastography

... TEG from the same patient shown in example 4. The heparin was reversed with protamine. The top curve represents a TEG with Heparinase (heparin activity eliminated) and the bottom trace is the same sample without Heparinase. Since both traces are identical all heparin was reversed by protamine. • Tre ...
An Update From COBM - American Society of Anesthesiologists
An Update From COBM - American Society of Anesthesiologists

... Single donor pheresis-derived platelets minimize the number of donor exposures for the transfusion recipient and have become the primary source of platelets in the US. i Platelets should be stored at room temperature (20º to 24ºC) for up to five days with continuous gentle agitation to facilitate g ...
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Platelet



Platelets, also called thrombocytes, are a component of blood whose function (along with the coagulation factors) is to stop bleeding by clumping and clogging blood vessel injuries. Platelets have no cell nucleus: they are fragments of cytoplasm which are derived from the megakaryocytes of the bone marrow, and then enter the circulation. These unactivated platelets are biconvex discoid (lens-shaped) structures, 2–3 µm in greatest diameter. Platelets are found only in mammals, whereas in other animals (e.g. birds, amphibians) thrombocytes circulate as intact mononuclear cells.On a stained blood smear, platelets appear as dark purple spots, about 20% the diameter of red blood cells. The smear is used to examine platelets for size, shape, qualitative number, and clumping. The ratio of platelets to red blood cells in a healthy adult is 1:10 to 1:20. The main function of platelets is to contribute to hemostasis: the process of stopping bleeding at the site of interrupted endothelium. They gather at the site and unless the interruption is physically too large, they plug the hole. First, platelets attach to substances outside the interrupted endothelium: adhesion. Second, they change shape, turn on receptors and secrete chemical messengers: activation. Third, they connect to each other through receptor bridges: aggregation. Formation of this platelet plug (primary hemostasis) is associated with activation of the coagulation cascade with resultant fibrin deposition and linking (secondary hemostasis). These processes may overlap: the spectrum is from a predominantly platelet plug, or ""white clot"" to a predominantly fibrin clot, or ""red clot"" or the more typical mixture. The final result is the clot. Some would add the subsequent clot retraction and platelet inhibition as fourth and fifth steps to the completion of the process and still others a sixth step wound repair.Low platelet concentration is thrombocytopenia and is due to either decreased production or increased destruction. Elevated platelet concentration is thrombocytosis and is either congenital, reactive (to cytokines), or due to unregulated production: one of the myeloprolerative neoplasms or certain other myeloid neoplasms. A disorder of platelet function is a thrombocytopathy.Normal platelets can respond to an abnormality on the vessel wall rather than to hemorrhage, resulting in inappropriate platelet adhesion/activation and thrombosis: the formation of a clot within an intact vessel. These arise by different mechanisms than a normal clot. Examples are: extending the fibrin clot of venous thrombosis; extending an unstable or ruptured arterial plaque, causing arterial thrombosis; and microcirculatory thrombosis. An arterial thrombus may partially obstruct blood flow, causing downstream ischemia; or completely obstruct it, causing downstream tissue death.
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