Hemostasis Flashcards

1
Q

Hemostasis

A

Physiologic coagulation of blood in injured vessels to prevent bleeding.

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2
Q

Describe steps in hemostasis

A
  1. Vascular constriction
  2. Formation of platelet plug
  3. Formation of blood clot
  4. Fibrous organization
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3
Q

Cold water step 1 of hemostasis

A

Injured vessels produce thromboxane A2. Vasoconstrict smooth muscles of vessel.

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4
Q

Cold water step 2 of hemostasis

A

Platelets adhere to exposed subendothelial collagen. Recruit other platelets; fibrinogen assists platelet-platelet adhesion.

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5
Q

Cold water step 3 of hemostasis

A

Intrinsic, extrinsic, and combined pathway form blood clot.

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6
Q

Cold water step 4 of hemostasis

A

Fibroblasts complete organization of clot into fibrous tissue in 1-2wks.

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7
Q

Petechiae

A

Small, purplish, hemorrhagic spots on skin (thrombocytopenia, febrile illnesses).

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8
Q

Purpura

A

Rash where blood cells leak into skin or mucous membranes (disorders of coagulation/thrombosis).

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9
Q

Vasculitis

A

Inflammation of blood vessels

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10
Q

Hematoma

A

Swollen mass of extravasated (us. clotted) blood.

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11
Q

Ecchymosis

A

Superficial bleeding under skin or mucous membrane.

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12
Q

Thrombosis

A

Formation or presence of blood clot within vascular system.

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13
Q

Embolism

A

Sudden obstruction of blood vessel by debris (clot, choloesterol plaque, injected substances).

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14
Q

Infarction

A

Death of tissue from blood supply deprivation.

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15
Q

Describe conversion of prothrombin to thrombin

A

Factor Xa; where intrinsic and extrinsic pathways meet.

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16
Q

Describe conversion of fibrinogen to fibrin

A

Thrombin catalyzes. Fibrin stabilized and solidifies aggregates to final thrombus.

17
Q

Describe lysis of blood clot

A

Fibrinolytic system: plasminogen converted to plasmin - breaks up clot; thrombin triggers thromin-activatable fibrinolysis inhibitor - cleaves fibrin clot.

18
Q

Desribe role of vitamin K in formation of blood clots

A

Required by 5 important clotting factors: prothrombin, Factor VII, IX, X, protein C. Insufficiency can lead to serious bleeding.

19
Q

Hemophilia

A

Bleeding disease of varying severity seen with mild to severe trauma. Treated with Factor VIII or IX (depending on type, but expensive). X-linked; males only.

20
Q

DVT

A

Endothelial surface roughened (arteriosclerosis, infection, trauma) initiating clotting process. Flow of blood is slowed (treated with t-Pa or anticoags).

21
Q

Thrombocytopenia

A

Low platelet count. Purpura on skin. Tx include whole blood transfusion or splenectomy.

22
Q

Pulmonary embolism

A

Part of thrombus breaks off (embolus) and travels through right side of heart blocking pulmonary arteries. Tx t-Pa or anticoags.

23
Q

Disseminated intravascular coagulation

A

Dying tissue or trauma causes release of tissue factor initiating widespread clotting mechanism. Can occlude peripheral vessels. Caused by septicemia.

24
Q

Bleeding test

A

Cuts made on forearm and time to stop bleeding measured. Not sensitive nor specific, can be influenced by meds and thrombocythemia; not commonly used.

25
Platelet count
Determine concentration of platelets in blood. Normal range 150-450,000/ul. Below 20,000 = mild spontaneous bleeding.
26
Thrombocythemia
Elevated platelet count
27
Thrombocytopenia
Decreased platelet count
28
Partial thromboplastin time (pTT)
Used to screen for deficiencies and inhibitions of factors in intrinsic and common pathway. Used to assess pts response to heparin therapy.
29
Prothrombin time
Time clot takes to form after addition of calcium and thromboplastin (Ca activator). Assess extrinsic and common pathway.
30
D-dimer
Antigen formed with fibrin degradation. Used to diagnose or rule out thrombosis in pts. Positive test rules in, but no infor on location. Neg test rules out.
31
Platelet function test
Measures ability of platelets to aggregate. (Not worrying about warm water shizz)
32
Mechanisms which prevent excessive thrombosis
Fibrolytic system dissolves and remodels fibrin clot. Natural inhibitors: Antithrombin and vitamin K dependent proteins C and S (inhibit thrombin). Heparin and antithrombin medication: Inhibit coagulation cascades by speeding up process and inactivating Factors, respectively. Tissue factor pathway inhibitor: Inhibits extrinsic pathway PG2 and NO: Generated by endothelial wall prevent thrombosis. Plasminogen activators: Limit platelet aggregation.
33
Describe hereditary causes of thrombosis
Factor V Leiden, Prothrombin mutation, anticoagulation deficiencies, fibrinolytic defects (rare).
34
Describe acquired causes of thrombosis
Trauma, medications (OCs), malignancy, orthopedic surgery, infection (rare), thrombocytosis and myeloproliferation, antiphospholipid antibodies.