Physiology: Application - Haemostasis Flashcards

1
Q

what is haemostasis

A

arrest of bleeding and maintenance of vascular patency

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2
Q

components of normal haemostatic system (what can happen)

A
  • formation of platelet plug
  • formation of fibrin clot
  • fibrinolysis
  • anti-coagulant defences
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3
Q

how and where are platelets formed

A

formed in bone marrow by budding from megakarocytes

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4
Q

describe how a platelet plug is formed

A

endothelial damage exposes collagen and releases VWF and other proteins, platelets have receptors to these and attach at the site of injury
platelets secrete chemicals leading to platelet aggregation at sit of injury

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5
Q

causes of failure of platelet plug formation (4)

A
  • vascular
  • low platelet count (thrombocytoenia)
  • decreased platlet function
  • VWF
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6
Q

what are the consequences of failure of platelet plug formation (4)

A
  • spontaneous bruising and purpura
  • mucosal bleeding
  • intracranial haemorrhage
  • retinal haemorrhage
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7
Q

what is primary haemostasis

A

platelet plug formation

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8
Q

what is secondary haemostasis

A

fibrin clot formation

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9
Q

describe the process of fribrin clot formation

A
  • TF and VIIa initiate clotting
  • V and Xa propagate prothrombin to thrombin
  • this changes fibrinogen to fibrin which causes the clot
  • thrombin amplifies the pathway via VIII and IXa
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10
Q

what are the causes fibrin clot failure (3)

A
  • single clotting factor deficiency (hereditary)
  • multiple clotting factor deficiencies (acquired)
  • increased fibrinolysis
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11
Q

what is fibrinolysis

A

breakdown of fibrin in blood clot

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12
Q

describe fibrinolysis

A
  • tpa activates plasmin from plasminogen

- plasmin changes fibrin to fibrin degredation products

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13
Q

what are the consequences of failure of fibrin clot formation

A
  • no characteristic syndrome
  • causes bleeding
  • primary or secondary haemostatic failure
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14
Q

what does the bleeding pattern in fibrin clot failure depend on

A
  • if its single or multiple abnormalities

- clotting factors involved

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15
Q

name 2 naturally occuring anto-coagulants

A
  • serine protease inhibitors

- proteins C and S

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16
Q

how do serine protease inhibitors work (anti-thrombin III)

A
  • anti-thrombin III inhibits clotting factors TF/VIIa, V/Xa, VIII/IXa and thrombin
  • this stops fibrin clot formation
17
Q

how to proteins C and S work

A
  • activated by thrombin and bind to thrombomodulin

- inhibit clotting factors V/Xa and VIII/IXa

18
Q

what is thrombomodulin

A

thrombin co-factor that decreases coagulation by converting thrombin to and anti-coagulation enzyme

19
Q

describe arterial thrombus and its treatment

A
  • atherosclerosis
  • platelet rich
  • aspirin and anticoagulants, modify atherosclerotic risk factors
20
Q

describe venous thrombus and its treatment

A
  • plateltes not activated- coagulation cascade activated, fibrin rich clot
  • heparin, warfarin or new O anticoagulants
21
Q

what is virchows triad

A
  • factors that contribute to coagulation

- blood stasis, hypercoagulation and endothelial injury

22
Q

what happens with unstable atherosclerotic plaques when they rupture

A
  • platlets are activated causing an actute thrombus

- sudden symptom onset

23
Q

where might and atherosclerotic rupture happen, what are the assoc. disease and what are the consequences of that

A
  • coronary arteries, unstable angina/MI
  • cerebral arteries, stroke
  • leads to acute organ ischaemia and necrosis
24
Q

describe the symptoms of DVT

A
  • limbs feel swollen, hot or tender

- pitting oedema

25
Q

what can happen as a consequence of PE

A
  • pulmonary infarct, pleuritic chest pain, CV collapse/death
  • hypoxia
  • R heart strain