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21 Cards in this Set

  • Front
  • Back
bernard-soulier syndrome
defect in GpIb receptor on platelet so that platelet cannot bind or identify von Willebrand factor
glanzmann thrombasthenia
defect in GpIIb-IIIa receptor on platelet so that fibrinogen cannot bind and platelet plug cannot be secured
von Willebrand disease
vWF defect where it is not expressed so platelets don't know where to bind to form plug
point of coagulation cascade
production of thrombin in order to convert fibrinogen to fibrin
intrinsic pathway of coagulation initiation of pathway
hageman factor (factor XII)
point of fibrinolytic system?
plasmin to breakdown fibrin to remove clot when healing is done
relative size of hemorrhage
petechiae < pupura (>3mm) < echymoses (>1cm)
alpha granules
granules in platelets that have P-selectin and a ton of clotting factors
dense bodies
granuels in platelets that contain chemical support for clotting factors (histamine, ADP, ATP, Ca)
what two molecules are necessary for primary plug
ADP, thromboxane A2
Factor V leiden, prothrombin gene mutation
hypercoagulation factors
HIT Syndrome (Heparin-Induced Thrombocytopenia)
Ab formed against heparin and excessive coagulation in limbs
Lines of Zahn
histological layers of platelets and fibrin found in thrombus
thrombus vs postmortem clot?
thrombus - firm, lines of Zahn
postmortem clot - red jelly, chicken fat-like material
Pulmonary embolism cause?
deep vein thromboses in leg
decompression sickness
nitrogen dissolved in blood because of rushed ascension. Caisson disease is chronic form of this disease. gas emboli.
shock
cardiovascular collapse involving hypotension, impaired tissue perfusion, hypoxia
types of shock
cardiogenic - heart is broke
hypovolemic shock - not enough blood
septic shock - bacterial infection
cytokine mediator causing shock?
TNF
cause of infarcts?
thrombotic or embolic occlusion of artery or vein
white (anemic) infarct
red (hemorrhagic) infarct
white - occlusion of artery with one input
red - occlusion of vein with system with more than one input