CH 4: Hemodynamic Disorders Flashcards
define hemostasis
blood clotting at the site of an injury
define edema
accumulation of fluids in the tissues
define effusions
accumulation of fluids in cavities
what are the two main conditions that cause an increase in hydrostatic pressure and therefore edema
deep vein thrombosis
congestive heart failure
peau d-orange breast cancer
blockage of subareolar lymphatics due to cancer
causes the breast to appear like an orange
what are the three most common sites for edema
subcutaneous tissues
lungs
brain
what is non-pitting (dependent) edema
accumulation of protein rich fluid
what is pitting edema
accumulation of protein poor fluid
what are interlobular septal markings in a lung indicative of
edemic change
likely excess fluid in the lymphatics that present with severe pulmonary edema
define hydrothorax
effusion in pleural cavity
define hemothorax
effusion in pleaural cavity containing blood
define hydropericardium or pericardial effusion
effusion in pericardium
define hemopericardium
effusion into the pericardium containing blood
define hydroperitoneum
effusion into the peritoneal cavity (ascites)
define hemoperitoneum
effusion into the peritoneal cavity containing blood
what is hyperemia
arteriolar dilation causes increased blood flow
tissue appears red due to engorgement of oxygenated blood (erythema)
what is congestion
impaired outflow of venous blood from tissue
tissue spreads a blue-red color (cyanosis) due to deoxygenated hemoglobin
“nutmeg liver”
chronic passive congestion of the liver
shows central congestion with hemorrhagic necrosis
what are the three required things for each step in the coagulation cascade
enzyme
substrate
cofactor
Coumadin
anticoagulant
vitamin K
cofactor
disorders of primary hemostasis affect what
platelets
what is affected in disorders of secondary hemostasis
clotting factors
what are the two vWF deficiency disorders
von Willebrand disease
Bernard-soulier syndrome
what are three factors that affect platelet adhesion
platelet changes shape from disc to spike
platelet releases granular contents
platelet aggregate
mutations in which clotting factor lead to hemophilia A
CF 8