Nur 612 Exam pt 3 Questions with Correct Answers 100% Verified By Experts| Latest Update
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thrombocytopenia a condition in which there is an abnormally small number of platelets
circulating in the blood.
caused by decrease thrombopoietin, increase sequestration of platelets in spleen, or decrease
in platelet survival
immune thrombocytopenia purpura autoimmune disease. increase of platelets lead to
antibody formation. usually follows viral infection in kids. Clotting factors are not involved
Hemophilia A Factor VIII deficiency. X linked recessive
Hemophilia B Factor IX deficiency. x linked recessive
hemorrhagic telanglectasia inherited tendency to bleed from localized lesions of the
capillaries
autosomal dominant
vitamin c deficiency poor collagen synthesis
senile purpura elderly bruising
DIC wide spread coagulation and bleeding. massive activation of coagulation sequence that
consumes all coagulation and proteins leading to severe hemorrhagic affects (consumptive
process)
RBC no organelles
bioconcave
flexible
, contains hgb
Iron required for hgb synthesis and oxygen.
transferrin Protein that transports iron in blood.
ferritin protein that stores iron. primarily in liver
Billirubin converted by heme molecule and transported to liver. Removed by rendered
water soluble (conjugated) for elimination in the bile
conjugated water soluble
Methmoglobin does not hold oxygen
G6PD deficiency A hereditary condition in which red blood cells break down when the body
is exposed to certain drugs.
same letter blood type and antigen
blood type A has what antibodies B
D antigen present Rh positive
chronic anemia Gi blededing. generally well compensated until oxygen compacity becomes
low
normal to low HCT with low MCV
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thrombocytopenia a condition in which there is an abnormally small number of platelets
circulating in the blood.
caused by decrease thrombopoietin, increase sequestration of platelets in spleen, or decrease
in platelet survival
immune thrombocytopenia purpura autoimmune disease. increase of platelets lead to
antibody formation. usually follows viral infection in kids. Clotting factors are not involved
Hemophilia A Factor VIII deficiency. X linked recessive
Hemophilia B Factor IX deficiency. x linked recessive
hemorrhagic telanglectasia inherited tendency to bleed from localized lesions of the
capillaries
autosomal dominant
vitamin c deficiency poor collagen synthesis
senile purpura elderly bruising
DIC wide spread coagulation and bleeding. massive activation of coagulation sequence that
consumes all coagulation and proteins leading to severe hemorrhagic affects (consumptive
process)
RBC no organelles
bioconcave
flexible
, contains hgb
Iron required for hgb synthesis and oxygen.
transferrin Protein that transports iron in blood.
ferritin protein that stores iron. primarily in liver
Billirubin converted by heme molecule and transported to liver. Removed by rendered
water soluble (conjugated) for elimination in the bile
conjugated water soluble
Methmoglobin does not hold oxygen
G6PD deficiency A hereditary condition in which red blood cells break down when the body
is exposed to certain drugs.
same letter blood type and antigen
blood type A has what antibodies B
D antigen present Rh positive
chronic anemia Gi blededing. generally well compensated until oxygen compacity becomes
low
normal to low HCT with low MCV
