anemia patho - Exam 1B Flashcards
abnormal anemia
sickle cell disease
decreased Hgb content
loss of iron & loss of key nutrients
hypochromic/pale
decreased number of circulating erythrocytes
decreased production
increased destruction
blood loss
iron is essential for
normal hgb production
folate & B12 are necessary for
normal DNA synthesis of RBCs
in megaloblastic anemia, MCV is
increased
in iron def anemia, MCV is
decreased
clinical manifestations of all anemias (mild - mod)
-fatigue/weakness
-tachycardia
-dyspnea
clinical manifestations of all anemias (mod - sev)
-increased HR & RR
-hypotension
-pallor
-faintness
-cardio probs
etiologies of IDA
decreased intake, impaired absorption, increased demand and excessive loss
people at risk for IDA
people w/ poor intake, elderly, teens with heavy periods
IDA clinical manifestations
-smooth tongue
-glossitis
-mouth ulcers
-cheilosis
-koilonychia
-pica
in childhood cognitive deficits
megaloblastic anemia is most common in the
elderly
causes of B12 deficiency anemia
-atrophic gastritis , IF not produced
-crohns, celiac
-pernicious anemia (autoimmune)
clinical manifestations of B12 def anemia
-neuropathy
-ataxia (poor muscle control)
-glossitis
-dementia/psychosis
folate deficiency is caused by
decreased intake, not absorption
-alcoholism bc folate is stored in liver
-diet
-cirrhosis
increased needs like during pregnancy & intake
anemia of chronic kidney disease is caused by
impaired erythropoietin production epo is made in the kidneys & is released to tell bone marrow to make more RBCs
aplastic anemia is caused by
bone marrow stem failure d/t autoimmune disease
-chemo/radiation
-complicated infection
clinical manifestations of aplastic anemia
low RBCs, WBCs & platelets
treatment for aplastic anemia
whole blood transfusion, bone marrow transplant, immunosuppressants, drugs to stim erythropoiesis
what is acquired hemolytic anemia & what causes it
premature destruction of RBCs caused by external agent
-autoimmune attack
-blood incompatibilities
-drug reaction
-severe burn
clinical manifestations of acquired hemolytic anemia
-low hgb
-increased reticulocyte (immature RBC) count
-mild jaundice
-hemoglobinuira
triggers of sickle cell anemia
dehydration, stress, high altitudes, fever, extreme temps
clinical manifestations of sickle cell anemia
-swelling of hands & feet
-pain
-clogged vessels
treatment of sickle cell anemia
1) oxygen
2) hydration
3) pain mgt
antimetabolite drugs
blood transfusion
genetic counseling
thalassemia
genetic disorder occurring mostly in person of mediterranean descent
-severe cases can lead to death in childhood d/t heart failure, live to 30s w/ treatment
lack of one of two proteins that make up hemoglobin, alpha & beta globin
clinical manifestations of thalassemia
-delayed growth
-fatigue
-dyspnea
-hepatomegaly
-splenomegaly
-bone deformities
-jaundice
occult blood loss
GI bleed, retropertoneal bleed
in secondary polycythemia, increased blood viscosity & volume causes
-HTN (headaches, low concentration, ruddy face, cyanosis)
-DVT
-hemorrhage
-angina
-cerebral insufficiency
-tIA
in secondary polycythemia, hyper-metabolism causes
-night sweats
-weight loss
in secondary polycythemia, increase RBC and H&H cause
-itching (pruritus)
-pain in fingers and toes