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66 Cards in this Set

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pseudo anemia maybe from
over hydration rehydration of a dehydrated pt.
IV fluid in specimen, pregnancy, hypoalbuminemia, laboratory error
factor deficiency anemia, caused by?
low: iron, B12, folic acid, or a combo of all three
production defect anemia
failure of blood forming organs to produce or or deliver mature RBC's
causes of production defect anemias
marrow fibrosis, neoplasm, chem toxins, severe infection, chronic renal disease, widespread malignancy, rheumatoid collagen diseases, hypothyroidism.
depletion anemia can be from;
peripheral blood loss. hemorrhage(acute or chronic).
hemolytic anemia/ hypersplenism
classification of anemia by RBC morphlogy
Microcytic, normocytic, macrocytic
%iron in hemoglobin?
70%
amt. inron consumed/absorbed
10mg/day consumed. 10% absorbed(1mg/day)
absorption of Iron is increased by?
absorption is inthe duodenun/jejunum. ingestin of Vit C. taking iron supplements 45-60minutes before eating.
Fe+ absorption is decreased by?
coffee, tea, dairy, and high fiber foods
states of iron
ingested as ferric, converted to ferrous. (fick/ferrus)
daily loss of Iron
men 1 mg/day
women 1mg/day
menstruating 2mg/day
Iron storage (by %)
70% in hemoglobin, 30% in bone marrow, liver, spleen, reticulum cells(60% as ferritin, 40% as hemosiderin)
M/CC bleeding in men:
GI bleeding. -40peptic ulcer. +40 carcinoma.
hemorrhoids
tests for GI bleeding
endoscopy, stool guaiac test, barium enema, sigmoidoscopy, colonoscopy
M/CC bleeding in women;
GI or vag. 20-50% menstruating women are Fe defficient.
factor deficiency Anemia blood smear;
may appear normal in early phase.

will be microcytic/hypochromic in later stages.
factor deficiency A. RBC indices
-MCV. +RDW. MCH and MCHC may or may not change.
Factor Deficiency A. Reticulocytes
normal in uncomplicated chronic iron def. reticulocytsis is possible w/ acute blood loss.
Serum Iron
sensitive indicator of possible iron defiiency. test is for iron bound to serum(transferrin) so levels depend on iron AND transferrin. levels vary w/ time of day a.d vary day to day.
Decreased serum Iron=
*Iron Deficiency
*Anemia of severe Chronic dz.( rheumaoid-collagen diseases, extensive malig, uremia, cirrhosis, severe chronic infection.)
*3rd tri
*severe stress
Serum Iron w/ Pregnancy
*-during 3rd trimester.
*+1st trimester.(transferrin is elevated by estrogen)
Increased Serum Iron=
*hemolytic anemia
*Fe overload
*estrogen Therapy(+transferrin)
*acute hepatitis
*parenteral Fe therapy
*thalassemia minor
*IM Fe-dextran infusion.
Megaloblastic A. and Fe deficiency
-Fe maybe unmasked by folate or B12 therapy
Total Iron Binding Capacity (TIBC)
*estimates Serum Transferrin
*+in uncomplicated chronic -Fe.
*+ w/ + transferrin
*- w/ - transferrin
Transferrin Saturation (TS)
- %TS is MORE SENSITIVE for IDA than Serum Iron or TIBC...bu it is LESS Specific.
Chronic Iron def. A. (IDA) test results
*- Serum Iron
*+ TIBC
* increases the unsaturated binding capacity or transferrin and lowers the % iron bound transferrin
Serum Ferritin
*major Fe storage compound
*MOST SENSITIVE test for for -Fe
Interpretation of Serum Ferritin
+10ng/ml is diagnostic for -Fe.
factors elevating Serum ferritin
*acute inflammation
* infection
*trauma
*transfusions
*megaloblastic a.
*hemolytic a.
*Fe Overload
*chronic viral Hep.
Free Erythrocyte Proporphyrin aka Zinc Protoporphyrin(ZPP)
*involved in last step of heme synthesis.
* if no Fe available, Zinc bids with protoporphyrin.
*+ w/ -Fe, Pb poison, infections, inflammation, malignancies, chron Liver dz., hemolytic anemia.
Bone Marrow Iron Stain
THE GOLD STANDARD for -Fe.
* most sensitive/specific/reliable
Dx. of Chronic Fe def.
* anemia w/ -MCV and +RDW
Interpretation of Chronic Iron Def.
*-SI & -TIBC= chronic Dz.
*- SI & + TIBC= low Fe
*- DI & -%T= thalassema minor
B12 deficiency causes
*lask of Intrinsic factor
*low gastric acid
*malabsorption syndrome
*bacterial overgrowth(dysbiosis)
*fish tapeworm
*pacreatic disease
*drug interference
*vegan diet
factors that can make b12 appear low
*++Vit C dose
*prgnancy
*folic Acid deficiency
*chronic -Fe
False elevation of B12
*Liver dz
*Myeloproliferative disorder w/ inc. WBCs
Megaloblastic Anemia causes
caused by *-b12 or -folic acid
Megaloblastic changes;
*enlargement of RBC precursors
*+ RBC destruction in marrow
*leukopenia
*anemia
*thrombocytopenia
*bandeutrophils
*....see pg 58
B12 deficiency causes
*lask of Intrinsic factor
*low gastric acid
*malabsorption syndrome
*bacterial overgrowth(dysbiosis)
*fish tapeworm
*pacreatic disease
*drug interference
*vegan diet
factors that can make b12 appear low
*++Vit C dose
*prgnancy
*folic Acid deficiency
*chronic -Fe
False elevation of B12
*Liver dz
*Myeloproliferative disorder w/ inc. WBCs
Megaloblastic Anemia causes
caused by *-b12 or -folic acid
Megaloblastic changes;
*enlargement of RBC precursors
*+ RBC destruction in marrow
*leukopenia
*anemia
*thrombocytopenia
*bandeutrophils
*....see pg 58
***megaloblastic anemia
Methylmalonic acid (MMA)
functional test for -B12
*MMa needs B12 to convert to succinate
+MMA=-B12
MMA is + even when serum B12 is normal(60%)
Megaloblastic anemia findings
+MMA
*+MCV
*+serum lactic dehydrogenase(LDH)=cell damage
LDH means?
LDH=cell damage
Pernicious Anemia is from?
atrophis gastritis causes -HCL, and IF deficiency
pernicious A. lab findings
macrocytic anemia w/ oval macrocytes and megaloblastic changes in bone marrow
patients most likely to have pernicious anema
northern europeans ages +40
Shilling test
definitive for pernicious anemia
may have 29% false +
Shilling test
pernicious anemia
*radioactive B12 given
folowed by "flushing dose"
Urine collected for 24 hours
*-8% recovery of radioactive b12 suggests PA
*+8% recovered with IF confirms dx.
***folic acid deficiency
shilling test required to distinguish from PA
treating PA w/ folate
may aleviate symptoms of -folic acid but -b12 will still causeneuro damage.
Folic Acid Deficiency causes:
*-dietary FA
*chronic OH-
*malabsorption
*pregnancy
*oral contreceptves
*Other drug interference
Pyridoxine Def.
*B6 is needed for heme synthesis
*anemia will resmble chronic -Fe
B6(pyridoxine) def. classification
sideroblastic anemia
*seen in bonemarow
*normoblasts w/ iron-staining cytoplasmic granules that form ring around nucleus
Production Defect anemia
*failure of marow to incorporate adequate supplies of raw material
* failure of marrow to release RBCs
*destruction of RBC precursors in the marrow.
Production Defect a.
Myelofibrosis
replacement of marrow by fibrosis
production defect anemia neoplasm
replacement of marrow by cancer cells
Production Defect A. lab signs
*normocytic/normochromic
*
multiple myeloma (production defect a.)
neoplasm of plasma cells leading to rouleaux formation, plasma cells in peripheral blood and hyerglobulinemia
aplastic anemia (pda)
-marrow fxn w/o cell abnormality or replacement
aplastic anemia (pda) causes
radiation, chemicals, cytotoxic drugs, medications, ebv, rubella, herpes zoster, hep c, thmoma, etc...
what % of PDA is idiopathic?
50%
PDA findings
serum Fe and TIBC are decreased