DLM Flashcards

1
Q

CBC-Hemoglobin

A

12-18g/dL

Indication of oxygen transport capacity of blood

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2
Q

CBC- Hematocrit

A

38-54% Percent of blood composed of erythrocytes- 3x HGB

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3
Q

CBC- MCV

A

Average volume of RBC
Macrocytic- large cells- due to B12 or folic acid deficiency
Microcytic- small cells- due to iron deficiency

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4
Q

CBC- Platelet Count

A
150,000-450,000
Number of platelets in blood sample.
Thrombocytopenia-
viral illness, warfarin, petechiae
Thrmobocythemia- Risk of DVT, PE- estrogen, smoking, sedentary
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5
Q

CBC- Mean Cell Hemoglobin (MCH)

A

27-33 picogram

Amount of hemoglobin in 1 RBC- used with MCHC to determine iron deficiency

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6
Q

CBC- Mean cell hemoglobin concentration (MCHC)

A

33-37 g/dL

Hypochromic indicates iron deficiency

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7
Q

CBC- Red cell distribution width

A

Distribution of size of RBCs- wide indicates varied cell sizes- mixed anemia or thalassemia

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8
Q

CBC- White blood cell count

A

500-10,000mm2

Number of leukocytes in volume of blood- order differential to determine types of WBCs

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9
Q

CBC- WBC differential

A

PMNs, Band neutrophils- Acute infection,
lymphocytes- viral infection,
monocytes- chronic infection,
eosinophils- allergy/worms basophils- chronic inflammation.

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10
Q

Normocytic anemia

A

Hgb &Hct-low, MCV- normal

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11
Q

Microcytic anemia

A

Hgb &Hct-low, MCV & MCHC- decreased

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12
Q

Macrocytic anemia

A

Hgb &Hct-low, MCV increased

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13
Q

Polycythemia

A

Hgb & Hct- high

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14
Q

Leukocytosis

A

WBC increased- differential indicates type and reason

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15
Q

Leukopenia

A

WBC decreased- differential leads to reason

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16
Q

Thrombocytosis

A

Platelets >400,000- risk of excessive clotting

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17
Q

Thrombopenia

A

Low platelet- risk of uncontrolled bleeding

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18
Q

CBC- left shift

A

Increase in number of band (immature) cells. Indicates infection, leukemia, myeloprolifereative disorders, myelofibrosis, hemorrhage

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19
Q

Fresh whole blood

A

All blood components- Indicated for hemorrhage >25% blood loss, cardiac surgery, emergencies

20
Q

Packed RBC

A

RBCs with small amt plasma and variable leukocytes- indicated to raise hematocrit, increase O2 carrying capacity

21
Q

Leukocyte poor blood

A

Decreased leukocyte levels- to reduce risk of agglutination rxn

22
Q

Frozen packed RBC

A

Stored for 10 years, preserve rare blood types- pts with severe retains to plasma protein

23
Q

Autologus packed RBC

A

Patients own blood stored for future use- elective surgery, stored 35 days before freezing

24
Q

Hemolytic transfusion reaction-

A

Mismatch of ABO blood typing- fever, chills, HA, hypotension. Prevention- hydration & diuresis

25
Anaphylactic reaction
IgE mediated response to incompatible blood- shock, vasodilation. T with epi, airway mgmt, steroids
26
Bone marrow biopsy
Diagnosis of leukemias- unexplained anemia, thrombocytopenia, leukopenia
27
Lymph node biopsy
Diagnosis of lymphoma based on cellular morphology
28
Total Iron Binding Capacity
Measures iron bound to transferrin- Increased in iron deficiency anemia
29
Serum Ferritin
Indirect measure of iron stores- markedly reduced in iron deficiency anemia
30
CBC
Low Hgb & Hct- indicates which type and deficiencies. Initial test
31
Hemoglobin electrophoresis
Determination of types of hemoglobin present- Id thalassemia
32
MMA
Metabolic intermediary of Vit B12- indicates anemia assoc with deficiency
33
Reticulocyte count
Immature, nucleated RBCs- high in anemia- can't complete making the cells
34
Bilirubin
Hemoglobin converted into bilirubin- high bilirubin indicates hemolytic anemia
35
Bone marrow biopsy
Gold standard- invasive & expensive, only used with unexplained anemia- find errors in RBC factory
36
Prothrombin Time
Extrinsic & common pathway- factors II, V, VII & X. Measures time to clot- increased time indicates abnormal. Less useful than INR.
37
INR
Ratio of patient PT vs mean normal. More sensitive than PT. Monitor patients on warfarin. Measures extrinsic & common pathway factors
38
aPTT
Screening test for deficiency & inhibitors of intrinsic pathway factors (VIII, IX, XI & XII) and common pathway. Report of clotting time, in seconds. Prolongation abnormal- heparin therapy, lupus,
39
Bleeding time
Measure of platelet fxn. Not specific or sensitive. Small cuts on forearm and measure bleeding time. Not used
40
D-dimer
Rule out thromboembolism. Elevated in VT, but not specific marker as may be elevated in other conditions. Measures fibrin degradation products.
41
Fibrin split products
Increase may indicate primary or secondary fibrinolysis. Clot break down
42
Factor assays
Determine etiology of prolonged PT or PTT, acquired or hereditary- hemophilias
43
Direct Coombs
Detects antibody mediated destruction of RBCs- hemoytic uremic syndrome, Rh hemolytic disease
44
Indirect Coombs
Detects presence of antibodies in body prior to transfusion, pregnancy
45
Mixing study
Determine if abnormal PT/PTT is due to factor deficiency or antibody inhibitor. Correction of PT/PTT with normal plasma suggest factor deficiency. Failure to correct suggests ab inhibitor.