Ch. 23 in class notes Flashcards

(57 cards)

1
Q

look at first in cbc with rbc

A

hemoglobin- see anemia or polycythemia

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2
Q

rbc #

A

5 million

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3
Q

hemoglobin and hematocrit

A

look at the same time- 1. determine anemia vs polycythemia 2. mcv (microcytic less than 80 or normocytic or macrocytic over 120)

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4
Q

microcytic size

A

80

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5
Q

macrocytic size

A

120

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6
Q

if microcytic

A

iron deficiency, thalassemia

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7
Q

if high ferritin and high iron and serum iron is low

A

anemia of chronic disease

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8
Q

total iron binding capacity low

A

anemia of chronic disease

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9
Q

thalassemia confiremed by

A

hemoglobin electrophoresis

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10
Q

variation btw lg and sm cells. if rate is high means the bone marrow is stimulated. is the case in…

A

rdw/fe deficiency

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11
Q

normal rdw

A

thalassemia

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12
Q

target cells

A

thalassemia

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13
Q

high reticulocytes

A

losing blood or blood destroyed from overactive spleen (hemolysis) (normocytic)

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14
Q

low reticulocytes (normocytic)

A

low production of rbc- ckd lowering erythropoietin, aplastic anemia

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15
Q

ow hemoglobin and hematocrit and normal MCV but have low reticulocytes. normal kidney function

A

could be early fe def deficiency bc typically microcytic but normocytic so early

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16
Q

macrocytic above 100 what do first

A

smear (ex. hypersegmented) then b12 test and folate test

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17
Q

if normocytic what do u do

A

reticulocytes

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18
Q

b12 sx

A

neurologic

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19
Q

drugs and liver disease can cause

A

macrocytic

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20
Q

if high reticulocyte expect hemolysis test for

A

bc hemoglobin broken into heme and bilirubin so have high LDH and high bilirubin

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21
Q

what protein gets attached to hemoglobin

A

haptoglobin

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22
Q

expect high or low haptoglobin if?

A

low

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23
Q
A

sicklecell anemia
spherocytosis
g6pd
?

24
Q

g6pd

A

beans? trigger hemolysis

25
hemolytic and aquired
thrombotic thrombocytic p... (ttp)(microangioblastic hemolysis. bc squeeze into capillaries) DIC
26
hypoxia JAK2 mutation
polycythemia
27
maintains RBC shape
Spectrin-ankyrin cytoskeleton
28
2 α + 2 β chains; each with a heme unit (Fe²⁺ binds O₂).
hemoglobin A
29
: 2 α + 2 γ chains → ↑ O₂ affinity (important for fetal gas exchange).
hemoglobin F
30
what regulates hemoglobin synthesis?
iron availibility
31
index of marrow activity
reticulocyte count
32
bone marrow reacting appropriately rest, determine if bone marrow biopsy is needed
Reticulocyte Index
33
high unconjugated bilirubin
jaundice
34
what rbc rely on for atp
anaerobic glycolysis bc lack mitochondria
35
reduces Hb’s affinity for O₂ → enhances tissue oxygen delivery.
2,3-DPG
36
protects against oxidatice damage in rbc
G6PD
37
Oxidative stress → Heinz bodies → hemolysis (e.g., G6PD deficiency).
38
mix donor RBCs + recipient serum → observe for agglutination
crossmatch
39
screen for antibodies in recipient
indirect coombs
40
detects antibodies bound to RBCs
direct coombs
41
Hb <7 g/dL or symptomatic anemia
transfusion indications
42
transfuse for massive acute loss
whole blood
43
transfude if anemic to increase o2 delivery
PRBCs
44
transfuse if thrombocytopenia under 10k or active bleeding
platelets
45
transfuse if coagulation factor replacement
ffp
46
transfuse if fibrinoge, vwf, factor 8
cryoprecipitate
47
acute lung injury
TRALI
48
...
taco
49
cause abo incompartibility to intravascular hemolysis
Acute Hemolytic Transfusion Reaction (AHTR)
50
Symptoms (within minutes): fever, chills, back pain, hypotension, hemoglobinuria
AHTR
51
Labs: ↑ LDH, ↓ haptoglobin, hemoglobinemia, positive Coombs
ahtr
52
Complications: DIC, renal failure, death
ahtr
53
Donor anti-leukocyte antibodies trigger capillary leak Onset <6 hrs → hypoxia, bilateral infiltrates, normal CVP
trali
54
Volume overload, esp. in elderly, heart failure Onset <6 hrs → dyspnea, ↑ CVP, BNP ↑, pulmonary edema
taco
55
immune
trali
56
fluid volume excess
taco
57