TEST 2- Anemia Flashcards

(28 cards)

1
Q

Anemia definition

A

Anemia is defined as a reduction in the number of red blood cells (RBCs), hemoglobin concentration, or hematocrit. In general, a hemoglobin concentration in adults below 13.6 g/dL for men or below 12 g/dL for women suggests anemia.

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2
Q

Symptoms of anemia

A

Asymptomatic generally until hgb <7.5= Fatigue, malaise, headache, dyspnea, irritability, and mild decrease in exercise tolerance

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3
Q

Normal RBC

A

male: 4.7-6.1
Female: 4.2-5.4

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4
Q

Normal hemoglobin

A
  1. 8-17.2

female: 12.1-15.1

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5
Q

Hematocrit

A

male: 41-50%
Female: 36-44%
rule of thumb: 1 hgb for every 3 hct

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6
Q

MCV

A

normal: 80-100

volume of RBC: tells you how big the RBC is. allows for classification of anemia:

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7
Q

MCHC

A

normal: 32-36

concentration of hgb in RBC’s: tells you how colorful RBC’s are (Pale, dark, normal).

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8
Q

Reticulocyte count

A

normal 0.5-2%. baby RBC’s. marrow production of RBC’s differentiate if anemia is related to decreased production or increased loss.

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9
Q

hgb electrophoresis

A
shows percentage of subclass of hgb
helps identify thalassemias
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10
Q

Rdw

A

12.2-16.1 in females
11.8-14.5 in males
rbc distribution. tells you variance in size of RBC (lets you know if there are a lot of reticulocytes or not)

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11
Q

TIBC

A

transferrin iron binding capacity
normal: 250-420
indirectly measures amount of transferrin
indicates the availability of binding sites on the protein for iront ransport

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12
Q

Serum ferritin

A

10-120 ng/ml in females
20-250 in males
total body iron stores
first level to become abnormal when iron stores are becoming depleted.

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13
Q

Serum iron

A

50-170 females
65-175 males
amount of iron bound to transferrin

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14
Q

Transferrin saturation percentage

A

20-50%

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15
Q

Types of anemia

A

Microcytic hypochromic- MCV <80, decreased MCHC
Macrocytic, normochromic: MCV >100 normal MCHC
Normocytic, normochromic: MCV: 80-100, normal MCHC

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16
Q

IDA is most common in..

A

Young children and pregnant women.

most common anemia in the world- usually nutrient deficiency

17
Q

What diagnostic test when considering anemia..

A
number 1: CBC
peripheral smear
reticulocyte count
ferritin
TIBC
serum iron
transferrin
stool for occult blood x3
electrophoresis
Iron studies- to differentiate between microcytic d/t IDA versus ACD, thalassemia, etc.
18
Q

What leads to mild IDA

A

inadequate diet, normal/heavy menses, blood donation, malabsorption, periods of rapid growth, pregnancy

19
Q

what leads to moderate to severe IDA (symptomatic)

A

chronic blood loss, PUD, varices, malignancy, diverticulitis, severe menorrhagia, severe malabsorption.

20
Q

Labs for IDA

A

CBC w diff, ferritin, iron, TIBC,

HGB will be low, ferritin will be low, iron can be low, tibc high, transferrin saturation low.

21
Q

Management for IDA

A

1st line: treat underlying cause!!
If severe, or malabsorption syndrome/unable to tolerate PO- consider IV iron AND REFER to hematologist.
replace iron: oral: 150-200mg daily until anemia corrected. Continue empirically until ferritin level is over 50.
side effects: nausea, constipation, upper gi discomfort, black stools, diarrhea.
iron absorption is optimum when taken 30 minutes before meals with vit. C. No dairy or calcium 1-2 hours after taking iron.
start on a low dose and increase slowly. Once ferritin levels have increased, hgb should follow in 1-2 weeks. MCV in 1-2 months.
ferrous sulfate 325mg= 65mg of elemental iron for ida give 750-1500mg/day divided BID-QID
for kids: 1mg/kg/day
pregnancy: supplementation almost always required. best indicator is serum ferritin.
older adults: if IDA throughoughy evlauate for GI cancers.
incrase iron rich foods, screen for nsaid overuse, strict vegetarians need supplementation.

22
Q

symptoms specific to IDA

A

if severe: paresthesia, sore tongue, brittle nails, spoon shaped nails, pica

(other symptoms if severe (general anemia symptoms): fatigue, exercise intolerance, weak, palpitations, irritability headaches)

23
Q

What is Thalassemia?

A

Inherited blood disorder that affects how the body makes hemoglobin. Microcytic, hypochromic (MCV<80, decreased MCHC).

24
Q

Thalassemia Alpha types

A

Alpha: 4 genes (two from each parent)
Silent carrier: 1 gene affected, asymptomatic, normal hgb and rbc.
Alpha thalassemia minor (trait): two genes affected, carrier, mild anemia, asymptomatic
Hemoglobin H disease: three genes affected, moderately to severely anemic
Alpha thalassemia major (hydrops fetalis): four genes affected, leads to premature births that are either stillborn or die shortly after birth → incompatible with life

25
Beta
Autosomal recessive Affected people: Mediterranean, Middle Eastern, African, Asian 2 genes (one from each parent) involved Beta thalassemia minor (trait): one gene affected Beta thalassemia intermedia: two genes affected, moderate anemia Beta thalassemia major (Cooley’s anemia): two genes affected, severe anemia
26
CM of Beta Thalassemia intermedia/major
``` Short stature Abnormal facies Cranial marrow expansion - trying to make more RBCs Pallor, jaundice, enlarged spleen, liver, or heart Beta thalassemia intermedia Moderate microcytic, hypochromic anemia Not transfusion dependent Beta thalassemia major Severe anemia Transfusion dependent ```
27
Thalassemia Alpha Major
Alpha → incompatible with life
28
Labs for Thalassemia
Anemia ⬇ MCV ✔ iron studies Hemoglobin electrophoresis (⬆ levels of hemoglobin A2) >3.5%- p.751 (primary diagnostic) Alpha globin DNA mutation (REFER for this if thalassemia is suspected, test not readily available) Mentzer index <13