Anemia Flashcards

0
Q

Autoimmune Hemolytic Anemia

A

Warm Agglutinins - IgG

Cold Agglutinins - IgM

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1
Q

Approach to anemia

A
  1. Check the WBC and platelets to see if they are abnormal
    - coagulation, marrow or complex problem
  2. Check the MCV to determine micro or macrocytic anemia
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2
Q

Lab tests used to evaluate anemia

A
Retic count
Serum folate/B12
Serum iron, TIBC, ferritin
Serum transferin receptor concentration
ESR, CRP fibrinogen and haptoglobin
Serum creatinine
Erythropoietin
TSH
LDH, bilirubin, haptoglobin
Urine hemosederin and hemoglobin
SPEP, UPEP and quantitative immunoglobulins
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4
Q

Retic count

A

High - bleeding, hemolysis
Low - hypo proliferative bone marrow
>100, 100/uL - increased erythropoiesis and shift in reticulocyte pool from marrow to peripheral blood - bleeding, hemolysis, response to treatment
- calculate RPI - <2 implies inadequate bone marrow response

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5
Q

Folate/B12

A

Detects deficiency in macrocytic anemia

- will show hyper segmentation of neutrophils

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5
Q

ESR, CRP fibrinogen and haptoglobin

A

acute phase reaction due to inflammatory cytokines,

  • decrease erythropoietin production,
  • decrease responsivemess to erythropoietin
  • block iron transport
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6
Q

Serum creatinine

A

high - underproduction of erythropoietin

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7
Q

Serum iron, TIBC, ferritin

A

Low serum iron - iron deficiency, anemia of chronic disease or inflammation
iron deficiency - high TIBC, low ferritin, low % sat
chronic disease - low TIBC, normal/high ferritin, low/normal transferrin
inflammation - low TIBC

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8
Q

Erythropoietin

A

rises logarithmically above normal levels in relation to decreasing hematocrit

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9
Q

TSH

A

hypothyroidism which can cause anemia

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10
Q

Haptoglobin, LDH, bilirubin

A

Hemolysis:

  • Hapto < 20 - hemolysis
  • elevated LDH and total bilirubin levels
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11
Q

Urine hemosiderin and hemoglobin

A

intravascular hemolysis

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12
Q

SPEP, UPEP, immunoglobulins

A

possible plasma cell myeloma or lymphoma

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13
Q

Intravascular hemolysis

A

Hemolysis associated with cold agglutinin disease (IgM) or thrombotic microangiopathy

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14
Q

Extravascular hemolysis

A

Hemolysis mediated by the spleen

supported by IgG - spleen, macrophages, cells opsinized, phagocyte activity

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15
Q

Ddx for Microcytic Anemia

A
Iron deficiency anemia - increased RDW
a-thalassemia trait - normal RDW
B-thalassemia trait
B-thalassemia intermedia
Sickle cell-B-thalassemia
16
Q

Ddx for Megaloblastic Anemia

A

Folate deficiency
VB12 deficiency
Drug-induced changes in erythrocytes
Erythroleukemia

17
Q

Ddx for Hemolytic Anemia

A
Membrane defect
Enzymopathy
Hemoglobinopathy
Autoimmune hemolytic anemia
Erythrocyte fragmentation (TTP, HUS, DIC
Infection - malaria
Hypersplenism
18
Q

DDx for Normocytic anemia

A
Acute blood loss
CKD
Red cell aplasia
Malignancy
Alcoholic liver disease
Anemia of inflammation
Hemolytic anemia
19
Q

Treatment of sickle cell

A

hydroxyurea

20
Q

Complications of Hodgkin’s

A

Myelodysplastic syndrome and acute leukaemia in 3 - 11 years

21
Q

Human parovirus B19

A

Server chornic anemia in HIV patients
- lg multinucleated dysplastic proerythroblasts
- cessation of erythropoiesis with associated reticulocytopenia
Dx: paravirus in serum
Tx: IV immunoglobin

22
Q

Thalassemia

A

Betathalassemia - increased A2

23
Q

Symptoms of multiple myeloma

A

Anemia
Hypercalcemia
Renal dysfunction
Total protein level is increased in the presence of normal albumin

24
Q

Causes of Nucleated RBC

A

sickle cell disease/thalassemia
Myelofibrosis/metastatic disease
Sepsis/Life threatening trauma

25
Q

Diagnosis of hemolytic anemia

A

Elevated retic count
Elevated LDH
Elevated indirect bilirubin