Anemia Flashcards

1
Q

Examination

A

Heart rate
Pallor: nailbeds, conjunctiva, oral mucosa
Jaundice
Signs of liver disease
Hemorrhoid so
Orthodontic changes
Strophic glossitis (smooth, shiny tongue)
Loss of proprioception and paresthesia’s (meglobalism, B12)
Evidence of chronic disease (renal/hepatic/GI/cancer)
Petechiae/Ecchymosis
Enlarged spleen

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2
Q

Anemia by Etiology

A

Blood loss

  • acute
  • chronic

Decreased production

  • B12, folic acid, Fe deficiency
  • infiltration of marrow by neoplasia
  • aplastic anemia

Increased destruction
* hemolytic anemias

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3
Q

Microcytic

A

Fe deficiency
Thalassemia
Lead poisoning

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4
Q

Normocytic

A

Chronic disease
Renal disease
Infections
Acute blood loss

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5
Q

Macrocytic

A

B12, folic acid deficiency

Abnormal DNA synthesis

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6
Q

Macrocytic Anemia

A

*Deficiency of vitamin B12
*Deficiency of folic acid
Drugs affecting DNA synthesis
Inherited disorders of DNA synthesis
*Liver disease
Hypothyroidism
Hypopituitarism
Accelerated erythropoiesis (reticulocytes)
Hypogastric and aplastic anemia
Infiltrated bone marrow
Acute leukemia

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7
Q

Normocytic Anemia

A
Anemia of chronic dx
Endocrine etiology
Acute blood loss
*Renal failure
Hyperspace sim
Neonatal anemia
Hemolysis
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8
Q

Decreased Production RBC’s

A

Infiltration of marrow: neoplasia, myelofibrosis
Hyperplastic marrow: B12, folate, Fe deficiency
Aplastic/hypoplastic marrow - pure RBC aplasia: acquired acute RBC hypoplasia
Aplastic/hypoplastic marrow - familial: Diamond-Blackfan, Fanconi, Congenital pancytopenia
Aplastic/hypoplastic marrow (drugs/idiopathic): antibiotics, Dilantin, viral hepatitis
Aplastic/hypoplastic marrow - dose related: heavy metals, benzene, antimetabolites

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9
Q

Hemolytic Causes

A
Sickle cell
Hereditary spherocytosis
G6PD
Pyruvate Kinase deficiency
Microangiopathic disorders: DIC, Hemolytic uremic syndrome, TTP
Mechanical hemolysis
Paroxysmal Nocturnal hemoglobinuria
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10
Q

Intracorpuscular Defect: Hereditary

A
  • hereditary spherocytosis
  • hereditary elliptocytosis
  • hemoglobinopathies
  • thalassemias
  • congenital dyserythropoietic anemias
  • hereditary RBC enzymatic deficiencies
  • rarer hereditary abnormalities
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11
Q

Intracorpuscular Defect: Acquired

A
  • vitamin B12 and folic acid deficiency
  • paroxysmal nocturnal hemoglobinuria
  • server iron deficiency
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12
Q

Extracorpuscular Defect

A
  • physical agents: burns, cold exposure
  • traumatic: prosthetic heart valves, march hemoglobinuria, disseminated intravacular coagulation (DIC), graft rejection
  • chemicals: drugs and venoms
  • infectious agents: malaria, toxoplasmosis, mononucleosis, hepatitis, primary atypical pneumonia, clostridial infections, bartonellosis, leishmaniasis
  • hepatic and renal disease
  • collagen vascular disease
  • malignancies: particularly hematologist neoplasia
  • transfusion of incompatible blood
  • hemolytic disease of the newborn
  • cold hemagglutinin disease
  • autoimmune hemolytic anemia Thrombotic thrombocytopenic purpura (TTP) and hemolytic-uremic syndrome (HUS)
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13
Q

Nutritional Etiologies

A

Iron deficiency
Vitamin B12 deficiency
Folate deficiency
Starvation and generalized malnutrition

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14
Q

Physical Etiologies

A

Trauma
Burns
Frostbite
Prosthetic valves and surfaces

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15
Q

Past Medical History

A
Ethnicity
Black/tar colored stool
Bleeding
Fatigue easily
Transfusions
History of jaundice
Females- menstrual flow
Medications
Pica - iron deficiency anemia
Clay eating - bind with iron => deficiency
OTC
Diet
Travel history
History of illness (acute and chronic)
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