Hemotology Flashcards

1
Q

normal HGB for male and female

A

male: 15 ish
female: 13 ish

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2
Q

normal HCT

A

multiply by 3
35-45

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3
Q

WBC count

A

4-10

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4
Q

platelets normal

A

150-400

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5
Q

what platelet count can lead to spontaneous bleeding

A

less than 20,000

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6
Q

causes of thrombocytopenia

A

-decreased platelet production (decreased bone marrow function)
-acute viral infections (EBV, rubella, CMV, HIV)
-autoimmune disease
-nutritional deficiencies
-radiation therapy/chemotherapy
-disseminated intravascular coagulation
-hyperslenism
(1/3 of platelets are stored in the spleen)

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7
Q

what does the spleen do

A

filter and clean blood, serves as a reservoir for blood, part of the immune system

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8
Q

what is Immune thrombocytopenia purpura (ITP)

A

immune disorder, common in children, platelets accumulate and are destroyed by phagocytes in the spleen and other lymphoid tissues
treatment: childrens rarely need treatment
adults: steroids, blood transfusions, splenectomy (rarely)

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9
Q

what is TTP
(thromboti thrombocytopenic purpura)

A

this is worse than ITP
-less common
-enhanced aggregation of platelets. with form clots!
-characterized by: hemolytic anemia, thrombocytopenia, fever not associated with infection, neuro and renal abnormalities
-caused by a deficiency in enzyme ADATS13
-medical emergency!!

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10
Q

what is the purpose of WBCs? what are the two types

A

defend body against infection, remove debris
agranular: T-cell, B-cell NK cell lymphocytes, monocytes
granular: basophils, neutrophils, eosinophils

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11
Q

what does a left shift mean?

A

that there are more young neutrophils
more bands (immature) than segs (matture)
it means that there is a bacterial infection

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12
Q

manifestations of neutropenia

A

frequent infection, purulent drainage might not occur,
-they might not get a fever in the same way (a low grade fever could be very significant)

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13
Q

what does a reticulocyte count mean?

A

it means that your body is throwing out immature red blood cells because the mature ones are used up

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14
Q

examples of anemias of deficient RBC production

A

-iron deficiency
-b12 deficiency
-megaloblastic (folic acid deficiency and cobalamin)
-aplastic anemia
-anemia from medications, such as chemotherapy, thalassemia

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15
Q

examples of hemolytic anemias

A
  • destruction of rbc’s
    -sickle cell disease
    -enzyme deficiency
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16
Q

s/s of iron deficiency anemia

A

pale skin, fatigued, tachypnea, tachycardi, inflamed tongue, inflamed lips

17
Q

diagnosis of iron deficiency anemia and treatment

A

-CBC will be low
-iron studies will be low
-total iron binding capacity will be HIGH
**Microcytic, hypo-chromic **
to treat, we replace iron by giving supplements, or for severe a transfusion of packed RBCs

18
Q

oral iron supplements education

A

-to enhance absorption, take one hour before meals, take with vitamin C or orange juice
-undiluted iron may stain teeth
-GI side effects are common
-stools will be black

19
Q

megaloblastic anemias

A

‘Ba’Ba’
Big red blood cells
includes coBalamin (vit B12), folic acid anemia
Macrocytic, normochromic

20
Q

pernicious anemia

A

autoimmune disorder that leads to destruction of the gastric mucosa and loss of parietal cells
-leads to lack of intrinsic factor necessary for absorption of vitamin b12

people at risk: chronic gastritis, chronic alcoholism, gastrectomy, ilium resection, illium inflammation or neoplasm

21
Q

thalassemias

A

autosomal recessive blood disorder common in ethnic grous near mediterranean
-reduction in production of normal hemoglobin

22
Q

interprofessional care of thalassemia

A

-blood transfusions
-iron chelation (binds to iron and reduces iron overload)
-folic acid and zinc supplements

23
Q

hemolytic anemias S/S

A

jaundice and dark urine

-increased schistocytes
-increased reticulocytes
-increase LDH
-decreased Haptoglobin

24
Q

Treatment and Management of Acquired Hemolytic Anemia

A

-determine and treat causative agent
-supportive care
-emergency preparedness (hydration, electrolyte replacement, corticosteroids, blood products, splenectomy)
-medications such as rituximab and eculizumab

25
Q

what is acute chest syndrome

A

a complication of sickle cell disease
-acute pulmonary complications like pneumonia, tissue infarction, fat embolism
characterized by fever, chest pain, cough, dyspnea
can lead to pulmonary hypertension, heart failure, miocardial infarction AND MORE

26
Q

aplastic anemia

A

bone marrow & blood stem cells are damaged
pancytopenia
-congenital or acquired