anemia patho - Exam 1B Flashcards

(31 cards)

1
Q

abnormal anemia

A

sickle cell disease

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2
Q

decreased Hgb content

A

loss of iron & loss of key nutrients
hypochromic/pale

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3
Q

decreased number of circulating erythrocytes

A

decreased production
increased destruction
blood loss

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4
Q

iron is essential for

A

normal hgb production

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5
Q

folate & B12 are necessary for

A

normal DNA synthesis of RBCs

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6
Q

in megaloblastic anemia, MCV is

A

increased

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7
Q

in iron def anemia, MCV is

A

decreased

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8
Q

clinical manifestations of all anemias (mild - mod)

A

-fatigue/weakness
-tachycardia
-dyspnea

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9
Q

clinical manifestations of all anemias (mod - sev)

A

-increased HR & RR
-hypotension
-pallor
-faintness
-cardio probs

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10
Q

etiologies of IDA

A

decreased intake, impaired absorption, increased demand and excessive loss

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11
Q

people at risk for IDA

A

people w/ poor intake, elderly, teens with heavy periods

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12
Q

IDA clinical manifestations

A

-smooth tongue
-glossitis
-mouth ulcers
-cheilosis
-koilonychia
-pica
in childhood cognitive deficits

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13
Q

megaloblastic anemia is most common in the

A

elderly

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14
Q

causes of B12 deficiency anemia

A

-atrophic gastritis , IF not produced
-crohns, celiac
-pernicious anemia (autoimmune)

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15
Q

clinical manifestations of B12 def anemia

A

-neuropathy
-ataxia (poor muscle control)
-glossitis
-dementia/psychosis

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16
Q

folate deficiency is caused by

A

decreased intake, not absorption
-alcoholism bc folate is stored in liver
-diet
-cirrhosis
increased needs like during pregnancy & intake

17
Q

anemia of chronic kidney disease is caused by

A

impaired erythropoietin production epo is made in the kidneys & is released to tell bone marrow to make more RBCs

18
Q

aplastic anemia is caused by

A

bone marrow stem failure d/t autoimmune disease
-chemo/radiation
-complicated infection

19
Q

clinical manifestations of aplastic anemia

A

low RBCs, WBCs & platelets

20
Q

treatment for aplastic anemia

A

whole blood transfusion, bone marrow transplant, immunosuppressants, drugs to stim erythropoiesis

21
Q

what is acquired hemolytic anemia & what causes it

A

premature destruction of RBCs caused by external agent
-autoimmune attack
-blood incompatibilities
-drug reaction
-severe burn

22
Q

clinical manifestations of acquired hemolytic anemia

A

-low hgb
-increased reticulocyte (immature RBC) count
-mild jaundice
-hemoglobinuira

23
Q

triggers of sickle cell anemia

A

dehydration, stress, high altitudes, fever, extreme temps

24
Q

clinical manifestations of sickle cell anemia

A

-swelling of hands & feet
-pain
-clogged vessels

25
treatment of sickle cell anemia
1) oxygen 2) hydration 3) pain mgt antimetabolite drugs blood transfusion genetic counseling
26
thalassemia
genetic disorder occurring mostly in person of mediterranean descent -severe cases can lead to death in childhood d/t heart failure, live to 30s w/ treatment **lack of one of two proteins that make up hemoglobin, alpha & beta globin**
27
clinical manifestations of thalassemia
-delayed growth -fatigue -dyspnea -hepatomegaly -splenomegaly -bone deformities -jaundice
28
occult blood loss
GI bleed, retropertoneal bleed
29
in secondary polycythemia, increased blood viscosity & volume causes
-HTN (headaches, low concentration, ruddy face, cyanosis) -DVT -hemorrhage -angina -cerebral insufficiency -tIA
30
in secondary polycythemia, hyper-metabolism causes
-night sweats -weight loss
31
in secondary polycythemia, increase RBC and H&H cause
-itching (pruritus) -pain in fingers and toes