Clinical Care of the Hematologic System Flashcards

1
Q

anemia is defined by a value less than what in:

Males

Females

A

Less 41%, males

Less than 37% in females

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2
Q

a ferritin lab value of what indicated anemia

A

less than 12 mcg/L ferritin

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3
Q

most common cause of iron deficiency anemia

A

bleeding

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4
Q

what is the most common type of anemia word wide

A

Iron deficiency

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5
Q

what increases chances of iron anemia

A

menstruation

pregnancy

frequent blood donations

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6
Q
  • Fatigue
  • Tachycardia
  • palpitation
  • tachypnea
  • cheilosis
  • Dysphasia (due to esophageal webs)
  • Pica( ice chips)

What is the DX

A

Iron Anemia

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7
Q

if a patient is given Ferrous Sulfate what else will be prescribed

A

stool softener or laxative

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8
Q

Ferrous Sulfate turns the stool what color

A

black

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9
Q

how much vitamin B12 does the liver contain

A

2000 - 5000 mcg

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10
Q

B12 vitamin develops after how many years after abortion is ceased

A

3 years

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11
Q

daily loss of vitamin B12 is

A

3-5 mcg/dL

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12
Q

Vitamin B12 is rare and only seen in what population

A

Vegans

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13
Q

What are physical findings for B12 deficiency

A

Glossitis

Anorexia

Late stage appears:

Pale

Paresthesia

difficulty w/ balance

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14
Q

whats a hallmark CBC with Diff for B12 deficiency

A

Megaloblastic anemia

with characteristic find of macro-ovalocyte with hyperpigminted neutrophils

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15
Q

what lab value is overly B12 deficiency

what lab value will show B12 deficient symptoms

A

170 pg/mL

100 pg/mL

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16
Q

whats the treatment for B12 deficiency

A

IM injection of vitamin B12

  • daily for 1st week
  • weekly 1st month
  • Monthly for life
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17
Q

what are the intrinsic pathways

A

12

11

8

9

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18
Q

what are the extrinsic pathways

A

7

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19
Q

Hemophilia A is Congenital Deficiency of coagulation of factor

A

Congenital Deficiency of coagulation of factor 8

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20
Q

Hemophilia B is Congenital Deficiency of coagulation of factor

A

Congenital Deficiency of coagulation of factor 9

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21
Q

what a complications of both coagulopathies

A

recurrent hemarthroses or
arthropathy

inhibitory antibodies to factor 8 or 9

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22
Q

complications of both coagulopathies is due to

A

infection with HIV or Hep C blood products

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23
Q

what is disseminated intravascular coagulation

A

its a systematic process with the potential for causing thrombosis and hemorrhage

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24
Q

what are common manifistation for disseminated intravascular coagulation

A

ecchymosoes

blood ozzing

venous thrombosis

arterial theombosis

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25
what are common causes of disseminated intravascular coagulation
Sepsis Malignancy trauma
26
what is the go to medication to treat disseminated intravascular coagulation
Heparin
27
what are complications of disseminated intravascular coagulation
Anemia Massive hemorrhage
28
what is G6PD
hereditary enzyme defect that causes episodic anemia because of RBC to deal with oxidative stresses
29
In G6PD oxidized hemoglobin dentures and forms precipitations called
Heinz bodies
30
Heinz bodies cause membrane damage which leads to removal by what organ
Spleen
31
G6PD is exacerbated by what drug
primaquine nitrofurantoin aspirin
32
what is a consideration of military G6PD members
red dog tags ans warning on front of the health record
33
what is Hemoglobinopathies / Sickle cell
a anemia austosomal recessive disorder in which an abnormal hemoglobin S
34
hemoglobin S is carried in what percent of African Americans
8%
35
what are S/S of Hemoglobinopathies / Sickle cell
jaundice Gallstones Hepatosplenmegly poor healing ulcers
36
what are s/s of acute Hemoglobinopathies / Sickle cell
pain in bones (especially back, long bones chest)
37
acute Hemoglobinopathies / Sickle cell last for how long
hours to days
38
acute Hemoglobinopathies / Sickle cell labs have a hallmark of
hyposplenism such as Howell-Jolly bodies and target cells
39
when acute painful episodes occur what should be the precipitating factors
keep hydrated and prevent hypoxemia search for underlying factors
40
what are considerations sickle cell trait
painful episodes with vigorous exertion or high altitudes
41
what is acute leukemia
malignancy of the hematopoietiuc progenitor cell
42
acute leukemia is classified into what two subcategories
Acute myeloid leukemia (AML) or acute lymphoblastic leukemia (ALL)
43
what type of acute leukemia comprises 80% of childhood leukemias and 20% of adult leukemias
acute lymphoblastic leukemia (ALL)
44
what type of acute leukemia is primarily an adult disease
Acute myeloid leukemia (AML)
45
what are S/S of acute leukemia
fatigue bleeding in the skin and mucosal surfaces such as gingiva epitaxis menorrhagia enlagrment of the liver, spleen, lymph nodes bone tenderness (sternum, tibia, femur)
46
whats a DXx for acute leukemia
Pertussis (whooping cough)
47
what are lab hallmarks for acute leukemia
pancytopenia with circulating blast
48
do you retain or medevac acute leukemia
medevac
49
what is Leukocytosis / Leukopenia
Leukocytosis high white cell count Leukopenia low white cell count
50
if a patient has determined to have Leukocytosis with a high lymphocytes what is the cause
viral infection Immune disease stress
51
if a patient has determined to have Leukocytosis with a high Eosinophils what is the cause
Skin diseasse drug reaction parasite infection asthma
52
if a patient has determined to have Leukocytosis with a high basophils what is the cause
chronic myeloid lukemia
53
if a patient has determined to have Leukocytosis with a high monocytes what is the cause
infection autoimmune disease
54
1 etiologies for leukopenia is ethnic neutropenia at what percent does it affect black and whites
4. 5% blacks | 0. 7% whites
55
what are S/s of leukopenia
fever jaundice rash
56
What is thromnoctopenia
low amount of circulating platlets
57
the risk of spontaneous bleeding doe not typically increase until platelet count falls below what
10,000 to 20,000 mcL or unless pt has Dysfunctional platelets
58
what are causes of thromnoctopenia
bone marrow failure medications bone marrow malignancy
59
what helps determine weather a deficiency is platelets issue rather than a coagulopathy
petchia
60
what is Thrombocytosis
abnormal high amount of thrombocytes 450,000
61
what are the two different types of thrombocytosis
reactive tthrombocytosis Autonomus thrombocytosis
62
what is a S/S of thrombocytosis
erthromelgia (see with painful burning of hands with erythemia)
63
what is the treatment plan for thrombocytosis
refer to hemotology of there is no infectious cause or does not resolve in 2-4 weeks.