Hematology Flashcards

(47 cards)

1
Q

Polyheme

A

Does not have to be refrigerated and is universal

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2
Q

Types of infusion

A

Whole blood
Packed Red Cell’s
Fresh Frozen Plasma
Clotting Factors

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3
Q

What are the 5 areas that form blood

A

Red bone marrow (all types of erythrocytes formed here)

Yellow bone marrow (produces white cells)

Lymph nodes (produces lymphocytes and antibodies)

Spleen (Stores large quantities of blood & produces lymph, plasma cells and antibodies)

Liver (during intrauterine life)

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4
Q

What % of blood is RBC

A

95%

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5
Q

Plasma

A

fluid portion of blood (92% water)

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6
Q

RBC life span

A

120 days

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7
Q

RBC production cycle

A

Starts with one cell in the red marrow and divides into 16 then develop

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8
Q

WBC’s

A

5-10K cells/mm3

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9
Q

Platelets

A

Thrombocytes that travel to site of damage, swell and adhere to damaged vessel wall

Will start clotting cascade if damage too great.

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10
Q

Hematocrit

A

measures fraction of blood volume cantaining RBC’s
40-50% in males
35-45% in females

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11
Q

Hemoglobin

A

14-18% in males

12-16% in females

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12
Q

Anemia

A

poor O2- concentration of hemoglobin or RBC’s is below normal.

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13
Q

Precipitating causes of anemia

A

Chronic or acute blood loss
Decrease erythrocyte production
Increased destruction of erythrocyte

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14
Q

Common forms of anemia

A

Iron-deficiency anemia
Hemolytic anemia
Aplastic
Pernicious

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15
Q

Iron-deficiency anemia

A

Bone marrow roduces small and pale RBC’s with reduced O2 carrying capacity

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16
Q

Most common causes of iron deficiency anemia

A

Menstruation
GI Bleeds – stress, infection, alcoholics
Iron poor diet in kids

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17
Q

Hemolytic Anemia types

A

Inherited and aquired

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18
Q

Inherited

A

Often abnormal rigidity of cell membrane causing smaller cells
Cells trapped in the smaller blood vessels (often spleen) and destroyed by macrophages

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19
Q

Examples of Inherited hemolytic anemia

A

Sickle cell
Thalassemia
Glucose-6-phosphate dehydrogenase

20
Q

3 conditions of aquired

A

Normal RBC’s disrupted due to mechanical forces (blood clots, atherosclerosis)
Autoimmune disorders which can destroy RBC’s with antibodies
RBC’s destroyed by microorganisms in the blood (ie malaria)

21
Q

Other anemias

A

Aplastic
Failure to produce RBC’s
Pernicious (usually inherited)
Lack of vitamin B, needed for cell division

22
Q

Anemia S/S

A
SOB
Chest pain
Fever
Pale
Fatigue, lethargy
Headaches
Sore mouth or tongue
Brittle nails
Cutaneous bleeding
Bleeding from mucous membranes
23
Q

Anemia Dx

A

History, blood tests, bone marrow biopsy

24
Q

Leukemia

A

Cancer of Hematopoietic Cells – abnormal cells develop

25
Leukemia more common
Males and caucasians, children and young adults
26
Leukemia mortality in children
50%
27
Leukemia classified by type of WBC
Acute lymphoblastic leukemia (ALL)--Usually in kids | Acute myeloblastic leukemia (AML)--Usually middle age adults
28
Leukemia S/S
``` FREQUENT BRUISING Fatigue Infections secondary to low levels of Neutrophils (WBC) Bone pain Elevate temperature and diaphoresis Heat intolerance Abdominal fullness Bleeding Headache Weight loss Night sweats Enlarged lymph nodes, spleen, liver and testes ```
29
Dx Leukemia
``` Bone marrow biopsy Severity assessed by Degree of liver and spleen enlargement Anemia Lack of platelets in the blood ```
30
Rx of Leukemia
Transfusion of blood and platelets Antibiotic therapy Anticancer drugs - chemotherapy Radiation
31
Lymphomas
``` Any neoplastic disorder of lymph tissue Two types Hodgkin's Non-Hodgkin’s Malignant ```
32
Hodgkin's Lymphoma
Abnormal function of B cells | more common in males, in 20's and then 55-70
33
Hodgkin's S/S
Swollen lymph Fatigue Chills Night sweats
34
Non-Hodgkin's Lymphoma
Vary in malignancy according to nature and activity of normal cells At least 10 types Classified low to high grade Cause unknown
35
Multiple Myeloma
Malignant neoplasm of the bone marrow Composed of plasma cells Production of large amounts of protein Increases viscosity of blood
36
Multiple Myeloma S/S
``` Destroys bone tissue causing Pain – early Fractures - early Hypercalcemia Skeletal deformities ```
37
Multiple Myeloma
rare before 40
38
Polycythemia
Increase in total RBC mass
39
2 types of polycythemia
Secondary—due to hypoxia | Primary—due to unknown reasons
40
Secondary Polycythemia
Naturally present in people who live or visit high altitude areas
41
Primary Polycythemia
Polycythemia Vera Condition occurs in those >50 years old Increased blood production causes blood to thicken and cause hands and feet to have red-purple complexion
42
Hemophilia
Group of inherited bleeding disorders | Loss of 1 of 13 clotting factors
43
Type A and B hemophilia
A—loss of factor VIII – most common | B—loss of factor IX AKA Christmas disease
44
Sickle Cell Disease
Sickle Hemoglobin has a flawed chemical structure that results in erythrocyte deformity when oxygen levels are low. Chronic Sickle Cell = Chronic Hemolytic Anemia
45
Sickle Cell S/S
``` PAIN DUE TO HYPOXIA EXCRUCIATING BONY DEFORMITIES Increased weakness Aching CP with SOB Sudden severe abdominal pain Icteric sclera Fever Arthralgia ```
46
Sickle Cell (vaso-occlusive) Crisis
``` DEHYDRATION INFECTION STRESS TRAUMA Exposure to temperature extremes Hypoxia Strenuous physical activity ```
47
Sickle Cell Rx
Treatment – Pain management, oxygen, fluids, rest and normothermic temperature