Hematology Flashcards

(95 cards)

1
Q

Common signs and symptoms of hematologic disorders:

A

Weakness, fatigue, and general malaise, pallor of the skin and mucous membranes (conjunctivae, oral mucosa)

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2
Q

In hematological disorders, when the hemoglobin level is low, the heart attempts to compensate by?

A

pumping faster and harder to deliver more blood to hypoxic tissue.

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3
Q

In hematological disorders, increased cardiac workload can result in

A

tachycardia, palpitations, dyspnea, dizziness, orthopnea, and exertional dyspnea

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4
Q

In hematological disorders, heart failure may eventually develop d/t

A

an enlarged heart (cardiomegaly) and liver (hepatomegaly) and by peripheral edema.

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5
Q

In hematological disorders, pernicious anemia affects the:

A

central and peripheral nervous systems

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6
Q

Neuro assessments in hematological disorders should include:

A

the presence and extent of peripheral numbness, paresthesias, ataxia, poor coordination, and confusion.

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7
Q

In hematological disorders, delirium can sometimes occur from:

A

other types of anemia, particularly in older adults

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8
Q

This hematological disorder is congenital but typically idiopathic:

A

Aplastic anemia

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9
Q

Aplastic anemia is a disorder caused by

A

a decrease in or damage to marrow stem cells, damage to the microenvironment within the marrow, and replacement of the marrow with fat.

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10
Q

In aplastic anemia, Stem cell damage is caused by the body’s T cells

A

mediating an inappropriate attack against the bone marrow, resulting in bone marrow aplasia (i.e., markedly reduced hematopoiesis).

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11
Q

insidious- bone marrow failure (may be first real knowledge), purpurus, renal hemorrhage, splenomegaly are all symptoms of

A

Aplastic Anemia

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12
Q

Pernicious Anemia is an absence of

A

intrinsic factor

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13
Q

In pernicious anemia, Intrinsic factor is normally secreted by

A

cells within the gastric mucosa; it binds with dietary vitamin B12 and travels with it to the ileum, where the vitamin is absorbed

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14
Q

In pernicious anemia, without intrinsic factor, orally consumed vitamin B12 cannot be

A

adequately absorbed, and erythrocyte production is eventually diminished.

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15
Q

bleeding from ulcers, gastritis, inflammatory bowel disease, or GI tumors in men and postmenopausal women is most commonly caused by:

A

iron deficiency anemia

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16
Q

smooth, red tongue, brittle and ridged nails, and angular cheilitis: these are all signs of?

A

Severe or prolonged iron deficient anemia

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17
Q

A health history should be obtained for individuals with iron deficient anemia when they have a history of:

A

multiple pregnancies, GI bleeding, and pica

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18
Q

Mortality rate for this disorder can exceed 80%

A

DIC

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19
Q

Causes of DIC:

A

Sepsis, trauma, cancer, abruptio placentae, allergic reactions

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20
Q

2/3 of DIC cases are initiated by:

A

an infection or a malignancy

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21
Q

an infection or a malignancy

A

inflammation and coagulation within the vasculature

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22
Q

In DIC, the excessive clotting triggers the fibrinolytic system to

A

release fibrin degradation products, which are potent anticoagulants

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23
Q

Compromised organ function or failure, Ischemia, and bleeding (less common) are clinical manifestations of:

A

DIC

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24
Q

What will be tested to diagnose DIC?

A

low platelet and fibrinogen levels; prolonged PT, aPTT, and thrombin time; D-dimer

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25
Because of bacterial proliferation, blood administration should not exceed _ hours:
4
26
How often does blood tubing need to be changed in order to decease chances or bacterial contamination?
after every 2 units transfused
27
How many mL of blood and anticoagulants does a single unit of whole blood contain?
450mL whole blood, 50mL of an anticoagulant
28
What % of PRBCs are made up of hematocrit?
70% (very concentrated)
29
What temperature are PRBCs stored at?
4C, 39.2F
30
How long can PRBCs be stored before they can be discarded?
42 days with a special preservative
31
To prevent clumping, platelets are:
gently agitated while stored
32
What temperature are platelets stored at?
must be stored at room temperature because they cannot withstand cold temperatures
33
Why is plasma immediately frozen?
to maintain the clotting factors
34
How long does plasma last?
1 year if it remains frozen
35
The blood product can be further pooled and processed into blood derivatives of albumin, immune globulin, factor VIII, and factor IX.
Plasma
36
When is FFP given?
planned surgery or invasive procedure in the presence of abnormal coagulation tests, for the reversal of warfarin in the presence of active bleeding or planned procedure when vitamin K is inadequate For thrombotic thrombocytopenic purpura, and congenital or acquired factor deficiency with no alternative therapy. trauma patients requiring massive transfusion and warfarin-related intracranial hemorrhage
37
What is the greatest cause of transfusion reactions?
patient is transfused an incompatible unit of blood product
38
Transfusion reactions are most frequently due to:
presence of donor leukocytes within the blood component unit (PRBCs or platelets)
39
What should the RN do when a transfusion reaction occurs?
•Assess •Stop •Notify the primary provider and implement prescribed treatments. Continue to monitor Notify blood bank •Return blood and tubing to lab (or blood bank as per policy) •Obtain any samples needed •Document
40
The majority of anemias are considered:
benign
41
iron deficiency, renal disease anemia, and aplastic anemia are considered:
proliferative anemias (all involve decreased production)
42
Hemolytic anemias are characterized by
break down
43
plasma is yellow because
there are no red blood cells
44
albumin is a
plasma protein
45
Hematopoiesis is the complex process of:
the formation and maturation of blood cells
46
the primary site for hematopoiesis is:
bone marrow
47
Glucose is carried by
erythrocytes
48
Hematopoietic stem cells break down in which cells?
blood cells, myeloid stem cells, and lymph stem cells
49
the average average lifespan of a RBC is?
120 days
50
Eosinophils are released during:
inflammatory response to fight infection
51
Eosinophils are elevated with:
allergies, autoimmune disorders, infections, tumors, fungus, virus
52
alpha, beta, and gamma cells make up:
globulin cells
53
used to form red blood cells when there is a low number
epogen (medication)
54
Iron deficiency occurs in bariatric surgery because?
there is less stomach acid following bariatric surgery and iron needs acid to aid in its absorption
55
Vitamin K is given to patients with:
very high INR level
56
In DIC, fingertips die from?
clotting
57
D dimer is drawn a lot to determine if patient has:
pulmonary embolism
58
aPTT needs to be drawn every _ hours to assess if the rate needs to be changed
6
59
Therapeutic phlebotomy is used to treat:
polycythemia vera (this causes an elevated RBC volume- causes lower perfusion and blood clots because its too thick)
60
Apheresis is the removal of:
blood plasma from the body by the withdrawal of blood, its separation into plasma and cells, and the reintroduction of the cells, used especially to remove antibodies in treating autoimmune disease
61
PRBC infusion should always be done using a __ gauge needle or large for insertion in large vein
20 (pink tip)
62
criteria for PRBC infusion
use normal saline transfusion because it is isotonic, check VS frequently for reaction, always check hospital policy for run time
63
normal hemoglobin Lab levels:
10-14 female, 12-16 male
64
Chronically high hemoglobin is caused by:
dehydration, burns (fluid volume deficit), polycythemia (blood removal)
65
normal Prothrombin time- INR:
10-13 seconds
66
INR needs to be 3-4 seconds in patients with an
artificial heart valve
67
Myelo- means:
marrow of the spinal cord
68
Lympho- means:
fluid that contains white blood cells
69
Acute leukemias occur in ________ population
younger
70
Chronic leukemia occurs in ______ population
older
71
Normal value of Hct
male 42-52%, female 35-47%
72
Normal value of WBC
4500-110,000 (mm3)
73
Normal value of platelets
150,000-450,000 (mm3)
74
Normal value of Hgb
male 13-18g/dL, female 12-16g/dL
75
Clinical Manifestations of ___________ include: Bleeding from mucous membranes, venipuncture sites, GI and GU tracts. Bleeding ranges from minimal occult internal bleeding to profuse hemorrhage from all orifices
DIC
76
What is the treatment for DIC?
Treatment Treat underlying cause Oxygenation Replace fluids Correct electrolyte imbalances Vasopressors FFP & PLATELETS Heparin (questionable)
77
The following labs are used to diagnose which condition? ``` Platelets (drop) Clotting factors (drop) D-dimer (increase) PT & aPTT (increase) Lab values + scoring system ```
DIC
78
This kind of anemia is genetic; Inability to properly utilize vitamin B12 (needed for development of RBC's) d/t lack of intrinsic factor from GI tract - cannot absorb B12
Pernicious anemia
79
This kind of anemia is caused by a decrease in/damage to marrow stem cells, leading to a replacement of marrow with FAT; Usually idiopathic, toxic materials, viral infection or pregnancy can trigger
Aplastic anemia
80
Symptoms of anemia:
fatigue, pallor, dyspnea, bruising
81
Stem cell transplant and immunosuppressive therapy are involved in the treatment of:
aplastic anemia
82
Diagnostics for aplastic anemia include:
``` Diagnostics CBC revealing pancytopenia Neutrophil count <1500 Hgb <10g/dL Platelets <50,000 Bone marrow aspirate showing marrow replaced with fat ```
83
____________ needed for RBC formation; Low intake, high demand for _________ in the body, malabsorption can lead to deficiency
folic acid
84
Folic acid levels in serum and within the red blood cells
folic acid deficiency diagnostics
85
This kind of anemia is characterized by erythrocytes losing its round, pliable, biconcave disc shape; adheres to endothelium of small vessels and each other Increased blood viscosity Decreased oxygen
Sickle cell anemia
86
Genetic - caused by inheritance of the hemoglobin gene. Usually from African descent.
sickle cell anemia
87
Treatment for sickle cell anemia
Treatment Hydroxyurea Folic acid replacement RBC transfusions
88
The following symptoms are manifestations for? ``` Anemia Jaundice Enlargement of bones of face/skull Tachycardia Cardiac murmurs Cardiomegaly Dysrhythmias Heart failure Thrombus formation ```
Sickle cell anemia
89
________ is characterized by increased volume of RBC’s Primarily; secondary – Reduced oxygen/neoplasms, excessive production of erythropoietin, more RBC’s
Polycythemia
90
``` In ___________ you can see: Can be asymptomatic Fatigue Headache Dizziness SOB Inability to concentrate ```
Polycythemia
91
In order to be diagnosed with polycythemia:
Hct >55% in males and 50% in females
92
Treating the primary condition and | therapeutic phlebotomy are treatments for which blood disorder?
Polycythemia
93
``` This blood disorder is inherited: Subclass A & B A caused by deficient/defective factor VIII B caused by deficient/defective factor IX ```
Hemophilia
94
Clinical manifestations of hemophilia include:
BLEEDING | Hemorrhages in various parts of the body but 75% occurs in joints
95
``` Treatment of ___________ includes: Recombinant forms of factor VIII and X FFP Neutralizing antibodies to factor concentrate Immunosuppression therapy ```
Hemophilia