Hematologic System Flashcards

1
Q

Hematology

A

branch of science studies the form, structure and function of blood and blood-forming tissues

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2
Q

Hematologic system integrated with what systems?

A

immune and lymphatic

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3
Q

Function of hematologic system

A

deliver formed elements to tissues for cellular metabolism, defense against injury and invading microorganisms and acid-base balance

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4
Q

T/F: lymph nodes are part of the hematopoietic system

A

true

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5
Q

Signs and Symptoms of hematologic disease

A

edema
infarction (tissue necrosis)
thrombus
embolus
lymphedema
bleeding and bruising
shock
splenomegaly

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6
Q

thrombus vs embolus

A

thrombus is a solid mass of clotted blood and embolus is a clot that moves within a blood vessel to lodge at a site distant from its place of origin

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7
Q

Lymphedema

A

chronic swelling of an area from accumulation of interstitial fluid (edema)

swelling because fluid build-up

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8
Q

Bleeding and bruising occur from ____

A

trauma

normal response

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9
Q

When does shock occur?

A

when the circulatory system is unable to maintain adequate pressure in order to perfuse organs

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10
Q

Common clinical signs of shock

A

tachycardia, tachypnea, cool extremities, decreased pulses, decreased urine output, altered mental status

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11
Q

Lymph nodes are mobile or immobile? Small or large?

A

small and mobile, rubbery feel

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12
Q

What declines with age in the hematopoietic system?

A

the percentage of the marrow space occupied by hematopoietic (blood-forming) tissue declines progressively

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13
Q

T/F Blood composition changes drastically with age

A

F: changes little

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14
Q

Anemias are a state or symptom of many diseases that result in

A

a reduction of the oxygen-carrying capacity of the blood (bc abnormality in the quantity or quality of RBC)

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15
Q

Anemia pathogenesis can be ______

A

multifactorial

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16
Q

Three main causes of Anemia

A

excessive blood loss (hemorrhage)

destruction of erythrocytes (hemolytic)

decreased production of erythrocytes

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17
Q

How is anemia classified?

A

morphology

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18
Q

What can cause excessive blood loss in PT setting?

A

slow and chronic GI blood loss from medication (aspirin or NSAIDs)

GI disorders

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19
Q

What causes an increased destruction of erythocytes?

A

congenital or acquired disorders

20
Q

*Decreased production of erthrocytes

A
  1. lack of erythropoietin
  2. inability of bone marrow to respond to erythropoietin and make RBC
  3. nutritional deficiency (iron, B12, folate)
  4. anemia of chronic disease
  5. chronic kidney disease
  6. bone marrow disorders
  7. radiation-induced bone marrow failure
21
Q

What is erythropoietin?

A

hormone produced in the kidney that stimulates the production and maturation of RBC

22
Q

Signs and Symptoms associated with anemia are related to the _____ of anemia and the ______ over which the erythrocytes were lost

A

severity

amount of time

23
Q

Symptoms of Mild vs Moderate Anemia

A

mild - vague symptoms

moderate - cant supply body tissues, tachycardia (trying to compensate for low blood oxygen), dyspnea, weakness, fatigue, pallor

24
Q

koilonychia is a symptom of

A

moderate anemia

spoon nails

25
more Clinical manifestations of moderate anemia
change in skin tone *lack of exercise tolerance dementia neuropathies pain or paresthesia lack of locomotion CNS - personality changes, dementia liver and kidney damage **cardiac ischemia - risk for heart attack
26
Diagnosis of anemia uses
complete blood count (RBC) - % of blood volume composed of RBCs and other factors (hemoglobin) reticulocyte count (amount of new RBCs) STUDY TABLE CBC
27
What is important to know as the PT with a patient with anemia?
know the underlying cause to recognize red flags and adjust the program or medical referal
28
Anemic people have _____ exercise tolerance
decreased
29
Hemostasis
arrest of bleeding after blood vessel injury using blood vessel wall, platelets and coagulation proteins
30
Primary hemostasis
formation of a platelet plug at the site of the vascular injury
31
Willebrand factor (VWF) and platelets are required in
primary hemostasis
32
function of willebrand factor
mediates initial adhesion of platelets at bleeding injuries binds and stabilizes blood clotting factor VIII
33
defects in VWF can cause
bleeding
34
defects in primary hemostasis (two condition names)
von Willebrand disease (dysfunction in VWF) thrombocytopenia (decrease in platelets)
35
Bleeding caused by platelet disorders or VWD is characterized by
easy bruising or mucosal bleeding
36
Thrombocytopenia is a platelet blood count below
150,000
37
Hemophilias is a defect of ____ hemostasis
secondary
38
Secondary hemostasis is triggered when
vascular damage exposes tissue factor *necessitates the presence of clotting factors
39
Defects in secondary hemostasis result from
clotting factor deficiencies or dysfunction
40
People with _____ hemostasis have more serious bleeding
secondary
41
Hemophillias
bleeding disorder inherited as an X-linked autosomal recessive trait
42
Hemophilia A (% and clotting factor)
80%, clotting factor VIII
43
Hemophilia B (% and clotting factor)
15%, clotting factor IX
44
Concentrations of coagulation factors - normal mild moderate severe
normal 50-150% mild 6-30% moderate 1-5% severe < 1%
45
Mild hemophilia (__%) what happens?
15 spontaneous bleeding is rare and joint and deep muscle bleeding are uncommon
46
Moderate hemophilia (___%) what happens
15 spontaneous hemorrhage not usually a problem *major bleeding episodes can occur after minor trauma
47
Severe hemophilia (__%) what happens
60 may bleed spontaneously or with slight trauma, particularly into joints and deep muscle