Ch 25 Hematologic Emergencies Flashcards

1
Q

Disease processes that breakdown RBC’s

A

Hemolytic Disorders

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2
Q

Bleeding and Clotting abnormalities

A

Hemostatic Disorders

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3
Q

Total body weight in fluids is approx 5-6L, how much of that fluid is plasma?

A

8%

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4
Q

Primary Function of blood (pg 1536)

A

Carry O2 & nutrients to cells
Transport CO2 & nitro from cells to lungs and kidney to dispose of
Carry hormones from endocrine glands to target tissues
Regulate body temp
Regulate pH
Keep electrolytes balanced
Regulate immune system through WBC’s & antibodies
Form clots through platelets

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5
Q

2 main components of blood

A

Plasma accounts for 55% of total blood volume: it is 92% water, 8% proteins, electrolytes, glucose, clotting factors

Formed Elements is 45% of total blood volume: it is 99% RBC’s, 1% WBC’s & Platelets

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6
Q

Refers to the secretion of antibodies called immunoglobulins, which recognizes a specific antigen.

A

Humoral Immunity

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7
Q

Macrophages & T cells attack & destroy pathogens or foreign substances

A

Cell-mediated immunity

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8
Q

Derived from stem cells, have an average of 7-10 days, 2/3 circulate the body, the rest is stored in the spleen.

A

Platelets

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9
Q

What is responsible for clotting of the blood?

A

Platelets

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10
Q

Condition in which the body produces too many platelets, which can lead to dangerous clotting conditions, such as thrombosis

A

Thrombocytosis

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11
Q

Primary site for cell production

A

Bone Marrow (long bones, pelvis, skull, & vertebrae)

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12
Q

Which organ produces the clotting factors found in blood?

A

Liver.
It also breaks down old RBC’s and turns them into bile.

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13
Q

Organ vital for breaking down RBC’s, producing lymphocytes, stores 1/3 of body’s platelets.

A

Spleen

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14
Q

Genetic disorder that is identified by the abnormal, oblong shape of the RBC’s. This shape makes the RBC’s poor carriers of O2, making them highly susceptible to hypoxia.

A

Sickle Cell Disease

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15
Q

Potential S/S of Sickle Cell emergency

A

Pain, fatigue, pale or jaundice skin, SOB, fever

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16
Q
A

Hemophilia

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17
Q
A

Polycythemia

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18
Q

Medical Care for Pts w/suspected blood disorder related complaints

A

O2
Fluids
EKG
Transport
Comfort
Pharmacology (pain meds)
Psychological Support

19
Q

Life expectancy for someone w/ Sickle Cell Disease

20
Q

The odd shape of “sickle cells” could become lodged within small blood vessels, causing a thrombosis. This crisis occurs when blood flow to and organ becomes restricted, causing pain, ischemia, and organ damage.

A

Vasoocclusive Crisis

21
Q

Considered a vasoocclusive crisis that presents to the lungs. Could have CP, fever, SOB, cough.

A

Acute Chest Syndrome

22
Q

This is a life threatening complication of Sickle Cell, when blood flow is cut off to the spleen, trapping blood within the spleen, resulting in a hard, painful, bloated abdomen. Pt can also present w/weakness, pallor, tachypenia, tachycaridia.

A

Splenic Sequestration Crisis

23
Q

Treatment for sickle cell crisis involves…..

A

Keeping pt warm, cold can increase suckling of cells

O2, d/t perfusion being decreased by sickled cells

IV fluids, to help flush damaged cells from the organs

Pain Management

24
Q

Hemoglobin or RBC’s at decreased levels in the blood, commonly associated with/an underlying condition or acute blood loss

25
Q

Most common type of anemia, typically caused from GI bleeds or menstrual bleeding in females

A

Iron-deficiency anemia

26
Q

S/S of someone w/anemia or low hemoglobin levels

A

Fatigue
SOB
Pallor

27
Q

Conditions that can result in more frequent infections, fevers, cutaneous bleeding and nosebleeds

A

Leukopenia (decrease in WBC production)

Thrombocytopenia (decrease in RBC production)

28
Q

Treatment for someone with anemia

A

O2, decreased RBC’s & hemoglobin, mean decreased oxygen carrying capacity

29
Q

Malignancies of the lymph nodes and/or spleen.

A

Lymphomas - usually characterized by swollen lymph nodes.

    1.) Non-Hodgkin 
     2.) Hodgkin
30
Q

Overabundance of RBC’s, resulting in blood viscosity & volume

A

Polycythemia

31
Q

Hyperviscosity increases the potential for ……

A

Thrombus Formation
Stroke
MI

32
Q

Polycythemia pts may present with….

A

AMS (CVA)
Respiratory distress
Tachycardia

33
Q

Condition in which massive injury or trauma, uncontrolled bleeding, your body loses all the fibrin and becomes unable to clot

A

Disseminated Intravascular Coagulation

34
Q

Bleeding disorder in which clotting does not occur or is insufficient.

A

Hemophilia

35
Q

A common and major cause of death for pts w/hemophilia.

A

Spontaneous Intracranial bleeding

36
Q

Cancer of bone marrow

A

Multiple Myeloma

37
Q

Highly complex process that allows the body to stop bleeding, coagulation, and platelet plugging.

A

Hemostasis

38
Q

Why do you have to pee when you get cold?

A

Baroreceptors

Vasoconstriction, When blood shunts blood from skin, raises BP, something else

To maintain BP

But i didn’t catch all that was said. Have no idea what he’s talking about.

39
Q

Can become any type of cell

A

Stem Cells

40
Q

RBC production is stimulated by….

A

Erythropoietin

41
Q

Breaks down RBC’s and converts them into bile

42
Q

When a pt receives a blood type different than his/her own, ca cause anaphylactic reactions, happens rapidly & causes circulatory collapse

A

Transfusion Reactions

43
Q

Can only receive O- blood?

44
Q

Complications of Transfusion Incompatibility

A

Hemolytic reaction
Febrile Reaction
Allergic Reation
Lung injury
Circulatory Overlaod
Bacterial Infection