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91 Cards in this Set

  • Front
  • Back
What is the consistency of blood?
45% blood cells
55% blood plasma
What is the volume of blood?
10-12 pints
What are erythrocytes?
Red Blood Cells
What is the function of red blood cells?
Transport oxygen and carbon dioxide
What are Leukocytes?
White blood cells
What is the function of WBC's?
Body defenses: destruction of bacteria and viruses
What are thrombocytes?
platelets
What do thrombocytes do?
initiate blood clotting
A body process that arrests the flow of blood and prevents hemorrhage is known as...
homeostasis
How can blood become thicker?
if fluid intake is limited
How are blood types determined?
by the presence or absence of specific antigens on the outer surface of the RBC
What blood type is the universal recipient?Ty
Type AB
What blood type is the universal donor?
Type O
Where are RH antibiodies located?
on the surface of the RBC
RH positive means...
RH antibodies are present
RH negative means...
RH antibiodies are NOT present
Immature neutrophils are called...
Bands
"A shift to the left" means...
There is an infection
What is the function of the lymphatic system?
Maintenance of fluid balance
Production of lymphocytes
Absorption and transportation of lipids from the intestine to the bloodstream
What is lymph?
Lymph is a specialized fluid formed in the tissue spaces transported by way of the lymphatic vessels and reenters the circulatory system
What are lymph nodes?
Act as filters, keeping particulate matter such as bacteria from entering bloodstream
In regards to lymphatic tissue, what do the tonsils do?
Produce lymphocytes and antibodies: trap bacteria
In regards to lymphatic tissue, what does the Spleen do?
Reservoir for blood; forms lymphocytes, monocytes, and plasma; destroys worn-out RBCs; removes bacteria by phagocytosis
In regards to lymphatic tissue, what does the Thymus do?
Immune system before and a few months after birth; atrophies at puberty
What are diagnostic tests used for Disorders of the Hematological and Lymphatic System?
Complete blood count (CBC)
Red cell indices
Peripheral smear
Schilling test
Megaloblastic anemia profile
Lymphangiography
Bone marrow aspiration or biopsy
What is anemia?
Disorder characterized by RBC and hemoglobin and hematocrit levels below normal range

Causes delivery of insufficient amounts of oxygen to tissues and cells
What are types of anemia?
Blood loss
Impaired production of RBCs
Increased destruction of RBCs
Nutritional deficiencies
What are clinical manifestations of anemia?
Anorexia
Dyspepsia
Cardiac dilation
Disorientation
Shortness of breath
Dyspnea
Fatigue
Headache
Insomnia
Pallor
Palpitation
Systolic murmur
Tachycardia
Vertigo
What is the medical management for anemia?
Depends on the cause
Correction of the disease process may correct or lessen the anemic condition
Treatment is often specific to the particular anemia
What is Hypovolemic anemia?
(Blood loss anemia)

Abnormally low circulating blood volume due to blood loss
(500 ml loss can be tolerated;1000 ml loss can cause severe complications)
~Severity and signs and symptoms depend on how rapid the blood is lost
Hypovolemic anemia:
Clinical manifestations
Weakness
Stupor; irritability
Pale, cool, moist skin
Hypotension
Tachycardia (rapid, weak, thready pulse)
Hypothermia
Hemoglobin less than 10 g/100 ml
Hematocrit less than 40%
Hypovolemic anemia:
Medical management/nursing interventions
Control bleeding
Treat shock
O2, elevate lower extremities, keep warm
Replace fluid
Blood transfusion, plasma, dextran, lactated Ringer’s
Monitor vital signs
What is pernicious anemia?
Absence of the intrinsic factor
Intrinsic factor is essential for the absorption of vitamin B12
A deficiency in B12 affects what?
affects growth and maturity of all body cells
How is Vitamin B12 is also related to nerve myelination?
May cause progressive demyelination and degeneration of nerves and white matter
Pernicious anemia: Clinical manifestations/assessment
Extreme weakness
Dyspnea
Fever
Hypoxia
Weight loss
Jaundice (destruction of RBCs)
Pallor
GI complaints
Dysphagia
Sore, burning tongue
Smooth and erythematous
Neurological symptoms
Tingling of the hands and feet
Disorientation
Personality changes; behavior problems
Partial or total paralysis
Pernicious anemia:
Medical management/nursing interventions
Vitamin B12 (cyanocobalamin) 1000 units
Folic acid supplement
Iron replacement
RBC transfusion
Diet: high in protein, vitamins, and minerals
Explain dosing schedules for Vitamin B12 (cyanocobalamin) for pernicious anemia
Daily for 1 week
Weekly for 1 month
Monthly for life
What is Aplastic anemia?
Decrease of bone marrow function
-can be primary or secondary
What is primary aplastic anemia?
Congenital
What is secodary aplastic anemia?
Viral invasion
Medications
Chemicals
Radiation; chemotherapy
Aplastic anemia:
Clinical manifestations/assessment
Pancytopenic
Repeated infections with high fevers
Fatigue, weakness, malaise
Dyspnea
Palpitations
Bleeding tendencies
Aplastic anemia:
Medical management/nursing interventions
Identify and remove cause
Platelet transfusion for severe thrombocytopenia
Splenectomy for hypersplenism
Steroids and androgens
Antithymocyte globulin
Bone marrow transplant
What is iron deficiency anemia?
RBCs contain decreased levels of hemoglobin
Excessive iron loss
Caused by chronic bleeding—intestinal, uterine, gastric
Iron deficiency anemia:
Clinical manifestations/assessment
Pallor
Fatigue; weakness
Shortness of breath
Angina; signs and symptoms of heart failure
Glossitis; burning tongue
Pagophagia
Headache
Paresthesia
Iron deficiency anemia:
Medical management/nursing interventions
Ferrous sulfate 900 mg daily
Oral or injection (Z-track)
Ascorbic acid
Diet high in iron
What is Sickle Cell anemia?
An abnormal, crescent-shaped RBC
Severe, chronic, incurable condition
Sickle cell anemia is what type of disease?
Homozygous
Sickle cell anemia is what trait?
Heterozygous
Sickle cell anemia:
Clinical manifestations/assessment
Precipitating factors
Loss of appetite
Irritability
Weakness
Abdominal enlargement
Joint and back pain
Edema of extremities
Sickle cell anemia:
Medical management/nursing interventions
No specific treatment—alleviate symptoms
Oxygen
Rest
Fluids
Analgesics
Bone marrow transplant
What is Agranulocytosis?
Severe reduction in the number of granulocytes
WBC less than 200/mm3
Medications
Chemotherapy
Radiation
Neoplastic disease
Viral and bacterial infections
Agranulocytosis:
Clinical manifestations/assessment
Symptoms of infection
Ulcerations of mucous membranes
Bronchial pneumonia
Urinary tract infection
Agranulocytosis:
Medical management/nursing interventions
Remove cause of bone marrow depression
Prevent or treat infections
Meticulous handwashing
Strict asepsis
What is Leukemia?
Malignant disorder of the hematopoietic system
Excess leukocytes accumulate in the bone marrow and lymph nodes
Cause unknown
How is Leukemia classified?
Acute or chronic
Proliferating cells (lymphocytic, monocytic, myelogenous)
Leukemia:
Clinical manifestations/assessment
Anemia
Thrombocytopenia; leukopenia
Enlarged lymph nodes
Splenomegaly
Leukemia:
Medical management/nursing interventions
Chemotherapy; radiation
Bone marrow transplant
Medications: chlorambucil (Leukeran), hydroxyurea, corticosteroids, cyclophosphamide (Cytoxan)
What is Thrombocytopenia?
Condition in which the number of platelets is reduced below 100,000/mm3; may be due to decreased production or decreased survival
Thrombocytopenia:
Clinical manifestations/assessment
Petechiae
Ecchymoses
Platelets below 100,000/mm3
Bleeding from mucous membranes
Thrombocytopenia:
Medical management/nursing interventions
Corticosteriod therapy
Splenectomy
Gamma globulin
Immunosuppressive drugs
Platelet transfusions
Avoid trauma
What is Hemophilia?
Hereditary coagulation disorder, characterized by a disturbance of clotting factor
Hemophilia A; hemophilia B
X-linked hereditary trait
Hemophilia:
Clinical manifestations/assessment
Internal and external bleeding
Hemarthrosis
Excessive blood loss from small cuts and dental procedures
Hemophilia:
Medical management/nursing interventions
Minimize bleeding—avoid trauma
Relieve pain—no aspirin
Transfusions
What are different transfusions for hemophilia?
Factor VIII or IX concentrate
Cryoprecipitate (rich in factor VIII)
Manufactured factor VIII or IX
What is von Willebrand’s disease?
Inherited bleeding disorder characterized by abnormally slow coagulation of blood; mild deficiency of factor VIII
Similar to hemophilia; not limited to males
von Willebrand’s disease:
Clinical manifestations/assessment
Spontaneous episodes of
GI bleeding
Epistaxis
Gingival bleeding
von Willebrand’s disease:
Medical management/nursing interventions
Cryoprecipitate
Fibrinogen
Fresh plasma
Desmopressin (DDAVP)
Minimize bleeding—avoid trauma
Relieve pain—no aspirin
What is Disseminated intravascular coagulation?
Overstimulation of clotting and anticlotting processes in response to disease or injury
Disseminated intravascular coagulation:
Clinical manifestations/assessment
Bleeding; hemoptysis
Dyspnea
Diaphoresis
Cold, mottled digits
Purpura on the chest and abdomen
Petechiae
Disseminated intravascular coagulation:
Medical management/nursing
Treat underlying cause
Cryoprecipitate
Heparin
Protect from bleeding and trauma
What is Multiple myeloma?
Malignant neoplastic immunodeficiency disease of the bone marrow
Multiple myeloma:
Clinical manifestations/assessment
Bone pain; pathological fractures
Infection
Anemia; bleeding
Hypercalcemia
Renal failure
Multiple myeloma:
Medical management/nursing interventions
Symptomatic; not curable
Radiation
Chemotherapy
Corticosteroids
IV fluids
What is Lymphangitis?
Inflammation of one or more lymphatic vessels
Usually occurs from acute streptococcal or staphylococcal infection in an extremity
Lymphangitis:
Clinical manifestations/assessment
Fine red streaks from the affected area
Edema
Chills; fever
Local pain
Headache; myalgia
Lymphangitis:
Medical management/nursing interventions
Penicillin
Moist heat
Elevate extremity
What is Lymphedema?
Primary or secondary disorder
Accumulation of lymph in the soft tissue
Lymphedema:
Clinical manifestations/assessment
Massive edema and tightness of affected extremity
Pain
Lymphedema:
Medical management/nursing interventions
Diuretics
Antibiotics
Compression pump
Elastic stocking or sleeve
Restricted sodium diet
Avoid constrictive clothing
Meticulous skin care
What is Malignant lymphoma?
Non-Hodgkin’s lymphoma
Neoplastic disorder of lymphoid tissue
Tumors usually start in lymph nodes and spread to lymphoid tissue in the spleen, liver, GI tract, and bone marrow
Malignant lymphoma:
Clinical manifestations/assessment
Painless, enlarged cervical lymph nodes
Fever; susceptibility to infection
Weight loss; anorexia
Anemia
Pruritus
Fatigue
Malaise
Malignant lymphoma:
Medical management/nursing interventions
Accurate staging of the disease is crucial to determine treatment regimen
Radiation
Chemotherapy
Bone marrow transplant
Tumor necrosis factor (TNF)
What is Hodgkin’s disease?
Inflammatory or infectious process that develops into a neoplasm
Affects males twice as frequently as females
Reed-Sternberg cells
Hodgkin’s disease:
Clinical manifestations/assessment
Enlargement of cervical lymph nodes
Anorexia
Weight loss
Pruritus
Low-grade fever
Night sweats
Anemia
Leukocytosis
Hodgkin’s disease:
Medical management/nursing interventions
Stage I or II (localized)
Radiation
Stage III or IV (generalized)
Chemotherapy
Combination
Malignant lymphoma:
Clinical manifestations/assessment
Painless, enlarged cervical lymph nodes
Fever; susceptibility to infection
Weight loss; anorexia
Anemia
Pruritus
Fatigue
Malaise
Malignant lymphoma:
Medical management/nursing interventions
Accurate staging of the disease is crucial to determine treatment regimen
Radiation
Chemotherapy
Bone marrow transplant
Tumor necrosis factor (TNF)
What is Hodgkin’s disease?
Inflammatory or infectious process that develops into a neoplasm
Affects males twice as frequently as females
Reed-Sternberg cells
Hodgkin’s disease:
Clinical manifestations/assessment
Enlargement of cervical lymph nodes
Anorexia
Weight loss
Pruritus
Low-grade fever
Night sweats
Anemia
Leukocytosis
Hodgkin’s disease:
Medical management/nursing interventions
Stage I or II (localized)
Radiation
Stage III or IV (generalized)
Chemotherapy
Combination