Disorders Of The Hematopoietic System Flashcards

1
Q

It is used to treat or prevent folate deficiency anemia. Helps the body make healthy red blood cells and is found in certain foods.

A

Folic Acid

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2
Q

Pernicious anemia is low in what vitamin?

A

Vitamin B12

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3
Q

Helps keep your body’s and nerve cells healthy and helps make DNA

A

Vitamin B12

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4
Q

Helps to turns food into energy and to keep the nervous system healthy. Your body can’t make it itself, normally get it from food

A

Thiamine

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5
Q

Helps to prevent blood clots from forming

A

Warfarin

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6
Q

Prevent and treat harmful blood clots. Helps keep blood flowing smoothly by lowering the activity of clotting protein in the blood

A

Enoxaparin

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7
Q

Decreases the clotting ability of the blood and helps prevent harmful clots from forming in the blood vessels

A

Apixaban

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8
Q

Decreases the clotting ability of the blood and help prevent harmful clots from forming in the blood vessels

A

Rivaroxaban

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9
Q

-Patho: Deficiency of erythrocytes or hemoglobin
-Causes: Blood loss, inadequate RBC production/volume, destruction of RBCs

A

Anemia

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10
Q

-Patho/Causes: sudden loss or chronic loss of small amounts of blood
-Signs and Symptoms: extreme pallor, tachycardia, hypotension, reduced urine output, altered consciousness, fatigue, chills, rapid respiratory rate (INSERT TABLE 31-2)
-Medical Management:
-Blood transfusions: treating underlying condition or chronic blood loss
- Administration of oral, IV, or IM iron: to restore hemoglobin
- Assessment: History, vital signs (how’s the HR, RR, CBC results) laboratory test results, physical examination, intake and output
-Nursing Diagnosis: Imbalanced body temperature; Activity Intolerance
-Interventions:
-Monitor results of CBC (how high or low hemoglobin and hematocrit)
-Assess vital signs; hypotension, tachycardia
-Monitor intake and output
-small frequent meals

A

Hypovolemic Anemia

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11
Q

Hemolytic Anemia

A

-Patho: Malaria, sickle cell; chronic premature erythrocyte destruction
-Signs and Symptoms: Jaundice, enlarged spleen, shock
-Microscopic examination; Coombs’ test (direct antiglobulin test)
-Medical Management: removing the cause; corticosteroids; blood transfusions
-Surgical Management: Splenectomy
-Nursing Management: Health history, supportive care, medication, teaching measures of self care, arrange follow up evaluations/care (making appointments or transportation to appointments)

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12
Q

-Patho: hereditary hemolytic anemia
-Types: alpha-thalassemias- (Southeast Asia/Africa), Beta-thalassemias- (mediterranean)
-Signs and Symptoms: Cooley’s anemia (beta): bronzing of the skin (from hemolysis)
-Medical Management: Symptomatic, frequent transfusions, iron chelation therapy (removing iron/heavy metals from the body)
Nursing Management: Bed rest, protect from infection, closely monitor before, during and after blood transfusion (LPN WONT ADMIN BLOOD TRANSFUSIONS)

A

Thalassemia’s

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13
Q

-Patho: lack of intrinsic factor (glycoprotein made by parietal cells) necessary for absorption of vitamin B12
-Degenerative changed on nervous system
-Secondary to surgical removal of stomach or small bowel resection (illium is where vitamin B12 is absorbed)
-Signs and Symptoms: Stomatitis (inflammation of mouth), glossitis (inflammation of tongue), digestive disturbances; diarrhea; dyspnea with minimal exertion, jaundice, irritability, confusion, depression, numbness and tingling in the arms and legs, ataxia
-Diagnostics: Blood and bone marrow studies; Schilling Test (confirms diagnosis-rare), blood smear (assess maturity of erythrocytes)
-Medical Management: IM vitamin B12; physical therapy for permanent neurologic deficits
Nursing Management:
-Stomatitis and Glossitis: soft, bland diet; small, frequent meals (to help with fatigue); oral care
-Permanent neurologic deficit: encourage and assist with ambulation, supervision
-Teaching: administration of vitamin B12, diet

A

Pernicious Anemia

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14
Q

-Signs and Symptoms: reddish-purple face and lips, fatigue, weakness, exertional dyspnea
-Diagnostics: elevated blood cell count, platelets and WBC counts elevated, abnormal serum K+ and uric acid
-Medical Management: phlebotomy (drain), radio phosphorus, and radiation therapy

A

Exocytosis

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15
Q

increase in circulating erythrocytes, leukocytes & platelets; Rapid proliferation of blood cells produced by the bone marrow; cause is unknown

A

Polycythemia vera

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16
Q

-Patho: proliferation of leukocytes, usually in immature form
-Four types according to dysfunctional bone marrow stem cell line (Acute and Chronic forms of lymphocytic and myelogenous leukemia)
-Precipitating factors: genetic correlation
-Signs and Symptoms: Severe anemia (rapid leukocyte proliferation causes a decrease in RBC & Plt), infections, fatigue, easy bruising, fever, enlarged spleen and lymph nodes, internal or external bleeding
-Medical Management: Antineoplastic drugs, transfusions, Transplantation: bone marrow; stem cell
-Nursing Process: The client with Leukemia
-Assessment: history of symptoms; physical assessment, laboratory results; assess neutrophil
-Diagnosis and Planning: Risks: infection, hemorrhage, activity intolerance, disturbed body image, anxiety, and fear
-Interventions: Monitor platelet counts; Assess for signs of bruising and petechiae(unknown bruises or are they getting bigger); report hematuria or epistaxis; Acknowledge client’s anxieties and fears; Educate patient regarding bleeding risk: electric razors, avoid cuts, prolonged pressure to needle sticks, etc Neutropenic Precautions (If low we are putting the neutropenic precautions in place; no visitors, wash hands, mask up if they are leaving the room)

A

Leukocytosis: Leukemia

17
Q

-Patho: malignancy involving plasma cells; Osteoclasts break down bone cells, resulting in increased blood calcium and pathologic fractures (calcium is going into blood)
-Osteolytic tumors: “punched-out” or “honeycomb” appearance in bones
-Signs and Symptoms: Pain, infection, symptoms of anemia, bruising, nosebleeds, renal calculi
-Diagnostics: skeletal radiographic studies: bone lesions (looking for that honeycomb appearance); elevated serum calcium levels, bone marrow aspiration
-Medical Management: Steroids, anticancer drugs, antibiotics, Analgesics, blood transfusions, Back braces, body casts (for support of the bones)
-Surgical Management: transplantation: bone marrow; stem cell (see Table 31-4)
-Nursing Management: Assess pain, signs of infection (fever, fatigue), fatigue, bleeding, thrombus formation, urine; Analgesics, ambulation (maybe need a walker), fluid intake, safety paramount (fall risk as their bones are breaking down), Prevent infection (hand washing, wearing a mask)

A

Multiple Myeloma

18
Q
A
19
Q

-Patho: decreased production of granulocytes, Neutrophils, basophils, eosinophils (types of lymphocytes). Sulfonamides, antineoplastics, psychotropics are at a great risk for decreased granulocytes which can cause infection like fungal, yeast, bacterial
-Decreased granulocytes place the client at risk for infection
-Signs and Symptoms: Fatigue, fever, chills, headache, opportunistic infections
-Medical Management: remove cause; drugs: human granulocyte colony-stimulating factor (peg/Filgatrim)
-Nursing Management: drug assessment(what drugs are they taking; is that what is the cause), protective isolation (neutropenic); visitor restriction

A

Agranulocytosis

20
Q

-Patho: pancytopenia: numbers of all cells reduced. Aplasia: failure to develop
-Causes: unknown, autoimmune, exposure to toxic chemicals, radiation, drug therapy
-Signs and Symptoms: Weakness, fatigue, opportunistic infections, Unusual bleeding, petechiae, ecchymosis, Enlarged spleen/abdominal pain
-Diagnostics: blood cell count (CBC; H/H); bone marrow aspiration
-Medical Management: Withdrawal of causative agent, Transfusions, antibiotics, corticosteroids, Transplantations: bone marrow; autologous stem cell (Own stem cells)
-Nursing Management: History, physical assessment(look at skin, diet), symptoms, Infection prevention measures/isolation, Nutrition; modify oral hygiene (use soft toothbrush and not brush too hard to avoid a cut in mouth to prevent bleeding/infection), Monitoring of blood transfusion (frequent transfusions increase risk for reaction

A

Pancytopenia: Aplastic Anemia

21
Q

-Patho: platelet manufacture by bone marrow is decreased or platelet destruction by the spleen is increased
-Causes: leukemia; malignant blood diseases, severe infection
-Signs and Symptoms: purpura, bleeding, internal hemorrhage
-Medical Management: identify and treat cause; corticosteroids, transfusions
-Surgical Management: splenectomy
-Nursing Management: Manage/minimize bleeding(avoid falling); Adverse drug reactions; taper corticosteroid dosage and frequency

A

Thrombocytopenia

22
Q

-Patho: absence or reduction in clotting factor; inherited: mother to son
-Signs and Symptoms: oozing; severe bleeding, bleeding in joints
-Diagnostics: coagulant factor assay; shows deficiency in factor
-Medical Management: transfusions, thrombin/fibrin application to blood, fresh frozen plasma, direct pressure, factor concentrats
-Nursing Management: health history; physical assessment; vital signs, prevent trauma, minimize bleeding; reduce pain or discomfort
-Teaching: conserve energy; ways to prevent further episodes, blood transfusion monitoring for blood

A

Hemophilia

23
Q

A client is found to have a low hemoglobin and hematocrit when laboratory work was performed. What does the nurse understand the anemia may have resulted from?

A

Blood loss; Abnormal erythrocyte production; Destruction of normally formed red blood cells

24
Q

A client who has undergone a hemigastrectomy has been diagnosed with pernicious anemia. The client asks the nurse what might have caused her problem. Which of the following is the nurse’s best response?

A

“You are no longer able to absorb vitamin B12 because of your surgery.”