Wk. 4 - Care of Adults with Hematology Cancer

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33 Terms

1
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What is neutropenia?

A condition characterized by an abnormally low number of neutrophils, increasing the risk of infection.

2
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How is mild neutropenia classified based on ANC levels?

ANC 1,000-1,500 cells/mmÂł

3
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How is moderate neutropenia classified based on ANC levels?

ANC 500-1,000 cells/mmÂł

4
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How is severe neutropenia classified based on ANC levels?

ANC <500 cells/mmÂł

5
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How is the Absolute Neutrophil Count (ANC) calculated?

ANC = (% Neutrophils + % Bands) x WBC/100

6
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A patient has a WBC count of 2,000/µL, neutrophils at 40%, and bands at 5%. What is their ANC?

900 cells/mmÂł

7
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Why do neutropenic patients often lack classic signs of infection?

Because they have a reduced immune response, leading to minimal inflammation.

8
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What is the most significant indicator of infection in neutropenic patients?

Low-grade fever (>100.4°F or 38°C).

9
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What are three other signs of infection in neutropenic patients?

Sore throat, skin infections, pain during urination

10
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What is the first step in managing febrile neutropenia?

Administer broad-spectrum IV antibiotics within 1 hour of fever onset.

11
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Name three additional steps in managing febrile neutropenia.

Collect samples, monitor virals, administer colony-stimulating factors

12
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What type of isolation is required for a patient with severe neutropenia?

Protective isolation with a HEPA-filtered private room.

13
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What dietary precautions should neutropenic patients follow?

Avoid raw meats, eggs, and unwashed fruits/vegetables, consume pasteurized dairy products.

14
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Why should neutropenic patients avoid crowds and sick individuals?

To reduce exposure to infections due to their weakened immune system.

15
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What is the primary pathophysiology of Acute Myeloid Leukemia (AML)?

Uncontrolled proliferation of myeloblasts (immature WBCs).

16
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What are three clinical manifestations of AML?

Fatigue, frequent infections, bleeding/bruising

17
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What is a key diagnostic finding in AML?

Bone marrow biopsy showing hypercellular marrow with myeloblasts.

18
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What is the primary treatment approach for AML?

Combination chemotherapy and hematopoietic stem cell transplantation (HSCT).

19
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How does Chronic Lymphocytic Leukemia (CLL) differ from AML?

CLL progresses slowly and involves mature but ineffective B lymphocytes.

20
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What is a hallmark diagnostic feature of CLL on a blood smear?

Smudge cells.

21
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How is early-stage CLL managed?

Observation if asymptomatic; chemotherapy if disease progresses.

22
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What is the defining characteristic of Hodgkin’s Lymphoma?

Presence of Reed-Sternberg cells in lymph nodes.

23
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What are the classic “B symptoms” of Hodgkin’s Lymphoma?

Fever, night sweats, unexplained weight loss.

24
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What is the primary treatment for Hodgkin’s Lymphoma?

Combination chemotherapy (ABVD regimen).

25
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How does Non-Hodgkin’s Lymphoma (NHL) differ from Hodgkin’s?

NHL lacks Reed-Sternberg cells and is more common.

26
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What is the treatment for indolent (low-grade) NHL?

Watchful waiting, radiation, or monoclonal antibodies.

27
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What is the treatment for aggressive (high-grade) NHL?

Combination chemotherapy and stem cell transplant.

28
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What is the hallmark pathophysiology of multiple myeloma?

Malignant plasma cells proliferate in bone marrow, damaging bones and producing M protein.

29
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What does the acronym "CRAB" stand for in multiple myeloma symptoms?

Calcium elevation (hypercalcemia), Renal failure, Anemia, Bone pain/fractures.

30
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What is a key diagnostic marker of multiple myeloma found in urine?

Bence-Jones protein.

31
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What medications are used to prevent bone breakdown in multiple myeloma?

Bisphosphonates (e.g., Pamidronate).

32
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What is the mechanism of action of Epoetin Alfa (Epogen®)?

Stimulates RBC production in bone marrow.

33
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What is the main side effect of Filgrastim (Neupogen®)?

Bone pain due to increased neutrophil production.