305. Leukeamia Flashcards

1
Q

How do you approach a leukeamic patient that feels unwell?

A

Take seriously, can deteriorate quickly

Bloo dcultures, FBC, U&E’s, LFt’s, Ca2+, glucose and clotting

Consider CNS bleeding

Discuss with patient aims of treatment

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2
Q

What neutropenic regimen should they abide by when in hospital?

A

Full barrier nursing

Avoid IM injections

Look for infection (mouth, axillae, perineum, IVI site)

Check FBC, platelets, INR, U&E, LFT, LDH,CRP, cultures, CXR

Wash perineum after defication

Oral hygiene (mouthwash every 2 hours)

Check vital signs 4 hourly

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3
Q

How do you use antibiotcs in those who are neutropenic

A

If fever then give piperacillin tazobactam and vancomycin

If fever persists despite antibiotics consider CMV or Fungi

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4
Q

What is tumour lysis syndrome?

A

Results in a high potassium, high urate and AKI. Low calcium

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5
Q

What is Hyperviscocity in those with leukaemia?

A

WCC can exceed 100 leading to thrombi forming in the brain, lung and heart.

Lower WBC with hydroxycarbamide or leukapheresis

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6
Q

What is DIC

A

Release of pro coagulants into the circulation causes widespread activation of coagulation consuming factors

Fibrin strands fill small vessels

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7
Q

What are the causes of DIC

What are the signs of DIC

A

Malignancy, Sepsis, Trauma, obstetric events

Bruising, bleeding, renal failure

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8
Q

What are the tests for DIC

A

Plateltes, prthrombin time, APTT, decreased fibronogen. Increase of fibrin

Schisctocytes

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9
Q

How is DIC treated?

A

Treat the cause

Replace platelets if <50.

Cryoprecipitate

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10
Q

How should sepsis be prevented in those with neutropenia?

A

Can give fluoroquinolone before neutropenia gets serious

Granulocyte colony stimulators can increase production of WBC

Herpes,pneumocystis and CMV prophylaxis has a role

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11
Q

What are the four main classes of leukemia?

A

Acute lymphoid luekemia- affects young and under 40’s

Acute myeloid leukemia-high mortality

Chronic myeloid leukemia- three stages

Chronic lyphoblastic leukemia- most common

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12
Q

What is acute myeloid leukemia?

A

A malignancy of lymphoid cells affecting B or T lymphocytes causing uncontrolled maturation of blast cells

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13
Q

What are the important associations with acute lymphoid leukemia?

A

Ionizing radiation dueing pregnancy

Down’s syndrome

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14
Q

What are the signs of Acute lymphoblastic leukemia?

A

Marrow failure- pancytopenia

Infilatration- hepato/splenomegaly, lymphadenopathy, CNS, Orchidomegaly

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15
Q

What are common infections that those with ALL might encounter?

A

Chest, mouth, perineum and skin

Bacterial septicaemia

Zoster

CMV

measles

Candidiasis

Pnemocystis pneumonia

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16
Q

What tests are undertaken in ALL?

A

Blast cells seen on blood film

CXR and CT scan for mediastinal and abnormal lymphadenopathy

Lumbar puncture for CNS involvement

17
Q

What support can you give to those with ALL?

A

Blood/platelet transfusions

IV fluids

Allopurinol

Subcutanous port/hickman line

18
Q

Discuss the treatment for ALL?

A

4 chemotherapy stages:

Remission inducing
Consolidation
CNS prophylaxis
Maintenance

Matched related allogenic marrow transplantation

19
Q

What indicates a poor prognosis in ALL?

A

Adult, male

Philadelphia chromosome (chromosomes 9 and 22)

Presentation with CNS signs

low Hb, low WCC

20
Q

What is chronic myeloid leukemia?

A

Uncontrolled proliferation of myeloid cells.

Occurs mainly in those 40-60

21
Q

What is different about CML and ALL with regards to genetic

A

Those with the Philadelphia chromosome do better in CML

22
Q

What are the stages of chronic myeloid leukemia?

A

Chronic phase- lasts months or years, hardly any symptoms-30% detected by chance

Accelerated phase- increasing symptoms of spleen size and difficulty controlling counts

Blast transformation features of acute leukemia and death

23
Q

What are the signs and symptoms of CML?

A
Weight loss
Tiredness
Fever 
Sweats
gout
splenomegaly
hepatomegaly
bruising
anaemia
24
Q

What are the tests involved in chronic myeloid leukemia?

A

Increased white blood cells

Increased spectrum of myeloid cells- increased neutrophils, monocytes, basophils, eosinophils

Increased urate and b12

Hypercellular bone marrow

25
Q

How is CML treated?

A

Imatinib, specifically targeted biologic to BCR-ABL

2nd generation bcr-abl drugs e.g. dasatinib and nilotib

Similar treatment to ALL, chemo (doesn’t have good outcomes), allogenic transplant (better in younger patients)