Haematology Flashcards

1
Q

What to rx if DVT likely

A

straight to DOAC

lmwh no longer recommended as it means patient doesnt need to switch to alt treatment for 3/6 months (provoked/unprovoked)

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2
Q

Wells score of 2 or more means what

A

DVT likely
Do leg USS ideally within 4 hours
If not possible, do d-dimer and commence DOAC whilst waiting
If USS neg but DVT likely, await d-dimer
If scan neg but d dimer pos, stop DOAC and offer repeat scan in 1 week

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3
Q

If WELLs score 1, what does this mean?

A

Unlikely DVT
Do d-dimer, if d-dimer negative = good
if d-dimer positive, do USS

If waiting longer than 4 hours for anything and DVT a suspicion, commence DOAC as can always stop

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4
Q

What to rx if DOAC not suitable for a patient in the mx of DVT

A

LMWH followed by dabigatran or edoxaban OR LMWH followed by a vitamin K antagonist (VKA, i.e. warfarin)

think severe renal impairment (eGFR <15), metallic heart valve, or ventricular thrombus, APS, pregnant

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5
Q

Provoked VTE - duration of anticoagulation

A

3 months

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6
Q

Unprovoked VTE - duration of anticoagulation

A

6 months

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7
Q

Sequestration crises in sickle cell - what is it?

A

sickling within organs such as the spleen or lungs causes pooling of blood with worsening of the anaemia
associated with an increased reticulocyte count

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8
Q

Sickle cell aplastic crisis - what is it?

A

caused by infection with parvovirus
sudden fall in haemoglobin
bone marrow suppression causes a reduced reticulocyte count

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9
Q

what is an acute chest syndrome in sickle cell disease

A

vaso-occlusion within the pulmonary microvasculature → infarction in the lung parenchyma
dyspnoea, chest pain, pulmonary infiltrates on chest x-ray, low pO2
management
pain relief
respiratory support e.g. oxygen therapy
antibiotics: infection may precipitate acute chest syndrome and the clinical findings (respiratory symptoms with pulmonary infiltrates) can be difficult to distinguish from pneumonia
transfusion: improves oxygenation

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10
Q

What is a thrombotic crisis in sickle cell disease

A

also known as painful crises or vaso-occlusive crises
precipitated by infection, dehydration, deoxygenation (e.g. high altitude)
painful vaso-occlusive crises should be diagnosed clinically - there isn’t one test that can confirm them although tests may be done to exclude other complications
infarcts occur in various organs including the bones (e.g. avascular necrosis of hip, hand-foot syndrome in children, lungs, spleen and brain

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11
Q

Called to see a patient, trasnfusion recently started. Febrile and anxious, otherwise obs fine

A

Non-haemolytic febrile reaction
Give paracetamol, slow or stop transfusion
Monitor

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12
Q

Transfusion commenced, patient develops uritcaria and pruritis

A

Minor allergic reaction
Stop transfusion, antihistamine, monitor

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13
Q

Hypotension, angioedema, wheeze, SoB post commencement of transfusion

A

Anaphylaxis
Stop transfusion, adrenaline IM, ABC support (fluids, 02)

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14
Q

Fever, abdominal pain, hypotension post commencement of transfusion

A

Acute haemolytic reaction
ABO incompatibility
Stop transfusion
Check blood products
Fluid resus

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15
Q

Pulmonary oedema, HTN, background HF in Hx, recent start of transfusion

A

Transfusion-associated circulatory overload (TACO)

Slow, stop, Consider intravenous loop diuretic (e.g. furosemide) and oxygen

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16
Q

Hypoxia, pulmonary infiltrates on chest x-ray, fever, hypotension post commencement of transfusion

A

Transfusion-related acute lung injury (TRALI)

Non-cardiogenic pulmonary oedema thought to be secondary to increased vascular permeability caused by host neutrophils that become activated by substances in donated blood

Stop the transfusion

Oxygen and supportive care

17
Q

What is polycythaemia rubra vera

A

a myeloproliferative disorder caused by clonal proliferation of a marrow stem cell leading to an increase in red cell volume, often accompanied by overproduction of neutrophils and platelets

18
Q

Mutation in what gene results in Pcrv

A

JAK 2 mutation

19
Q

Features of PCRV

A

pruritus, typically after a hot bath
splenomegaly
hypertension
hyperviscosity
arterial thrombosis
venous thrombosis
haemorrhage (secondary to abnormal platelet function)
low ESR

20
Q

What is hodgkins lymphoma

A

a malignant proliferation of lymphocytes characterised by the presence of the Reed-Sternberg cell. It has a bimodal age distributions being most common in the third and seventh decades

21
Q

What are the B cell symptoms

A

fever
night sweats
weight loss

22
Q

What is the relevance of B cell symptoms

A

poor prognosis

23
Q

large spleen, abdo pain, sickle cell disease, anaemia

A

sequestrant crisis

24
Q

why is warfarin contraindicated in pregnancy?

A

teratogenic
thats why LMWH is used in DVT tx

25
Q
A