2011 exam Flashcards

1
Q

haemolytic disease for newborn - does anti D - extra or intra vascular

A

extravascular

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2
Q

Additional tests you ask the blood bank to complete on baby and mother

A

?

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3
Q

Clinical symptoms of leukaemia

how to confirm?

A
  • tiredness
  • severe brusing
  • unusual bleeding from gums
  • low haemoblobin
  • lowplatelets
  • low nuetrophils

Anaemia - fatigue, dyspnoea , chest pain
Neutropenia - infection, wounds slow to heal as less good white blood cells
Thrombocytopenia - bruising and bleeding
Bone marrow pain
Enlarger liver, spleen, lymph nodes
Gums

  • take a bone marrow examination and could do bone marrow morphology – see if more than 20% are myeloid or lymphoid
  • aspirate
  • trephine
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4
Q

Would it benefit to give G-CSF colony stimulating factor? side effects?

A

G-CSF - is a haemoatopoitic growth factor, that redcues the impact of neutropenia bu stimulating bone marrow to make more neutrophils

-have seen that this can benefit patients by increasing number of neutrophils, so that the patient can fight of infections better and not get as sick

risk factors - ??

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5
Q

Risk factors for leuakaemia

A

congenital / inherited risk factors - e.g down sydrome have an increased incidence
viral infections
radiation
chemical/dna damaging drugs

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6
Q

Transfusion support is critical in management of patients with acute leukaemia. Outline blood products that could be used by this patient and when they may be prescribed?

A
  • platelets

- red cells

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7
Q

general / supportive care for leukaemia

A

General/ supportive care
-intensive transfusion support - red cells, platelets

management of infection
-ID and lab support, antibiotic therapy

Chemotherapy

Stem cell transplantation

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8
Q

what is another cause of macrosytic anaemia

A

liver disease

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9
Q

Risk factors for DVT

A

Stasis of blood
immobility - post op, plane
Pressure - (blockages) catheter, tumour obstruction
Increased viscosity - polycthaemia, dehydration, EPO

Blood hyper coagulability
increased procoagulants
decrease in inhibitors
impaired fibrinolysis (rare)

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10
Q

Hereditary abnormalities which may increase the risk of DVT, how common are these?

A

Inherited thrombophilia - increased tendency to develop VT

  1. Factor V leiden
    - most common hereditary cause (4% northern europeans)
    - Where protein C is unable to cleave factor 5a
    - this slows down production of activated 10a
  2. APCR gene - heterozygotes carry a 3-7 fold increased risk of thrombosis
    - homozygotes carry a 50-100 fold increase risk of thrombosis
  3. deficiencey of inhibitors - e.g antithrombin, protein C, protein S
  4. increased factor levels - e.g prothrombin gene mutation 20210a
    - elevated factor 8

if you have both factor 5 leiden and are homozygotes for apcr - have an 80 relative risk comapared to a normal person

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11
Q

what are the causes of a prolonged APPT with a normal PT?

A
  1. lupus anticagulant
  2. (rare) Autoimmune disease, making an inhibitor bind onto a clotting factor (usually 8) - causes “aquired haemophilia”
  3. Heparin (drugs), these are inhibitors of coagulation system
    - can cause bleeding
    - upregulates the affect of anti-thrombin
    - so it blocks activated thrombin
    - because it is blocking the activated protein, it doesnt overcome the effect of the inhibitor and this is why 1 + 1 is prolonged

Also - Dibigatran

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12
Q

How can you distinguish between dibigatran and heparin

A

-both have prolonged APPT, and 1 + 1, however if you add protamine this will correct heparin but not dibigatran

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13
Q

How can you have deficiencies with common pathway factors, with a normal APPT ? (but have an abnormal PT)

A
  • because APPT is less sensitive that prothrombin time
  • prothrombin will be prolonged if factors are reduced to 40-50%
  • but APPT is less sensitive then that, so if have mild common factor deficiencies, the APPT can be normal with a mild prolongation of PT time
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14
Q

What further micro test to obtain more info>

A

Disc suceptibility testing

  • on an agar dish, place bacteria all over
  • then place an antibiotic disc that you want to test suceptibility onto the agar
  • this will difuse into agar in a conc gradient
  • then can measure the distance around the disc to see the suceptibility of antibiotic to that certain bacterium grown
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15
Q

What further micro test to obtain more info>

A

Disc suceptibility testing

  • on an agar dish, place bacteria all over
  • then place an antibiotic disc that you want to test suceptibility onto the agar
  • this will difuse into agar in a conc gradient
  • then can measure the distance around the disc to see the susceptibility of antibiotic to that certain bacterium grown
  • then can use thsi info to presribe antibiotics
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16
Q

Most likely cauase of meningitis
-gram stain and virulence factors

-how to identify in lab

A

Streptococcus pneumonia - older

  • gram positive
  • polysacharide external capsule - can escape phagocytosis , many different capsule serotypes - prevents opsonisation
  • has pneumolysin - can destory human cells

-gram positive, cataluse negative, alpa haemoliticm optochin sensitivity

niseria meningitides - young children

  • gram negative cocci
  • thcik polysacharide capsule, prevents opsonisation
  • Factor H - can bind to this on human cells, and down regulates complement forming

epidemiology of organism - majority infectes young maori and pacfic children

17
Q

How should patient be treated?

A

dexmotrexane (antiinflammatory) then anitbiotics (penicilin)

18
Q

Innate and adaptive system responses to bacterial infections

A

Innate - physical barrier, microbial factors - lysozyme, complement,

Adaptive
-inflammation

19
Q

Principles of immunisation with inactivated bacterial vaccines

A

Inactivated vaccines consist of -polysacharide capsule

  • combinant
  • protein based
  • whole bacteria or parts of it
  • toxin
  • modify in lab
  • get immune response
  • but not as strong
  • not lifelong
  • need to repeat immunisation
  • antibody response increases over no. times give vaccine
20
Q

candida albicans

  • how to look this up in lab
  • what do we use for treatment>
A

-black yeasts w psuedohyphae on gram stain

=grows well on blood agar