HAEMATOLOGY Flashcards

1
Q

Definition of anaemia

A

Low haemoglobin

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2
Q

Interpreting FBC

A

Hb, White cell, platelets

MCV - clue of cause of anaemia

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3
Q

How do you classify anaemia

A

Size of red cells

Microcytic - iron deficiency (95% of microcytic caused by this)

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4
Q

How do you classify anaemia

A

Size of red cells
Microcytic - iron deficiency (95% of microcytic caused by this)
Macrocytic - B12/ folate deficiency
Normocytic - blood loss

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5
Q

Macrocytosis without anaemia causes

A

Liver disease
Hyperthryroid
Excess alcohol use

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6
Q

Sickle cell anaemia

A

Autosomal recessive

Single point mutation

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7
Q

Key feature of sickle cell

A

Painful vaso occlusive crises

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8
Q

Triggers for sickle cell crises

A

Infection
Cold weather
Hypoxia

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9
Q

What would you see on a smear for sickle cell

A

Target cells

erythroblasts - dont usually see these in normal population represent high turnover in marrow

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10
Q

what is myelodysplasia

A

disease of elderly
pre-malignant condition
bone marrow not working properly

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11
Q

what is lymphoma

A

malignancy of lymphocytes in lymph nodes

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12
Q

symptoms of hodgkins lymphoma

A

B symptoms

painless lymphadenopathy

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13
Q

types of non -hodgkins lymphoma

A

high (acute/ progress rapidly, but curable) or low grade (slow progression but incurable)

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14
Q

symptoms of hodgkins lymphoma

A

B symptoms
painless lymphadenopathy
4 sub types

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15
Q

what is myeloma

A

proliferation of plasma cells

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16
Q

causes of thrombocytosis

A

bleeding, malignancy, inflammation, infection

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17
Q

warfarin

A

slow on and off

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18
Q

test for haemophillia

A

factor 8 and 9

APTT

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19
Q

treatment of pernicious anaemia with hb very low

A

still dont transfuse as will have acquired deficiency slowly over time, if transfuse quickly can tip into heart failure (if elderly and features of hf)

20
Q

neurological manifestations of folate

21
Q

blood components from one donation

A

red cells
platelets
fresh frozen plasma
cryprecipitate (used to replace fibringogen)

22
Q

complications of blood transfusions

A
fluid overload
viral infection 
bacterial infection
incompatibility reaction 
iron overload
23
Q

risk factors for vte

A
surgery 
obesity 
immobility
cancer 
cocp
pregnancy
24
Q

treatment for pe

A

rivaroxiban for 3 months
15 mg for 3 weeks then 20 mg for remainder
different dose after 3 weeks

25
treatment for pe
``` rivaroxiban for 3 months 15 mg for 3 weeks then 20 mg for remainder different dose after 3 weeks provoked 3 months unprovoked 6 months ```
26
what is the action of tranexamic acid
Anti-fibrinolytic | Stops (prevents) the breakdown of clots
27
what is a direct and indirect coombs test | What is an indirect coombs test used for
Direct tests for antibody on RBC surface | Indirect tests for antibodies in blood, this one is used to diagnose reactions to blood transfusion.
28
What is the response to protamine sulphate by 1) heparin 2) LMWH 3) Fondaparinux
1) Complete response 2) Partial response 3) No response
29
Why are LMWH and fondaparinux preferred to unfractioned heparin
``` Better pharmacokinetics (stable half lives regardless of dose so dont need daily monitoring) Less adverse reactions - lower risk of HIIT because dont have mechanism of action on thrombin (which is mechanism of action that caused thrombocytopaenia) ```
30
Management of major haemorrhage
Activate major haemorrhage protocol Administer high flow oxygen Insert 2 wide bore peripheral cannulae and provide fluid resuscitation. Contact key personnel, including experts to treat bleeding cause. Arrest bleeding and treat underlying cause as soon as possible. Request laboratory investigations and perform Point of Care Tests where available, including blood gas analysis and viscoelastic tests (ROTEM/ TEG). Transfuse red cells to maintain a haemoglobin level of 70-90 g/L Administer tranexamic acid within 3 hours of onset of haemorrhage unless complicated by disseminated intravascular coagulation Transfuse FFP empirically if estimated blood loss greater than 20% blood volume or if microvascular bleeding Anticipate the need for additional blood components (including red cells, FFP, platelets and cryoprecipitate) Use cell salvage where available and appropriate When bleeding is under control additional doses of FFP should be based on results
31
what are the complications of major haemorrhage
``` thrombocytopaenia hypothermia hypocalcaemia hyperkalaemia ARDS coagulopathy ```
32
what bloods should you take during major haemorrhage
FBC - Hb, infection, platelets Clotting - PT, APTT, including Fibrinogen (DIC) Group and save - group blood Cross match - cross matched blood Calcium - needed for coagulation factors to work ABG - ongoing Hb and electrolytes
33
How should blood be given in major haemorrhage
2 units RBC (O negative emergency) 1 unit of FFP to every 2 units of RBC Platelets if fall below <75 Cryo only if fibrinogen is not correcting by FFP and is <1.5
34
what is fibrinogen concentrate indicated for
Fibrinogen supplementation in patients with congenital hypofibrinogenaemia; as prophylaxis before surgical procedures, or to treat bleeding Correction of low fibrinogen levels due to acquired bleedingdisorders in Europe and in the Republic of Ireland, although not yet licensed for this indication in the UK. Alert!! Fibrinogen concentrate can cause widespread thrombi, if administered inappropriately or in excessive dose. A critically low fibrinogen level should be confirmed beforehand.
35
What are the common acute transfusion reactions
``` Febrile, allergic, hypotensive reactions Acute haemolytic transfusion reaction TACO - circulatory overload TA Lung injury Transfusion related dyspnea Septic shock - from bacterial contaminant ```
36
what are the common delayed transfusion relactions
Haemolytic reactions from pregnancy or previous transfusion Graft vs host disease Iron overload Post transfusion purpura
37
Outline the management of a suspected acute red cell transfusion reaction
STOP THE TRANSFUSION Rapidly assess patient A-E (observations and interventions as necessary) Any concerns - call for help Check component and patient are correct/ correct blood has been given Commence medical treatment as necessary eg salbutamol for bronchospasm Send giving set to blood bank for coombs test Document event Report on local incident management Report to SHOT
38
How should you manage a transfusion reaction
STOP the transfusion Maintain IV access Undertake rapid clinical assessment including ABC (Airway, Breathing, Circulation) If appropriate, call for help Check identification details between the patient, their identity band and the compatibility label of the blood component Visually assess the unit looking for evidence of unusual clumps or discolouration and check the expiry date Check standard observations.
39
management of severe transfusion reaction
Call for help/medical staff immediately Disconnect the component and giving set from the patient and retain for further investigation Maintain IV access with physiological saline and use blood pressure, pulse and urine output to guide fluid administration Ensure the airway is patent, and if the patient is severely dyspnoeic give high flow oxygen through a mask with a reservoir. Shock/severe hypotension associated with wheeze/stridor i.e. anaphylaxis Shock/severe hypotension without clinical signs of anaphylaxis or fluid overload i.e. ABO incompatibility or bacterial contamination Severe dyspnoea without shock i.e. TRALI or TACO (Transfusion Related Acute Lung Injury or Transfusion Associated Circulatory Overload).
40
Treatment of moderate transfusion reactions
Moderate febrile symptoms Differential diagnosis is similar to severe ATR In most cases the transfusion will be discontinued. If the transfusion is resumed then the patient should be monitored closely. Moderate allergic symptoms Symptoms may include angioedema and dyspnoea but not sufficiently severe to be life-threatening. Antihistamines should be given. Consider oxygen therapy and inhaled salbutamol.
41
Treatment of mild transfusion reaction
In mild ATR, medical staff should be informed, but the transfusion may be continued with appropriate treatment and close observation. Treat mild febrile reactions with oral paracetamol (500-1000mg in adults). Treat mild allergic reactions with antihistamines and slow the transfusion rate. BEST PRACTICE POINT A mild reaction may be the early stages of a severe reaction - DON’T IGNORE IT. Observe the patient closely
42
investigations for moderate-severe transfusion reactions
Full Blood Count (FBC) Urea and Electrolytes (U&Es), Liver Function Test (LFTs) Urine analysis (for haemoglobinuria, to exclude haemolysis)
43
what is the threshold and considerations for transfusing platelets
Well patient / no RFs - if fall below 10 (as long as plts are >5 there shouldnt be any increased risk of bleeding in the absence of any other RFs) If RFs - transfuse at <20 If having surgery <50 If having anything to do with brain eyes - <100 Epidural - <80 Severe bleeding <50 Multiple trauma incl intracerebral bleed <100
44
what are the indications for cryo
< fibrinogen von willebrands disease factor 8 and 13 deficiency DIC
45
why is cryo preferred in fibrinogen replacement to FFP
15 mls of cryo Can keep replacing without overload Higher concentration of fibrinogen in cryo (250mg in 10 mls) than FFP (400 mg in 200 mls)