Haemotopietic System Flashcards

1
Q

Erythrocytosis

A

Increased erythrocytes

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2
Q

Lymphocytosis

A

Increased lymphocytes

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3
Q

Erythropenia

A

Deficiency if erythrocytes

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4
Q

Lymphopenia

A

Deficiency of lymphocytes

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5
Q

Monocytosis

A

Increased monocytes

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6
Q

Monopenia

A

Deficiency of monocytes

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7
Q

Neutrophilia

A

Increase in neutrophils

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8
Q

Anaemia

A

Erythropoietin secreted from kidneys in response to low circulating oxygen

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9
Q

Regenerative anaemia

A

Bone marrow responds to replace cells (problem isn’t with bone marrow) e.g. haemolysis (bursting red blood cells)

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10
Q

Non-regenerative anaemia

A

Bone marrow does not respond to replace cells

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11
Q

Haemorrhage

A

Acute blood loss due to internal or external trauma (organ rupture, poisoning e.g. warfarin)

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12
Q

Chronic blood loss

A

Haematuria, melaena, epistaxis, neoplasia, parasite burden

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13
Q

Haemolysis

A

Immune mediated disease e.g. autoimmune haemolytic anaemia

Cellular parasites e.g. mycoplasma haemofelis

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14
Q

Medullary disorders

A

Bone marrow hypoplasia (underdeveloped bone marrow/bone marrow tumour)

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15
Q

Extramedullary disorders

A

Rental disease
FIV
FeLV

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16
Q

Clinical signs of anaemia

A
Pallor mucous membranes
Lethargy 
Dyspnoea / tachypnoea 
Exercise intolerance 
Syncope; fainting, collapse, death
Tachycardia +/- haemic (anaemia induced murmur)
17
Q

Diagnostic testing for anaemia

A

History and full physical examination
Blood tests for biochemistry, haematology including reticulocytes and platelet counts e.g. PCV + reticulocyte count (immature rbc)
Blood smear
Blood tests for coagulopathies/immune mediated diseases
Bone marrow biopsy
Radiograph/ultrasound

18
Q

How long does it take for erythroblast to become erythrocyte

19
Q

Treatment for anaemia

A

Control active haemorrhage
Whole blood transfusions/colloids
Medication e.g. erythropoietin, steroids, chemo

20
Q

Nursing care for anaemia patient

A
Monitor vital and clinical signs 
Keep quiet and avoid stress
General care of trauma patient 
Medication prescribed by vet
Diet with haematinics e.g iron and vit b
21
Q

Haemostasis

A

Prevents excessive blood loss from damaged vessels. Liver produces all clotting factors except Von Williband

22
Q

Primary haemostasis

A

Slowing down (clumping everything together)

23
Q

Secondary haemostasis

A

Forming of the clot using clotting factors

24
Q

What is Von willebrand disease

A

Common hereditary coagulopathy

Protein linking platelets to sub-endothelium and assists platelet aggregation

25
What is haemophilia A
Effects dogs but bitches can carry German shepherds Factor VIII deficiency
26
Immune mediated thrombocytopenia
Causes destruction of platelets
27
Anticoagulant rodenticide poisoning
Rat bait contains warfarin causing reduction in vitamin k
28
What can liver disease cause
Severe liver dysfunction e.g. cirrhosis
29
Disseminated intravascular coagulation
Development of tiny clots in blood exhausting all the clotting factors Due to secondary cause pancreatitis, haemangiosarcoma, septic shock
30
Clinical signs of coagulopathies
``` Petechial or ecchymotic haemorrhages Epistaxis Melaena Haematuria Haematomas Prolonged bleeding from cuts/venipuncture Bleeding into body cavity/joints Bleeding after shedding teeth Delayed bleeding after venipuncture ```
31
Diagnosis of coagulopathies
History and full physical examination Blood test - biochem and haematology including reticulocyte and platelet counts Blood tests for coagulopathies e.g. activated clotting time, Von willebrands, buccaneer mucosal bleeding time
32
Treatment of coagulopathies
Plasma, platelet rich plasma or whole blood transfusion | Medication e.g. steroids, desmopressin, vit k, heparin
33
Nursing care for coagulopathies
``` Monitor vital and clinical signs Keep quiet and avoid stress Handle with care Administer medication prescribed by vet Venipuncture must not be done using jugular ```