SA Bloodwork Cases Flashcards

(37 cards)

1
Q

what is done with every CBC

A

blood smear

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2
Q

what tests are needed to evaluate urine

A

chem + UA
USG

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3
Q

what signals a mature neutrophilia

A

increased number of segs

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4
Q

what is associated with an elevated mature neutrophilia

A

inflammation
stress
fear
neoplasia

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5
Q

what is associated with a decreased mature neutropenia

A

overwhelming infection/inflammation

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6
Q

what is a physiologic leukocytosis

A

neutrophilia
lymphocytosis

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7
Q

what creates a physiologic leukocytosis and in what species is it commonly seen

A

fear - cats

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8
Q

what is a stress/corticosteroid leukogram

A

mature neutrophilia, monocytosis, and lymphopenia

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9
Q

in what species is a stress/ corticosteroid leukogram common in

A

dogs

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10
Q

what signals an inflammatory leukogram

A

> 1000 bands
decrease in WBCs

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11
Q

what can an extreme neutrophilic leukocytosis signal

A

pyometra
ehrilichia
hepatozoanosis
fungus

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12
Q

what would signal a leukemia on a CBC

A

> 50,000

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13
Q

Types of anemia that are regenerative

A

hemorrhage/ blood loss
hemolysis

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14
Q

what test can be used to determine true rouleaux formation

A

saline test - rouleaux will separate

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15
Q

what can you use to evaluate precursors and normal development and maturation process of all cell lines as well as any abnormal processes

A

bone marrow
aspirates / biopsy

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16
Q

what are possible causes of petechia

A

thrombocytopenia
thrombopathy
infection/inflammation

17
Q

reasons for thrombocytopenia

A

increased destruction
decreased production
increased consumption
sequestratio n

18
Q

what are types of thrombopathy

A

inherited
vWB factor
acquired with drugs, uremia, liver disease or dysproteinemias

19
Q

what are basic primary coagulation issues

A

platelets and vasculature

20
Q

what are basic secondary coagulation issues

A

coagulation factors
anti-thrombotic and fibrinolytic

21
Q

clinical signs of primary hemostatic disorders

A

petechia
ecchymosis
mucosal bleeds
epistaxis

22
Q

clinical signs of secondary hemostatic disorders

A

hemoabdomen
hemothorax
melena
hematemesis

23
Q

components of virchow’s triad

A

stasis
endothelial injury
hypercoagulability

24
Q

platelet testing

A

platelet count
platelet function (thrombopathies)
Buccal Mucosal Bleeding Time
Clot retraction
aggregation

25
what does a hypercoagulation pattern look like on a TEG
RK decreased MA angle increased * basically looks like a fat oval
26
increased BMBT decreased platelet count
thrombocytopenia
27
increased BMBT everything else normal
thrombocytopathia
28
increased BMBT possible increased ACT possible increased PTT
vWD
29
normal BMBT increased ACT increased PTT
hemophilias
30
possible increased BMBT increased ACT increased PT increased PTT possible decrease platelet count possible decreased fibrinogen possible increased FDPs
rodenticide
31
everything increased decreased platelet count possible decrease fibrinogen
DIC
32
possible increased BMBT increased ACT possible increased PT increased PTT possible decrease platelet count possible decrease fibrinogen normal FDPs
liver disease
33
what does APTT and PTT evaluate
intrinsic and common pathways
34
what does PT evaluate
extrinsic and common
35
which clotting factor will run out first and therefore we should test for in cases of time
7
36
which tests should be run to test factor 7
PT ACT could track it in the common pathway but non-specific
37