Exam 5 Coagulation Flashcards

1
Q

what is a reticulocyte count

A

reticulocyte= immature RBC in circulation

reported as % of RBCs

indicated bone marrow response

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2
Q

what does an increase reticulocyte count mean?

a decreased??

A

increased: body producing more immature RBCs and putting into circulation because they are needed
ex: after anemia treatment, in response to hemorrhage
decreased: less new RBCs being made

Ex: leukemia, decreased B12, Fe deficiency, anything that would shut down bone marrow response

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3
Q

What are examples of increased reticulocyte count

A

ex: after anemia treatment,

in response to hemorrhage

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4
Q

what are examples of decreased reticulocytes

A

Ex:
leukemia,

decreased B12,

Fe deficiency,

anything that would shut down bone marrow response

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5
Q

name some causes of poor coagulation

A

genetic

acquired

medication induced (heparin, warfarin)

low platelets

coagulation factor deficiency (Von willebrand disease, hemophilia)

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6
Q

name some causes of excess coagulation

A

genetic

acquired

medication induced (estrogens)

factor leiden mutation

malignancy

inflammation

impaired circulation

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7
Q

steps of hemostasis

A

`.1. tissue injury

  1. platelet response / tissue factor
  2. platelet adhesion, activation and aggregation, coagulating factors = plug formed
  3. fibrin degrades (plasminogen/ plasmin) and clot dissolution
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8
Q

how long do platelets last in circulation

A

7-10 days

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9
Q

what is the first line test in relation to bleeding/clotting

A

platelet count

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10
Q

what is too many platelets called?

too few?

A

too many: thrombocytosis

  • can be caused by cancer, meds, splenectomy
  • can result in clots

too few: thrombocytopenia
- can be caused by cancer, meds, lisinopril, infection (use them up), Idiopathic thrombocytopenia

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11
Q

what is prothrombin time (PT)

A

assess EXTRINSIC and common pathways

reported in # of seconds take to clot

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12
Q

what increases PT

A

WARFARIN

anticoagulants

salicylates

Vit K def

liver disease

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13
Q

what is Internationalized normalized ration (INR)

A

standardization of reporting for PT (prothrombin time)

anticoagulation therapy is adjusted based on INR goals
- aka we want some ppl to bleed a little bit more (why we put them on warfarin)

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14
Q

what is activated partial thromboplastin time (aPTT)

A

assess INTRINSIC and common pathway

reported as # seconds takes to clot

helps monitor: HEPARIN
and fast acting meds, usually inpatient!!!!!!!!!!!!!!

collect via venipuncture

active part makes it faster

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15
Q

what increases aPTT

A

Heparin

liver disease

hemophilia A and B

von willebrands

DIC

Vit K def

AKA increasing aPTT= increasing the amount of time it takes to clot = if it increases means harder to clot

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16
Q

are coagulating factors a first line test

A

no

they are useful for further investigation of unexplained bleeding

$$$

before you run pt should have a family Hx of bleeding disorder and current bleeding probs

17
Q

how are coagulation factors reported

A

by the factor as a %

18
Q

what is the factor V leiden mutation test

when should you run it

A

tests for an inherited defect in coagulation factor (resistant to clot breakdown)

should run if:

  • thrombosis (esp. if young)
  • unusual clotting and family hx

sample
-blood OR cells

NOT a first line test

19
Q

what is the most common HYPER coagulative inherited disorder

A

factor V leiden mutation

20
Q

what is the Coombs test

direct vs indirect

A

NOT A COAGULATION TEST

checks for RBC immune reaction/Abs

DIRECT: checks for Abs on RBCs
- AFTER suspected transfusion reaction or immune hemolysis

INDIRECT: checks for Abs in pt serum
-PRIOR to transfusion cross matching

21
Q

what test for a 76 yr old man on warfarin

A

PT/INR

22
Q

what test for a pt that needs a transfusion

A

Coombs

23
Q

what test for pt with iron deficiency anemia

A

CBC

reticulocyte

Fe

24
Q

what test for patient post thrombotic stroke and fam hx blood clots

A

factor 5 leiden mutation

25
Q

what test for a pt with severe post part hemorrhage intial?

secondary?

A

intial: CBC, PT, aPTT
secondary: coagulation factors, von willebrand

26
Q

what does heparin do

A

increases PTT (intrinisic, inpatient)

27
Q

what does warfarin do

A

increases PT and INR (warfarin= extrinisc pathway, outpatient)

28
Q

76 y/o male takes warfarin for chronic atrial fib and has a history PE

which labs would be useful to monitor pt

A

PT
INR

no need to get platelet or CBC

29
Q

what foods cause you INR to go donw

A

vit k veggies (Avocado)

green tea

30
Q

female to clinic for follow up post hospitalization for thrombotic stroke, non smoker, normal BP, fam history of blood clots

what labs would be useful initially

what to do if think inherited

A

platelet count with CBC
PT/INR
PTT

to see if inherited disorder: factor 5 Leiden (fam history clotting)

31
Q

female referred by OB/Gyn after severe post partum hemorrhage requiring repeat transfusions
pt admits heavy menses in early life
grandma had sim issues
father has severe nose bleeds

which labs would be good initially

which would be appropriate second line labs

A

initially:
- platelet count with CBC
- PTT
- PT/INR

second line: coagulation factors (bc family history bleeding)