Pics 1: coag/plt/throm Flashcards

Coag, platelets, thrombosis

1
Q

Bethesda Assay
How it works

A
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2
Q

Differentiating causes of long aPTT
Congenital vs Acquired hemophilia
Congenital +inh
Lupus inhibitor
Heparin effect

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3
Q

Lupus inhibitor: what it acts on

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4
Q

Mechanisms of anticoagulants, and examples
Xa
IIa
Xa and IIa
VKA

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5
Q

Trials for APS, warfarin for triple positive

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6
Q

Half lives of Vit K dependent factors
Why it matters

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7
Q

Warfarin indications

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8
Q

DOACs pros/cons

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9
Q

DOAC reversal

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10
Q

Anticoagulant with altered GI anatomy

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11
Q

CAT: who can’t get DOAC
which societies?

A
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12
Q

Primary, secondary hemostasis and fibrinolysis
Testing for each part

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13
Q

Coagulation cascade

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14
Q

Clinical scenarios: Isolated long aPTT

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15
Q

Clinical scenarios: isolated long PT/INR

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16
Q

Scenarios with long aPPT and PT/INR

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17
Q

Coag testing abnormalities: summary table

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18
Q

Hemophilia genetics

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19
Q

Hemophilia complications

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20
Q

Hemophilia: percentage increase with doses of FVIII or FIX

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21
Q

Types of extended half life coagulation factor products

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22
Q

MOA emicizumab

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23
Q

Hemophilia rebalancing therapies

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24
Q

Gene therapies for hemophilia
MOA?

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25
Q

Rare factor deficiencies table

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26
Q

HHT therapies

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27
Q

Delta/Dense granule contents

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27
Q

PFA-100
what agonists?
Simple results?

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27
Q

Vascular bleeding disorders

A

Also EDS

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28
Q

Steps of platelet function

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28
Q

Alpha granule contents

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29
Q

Platelet aggregometry: types of agonists
Which are strong?

A
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30
Q

Example plt agg
P2Y12 inh
ASA effect

A
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30
Q

Example plt agg
VWD2B/plt type VWD
collagen issues [GPVI]

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31
Q

Possible inherited bleeding disorder flow sheet

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32
Q

Testing modalities for platelet disorders

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33
Q

Specific disorders of platelets
Plt count
smear
aggs
other tests
which gene

A
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34
Q

Specific disorders of platelets
Plt count
smear
aggs
other tests
which gene

A
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35
Q

Inherited plt disorders:
Schema of the platelet

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36
Q

Bernard soulier vs Glanzmann

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36
Q

Storage pool defects vs signalling defects

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37
Q

Acquired plt dysfunction: meds and foods

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37
Q

Acquired platelet dysfunction: meds

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38
Q

Qualitative platelet defects
Differential of Inherited vs Acquired

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39
Q

Qualitative platelet defects
Differential of Inherited vs Acquired
In picture form

A
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40
Q

VWD and lab values for each type

A
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41
Q

VWD and inheritance
Also blood groups and effect on VWF

A
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42
Q

Quantitative VWD subtypes

A
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43
Q

Qualitative VWD subtypes

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44
Q

VWD Dx summary

A

Use BAT
Use newer assay than Risto if have it
Level <50% and bleeding -> VWD
DDAVP with 1h and 4h for Type 1C Dx

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45
Q

VWD Treatment summary

A
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46
Q

VWD diagnosis flowsheet

A
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47
Q

Flowsheet diagnosis of suspected Type 2B VWD

A
48
Q

Type 2 VWD diagnosis recommendations

A
49
Q

Type 2 VWD treatments recommendations

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50
Q

VWD diagnosis summary from slides

A
51
Q

Pneumonic for VWD types

A
52
Q

Type 2 VWD treatments recommendations

A
53
Q

fibrin formation and degradation

A
53
Q

Mechanisms picture, quantitative VWD

A
54
Q

VWD table ASH SAP

A
55
Q

Mechanisms picture, qualitative VWD

A
56
Q

Coag cascade and corresponding lab tests

A
57
Q

VWF multiyear analysis examples

A
58
Q

FVIII concentrates

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59
Q

FIX concentrates

A
60
Q

Bypassing agents in bleeding: table from ASH SAP

A
61
Q

Rare factor deficiencies ASH SAP table

A
62
Q

Normal platelet function diagram

A
63
Q

Schematic of platelet function [picture]
and where disorders are involved

A
63
Q

List of all inherited plt disorders
Know main categories

A
64
Q

Acquired defects in platelet function

A
65
Q

TTP vs aHUS

A
66
Q

iTTP diagnosis

A
67
Q

Prediction tools for TTP

A
68
Q

Treatment pillars of TTP

A
69
Q

Treatment TTP, acute inpt, acute inpt/outpt, remission

A
70
Q

aHUS manifestations by organ system

A
71
Q

Risk of aHUS by mutation and triggers

A
71
Q

aHUS pathogenesis: complement balance beam

A
72
Q

Stopping terminal complement inhibitor flow chart

A
73
Q

Conditions associated with DIC

A
73
Q

aHUS summary

A
74
Q

Mgmt DIC

A
75
Q

TMA in cancer: etiologies, 3 types

A
76
Q

TMA in cancer, workup and mgmt

A
77
Q

Summary slide cancer associated TMA

A
78
Q

HIT activation: multiple pan cellular mechanisms

A
78
Q

TMA summary slide

A
79
Q

Other TMAs that are/can be complement mediated

A
80
Q

Catastrophic APS

A
81
Q

D-ITP vs HIT: timeline and clinical picture

A
81
Q

Thrombosis types in HIT

A
82
Q

4Ts score in HIT

A
83
Q

Treatment HIT: 2 dos, 2 donts, 2 diagnostics

A
84
Q

Warfarin induced limb gangrene
Why happens [pathophys]?

A
85
Q

HIT boards review pearls

A
85
Q

Anti-PF4 disorders
There are 5!

A
86
Q

Pathogenesis ITP
5 mechanisms

A
87
Q

1L mgmt of ITP
drug/dose/time to response/side effects

A
87
Q

MOA of steroids in ITP
Multiple effects on immune system

A
88
Q

2L mgmt ITP
Rx, RR, longterm remission rates

A
89
Q

Drug induced ITP summary

A
90
Q

ITP boards summary slide

A
91
Q

Treatments summary for ITP

A
91
Q

DDX TMA flowsheet

A
92
Q

Complement alternative pathway

A
93
Q

iTTP pathogenesis picture

A
94
Q

Classifications of TMAs
Known vs unknown etiologies

A
95
Q

HIT incidence by population and which drug exposed to

A
96
Q

Testing for ITP
from working group recommendations

A
97
Q

ITP
Primary
secondary
phases

A
98
Q

PE management flow sheet

A
99
Q

Recurrence triangle
with percentages

A
100
Q

Recurrence triangle
with modifiers of level on triangle

A
101
Q

Test in thrombophilia:
which to do
Common/classic/acquired/other

A
102
Q

who to consider thrombophilia testing

A
103
Q

False testing of Protein C, S, AT
Why acquired deficiency and which ones?

A
104
Q

New Sydney criteria for antiphospholipid syndrome diagnosis

A
105
Q

Effects of DOACs on coag testing

A
106
Q

Family members: who to test when family member has a thrombophilia

A
107
Q

Conditional recommendations of when to maybe test for inherited thrombophilia

A
108
Q

Inherited thrombophilias summary slide

A
109
Q

Threshold model of thrombosis risk

A
110
Q

Factors favouring extended or limited anticoagulant therapy in patients with unprovoked VTE

A
111
Q

Main questions for unexplained arterial thrombosis in the young
4 main parts/sections

A
112
Q

Reasons for and against thrombophilia testing

A
113
Q

Inherited thrombophilias and estimated prevalence and RR for VTE manifestations

A
114
Q

Management of supra therapeutic INR in pt on VKA

A
115
Q

DOACs and their properties table

A