Benign and Thrombosis Flashcards

(137 cards)

1
Q

May Hegglin anomaly morphology

A

Large thrombocytes
Dohle bodies

Usually ASx

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2
Q

Wiskot Aldreich syndrome PB morphology

A

Micro thrombocytopenia
X linked
Eczema

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3
Q

When to start warfarin after HIT

A

When PLT normalize

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4
Q

Temporary Tx of TTP if PEX is not available

A

FFP

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5
Q

Tx of HELLP/Pre-eclampsia

A

Delivery at 34 weeks

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6
Q

Clues for psychogenic pupura

A

Psychiatric illness
Areas that are accessible to pt

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7
Q

Tx of MGUS associated VWD

A

IVIG
DDAVP

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8
Q

Dosing of FIX

A

1U/kg for 1% change

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9
Q

Dosing of FVIII

A

1U/kg for 2% change
(Half of FIX)

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10
Q

Titer of Ab in hemophilia pts requiring bypassing agents

A

5 BU

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11
Q

Immune tolerance therapy SE

A

Allergic reactions
Nephrotic syndrome

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12
Q

Abciximab SE

A

Thrombocytopenia

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13
Q

Dosing of DDAVP

A

Intranasal 150 mcg
IV/SC 0.3 mcg/kg max 20 mcg

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14
Q

Goal of FEIBA Tx

A

To control bleeding
not to correct aPTT

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15
Q

Superwarfarin PK

A

Longer half life

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16
Q

Prolonged reptilase time

A

Dysfibrinogenemia

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17
Q

Management of weak thrombophilias in pregnancy

A

No rule for antepartum AC
If FHx- Postpartum AC
w/o FHx no Tx

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18
Q

Duration of AC after HIT without VTE

A

1 month

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19
Q

Duration of AC after HIT with VTE

A

3 months

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20
Q

Target INR in Mechanic vlaves

A

Aortic- 2.5
Mitral- 3

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21
Q

When to consider dysfibrinogenemia

A

Hemmorhagic and thrombotic meinfistation

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22
Q

Role of vitamin supplementation for MTHFR

A

No benefit
MTHFR mutation is probably not meaningful

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23
Q

Management of PVT

A

Depending on bleeding and thrombosis risk
w&w may be appropriate if ASx
DOACs are effective

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24
Q

Polycythemia effect on PT

A

Increases PT/INR
Check with less citrate to get the right result

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25
Tx of SVT proximal to junction with deep vein
Same as DVT
26
Tx of SVT of >5 cm
Prophylactic AC for 45 days Fundaparinox 2.5/rivaroxaban 10
27
Indications for phlebotomy in hemochromatosis
Ferittin > 200 or Organ damage
28
DM drug affecting B12 metabolism
Metformin Supplement calcium to overcome
29
Which test is more specific for spherocytosis
EMA More sensetive and specific than osmotic frgaility
30
Test for eliptocytosis
Spectrin analysis
31
Zinc excess effect
Copper and iron defficiency
32
EPO ressistance in dialysis pts
Consider hyperparathyroidism PTH can cause BM fibrosis
33
p50
Checks Hb affinity High (right shift) means less affinity Acidosis, 2,3 BPG, CO2
34
Tx of methemoglobinemia
Methylene blue
35
Problamatic mutation in hemochromatosis
C282Y H63D is usually benign
36
McLeod phenotype
Absence of Kell group X linked Acanthocytosis and a compensated hemolytic state Progressive neurologic deterioration
37
Passenger lymphocytes hemolysis
Can be delayed Usually due to ABO mismatch
38
Tx of erythrocytosis post kidney transplant
ACEi
39
Tx of Sideroblastic anemia
B6
40
Tx of aplastic crisis due to Parvo in HS pts
Supportive care
41
Emergent Tx of CAD
Plasmapheresis
42
Prognosis of aplastic anemia during pregnancy
50% will recover spontaneously
43
Predictors for response to IST in aplastic anemia
IFN-gamma on T cells
44
VTE and ATE risk in cancer (timing)
VTE continuous ATE around diagnosis
45
Which anti-PLT is resistant to Tx with PLT
Ticagrelor (Reversable inhibitor so less amendable to PLT transfusion)
46
Transfusion of fresh vs stored RBC in critically ill patients
No decrease in 90 days mortality
47
Presentation of partial D phenotype
D-positive patient with anti-D after transfusion
48
Implications of partial D phenotype
As donor D+ As receipent (pregnancy) D-
49
Presentation of weak D phenotype
D+ pt testing on occasions as D-
50
P value
Probability of obtaining test results at least as extreme as the result actually observed, under the assumption that the **NULL HYPOTHESIS** is correct
51
Highest risk Ab for HDFN
D, c, Kell, E c+E- very high risk
52
Rivaroxaban dose adjustment
CrCL< 50
53
Dabigatran dose adjustment
CrCL< 30 But caution in CrCL< 50
54
Edoxaban dose adjustment
Weight < 60 kg CrCL< 50
55
L-glutamine in SCD
As adjuvant to HU Prevention of vaso-occlusive pain in patients with frequent episodes
56
Mesenteric venous thrombosis Tx benefit of AC
OS Recalnulization in most pts Lowers bleeding!
57
Duraion of AC in Mesenteric venous thrombosis
3-6 months longer if thromophilia present
58
Source of plasma transfusion in pts with unknown blood type
A
59
CAD ab
Anti-I EBV related- anti-i (not present in adults)
60
CAD hemolysis type
Usually extra-vascular in the liver May be intravascular if high titer
61
Leukoreduction benefit
FNHTR CMV Alloimmunization TRIM
62
Bernard Soulier vs Glazman defect
BS- GPIb-IX-V complex Glanzman- GPIIb/IIIa
63
PLT adhesion vs aggregation
Adhesion- VWF and GPIb Aggregation- GPIIb-IIIa
64
Upper vs lower limb DVT
Less PE with upper Same rate of PTS
65
Hb goal in thalassemia major pts
Pretransfusion- 9-10 Post transfusion- 13-14
66
Causes of ovarin vein thrombosis
Pelvic infection Surgery Ovarian cancer MPN
67
A2 blood type
Can have anti-A1 in their serum May cause hemolysis after A transfusion
68
Causes of reduction in ATIII
PEG-Asp Infection Liver failure Nephrotic syndrome
69
Causes of reduction in protein C
Infection Liver failure CKD
70
Factors effecting APCR test
Elevated FVIII Reduced PS Estogen Sepsis
71
FXI inheritance
AR
72
Periopertive management of mild hemophilia A
DDAVP If major surgery FVIII
73
Blood components in cryoprecipitate
Fibrinogen Factor VIII vWF Factor XIII Fibronectin
74
Complications of treatment with iron chelators
Deferoxamine: retinopathy and auditory toxicity Deferiprone- agranulocytosis Deferasirox- GI, rash, LFT
75
Granulocytes storage time
24 hours
76
p50
High means lower effinity to O2 (right shift) 2,3 BPG, acidosis- raise p50 Causing O2 to dissocate to the tissue
77
Acute hemolysis after PLT transfusion
Usually ABO incompatibilty due to ab in plasma of transfused PLT Washing can reduce risk
78
Dense granules of platelets compusition
ADP, ATP, Ca, serotonin
79
EBV related CAD IgM
Anti-i
80
Indications for transfusion in SCD
ACS not responding CVA prevention Preoperative
81
Prothrombin mutation location
Non coding region
82
Bashophilic stiplling
Aggregates of ribosomal RNA Seen in Lead poisoning, sideroblastic anemia
83
Couagulation factor with shortest half life
FVII
84
Weak A blood type
An impairement in the function of glycosyltransferase (Baby can be A even if both parents are O- bcs one of them is actually weak A)
85
Storage lesions in stored blood products
Decreased 2,3DPG and ATP Decreased pH Increased K
86
Risk of VTE among thrombophilia pts on estrogen
X35
87
Protein defects in HS
Ankyrin, band 3, β-spectrin, α-spectrin, and protein 4.2
88
Aspirin vs LMWH in orthopedic pts
Non inferior post fracture More VTE with aspirin after TKR and hip surgery
89
Risks for post-splenectomy sepsis
Older age Hem condition (including thalassemia)
90
Adsorption results interpetation
If positive- allo ab If negative- auto ab
91
Elution results interpetation
If positive- auto ab If negative- allo ab
92
Use of enzymes in adsoption technique
Removal of auto antigens while maintaining allo antigens on RBCs
93
Plasmaphersis in myesthenia gravis solution
Albumin
94
PLT refractoriness threshold
5K
95
Refractoriness to oral iron therapy def.
Hb increment < 1 g% after 4 weeks of therapy
96
Typical increment after PLT transfusion
30K
97
Osmotic fragility curve in HS
Right shift Not stable in high osmolarity
98
Lack of anti-A,B after transplant
May be due to donor-receipent mismatch in ABO Transfuse matched blood products Or O- Can try crossing after cooling of blood sample. Bcs IgM is more active at cold temperature.
99
Splenectomy benefits and risk in thalassemia
Improves- Hb, PLT, decreases hemolysis and reduces extramedullary hematopoiesis Risks- VTE, worsening PHTN
100
HIT without heparin Tx
Post COVID19 vaccine Post adenovirus infection
101
Causes of methemoglobinemia
Dapsone, nirtrite
102
FVIII trarget pre surgrey in Hem A pts
80-100%
103
PCC dosage
25-50U/kg
104
Andexanet alpha study
ANNEXA-I Composite outcome of hematoma volume and nuerologic det in 12 hours No advantage in long term neurologic outcomes 10% VTE vs 5%
105
Prax-bind dosage
5 mg can repeat (2 separate doses of 2.5 in 15 minutes)
106
Which cougulation factor does not change during pregnancy
ATIII PC FV
107
Risk factors for catheter associated thrombosis in cancer patients
Type of cancer (HL, esophageal, ovrian)
108
Risk factor for PTS
F Obesity Older age
109
Factors to follow in PEX
Fibrinogen Ca
110
Dosage of caplacizumab
11 mg (Practically 10 mg) First dose IV Then SC
111
Management of distal DVT
FU can be exceptable
112
Coumadin in cancer associated thrombosis
Was compared to LMWH Inferior
113
DOAC after bariatric surgery
Not in the first month Apixaban is probably the safest
114
Factors to prefer LMWH vs DOAC in CAT
GI/GU cancer Thrombocytopenia Absorption problems/vomiting Drug interactions Known planned procedures
115
Cougulation factors that are elevated in pregnancy
F7-10 FV does not change
116
INR for epidural
1.5
117
Management of reccurent abortions in obstetric APLS
Increase dose to 1mg/kg qd Increase apirin to bid Add plaquenil IVIG Steroids
118
Tx of superficial vein thrombosis > 5 cm
Fundaparinox 2.5 Rivaroxaban 10 LMWH? For 45 days
119
Tx of congenital TTP
Recombinant ADAMTS13 IV cTTP Phase III vs SOC ADAMTS13 levels were 100% and TTP events were rare
120
Andexanet alpha mechanism of action
Recombinant Xa that seaquesters anti-Xa
121
Caplacizumab mechanism of action
Targets the A1-domain of vWF Inhibiting the interaction between vWF and platelets
122
aHUS complement levels
Low c3 with normal c4
123
aHUS special blood tests
Soluble c5b-9 Flow with CD46 positive Low Factor H and Factor I PEP IEP FLC
124
What to do if aHUS pt does not improve his AKI even though hemolysos is better
Kidney biopsy to diagnose TMA vs other etiologies for CKD
125
Duration of Tx of eculozumab in aHUS
3-4 months after hematologic count recovery
126
What to do if aHUS pt is on continous dialysis
Stop eculizumab
127
What differentiates aHUS and TTP presentation
aHUS- HTN, Renal TTP- Deep thrombocytopenia, fever
128
Tx of HTN in aHUS
ACEi/ARB
129
Dosing of andexanet-alpha
400-800 mg depeding on rtime from presentation and dosing
130
Hemocysteine levels in MAHA
Cobalamin C deficiency HUS
131
MGUS associated aHUS
Anti-factor H AI Treat with eculizumab+rituximab
132
FVII deficiency ethnicty
Maroco Prasia
133
Coagulation system prevalent in bleeding from endothel
Hyperfibrinolysis
134
Pt with factor deficiency receiveing plasma
Always consider development of inhibitors
135
FFP dosing
15-20 ml/kg
136
rFVII dosing
15-30 mcg/kg
137
Rexposure to heparin in HIT pts
In short exposure (CABG) Most will not develop antibodies