Coagulation disorders Flashcards

(44 cards)

1
Q

Warfarin Major bleed T

A

Stop W
Cit K IV 5mg (phytomenodione K1)
Prothrombin Complex Bereplex 50u/kg

(cant: FFP)

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2
Q

Warfarin Minor bleed T

A

Stop W
Vit K IV 1-3mg (phytomenodion K1)
Repeat in 24hr if INR still high
Restart warfarin INR

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3
Q

INR 5-8 (no bleed)

A

Omit 1-2 doses

Adjust after

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4
Q

INR 8+ (no bleed)

A

Stop W
Vit K oral 1-5mg (swallow IV prep phytomenodione K1)
Repeat in 24hr if INR still high

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5
Q

Warfarin mechanism

A

Vit K dependent factors
2,7,9,10
Protein C + S

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6
Q

Warfarin half life

A

> 40hr

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7
Q

INR aim post 1st VTE

A

provoked: 2-3 for 3m
unprovoked: 2-3 for 6m

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8
Q

INR aim post recurrent VTEs no treatment

A

2-3 for life

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9
Q

INR aim recurrent VTEs ON treatment

A

3-4 for life

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10
Q

INR aim on HEART VALVES

A

Mechanical Aortic 2-3

Mechanical mitral 2.5-3.5

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11
Q

Describe Intrinsic pathway

A
Eposed collagen
12a hageman
11a
9a + 8a
10a + 5a
2a thrombin
1a + 13a
fibrin clot
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12
Q

Describe extrinsic pathway

A
tissue damage
7a + tissue factor thromboplastin 3
10a + 5a
2a thombin
1a + 13a
Fibrin clot
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13
Q

Vit K factors

A

7, 9, 10, 2

protein C + S

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14
Q

Thrombomodulin

A

+ 2a thrombin + Protein S
causes Protein C -> Active protein C
INHIBITs 5a + 8a

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15
Q

Antithrombin 3

A

Binds heparin
HMWH/ unfractionated: 2,9,10,11,12 (IV)
LMWH: 10a only (SC)

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16
Q

Tissue Factor Pathway inhibitor

A

Inhibts 7aTF

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17
Q

Fibrinolysis (tPa)

A

tPa
Plaminogen to Plasmin
Fibrin to Fibrinogen

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18
Q

Measuring intrinsic

19
Q

Measuring extrinsic

20
Q

Thrombin functions

A

Activates 11, 8, 5 and 13

+thrombomodulin & protein S -> activate Protein C

21
Q

Haemophilia A

A

Low Factor 8

A8

22
Q

Haemophilia B

A

Low Factor 9

B9

23
Q

Haemophilia inheritence

A
X linked (male only)
female carry
24
Q

Haemarthrosis

25
Christmas disease
Haemophilia B9
26
Haemophilia bloods
``` High APPT (intrinsic) normal PT (extrinsic) normal vWF Low 8 (A) or 9(B) ```
27
haemophilia A T
Replace A8 | Demopression increases 8
28
haemophilia B T
Replace B9
29
Variant CJD risk
Haemophilia
30
Chronic arthropathies
Haemophilia
31
``` High APPT (intrinsic) normal PT (extrinsic) normal vWF Low 8 (A) or 9(B) ```
Haemophilia
32
High APPT, normal PT low vWF Low 8
vW disease
33
No 1 bleeding disorder
vW disease
34
vW disease types
1-partial drop in vWF 2-abnormal vWF 3-NovWF
35
vW disease inheritence
``` Autosomal dominant (type 3-no vWF is AR) ```
36
vW disease T
Desmopression inreases vWF + 8 vW rich factor 8/ vWF concentrate TRANEXAMIC ACID
37
Thrombophilia primary causes
``` LOW Protein C Protein S Antithrombin 3 Factor 5 Leiden (active protein C cant break 5a down) ```
38
commonest heritable thrombophilia
Factor 5 Leiden (active protein C cant break 5a down)
39
Virchows triad
Venous stasis Hypercoagulation Vascular injury
40
Homan's sign
Pain dorsiflexion in calf DVT | risk of dislodgeing
41
VTE treatment
1. LMWH/ Fondaparinux for 5d+ AND INR >2.0 for 24hr 2, within 24hr start WARFARIN -Provoked 3month -Unprovoked 6months CANCER - LMWH 6months + compression stocking 2yrs Unprovoked = screen for cancer -exam, CXR, FBC, Ca2+, LFTs, urinalysis +/- >40yr CTCAP/ mammography Unprovoked = screen for thrombophilia + antiphospholipid if their on gna be on lifelong warfarin USS review in 1 week
42
Thrombophilia secondary cuases
Immobility, surgery, malignany, smoking, pregnancy ANTI-PHOSPHOLIPID SYNDROME Oestrogens (COCP)
43
Prophylaxis on flights
Aisle seat Ankle exercises Stockings
44
VTE investigations
Two level Wells score | 2+ = USS