Title: Venous thromboembolism Treatment and secondary prevention
1Venous thromboembolism Treatment and secondary
prevention
DVT
PE
Deep vein insufficiency
Post-thrombotic syndrome
Pulmonary hypertension
Death
Ulcus cruris
Chronic PE
2Deep vein thrombosis
Common femoral vein
Thrombus
Proximal
Knee
Distal
3Treatment and secondary prevention of VTE
VTE event
Acute
Continue
Heparin or LMWH together with a VKA (e.g.
warfarin) until an INR of 2.0-3.0 is achieved
VKA (e.g. warfarin)INR 2.0-3.0
4VTE - treatment options
Acute
Long-term
- Anticoagulation
- - UFH/LMWH
- Thrombolysis
- Thrombectomy
- Inferior vena cava filters (IVCF)
- Anticoagulation- VKAs (e.g. warfarin)- LMWH
- Stockings
57th ACCP recommendations- Initial treatment for
acute DVT or PE
- Confirmed DVT or non-massive PE
- Initial treatment with sc LMWH or iv UFH (or sc
if DVT) Grade 1A for at least 5 days Grade
1C - Start VKA with LMWH or UFH on day 1 Grade 1A
- Stop LMWH or UFH when INR stable gt2.0 Grade 1A
- High clinical suspicion of VTE
- Anticoagulation until outcome of diagnostic
tests Grade 1C
Büller H et al. Chest 2004126401S428S
6Treatment and secondary prevention of VTE
VTE event
Decision point
How long?
Acute
Continue
Heparin or LMWH together with a VKA (e.g.
warfarin) untill an INR of 2.0-3.0 is achieved
VKA (e.g. warfarin)INR 2.0-3.0
3-6-12 months or lifelong
Risk of VTE (5-7/year) vs. Risk of bleeding
(3-4/year)
77th ACCP recommendations- Long-term treatment
for DVT or PE
- First episode with a transient risk factor
- 3 months after distal or proximal DVT Grade 1A
- At least 3 months after PE Grade 1A
- First episode of idiopathic DVT/PE
- VKA for at least 612 months Grade 1A but
consider indefinite duration Grade 2A - Two or more episodes of DVT/PE
- Suggest indefinite treatment Grade 2A
- Target INR 2.5 (range 2.03.0) Grade 1A
Büller H et al. Chest 2004126401S428S
8Long-term treatment of DVT
- Recurrence rate of VTE in patients with DVT
dependent on Underlying risk factors for DVT
Duration of treatment - Decision regarding duration of treatmentdependent
on Underlying risk factors for DVT Risk of
haemorrhage from oral anticoagulation Patient
preference - Numerous regimens studied to improve benefit of
long-term treatment while reducing the dose
9Recurrence of VTE after stopping oral
anticoagulation
3 months treatment
Event rate ()
15
10
5
0
0
3
6
12
24
Months
10Recurrence of VTE after stopping oral
anticoagulation
3 months treatment
Event rate()
6 months treatment
15
10
5
0
0
3
6
12
24
Months
11Recurrence of VTE after stopping oral
anticoagulation
3 months treatment
Event rate()
6 months treatment
1 year treatment
15
10
5
0
0
3
6
12
24
Months
12Optimal duration of anticoagulation after VTE
LongOAC
ShortOAC
Reference
No. ofpatients
Followup
Recurrent VTE
Major bleeding
months
months
months
LongOAC
ShortOAC
LongOAC
ShortOAC
DURAC I 897 6 1.5 24 9.5 18.1 1.1 0.2 LAFIT 16
2 27 3 10 1.3 27.4 3.8 0.0 WODIT-DVT 267 12 3
12 3.0 8.3 3.0 0.8 WODIT-PE 326 6-12 3 32.7 4.
1 9.1 1.8 0.0 DOTAVK 539 6 3 15 8.7 8.1 2.6
1.9 DURAC II 227 Indefinite 6 43 2.6 20.7 8.6
2.7
OAC, oral anticoagulation
13Intensity of anticoagulant therapy
Recurrent VTE Cumulative event rate ()
0.25
Placebo - PREVENT
0.20
0.15
Low INR PREVENT
0.10
Low INR ELATE
0.05
Conventional INR - ELATE
0.00
0
1
2
3
4
Years of follow-up
Ridker PM et al. N Engl J Med 2003
3481425-34 Kearon C et al. N Engl J Med
2003349631-9