How to approach a patient with venous thrombosis? · How to approach a patient with venous...
Transcript of How to approach a patient with venous thrombosis? · How to approach a patient with venous...
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How to approach a patient
with venous thrombosis?
ISTH advanced course in thrombosis & hemostasis, March 2014
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Vein thrombosis: sites
- thrombosis may
occur in any vein.
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VT treatment goals: to ...
- prevent thrombus growth
- re-establish vein patency
- reduce immediate complications(embolisms, pain, inflammation)
- reduce long-term complications(post-thrombotic syndrome)
- prevent recurrent events
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VT treatment: phases
Acute treatment
Follow-up phase
Long-term treatment/prophylaxis
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Acute VT treatment: options
VTestablished
thrombectomy/thrombolysis
pain controlcompression
anticoagulanttreatment
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DVT: anticoagulant treatment
- prevents thrombus growth
- improves thrombus resolution
- reduces immediate complications
clear evidence from RCTs
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Initial anticoagulant management
DVT
UFH*/Argatroban
increased risk of bleeding?
yes
LMWH/fondaparinux/Apixaban/Rivaroxaban
no
* APTT-adjusted
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Predictors of bleeding- previous major surgery (< 7 days)
- previous stroke (< 6 weeks)
- bleeding history
- anti-platelet agents
- severe liver disease (INR > 1.8)
- platelet count < 50.000/µl
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Renal vein thrombosis (RVT)
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Renal vein thrombosis (RVT)
- relatively uncommon
- predominantly a disease of children
- in newborns the 3rd most prevalent cause of TE
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Renal vein thrombosis (RVT)RVT
bilateral and
renal impairment
t-PA fibrinolysis1-2 mg/kg b.w./24h
anticoagulanttherapy (UFH/LMWH)
yes no
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Renal vein thrombosis (RVT)RVT
bilateral and
renal impairment
t-PA fibrinolysis1-2 mg/kg b.w./24h
for max. 3 days
anticoagulanttherapy (UFH/LMWH)
yes no
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Renal vein thrombosis (RVT)unilateral RVT
renal impairment
full dose(LMWH/UFH)
prophylactic dose(LMWH/UFH)
yes no
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Renal vein thrombosis (RVT)
- relatively uncommon
- predominantly a disease of children
- in newborns the 3rd most prevalent cause of TE
- low risk of recurrence
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Renal vein thrombosis (RVT)RVT
anticogulanttreatment
terminated after 3 months
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Portal vein thrombosis
Risks:portal hypertensionspleen infarctionbowel infarctionliver failure
may be asymptomatic
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Portal vein thrombosis (PVT)PVT
acute?
full-dose LMWH/UFH
prophylacticLMWH/UFH*
yes no
* depending on thrombus resolution
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Portal vein thrombosis
Risks:portal hypertensionspleen infarctionbowel infarctionliver failure
may be asymptomatic
risk of recurrence:5% per year w/o anti-coagulation
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Upper extremity DVT (UEDVT)
incidence:≈ 5 – 10% of VT
symptoms:arm swelling, pain,discolloration
complications:PE (≈ 5%)PST of the arm
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UEDVT: specific risk factors
- central venous catheter(≈ 75% of UEDVT)
- insertion of a pace maker
- thoracic outlet syndrome (TOS)
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UEDVT: treatment approach
UEDVT with CVT
remove CVT
CVT, central venous catheter
LMWH/fondaparinux/UFHfor 3 months
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UEDVT: treatment approach
unprovoked UEDVT
TOS screening
TOS, thoracic outlet syndrome
anticoagulationfor at least 3 months
anticoagulationuntil surgery
positivenegative
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Vein thrombosis: sites
- Deep vein thrombosis (DVT)
- Renal vein thrombosis
- Splanchnic vein thrombosis(mesenteric/portal)
- upper extremity DVT (UEDVT)(Paget-von-Schroetter disease)
- Retinal vein thrombosis
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Retinal vein thrombosis
associated withhypertension?
* no RCT available
anti-hypertensivetreatment
anticoagulation atprophylactic dose
for 2-6 weeks*
noyes
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VT treatment: phases
Acute treatment
Follow-up phase
Long-term treatment/prophylaxis
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Cancer and thrombosis
* Boccaccio C et al., Nature 2005; 434: 396 - 400
Trousseau-mouse*
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Cancer screening
- Occult cancer is a thrombophilic risk factor.
This justifies a cancer screening in patients presenting with a spontaneous thrombosis
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Cancer and thrombosis
Timp JF et al. Blood 2013, 122: 1712 - 1723
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VT treatment: phases
Acute treatment
Follow-up phase
Long-term treatment/prophylaxis
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VT: recurrence
- The risk of recurrence is high in patients
fulfilling the clinical criteria of thrombo-
philia (approx. 30% over 10 years).
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Thrombophilia: clin. criteria
- unprovoked event
- first thrombotic event at young age
- thrombosis at uncommon site
- familial history
- recurrent events
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Thrombophilia likely
- Should the patient referred to extendedanticoagulant treatment w/o furtherscreening?
- Do we need a thrombophilia screen?If yes, which parameters should beincluded?
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Christiansen SC et al. JAMA 2005; 293: 2352 - 2361
Incidence of recurrent thrombosis
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Thrombophilia work-up (I)
- Lupus anticoagulant/APA
- Jak-2-polymorphism (splanchnic VT)
- PNH-testing
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Clinical decision finding
LA/APA positivePNH positive
extension of anticoagulanttreatment
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Thrombophilia work-up (II)
- APC-resistance/FV-Leiden
- Antithrombin
- Protein-C-/-S-deficiency
- Prothrombin-G20210A-mutation
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Clinical decision finding (II)
first unprovoked DVT
strong thrombophilicrisk factor (AT-deficiency)
argues pro indefinite oral anticoagulant treatment
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Long-term management
oral anticoagulant treatment> 1 year
re-evaluation ofthe risk-benefit ratio
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- Thrombosis may occur at any vein.
- Anticoagulant treatment is the treatment ofchoice for nearly all types of venous thrombosis.
- The risk of reccurrence depends on the loca-lisation of thrombosis.
- In patients receiving extended oral anti-coagulant treatment the risk-benefit ratioshould be regularly re-evaluated.
Conclusion