Skip to main content
Log in

Therapie der Beinvenenthrombose

Wann welche Substanzen?

Antithrombotic treatment of deep vein thrombosis

  • Schwerpunkt: Was ist gesichert in der Therapie?
  • Published:
Der Internist Aims and scope Submit manuscript

Zusammenfassung

Bei der antithrombotischen Therapie der tiefen Venenthrombose (TVT) unterscheidet man eine initiale Phase mit sofort wirksamen Antithrombotika und eine anschließende längerfristige Sekundärprophylaxe. Für die Initialbehandlung hat sich die s.c.-Gabe von niedermolekularen Heparinen durchgesetzt, wobei die Kontraindikation der Niereninsuffizienz beachtet werden muss, die zur Kumulation führen könnte. Als neues, sofort wirksames Antithrombotikum steht in Kürze das synthetische Pentasaccharid Fondaparinux zur Verfügung. Die Sekundärprophylaxe der TVT mit Vitamin-K-Antagonisten ist hocheffektiv. Auch nach aktuellen Studien ist der dabei anzustrebende Zielbereich eine INR von 2,0–3,0. Die Dauer der oralen Antikoagulation richtet sich nach dem mutmaßlichen Rezidivrisiko. Wegen des engen therapeutischen Fensters der Vitamin-K-Antagonisten wird bei Patienten mit erhöhtem Blutungsrisiko zunehmend niedermolekulares Heparin zur Sekundärprophylaxe eingesetzt, meist in der halben therapeutischen Dosis. Derzeit werden zahlreiche neue Antithrombotika geprüft, die möglicherweise in absehbarer Zeit die Thrombosetherapie weiter vereinfachen und sicherer machen könnten.

Abstract

Current antithrombotic therapy of deep vein thrombosis (DVT) consists of an initial course of heparin, followed by the secondary prevention with oral anticoagulation (OAC). Low molecular weight heparin has several advantages over unfractionated heparin, however, renal insufficiency has to be observed to avoid accumulation. The synthetic pentasaccharide Fondaparinux is a factor Xa inhibitor, that will shortly be available for the initial treatment of DVT. Oral anticoagulation with vitamin K antagonists (VKA) is highly effective, the standard target INR is 2.0–3.0. For a first episode of DVT the duration of OAC usually is six months, but has to be adjusted according to the estimated risk for recurrence. Because of the narrow therapeutic window of VKA, low molecular weight heparins are increasingly being used for secondary prevention in patients with an increased risk for bleeding, mostly in 1/2-therapeutic dose. At present, several new antithrombotic agents are being studied and may become available shortly for DVT treatment.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Abb. 1
Abb. 2a, b

Literatur

  1. van Den Belt AG, Prins MH, Lensing AW, Castro AA, Clark OA, Atallah AN, Burihan E (2000) Fixed dose subcutaneous low molecular weight heparins versus adjusted dose unfractionated heparin for venous thromboembolism. Cochrane Database Syst Rev: CD001100

    Google Scholar 

  2. van Dongen CJ, Mac Gillavry MR, Prins MH (2003) Once versus twice daily LMWH for the initial treatment of venous thromboembolism. Cochrane Database Syst Rev: CD003074

    Google Scholar 

  3. Bauersachs RM, Lindhoff-Last E, Wolff U, Ehrly AM (1998) Aktuelles Management der tiefen Venenthrombose. Med Welt 49: 194–215

    Google Scholar 

  4. Pettila V, Leinonen P, Markkola A, Hiilesmaa V, Kaaja R (2002) Postpartum bone mineral density in women treated for thromboprophylaxis with unfractionated heparin or LMW heparin. Thromb Haemost 87: 182–186

    CAS  PubMed  Google Scholar 

  5. Greinacher A (2003) Heparininduzierte Thrombozytopenie. Dtsch Ärztebl 100: A-2220–2229

  6. Montalescot G, Philippe F, Ankri A et al. (1998) Early increase of von Willebrand factor predicts adverse outcome in unstable coronary artery disease: beneficial effects of enoxaparin. French Investigators of the ESSENCE Trial. Circulation 98: 294–299

    CAS  PubMed  Google Scholar 

  7. Hirsch D, Lee T, Morrison R, Carlson, Goldhaber S (1996) Shortened hospitalization by means of adjusted-dose subcutaneous heparin for deep venous thrombosis. Am Heart J 131: 276–278

    Article  CAS  PubMed  Google Scholar 

  8. Büller HR, Davidson BL, Decousus H et al. (2004) Fondaparinux or enoxaparin for the initial treatment of symptomatic deep venous thrombosis: a randomized trial. Ann Intern Med 140: 867–873

    PubMed  Google Scholar 

  9. Büller HR, Davidson BL, Decousus H et al. (2003) Subcutaneous fondaparinux versus intravenous unfractionated heparin in the initial treatment of pulmonary embolism. N Engl J Med 349: 1695–1702

    Article  CAS  PubMed  Google Scholar 

  10. Magnani H (1993) Heparin-induced thrombocytopenia (HIT): an overview of 230 patients treated with orgaran (Org 10172). Thromb Haemost 70: 554–556

    CAS  PubMed  Google Scholar 

  11. Schulman S, Rhedin AS, Lindmarker P et al. for the Duration of Anticoagulation Trial Study Group (1995) Comparison of six weeks with six months of oral anticoagulant therapy after a first episode of venous thromboembolism. N Engl J Med 332: 1661–1665

    Article  CAS  PubMed  Google Scholar 

  12. Bauersachs RM (2003) Was ist gesichert in der Therapie? Therapie und Sekundärprophylaxe der venösen Thromboembolie mit Vitamin-K-Antagonisten. Internist (Berl) 44: 1491–1499

    Google Scholar 

  13. Landefeld CS, Beyth RJ (1993) Anticoagulant-related bleeding: clinical epidemiology, prediction, and prevention. Am J Med 95: 315–328

    Article  CAS  PubMed  Google Scholar 

  14. Agnelli G (2004) Long-term low-dose warfarin use is effective in the prevention of recurrent venous thromboembolism: no. J Thromb Haemost 2: 1038–1040

    CAS  PubMed  Google Scholar 

  15. Palareti G, Leali N, Coccheri S et al. (1996) Bleeding complications of oral anticoagulant treatment: an inception-cohort, prospective collaborative study (ISCOAT). Italian Study on Complications of Oral Anticoagulant Therapy. Lancet 348: 423–428

    Article  CAS  PubMed  Google Scholar 

  16. Kearon C, Ginsberg JS, Kovacs MJ et al. (2003) Comparison of low-intensity warfarin therapy with conventional-intensity warfarin therapy for long-term prevention of recurrent venous thromboembolism. N Engl J Med 349: 631–639

    Article  CAS  PubMed  Google Scholar 

  17. Ridker P et al. for the PREVENT Investigators (2003) Long-term, low-intensity warfarin therapy for the prevention of recurrent venous thromboembolism. N Engl J Med 348: 1425–1434

    Article  CAS  PubMed  Google Scholar 

  18. Kearon C, Ginsberg JS, Kovacs M et al. (2003) Influence of thrombophilia on efficacy of warfarin for prevention of recurrent venous thromboembolism: results from a randomized trial. J Thromb Haemost 1 [Suppl]: OC002

  19. Crowther MA, Ginsberg JS, Julian J et al. (2003) A comparison of two intensities of warfarin for the prevention of recurrent thrombosis in patients with the antiphospholipid antibody syndrome. N Engl J Med 349: 1133–1138

    Article  CAS  PubMed  Google Scholar 

  20. Vink R, Kraaijenhagen RA, Levi M, Buller HR (2003) Individualized duration of oral anticoagulant therapy for deep vein thrombosis based on a decision model. J Thromb Haemost 1: 2523–2530

    CAS  PubMed  Google Scholar 

  21. Lindhoff-Last E, Sohn C, Ehrly AM, Bauersachs RM (2000) Aktuelles Management der Thromboembolie in Schwangerschaft und Wochenbett. Zentralbl Gynäkol 122: 4–16

  22. Arcelus JI, Caprini JA, Monreal M, Suarez C, Gonzalez-Fajardo J (2003) The management and outcome of acute venous thromboembolism: a prospective registry including 4011 patients. J Vasc Surg 38: 916–922

    Article  PubMed  Google Scholar 

  23. van der Heijden JF, Hutten BA, Buller HR, Prins MH (2002) Vitamin K antagonists or low-molecular-weight heparin for the long term treatment of symptomatic venous thromboembolism. Cochrane Database Syst Rev: CD002001

    Google Scholar 

  24. Pineo GF, Hull RD (2003) Tinzaparin in the treatment of venous thromboembolism. Expert Opin Pharmacother 4: 2355–2362

    Article  CAS  PubMed  Google Scholar 

  25. Meyer G, Marjanovic Z, Valcke J et al. (2002) Comparison of low-molecular-weight heparin and warfarin for the secondary prevention of venous thromboembolism in patients with cancer: a randomized controlled study. Arch Intern Med 162: 1729–1735

    Article  CAS  PubMed  Google Scholar 

  26. Lee AY, Levine MN, Baker RI et al. (2003) Low-molecular-weight heparin versus a coumarin for the prevention of recurrent venous thromboembolism in patients with cancer. N Engl J Med 349: 146–153

    Article  CAS  PubMed  Google Scholar 

  27. Ginsberg JS, Bates SM (2003) Management of venous thromboembolism during pregnancy. J Thromb Haemost 1: 1435–1442

    Article  CAS  PubMed  Google Scholar 

  28. Sanson BJ, Lensing AWA, Prins MH et al. (1999) Safety of low-molecular-weight heparin in pregnancy: A systematic review. Thromb Haemost 81: 668–672

    CAS  PubMed  Google Scholar 

  29. Hach-Wunderle V, Bauersachs R, Landgraf H, Schellong S, Schweizer J, Wuppermann T (2002) Leitlinien der Deutschen Gesellschaft für Angiologie: Venöse Thromboembolie. VASA S60: 1–19

    Google Scholar 

  30. Brill-Edwards P, Ginsberg JS, Gent M, Hirsh J, Burrows R, Kearon C, Geerts W, Kovacs M, Weitz JI, Robinson KS, Whittom R, Couture G (2000) Safety of withholding heparin in pregnant women with a history of venous thromboembolism. N Engl J Med 343: 1439–1444

    Article  CAS  PubMed  Google Scholar 

  31. Greer IA (2004) Prevention of venous thromboembolism in pregnancy. Eur J Med Res 9: 135–145

    CAS  PubMed  Google Scholar 

  32. Bauersachs RM, für die EThIG Trialist Group (2004) EThIG Studie: Risikoschwangere erfolgreich antikoagulieren. Vascular Care 6: 28–41

    Google Scholar 

  33. Eriksson H, Wahlander K, Gustafsson D, Welin LT, Frison L, Schulman S (2003) A randomized, controlled, dose-guiding study of the oral direct thrombin inhibitor ximelagatran compared with standard therapy for the treatment of acute deep vein thrombosis: THRIVE I. J Thromb Haemost 1: 41–47

    Article  CAS  PubMed  Google Scholar 

  34. Huisman MV, on behalf of The THRIVE II&V Investigators (2003) Efficacy and safety of the oral direct thrombin inhibitor ximelagatran compared with current standard therapy for acute symptomatic deep vein thrombosis, with or without pulmonary embolism: a randomized, double-blind, multinational study. J Thromb Haemost 1 [Suppl 1]: OC003

  35. Schulman S, Wahlander K, Lundstrom T, Clason SB, Eriksson H (2003) Secondary prevention of venous thromboembolism with the oral direct thrombin inhibitor ximelagatran. N Engl J Med 349: 1713–1721

    Article  CAS  PubMed  Google Scholar 

  36. The Persist Investigators (2004) A novel long-acting synthetic factor Xa inhibitor (SanOrg34006) to replace warfarin for secondary prevention in deep vein thrombosis. A Phase II evaluation. J Thromb Haemost 2: 47–53

    PubMed  Google Scholar 

  37. Kearon C, Hirsh J (1997) Management of anticoagulation before and after elective surgery. N Engl J Med 336: 1506–1511

    Article  CAS  PubMed  Google Scholar 

  38. Ridker PM (2004) Long-term low-dose warfarin use is effective in the prevention of recurrent venous thromboembolism: yes. J Thromb Haemost 2: 1034–1037

    CAS  PubMed  Google Scholar 

Download references

Interessenkonflikt:

Keine Angaben

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to R. M. Bauersachs.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Bauersachs, R.M. Therapie der Beinvenenthrombose. Internist 45, 1345–1355 (2004). https://doi.org/10.1007/s00108-004-1302-8

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00108-004-1302-8

Schlüsselwörter

Keywords

Navigation