Zusammenfassung
Aufgrund ihrer verwandten Pathophysiologie werden die tiefe Beinvenenthrombose sowie die Lungenarterienembolie unter dem Begriff „venöse Thrombembolien“ (VTE) zusammengefasst. Während die Inzidenz dieser Erkrankungen durch den demographischen Wandel sowie die verbesserte Diagnostik seit Jahren zunimmt, sinken Morbidität und Mortalität. Dies ist v. a. Folge sensitiverer Diagnostik, verbesserter Risikostratifizierung sowie effektiverer Strategien zur Antikoagulation, deren Ziel die Verhinderung früher Ereignisse bis hin zum Tod sowie die Prävention von Rezidiven darstellt. Die Antikoagulationstherapie sollte entweder zunächst mit Heparinen (unfraktioniert oder niedermolekular), Fondaparinux oder auch direkten oralen Antikoagulanzien begonnen werden. Patienten mit einem Rezidivereignis qualifizieren sich für eine dauerhafte Antikoagulation. Bei einem Erstereignis sollte die Antikoagulationstherapie für mindestens 3 Monate erfolgen (Erhaltungstherapie). Nachfolgend kann in Abhängigkeit vom individuellen Risiko (Rezidiv, Blutung) eine verlängerte Erhaltungstherapie im Sinne der Sekundärprävention sinnvoll sein. Hierzu sind mittlerweile auch Nicht-Vitamin-K-abhängige Antikoagulanzien (NOAK) zugelassen. Aufgrund des wahrscheinlich dauerhaft hohen Rezidivrisikos von bis zu 10 % pro Jahr nach Absetzen der Antikoagulation, unzureichender Scores zur Abschätzung des Blutungsrisikos sowie vielversprechender Sicherheitsprofile von NOAK in der Sekundärprävention ist zukünftig von einer Zunahme länger (>3–6 Monate) bis dauerhaft (>1 Jahr) antikoagulierter Patienten nach thromboembolischen Erkrankungen auszugehen.
Abstract
Deep vein thrombosis and pulmonary artery embolisms share pathophysiological features and are therefore collectively referred to as venous thromboembolisms (VTE). While the incidence of VTE has been increasing for years as a result of demographic changes and improved diagnostics, the morbidity and mortality are decreasing. This is particularly due to more sensitive diagnostics, improvements in risk stratification and more effective anticoagulation strategies. The aim of effective anticoagulation therapy is the avoidance of early events up to death and prevention of recurrent events. Anticoagulation treatment should be started with either heparins (unfractionated or low molecular weight), the pentasaccharide fondaparinux or direct oral anticoagulants. Patients with recurrent events qualify for indefinite anticoagulation treatment. For a first episode of VTE anticoagulation treatment for at least 3 months is recommended (maintenance therapy). Subsequently, prolonged maintenance therapy for secondary prevention can be meaningful, depending on the individual patient risk (provoked event, risk for recurrence or bleeding). The non-vitamin K antagonist oral anticoagulants (NOACs) have now also been approved for this indication. As a result of a probably permanently high risk for recurrent events of up to 10% per year after cessation of anticoagulation, insufficient scores for estimation of the risk of bleeding and recent data documenting the safety and efficacy of NOACs for secondary prevention, a shift towards prolonged anticoagulation of 3–6 months or even indefinite (>1 year) treatment can be anticipated for patients after thromboembolic diseases.
Literatur
Cohen AT, Agnelli G, Anderson FA et al (2007) Venous thromboembolism (VTE) in Europe. The number of VTE events and associated morbidity and mortality. Thromb Haemost 98:756–764
Konstantinides SV, Barco S, Lankeit M, Meyer G (2016) Management of pulmonary embolism: an update. J Am Coll Cardiol 67:976–990
Wells PS, Ginsberg JS, Anderson DR et al (1998) Use of a clinical model for safe management of patients with suspected pulmonary embolism. Ann Intern Med 129:997–1005
AWMF (2015) AWMF Leitlinien-Register Nr. 065/002. Diagnostik und Therapie der Venenthrombose und der Lungenembolie. http://www.awmf.org/leitlinien/detail/ll/065-002.html (Erstellt: 10. Okt. 2015). Zugegriffen: 20. Oktober 2017
The Task Force for the Diagnosis and Management of Acute Pulmonary Embolism of the European Society of Cardiology (ESC) (2014) 2014 ESC Guidelines on the diagnosis and management of acute pulmonary embolism. Eur Heart J 35:3033–3080
Research Committee of the British Thoracic Society (1992) Optimum duration of anticoagulation for deep-vein thrombosis and pulmonary embolism. Lancet 340:873–876
Schulman S, Kearon C, Kakkar AK et al (2009) Dabigatran versus warfarin in the treatment of acute venous thromboembolism. N Engl J Med 361:2342–2352
Bauersachs R, Berkowitz SD, Brenner B et al (2010) Oral rivaroxaban for symptomatic venous thromboembolism. N Engl J Med 363:2499–2510
Büller HR, Prins MH, Lensin AW et al (2012) Oral rivaroxaban for the treatment of symptomatic pulmonary embolism. N Engl J Med 366:1287–1297
Agnelli G, Büller HR, Cohen A et al (2013) Oral apixaban for the treatment of acute venous thromboembolism. N Engl J Med 369:799–808
Büller HR, Decousus H, Grosso MA et al (2013) Edoxaban versus warfarin for the treatment of symptomatic venous thromboembolism. N Engl J Med 369:1406–1415
Chan CM, Woods C, Shorr AF (2010) The validation and reproducibility of the pulmonary embolism severity index. J Thromb Haemost 8:1509–1514
Donzé J, Le Gal G, Fine MJ et al (2008) Prospective validation of the pulmonary embolism severity index. A clinical prognostic model for pulmonary embolism. Thromb Haemost 100:943–948
Vanni S, Nazerian P, Pepe G et al (2011) Comparison of two prognostic models for acute pulmonary embolism: clinical vs. right ventricular dysfunction-guided approach. J Thromb Haemost 9:1916–1923
Cossette B, Pelletier ME, Carrier N et al (2010) Evaluation of bleeding risk in patients exposed to therapeutic unfractionated or low-molecular-weight heparin: a cohort study in the context of a quality improvement initiative. Ann Pharmacother 44:994–1002
van Dongen CJ, van den Belt AG, Prins MH et al (2004) Fixed dose subcutaneous low molecular weight heparins vs. adjusted dose unfractionated heparin for venous thromboembolism. Cochrane Database Syst Rev. https://doi.org/10.1002/14651858.CD001100.pub2
Stein PD, Hull RD, Matta F et al (2009) Incidence of thrombocytopenia in hospitalized patients with venous thromboembolism. Am J Med 122:919–930
Middedorp S (2011) How I treat pregnancy-related venous thromboembolism. Blood 118:5394–5400
Fahrni J, Husmann M, Gretener S, Keo HH (2015) Assessing the risk of recurrent venous thromboembolism—a practical approach. Vasc Health Risk Manag 11:451–459
Agnelli G, Prandoni P, Becattini C et al (2003) Extended oral anticoagulant therapy after a first episode of pulmonary embolism. Ann Intern Med 139:19–25
Kearon C, Akl EA (2014) Duration of anticoagulant therapy for deep vein thrombosis and pulmonary embolism. Blood 123:1794–1801
Tosetto A, Iorio A, Marcucci M et al (2012) Predicting disease recurrence in patients with previous unprovoked venous thromboembolism: a proposed prediction score (DASH). J Thromb Haemost 10:1019–1025
Eichinger S, Heinze G, Jandeck LM et al (2010) Risk assessment of recurrence in patients with unprovoked deep vein thrombosis or pulmonary embolism: the Vienna prediction model. Circulation 121:1630–1636
Rodger MA, Kahn SR, Wells PS et al (2008) Identifying unprovoked thromboembolism patients at low risk for recurrence who can discontinue anticoagulant therapy. CMAJ 179:417–426
Kearon C, Spencer FA, O’Keeffe D et al (2015) D‑dimer testing to select patients with a first unprovoked venous thromboembolism who can stop anticoagulant therapy: a cohort study. Ann Intern Med 162:27–34
Klok FA, Niemann C, Dellas C et al (2016) Performance of five different bleeding-prediction scores in patients with acute pulmonary embolism. J Thromb Thrombolysis 41(2):312–320
Riva N, Bellesini M, Di Minno MN et al (2014) Poor predictive value of contemporary bleeding risk scores during long-term treatment of venous thromboembolism. A multicentre retrospective cohort study. Thromb Haemost 112:511–521
Kearon C, Gent M, Hirsh J et al (1999) A comparison of three months of anticoagulation with extended anticoagulation for a first episode of idiopathic venous thromboembolism. N Engl J Med 340:901–907
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
Becattini C, Agnelli G, Schenone A et al (2012) Aspirin for preventing the recurrence of venous thromboembolism. N Engl J Med 366(21):1959–1967
Brighton TA, Eikelboom JW, Mann K et al (2012) Low-dose aspirin for preventing recurrent venous thromboembolism. N Engl J Med 367:1979–1987
Schulman S, Kearon C, Kakkar AK et al (2013) Extended use of dabigatran, warfarin, or placebo in venous thromboembolism. N Engl J Med 368:709–718
Weitz JI, Lensing AWA, Prins MH et al (2017) Rivaroxaban or aspirin for extended treatment of venous thromboembolism. N Engl J Med 376:1211–1222
Agnelli G, Büller HR, Cohen A et al (2013) Apixaban for extended treatment of venous thromboembolism. N Engl J Med 368:699–708
Raskob G, Ageno W, Cohen AT et al (2016) Extended duration of anticoagulation with edoxaban in patients with venous thromboembolism: a post-hoc analysis of the Hokusai-VTE study. Lancet Haematol 3(5):e228–e236. https://doi.org/10.1016/S2352-3026(16)00023-5
Lee AY, Levine MN, Baker RI et al (2003) Low-molecular-weight heparin vs. a coumarin for the prevention of recurrent venous thromboembolism in patients with cancer. N Engl J Med 349:146–153
Lee AY, Kamphuisen PW, Meyer G et al (2015) Tinzaparin vs warfarin for treatment of acute venous thromboembolism in patients with active cancer: a randomized clinical trial. JAMA 314:677–686
Vedovati MC, Germini F, Agnelli G et al (2015) Direct oral anticoagulants in patients with VTE and cancer: a systematic review and meta-analysis. Chest 147:475–483
van Es N, Di Nisio M, Bleker SM et al (2015) Edoxaban for treatment of venous thromboembolism in patients with cancer. Rationale and design of the Hokusai VTE-cancer study. Thromb Haemost 114:1268–1276
Bates SM, Greer IA, Middeldorp S et al (2012) VTE, thrombophilia, antithrombotic therapy, and pregnancy: antithrombotic therapy and prevention of thrombosis, 9th ed: American College of Chest Physicians evidence-based clinical practice guidelines. Chest 141:e691S–e736S
Chan WS, Rey E, Kent NE et al (2014) Venous thromboembolism and antithrombotic therapy in pregnancy. J Obstet Gynaecol Can 36:527–553
Gibson PS, Powrie R (2009) Anticoagulants and pregnancy: when are they safe? Cleve Clin J Med 76:113–127
Kearon C (2012) A conceptual framework for two phases of anticoagulant treatment of venous thromboembolism. J Thromb Haemost 10(4):507–511
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P.W. Radke und M. Möckel haben Honorare für Vorträge und Beratungsleistungen von den Firmen Bayer Healthcare, Boehringer Ingelheim, Bristol-Myers Squibb und Daiichi-Sankyo erhalten.
Dieser Beitrag beinhaltet keine von den Autoren durchgeführten Studien an Menschen oder Tieren.
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Radke, P.W., Möckel, M. Strategien zur Antikoagulation bei Patienten mit tiefer Beinvenenthrombose und Lungenarterienembolie. Herz 43, 34–42 (2018). https://doi.org/10.1007/s00059-017-4655-1
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DOI: https://doi.org/10.1007/s00059-017-4655-1