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DOI: 10.1055/s-0038-1655325
Therapie der akuten tiefen Beinvenenthrombose mit niedermolekularen Heparinen
Publication History
Publication Date:
27 June 2018 (online)
Zusammenfassung
Die akute tiefe Beinvenenthrombose ist eine häufige Erkrankung. Die klassische Behandlung besteht aus einer initialen Phase mit Heparin sowie einer Langzeittherapie mit oralen Antikoagulanzien. Die Therapie mit Heparin muß rasch begonnen werden, innerhalb von 24 Stunden im therapeutischen Bereich liegen und über 5 bis 7 Tage weitergeführt werden, bis die orale Antikoagulation ihrerseits im therapeutischen Bereich liegt. Zahlreiche Studien zeigten, daß die Therapie mit subkutan applizierten niedermolekularen Heparinen mindestens so wirksam und sicher ist wie die herkömmliche parenterale und labormäßig kontrollierte Gabe von unfraktioniertem Heparin. Die niedermolekularen Heparine haben jedoch den Vorteil der einfacheren Anwendung und der geringeren Rate von immunologisch-bedingter Thrombozytopenie. Sie stellen heute die Therapie der ersten Wahl dar bei der initialen Behandlung der akuten tiefen Beinvenenthrombose. Sie bieten außerdem die Möglichkeit der ambulanten bzw. der verkürzten stationären Therapie.
Eine Thrombolyse sollte nur in Ausnahmefällen durchgeführt werden, da sie mit einem höheren Blutungsrisiko verbunden ist und bezüglich klinisch relevanter Endpunkte der Therapie mit Heparinen nicht überlegen ist.
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LITERATUR
- 1 Anonymous. A randomised trial of subcutaneous low molecular weight heparin (CY 216) compared with intravenous unfractionated heparin in the treatment of deep vein thrombosis. A collaborative European multicentre study. Thromb Haemost 1991; 65: 251-6.
- 2 Basu D, Gallus A, Hirsh J, Cade J. A prospective study of the value of monitoring heparin treatment with the activated partial thromboplastin time. N Engl J Med 1972; 287: 325-7.
- 3 Brandjes DPM, Btiller HR, Heijboer H. et al. Randomised trial of effect of compression stockings in patients with symptomatic proximal-vein thrombosis. Lancet 1997; 349: 759-62.
- 4 Brandjes DPM, Heijboer H, Biiller HR, de Rijk M, Jagt H, ten Cate JW. Acenocoumarol and heparin compared with acenocoumarol alone in the initial treatment of proximalvein thrombosis. N Eng J Med 1992; 327: 1485-9.
- 5 Bratt G, Aberg W, Johansson M, Törnebohm E, Granqvist S, Lockner D. Two daily subcutaneous injections of Fragmin as compared with intravenous standard heparin in the treatment of deep venous thrombosis (DVT). Thromb Haemost 1990; 64: 506-10.
- 6 Brownell Wheeler H, Anderson FAJ. Diagnostic methods for deep vein thrombosis. Haemostasis 1995; 25: 6-26.
- 7 Dolovich L, Ginsberg JS. Low molecular weight heparins in the treatment of venous thromboembolism. Vessels 1997; 03: 4-11.
- 8 Elliot MS, Immelman EJ, Jeffery P. et al. A comparative randomized trial of heparin versus streptokinase in the treatment of acute proximal venous thrombosis: an interim report of a prospective trial. Br J Surg 1979; 66: 838-43.
- 9 Fiessinger JN, Lopez-Fernandez M, Gatterer E. et al. Once-daily subcutaneous dalte-parin, a low molecular weight heparin, for the treatment of acute deep vein thrombosis. Thromb Haemost 1996; 76: 195-9.
- 10 Gallus A, Jackaman J, Tillet J. et al. Safety and efficacy of warfarin started early after submassive venous thrombosis or pulmonary embolism. Lancet 1986; 02: 1293-6.
- 11 Ginsberg JS. Management of venous thromboembolism. N Engl J Med 1996; 335: 1816-28.
- 12 Goldhaber SZ, Meyerovitz MF, Green D. et al. Randomized controlled trial of tissue plasminogen activator in proximal deep venous thrombosis. Am J Med 1990; 88: 235-40.
- 13 Hansson P-O, Welin L, Tibblin G, Eriksson H. Deep vein thrombosis and pulmonary embolism in the general population. Arch Intern Med 1997; 157: 1665-70.
- 14 Hirsh J. Heparin. N Engl J Med 1991; 324: 1565-74.
- 15 Hirsh J, Levine MN. Low molecular weight heparin. Blood 1992; 79: 1-17.
- 16 Hommes DW, Bura A, Mazzolai L, Büller HR, ten Cate JW. Subcutaneous heparin compared with continuous intravenous heparin administration in the initial ttreatment of deep vein thrombosis. A meta-analysis. Ann Int Med 1992; 116: 279-84.
- 17 Hull RD, Raskob GE, Hirsh J. et al. Continuous intravenous heparin compared with intermittent subcutaneous heparin in the initial treatment of proximal vein thrombosis. N Eng J Med 1986; 315: 1109-14.
- 18 Hull RD, Raskob GE, Pineo GF. et al. Subcutaneous low-molecular-weight heparin compared with continuous intravenous heparin in the treatment of proximal-vein thrombosis. N Engl J Med 1992; 326: 975-82.
- 19 Hull RD, Raskob GE, Rosenbloom D. et al. Heparin for 5 days compared with 10 days in the initial treatment of proximal-vein thrombosis. N Eng J Med 1990; 322: 1260-6.
- 20 The Columbus Investigators. Low-molecular-weight heparin in the treatment of patients with venous thromboembolism. N Engl J Med 1997; 337: 657-62.
- 21 Kakkar VV, Flanc C, Howe CT, O’Shea M, Flute PT. Treatment of deep vein thrombosis. A trial of heparin, streptokinase, and Alvin. Br Med J 1969; 01: 806-10.
- 22 Kakkar VV, Lawrence D. Hemodynamic and clinical assessment after therapy for acute deep vein thrombosis. Am J Surg 1985; 150: 54-63.
- 23 Koopman MM, Prandoni P, Piovella F. et al. Treatment of venous thrombosis with intravenous unfractionated heparin administered in the hospital as compared with subcutaneous low-molecular-weight heparin administered at home. The Tasman Study group. N Engl J Med 1996; 334: 682-7.
- 24 Koopman MMW, Kraaijenhagen RA, Büller HR. The feasibility of low molecular weight heparin treatment of venous thromboembolism at home. Vessels 1997; 03: 12-7.
- 25 Leizorovicz A, Simonneau G, Décousus H, Boissel JP. Comparison of efficacy and safety of low molecular weight heparins and unfractionated heparin in initial treatment of deep venous thrombosis: a meta-analysis. BMJ 1994; 309: 299-304.
- 26 Lensing AW, Prins MH, Davidson BL, Hirsh J. Treatment of deep venous thrombosis with low-molecular-weight heparins. A meta-analysis. Arch Intern Med 1995; 155: 601-7.
- 27 Lensing AWA, Hirsh J. Rationale and results of thrombolytic therapy for deep vein thrombosis. In: Vascular Diagnosis. Bernstein EF. (eds) St. Louis; Mosby-Year Book: 1993: 875-9.
- 28 Lensing AWA, Hirsh J, Biiller HR. Diagnosis of venous thrombosis. In: Hemostasis and Thrombosis, basic principles and clinical practice. Colman RW, Hirsh J, Marder VJ, Salzman EW. (eds) 3rd. edition. Philadelphia: JP Lippincott; 1994: 1297-321.
- 29 Levine M, Gent M, Hirsh J. et al. A comparison of low-molecular-weight heparin administered primarily at home with unfractionated heparin administered in the hospital for proximal deep-vein thrombosis. N Engl J Med 1996; 334: 677-81.
- 30 Lindmarker P, Holmstrom M, Granqvist S, Johnsson H, Lockner D. Comparison of once-daily subcutaneous Fragmin with continuous intravenous unfractionated heparin in the treatment of deep vein thrombosis. Thromb Haemost 1994; 72: 186-90.
- 31 Luomanmaki K, Granqvist S, Hallert C. et al. A multicentre comparison of once-daily subcutaneous dalteparin (low molecular weight heparin) and continuous intravenous heparin in the treatment of deep vein thrombosis. J Int Med 1996; 240: 85-92.
- 32 Porter JM, Seaman AJ, Common HH, Rosch J, Eidemiller LR, Calhoun AD. Comparison of heparin and streptokinase in the treatment of venous thrombosis. Am Surg 1975; 41: 511-9.
- 33 Prandoni P, Lensing AW, Biiller HR. et al. Comparison of subcutaneous low-molecular-weight heparin with intraveneous standard heparin in proximal-vein thrombosis. Lancet 1992; 339: 441-5.
- 34 Prandoni P, Vigo M, Cattelan AM. et al. Treatment of deep vein thrombosis by fixed doses of a low-molecular-weight heparin (CY216). Haemostasis 1990; 20 (suppl) 220-3.
- 35 Robertson BR, Nilsson IM, Nylander G. Value of streptokinase and heparin in treatment of acute deep venous thrombosis. Acta Chir Scand 1968; 134: 203-8.
- 36 Robertson BR, Nilsson IM, Nylander G. Thrombolytic effect of streptokinase as evaluated by phlebography of deep venous thrombi of the leg. Acta Chir Scand 1970; 136: 173-80.
- 37 Schulman S, Granqvist S, Juhlin-Dannfelt A, Lockner D. Longterm sequelae of calf vein thrombosis treated with heparin or low-dose streptokinase. Acta Med Scand 1986; 219: 349-57.
- 38 Simonneau G, Charbonnier B, Décousus H. et al. Subcutaneous low-molecular-weight heparin compared with continuous intravenous unfractionated heparin in the treatment of proximal deep vein thrombosis. Arch Intern Med 1993; 153: 1541-6.
- 39 Siragusa S, Cosmi B, Piovella F, Hirsh J, Ginsberg JS. Low-molecular-weight heparins and unfractionated heparin in the treatment of patients with acute venous thromboembolism: results of a meta-analysis. Am J Med 1996; 100: 269-77.
- 40 Cate JW, Koopman MMW, Prins MH, Biiller HR. Treatment of venous thromboembolism. Thromb Haemost 1995; 74: 197-203.
- 41 Tsapogas MJ, Peabody RA, Wu KT, Karmody AM, Devaraj KT, Eckert C. Controlled study of thrombolytic therapy in deep vein thrombosis. Surgery 1973; 74: 973-84.
- 42 Turpie AGG, Levine MN, Hirsh J. et al. Tissue plasminogen activator (rt-PA) vs heparin in deep vein thrombosis. Chest 1990; 97: S172-5.
- 43 Warkentin TE, Levine MN, Hirsh J. et al. Heparin-induced thrombocytopenia in patients treated with low-molecular-weight heparin or unfractionated heparin. N Engl J Med 1995; 332: 1330-5.
- 44 Weitz JI. Low-molecular-weight heparins. N Engl J Med 1997; 337: 688-97.
- 45 Wells PS, Hirsh J, Anderson DR. et al. Accuracy of clinical assessment of deep-vein thrombosis. Lancet 1995; 345: 1326-30.
- 46 Young E, Prins MH, Levine MN, Hirsh J. Heparin binding to plasma proteins. An important mechanism for heparin resistance. Thromb Haemost 1992; 67: 639-43.