Anticoagulation with the low-molecular-weight heparin dalteparin (Fragmin®) in atrial fibrillation and TEE-guided cardioversion

被引:9
作者
Bechtold, H
Gunzenhauser, D
Sawitzki, H
Fung, S
Janssen, D
机构
[1] Reg Hosp Crailsheim, Dept Internal Med, D-74564 Crailsheim, Germany
[2] Heart Ctr Lake Constance, CH-8280 Kreuzlingen, Switzerland
[3] Pharmacia GmbH, D-91056 Erlangen, Germany
[4] Med I Scene Concept GmbH, D-91085 Weisendorf, Germany
来源
ZEITSCHRIFT FUR KARDIOLOGIE | 2003年 / 92卷 / 07期
关键词
anticoagulation; dalteparin; atrial fibrillation; cardioversion; echo cardiography;
D O I
10.1007/s00392-003-0939-y
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Cardioversion (CV) in atrial fibrillation can cause arterial embolism. Effective anticoagulation clearly reduces the risk. In practice, in every third case anticoagulation is not in line with the recommendations. Simplification can be achieved, and time gained, by transesophageal echocardiography (TEE) due to the shorter anticoagulation period prior to CV, and by use of low-molecular-weight heparin (LMWH) for anticoagulation. As yet little data is available on LMWH in cardioversion. The aim of this cohort study was to investigate the administration of a LMWH in this indication under everyday clinical conditions. Methods 125 patients treated as inpatients for atrial fibrillation or -flutter received the LMWH Fragmin(R) (dalteparin 2 x 100 anti-Xa units/kg, maximum doasage 2 x 10 000 anti-Xa units subcutaneously). In the presence of a relevant indication, TEE-guided CV was performed. The application of dalteparin was terminated as soon as effective anticoagulation had been achieved from phenprocoumon or once anticoagulation was no longer indicated. Results 125 patients with atrial fibrillation or -flutter received dalteparin for a median of 11 days (range of 3-41 days). TEE was performed in 39 patients. Five patients revealed a thrombus in the left atrial appendage in the TEE, and one patient died from suspected cerebral embolism over the further course. In the remaining 124 patients, no thromboembolic event was established. Successfully cardioverted were 26 of 34 patients (76%) who had no thrombus in the TEE. Serious adverse effects did not ensue. Conclusion Simple, well-tolerated and effective anticoagulation is possible with dalteparin in TEE-guided CV. Due to the methodic limitations of a cohort study and the low incidence of emboli, the efficacy of dalteparin in this indication needs to be further confirmed by prospective and randomized studies.
引用
收藏
页码:532 / 539
页数:8
相关论文
共 28 条
[1]   Antithrombotic therapy in atrial fibrillation [J].
Albers, GW ;
Dalen, JE ;
Laupacis, A ;
Manning, WJ ;
Petersen, P ;
Singer, DE .
CHEST, 2001, 119 (01) :194S-206S
[2]  
Antonielli E, 1997, G Ital Cardiol, V27, P803
[3]   Timing of thromboembolic events after electrical cardioversion of atrial fibrillation or flutter: A retrospective analysis [J].
Berger, M ;
Schweitzer, P .
AMERICAN JOURNAL OF CARDIOLOGY, 1998, 82 (12) :1545-+
[4]   Cardioversion of atrial fibrillation in the elderly [J].
Carlsson, J ;
Tebbe, U ;
Rox, J ;
Harmjanz, D ;
Haerten, K ;
Neuhaus, KL ;
Seidel, F ;
Niederer, W ;
Miketic, S .
AMERICAN JOURNAL OF CARDIOLOGY, 1996, 78 (12) :1380-1384
[5]  
El Gendi H, 2002, Minerva Cardioangiol, V50, P43
[6]   Long-term anticoagulation of outpatients with adverse events to oral anticoagulants using low-molecular-weight heparin [J].
Harenberg, J ;
Huhle, G ;
Piazolo, L ;
Giese, C ;
Heene, DL .
SEMINARS IN THROMBOSIS AND HEMOSTASIS, 1997, 23 (02) :167-172
[7]   Oral anticoagulants: Mechanism of action, clinical effectiveness, and optimal therapeutic range [J].
Hirsh, J ;
Dalen, JE ;
Anderson, DR ;
Poller, L ;
Bussey, H ;
Ansell, J ;
Deykin, D .
CHEST, 2001, 119 (01) :8S-21S
[8]   Heparin and low-molecular-weight heparin - Mechanisms of action, pharmacokinetics, dosing, monitoring, efficacy, and safety [J].
Hirsh, J ;
Warkentin, TE ;
Shaughnessy, SG ;
Anand, SS ;
Halperin, JL ;
Raschke, R ;
Granger, C ;
Ohman, EM ;
Dalen, JE .
CHEST, 2001, 119 (01) :64S-94S
[9]  
Horton JD, 1999, AM FAM PHYSICIAN, V59, P635
[10]   Antithrombotic therapy for venous thromboembolic disease [J].
Hyers, TM ;
Agnelli, G ;
Hull, RD ;
Morris, TA ;
Samama, M ;
Tapson, V ;
Weg, JG .
CHEST, 2001, 119 (01) :176S-193S