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心房颤动:低分子量肝素能发挥作用吗?

Atrial fibrillation: is there a role for low-molecular-weight heparin?

作者信息

Camm A J

机构信息

Department of Cardiological Sciences, St. George's Hospital Medical School, London, UK.

出版信息

Clin Cardiol. 2001 Mar;24(3 Suppl):I15-9. doi: 10.1002/clc.4960241306.

Abstract

Atrial fibrillation (AF) is the most common form of tachyarrhythmia and carries a significant risk of serious thromboembolic complications. Anticoagulation is used for long-term thromboprophylaxis and for short-term management in a number of clinical situations, among which is the medical or electrical cardioversion of AF to sinus rhythm. Current guidelines recommend prompt cardioversion with heparin cover for AF of <48 h duration, and several weeks of warfarin therapy prior to cardioversion when the duration of disease is longer. Recent animal and human studies, however, have shown that swifter cardioversion is likely to be more successful in achieving sinus rhythm and in reducing the risk of recurrence of AF. Other observations have demonstrated that thrombi can develop within a few hours of the development of AF. These considerations suggest that cardioversion should be carried out as early as possible in all cases, and that the most sensitive means of detecting atrial thrombi, currently transesophageal echocardiography (TEE), should be used to screen all patients prior to cardioversion. Within this context, there is growing interest in the use of low-molecular-weight heparin (LMWH) as an anticoagulant therapy in AF. Compared with unfractionated heparin, LMWH therapy does not involve prolonged intravenous administration, hospitalization, or laboratory monitoring; LMWH therefore has the potential to greatly simplify anticoagulation therapy for AF, especially pericardioversion. Recent studies have demonstrated that LMWH can be used safely and effectively in place of unfractionated heparin for acute treatment at the onset of AF and during early cardioversion. For example, in patients with AF, a strategy of immediate administration of dalteparin (100 IU/kg s.c. twice daily) continued for 11 days, combined with early TEE and immediate cardioversion in patients with no thrombus, resulted in sinus rhythm in 74% of patients after a median of 7 days. Low-molecular-weight heparin therapy may also find a role perioperatively and in selected patients, notably those with warfarin intolerance, as a replacement for warfarin following cardioversion. Controlled clinical studies are still required, however, to establish a firm, evidence-based foundation for the use of LMWHs in AF.

摘要

心房颤动(AF)是最常见的快速性心律失常形式,具有发生严重血栓栓塞并发症的重大风险。抗凝治疗用于长期血栓预防以及多种临床情况下的短期管理,其中包括将房颤转复为窦性心律的药物或电转复。当前指南建议,对于病程小于48小时的房颤,在肝素覆盖下迅速进行转复;而当病程较长时,在转复前进行数周的华法林治疗。然而,最近的动物和人体研究表明,更快的转复在实现窦性心律和降低房颤复发风险方面可能更成功。其他观察结果显示,在房颤发生后的数小时内即可形成血栓。这些考虑因素表明,在所有情况下都应尽早进行转复,并且应使用目前最敏感的检测心房血栓的方法——经食管超声心动图(TEE),在转复前对所有患者进行筛查。在此背景下,使用低分子量肝素(LMWH)作为房颤的抗凝治疗方法越来越受到关注。与普通肝素相比,LMWH治疗无需长时间静脉给药、住院或实验室监测;因此,LMWH有潜力极大地简化房颤的抗凝治疗,尤其是转复前后的治疗。最近的研究表明,LMWH可安全有效地替代普通肝素用于房颤发作时的急性治疗和早期转复期间。例如,在房颤患者中,采用立即皮下注射达肝素(100 IU/kg,每日两次)持续11天的策略,并结合早期TEE检查,对无血栓患者立即进行转复,中位7天后74%的患者恢复窦性心律。低分子量肝素治疗在围手术期以及某些特定患者(尤其是对华法林不耐受的患者)中,作为转复后华法林的替代药物可能也有作用。然而,仍需要进行对照临床研究,为LMWH在房颤中的应用建立坚实的循证基础。

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