Wolak Arik, Ayzenberg Yosef, Cafri Carlos, Gilutz Harel, Ilia Reuben, Zahger Doron
Department of Cardiology, Soroka Medical Center, Faculty of Health Sciences, Ben Gurion University of the Negev, P.O. Box 151, 84101 Beer Sheva, Israel.
Int J Cardiol. 2004 Aug;96(2):151-5. doi: 10.1016/j.ijcard.2003.05.032.
Enoxaparin has gained wide acceptance in patients with acute coronary syndromes. However, there is uncertainty regarding management of patients who require coronary intervention while on enoxaparin. Some physicians withhold the morning dose of enoxaparin prior to coronary intervention while others switch patients to unfractionated heparin. Both methods do not provide optimal anticoagulation in the hours preceding intervention. There are no published controlled data to assess the safety of coronary intervention using enoxaparin alone in patients with acute coronary syndromes.
We prospectively compared enoxaparin to unfractionated heparin during coronary angiography and intervention. Sixty four patients admitted to the coronary care unit (CCU) were given enoxaparin twice daily, including on the morning of procedure. Coronary angiography and intervention were performed without additional unfractionated heparin. The control group comprised of 52 patients admitted to Internal Medicine for an acute coronary syndrome. These were also given enoxaparin but the morning dose was withheld and unfractionated heparin was used during procedure.
Patients in both groups had similar baseline characteristics. No significant differences were observed between the two groups in procedural success rate, complications or bleeding. One year follow up showed similar rates of hospitalization and mortality.
Enoxaparin seems to offer safe and effective procedural anticoagulation in patients undergoing percutaneous intervention for acute coronary syndromes. Patients given enoxaparin can probably have coronary intervention without interruption of enoxaparin treatment and without additional procedural anticoagulation. These findings require confirmation in larger, randomized trials.
依诺肝素在急性冠脉综合征患者中已得到广泛认可。然而,对于正在使用依诺肝素的患者进行冠状动脉介入治疗时的管理存在不确定性。一些医生在冠状动脉介入治疗前停用依诺肝素的早晨剂量,而另一些医生则将患者换用普通肝素。这两种方法在介入治疗前的数小时内均未提供最佳抗凝效果。目前尚无已发表的对照数据来评估在急性冠脉综合征患者中单独使用依诺肝素进行冠状动脉介入治疗的安全性。
我们在冠状动脉造影和介入治疗期间前瞻性地比较了依诺肝素与普通肝素。入住冠心病监护病房(CCU)的64例患者每天接受两次依诺肝素治疗,包括在手术当天早晨。在不额外使用普通肝素的情况下进行冠状动脉造影和介入治疗。对照组由52例因急性冠脉综合征入住内科的患者组成。这些患者也接受依诺肝素治疗,但手术当天早晨停用依诺肝素,并在手术期间使用普通肝素。
两组患者的基线特征相似。两组在手术成功率、并发症或出血方面未观察到显著差异。一年随访显示住院率和死亡率相似。
对于接受经皮介入治疗的急性冠脉综合征患者,依诺肝素似乎能提供安全有效的手术抗凝作用。接受依诺肝素治疗的患者可能无需中断依诺肝素治疗且无需额外的手术抗凝即可进行冠状动脉介入治疗。这些发现需要在更大规模的随机试验中得到证实。