[糖蛋白IIb-IIa抑制剂(阿昔单抗)辅助治疗具有高血栓形成风险的冠状动脉血管成形术]。

V Matos, A M Marques, H Oliveira, D Ramos, P Lopes, M Camacho, A Gonsalves
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引用次数: 0

摘要

我们回顾性研究了糖蛋白IIb-IIIa抑制剂(阿昔单抗)对冠状动脉成形术(PTCA)中血栓并发症高风险患者的辅助治疗经验。患者与方法:1996年9月至1997年11月对210例患者行PTCA,其中38例(18%)给予阿昔单抗治疗。在55%的病例中,紧急干预(急性心肌梗死的原发性PTCA)。患者平均年龄为68.6±12岁,男性占71%。冠脉介入治疗的原因为:急性心肌梗死21例(55.3%),不稳定型心绞痛9例(23.7%),稳定型心绞痛8例(21%)。13例(34%)患者植入冠脉支架,4例(11%)患者使用主动脉内球囊泵。使用阿昔单抗的原因有:血栓病变22例(57.9%);其他B2/C型病变特征:6例(15.9%);球囊后PTCA急性闭合9例(23.7%),亚急性支架血栓1例(2.6%)。所有患者在干预开始时给予口服乙酰水杨酸和静脉注射肝素。手术结束时平均APTT为124±32秒。结果:根据APTT值的正常化,术后6小时切除动脉鞘(8 French)。这组患者的血管造影成功率为100%。1例患者在住院期间因左心室衰竭死亡。住院期间不需要重复血管成形术或冠状动脉旁路移植术。与使用阿昔单抗相关的主要并发症是:4例患者出血(需要输血)(10.5%);严重血小板减少(< 50,000血小板/mm3): 1例(2.6%);心包填塞(需要心包穿刺):1例(2.6%);股动脉假性动脉瘤(需要血管手术):1例(2.6%)。结论:在这一小群接受冠状动脉介入治疗的血栓并发症高风险患者中,使用阿昔单抗作为辅助治疗与手术成功率高相关,但以出血并发症的高发生率为代价。因此,在此过程中和之后必须特别小心,以提高使用该药物治疗的患者的安全性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Adjuvant therapy with a glycoprotein IIb-IIa inhibitor (abciximab) in coronary angioplasties with a high thrombotic risk].

Introduction: We retrospectively studied our experience with adjunctive therapy with glycoprotein IIb-IIIa inhibitor (abciximab) on patients with a high risk of thrombotic complications during coronary angioplasty (PTCA).

Patients and methods: From September 1996 to November 1997, we performed PTCA in 210 patients, and abciximab was given to 38 (18%) of them. The interventions were urgent (primary PTCA in acute myocardial infarction) in 55% of the cases. The mean age of patients was 68.6 +/- 12 years and 71% were male. The reasons for coronary intervention were: acute myocardial infarction in 21 patients (55.3%), unstable angina in 9 (23.7%) and stable angina in 8 (21%). Coronary stents were implanted in 13 patients (34%) and an intra aortic balloon pump was used in 4 (11%). The reasons for using abciximab were: thrombus containing lesion: 22 (57.9%); other type B2/C lesion characteristics: 6 (15.9%); acute closure post balloon PTCA: 9 (23.7%), sub-acute stent thrombosis: 1 (2.6%). Oral acetilsalicilic acid and intravenous heparin were given to all patients at the beginning of the intervention. The mean APTT was 124 +/- 32 seconds at the end of the procedure.

Results: The arterial sheaths (8 French) were removed six hours after procedure, according to the normalisation of APTT values. Angiographic success in this group of patients was 100%. One patient died during hospitalisation due to left ventricular failure. There was no need for repeated angioplasty or coronary bypass grafting during hospital stay. The main complications related to the use of abciximab were: bleeding (requiring transfusion) in four patients 10.5%); severe thrombocytopenia (< 50,000 platelets/mm3): 1 (2.6%): cardiac tamponade (requiring pericardiocentesis): 1 (2.6%) and pseudo-aneurysm of femoral artery (requiring vascular surgery): 1 (2.6%).

Conclusions: The use of abciximab as adjunctive therapy in this small group of patients undergoing coronary interventions with high risk of thrombotic complications is associated with high procedural success, but at the expense of high rates of bleeding complications. Therefore, special care must be applied during and after the procedure to enhance the safety of the patients treated with this drug.

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