Grijseels E W, Bouten M J, Lenderink T, Deckers J W, Hoes A W, Hartman J A, van der Does E, Simoons M L
Thoraxcentre, Department of Cardiology, Erasmus University Rotterdam, The Netherlands.
Eur Heart J. 1995 Dec;16(12):1833-8. doi: 10.1093/oxfordjournals.eurheartj.a060836.
To assess the practical application, safety and long-term outcome of pre-hospital thrombolytic intervention with either alteplase or streptokinase in patients with extensive myocardial infarction.
Prospective study.
Patients with chest pain of more than 30 min duration, presenting within 6 h of symptom onset and with electrocardiographic evidence of extensive evolving myocardial infarction.
Eligibility of patients was established by the general practitioner or the ambulance nurse using a standardized questionnaire with (contra-) indications for thrombolytic therapy. Computerized ECG was recorded by ambulance nurses. In the presence of extensive ST segment elevation (sum ST deviation of at least 1.0 mV), eligible patients received either 100 mg alteplase (n = 246) or 50 mg alteplase in the ambulance followed by 0.75 x 10(6) IE streptokinase in hospital (n = 90), or 1.5 x 10(6) IE streptokinase intravenously (n = 193).
Death and life-threatening complications (ventricular fibrillation, cardiac arrest) and side effects (hypotension, allergic reactions) during transportation to hospital and in the first 24 h following hospitalization, and survival up to 5 years follow-up.
From 1988-1993, 529 patients received thrombolytic treatment initiated pre-hospital. The time gained by pre-hospital administration of thrombolysis amounted to 50 min. The rate of complications during transportation and during the first 24 h after hospitalization was low. Hospital mortality was 2% and 1-year mortality 3%. Cumulative survival at 5 years was 92%. This was superior to the 84% 5-year survival observed in a matched group of 239 patients with similar baseline characteristics treated with alteplase in hospital.
Pre-hospital administration of either alteplase or streptokinase is feasible and safe and results in significant time gain. The long-term prognosis is excellent in spite of extensive evolving myocardial infarction upon admission.
评估院前使用阿替普酶或链激酶对广泛心肌梗死患者进行溶栓干预的实际应用情况、安全性及长期预后。
前瞻性研究。
症状发作6小时内出现胸痛持续超过30分钟且有广泛进展性心肌梗死心电图证据的患者。
由全科医生或救护护士使用具有溶栓治疗(禁忌)指征的标准化问卷确定患者是否符合条件。救护护士记录计算机化心电图。在出现广泛ST段抬高(ST段总偏移至少1.0 mV)时,符合条件的患者在救护车上接受100 mg阿替普酶(n = 246),或先在救护车上接受50 mg阿替普酶,随后在医院接受0.75×10⁶国际单位链激酶(n = 90),或静脉注射1.5×10⁶国际单位链激酶(n = 193)。
在转运至医院期间及住院后的头24小时内的死亡和危及生命的并发症(室颤、心脏骤停)及副作用(低血压、过敏反应),以及长达5年随访期的生存率。
1988年至1993年,529例患者接受了院前启动的溶栓治疗。院前溶栓治疗节省的时间达50分钟。转运期间及住院后头24小时内的并发症发生率较低。医院死亡率为2%,1年死亡率为3%。五年累积生存率为92%。这优于一组239例具有相似基线特征且在医院接受阿替普酶治疗的匹配患者中观察到的84%的五年生存率。
院前使用阿替普酶或链激酶是可行且安全的,并能显著节省时间。尽管入院时存在广泛进展性心肌梗死,但长期预后良好。