Daou Badih, Deprince Maureen, D'Ambrosio Robin, Tjoumakaris Stavropoula, Rosenwasser Robert H, Ackerman Daniel J, Bell Rodney, Tzeng Diana L, Ghobrial Michelle, Fernandez Andres, Shah Qaisar, Gzesh Dan J, Murphy Deborah, Castaldo John E, Mathiesen Claranne, Pineda Maria Carissa, Jabbour Pascal
Thomas Jefferson University Hospital, Department of Neurosurgery, Philadelphia, PA, United States.
Thomas Jefferson University Hospital, Department of Neurosciences Institute, Philadelphia, PA, United States.
Clin Neurol Neurosurg. 2015 Dec;139:264-8. doi: 10.1016/j.clineuro.2015.10.010. Epub 2015 Oct 21.
Recently, the FDA guidelines regarding the eligibility of patients with acute ischemic stroke to receive IV rt-PA have been modified and are not in complete accord with the latest AHA/ASA guidelines. The resultant differences may result in discrepancies in patient selection for intravenous thrombolysis.
Several comprehensive stroke centers in the state of Pennsylvania have undertaken a collaborative effort to clarify and unify our own recommendations regarding how to reconcile these different guidelines.
Seizure at onset of stroke, small previous strokes that are subacute or chronic, multilobar infarct involving more than one third of the middle cerebral artery territory on CT scan, hypoglycemia, minor or rapidly improving symptoms should not be considered as contraindications for intravenous thrombolysis. It is recommended to follow the AHA/ASA guidelines regarding blood pressure management and bleeding diathesis. Patients receiving factor Xa inhibitors and direct thrombin inhibitors within the preceding 48 h should be excluded from receiving IV rt-PA. CT angiography is effective in identifying candidates for endovascular therapy. Consultation with and/or transfer to a comprehensive stroke center should be an option where indicated. Patients should receive IV rt-PA up to 4.5h after the onset of stroke.
The process of identifying patients who will benefit the most from IV rt-PA is still evolving. Considering the rapidity with which patients need to be evaluated and treated, it remains imperative that systems of care adopt protocols to quickly gather the necessary data and have access to expert consultation as necessary to facilitate best practices.
最近,美国食品药品监督管理局(FDA)关于急性缺血性卒中患者接受静脉注射重组组织型纤溶酶原激活剂(IV rt-PA)资格的指南已被修订,且与最新的美国心脏协会(AHA)/美国卒中协会(ASA)指南不完全一致。由此产生的差异可能导致静脉溶栓患者选择上的差异。
宾夕法尼亚州的几个综合卒中中心共同努力,以阐明并统一我们自己关于如何协调这些不同指南的建议。
卒中发作时的癫痫、既往亚急性或慢性的小卒中、CT扫描显示累及大脑中动脉区域超过三分之一的多叶梗死、低血糖、轻微或迅速改善的症状不应被视为静脉溶栓的禁忌证。建议遵循AHA/ASA关于血压管理和出血素质的指南。在过去48小时内接受过Xa因子抑制剂和直接凝血酶抑制剂治疗的患者应排除接受IV rt-PA治疗。CT血管造影在识别血管内治疗候选者方面有效。在有指征的情况下,应选择咨询和/或转诊至综合卒中中心。患者应在卒中发作后4.5小时内接受IV rt-PA治疗。
确定最能从IV rt-PA治疗中获益的患者的过程仍在不断发展。考虑到患者需要快速接受评估和治疗,护理系统采用方案快速收集必要数据并在必要时获得专家咨询以促进最佳实践仍然至关重要。