Zaman Babar Masood Uz, Khan Ammar Zaman, Hakim Haris, Gilani Jaleed, Wasay Mohammad
Department of Neurology, Aga Khan University Hospital, Karachi.
Department of general Surgery, Benazir Bhutto Hospital, Rawalpindi.
J Pak Med Assoc. 2019 Nov;69(11):1705-1710. doi: 10.5455/JPMA.282873..
To determine the utilisation of intravenous tissue plasminogen activator at a certain dose for ischaemic stroke thrombolysis and to compare the outcomes with those of a different dosage mentioned in literature.
The retrospective study was conducted at the Aga Khan University Hospital, Karachi, and comprised medical records from January, 2007, to October, 2016, of all patients having received intravenous tissue plasminogen activator for ischaemic stroke thrombolysis. Primary safety outcome variables included symptomatic intracerebral haemorrhage after the start of treatment (0.6mg/kg) and death within three months as per the modified Rankin scale 6. Secondary efficacy outcome variable was functional independence as per modified Rankin scale 0-2 at three months. The outcomes were compared with those mentioned in literature with a dose of 0. 9mg/kg.
Of the 79 patients, 52 (66%) were male and 27 (34 %) were female. Median pre-treatment tissue plasminogen activator score was 12 (interquartile range: 8-15). Overall utilisation of t-PA remained at 1.7%. Symptomatic intracerebral haemorrhage was not seen in our cohort while it was seen in 107 (1.7%) patients at the higher dose. Using another definition, it was seen in 3 (3.8%) patients versus 468 (7.3%) patients at the higher dose. Functional independence was seen in 40 (50.6%) patients at three months compared to 3362 (54.8%) patients at the higher dose.
Low-dose intravenous thrombolytic therapy for ischaemic stroke patients was found to be safe and efficacious, and yielded comparable results with those obtained at a higher dose..
确定特定剂量静脉注射组织型纤溶酶原激活剂用于缺血性中风溶栓的使用情况,并将结果与文献中提及的不同剂量的结果进行比较。
这项回顾性研究在卡拉奇的阿迦汗大学医院进行,纳入了2007年1月至2016年10月期间所有接受静脉注射组织型纤溶酶原激活剂进行缺血性中风溶栓的患者的病历。主要安全性结局变量包括治疗开始后(0.6mg/kg)的症状性颅内出血以及根据改良Rankin量表6级在三个月内的死亡情况。次要疗效结局变量是三个月时根据改良Rankin量表0-2级的功能独立性。将这些结果与文献中提及的0.9mg/kg剂量的结果进行比较。
79例患者中,52例(66%)为男性,27例(34%)为女性。治疗前组织型纤溶酶原激活剂评分中位数为12(四分位间距:8-15)。t-PA的总体使用率保持在1.7%。在我们的队列中未观察到症状性颅内出血,而在高剂量组中有107例(1.7%)患者出现。使用另一种定义,在低剂量组中有3例(3.8%)患者出现,而在高剂量组中有468例(7.3%)患者出现。三个月时,40例(50.6%)患者实现了功能独立,而高剂量组中有3362例(54.8%)患者实现了功能独立。
发现低剂量静脉溶栓治疗缺血性中风患者是安全有效的,并且产生了与高剂量治疗相当的结果。