首页> 外文期刊>Southern Medical Journal >Intraventricular administration of rt-PA in patients with intraventricular hemorrhage.
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Intraventricular administration of rt-PA in patients with intraventricular hemorrhage.

机译:脑室内出血患者的rt-PA的脑室内给药。

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OBJECTIVE: Intraventricular hemorrhage (IVH) represents a clinicopathologic entity with a dismal prognosis. The associated mortality rate has been reported as high as 80%; the morbidity is also quite high. The use of various fibrinolytic agents (streptokinase, urokinase, and recombinant tissue-type plasminogen activator [rt-PA]) has been reported in a small number of clinical series with a very limited number of participants, yielding significant variability regarding inclusion criteria, treatment protocol, and outcome analysis. METHODS: In our prospective study, we report our experience using rt-PA in 21 patients with IVH. Patients with IVH of aneurysmal or arteriovenous malformation origin were excluded. Intraventricular administration of rt-PA was initiated within 24 hours after the ictal event (dose, 3 mg every 24 hours) through a ventricular catheter. The patients' intracranial and cerebral perfusion pressures, cerebrospinal fluid (CSF) cell count, and head CT scans with emphasis to frontal horn dimension and inner cranium diameter at the same level ratio were collected and analyzed. RESULTS: Good outcome was observed in 47.5% of our patients, whereas 28.5% died and 24.0% survived with severe disability. The development of rt-PA-associated complications was as follows: new hemorrhage in 19%, infection in 14.3%, and CSF pleocytosis in 100% of patients. Permanent CSF shunt was required in 40%. The intermediate (3-month) follow up of our survivors showed no significant outcome changes compared with the immediate (1-month) follow up. CONCLUSIONS: Intraventricular administration of rt-PA appears to be beneficial in cases of IVH even though it is occasionally associated with serious complications. Further multi-institutional studies are required for validating this treatment modality and standardizing its parameters.
机译:目的:脑室内出血(IVH)代表预后不良的临床病理学实体。据报道,相关的死亡率高达80%。发病率也很高。在少数临床系列报告中报告了使用多种纤溶酶试剂(链激酶,尿激酶和重组组织型纤溶酶原激活剂[rt-PA])的情况,参与者数量非常有限,在纳入标准,治疗方法方面存在很大差异方案和结果分析。方法:在我们的前瞻性研究中,我们报告了21例IVH患者使用rt-PA的经验。患有动脉瘤或动静脉畸形的IVH患者被排除在外。在发作事件发生后24小时内(剂量,每24小时3 mg)通过心室导管开始rt-PA的脑室内给药。收集并分析患者的颅内和脑灌注压力,脑脊液(CSF)细胞计数以及在相同水平比例下侧重于额角尺寸和内部颅骨直径的头部CT扫描。结果:在我们的患者中有47.5%的患者观察到了良好的预后,而有严重残疾的患者中有28.5%的患者死亡,24.0%的患者存活。 rt-PA相关并发症的发展如下:新出血19%,感染14.3%,CSF胞吞症100%。 40%需要永久性CSF分流。与立即(1个月)随访相比,我们幸存者的中期(3个月)随访没有明显的预后改变。结论:rt-PA的脑室内给药似乎对IVH有益,即使偶尔伴有严重并发症。需要进一步的多机构研究来验证这种治疗方式并使其参数标准化。

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