首页> 外文期刊>Neurosurgery >Intraventricular thrombolysis speeds blood clot resolution: results of a pilot, prospective, randomized, double-blind, controlled trial.
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Intraventricular thrombolysis speeds blood clot resolution: results of a pilot, prospective, randomized, double-blind, controlled trial.

机译:脑室内溶栓治疗可加速血凝块溶解:一项前瞻性,前瞻性,随机,双盲,对照试验的结果。

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OBJECTIVE: Animal models and clinical studies suggest that intraventricular thrombolysis improves clot resolution and clinical outcomes among patients with intraventricular hemorrhage. However, this intervention may increase the rates of rebleeding and infection. To assess the safety and efficacy of intraventricular thrombolysis, we conducted a pilot, randomized, double-blind, controlled, multicenter study. METHODS: Patients with intraventricular hemorrhage requiring ventriculostomy were randomized to receive intraventricular injections of normal saline solution or urokinase (25000 international units) at 12-hour intervals. Injections continued until ventricular drainage was discontinued according to prespecified clinical criteria. Head computed tomographic scans were obtained daily, for quantitative determinations of intraventricular hemorrhage volumes. The rate of clot resolution was estimated for each group. RESULTS: Twelve subjects were enrolled (urokinase, seven patients; placebo, five patients). Commercial withdrawal of urokinase precluded additional enrollment. The urokinase and placebo groups were similar with respect to age (49.6 versus 55.2 yr, P = 0.43) and presenting Glasgow Coma Scale scores (7.14 versus 8.00, P = 0.72). Randomization to the urokinase treatment arm (P = 0.02) and female sex (P = 0.008) favorably affected the clot resolution rate. The sex-adjusted clot half-life for the urokinase-treated group was reduced 44.6%, compared with the value for the placebo group (4.69 versus 8.48 d). CONCLUSION: Intraventricular thrombolysis with urokinase speeds the resolution of intraventricular blood clots, compared with treatment with ventricular drainage alone.
机译:目的:动物模型和临床研究表明,脑室内溶栓可改善脑室内出血患者的血凝块分辨率和临床结局。但是,这种干预可能会增加再出血和感染的发生率。为了评估脑室内溶栓的安全性和有效性,我们进行了一项先导,随机,双盲,对照,多中心研究。方法:需要进行脑室造口术的脑室内出血患者,每隔12小时随机接受一次脑室内注射生理盐水或尿激酶(25000国际单位)。继续注射直至根据预先指定的临床标准停止心室引流。每天进行头颅计算机断层扫描,以定量测定脑室内出血量。估计每组的血块消退率。结果:招募了十二名受试者(尿激酶,七名患者;安慰剂,五名患者)。尿激酶的商业撤回排除了额外的入组。尿激酶和安慰剂组在年龄方面相似(49.6岁对55.2岁,P = 0.43),并且表现出格拉斯哥昏迷量表评分(7.14对8.00,P = 0.72)。尿激酶治疗组(P = 0.02)和女性(P = 0.008)的随机分组有利地影响了凝块的分辨率。与安慰剂组相比,经尿激酶治疗的组经性别调整的血凝块半衰期减少了44.6%(4.69对8.48 d)。结论:与单纯心室引流相比,尿激酶脑室内溶栓可加快脑室内血块的消退。

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