Du Bo, Shan Ai-Jun, Zhang Yu-Juan, Wang Jin, Peng Kai-Wen, Zhong Xian-Liang, Peng Yu-Ping
Department of Neurosurgery, Nanfang Hospital, Southern Medical University, Guangzhou; Department of Emergency Medicine, Shenzhen People's Hospital, The Second Affiliated Hospital of Jinan University, Shenzhen, Guangdong Province, China.
Department of Emergency Medicine, Shenzhen People's Hospital, The Second Affiliated Hospital of Jinan University, Shenzhen, Guangdong Province, China.
Neural Regen Res. 2018 Jun;13(6):999-1006. doi: 10.4103/1673-5374.233442.
The mortality rate of acute severe intraventricular hematoma is extremely high, and the rate of disability in survivors is high. Intraventricular hematoma has always been a difficult problem for clinical treatment. Although minimally invasive endoscopic hematoma evacuation is widely used to treat this disease, the technique still has room for improvement. Equipment for the intra-neuroendoscopic technique (INET) consists of two of our patented inventions: a transparent sheath (Patent No. ZL 200820046232.0) and a hematoma aspirator (Patent No. ZL 201520248717.8). This study explored the safety and efficacy of INET by comparing it with extraventricular drainage in combination with urokinase thrombolytic therapy. This trial recruited 65 patients with severe intraventricular hemorrhage, including 35 (19 men and 16 women, aged 53.2 ± 8.7 years) in the INET group and 30 (17 men and 13 women, aged 51.5 ± 7.9 years) in the control group (extraventricular drainage plus urokinase thrombolytic therapy). Our results showed that compared with the control group, the INET group exhibited lower intraventricular hemorrhage volumes, shorter intensive care-unit monitoring and ventricular drainage-tube placement times, and fewer incidences of intracranial infection, secondary bleeding, and mortality. Thus, the prognosis of survivors had improved remarkably. These findings indicate that INET is a safe and efficient new method for treating severe intraventricular hematoma. This trial was registered with ClinicalTrials.gov (NCT02515903).
急性重症脑室内血肿的死亡率极高,幸存者的致残率也很高。脑室内血肿一直是临床治疗中的难题。尽管微创神经内镜血肿清除术被广泛用于治疗该疾病,但该技术仍有改进空间。神经内镜技术(INET)的设备由我们的两项专利发明组成:一个透明鞘管(专利号:ZL 200820046232.0)和一个血肿抽吸器(专利号:ZL 201520248717.8)。本研究通过将INET与脑室外引流联合尿激酶溶栓治疗进行比较,探讨了INET的安全性和有效性。该试验招募了65例重度脑室内出血患者,其中INET组35例(男性19例,女性16例,年龄53.2±8.7岁),对照组(脑室外引流加尿激酶溶栓治疗)30例(男性17例,女性13例,年龄51.5±7.9岁)。我们的结果表明,与对照组相比,INET组的脑室内出血量更低,重症监护病房监测和脑室引流管放置时间更短,颅内感染、继发性出血和死亡率的发生率更低。因此,幸存者的预后有了显著改善。这些发现表明,INET是一种治疗重度脑室内血肿的安全有效的新方法。该试验已在ClinicalTrials.gov(NCT02515903)注册。