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使用粒细胞集落刺激因子动员干细胞治疗急性缺血性卒中:一项随机对照试点研究。

Mobilization of Stem Cells Using G-CSF for Acute Ischemic Stroke: A Randomized Controlled, Pilot Study.

作者信息

Prasad Kameshwar, Kumar Amit, Sahu Jitendra Kumar, Srivastava M V P, Mohanty Sujata, Bhatia Rohit, Gaikwad Shailesh B, Srivastava Achal, Goyal Vinay, Tripathi Manjari, Bal Chandrashekar, Mishra Nalini Kant

机构信息

Department of Neurology, Room No. 704, Neurosciences Centre, All India Institute of Medical Sciences, Ansari Nagar, New Delhi 110029, India.

出版信息

Stroke Res Treat. 2011;2011:283473. doi: 10.4061/2011/283473. Epub 2011 Oct 11.

Abstract

Background. There is emerging evidence to support the use of granulocyte colony-stimulating factor (G-CSF) therapy in patients with acute ischemic stroke. Aims. To explore feasibility, safety, and preliminary efficacy of G-CSF therapy in patients with acute ischemic stroke. Patients and Method. In randomized study, 10 patients with acute ischemic stroke were recruited in 1 : 1 ratio to receive 10 μg/kg G-CSF treatment subcutaneously daily for five days with conventional care or conventional treatment alone. Efficacy outcome measures were assessed at baseline, one month, and after six months of treatment included Barthel Index (BI), National Institute of Health Stroke Scale, and modified Rankin Scale. Results. One patient in G-CSF therapy arm died due to raised intracranial pressure. No severe adverse effects were seen in rest of patients receiving G-CSF therapy arm or control arm. No statistically significant difference between intervention and control was observed in any of the scores though a trend of higher improvement of BI score is seen in the intervention group. Conclusion. Although this study did not have power to examine efficacy, it provides preliminary evidence of potential safety, feasibility, and tolerability of G-CSF therapy. Further studies need to be done on a large sample to confirm the results.

摘要

背景。有新出现的证据支持在急性缺血性中风患者中使用粒细胞集落刺激因子(G-CSF)治疗。目的。探讨G-CSF治疗急性缺血性中风患者的可行性、安全性和初步疗效。患者与方法。在一项随机研究中,10例急性缺血性中风患者按1∶1比例招募,一组接受常规护理并每日皮下注射10μg/kg G-CSF,共5天,另一组仅接受常规治疗。在基线、治疗1个月和6个月后评估疗效指标,包括巴氏指数(BI)、美国国立卫生研究院卒中量表和改良Rankin量表。结果。G-CSF治疗组有1例患者因颅内压升高死亡。接受G-CSF治疗组或对照组的其他患者未出现严重不良反应。尽管干预组的BI评分有更高改善的趋势,但在任何评分中干预组和对照组之间均未观察到统计学上的显著差异。结论。尽管本研究没有足够的检验效能来检测疗效,但它提供了G-CSF治疗潜在安全性、可行性和耐受性的初步证据。需要进行更大样本量的进一步研究以证实结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e75d/3191816/3ea67dd1eb6b/SRT2011-283473.001.jpg

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