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脑苷肌肽注射液(凯洛欣)治疗新生儿缺氧缺血性脑病疗效观察 被引量:3

The effect of cattle encephalon glycoside and ignotin injection on neonates with hypoxia-ischemia encephalopathy
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摘要 目的:观察脑苷肌肽注射液(凯洛欣)治疗新生儿缺氧缺血性脑病(HIE)的疗效。方法:将患几分为治疗组(凯洛欣组)与对照组,两组病例均根据病情给予吸氧、止惊、降颅压及能量合剂等支持治疗和对症处理,并及时纠正酸中毒、低血压、低血糖等。治疗组给予凯洛欣2mL,加入100g·L^-1葡萄糖注射液20mL中静脉滴注,1次/d,7d为1个疗程,连用1~2个疗程。结果:治疗组62例中显效42例,有效15例,无效5例,总有效率91.93%。对照组50例中显效15例,有效22例,无效13例,总有效率74.0%。两组差异有显著性意义(P〈0.05)。结论:应用凯洛欣治疗新生儿缺氧缺血性脑病临床效果显著,能在短期内消除症状,提高疗效,促使受损脑细胞早日恢复,缩短病程且副作用少。 e.To investigation the effect of cattle encephalon glycoside and ignotin injection(CEGI) to sedative, intracranial pressure reduction, and energy mixture. The rectification of acidosis, hypotension and hypoglycemia was also same in the two groups according to patients' condition. Besides, in CEGI group, 2 mL CEGI was added into 10% GS 20 mL ivgtt qd for 7days in one period. Another 1 - 2 periods were applied continually. Results: The total efficiency in CEGI group was 91.9% (42 neonates improved obviously, 15 improved, and 5 had no effect in all 62 newborns), compared with 74. 0% in control group ( 15 neonates improved obviously, 22 improved, and 13 had no effect in 50 newborns), with significant statistic difference between two groups ( P 〈 0. 05 ). Conclusion: There are obviously positive clinic benefits of CEGI in HIE therapy. CEGI can eliminate symptoms quickly, improve therapeutic effects, make impaired brain cell recover earlier with little side effects. This therapy deserves to be widely used in practice.
作者 朱玲玲
出处 《药学与临床研究》 2007年第6期476-478,共3页 Pharmaceutical and Clinical Research
关键词 凯洛欣 缺氧缺血性脑病 新生儿 Encephalon glycoside and ignotin injection Hypoxia ischemia encephalopathy(HIE) Neonate
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  • 1汤泽中,周丛乐,虞人杰.新生鼠缺氧缺血脑损伤脑细胞凋亡与钙超载的研究[J].中华儿科杂志,2001,39(1):18-20. 被引量:47
  • 2Fukumoto S, Mutoh T, Hasegawa T, et al. GD3 synthase gene expression in PC12 cells results in the continuous activation of TrkA and ERK1/2 and enhanzed proliferation[J]. J Biol Chem, 2000,275(8):5832- 5838.
  • 3Tan WK, Williams CE, Gunn AJ, et al. Pretreatment with monosialoganglioside GM1 protects the brain of fetal sheep against hypoxic-ischemic injury without causing systemic compromise[J].Pediatric Res, 1993,34(1):18 - 22.
  • 4Rocca WA, Dorsey FC, Grigoletto F, et al. Design and baseline results of the monosialoganglioside Early Stroke Trial[J]. Stroke,1992,23(4):519 - 526.
  • 5Lenzi GL, Grigoletto F, Gent M, et al. Early treatment of stroke with monosialoganglioside GM1: efficacy and safety results of the early stroke results of the Early Stroke Trial[J]. Stroke, 1994,25(8)1552- 1558.
  • 6Alter M. GM1 ganglioside for acute ischemic stroke. Trial design issues[J]. Ann N Y Acad Sci, 1998,845:391- 401.
  • 7Palestini P, Pitto P, Ferraretto A, et al. Change of ganglioside accessibility at the plasma membranc surfacc of cultured neurons,following protein kinase C activation[J]. Biochemistry, 1998,37(9):3143 - 3148.
  • 8Avrova NF, Victorov IV, Tyurin VA, et al.Inhibition of glutamate - induced intensification of free radical reactions by gangliosides: possible role in their protective effect in rat cerebellar granule cells and brain synaptosome[J].Neurochem Res, 1998,23(7):945 - 952.
  • 9Ryu BR, Choi DW, Hartley DW, et al. Attenuation of cortical neuronal apoptosis by gangliosides[J]. J Pharmacol Exp Ther, 1999,290(2):811 - 816.
  • 10Furuse H, Waki H, Kaneko K, et al. Effect of the mono -and tetrasialogangliosides, GM1 and GQ1b, on long-term potentiation in the CA1 hippocampal neurons of the guinea pig[J]. Exp Brain Res, 1998,123(3):307 - 314.

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