甲磺酸罗比卡因用于肌间沟臂从神经阻滞的临床观察

我们通过对不同浓度的甲磺酸罗比卡因应用于肌间沟臂丛神经阻滞的麻醉效果及不良反应的比较,验证甲磺酸罗比卡因临床应用的有效性和安全性。资料与方法一般资料60例ASAⅠ~Ⅱ级,年龄18~55岁,体重50~70kg,拟行上肢手术患者,男39例,女21例。入选患者均无局麻药过敏史,无服用肝素类     

神经内镜下行三脑室底造瘘术治疗梗阻性脑积水的并发症分析和防治

目的:分析神经内镜下三脑室底造瘘术(ETV)的手术并发症原因,探讨其防治要点。方法:通过回顾性分析2004年9月至2006年2月应用ETV连续治疗梗阻性脑积水55例的手术并发症,对ETV的常见并发症的原因做了探讨。结果:54例患者ETV得以完成,术后50例患者恢复良好,脑积水症状明显减轻或消失。4例患者症状复发或加重,行脑室腹腔分流术。术后并发症包括硬膜下积液8例,发热15例,2例伴有脑膜刺激征为颅内感染,癫痫1例,硬膜外出血1例,头皮下积液8例。结论:熟悉三脑室底的解剖结构,选择合适的造瘘方法,并注意手术前后脑脊液动力学的变化,可以减少三脑室底造瘘治疗梗阻性脑积水的手术并发症。     

关节软骨损伤的治疗（上）

关节软骨属于透明软骨，自身没有血供，无淋巴引流，无神经分布，软骨细胞是高度分化的组织细胞，成熟的关节软骨中软骨细胞的分裂能力非常有限，因此软骨损伤后修复能力差。早在1743年Hunter就提出“骨软骨一旦破坏，就不能得到修复”的观点，而关节软骨损伤及其修复问题，长期以来也一直是困扰骨科基础研究与临床治疗的棘手问题。随着社会的现代化进程和人口的老龄化，由于外伤和退变引起的关节软骨损伤患者显著增多，为此如何解决关节软骨修复的问题日益显得重要。     

神经干细胞的端粒酶活性与其增殖分化的关系

目的探讨体外培养的神经干细胞端粒酶活性与细胞增殖、分化的关系,以及细胞分化后端粒酶逆转录酶的表达情况。方法采用无血清培养法从新生大鼠脑皮质分离培养神经干细胞；通过免疫荧光细胞染色鉴定神经干细胞；细胞计数法检测细胞的增殖情况；TRAP-ELISA法测定神经干细胞的端粒酶活性：RT-PCR法和Western-blot法测定细胞分化前后的端粒酶逆转录酶的表达。结果从新生大鼠脑皮质分离培养的神经干细胞具有端粒酶活性；体外培养12周内,神经干细胞的端粒酶活性未见变化,细胞的增殖速率亦未见明显不同；神经干细胞分化后端粒酶活性丧失,端粒酶逆转录酶的mRNA和蛋白质也均未见表达。结论在体外培养过程中,大鼠脑神经干细胞的端粒酶活性和细胞增殖速率未见变化；神经干细胞分化后端粒酶活性丧失,可能是由于端粒酶逆转录酶停止表达所致。     

胰胆管返流的X线诊断及临床意义

胰胆管返流征象在以往常规上消化道钡餐检查中显示不甚清楚，近年来随着高清晰数字胃肠机的应用，此征象在行上消化道钡餐检查中经常见到，但胰胆管返流征象的X线诊断是否有临床意义却少有报道。我们自1999年至今收集到96例并与CT、B超、实验室及临床进行了对比分析和探讨，现报告如下。     

RF钉治疗胸腰椎骨折患者术后疼痛程度与神经功能评估

胸、腰椎骨折脱位约占脊柱损伤的82．5％～96．2％。随着交通事故的增加和建筑业的繁荣，胸、腰椎骨折越来越多，且爆裂性骨折的比例也在增加，并多伴有脊髓损伤。应用RF钉治疗胸、腰椎骨折并对术后疼痛程度及神经功能进行评估，效果良好。     

上胸椎前方手术入路的解剖及其临床意义

目的研究上胸椎与其毗邻组织结构的解剖关系,为探讨上胸椎前方手术入路提供参考.方法取20具经防腐处理的尸体标本,模拟上胸椎前路手术,部分劈开胸骨,并分别经不同的血管、神经间隙显露椎体,比较不同的血管、神经间隙入路的暴露范围及其优缺点.观察上胸椎毗邻的血管、神经等组织结构的走行及其与椎体的对应关系.结果头臂干外侧间隙入路（头臂干与右头臂静脉、左头臂静脉根部之间的间隙）95%可显露达T3椎体以下,而头臂干内侧间隙入路（气管食道鞘与头臂干、左头臂静脉之间的间隙）只有45%可显露达T3椎体以下.上腔静脉与升主动脉之间的间隙只能在直视下显露T4,并且视野狭小.右喉返神经在T1,2水平从迷走神经发出,绕过锁骨下动脉斜行走向内上,在T1椎体上缘水平附近走向气管食道沟.胸导管75%在T1椎体到T1-2椎间盘水平入左侧静脉角,约50%最高点达T1水平.左头臂静脉55%平T3椎体水平从上腔静脉发出.主动脉弓主干约80%在T3-4椎间盘水平横过椎体.结论头臂干外侧间隙入路操作简单、显露清楚,可以很容易地显露T3和T4椎体;头臂干外侧间隙与头臂干内侧间隙相比,可多显露0.5～1个椎体.但由于迷走神经穿过此间隙并在此发出心支,所以应注意保护迷走神经.在右侧施行T1,2水平手术时易损伤右喉返神经.在采用左侧入路时应注意胸导管的走行,避免损伤胸导管.     

Effect on peripheral nerve vivo with human insulin-like regeneration by transgene in growth factor-1

BACKGROUND: Human insulin-like growth factor (hIGF-1) has been successful in treating peripheral nerve injury, but it is still unclear whether hIGF-1 after transgene in vivo has the effect on promoting the regeneration of peripheral nerve. OBJECTIVE: To observe the effect of hIGF-1 on the regeneration of peripheral nerve by transgene in vivo with electrophysiology, histological morphology and ultromicro morphology. DESIGN: A univariate design. SETTINGS: Jilin Institute of Surgery, China-Japan Friendship Hospital Affiliated to Jilin University; School of Basic Medical Sciences, Jilin University. MATERIALS: Thirty male adult Wistar rats of grade Ⅱ, weighing 200-250 g, were provided by the Animal Experimental Center of Jilin University [certification number: SCXK-(Ji)20030001]. The rats were raised in the environment at the temperature of 25 ℃ and humidity of 70%. All the rats were randomly divided into hIGF-1-treated group, treatment control group and blank control group, 10 rats in each group. Positive liposomes (mass concentration of 2 g/L) and pcDNA3.1 (mass concentration of 1 g/L) were purchased from Beijing Yuanpinghao Company; pcDNAhIGF-1 (mass concentration of 1 g/L) was provided by Dr. Shen from the School of Public Health of Jilin University. The liposomes were mixed with plasmids with the mass ratio of 1.5 to 10.Operative microscope was made by Jiangsu Zhenjiang Microsurgical Instrument Factory; EMB-5304K electromyogram (EMG) evoked potential meter by Nihon Kohden Corporation. HPIAS-1 000 high-acuity color pathological imaging analytical system (Japan) and JEM-1200EX transmission electron microscope (Japan) were also used. METHODS: The experiments were carried out in Jilin Institute of Surgery from April to June in 2004. ① All the rats were anesthetized, and the right sciatic nerve was exposed, and it was clipped with a clip at 5 mm below the piriform muscle for 3 times, 10 s for each time. The pressed width was 3 mm, and formed as membrane under operating microscope (×6). Rats in the hIGF-1-treated group were subepineurially injected with the mixture of pcDNAhIGF-1 and positive liposomes (10 μL) immediately, those in the treatment control group were injected with the mixture of pcDNA3.1, positive liposomes and distilled water (10 μL), and those in the blank control group were not given any injection. ② The sciatic nerve functional indexes (SFI) were measured within 56 days postoperatively according to the methods used by Shen et al. ISFI=0 was taken as normal, and ISFI=-100 as completely damaged. EMG evoked potential meter was used to record the electrophysiological changes of the regenerated nerve fibers. The indexes of histological morphology in 5 randomly selected sights were determined with the color pathological imaging analytical system, and the ultrostructures of the regenerated nerve fibers were also observed. MAIN OUTCOME MEASURES: ① Comparison of the SFI within 56 days postoperatively; ② Comparison of the electrophysiology, histological morphology and ultrastructure of the regenerated nerve fibers 56 days postoperatively. RESULTS: All the 30 Wistar rats were involved in the analysis of results. ① SFI: The SFI values were gradually increased as time prolonged in all the three groups, and the changes were more obvious after 24 days, the SFI values recovered better at each time point in the hIGF-1-treated group than in the other two groups. ② Eelectrophysiological results of right sciatic nerve: The latency of motor evoked potential (MEP) was close between the treatment control group and the blank control group [(2.55±0.36), (2.65±0.55) ms, P > 0.05], but higher in the hIGF-1-treated group [(2.14±0.22) ms] than in the blank control group (P < 0.01). The amplitude and conduction velocity of MEP in the treatment control group [(6.67±0.69) mV, (29.57±4.06) m/s] were close to those in the blank control group [(6.60±0.59) mV, (29.22±3.20) m/s, P > 0.05], but those in the hIGF-1-treated group [(7.81±0.84) mV, (36.91±4.37) m/s] were larger or faster than those in the blank control group (P < 0.01). ③ Results of the pathological image analysis of the regenerated nerve fibers: The axonal diameter, thickness of myelin sheath of the regenerated nerve fiber and the number of myelinated nerve fiber in the treatment control group [(2.28±0.33) μm, (1.08±0.18) μm2, (71.80±8.25) fibers] were close to those in the blank control group [(2.18±0.29) μm, (1.03±0.15) μm2, (68.60±8.55) fibers] (P > 0.05), and those in the hIGF-1-treated group [(3.03±0.35) μm, (1.65±0.24) μm2, (88.20±8.82) fibers] were obviously larger or more than those in the blank control group (P < 0.01). ④ Ultrastructure of the regenerated nerve fibers of sciatic nerve: In the hIGF-1-treated group, the regenerated fibers of sciatic nerve were more and mature, manifested by thicker nerve fibers, thicker and evener myelin sheath, which were better than those in the other two groups. CONCLUSION: The results of the quantitative parameters of the electrophysiology, gross histological morphology and ultrostructural changes in the process of repairing damaged peripheral nerve indicate that transgene in vivo with hIGF-1 can promote the neural regeneration after peripheral nerve injury.     

平面三角针治疗尺骨鹰嘴骨折10例

尺骨鹰嘴骨折是较常见的肘关节损伤，临床上治疗方法较多，我科自1995年以来利用平面三角针治疗10例，经临床观察，疗效满意，报告如下：     

接受人工通气新生儿中吗啡对动脉血压的影响

目的:研究在接受人工通气的新生儿中连续吗啡静滴对动脉血压的影响。设计:盲法随机安慰剂对照试验。机构:两个中心的三级新生儿重症监护病房。病例:共有144名接受人工通气的新生儿,入选标准为出生后年龄<3d、人工通气<8h并有留置动脉导管,剔除标准为严重窒息、严重脑室内出血、