截石位手术床腿架万向移动装置的研制

目的：设计一种调节方便,升降安全的截石位手术床腿架。方法：将气弹簧结构应用于截石位腿架中,进行腿架的升降调节,取代原有的通过拧螺丝调节的方法,并将新型腿架应用于泌尿外科80例截石位手术中。结果：此新型腿架单人操作即可,升降调节时无需将患者腿部抬起,操作方便、节省人力,80例手术无1例发生腿部滑落,操作者使用后效果满意。结论：此新型专利解决了截石位腿架调整操作费力及存在安全隐患的问题,值得临床推广使用。     

Haplotype-based study of the association of alcohol and acetaldehyde-metabolising genes with alcohol dependence (with or without comorbid anxiety symptoms) in a Cape Mixed Ancestry population

Alcohol dependence (AD) has a large heritable component. Genetic variation in genes involved in the absorption and elimination of ethanol have been associated with AD. However, some of these polymorphisms are not present in an African population. Previous studies have reported that a type of AD which is characterized by anxious behaviour may be a genetically specific subtype of AD. We investigated whether variation in genes encoding cytochrome P450 2E1 (CYP2E1) or acetaldehyde-metabolising enzymes (ALDH1A1, ALDH2) might alter the risk of AD, with and without symptoms of anxiety, in a Cape population with mixed ancestry. Eighty case control pairs (one with AD, one without AD) were recruited and individually matched for potential confounders. Genotype data were available for 29 single-nucleotide polymorphisms (SNPs) across the three genes. Linkage disequilibrium D′ values were evaluated for all pairwise comparisons. Allele and haplotype frequencies were compared between cases and controls using a χ ² test. The ACAG haplotype in block 4 of the ALDH1A1 gene provided evidence of an association with AD (p?=?0.03) and weak evidence of an association with AD without symptoms of anxiety (p?=?0.06). When a genetic score was constructed using SNPs showing nominal evidence of association with AD, every extra risk allele increased the odds of AD by 35 % (OR 1.35, 95%CI 1.08, 1.68, p?=?0.008) and the odds of having AD with anxiety symptoms increased by 53 % (OR 1.53, 95%CI 1.14, 2.05, p?=?0.004). Although our results are supported by previous studies in other populations, they must be interpreted with caution due to the small sample size and the potential influence of population stratification.     

Pharmacokinetic and Pharmacodynamic Properties of a Micro-Dose Nasal Spray Formulation of Desmopressin (AV002) in Healthy Water-Loaded Subjects

Pharmaceutical Research - For some biological systems, there exist several models with somewhat different features and perspectives. We propose an evaluation method for NLME models by analyzing...     

Immunohistochemical localization of ORL-1 in the central nervous system of the rat

A novel member of the opioid receptor family (ORL-1) has been cloned from a variety of vertebrates. ORL-1 does not bind any of the classical opioids, although a high affinity endogenous agonist with close homology to dynorphin has recently been identified. We have generated a monoclonal antibody to the N-terminus of ORL-1 to map areas of receptor expression in rat central nervous system (CNS). Intense and specific immunolabeling was observed in multiple areas in the diencephalon, mesencephalon, pons/medulla, and spinal cord. In the telencephalon, intense labeling was observed in the neuropil throughout layers II–V in the neocortex, the anterior olfactory nuclear complex, the pyriform cortex, the CA1–CA4 fields and dentate gyrus of the hippocampus, and in many of the septal and basal forebrain areas. In contrast to other members of the opioid receptor family, light labeling for ORL-1 was observed in telencephalic areas such as caudate-putamen. In the cerebellum, ORL-1 immunoreactivity was only observed in the deep nuclei. Throughout the CNS the majority of labelling was localized to fiber processes and fine puncta, although labeled scattered perikarya were observed in a few brain areas such as the hilus dentate in the hippocampus and some nuclei in the brainstem and spinal cord. The present mapping study is consistent with the reported distribution of ORL-1 mRNA and provides the first immunohistochemical report on anatomical and cellular distribution of ORL-1 receptor in the rat CNS. © 1996 Wiley-Liss, Inc.     

左腋动脉和臂丛神经走行变异1例

笔者在标本解剖操作观察腋窝结构时发现1例左侧腋动脉与臂丛神经位置及走行出现变异,既往文献报道的变异多为腋动脉发出的分支与臂丛神经之间的位置与走行之间变异^[1-3],本次解剖观察发现腋动脉与臂丛神经的内侧束、外侧束和后束之间的位置关系出现变异,与既往报道有所不同,现报告如下。     

自体外周血造血干细胞联合自体骨髓移植治疗难治性淋巴瘤的临床分析

本研究通过回顾性分析自体外周造血干细胞移植、自体骨髓移植及二者联合移植在治疗难治性恶性淋巴瘤的疗效、毒副作用、造血和免疫功能恢复速度等临床方面的差异,总结归纳三种不同移植方式在治疗难治性淋巴瘤方面的优劣。68例难治性恶性淋巴瘤患者接受了大剂量放化疗结合自体造血干细胞移植治疗,其中10例患者为单一自体骨髓移植（autologous bone marrow transplantation,ABMT）,46例患者为单一自体外周血造血干细胞移植（autologous peripheral blood hematopoietic stem cell transplantation,APBHSCT）,12例患者为自体外周血造血干细胞联合自体骨髓移植（autologous peripheral blood hematopoietic stem cells transplantation combined with autologous bone marrow transplantation,APBHSCT＋ABMT）。结果表明：ABMT、APBHSCT、APBHSCT＋ABMT的治疗有效率和1、3、5年生存率分别为（90％和75％、57．1％、33．3％）;（86．4％和74．4％、54．2％、38．1％）;（83．3％和72．7％、55．6％、40％）。白细胞恢复时间分别为13天、11天、8天,血小板恢复时间分别为17天、14天、9天。在移植后3个月、6个月、1年时检测ABMT、APBHSCT、APBHSCT＋ABMT患者T细胞亚群正常率分别为（0％、33．3％、60％）,（10．8％、32％、73．9％）,（27．3％、55．6％、85．7％）。结论：自体外周血造血干细胞联合自体骨髓移植与单一自体外周造血干细胞移植治疗难治性恶性淋巴瘤的临床疗效和毒副作用当,但联合造血干细胞移植（APBHSCT＋ABMT）患者的造血功能恢复略快,有利于拓宽年龄偏大和造血功能受损患者移植方式的选择。     

社区护理人员开展健康教育的调查分析

目的 通过了解新疆石河子市社区卫生服务机构护理人员开展健康教育的现状,分析影响因素,为社区护士科学有效地开展健康教育提供依据.方法 采用问卷调查,对本市社区卫生服务机构的151名护理人员进行了调查.结果 社区护士普遍开展了健康教育,主要是通过健康咨询的方式宣传健康的生活方式和慢性病的防治知识,护士在健康教育过程中面临的最大困难依次是缺少资金、社区居民观念跟不上和缺少社区护士.结论 社区健康教育的对象主要为服务站的就诊者,内容和形式单一,且不够深入,社区护士缺乏健康教育的理论与技能,在健康教育与健康促进方面没有发挥应有的作用,应引起社区护理管理者的重视,制定切实可行的措施,发挥社区护士在健康教育中的作用.     

肢带型肌营养不良的MRI表现

目的 观察肢带型肌营养不良的MRI表现。方法 回顾性分析7例经临床及病理检查确诊为肢带型肌营养不良患者的MRI资料,观察双侧大腿肌群脂肪沉积与炎性水肿情况,采用4分法进行评价。并进行统计学分析。结果 肢带型肌营养不良患者大腿肌群MRI均可见脂质沉积和炎性水肿性改变。不同肌肉间脂肪沉积(χ²=75.596,P<0.01)与炎性水肿差异均有统计学意义(χ²=41.368,P<0.01),双侧大腿肌群间脂肪沉积与炎性水肿差异均无统计学意义(P均>0.05)。结论 肢带型肌营养不良患者大腿肌群MRI信号特点及分布具有一定特征,MR检查有助于疾病的诊断。