中外护理高等教育的文献研究

目的分析国内外护理高等教育研究的现状、热点和发展趋势,为我国护理高等教育提供参考。方法利用PubMed和CNKI检索发达国家(美国、英国)和发展中国家(土耳其、泰国、中国)2000年4月21日至2010年4月21日发表的关于护理高等教育的文献。结果 PubMed收录护理高等教育研究文献1514篇,CNKI收录1070篇。中国关于教学方法的研究多于国外;国内外都比较关注计算机辅助学习(CAL)教学法的研究。课程设置方面,中国的实习模式局限于对早期接触临床或穿插实习2种模式的研究,国外则包括以社区为基础、服务中学习等多种模式。国外课程内容的研究具有时代性,而中国还主要集中在对专业基础课等的研究。国外师资的研究多于国内。国外存在多种形式的评价模式,中国对评价模式的研究还是空白。中国关于培养目标的研究较国外多。结论各国对护理高等教育的研究侧重点不同,中国可借鉴国外先进的教学经验,在教学方法、课程设置、师资、教育评价、培养目标5个方面进行改进,以提高我国护理高等教育教学质量。     

老年血液透析患者不同超滤量状态下血压及心功能的观察与护理

目的:探讨老年尿毒症血液透析患者不同超滤量状态下对血压及心功能影响的观察与护理.方法:选取108名老年血液透析患者,接其超滤量小于2.5Kg或大于2.5Kg,设为A、B两组,透析时按干体重定超滤量,观察不同超滤量状态下对血压及心功能的影响,并分别进行针对性护理.结果:两组患者在透析前后血压及左心室舒张末期内径(LVDd)、射血分数(EF)有差异,P＜0.01.结论:老年患者对容量负荷耐受性差,超滤量大,容易有血压波动、心功能损害;针对性的护理可防范不良反应,减少心血管事件发生.     

Genome-wide copy number variation association study suggested VPS13B gene for osteoporosis in Caucasians

Summary

Osteoporotic fracture (OF) is a serious outcome of osteoporosis. Important risk factors for OF include reduced bone mineral density and unstable bone structure. This genome-wide copy number variation association study suggested VPS13B gene for osteoporosis in Caucasians.

Introduction

Bone mineral density (BMD) and femoral neck cross-sectional geometric parameters (FNCSGPs) are under strong genetic control. DNA copy number variation (CNV) is an important source of genetic diversity for human diseases. This study aims to identify CNVs associated with BMD and FNCSGPs.

Methods

Genome-wide CNV association analyses were conducted in 1,000 unrelated Caucasian subjects for BMD at the spine, hip, femoral neck, and for three FNCSGPs —cortical thickness (CT), cross-section area (CSA), and buckling ratio (BR). BMD was measured by dual energy X-ray absorptiometry (DEXA). CT, CSA, and BR were estimated using DEXA measurements. Affymetrix 500K arrays and copy number analysis tool was used to identify CNVs.

Results

A CNV in VPS13B gene was significantly associated with spine, hip and FN BMDs, and CT, CSA, and BR (p?<?0.05). Compared to subjects with two copies of the CNV, carriers of one copy had an average of 14.6%, 12.4%, and 13.6% higher spine, hip, and FN BMD, 20.0% thicker CT, 10.6% larger CSA, and 12.4% lower BR. Thus, a decrease of the CNV consistently produced stronger bone, thereby reducing osteoporotic fracture risk.

Conclusions

VPS13B gene, via affecting BMD and FNCSGPs, is a novel osteoporosis risk gene.     

改良消蚀法制备脱细胞真皮基质微粒及其生物相容性评价

目的:利用改良消蚀法制备一种新型脱细胞真皮基质(Acellular dermal matrix,ADM)微粒,并对其相容性加以评价,为组织工程微粒皮肤的制备奠定研究基础。方法:应用机械法切除猪真皮乳头层,结合消蚀法和冻融法除去网状真皮中的所有细胞制备成ADM,将ADM搅碎成颗粒状,对其做细胞毒性实验和皮下埋藏实验检验其相容性。结果:该方法制备的ADM微粒韧性好,细胞去除完全,胶原三维稍松散但结构完整,无基底膜和乳头层。细胞毒性实验显示其基本无毒性,成纤维细胞在ADM微粒上增殖良好,皮下埋藏试验未见明显排异反应,ADM微粒能诱导血管和成纤维细胞长入。结论:用改良消蚀法制备的ADM微粒抗原性低、相容性好,可以作为组织工程微粒皮肤的支架和填充材料。     

经胸乳径路腔镜甲状腺切除术91例

目的：探讨经胸乳径路腔镜甲状腺手术的临床效果。方法：全麻下行胸乳径路腔镜甲状腺切除术91例,其中结节性甲状腺肿48例,甲状腺腺瘤38例,甲状腺乳头状癌5例。结果：91例均顺利完成手术,手术时间50～195min,平均（120.5±29.6）min;术后发生颈部皮下积液和一过性声音嘶哑各1例。随访2～44个月,中位数21个月,无复发,患者对手术及美容效果均表满意。结论：胸乳径路腔镜甲状腺切除术是安全可行的,具有很好的美容效果。     

不同浓度罗哌卡因腹横肌平面阻滞用于剖宫产术后镇痛的效果

目的探讨不同浓度罗哌卡因腹横肌平面(transversus abdominis plane,TAP)阻滞用于剖宫产术后镇痛的效果。方法选择ASAⅠ或Ⅱ级剖宫产产妇150例,随机均分为三组:A组、B组和C组术后双侧TAP分别注射0.25%、0.20%、0.15%罗哌卡因1.5mg/kg,并使用PCIA。观察和记录术后4、8、12、24和48h产妇VAS评分。并记录产妇镇痛满意率、镇痛泵按压次数及发生TAP相关并发症(穿破腹膜入腹腔、腹壁严重损伤、感染出血、局麻药误入血管及局麻药中毒)。结果与C组比较,术后不同时点A组产妇VAS评分明显降低(P0.05)。术后不同时点A组和B组VAS评分差异无统计学意义。与C组比较,A组和B两组产妇对镇痛满意率明显增加、镇痛泵按压次数明显减少(P0.05)。三组产妇未发生穿破腹膜入腹腔、腹壁严重损伤、感染出血、局麻药误入血管及局麻药中毒等TAP相关并发症。结论 0.20%以上罗哌卡因TAP阻滞联合PCIA用于剖宫产术后镇痛是安全有效的。     

Paracrine factors from mesenchymal stem cells: a proposed therapeutic tool for acute lung injury and acute respiratory distress syndrome

Despite extensive researches in acute lung injury (ALI) and acute respiratory distress syndrome (ARDS), current pharmacological therapies and respiratory support are still the main methods to treat patients with ALI and ARDS and the effects remain limited. Hence, innovative therapies are needed to decrease the morbidity and mortality. Because of the proven therapeutic effects in other fields, mesenchymal stem cells (MSCs) might be considered as a promising alternative to treat ALI and ARDS. Numerous documents demonstrate that MSCs can exert multiple functions, such as engraftment, differentiation and immunoregulation, but now the key researches are concentrated on paracrine factors secreted by MSCs that can mediate endothelial and epithelial permeability, increase alveolar fluid clearance and other potential mechanisms. This review aimed to review the current researches in terms of the effects of MSCs on ALI and ARDS and to analyse these paracrine factors, as well as to predict the potential directions and challenges of the application in this field.     

Patients with multiple morphological abnormalities of the sperm flagella harbouring CFAP44 or CFAP43 mutations have a good pregnancy outcome following intracytoplasmic sperm injection

Multiple morphological abnormalities of the sperm flagella (MMAF) are a rare type of male infertility. Mutations in DNAH1, CFAP43 and CFAP44 are the main aetiology of the disorder. Previously, good intracytoplasmic sperm injection (ICSI) outcomes were reported for MMAF patients with DNAH1 mutations. However, the ICSI prognosis for MMAF patients with CFAP43 or CFAP44 mutations was not known. We designed a retrospective cohort study. Molecular genetic testing identified six MMAF patients with biallelic CFAP44 (CFAP44⁺ group) or CFAP43 mutations and 12 patients with homozygous or compound heterozygous DNAH1 mutations (DNAH1⁺ group). A control group consisted of age‐matched, non‐MMAF men. For MMAF patients carrying CFAP44 mutations, the recorded rates of fertilisation, transferable embryos, pregnancy and delivery after ICSI were 76.47%, 88.46%, 50.0% and 50.0% respectively. The fertilisation rate was significantly higher in the CFAP44⁺ group than in the DNAH1⁺ group (76.47% vs. 54.5%, p = 0.0196). There were no statistically significant differences in the rates of transferable embryos, implantation, clinical pregnancy and miscarriage between the CFAP44⁺ group and either the DNAH1⁺ group or the age‐matched control group. Our results support a good ICSI prognosis for MMAF patients carrying CFAP44 or CFAP43 mutations.     

钙调蛋白及其突变体与电压门控钠离子通道1.2异亮氨酸-谷氨酰胺基序的结合作用

目的: 探讨在不同钙离子浓度下电压门控钠离子通道（Na_V）1.2与钙调蛋白（CaM）的结合,并分析CaM的钙离子结合位点突变后与Na_V1.2结合能力的变化。方法: 应用PCR技术构建Na_V1.2蛋白片段异亮氨酸-谷胺酰胺（IQ）基序的cDNA,采用QIAGEN点突变技术构建CaM突变体（CaM₁₂、CaM₃₄、CaM₁₂₃₄）,应用牵出（pull-down）试验技术检测有钙（100 nmol/L钙离子浓度）和无钙条件下Na_V1.2 IQ与CaM及其突变体（CaM₁₂、CaM₃₄、CaM₁₂₃₄）的结合情况。结果: CaM与Na_V1.2 IQ在无钙和有钙情况下均可互相结合,而单独重组谷胱甘肽-S-转移酶（GST）不具有与CaM结合的能力。无钙条件下CaM与Na_V1.2 IQ的结合量大于有钙条件下两者的结合量（P < 0.05）;无钙条件下,CaM野生型与Na_V1.2 IQ结合量大于CaM突变体与Na_V1.2 IQ的结合量,其中CaM₁₂₃₄的结合能力在三个突变体中最弱（P < 0.05）。结论: CaM及其突变体对Na_V1.2 IQ的结合具有钙离子依赖性,这一CaM调控Na_V1.2新机制为离子通道疾病研究提供了一定依据。