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在身体接触性项目高水平运动员中,与柔韧性、形体、加速、临床缺陷和即往损伤相关的运动损伤
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作者 高崇玄 《体育科学》 CSSCI 北大核心 2003年第2期140-140,共1页
关键词 身体接触性项目 高水平运动员 柔韧性 形体 加速 临床缺陷 运动损伤
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中医骨伤科临床缺陷专项整顿管理措施探讨
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作者 章蝶超 吴云芳 《中医药管理杂志》 2024年第11期209-211,共3页
目的:探讨和研究中医骨伤科临床缺陷专项整顿管理状况分析,通过管理措施提高骨科患者护理质量与水平。方法:随机选取医院2022年3月—2023年9月的139例骨科患者为研究对象,随机分为对照组69例与观察组70例,对照组患者根据常规的管理方法... 目的:探讨和研究中医骨伤科临床缺陷专项整顿管理状况分析,通过管理措施提高骨科患者护理质量与水平。方法:随机选取医院2022年3月—2023年9月的139例骨科患者为研究对象,随机分为对照组69例与观察组70例,对照组患者根据常规的管理方法及护理流程进行干预,观察组骨科护理患者给予中医骨伤科临床缺陷专项整顿管理措施及护理方法进行干预。比较两组患者的管理效果。结果:观察组中医骨伤科患者不良事件发生率显著低于对照组(P<0.05)。观察组中医骨伤科患者对护理质量评分显著高于对照组(P<0.05)。观察组中医骨伤科患者护理干预总满意率显著高于对照组(P<0.05)。结论:中医骨伤科临床缺陷调查中查对制度、低龄护理人员及护理人员配置情况问题较为突出,经过专项整顿管理干预后,中医骨伤科患者在护理不良事件发生情况、护理质量评分情况以及护理干预满意度情况均有不同程度的改善和好转,具有显著的应用效果。 展开更多
关键词 中医骨伤科 临床缺陷 专项整顿管理 实施效果
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神经内科常见临床护理缺陷的分析
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作者 李珍 王海霞 《辽宁中医药大学学报》 CAS 2006年第4期119-120,共2页
关键词 神经内科 临床护理缺陷 分析
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小学生的亚临床注意缺陷多动障碍及社会适应性
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作者 李庄阳 陈彩琦 《心理学进展》 2019年第7期1316-1323,共8页
探讨小学生注意缺陷多动障碍(ADHD)和亚临床ADHD问题的检出率及其与社会适应性的关系。以广州市、惠州市和澳门特别行政区的小学生为研究对象,让父母通过ADHD父母评定量表第4版,Conners父母用儿童行为量表,儿童适应行为评定量表以及自... 探讨小学生注意缺陷多动障碍(ADHD)和亚临床ADHD问题的检出率及其与社会适应性的关系。以广州市、惠州市和澳门特别行政区的小学生为研究对象,让父母通过ADHD父母评定量表第4版,Conners父母用儿童行为量表,儿童适应行为评定量表以及自编问卷对孩子的行为表现进行评定。结果发现,小学生亚临床ADHD的检出率相对ADHD较高,其行为适应问题与典型ADHD患者类似。因此,加强亚临床ADHD人群的临床和心理教育干预是非常迫切的。 展开更多
关键词 注意缺陷多动障碍 临床注意缺陷多动障碍 检出率 社会适应性
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临床护理服务缺陷原因分析及防范对策
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作者 王秀芝 《中国卫生产业》 2013年第9期51-51,53,共2页
目的分析临床护理缺陷的原因,探讨防范对策。方法对2011年1月—2012年10月发生的临床护理服务缺陷进行分析、调查。结果缺陷定性以护士的疏忽大意,责任心不强、对新设备操作不熟练,以及用错误发生之首。病区工作量大,治疗任务多、危重... 目的分析临床护理缺陷的原因,探讨防范对策。方法对2011年1月—2012年10月发生的临床护理服务缺陷进行分析、调查。结果缺陷定性以护士的疏忽大意,责任心不强、对新设备操作不熟练,以及用错误发生之首。病区工作量大,治疗任务多、危重病人多的科室为高危科室,新上岗的年轻护士是发生缺陷的高危人群。结论加强护士核心制度的培训,重视护理缺陷管理,加强年轻护士的培训和管理,合理配备人力资源,有效的降低护理风险,防范护理缺陷的发生。增强护士在临床工作中的预见性,为患者提供安全、舒适、有效的护理服务。 展开更多
关键词 临床护理服务缺陷 原因分析 预防对策
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白细胞介素-6、肿瘤坏死因子α和白细胞介素-10的产生与慢性血透病人的临床免疫缺陷状态相关
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作者 叶俊雅 Girndt-m +4 位作者 kohler-H Schiedhelm-Weick-E Schlaak-JF Meyer-Zum-Buschenfelde-KH Fleischer-B 《现代临床医学生物工程学杂志》 1996年第3期230-230,共1页
在慢性肾功能衰竭的病人中,单因子(Monokine)产生的改变是一个常见的特征.它们的临床关系尚未被证实.我们在此显示这些患者体外单核细胞受LPS刺激后,白细胞介素-6和肿瘤坏死因子α的过量产生与免疫缺陷的临床等级相关。白细胞介素-... 在慢性肾功能衰竭的病人中,单因子(Monokine)产生的改变是一个常见的特征.它们的临床关系尚未被证实.我们在此显示这些患者体外单核细胞受LPS刺激后,白细胞介素-6和肿瘤坏死因子α的过量产生与免疫缺陷的临床等级相关。白细胞介素-6和肿瘤坏死因子α的高水平引致免疫耐受状态.这就对乙型肝炎病毒疫苗无反应性.然而.具有良好免疫能力的患者的细胞因子显示与健康对照者有相同水平. 展开更多
关键词 白细胞介素-6 肿瘤坏死因子Α 白细胞介素-10 临床免疫缺陷 慢性肾功能衰竭 血液透析
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Hepatitis B and C virus co-infections in human immunodeficiency virus positive North Indian patients 被引量:7
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作者 Swati Gupta Sarman Singh 《World Journal of Gastroenterology》 SCIE CAS CSCD 2006年第42期6879-6883,共5页
AIM: To determine the prevalence of hepatitis B and C virus infections in human immunodeficiency virus (HIV) -positive patients at a tertiary care hospital in New Delhi, India. METHODS: Serum samples from 451 HIV ... AIM: To determine the prevalence of hepatitis B and C virus infections in human immunodeficiency virus (HIV) -positive patients at a tertiary care hospital in New Delhi, India. METHODS: Serum samples from 451 HIV positive patients were analyzed for HBsAg and HCV antibodies during three years (Jan 2003-Dec 2005). The control group comprised of apparently healthy bone-marrow and renal donors. RESULTS: The study population comprised essentially of heterosexually transmitted HIV infection. The prevalence Fate of HBsAg in this population was 5.3% as compared to 1.4% in apparently healthy donors (P 〈 0.001). Though prevalence of HCV co-infection (2.43%) was lower than HBV in this group of HIV positive patients, the prevalence was significantly higher (P 〈 0.05) than controls (0.7%). Triple infection of HIV, HBV and HCV was not detected in any patient. CONCLUSION: Our study shows a significantly high prevalence of hepatitis virus infections in HIV infected patients. Hepatitis viruses in HIV may lead to faster progression to liver cirrhosis and a higher risk of antiretroviral therapy induced hepatotoxicity. Therefore, it would be advisable to detect hepatitis virus coinfections in these patients at the earliest. 展开更多
关键词 Human immunodeficiency virus Hepatitis B Hepatitis C Hepatitis B surface antigen CO-INFECTIONS
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The Biology of Kaposi’s Sarcoma-Associated Herpesvirus and the Infection of Human Immunodeficiency Virus 被引量:1
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作者 Di QIN Chun LU 《Virologica Sinica》 SCIE CAS CSCD 2008年第6期473-485,共13页
Kaposi sarcoma-associated herpesvirus (KSHV),also known as human herpesvirus 8 (HHV-8),is discovered in 1994 from Kaposi's sarcoma (KS) lesion of an acquired immunodeficiency syndrome (AIDS) patient. In addition t... Kaposi sarcoma-associated herpesvirus (KSHV),also known as human herpesvirus 8 (HHV-8),is discovered in 1994 from Kaposi's sarcoma (KS) lesion of an acquired immunodeficiency syndrome (AIDS) patient. In addition to its association with KS,KSHV has also been implicated as the causative agent of two other AIDS-associated malignancies: primary effusion lymphoma (PEL) and multicentric Castleman’s disease (MCD). KSHV is a complex DNA virus that not only has the ability to promote cellular growth and survival for tumor development,but also can provoke deregulated angiogenesis,inflammation,and modulate the patient’s immune system in favor of tumor growth. As KSHV is a necessary but not sufficient etiological factor for KS,human immunodeficiency virus (HIV) is a very important cofactor. Here we review the basic information about the biology of KSHV,development of pathogenesis and interaction between KSHV and HIV. 展开更多
关键词 Kaposi sarcoma-associated herpesvirus (KSHV) BIOLOGY PATHOGENESIS HIV
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Intrahepatic cholestasis of pregnancy:When should you look further? 被引量:22
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作者 Winita Hardikar Shivani Kansal +1 位作者 Ronald P J Oude Elferink Peter Angus 《World Journal of Gastroenterology》 SCIE CAS CSCD 2009年第9期1126-1129,共4页
Pruritis with abnormal liver function tests is the classical presentation of intrahepatic cholestasis of pregnancy(ICP),a condition associated with significant fetal complications.Although the etiology of ICP is uncle... Pruritis with abnormal liver function tests is the classical presentation of intrahepatic cholestasis of pregnancy(ICP),a condition associated with significant fetal complications.Although the etiology of ICP is unclear in many cases,certain features of the clinical presentation should alert the practitioner to the possibility of an underlying metabolic defect, which may not only affect subsequent pregnancies, but may be an indicator of more serious subsequent liver disease.We report a kindred of Anglo-Celtic descent,among whom many members present with ICP,gallstones or cholestasis related to use of oral contraception.Genetic studies revealed a novel mutation in the ABCB4 gene,which codes for a phospholipid transport protein.The clinical significance of this mutation and the importance of identifying such patients are discussed. 展开更多
关键词 ABCB4 gene ABCB4 transporter PHOSPHOLIPIDS Cholestasis of pregnancy GALLSTONES
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Clinical analysis of primary central nervous system lymphoma with non-immune deficiency in 17 patients
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作者 Weiping Tao Zhiwei Wang Long Wu 《The Chinese-German Journal of Clinical Oncology》 CAS 2013年第1期40-42,共3页
Objective: The aim of this study was to investigate the clinical manifestations of primary central nervous system lymphoma (PCNSL) with non-immune deficiency and explore effective methods for its diagnosis and treatme... Objective: The aim of this study was to investigate the clinical manifestations of primary central nervous system lymphoma (PCNSL) with non-immune deficiency and explore effective methods for its diagnosis and treatment. Methods: The clinical, imaging and pathological data from 17 cases with PCNSL in our hospital from March 2006 to April 2009 were analyzed. The immunologic function test for all 17 cases was confirmed as normal. Four of them received stereotactie brain biopsy while the other patients were given full or partial resection. Fifteen of them were given both radiotherapy and chemotherapy after surgery. High-dose Methotrexate (HD-MTX) (2.0g/m2) was used via intravenous infusion once per week for three times. From week 4, patients began radiotherapy. Six cases with abnormal cerebrospinal fluid were given whole central nervous system radiotherapy, and 9 cases with normal cerebrospinal fluid were given only whole brain radiotherapy. Two of them were without any additional treatment after surgery. Sixteen of 17 cases were followed up for 9-48 months. Therapeutic efficacy, toxic and side effect were investigated. Results: Six cases, who were given HD-MTX chemotherapy and whole central nervous system radiotherapy, had grade 3 leukopenia, but other toxic and side effect above grade 3 were not observed. Two patients having no chemotherapy and radiotherapy recurred in one month, but there was only one recurred case in three months among 15 cases who had both chemotherapy and radiotherapy. One of them lost fellow-up. The 2-year survival rate was 69.2%. Conclusion: There is no specific clinical manifestation for PCNSL. The pathological examination is a reliable method to confirm PCNSL. Recurrence may occur after surgery alone, however, the combination of HD-MTX chemotherapy and radiotherapy is an effective and safe therapeutic option, which might improve the treatment efficiency and survival rate. 展开更多
关键词 central nervous system LYMPHOMA DIAGNOSIS TREATMENT
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Translational Benefits of Gene Therapy to Date
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作者 M Mary McMenamin 《Clinical oncology and cancer researeh》 CAS CSCD 2011年第1期10-15,共6页
Gene therapy is now a reality with a number of early phase clinical trials having been completed and several currently in progress. In spite of some early setbacks substantial progress has been made with treatment of ... Gene therapy is now a reality with a number of early phase clinical trials having been completed and several currently in progress. In spite of some early setbacks substantial progress has been made with treatment of several different diseases using a variety of delivery vectors and transgenes. Indeed for some diseases gene therapy is now the treatment of choice, in particular the inherited immune deficiencies. Treatment of ocular diseases and cancer are also showing great promise. Immune responses and insertional mutagenesis still pose problems but refinement of delivery systems and an increased understanding of oncogene activation should ensure that more successful protocols will emerge in the near future. Continuous progress suggests that a wider range of diseases can be treated with gene therapy in the future. 展开更多
关键词 gene therapy NEOPLASM clinical trial IMMUNOLOGY
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Clinical significance of"anti-HBc alone"in human immunodeficiency virus-positive patients 被引量:2
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作者 M~aTeresa Pérez-Rodríguez Bernardo Sopea +4 位作者 Manuel Crespo Alberto Rivera Teresa González del Blanco Antonio Ocampo César Martínez-Vázquez 《World Journal of Gastroenterology》 SCIE CAS CSCD 2009年第10期1237-1241,共5页
AIM: TO determine the prevalence and clinical relevance of isolated antibodies to hepatitis B core antigen as the only marker of infection (“anti-HBc alone”) among human immunodeficiency virus (HIV) type-1 infe... AIM: TO determine the prevalence and clinical relevance of isolated antibodies to hepatitis B core antigen as the only marker of infection (“anti-HBc alone”) among human immunodeficiency virus (HIV) type-1 infected patients. Occult hepatitis B infection frequency was also evaluated. METHODS: Three hundred and forty eight histories from 2388 HIV-positive patients were randomly reviewed. Patients with serological markers of hepatitis B virus (HBV) infection were classified into three groups: past hepatitis, "anti-HBc alone" and chronic hepatitis. Determination of DNA from HBV, and RNA and genotype from hepatitis C virus (HCV) were performed on "anti-HBc alone" patients. RESULTS: One hundred and eighty seven (53.7%) HIV-positive patients had markers of HBV infection: 118 past infection (63.1%), 14 chronic hepatitis (7.5%) and 55 "anti-HBc alone" (29.4%). Younger age [2.3-fold higher per every 10 years younger; 95% confidence intervals (Cl) 1.33-4.00] and antibodies to HCV infection [odds ratio (OR) 2.87; 95% CI 1.10-7.48] were factors independently associated with the "anti-HBc alone" pattern. No differences in liver disease frequency were detected between both groups. Serum levels of anti-HBs were not associated with HCV infection (nor viral replication or HCV genotype), or with HIV replication or CD4 level. No "anti-HBc alone" patient tested positive for HBV DNA. CONCLUSION: "Anti-HBc alone" prevalence in HIM- positive patients was similar to previously reported data and was associated with a younger age and with antibodies to HCV infection. In clinical practice, HBV DNA determination should be performed only in those patients with clinical or analytical signs of liver injury, 展开更多
关键词 Human immunodeficiency virus "Anti-HBcalone" Occult hepatitis Hepatitis B virus DNA Liverdisease
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纳米羟基磷灰石/聚酰胺66复合材料的研究及应用 被引量:14
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作者 温从游 孟纯阳 蒋电明 《中国组织工程研究》 CAS CSCD 2014年第3期464-469,共6页
背景:纳米羟基磷灰石在骨修复替代材料中有明显优势,但骨诱导活性低、力学性能差等缺陷限制了其临床应用。为克服弊端,国内外学者从仿生学等角度出发,以纳米羟基磷灰石为基础,掺杂、复合有机或无机材料,得到多种仿生复合材料。目的:综... 背景:纳米羟基磷灰石在骨修复替代材料中有明显优势,但骨诱导活性低、力学性能差等缺陷限制了其临床应用。为克服弊端,国内外学者从仿生学等角度出发,以纳米羟基磷灰石为基础,掺杂、复合有机或无机材料,得到多种仿生复合材料。目的:综述纳米羟基磷灰石/聚酰胺66复合材料的研究及应用进展。方法:应用计算机检索1987年1月至2012年12月PubMed数据库相关文章,检索词为"nano,hydroxyapatite,polyamide 66"。同时,计算机检索1987年1月至2012年12月中国期刊网全文数据库相关文章,检索词为"纳米,羟基磷灰石,聚酰胺66"。共检索到文献93篇,最终纳入符合标准的文献56篇。结果与结论:纳米羟基磷灰石/聚酰胺66复合材料具有良好的热稳定性、生物力学性能及生物相容性。目前,纳米羟基磷灰石/聚酰胺66复合材料研究及引用主要集中于人工椎体、人工椎板及椎间融合器等,并取得了良好临床治疗效果,但仍有很多问题尚需要解决,如诱导成骨、降解情况都缺少长期而详尽的随访资料,而且目前主要是通过细胞学、组织学等方面来评价其生物安全性,尚未涉及到分子水平。 展开更多
关键词 背景 纳米羟基磷灰石在骨修复替代材料中有明显优势 但骨诱导活性低、力学性能差等缺陷限制了其临床应用.为克服弊端 国内外学者从仿生学等角度出发 以纳米羟基磷灰石为基础 掺杂、复合有机或无机材料 得到多种仿生复合材料.目的 综述纳米羟基磷灰石 聚酰胺66复合材料的研究及应用进展.生物材料 骨生物材料 纳米 羟基磷灰石 聚酰胺66 人工椎体 人工椎板 椎间融合器 进展 863项目
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藤黄酸抗肿瘤作用机制及其纳米制剂的研究进展 被引量:12
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作者 白皎皎 陈新棉 +3 位作者 曾代文 汤明海 童荣生 蔡璐璐 《华西药学杂志》 CAS CSCD 2018年第6期656-659,共4页
藤黄酸是从植物藤黄中提取的主要有效活性成分,近年来发现藤黄酸对多种肿瘤有明显疗效,其作用机制较多,作用靶点广泛。但藤黄酸自身仍具有一些缺点,限制了其在临床上的应用。新型纳米技术能够克服藤黄酸的这些缺点,为藤黄酸新制剂的研... 藤黄酸是从植物藤黄中提取的主要有效活性成分,近年来发现藤黄酸对多种肿瘤有明显疗效,其作用机制较多,作用靶点广泛。但藤黄酸自身仍具有一些缺点,限制了其在临床上的应用。新型纳米技术能够克服藤黄酸的这些缺点,为藤黄酸新制剂的研究与开发提供了一种新方向。文中综述了近5年来国内外有关藤黄酸抗肿瘤机制以及其纳米制剂方面的进展,可为藤黄酸的进一步深入研究提供参考。 展开更多
关键词 藤黄酸 抗肿瘤 作用机制 纳米制剂 作用靶点 临床缺陷 靶向性 新方向 研究进展
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Glucose metabolic abnormality is associated with defective mineral homeostasis in skeletal disorder mouse model 被引量:1
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作者 ZOU JiangHuan XIONG XiWen +3 位作者 LAI BeiBei SUN Min TU Xin GAO Xiang 《Science China(Life Sciences)》 SCIE CAS CSCD 2015年第4期359-367,共9页
Bone was reported as a crucial organ for regulating glucose homeostasis. In this study, we found that Phex mutant mice(PUG), a model of human X-linked hypophosphatemic rickets(XLH), displayed metabolic abnormality in ... Bone was reported as a crucial organ for regulating glucose homeostasis. In this study, we found that Phex mutant mice(PUG), a model of human X-linked hypophosphatemic rickets(XLH), displayed metabolic abnormality in addition to abnormal phosphate homeostasis, skeletal deformity and growth retardation. Glucose tolerance was elevated with enhanced insulin sensitivity in PUG, though circulating insulin level decreased. Interestingly, bone mineral density defects and glucose metabolic abnormality were both rescued by adding phosphorus- and calcium-enriched supplements in daily diet. Serum insulin level, glucose tolerance and insulin sensitivity showed no differences between PUG and wild-type mice with rescued osteocalcin(OCN) following treatment. Our study suggested that OCN is a potential mediator between mineral homeostasis and glucose metabolism. This investigation brings a new perspective on glucose metabolism regulation through skeleton triggered mineral homeostasis and provides new clues in clinical therapeutics of potential metabolic disorders in XLH patients. 展开更多
关键词 glucose metabolism mineral homeostasis bone PHEX X-linked hypophosphatemic rickets
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