苯妥英钠血清浓度监测（31例报告）

报告31例口服DPH治疗的门诊癫痫病人RIA法血清DPH浓度监测结果。在随访中记录的临床治疗反应。病人平均药物剂量为4．39±1．19mg/kg／d，不同病人服用同一剂量DPH，其血清药物旅度可相差9倍。22例获良好(较好)的治疗反应，其平均有效血清药物浓度为24．1±10．1μg／ml。9例出现中毒反应；血清药物浓度在25μg／ml以上时可出现眼球震颤、视物模糊，共济失调。DPH血清浓度监测有功于实现个体化给药方案，提高疗效并避免中毒。     

家蚕的抗氟性及其与数量性状的相关研究

测定家蚕幼虫抗氟中毒的抵抗能力,4龄>3龄>2龄。强抗原种杂变组成的杂种一代,抗性介于两亲之间,弱抗原种杂交组成的杂种一代,其抗性表现出超亲的遗传现象,不同浓度的氟素对品种间的生长发育影响有着显著的差异,说明了品种间的抗氟能力存在着差别;抗氟性与DNV抗性有着显著的相关性;与茧质性状表现为不显著的正相关,抗氟性与蚕血中Ca~(2+)、Mg~(2+)含量无明显的相关关系。     

Microstructure of the non-rapid eye movement sleep electroencephalogram in patients with newly diagnosed Parkinson's disease: effects of dopaminergic treatment.

We investigated non-rapid eye movement (non-REM) sleep in patients with newly diagnosed Parkinson's disease (PD) who had never previously received dopaminergic medication. There were no significant differences in the conventional sleep parameters between de novo patients with PD and a healthy control group, but the length of stage 1 sleep and the number of awakenings increased significantly upon administration of dopaminergic drugs. Analyzing the quantitative electroencephalogram (EEG), we observed a significant reduction in the low-delta frequency range and a nonsignificant increase in the sigma frequency range in de novo patients with PD. The dopaminergic medication also nonsignificantly reduced the low-delta and sigma frequencies, the latter to the level of the controls. Possible mechanisms that may account for the observed differences are discussed. It is suggested that Parkinson's disease as well as the application of dopaminergic drugs exerts a desynchronizing effect on the sleep EEG that is reflected in a disruption of sleep continuity.     

Evaluation of a Swedish version of the Arthritis Self-Efficacy Scale.

There is a great need today for clinically useful instruments in the rehabilitation of chronic pain patients. The Arthritis Self-efficacy Scale measures patients' perceived self-efficacy to cope with the consequences of chronic arthritis. The aim of the present study was to evaluate a Swedish version of the Arthritis Self-efficacy Scale with respect to factor structure and reliability. Twenty-five chronic pain patients and twenty-four rheumatology patients were given a Swedish version of the Arthritis Self-efficacy Scale twice within a three week interval. The three factor structure of the scale was confirmed; Cronbach's alpha for internal consistency ranged between 0.82-0.91 and test-retest correlations ranged between 0.81-0.91, showing that the instrument satisfactorily met psychometric standards.     

The disability rating index: An instrument for the assessment of disability in clinical settings

The purpose of this study was to evaluate an instrument for assessment of physical disability, mainly intended for clinical settings, the Disability Rating Index (DRI). Healthy persons (n = 1092), both white and blue collar workers, and patients (n = 366) with different levels of physical capacity, were assessed. Most of the patients (n = 303) underwent rehabilitation programmes for neck/shoulder/low-back pain but some (n = 47) were arthritis patients waiting for hip or knee replacement surgery, or wheelchair patients with multiple sclerosis (n = 16). The reliability was investigated by test-retest studies, intra- and inter-rater and internal consistency studies. Five construct validity tests were carried out: a discrimination study; a converging validity test; a test for sensitivity to small alterations in health status; and two correlational validity tests. Correlation of the self-reported DRI to the actual performance in similar activities was carried out. Responsiveness was tested by correlation of the DRI before/after replacement surgery for arthritis. The test-retest correlations were 0.83–0.95 in the studies, including correlation of different versions. The intra- and inter-rater reproducibility was 0.98 and 0.99 respectively. The Kruskal-Wallis test in the discrimination study yielded p < 0.0001. More than 90% of the respondents completed the questionnaire correctly. Correlation of the DRI to the Functional Status Questionnaire was 0.46. The responsiveness was excellent, p = 0.0001. The DRI proved to be a robust, practical clinical and research instrument with good responsiveness and acceptability for assessment of disability caused by impairment of common motor functions.     

顺铂对结直肠癌肿瘤浸润淋巴细胞杀伤活性的影响

为在临床选择有效的免疫化疗方案提供一定的理论依据，作者以结直肠癌肿瘤浸润淋巴细胞（ＴＩＬ）和顺铂（ＣＤＤＰ）为研究对象，对１６名手术治疗的结直肠癌患者，分别观察ＣＤＤＰ体内注射及体外预处理ＴＩＬ和Ｒａｊｉ细胞对ＴＩＬ表面标志和杀伤活性的影响。流式细胞仪检测结果显示，静脉注射ＣＤＤＰ能增加结直肠癌ＴＩＬ中ＣＤ３＋／ＣＤ４＋和ＣＤ３＋／ＣＤ８＋细胞含量，同时增强ＴＩＬ体外杀伤Ｒａｊｉ细胞的活性；而体外以ＣＤＤＰ处理Ｒａｊｉ细胞能增强其对结直肠癌ＴＩＬ杀伤的敏感性。作者认为，对于联合应用ＴＩＬ和ＣＤＤＰ治疗结直肠癌的临床效果有必要进一步研究。     

基础医学教师课堂教学质量评价

为了了解本科教师的教学质量和教学效果 ,教学专家和学生评价了 14 7位基础医学教师。结果显示 ,讲师以上职称教师的教学质量明显好于初级职称教师 (P<0 .0 5 ) ,高级职称教师教学的科学性、艺术性和思想性明显好于讲师和助教 (P<0 .0 5 )。文章还对教学中存在的问题和对策进行了讨论。     

医院综合效益评价中的权数（三）——估计权数

在医院综合效益评价中，估计权数由评价专家根据经验对评价指标的重要程度的一种评估，这类数据通常用的ＡＨＰ法进行处理。本文用ＡＨＰ的递推算法计算估计权数，这种算法不仅计算简单，而且易达到一致性的要求，其估计的剩余误差小于ＡＨＰ法。     

超声定量检查技术新进展

近年来，超声定量检查技术在临床的应用为心血管疾病患者的心功能评估提供了量化的依据，本文介绍了超声诊断仪的使用部分最新定量检查技术。     

白芍总苷治疗口腔扁平苔藓的疗效评价研究

目的：观察羟氯喹及羟氯喹与白芍总苷两者合并治疗口腔扁平苔藓（OLP）的疗效,并且同时比较两种定性疗效评价方法,对OLP的损害程度和治疗效果进行评价。方法：随机选取两组初诊患者,分别采用羟氯喹及羟氯喹与白芍总苷治疗三个月,使用绝对数值标准和相对变化标准分别计算。结果：白芍总苷和羟氯喹联合用药,对OLP糜烂型和充血型损害有效。单用羟氯喹治疗OLP糜烂型和充血型损害无效。对于OLP斑纹型损害,两组均有效。白芍总苷和羟氯喹联合用药治疗OLP,可以减少羟氯喹的不良反应。采用＂绝对数值标准＂的定性评价方法与采用＂相对变化标准＂的定性评价方法相比,具有记录简便、评价准确的优点。结论：白芍总苷辅助治疗口腔扁平苔藓有效;绝对数值标准高效准确。