高效液相色谱/质谱法检测人尿中的糖皮质激素及其它兴奋剂

采用液相色谱/质谱(LC/MS)方法检测糖皮质激素、甾体和β2激动剂。本文采用Zorbax 30 mm×2.1mm,1.8μm短柱,对12种糖皮质激素、3种甾体和2种β2激动剂的液相色谱/质谱的测定方法进行了研究,建立了6分钟内快速检测人尿中多种糖皮质激素、甾体和β2激动剂的测定方法。检测限低于5ng/ml。该方法适用于兴奋剂的筛选及确证。     

颅内动脉瘤合并脑血管痉挛栓塞术后的观察与护理

目的:探讨颅内动脉瘤合并脑血管痉挛栓塞术后观察与护理的重要性。方法:本组36例颅内动脉合并脏血管痉挛患者入院72h内在全麻下行颅内动脉瘤栓塞术。术前、术中常规罂粟硷30mg/10ml持续静脉内泵入,术后持续泵入3d,给予尼莫通抗血管痉挛。术后第2天开始实施三高疗法,术后常规腰大池引流,放出血性脑脊液。结果:本组行颅内动脉瘤栓塞术后,32例恢复良好(可恢复工作,无明显神经系统功能障碍),2例持续昏迷自动出院;2例中度致残(轻度神经系统功能障碍,但生活能自理)。结论:利用护理手段干预4方面中的可控因素,如平均动脉压、颅内压、中心静脉压、血流速度(血液稀释度),使其控制在预设定目标范围内可保证脑的有效灌注压,预防CVS的发生。     

早期乳腺导管原位癌X线表现与预后生物学标记关系的研究

目的评价乳腺导管原位癌（DCIS）及DCIS伴微浸润的X线片表现，分析X线表现与预后生物学标记的相关性。方法对50例乳腺DCIS及45例DCIS伴微浸润的患者行X线检查，共62例行预后生物学标记，分析影像表现与孕激素受体（PR）、癌基因（C—erbB-2）、抑癌基因（p53）的相关性。用卡方检验进行统计学处理，并对有意义者行优势比（OR值）分析。结果（1）单独1个X线征象表现者62例；合并2个征象26例；阴性7例。（2）各种X线征象单独分析显示，62例有钙化的病灶中恶性钙化占73％（45例），其余为中间性钙化；钙化以簇状分布最为常见（36例），其次为段样分布（18例）。22例有肿块的病灶中，以卵圆形肿块最为常见（13例）；肿块的边缘表现为浸润、小分叶、清晰和模糊各为15、1、4和2例；等密度肿块占的比例较高（55％，12例）。结构扭曲7例，除1例外多与其他征象伴行；局灶性不对称占16％（15／95），可单独发生或与其他征象伴发。（3）将病灶的X线表现分成恶性钙化、中间性钙化和非钙化3组，PR与C-erbB-2在3组中的分布有统计性意义，PR阳性表达者X线上非钙化征象发生率是中间性钙化的11．00倍[χ^2=8．571，P=0．003；95％可信区间（CI）为1．998～60．572]、恶性钙化的8．80倍（χ^2=9．748，P=0．002；95％CI为2．024～38．253）；而C—erbB-2高表达者，恶性钙化是非钙化发生的12．35倍（χ^2=7．353，P=0．007；95％CI为1．447—105．443），中间性钙化的5．74倍（χ^2=4．977，P=0．026；95％CI为1．110～29．645）。结论乳腺DCIS及DCIS伴微浸润X线征象有特征。X线征象可以作为早期乳腺DCIS的一个预后因子。     

直肠癌根治会阴部造口术后二期股薄肌移植肛门成形

目的　回顾性总结32例直肠癌根治会阴部造口术后二期股薄肌移植肛门成形术的治疗效果。方法　采用Williams 5级评分法对重建前后肛门功能进行评价。结果　二期股薄肌移植肛门成形术前,32例患者肛门功能均在4级以上[4级28.4%(9/32),5级71.6%(23/32)],二期股薄肌移植肛门成形术后肛门功能明显好转。结论　二期股薄肌移植肛门成形术是直肠癌根治会阴部造口术后有效的肛门重建手段。     

Complex segregation analyses of bone mineral density in Chinese

China has the largest population in the world; approximately 7% of the total population suffers from primary osteoporosis. Osteoporosis is mainly characterized by low bone mineral density (BMD). In the present study, familial correlation and segregation analyses for spine and hip BMDs have been undertaken for the first time in a Chinese sample composed of 401 nuclear families with a total of 1,260 individuals. The results indicate a major gene of additive inheritance for hip BMD, whereas there is no evidence of a major gene influencing spine BMD. Significant familial residual effects are found for both traits, and heritability estimates (±SE) for spine and hip BMDs are 0.807(0.099) and 0.897(0.101), respectively. Sex and age differences in genotype‐specific average BMD are also observed. This study provides the first evidence quantifying the high degree of genetic determination of BMD variation in the Chinese.     

Treatment of severe subglottic laryngotracheal stenosis using hyoid graft with sternohyoid muscle flap]

OBJECTIVE: To evaluate the possibility and reliability of the hyoid-sternohyoid graft transfer in the correction of server subglottic laryngotracheal stenosis, and delineate the operation skills and clinical results. METHODS: Seven patients with severe subglottic stenosis underwent laryngotracheal reconstruction using the hyoid grafts with sternohyoid muscle flaps (HG-SHMF). Five of these patients had traumatic subglottic stenosis, one with scar tissue of unknown etiology arising in the subglottic region, another with tracheal narrowing caused by inhalation of hydrochloric acid. RESULTS: All seven patients were successfully decannulated with moderate good voice. The average time from reconstruction to decannulation was 15.4 months. The stent was endoscopically removed with a range of 3 to 22 months; the mean time required for stenting was 9.6 months. Two patients who received additional salvage reconstruction procedures because of graft or stent displacement were extubated with improved voices and satisfactory airway. CONCLUSIONS: The HG-SHMF transfer was a single-stage reconstruction, relatively simple procedure that can restore an adequate airway and a good voice. Patients undergoing laryngotracheal reconstruction with HG-SHMF must have regular, long-term follow-up since graft displacement and recurrent granulation tissue or scar reformation can cause restenosis after an initially successful surgery. This procedure should be used in a large number of patients to further test its reliability.     

甘露醇和低温对兔骨骼肌缺血再灌流损伤的保护作用

通过兔后肢缺血模型，观察了甘露醇和低温对骨骼肌缺血再灌流损伤的保护作用。结果：甘露醇和低温可以不同程度地降低再灌流后患肢静脉回流血中细胞内酶（ＣＰＫ、ＬＤＨ、ＡＳＴ）的活性和脂质过氧化反应终末代谢产物丙二醛（ＭＤＡ）的含量，减轻骨骼肌细胞超微结构的破坏。两者单独应用效果不明显（Ｐ＞０．０５），联合应用效果非常明显（Ｐ＜０．０１）。提示自由基介导的脂质过氧化反应参与骨骼肌缺血再灌流损伤，甘露醇和低温对其具有协同保护作用。     

中风后癫痫的临床研究

本文报告３６例中风后癫痫发作的临床和ＣＴ资料。通过回顾性病历复习和随访发现，中风后癫痫的发生率占同期住院中风患者的５．２６％，以蛛网膜下腔出血和脑栓塞发生癫痫比率最高，分别为１５％和１２．５％。癫痫发作与ＣＴ所见病灶分布密切相关，皮质病灶较皮质下病灶更易发生病病。癫痫发作可发生于中风后任何时期，但早期癫痫以出血性中风多见，而迟发性癫痫则更多见于脑梗塞患者。     

PAI－1糖基化位点突变体的构建及其在哺乳动物细胞中表达

Ⅰ型纤溶酶原激活物抑制剂（ＰＡＩ－１）是一种Ｍｒ为５０×１０３的单链糖蛋白，有３７９个氨基酸残基，３个Ｎ型糖基化位点。构建ＰＡＩ－１糖基化突变体，以便研究糖链的功能。用寡核苷酸定位突变技术将３个糖基化位点２０９，２６５，３２９位进行突变，把３个糖基化位点都发生了突变的ＰＡＩ－１ｃＤＮＡ组装到真核表达载体ｐＳＶ２中，得到真核表达质粒ｐＺＨ－ｐ１－Ｍ３Ｅ；在二氢叶酸还原酶缺陷型中国仓鼠卵巢细胞（ＣＨＯｄｈｆｒ－）中进行短暂表达，用发色底物法和夹心ＥＬＩＳＡ方法检测培养液中ＰＡＩ－１的活性和含量。结果：糖基化位点突变的ＰＡＩ－１能在ＣＨＯ细胞中表达，但表达水平及活性较低。非糖基化ＰＡＩ－１的活性和抗原分别为４．３４ＩＵ／ｍｌ和３．１５μｇ／Ｌ结论：用寡核苷酸定位突变方法获得了ＰＡＩ－１糖基化突变体，并且在ＣＨＯ细胞中得到表达。     

狭缝印迹杂交分析癌转移抑制基因nm23在人肺癌中的表达

为探讨癌转移抑制基因在人肺癌发生、发展中的作用，采用狭缝印迹杂交技术检测了不同部位、不同性质人肺组织中的ｎｍ２３－Ｈ１和ｎｍ２３－Ｈ２基因的ｍＲＮＡ表达。结果发现，ｎｍ２３－Ｈ１和ｎｍ２３－Ｈ２ＡＤＬＤＲ ＭｒｎａＧＥ ＤＰ ，ＦＴＪＢ