火器伤后胸心异物存留

目的：探讨火器伤后胸心异物存留摘除的指征、时机、方法及结果。方法：回顾性分析了３９例火器伤后胸心异物存留摘除者的一般资料、临床表现、不同处理方法的选择及效果。结果：１９例患者早期因凝固性血胸及肺持续漏气伴异物存留或异物存留伴胸腔及心包腔化脓性感染，在开胸清创时做了异物摘除；另２０例患者为胸伤伤情恢复后单纯异物存留，因异物位于肺门、心脏及大血管旁或远期并发症等，而后期开胸异物摘除。结论：火器性胸部穿透伤后，因异物本身或其他原因所致早期并发症者，应在开胸清创的同时摘除异物；胸伤伤情恢复而单纯胸心异物存留，应选择性摘除或因并发远期并发症而摘除。     

已婚育龄妇女避孕措施变化趋势分析

目的:了解已婚育龄妇女避孕措施的变化趋势,为指导计划生育服务工作提供科学依据。方法:收集1983~2005年苏州市已婚育龄妇女避孕方法的资料,并用统计软件对其变化趋势进行了分析。结果:已婚育龄妇女节育率在88.38%~92.94%范围波动,长效避孕措施现用率从75.19%下降至71.27%,而短效避孕措施从12.86%上升至17.11%。宫内节育器的现用率从50.09%上升到66.50%;避孕套从1.94%上升到14.21%;其他避孕方法的现用率均呈下降趋势,其中女性绝育现用率从24.42%下降到4.50%。结论:节育率维持在较高水平;长效避孕措施现用率下降而短效避孕措施现用率上升;避孕方法使用趋于多样化,需要提供满足个性化需求的指导和服务。     

心脏机械瓣膜置换术后分娩的临床研究

目的 探讨心脏机械瓣膜置换术后分娩的临床处理措施。方法 对19例心脏机械瓣膜置换手术后妊娠及分娩的资料进行回顾性分忻。结果 19例心脏机械瓣膜置换术后产妇均安全度过孕产期。分娩前后心功能Ⅰ～Ⅲ级，分娩时出血200～260m1，胎儿体重2950--3146g。无母婴死亡者，无胎儿出血以及畸形者。结论 心脏机械瓣膜置换术后心功能Ⅰ～Ⅲ级可安全度过孕产期。分娩采用剖宫产术为宜。妊娠期间口服抗凝剂(华法林)不增加分娩时母婴出血和新生儿畸形。     

某化工厂1987～2000年164例工伤事故调查分析

目的调查分析某化工厂工伤事故的分布规律及其危险因素,以便采取相应的预防干预措施。方法对1987～2000年该化工厂发生的工伤事故进行回顾性调查分析,建立数据库,并统计分析。结果 ①事故以轻伤为主,约占80.0％。②事故类别主要是灼烫烧伤和机械伤害,分别为工伤事故总数的35.8％、28.5％。③工伤伤害性质以骨折多见,约为总数的56.1％。④受伤工人的年龄分布以30～40岁段为主,约为总数的31.1％。⑤工伤事故原因中注意力不集中和违反操作规程分别为总数的43.0％,38.3％。结论12根据上述流行病学特点,采取相应的措施来减少工伤事故的发生。     

扩散管配制甲醛标准气体的研究

介绍了扩散法配制标准气体的方法。以三聚甲醛为原料，通过加热催化分解三聚甲醛蒸气，来配制甲醛标准气体。讨论了配制甲醛标准气体的准确性、稳定性、重复使用性，以及温度、扩散管几何尺寸、载气气流、配气源物质的量等因素对三聚甲醛扩散率的影响。本方法制备的甲醛标准气体，扩散率（２～５０μｇ／ｍｉｎ）测定总不确定度小于５％。     

宫颈癌组织中HPV16 E7序列多态性分析

目的探讨广东地区宫颈癌组织中HPV16肿瘤相关性抗原E7基因序列的多态性.方法采用通用引物PCR直接测序法对宫颈癌标本中的HPV分型,从含有HPV16型的标本中采用自行设计的多重引物通过巢式PCR扩增出HPV16E7,经DNA序列测定法检测其基因变异,进而寻找其热点突变.结果50例宫颈癌组织HPV-DNA的检出率为78%,其中HPV16和HPV18型混合感染18例,单纯HPV16型感染15例.33例含有HPV16型的标本中扩增出25例HPV16E7,其中17例647位核苷酸“T”变异“C”,导致相应的蛋白质由天冬氨酸变异为丝氨酸.结论广东地区宫颈癌组织中HPV16E7DNA序列发生碱基替换的区域主要在647位至846位,热点突变点为Nt647和Nt846.     

胆道支撑管显影材料的制备及体外细胞毒性评价

目的 探讨新型显影胆道支撑管材料制备的可行性，对构建出的材料进行体外细胞毒性评价和筛选。方法 选择具有X线下显影特性的基础材料A、B、C，分别与硅橡胶生胶共混炼，模压后分别得到相应的显影复合材料甲、乙、丙，经一段和二段硫化过程完成加工。采用MTT法作为体外细胞毒性评价的方法，测定参比对照材料和新材料的50％浓度的浸提液对小鼠成纤维细胞的增殖率的影响，确定细胞毒性级别。结果 新材料甲、乙、丙在x线下影像清晰。甲、乙材料的细胞毒性级别为零，丙材料细胞毒性级别为2。结论 构建出在X线下显影的弹性体材料可行。材料甲、乙是制造新型胆道支撑管的初选材料，材料丙无应用的价值。     

cis-Acting packaging motifs of porcine adenovirus type 3

The cis-acting packaging domain is required for selective encapsidation of adenovirus DNA into preformed empty capsids late in the viral life cycle. Earlier, it was demonstrated that the cis-acting packaging domain of porcine adenovirus type (PAdV)-3 is located between nucleotide position (nt) 212 and 531 at the left end genome which contains six AT/GC rich motifs. Removal of packaging domain from left end to the right end of the genome produced a viable mutant virus suggesting that the identified cis-acting packaging domain represents the DNA sequences required for selective packaging of PAdV-3 DNA, whose position and orientation appear to be flexible. Here, by constructing and analyzing a panel of virus mutants carrying deletions or linker scanning mutations in AT/GC rich sequences, we examined the significance of the continuous A/T or G/C sequences individually in the viral packaging process. In contrast to consensus bipartite structure (5'-TTTGN8CG-3') described for most of packaging motifs of human adenovirus type 5 (HAdV-5), the packaging motifs I, II, III, and IV of PAdV-3 displayed a tripartite structure in which the continuous A/T nucleotides were flanked by G/C-rich sequences. Mutations in both continuous A/T nucleotides and its flanking GC-rich sequences reduced the packaging efficiency of mutants to varying degrees. In addition, although the continuous A/T sequences were present in all of the packaging motifs, their significance in the packaging process appears to vary within each packaging motif.     

Determination of Copy Number of rRNA Genes in Pneumocystis carinii f. sp. hominis

Differential PCR was performed to determine the copy number of rRNA genes in Pneumocystis carinii f. sp. hominis. Two different reference genes, thymidylate synthase (TS) and beta-tubulin (BTU) genes, were used. Primers for the internal transcribed spacer (ITS) region of nuclear rRNA genes and either the TS or BTU gene were mixed together to perform PCR on seven different bronchoalveolar lavage specimens from patients with P. carinii pneumonia. The radioactivity derived from the incorporated radioactive nucleotides of each PCR product band was then used to calculate the copy number of the ITS relative to that of the TS or BTU gene. The copy number ratio between the ITS and the TS gene was determined to be 0.8, and that between the ITS and the BTU gene was also 0.8. These results suggest that the ITS has the same copy number as the TS or BTU gene. Since the copy number of the TS or BTU gene is presumed to be 1, the results also suggest that P. carinii f. sp. hominis has only one copy of the ITS and thus one copy of the nuclear rRNA genes. Therefore, two types of ITS sequences derived from a specimen would indicate that the patient is infected by two types of P. carinii f. sp. hominis.