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目的:总结外科手术室感染控制存在的问题,并分析相应的护理管理对策。方法:对我院2012年1月-2012年12月手术室感染高危因素进行总结分析,并提出相应的护理管理措施,比较外科手术室实施护理管理前后的感染情况。结果 外科手术室感染高危因素主要包括术前洗手不彻底、器械物品消毒不认真、医护人员流动管理不严格、以及患者自身的因素等;实施护理管理措施后感染率为2.39%(9例/376例),明显低于实施护理管理前的感染率9.52%(35例/368例),差异有统计学意义(P<0.05)。结论:在外科手术室加强护理管理可以明显的降低感染率,为患者在外科手术室的安全提供了保障。 相似文献
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目的:探讨产科病房安全管理的潜在隐患,并针对隐患采取防范措施,有效的控制产科病室医院感染的发生.方法:针对产科病房的安全隐患进行因素分析,并提出针对性护理预防措施.结果:对存在的护理问题和可能出现的差错苗头及时采取改进措施和效果评价反馈,将差错、事故消灭在萌芽中.结论:产科病房病区需配备具有高度责任心和有爱心的医护人员实施母、婴统一体的护理制度.在护理过程中强化防范意识;在健康教育中强化安全意识,贯彻以母婴为中心的思想,才能保证产科母婴病房的安全、舒适、和谐. 相似文献
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目的:对我院不安全用药行为进行监测与调查,分析临床用药问题中存在的风险因素,探讨医疗机构加强药品风险管理的措施,以减少临床用药的安全隐患。方法:采用调查问卷的方式,对我院部分科室就诊患者的用药情况进行问卷调查;应用“医院用药安全监测与评价”软件对我院医护人员在临床用药管理方面存在的风险因素进行评估,整理并分析调查结果。结果:在本次临床用药风险分析中,各因素所占比例为:医生:30.50%,药师:9.00%,护士:32.00%,患者:28.50%。了解临床用药各环节中存在的临床用药风险的医护人员占83.3%,但只有50.6% 的人员采取基本的防范措施。用药风险警示调查显示:PASS 警示有效率为57.5%;关联因素评价中人员因素的发生率最高55.16%;外界因素次之31.29%;药物因素发生率为26.95%。结论:医疗机构应当加强临床用药管理,识别、分析用药风险因素,强化合理用药意识及知识,努力构建临床用药风险控制系统,为医药护理人员及患者营造良好的医疗安全氛围,从而降低用药风险的发生,保障患者的用药安全。 相似文献
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摘要 目的: 对我院不安全用药行为进行监测与调查, 分析临床用药问题中存在的风险因素, 探讨医疗机构加强药品风险管理的
措施,以减少临床用药的安全隐患。方法: 采用调查问卷的方式,对我院部分科室就诊患者的用药情况进行问卷调查; 应用 “医院
用药安全监测与评价” 软件对我院医护人员在临床用药管理方面存在的风险因素进行评估, 整理并分析调查结果。结果: 在本次
临床用药风险分析中, 各因素所占比例为: 医生: 30.50%,药师: 9.00%, 护士: 32.00%, 患者: 28.50%。了解临床用药各环节中存在的
临床用药风险的医护人员占 83.3%,但只有 50.6% 的人员采取基本的防范措施。用药风险警示调查显示: PASS 警示有效率为
57.5%; 关联因素评价中人员因素的发生率最高 55.16%;外界因素次之 31.29%; 药物因素发生率为 26.95%。结论: 医疗机构应当
加强临床用药管理, 识别、分析用药风险因素, 强化合理用药意识及知识, 努力构建临床用药风险控制系统,为医药护理人员及患
者营造良好的医疗安全氛围, 从而降低用药风险的发生, 保障患者的用药安全。
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On the origin of the Hirudinea and the demise of the Oligochaeta 总被引:10,自引:0,他引:10
Martin P 《Proceedings. Biological sciences / The Royal Society》2001,268(1471):1089-1098
The phylogenetic relationships of the Clitellata were investigated with a data set of published and new complete 18S rRNA gene sequences of 51 species representing 41 families. Sequences were aligned on the basis of a secondary structure model and analysed with maximum parsimony and maximum likelihood. In contrast to the latter method, parsimony did not recover the monophyly of Clitellata. However, a close scrutiny of the data suggested a spurious attraction between some polychaetes and clitellates. As a rule, molecular trees are closely aligned with morphology-based phylogenies. Acanthobdellida and Euhirudinea were reconciled in their traditional Hirudinea clade and were included in the Oligochaeta with the Branchiobdellida via the Lumbriculidae as a possible link between the two assemblages. While the 18S gene yielded a meaningful historical signal for determining relationships within clitellates, the exact position of Hirudinea and Branchiobdellida within oligochaetes remained unresolved. The lack of phylogenetic signal is interpreted as evidence for a rapid radiation of these taxa. The placement of Clitellata within the Polychaeta remained unresolved. The biological reality of polytomies within annelids is suggested and supports the hypothesis of an extremely ancient radiation of polychaetes and emergence of clitellates. 相似文献
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Göran Malmberg 《Systematic parasitology》1990,17(1):1-65
Data on the ontogeny of the posterior haptor of monogeneans were obtained from more than 150 publications and summarised. These data were plotted into diagrams showing evolutionary capacity levels based on the theory of a progressive evolution of marginal hooks, anchors and other attachment components of the posterior haptor in the Monogenea (Malmberg, 1986). 5 + 5 unhinged marginal hooks are assumed to be the most primitive monogenean haptoral condition. Thus the diagrams were founded on a 5 + 5 unhinged marginal hook evolutionary capacity level, and the evolutionary capacity levels of anchors and other haptoral attachement components were arranged according to haptoral ontogenetical sequences. In the final plotting diagram data on hosts, type of spermatozoa, oncomiracidial ciliation, sensilla pattern and protonephridial systems were also included. In this way a number of correlations were revealed. Thus, for example, the number of 5 + 5 marginal hooks correlates with the most primitive monogenean type of spermatozoon and with few sensillae, many ciliated cells and a simple protonephridial system in the oncomiracidium. On the basis of the reviewed data it is concluded that the ancient monogeneans with 5 + 5 unhinged marginal hooks were divided into two main lines, one retaining unhinged marginal hooks and the other evolving hinged marginal hooks. Both main lines have recent representatives at different marginal hook evolutionary capacity levels, i.e. monogeneans retaining a haptor with only marginal hooks. For the main line with hinged marginal hooks the name Articulon-choinea n. subclass is proposed. Members with 8 + 8 hinged marginal hooks only are here called Proanchorea n. superord. Monogeneans with unhinged marginal hooks only are here called Ananchorea n. superord. and three new families are erected for its recent members: Anonchohapteridae n. fam., Acolpentronidae n. fam. and Anacanthoridae n. fam. (with 7 + 7, 8 + 8 and 9 + 9 unhinged marginal hooks, respectively). Except for the families of Articulonchoinea (e.g. Acanthocotylidae, Gyrodactylidae, Tetraonchoididae) Bychowsky's (1957) division of the Monogenea into the Oligonchoinea and Polyonchoinea fits the proposed scheme, i.e. monogeneans with unhinged marginal hooks form one old group, the Oligonchoinea, which have 5 + 5 unhinged marginal hooks, and the other group form the Polyonchoinea, which (with the exception of the Hexabothriidae) has a greater number (7 + 7, 8 + 8 or 9 + 9) of unhinged marginal hooks. It is proposed that both these names, Oligonchoinea (sensu mihi) and Polyonchoinea (sensu mihi), will be retained on one side and Articulonchoinea placed on the other side, which reflects the early monogenean evolution. Except for the members of Ananchorea [Polyonchoinea], all members of the Oligonchoinea and Polyonchoinea have anchors, which imply that they are further evolved, i.e. have passed the 5 + 5 marginal hook evolutionary capacity level (Malmberg, 1986). There are two main types of anchors in the Monogenea: haptoral anchors, with anlages appearing in the haptor, and peduncular anchors, with anlages in the peduncle. There are two types of haptoral anchors: peripheral haptoral anchors, ontogenetically the oldest, and central haptoral anchors. Peduncular anchors, in turn, are ontogenetically younger than peripheral haptoral anchors. There may be two pairs of peduncular anchors: medial peduncular anchors, ontogentically the oldest, and lateral peduncular anchors. Only peduncular (not haptoral) anchors have anchor bars. Monogeneans with haptoral anchors are here called Mediohaptanchorea n. superord. and Laterohaptanchorea n. superord. or haptanchoreans. All oligonchoineans and the oldest polyonchoineans are haptanchoreans. Certain members of Calceostomatidae [Polyonchoinea] are the only monogeneans with both (peripheral) haptoral and peduncular anchors (one pair). These monogeneans are here called Mixanchorea n. superord. Polyonchoineans with peduncular anchors and unhinged marginal hooks are here called the Pedunculanchorea n. superord. The most primitive pedunculanchoreans have only one pair of peduncular anchors with an anchor bar, while the most advanced have both medial and lateral peduncular anchors; each pair having an anchor bar. Certain families of the Articulonchoinea, the Anchorea n. superord., also have peduncular anchors (parallel evolution): only one family, the Sundanonchidae n. fam., has both medial and lateral peduncular anchors, each anchor pair with an anchor bar. Evolutionary lines from different monogenean evolutionary capacity levels are discussed and a new system of classification for the Monogenea is proposed.In agreeing to publish this article, I recognise that its contents are controversial and contrary to generally accepted views on monogenean systematics and evolution. I have anticipated a reaction to the article by inviting senior workers in the field to comment upon it: their views will be reported in a future issue of this journal. EditorIn agreeing to publish this article, I recognise that its contents are controversial and contrary to generally accepted views on monogenean systematics and evolution. I have anticipated a reaction to the article by inviting senior workers in the field to comment upon it: their views will be reported in a future issue of this journal. Editor 相似文献
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