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   效果比 在 消化系统疾病 分类中 的翻译结果: 查询用时:0.092秒
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效果比
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  effectiveness ratio
    RESULTS: The cost effectiveness ratio for 4 groups was HP eraduation: A 9.08, B 8.56, C 12.05, D 12.97;
    D组 :兰索拉唑 +丽珠胃三联 (枸橼酸铋钾 克拉霉素 替硝唑 )进行分析评价。 结果 :4组方案的成本 效果比 (C/E) ,HP消除 :A 9 0 8,B 8 5 6 ,C 12 0 5 ,D 12 97;
短句来源
    The cost effectiveness ratio of schemes E was the minimum,which was11.53yuan;
    E方案成本-效果比最低,为11. 53元;
短句来源
    Results:The cost effectiveness ratio of three regimens was 18.60,20.04 and 16.30,respectively.
    结果:A,B,C 3种方案的成本效果比(C/E)分别为18.60,20.04,16.30。
短句来源
    The cost effectiveness ratio were 108.61 and 76.35.Conclusion Homemade octreotide is better in the treatment of severe acute pancreatitis.
    成本-效果比分别是108.61和76.35。 结论国产奥曲肽是治疗重症急性胰腺炎的较佳方案。
短句来源
    The clinical efficacy indexes of these two groups are statistically analyzed and the cost effectiveness ratio as the appraisal index is calculated.
    统计两组临床疗效指标,同时计算其经济学的项目费用,并采用成本效果比为评价指标。
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  “效果比”译为未确定词的双语例句
    the cost-effectiveness ratios were 57.20 and 91.58 respectively(P<0.05).
    成本-效果比分别为57.20和91.58(P<0.05);
短句来源
    cost-effective- ness ratios obtained by sensitivity analysis were 45.76 and 73.26 respectively.
    经敏感度分析所得的成本-效果比分别为45.76和73.26。
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    The cost-profit ratio was 6.5/11.5 for the pantoprazole and omeprazole groups.
    而泮托拉唑组成本-效果比为6.5,明显低于奥美拉唑组(11.5)。
短句来源
    Results After 4 weeks treatment, the effective rate of rhGH and HSA was 75.0% and 83.3%,the cost-effectiveness ratios were 68.4? 51.0 respectively.
    结果 rhGH和HSA治疗肝硬化低蛋白血症 ,治疗后第 4周有效率分别为 75 .0 %、83.3% ,成本效果比分别为 6 8.4、5 1.0 ;
短句来源
    The schemes were evaluated with pharmacoeconomic cost-effectiveness analysis. RESULTS:The cost-effectiveness ratios of OMC,OFC,OFA,BFC for gastritis or duodenal ulcer were 16.19/17.33,17.30/13.93,11.40/10.56,11.17/10.75 respectively.
    结果 :OMC、OFC、OFA、BFC4组方案对胃炎/十二指肠溃疡的成本 -效果比为16 19/17 33、17 30/13 93、11 40/10 56、11 17/10 75。
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  effectiveness ratio
The cost-effectiveness ratio for tacrolimus is about 15.5 % better than for cyclosporin A.
      
In the other evaluated European countries treatment with simvastatin showed a favourable cost-effectiveness ratio independent of differences in local health care unit costs.
      
Conclusion: The results of this study show a combination of albumin 4 %-hydroxyethyl starch to replace plasma during plasma exchange to be the method presenting the lowest morbidity and the best cost/effectiveness ratio.
      
A cost-effectiveness ratio was computed for 176?stays with at least one organ failure, at hospital discharge and 6?months later.
      
The incremental cost-effectiveness ratio was US$?1,150 per life-year saved and the incremental cost-utility ratio was US$?4,100 per quality-adjusted life-year (QALY) saved, without discounting.
      
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ne hundred and six neonates born to HBeAg-Positive and HBsAg-Carrier motherswere randomly divided into two groups,In one group each infant received 20 μg perdose of yeast derived recombinant hepatitis B vaccine (recombinant vaccine)and eachinfant in the other group received 20 μg per dose of plasma derived hepatitis B vac-cine(plasma vaccine)on the day of birth,at 1 month and at 6 Inonths (three times). Physical examination and blood testing were performed for all infants at 6,12,24,36, and 48 months of age....

ne hundred and six neonates born to HBeAg-Positive and HBsAg-Carrier motherswere randomly divided into two groups,In one group each infant received 20 μg perdose of yeast derived recombinant hepatitis B vaccine (recombinant vaccine)and eachinfant in the other group received 20 μg per dose of plasma derived hepatitis B vac-cine(plasma vaccine)on the day of birth,at 1 month and at 6 Inonths (three times). Physical examination and blood testing were performed for all infants at 6,12,24,36, and 48 months of age. The results showed that the protective efficacy rates at 6,12,24,36,and 48 monthswere 66.7%,75.0% , 62.5%, 61.7% and 56.5% respectively for the recombinantvaccine group,and 57.7%, 75.5%, 51.1%, 40.5% and 23.8% respectively for plasmavaccine group.The differences of protective efficacy rates between the two groups werenot statistically significant by Chi-square test in the first two years,and were muchmore significant in the last two years. The study indicates that for the prevention of mother-infant transmission of hepa- titis B virus the protective efficacy of the recombinant vaccine and of the plasma va-ccine are approximate in the near future, and the long term efficacy of the recombinantvaccine is longer than that of the plasma vaccine.

已知血源乙型肝炎疫苗(简称血源疫苗)能有效地阻断乙型肝炎传播,个体接种后的免疫效果可持续至少3年。我们对血清HBeAg阳性和HBsAg携带者母亲分娩的106名新生儿随机分为二组,分别接受美国提供的由酵母菌提取的重组乙型肝炎基因疫苗(简称重组疫苗)和国产血源疫苗,以等剂量和同样的免疫顺序,作对照试验,分析二者对阻断母婴传播的长期效果。以保护性抗体的滴度≥10mIU/ml的持续存在分析保护效果,指出重组疫苗使用安全无明显副反应;近期的保护效果与血源疫苗相似,而远期效果比血源疫苗长。

In order to compare the effect of reducing jaundice on the patients with severe obstruction jaundice before whipple's operation and complication and mortality after whipple's operation. PTCD was performed in 36 patients and that bile is drained inside pody by means of connecting gallballder with jejunum through the bridge in 6 patients.We found that the later effect of reducing jaundice was better than that of PTCD method.Complication and mortilify after whipple's operation was lower in later's method than those...

In order to compare the effect of reducing jaundice on the patients with severe obstruction jaundice before whipple's operation and complication and mortality after whipple's operation. PTCD was performed in 36 patients and that bile is drained inside pody by means of connecting gallballder with jejunum through the bridge in 6 patients.We found that the later effect of reducing jaundice was better than that of PTCD method.Complication and mortilify after whipple's operation was lower in later's method than those of PTCD method.

为比较严重梗阻性黄疸病人术前减黄的效果、并探讨其与Whipplcs手术后合并症,死亡率的关系,对36例病人行PTCD减黄,6例行胆囊空肠体外架桥胆汁内引流术减黄、发现胆囊空肠体外架桥胆汁内引流出的减黄效果比PTCD好,且Whipples手术后并发症及死亡率低。

In order to search for specific therapeutic drugs against persistant infection of hepatitis B virus (HBV),a eukaryotic expression clone for the fusion protein(IL-2 preS) consisting in human interleukin-2(IL-2) and preS antigen(preS) was previously constructed and it was confirmed that IL-2 preS could be secreted from mammalian cells. In this study, the expression clone was used as gene vaccine and was innoculated Balb/c mice through regenerating muscles and normal muscles. The experimental results showed that...

In order to search for specific therapeutic drugs against persistant infection of hepatitis B virus (HBV),a eukaryotic expression clone for the fusion protein(IL-2 preS) consisting in human interleukin-2(IL-2) and preS antigen(preS) was previously constructed and it was confirmed that IL-2 preS could be secreted from mammalian cells. In this study, the expression clone was used as gene vaccine and was innoculated Balb/c mice through regenerating muscles and normal muscles. The experimental results showed that inoculation of IL-2 preS gene vaccine could induce the mice to produce antibodies against preS antigen. The antibody level could be detected 15 days post immunization,reached the highest level 45 days and didn't decrease 60 days. The regenerating muscular inoculation was more effective than the normal muscular inoculation and the antibody titerof the former was significantly higher than that of the latter. It indicated that IL-2 preS fusionprotein could be secreted in bodies,and suggested that IL-2 preS gene vaccine might be of multiple function,including induction of humoral and cellular immune responses,and double receptorlinking effects,in human bodies.

为了构建抗乙型肝炎病毒(HBV)持续性感染的特异性免疫治疗剂,我们曾构建了人白细胞介素-2(IL-2)与HBV前S(preS)抗原的融合蛋白(IL-2preS)的真核表达克隆,并证明IL-2preS融合蛋白能在哺乳动物细胞中分泌表达。本文以该克隆为基因疫苗,经正常肌肉组织内接种和再生性肌肉组织内接种进行基因免疫,实验结果证明接种IL-2preS基因疫苗能在动物体内诱导抗preS抗体产生,免疫后15天可检出抗体,45天时达高峰值,60天不见下降。再生性肌肉内的免疫效果比正常肌肉的好,所产生的抗体水平前者显著高于后者。结果表明IL-2pres融合蛋白能在机体内分泌表达。提示IL-2preS基因疫苗在人体内可能有多重生物功能,如诱导体液免疫与细胞免疫应答,双重导向作用和细胞膜受体交联效应等。

 
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