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hypothermia liquid
相关语句
  低温液体
     the temperature recovery ratio in 5 days was the highest in the intravenous drip hypothermia liquid group (p<0.05); the cooling inefficacy ratio was the lowest in the intravenous drip hypothermia liquid group.
     5天以内体温恢复率以静脉滴注低温液体组最高(P<0.05),降温无效率,静脉滴注低温液体组最低。
短句来源
     the temperature reiteration ratio was the lowest in the intravenous drip hypothermia liquid group;
     体温反复率以静脉滴注低温液体组最低;
短句来源
     Objective: The nursing technique of intravenous dripping hypothermia liquid was used to treat central hyperthermia.
     目的 :为有效治疗中枢性高热 ,研制静脉滴注低温液体这一护理新技术。
短句来源
     Methods 90 cases of burn and hi-heat were randomly divided into intravenous drip hypothermia liquid group, drug cooling group and physical cooling group . The indexes , such as the recovery ratio( in 60 minutes), reiteration ratio (in 60 minutes), the recovery ratio(in 5 days) and cooling inefficacy ratio( in 5 days), were compared and observed.
     方法将90例烧伤高热病人,随机分为静脉滴注低温液体组,药物降温组,物理降温组,以三组病人60min内体温恢复率、体温反复率、5天以内体温恢复率、降温无效率等指标进行对照观察。
短句来源
     Methods:30 healthy volunteers and 30 central hyperthermia patients were tested with intravenous dripping hypothermia liquid by searching chinese and forgein liferatures between Jan , 1983 and oct ,1994 as well as between Jan , 1989 and Jan ,1999. Results: There was sign ificant difference ( P <0.05) ,The efficieney rate was 100%.
     再次检索 1989年 1月至 1999年 1月 10年国内外文献 ,对研究结果进行验证和实证支持。 结果 :静脉滴注低温液体对中枢性高热有显著性疗效 (P <0 .0 5 ) ;
短句来源
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  “hypothermia liquid”译为未确定词的双语例句
     Clinical study of intravenous dripping hypothermia liquid
     静脉滴注低温液体的临床研究
短句来源
  相似匹配句对
     Clinical study of intravenous dripping hypothermia liquid
     静脉滴注低温液体的临床研究
短句来源
     Liquid Light
     液体光阀
短句来源
     Job liquid .
     工作液。
短句来源
     the temperature reiteration ratio was the lowest in the intravenous drip hypothermia liquid group;
     体温反复率以静脉滴注低温液体组最低;
短句来源
     Hypothermia Gluing Technologies
     低温型胶订技术
短句来源
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Objective: The nursing technique of intravenous dripping hypothermia liquid was used to treat central hyperthermia.This study was to test the effect of intravenous dripping hypothermia liquid on treatment central hyperthemia. Methods:30 healthy volunteers and 30 central hyperthermia patients were tested with intravenous dripping hypothermia liquid by searching chinese and forgein liferatures between Jan , 1983 and oct ,1994 as well as between Jan , 1989 and Jan ,1999. Results: There was sign...

Objective: The nursing technique of intravenous dripping hypothermia liquid was used to treat central hyperthermia.This study was to test the effect of intravenous dripping hypothermia liquid on treatment central hyperthemia. Methods:30 healthy volunteers and 30 central hyperthermia patients were tested with intravenous dripping hypothermia liquid by searching chinese and forgein liferatures between Jan , 1983 and oct ,1994 as well as between Jan , 1989 and Jan ,1999. Results: There was sign ificant difference ( P <0.05) ,The efficieney rate was 100%. Conclusion: Intravenous dripping hypothermia liqnid was effective, safety and advanced nuring techniques.

目的 :为有效治疗中枢性高热 ,研制静脉滴注低温液体这一护理新技术。方法 :检索 1983年 1月至 1994年 10月国内外文献 ,依据研究提示 ,设计静脉滴注低温液体治疗中枢性高热 ;对 30例健康志愿者和 30例中枢性高热患者进行静脉滴注低温液体研究 ;再次检索 1989年 1月至 1999年 1月 10年国内外文献 ,对研究结果进行验证和实证支持。结果 :静脉滴注低温液体对中枢性高热有显著性疗效 (P <0 .0 5 ) ;有效率 10 0 %。结论 :静脉滴注低温液体是一项有效、安全、先进的护理新技术。

Objective In order to cure and nurse the patients of burn and hi-heat , to explore the cooling effects on the patients of burn and hi-heat in 3 different ways. Methods 90 cases of burn and hi-heat were randomly divided into intravenous drip hypothermia liquid group, drug cooling group and physical cooling group . The indexes , such as the recovery ratio( in 60 minutes), reiteration ratio (in 60 minutes), the recovery ratio(in 5 days) and cooling inefficacy ratio( in 5 days), were compared and observed....

Objective In order to cure and nurse the patients of burn and hi-heat , to explore the cooling effects on the patients of burn and hi-heat in 3 different ways. Methods 90 cases of burn and hi-heat were randomly divided into intravenous drip hypothermia liquid group, drug cooling group and physical cooling group . The indexes , such as the recovery ratio( in 60 minutes), reiteration ratio (in 60 minutes), the recovery ratio(in 5 days) and cooling inefficacy ratio( in 5 days), were compared and observed. Results The recovery ratio was the best in the drug cooling group in an hour(p<0.01); the temperature reiteration ratio was the lowest in the intravenous drip hypothermia liquid group; the temperature recovery ratio in 5 days was the highest in the intravenous drip hypothermia liquid group (p<0.05); the cooling inefficacy ratio was the lowest in the intravenous drip hypothermia liquid group.Conclusion The intravenous drip hypothermia liquid is an effective and safe cooling method. It adapts to the patients of burn and hi-heat.

目的为有效地治疗和护理烧伤高热,探讨三种不同方法对烧伤高热病人的降温效果。方法将90例烧伤高热病人,随机分为静脉滴注低温液体组,药物降温组,物理降温组,以三组病人60min内体温恢复率、体温反复率、5天以内体温恢复率、降温无效率等指标进行对照观察。结果三组比较60min内体温恢复率以药物降温为佳(P<0.01);体温反复率以静脉滴注低温液体组最低;5天以内体温恢复率以静脉滴注低温液体组最高(P<0.05),降温无效率,静脉滴注低温液体组最低。结论静脉滴注低温液体是一项有效、安全的降温方法,适合烧伤高热病人应用。

BACKGROUND: Myocardial cell separation is the first step for extraction of myocardial cells to perform detecting technique based on venlricular cytology. Usually, not sufficient and high quality myocardial cells are extracted due to the limitations of instruments and separation method. Application of ultra-hypothermia liquid nitrogen storage for preservation of ventricular myocytes of adult rats is one of effective methods to solve the technical problems. OBJECTIVE: To probe into the feasibility of preparing...

BACKGROUND: Myocardial cell separation is the first step for extraction of myocardial cells to perform detecting technique based on venlricular cytology. Usually, not sufficient and high quality myocardial cells are extracted due to the limitations of instruments and separation method. Application of ultra-hypothermia liquid nitrogen storage for preservation of ventricular myocytes of adult rats is one of effective methods to solve the technical problems. OBJECTIVE: To probe into the feasibility of preparing ventricular myocyte suspension of adult rats with ultra-hypothermia liquid nitrogen storage. DESIGN: Separation of ventricular myocytes based on the experimental animals. SETTING: Department of Cardiology, First Affiliated Hospital of Guangzhou University of Traditional Chinese Medicine; Department of Traditional Chinese Medicine, Second Affiliated Hospital of Guangzhou Medical College. MATERIALS: The experiment was conducted in the laboratory of the Department of Cardiology and laboratory of Molecular Biology Laboratory, First Affiliated Hospital of Guangzhou University of Traditional Chinese Medicine, between October 2001 and April 2002. Totally 30 SD rats weighing 200 to 220 g were recruited. Krebs-Henseleit buffer solution (pH 7.4): NaCl 118 mmol/L, KCl 4.8 mmol/L, MgSO_4 1.2 mmol/L, KH2P04 1.2 mmol/L, NaHCO_3 25 mmol/L, glucose 11 mmol/L. METHODS: Open chest operation was performed on the anesthetized rats to take out their hearts. The remaining blood was washed, and the large vessels, atriums and right ventricle were removed. The left myocardium was cut into two parts, then put in the DMEM tube containing 600 mL/L of glycerol, frozen at 4℃ for 30 minutes, at-20℃ for 30 minutes, and at-80℃ for 30 minutes. Then they were stored in the liquid nitrogen at 196℃. When separating the ventricular myocytes, the myocytes of the Irozen left ventricle was taken from liquid nitrogen, then quickly put into 40℃ water; the heart was washed with DMEM; the left myocardium was cut into 1 mm×1 mm ×1 mm, followed by treatment in the Krebs-Hense-leil solution buffer for 10 minutes to separate the myocardial cells. The liquid containing myocardial cells was filtered with a 100-hole sieve for centrifugation at 800 r/min for 5 minutes. The supernatant was removed, then the sediment was washed twice with 0.1 mol/L of phosphate buffer solution, followed by centrifugation at 800 r/min for 5 minutes; the left myocardium fragment was treated again to obtain more left myocardial cells if necessary. The sediment was put gently on the Ficoll of 40 g/L at 400 r/ min for 4 minutes, and the supernatant was removed. The sediment was the bacilliform myocardial cells of high purity. MAIN OUTCOME MEASURES: Whether the high-purity myocardial cells which met the quality standard were separated or not. RESULTS: Myocardial cells of the adult rats were preserved with ultra-hypothermia liquid nitrogen storage and a sufficient number of bacilliform myocardial cells which met the quality standard were separated. CONCLUSION: It is feasible to separate myocardial cells with myocardium stored in liquid nitrogen, which can be used as a most basic experimental method in the study of molecular biology, and even genome research and proteome research based on cytology. The method is simple and easy to perform with low cost and consumption and short time, and it is suitable for the study of large sample size.

背景:进行一些以心肌细胞学为基础的检测技术,首先必需采用心肌细胞分离方法提取心肌细胞,由于使用器械的限制或分离方法的缺陷,往往提取不到足够数量和高质量的心肌细胞。采用超低温液氮保存的成年大鼠心室肌细胞分离法是解决这一技术问题有效的方法之一。 目的:探讨成年大鼠心室肌细胞超低温液氮保存分离法制备心肌细胞悬液的可行性。 设计:以实验动物为观察对象的心室肌细胞分离方法。 单位:广州中医药大学第一附属医院心内科和广州医学院第二附属医院中医科。 材料:实验于2001-10/2002-04在广州中医药大学第一附属医院内科实验室及细胞分子生物技术实验室完成。选用200~220g SD大鼠30只;Krebs-Henseleit缓冲液(pH7.4):NaCl 118mmol,L,KCl4.8mmol/L,MgSO_41.2mmol/L,KH_2PO_4 1.2 mmol/L,NaHCO_3 25 mmol/L,Glucose 11 mmol/L。 方法:麻醉大鼠开胸后,迅速取出心脏,置于冷Krebs-Henseleit液中,洗去残存的血液,弃去大血管、心房和右心室,将左心室肌剪成两块,然后置于含600mL/L甘油的DMEM的冻...

背景:进行一些以心肌细胞学为基础的检测技术,首先必需采用心肌细胞分离方法提取心肌细胞,由于使用器械的限制或分离方法的缺陷,往往提取不到足够数量和高质量的心肌细胞。采用超低温液氮保存的成年大鼠心室肌细胞分离法是解决这一技术问题有效的方法之一。 目的:探讨成年大鼠心室肌细胞超低温液氮保存分离法制备心肌细胞悬液的可行性。 设计:以实验动物为观察对象的心室肌细胞分离方法。 单位:广州中医药大学第一附属医院心内科和广州医学院第二附属医院中医科。 材料:实验于2001-10/2002-04在广州中医药大学第一附属医院内科实验室及细胞分子生物技术实验室完成。选用200~220g SD大鼠30只;Krebs-Henseleit缓冲液(pH7.4):NaCl 118mmol,L,KCl4.8mmol/L,MgSO_41.2mmol/L,KH_2PO_4 1.2 mmol/L,NaHCO_3 25 mmol/L,Glucose 11 mmol/L。 方法:麻醉大鼠开胸后,迅速取出心脏,置于冷Krebs-Henseleit液中,洗去残存的血液,弃去大血管、心房和右心室,将左心室肌剪成两块,然后置于含600mL/L甘油的DMEM的冻存管中,程序冷冻,即4℃30min,-20℃30min,-80℃30min,最后保存于-196℃的液氮中备用。分离心肌细胞时,从液氮中取出冻存的左心室肌,迅速放入40℃水浴中解冻;用DMEM清洗心脏;将左心室肌剪碎成1mm~3的小块,于冷Krebs-Henseleit液中吹打10min,以分离心室肌细胞;将含心肌细胞的悬液用100目网筛过滤,800r/min,离心5min。弃上清,0.1mol/L磷酸盐缓冲液清洗沉淀2次,800r/min离心5min;必要时可再次吹打左心室肌碎片以获得更多的左心室肌细胞;将沉淀轻轻加入40g/L的Ficoll上,400r/min离心4min,弃上清,沉淀即为高纯度的杆状的心肌细胞。 主要观察指标:是否分离出高纯度的符合质量的心肌细胞。 结果:采用成年大鼠心室肌细胞超低温液氮保存分离法,成功地分离出足够数量符合质量的杆状心肌细胞。 结论:运用液氮冻存的大鼠心室肌来分离心室肌细胞的方法是可行的,可作为以细胞学为基础一些分子生物学甚至基因组学、蛋白组学研究中的一种最基本的实验方法。该方法具有无需特殊昂贵设备、简单易行、消耗低廉、耗时短、适于大样本研究。

 
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