首页 | 本学科首页   官方微博 | 高级检索  
文章检索
  按 检索   检索词:      
出版年份:   被引次数:   他引次数: 提示:输入*表示无穷大
  收费全文   701篇
  免费   52篇
  国内免费   30篇
妇产科学   6篇
基础医学   16篇
口腔科学   5篇
临床医学   71篇
内科学   6篇
神经病学   3篇
特种医学   24篇
外科学   217篇
综合类   258篇
预防医学   30篇
眼科学   4篇
药学   126篇
  5篇
中国医学   7篇
肿瘤学   5篇
  2024年   1篇
  2023年   7篇
  2022年   12篇
  2021年   25篇
  2020年   25篇
  2019年   16篇
  2018年   8篇
  2017年   22篇
  2016年   28篇
  2015年   20篇
  2014年   50篇
  2013年   40篇
  2012年   37篇
  2011年   48篇
  2010年   38篇
  2009年   48篇
  2008年   38篇
  2007年   47篇
  2006年   38篇
  2005年   49篇
  2004年   38篇
  2003年   38篇
  2002年   29篇
  2001年   27篇
  2000年   15篇
  1999年   13篇
  1998年   6篇
  1997年   6篇
  1996年   1篇
  1995年   2篇
  1994年   2篇
  1993年   2篇
  1992年   1篇
  1991年   2篇
  1990年   2篇
  1989年   1篇
  1988年   1篇
排序方式: 共有783条查询结果,搜索用时 453 毫秒
1.

Background

The efficacy of dexamethasone in extending the duration of local anaesthetic block is uncertain. In a randomised controlled triple blind crossover study in volunteers, we tested the hypothesis that neither i.v. nor perineurally administered dexamethasone prolongs the sensory block achieved with ropivacaine.

Methods

Ultrasound-guided ulnar nerve blocks (ropivacaine 0.75% wt/vol, 3 ml, with saline 1 ml with or without dexamethasone 4 mg) were performed on three occasions in 24 male volunteers along with an i.v. injection of saline 1 ml with or without dexamethasone 4 mg. The combinations of saline and dexamethasone were as follows: control group, perineural and i.v. saline; perineural group, perineural dexamethasone and i.v. saline; i.v. group, perineural saline and i.v. dexamethasone. Sensory block was measured using a VAS in response to pinprick testing. The duration of sensory block was the primary outcome and time to onset of sensory block the secondary outcome.

Results

All 24 subjects completed the trial. The median [inter-quartile range (IQR)] duration of sensory block was 6.87 (5.85–7.62) h in the control group, 7.37 (5.78–7.93) h in the perineural group and 7.37 (6.10–7.97) h in the i.v. group (P=0.61). There was also no significant difference in block onset time between the three groups.

Conclusion

Dexamethasone 4 mg has no clinically relevant effect on the duration of sensory block provided by ropivacaine applied to the ulnar nerve.

Clinical trial registration

DRKS, 00014604; EudraCT, 2018-001221-98.  相似文献   
2.
甲磺酸罗比卡因与盐酸罗比卡因用于硬膜外阻滞的效应比较   总被引:10,自引:0,他引:10  
目的 评价甲磺酸罗比卡因用于硬膜外阻滞的效应和安全性。方法 45例择期行下腹或下肢手术病人,随机分别接受用甲磺酸罗比卡因(8.94 mg/ml,观察组)或盐酸罗比卡因(7.5mg/ml,对照组)施行的硬膜外阻滞。观察两组在感觉阻滞、运动阻滞、镇痛和肌肉松弛方面的效果,同时观察用药前后肝肾功能变化。结果 观察组和对照组感觉阻滞平面达到T6以上的病例分别为84.3%和76%(P>0.05),Bromage≥3级的病例分别90%和92%(P>0.05)。两组感觉阻滞平面固定时间、Bromage达到最大级别时间、最大级别维持时间和运动阻滞维持时间均无显著性差异(P>0.05)。两组镇痛及肌松满意率无显著性差异。观察组术中2例发生低血压,2例发生心动过缓,而对照组仅1例发生低血压。两组术后24 h天冬氨酸氨基转移酶(AST)、天冬氨酸转氨酶(ALT)、尿素氮(BUN)和肌酐(Cr)均在正常范围。结论 甲磺酸罗比卡因与盐酸罗比卡因行硬膜外阻滞的效应基本相同,且无明显毒性。  相似文献   
3.
Ropivacaine, a new long–acting amino–amide local anaesthetic agent, and bupivacaine, in various concentrations with or without addition of adrenaline, were tested in a randomized, double–blind study using intradermal wheals. Ten non–smoking, healthy, young male volunteers participated. In series I plain solutions of ropivacaine (0.25%, 0.5%, 0.75% and 1%) and bupivacaine (0.25%, 0.5% and 0.75%) were injected intradermally and in series II the same concentrations, with the addition of adrenaline 5 ug ml-1 ( 1 :200 000), were used. The same volunteers took part in both series, with an interval of at least three weeks between the experiments. Saline was included as control in both series. Pin–pricking was used to assess the dermal analgesia. Plain solutions of ropivacaine produced significantly longer durations of dermal analgesia than did plain solutions of bupivacaine, in all tested concentrations. A significant increase in duration was seen for both local anaesthetics when adding adrenaline. Local vascular effects at the injected areas were determined by visual inspection (nil, pink, pale). Local blanching (pale) was significantly more frequent for plain solutions of ropivacaine, in all tested concentrations. Local redness (pink) was significantly more frequent with plain bupivacaine, in a dose–dependent relation. An initial redness was frequently observed for both local anaesthetics containing adrenaline, followed by blanching at most sites.  相似文献   
4.
两种局麻药术后镇痛效果及副作用比较   总被引:2,自引:0,他引:2  
目的:观察比较0.2%罗哌卡因和0.15%布比卡因两种同麻药在硬膜外自控镇痛(PCEA)中的镇痛效果及副作用。方法:选用0.2%罗哌卡因和0.15%布比卡因两种同麻药用于PCEA中.对其效果进行对比分析。结果:0.2%罗哌卡因、0.15%布比卡因分别与0.1mg芬太尼联合用于PCEA中,镇痛效果确切.毒副作用轻微,并发症少。结论:将0.2%罗哌卡因替代0.15%布比卡因与0.1mg芬太尼合用后.病人术后行走能力的早期恢复可得到改善。  相似文献   
5.
6.
Introduction  Wide awake open carpal tunnel decompression is a procedure performed under local anesthesia. This study aimed to present the effect of various local anesthetics in peri and postoperative analgesia in patients undergoing this procedure. Materials and Methods  A total of 140 patients, with 150 hands involved, underwent carpal tunnel release under local anesthesia. Patients were divided in five groups according to local anesthetic administered: lidocaine 2%, ropivacaine 0.75%, ropivacaine 0.375%, chirocaine 0.5%, and chirocaine 0.25%. Total 400 mg of gabapentin were administered to a subgroup of 10 cases from each group (50 cases totally), 12 hours before surgery. Patients were evaluated immediately, 2 weeks and 2 months after surgery according to VAS pain score, grip strength, and two-point discrimination. Results  In all patients, pain and paresthesia improved significantly postoperatively, while the use of gabapentin did not affect outcomes. Grip strength recovered and exceeded the preoperative value 2 months after surgery, without any difference between the groups. No case of infection, hematoma, or revision surgery was reported. Conclusion  Recovery after open carpal tunnel release appears to be irrelevant of the type of local anesthetic used during the procedure. Solutions of low local anesthetic concentration (lidocaine 2%, ropivacaine 0.375%, and chirocaine 0.25%) provide adequate intraoperative analgesia without affecting the postoperative course.  相似文献   
7.
目的:将新型酰胺类局麻药罗哌卡因药效学与布比卡因进行比较。方法:选择行择期下肢手术病人40例,随机分成四组进行硬膜外麻醉,分别在硬膜外注入0.75%罗哌卡因(n=10例),0.5%罗哌卡因(n=10例)和0.75%布比卡因(n=10例),0.5%布比卡因(n=10例)15-18ml。分别观察感觉阻滞起效,最大运动阻滞,感觉、运动恢复时间及最高阻滞平面,最大Bromage评分及术中不良反应的情况。结果:罗哌卡因起效快,产生的麻醉平面广,镇痛、运动阻滞效果好。术中有低血压、心率减慢等副作用发生。结论:罗哌卡因应用于临床麻醉有可靠的麻醉性能及安全性,利用其感觉运动神经分离作用,利于病人术后早期活动,具有良好的临床应用前景。  相似文献   
8.
多区域浸润麻醉减轻腹腔镜胆囊切除术后早期症状   总被引:1,自引:0,他引:1  
目的探讨躯体、内脏局部浸润麻醉对择期腹腔镜胆囊切除术后疼痛、恶心症状的影响.方法随机将50例病人分为对照组和实验组,在门静脉周围和腹膜内分别浸润生理盐水66ml和罗吡卡因66ml;术后3h记录疼痛和恶心的程度、部位及所补充的哌替啶用量.结果罗吡卡因局部浸润可减轻术后3h的切口疼痛和恶心症状,但对腹内和肩部疼痛无明显效果;且术后3h所补充的哌替啶的用量显著减少.结论躯体、内脏局部浸润麻醉可减轻术后3h的切口疼痛、恶心及哌替啶用量.  相似文献   
9.
局麻药心脏毒性研究进展   总被引:13,自引:1,他引:13  
自从首例局麻药引发心脏毒性的病例报道以来,20多年来对局麻药的心脏毒性机理及治疗的研究从来没有终止过,本文旨在对局麻药心脏毒性的机理、比较及治疗进展作综述。  相似文献   
10.
Shah MK  Sia AT  Chong JL 《Anaesthesia》2000,55(10):1008-1013
Sixty patients in early labour were randomly allocated to one of three groups. The control group received intrathecal fentanyl 25 microg, the ropivacaine group received intrathecal fentanyl 25 microg and ropivacaine 2.5 mg while the bupivacaine group received intrathecal fentanyl 25 microg and bupivacaine 2.5 mg. The incidence of pruritus was 100% in controls, compared with 85% in the ropivacaine group (not significant) and 75% in the bupivacaine group (p = 0.003). The severity of pruritus was significantly less in the ropivacaine (p = 0.006) and bupivacaine (p = 0.001) groups. Most patients developed pruritus by 30 min. Pruritus above the abdomen was not reduced in patients receiving local anaesthetics. There were no significant differences in the mean pain visual analogue score, systolic blood pressure, maternal heart rate and upper level of reduced pin-prick sensation in the first 30 min. Intrathecal ropivacaine and, more so, intrathecal bupivacaine reduce the incidence and severity of pruritus from intrathecal fentanyl for labour analgesia.  相似文献   
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号