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Transabdominal sacrocolpopexy has been shown, in multiple long-term studies of its success and durability, to be the definitive treatment option for post-hysterectomy vaginal vault prolapse. It is, however, associated with greater morbidity than vaginal repair. We describe a minimally invasive technique for vaginal vault prolapse repair and present our experience with a minimum of one-year follow-up. The surgical technique involves five laparoscopic ports—three for the da Vinci robot and two for the assistant. After appropriate dissection a polypropylene mesh is attached to the sacral promontory and to the vaginal apex by use of Gore-Tex sutures. The mesh material is then covered by the peritoneum. Patient analysis focused on complications, urinary continence, patient satisfaction, and morbidity, with a minimum of 12 months follow-up. Forty-two patients with post-hysterectomy vaginal vault prolapse underwent robot-assisted laparoscopic sacrocolpopexy at our institute and 35 have a minimum of 12 months follow-up, with a mean follow-up of 36 months (range 12–48) in the group. Mean age was 67 (47–83) years and mean operating time was 3.1 (2.15–4.75) h for the entire cohort. All but one patient were discharged home on postoperative day one; one patient left on postoperative day two. One developed recurrent grade three rectocele, one had recurrent vault prolapse, and two suffered from vaginal extrusion of mesh. All patients were satisfied with their outcome. The robot-assisted laparoscopic sacrocolpopexy is a minimally invasive technique for vaginal vault prolapse repair, combining the advantages of open sacrocolpopexy with the reduced morbidity of laparoscopy. We observed reduced hospital stay, low occurrence of complications, and high patient satisfaction, with a minimum of 1-year follow-up. Most importantly, the long-term results of the robotic repair are similar to those of open repair, but with significantly less morbidity.  相似文献   
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Fossa navicularis strictures following radical prostatectomy are reported infrequently. We recently experienced a series of fossa strictures following robotic-assisted laparoscopic prostatectomy (RLP). We describe herein our experience to prevent fossa strictures and to determine its etiologic factors. From June 2002 to May 2006, 424 patients underwent robotic-assisted laparoscopic prostatectomy with the da Vinci surgical system. Fossa strictures were diagnosed based on the acute onset of obstructive voiding symptoms and bougie calibration. During our series, we switched from the intra-operative use of an 18 French (F) catheter to that of a 22 F one to avoid inadvertent stapling of the urethra when dividing the dorsal venous complex. After we observed a high incidence of fossa strictures, we reverted back to 18 F catheters during surgery. All patients had an 18 F catheter indwelling for 1 week after surgery. Parameters were evaluated using Fisher’s exact test and Student’s t-test for means. The 18 F catheter group of patients (n = 293) developed one fossa stricture, whereas the 22 F catheter group (n = 131) developed nine fossa strictures (P < 0.01). The fossa stricture rate in the 18 F group was 0.3% versus 6.9% in the 22 F group. The two groups had no differences in age, body mass index, cardiovascular disease, American Urological Association symptom score, urinary bother score, preoperative prostate-specific antigen, operative time, estimated blood loss, cautery use, prostate size, or catheterization time. Based on these results, a larger urethral catheter size – 20 F versus 18 F – during the intra-operative dissection would appear to increase the risk for fossa stricture by more than 20-fold. Statement of disclosure Dr. Thomas Ahlering is a meeting participant and lecturer for Intuitive Surgical Corp. The other authors have no direct or indirect commercial financial incentives associated with publishing the article. No research or project support funding was received.  相似文献   
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Abstract Robotics has been applied to the rehabilitation of patients suffering from upper limb-related diseases such as stroke, upper spinal cord injuries and neuromuscular diseases (e. g. muscular dystrophy) alone, or combined with appropriate orthotic devices. In all cases, expensive industrial manipulators, as much as relatively low-cost commercial systems with specific modifications have been used. However, no reference has been made in the literature on the technology of such devices. This article presents the development of a joystick-computer system for the control of a step motor. Further research can lead to the development of an extremely low-cost robotic arm which uses residual finger movement input and can be used by research centers with restricted funding. Reference is made to the technology on which the circuitry is based, as well as to the design concept of it.  相似文献   
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The loads needed to elicit a positive pivot shift test in a knee with an anterior cruciate ligament (ACL) rupture have not been quantified. The coupled anterior tibial translation (ATT), coupled internal tibial rotation (ITR), and the in situ force in the ACL in response to a valgus torque, an inherent component of the pivot shift test, were measured in 10 human cadaveric knee specimens. Using a robotic/universal force-moment sensor testing system, valgus torques ranging from 0.0 to 10.0 Nm were applied in nine increments on the intact and ACL-deficient knee in flexion ranging from 0 degrees to 90 degrees. At 15 degrees of knee flexion, the coupled ATT and ITR were significantly increased in the ACL-deficient knee when compared to the intact knee. Coupled ATT increased a maximum of 291% (6.7 mm, p<0.05), while coupled ITR increased a maximum of 85% (5.1 degrees, p<0.05). At 30 degrees, the increases in coupled ATT and ITR were significant at valgus loads of 3.3 Nm and greater with a maximum increase in coupled ATT of 137% (6.3 mm, p<0.05) and a maximum increase in coupled ITR of 38% (3.6 degrees, p<0.05). At 45 degrees, coupled ATT increased significantly (maximum of 69%, 4.4 mm, p<0.05), but only at torques > or =6.7 Nm. The in situ force in the ACL was less than 20 N for all flexion angles when a torque between 3.3 and 5.0 Nm was applied. Low valgus torque elicited tibial subluxation in the ACL-deficient knee with low in situ ACL forces, similar to a positive pivot shift test. Thus, application of a valgus torque may be suitable to evaluate ACL-deficient and ACL-reconstructed knees, since subluxation can be achieved with minimal harm to the ACL graft. This work is important in understanding one load component needed for the pivot shift examination; further studies quantifying other load components are essential for better comprehension of the in vivo pivot shift examination.  相似文献   
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We report the first case of post-cryotherapy salvage radical prostatectomy for local recurrence performed laparoscopically with the da Vinci robot. Total operative time was 210 minutes and blood loss was 50ml. There were no intraoperative or postoperative complications. The hospital stay was 24 hours and the Foley catheter was removed on postoperative day 7. The patient achieved a pad free status 4 weeks postoperatively. Pathology showed extensive disease, pT3bN0, Gleason score of 5+3 and positive margins. The patient continued on complete androgen deprivation therapy and his follow up PSA at 10 months was <0.1. Further studies are needed to evaluate both functional and oncological results with this approach.  相似文献   
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血管介入治疗作为一种微创治疗方法已被血管外科、心血管内外科及神经内外科等不同学科所广泛应用。传统血管介入手术依靠透视下手对导管导丝的操作,可持续性及精确性存在一定问题;同时操作者在长期X射线暴露及铅防护围裙负重中承担了较高的职业危害风险。血管介入机器人系统具有明显减少操作者X射线暴露、成像定位精准、操作准确稳定的优点,在减少器械与血管壁接触、操作颤抖的同时,增加操作者舒适感,目前已经成为医疗机器人的研究热点。笔者在此介绍血管介入手术机器人系统的图像导航、机械臂结构、力反馈及安全性能等关键技术,并对目前国内外血管介入手术机器人系统的研究进展进行阐述,通过临床应用阐明该技术在血管介入手术机器人系统中的重要意义,探讨关键技术的发展趋势。尽管技术的进步使得血管介入手术机器人系统有了长足发展,但需要看到的是,目前的介入手术机器人系统仍然存在较多不足:触觉力学反馈的缺乏使其在复杂困难病变、钙化病变、慢性闭塞病变中的应用受到了限制;同时缺乏适用操控各类目前已经商品化的导丝、导管、球囊、支架等血管腔内器具,频繁更换介入器材会导致手术时间的增加,进一步降低了手术的可操控性。人工智能与5G通信技术的快速发展,将为机器人系统辅助下的血管介入手术提供更加精准化、规范化的发展方向。并且在人工智能基础上,血管介入机器人系统与腔内影像设备的一体化融合及虚拟现实技术的应用将为精准血管介入提供更为广阔的前景,指明了血管介入手术机器人系统未来研究方向。血管介入手术机器人系统的发展,是符合目前对于精准医疗的趋势,为血管介入医师提供一种保护,但仍然需要更多的时间去完善、精进这项技术,同时需要制定其应用的适应证和禁忌证,建立标准程序,并通过大量临床试验来评估血管介入机器人系统的长期疗效,使得这项技术能够得到更广泛的应用。  相似文献   
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