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find Keyword "牵引" 40 results
  • Magnetic anchoring and traction technique-assisted thoracoscopic esophagectomy: Report of three cases

    Magnetic anchoring and traction technique is one of the core technologies of magnetic surgery. With the "non-contact" traction force of the outer magnet on the inner magnet, we can drive the inner magnet and the gripper to multiple directions, and pull tissue or organ to required position in operations, so as to get a clearer surgical field of view. On the basis of the previous animal experiments, we applied magnetic anchoring and traction device in 3 human (males aged 63-71 years) thoracoscopic esophagectomies. Using the magnetic anchoring device, we could pull the esophagus dorsally or ventrally to assist in exposing the anatomical plane without special equipment or pleural puncture for retraction of the esophagus. The interference between operating instruments reduced. The mean blood loss in operation was 83 mL, the mean total operation time was 253 min and the mean length of hospital stay was 10 d. Postoperative follow-up showed that all 3 patients had good short-term prognosis. There was no swellling or pain in magnetic anchoring zone of chest wall.

    Release date:2022-06-24 01:25 Export PDF Favorites Scan
  • An innovative exploration of endoscopic nipple-sparing mastectomy combined with immediate pre-pectoral implant-based breast reconstruction with TiLoop Bra via single axillary incision for breast cancer patients

    ObjectiveTo explore the surgical technique and preliminary results of endoscopic nipple-sparing mastectomy (E-NSM) and immediate pre-pectoral implant-based breast reconstruction (BR) with titanium-coated polypropylene mesh (TiLoop Bra) via single axillary incision for breast cancer patients.MethodsThe clinical data of 9 consecutive female patients who underwent E-NSM and immediate pre-pectoral implant-based BR with TiLoop Bra from March to May 2021 were retrospectively analyzed. The mean age of patients was 40.6 (22-60) years. The operation time, early complications were collected, and the patients' social and mental health, breast satisfaction and chest function before and after the operation were assessed with the BREAST-Q questionnaire.ResultsAll the patients had unicentric tumor with a mean diameter of 2.4 (0.6-4.7) cm. The mean distance from the tumor to the nipple was 2.5 (2-4) cm. There were 2 patients with tumor stage 0 and 7 patients with stageⅠ. The mean operation time was 161.1 (125-201) min, the mean blood loss was 41.1 mL and the hospital stay time was 1.5 d. There were 5 patients in the day-care unit. All the patients were successfully followed up with a median follow-up time of 1 (1-2) month. One (11.1%) patient with depigmentation of the nipple-areola complex caused by mild ischemia. None of the patients had incision complications, subcutaneous emphysema, hematoma, infection, nipple-areola or skin flaps necrosis, implant loss. During the follow-up period, no local/regional recurrence or distant metastasis was found. Chest well-being was decreased in the first month after the surgery compared with preoperative status, and the difference was statistically significant (P=0.001). There was no statistical difference in the breast satisfaction or psychosocial function scores between pre- and post-operation (P>0.05).ConclusionE-NSM and immediate pre-pectoral implant-based BR with TiLoop Bra via single axillary incision has minimal trauma, rapid postoperative recovery, short operation time, few early complications and good early cosmetic effect, and the short-term result is satisfactory.

    Release date:2021-09-18 02:21 Export PDF Favorites Scan
  • Clinical study for preoperative traction on impact of osteonecrosis of femoral head in patients with femoral neck fractures

    Objective To explore the impact of preoperative traction on the osteonecrosis of the femoral head (ONFH) in patients with femoral neck fractures. Methods Between February 2013 and May 2016, 120 patients with femoral neck fractures, who were treated with screw fixation, were collected. Sixty patients with fractures of Garden type Ⅰ and Ⅱ were non-displaced fracture group; 60 cases with fractures of Garden type Ⅲ and Ⅳ were displaced fracture group. The patients in 2 groups were randomly divided into traction and non-traction subgroups (n=30). There was no significant difference in gender, age, injury mechanism, damage side, the time from injury to operation, and fracture classification between 2 subgroups (P>0.05). Intracapsular pressure was recorded before operation. The quality of fracture reduction and the satisfaction ratio of screw implant were evaluated during operation. Visual analogue scale (VAS), Harris score, joint mobility, and the incidence of ONFH would be evaluated at 6 months, 1 year, and 2 years after operation. Results All incisions of 2 groups healed by first intention after operation. There was no infection or deep vein thrombosis of lower extremity. All patients were followed up 2 years. In displaced and non-displaced fracture groups, the intracapsular pressure of traction subgroups were higher than that of non-traction group (P<0.05); the differences of the quality of fracture reduction and the satisfaction ratio of screw implant were not significant (P>0.05) between 2 subgroups. At 6 months, 1 year, and 2 years after operation, VAS scores were higher in traction subgroup than in non-traction subgroup (P<0.05); and the joint mobility and Harris scores were lower in traction subgroup than in non-traction subgroup (P<0.05). X-ray films showed all fractures healed. Except for the non-displaced group at 6 months, the incidences of ONFH were higher in traction subgroup than in non-traction subgroup at other time points (P< 0.05). Conclusion Preoperative traction may increase the risk of ONFH, which can increase the intracapsular pressure and affect the blood supply of femoral head.

    Release date:2019-06-04 02:16 Export PDF Favorites Scan
  • Comparison of radiological changes after Halo-pelvic traction with posterior spinal osteotomy versus simple posterior spinal osteotomy for severe rigid spinal deformity

    ObjectiveTo compare the changes of scoliosis and kyphosis angles after Halo-pelvic traction with posterior spinal osteotomy versus simple posterior spinal osteotomy for severe rigid spinal deformity.MethodsA clinical data of 28 patients with severe rigid spinal deformity between January 2015 and November 2017 was retrospectively analyzed. Sixteen patients were treated by Halo-pelvic traction with posterior spinal osteotomy (group A) and 12 patients were treated with posterior spinal osteotomy only (group B). There was no significant difference between the two groups (P>0.05) in gender, age, body mass index, and preoperative pulmonary function, coronal and sagittal Cobb angles, and flexibility. The operation time, intraoperative blood loss, and complications were recorded. The coronal and sagittal Cobb angles were measured on X-ray films before operation (before traction in group A), at 10 days after operation, at last follow-up in the two groups and after traction in group A. The improvement rate of deformity after traction in group A, the correction rate of deformity after operation, and the loss rate of correction at last follow-up were calculated.ResultsAll patients were followed up 24-30 months (mean, 26.5 months). The operation time and intraoperative blood loss were significantly less in group A than in group B (t=7.629, P=0.000; t=8.773, P=0.000). In group A, 1 patient occurred transient numbness of both legs during continuous traction and 2 patients needed ventilator support for more than 12 hours. In group B, 7 patients needed ventilator support for more than 12 hours, including 1 patient with deep incision infection. The incidence of complications was 18.75% (3/16) in group A and 58.33% (7/12) in group B, and the difference between the two groups was significant (χ2=4.680, P=0.031). The coronal and sagittal improvement rates of deformity after traction in group A were 40.47%±3.60% and 40.70%±4.20%, respectively. There was no significant difference between the two groups (P>0.05) in the coronal and sagittal Cobb angles at 10 days after operation and at last follow-up, in the correction rate of deformity after operation, and in the loss rate of correction at last follow-up.ConclusionFor the severe rigid spinal deformity, Halo-pelvic traction with posterior spinal osteotomy and simple posterior spinal osteotomy can obtain the same orthopedic effect and postoperative deformity correction. However, the Halo-pelvic traction can shorten operation time, reduce blood loss and incidence of perioperative complications.

    Release date:2020-07-27 07:36 Export PDF Favorites Scan
  • A comparative study on effectiveness of closed reduction and internal fixation of intertrochanteric fracture assisted with skeletal tractor and traction table

    ObjectiveTo investigate the effectiveness and advantages of skeletal tractor in closed reduction and proximal femoral nail antirotation (PFNA) internal fixation of intertrochanteric fracture compared with traction table.MethodsThe clinical data of 86 patients with intertrochanteric fractures, who were treated with closed reduction and PFNA internal fixation between October 2016 and March 2018 and met the selection criteria, was retrospectively analysed. Among them, 44 cases were treated with skeletal tractor (trial group) and 42 cases were treated with traction table (control group). There was no significant difference between the two groups in gender, age, cause of injury, fracture side, AO classification, and degree of osteoporosis (P>0.05). The preoperative position time, operation time, intraoperative fluoroscopy times, intraoperative blood loss, fracture healing time, intraoperative and postoperative complications, and postoperative Harris score were compared between the two groups.ResultsThe operation was successfully completed in both groups. Compared with the control group, the patients in the trial group had shorter preoperative position time and operation time, fewer intraoperative fluoroscopy times, and less intraoperative blood loss (P<0.05). The patients were followed up 12-21 months in trial group (mean, 14.2 months) and 12-22 months in control group (mean, 14.3 months). Venous thrombosis of lower extremity occurred in 8 patients (3 cases of trial group and 5 cases of control group) after operation. Internal fixation failure occurred in 5 patients (2 cases of trial group and 3 cases of control group) during 1 year after operation. All fractures healed except for those with internal fixation failure, the fracture healing time was (11.6±2.9) weeks in trial group and (12.4±3.6) weeks in control group; and there was no significant difference between the two groups (t=1.250, P=0.214). At 1 year after operation, Harris score of the trial group was 86.2±5.9 and that of the control group was 84.1±6.1. There was no significant difference between the two groups (t=1.768, P=0.080).ConclusionCompared with traction table, skeletal tractor in closed reduction and PFNA internal fixation of intertrochanteric fracture can significantly shorten the preoperative position time and operation time, reduce the intraoperative fluoroscopy times, improve the operation efficiency, and have similar effectiveness.

    Release date:2020-04-29 03:03 Export PDF Favorites Scan
  • 腋窝入路腔镜下乳腺癌根治假体结合补片在一期乳房重建中的应用

    目的介绍腋窝入路腔镜下乳腺癌根治假体结合补片一期乳房重建术的手术方法及效果。方法回顾分析 2020 年 10 月—2021 年 2 月采用腋窝入路腔镜下乳腺癌根治假体结合补片一期乳房重建的 15 例女性患者临床资料。年龄 32~52 岁,平均 43 岁。术前临床分期:0 期 3 例,Ⅰ期 3 例,Ⅱ期 9 例。肿瘤均为单发,最大径 0.7~3.2 cm,平均 2.2 cm;肿瘤距离乳头 2~6 cm,平均 3.6 cm。术前及术后 1、3 个月采用 BREAST-Q 评分量表从乳房满意度、性满意度、胸部功能及心理社会健康方面评价疗效。结果术后切口均Ⅰ期愈合;出现乳房皮肤轻度缺血 1 例、皮下积液 1 例,均未出现切口并发症、皮下气肿、乳房内血肿形成、感染、乳头乳晕表皮层坏死、皮瓣坏死、假体和/或补片取出。患者均获随访,随访时间 5.0~9.5 个月,平均 7.6 个月。随访期间未发现肿瘤复发或转移。与术前相比,术后 1 个月乳房及性满意度、胸部功能、心理社会健康评分降低(P<0.05),但术后 3 个月乳房满意度、胸部功能评分差异已无统计学意义(P>0.05),性满意度、心理社会健康评分差异仍有统计学意义(P<0.05)。结论该术式创伤小、并发症少、术后恢复快、手术时间短、重建乳房外观较好,可获得满意疗效。

    Release date:2021-09-28 03:00 Export PDF Favorites Scan
  • Old Comprehensive Treatment of Patella Fractures Pxperience

    目的:探讨陈旧性髌骨骨折的最佳治疗方案。方法:我院1997.1~2007.12收治陈旧性髌骨骨折患者20例,均采用术前髌骨牵引、股四头肌锻炼,术中髌前纵形S切口、改良张力带固定骨折块,配合关节腔注射玻璃酸钠,术后早期行患肢CPM机功能锻炼。结果: 所有患者均获得随访,随访时间1.5~3.5年,平均2.2年。患者术后X片髌骨骨折块对位良好、关节面平整。术后切口甲级愈合,下床时间2d~21d,平均6.5d。骨折愈合时间3.0~6.5月,平均4.2月。术后1.5年膝关节HSS功能评分:优8例,良8例,可3例,差1例,优良率80%。结论: 术前牵引、术中正确处理骨折、术后术后早期锻炼等综合治疗陈旧性髌骨骨折疗效显著。

    Release date:2016-09-08 10:02 Export PDF Favorites Scan
  • 手术内固定治疗创伤性连枷胸对患者呼吸功能的影响

    目的观察连枷胸患者胸壁加压包扎、肋骨牵引和手术内固定的治疗效果。 方法纳入2001年1月至2010年6月解放军第一医院心胸外科收治的56例连枷胸患者,分为3组:牵引治疗组,14例,其中男10例、女4例,年龄(39.7±11.6)岁;包扎治疗组,12例,其中男11例、女1例,年龄(40.2±13.2)岁;手术内固定组,30例,其中男26例、女4例,年龄(42.6±12.5)岁。比较3组的治疗效果。 结果手术内固定组与牵引治疗组和包扎治疗组比较,除需呼吸机支持率与牵引治疗组差异无统计学意义(P>0.05)外,呼吸机通气时间、住ICU时间、胸腔引流管拔除时间均缩短(P<0.05),胸部并发症发生率及死亡率降低(P<0.05),动脉血氧分压(PaO2)、动脉血氧饱和度(SaO2)显著升高(P<0.01),肺挫伤评分下降明显;而牵引治疗组PaO2、SaO2及肺挫伤评分较入院时改善缓慢,胸壁加压包扎治疗组甚至有加重趋势。 结论大面积浮动胸壁的病理改变以胸腔容积减少为基础,胸壁加压包扎无治疗效果,甚至加重低氧;肋骨巾钳悬吊牵引固定对连枷胸缺氧内环境的改善效果不佳;手术切开复位内固定是改善大面积浮动胸壁呼吸功能障碍的有效方法。

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  • The development and recent status of the craniomaxillofacial surgery in China during past three decades

    The authors made a profound review on the development and the recent status of craniomaxillofacial surgery in China during past three decades. The emphases were placed on the following aspects: the modifications of the reconstructive procedure and minimal invasive mode, the researches on molecular genetic characteristics of the congenital craniofacial malformations, the clinical applications of three-dimensional digital computer-aided techniques (including three-dimensional printing and prefabricated template for precious osteotomies), the craniomaxillofacial defects reconstructing by using the distraction osteogenesis and osseous integrated titanium implant and prothesis, etc. Finally, the authors outlooked prospectively the future trends of the craniomaxillofacial surgery.

    Release date:2018-07-12 06:19 Export PDF Favorites Scan
  • The current status and progress of ocriplasmin in treating vitreomacular interface diseases

    As a potent collagenase activator, ocriplasmin is a recombinant truncated form of serine protease that retains the protease activity of plasmin. Pre-clinical animal experiments, clinical trials and recent clinical studies all indicated a promising outcome of intravitreal injection of ocriplasmin to treat vitreomacular interface diseases, including vitreomacular adhesion (VMA), vitreomacular traction (VMT) and full-thickness macular hole. Ocriplasmin was approved by the Food and Drug Administration of USA in the management of symptomatic VMA, and by the European Medicines Agency in treating VMT-associated macular hole with less than or equal 400 μm. Further randomized controlled clinical trials are needed for further comprehensive observation and evaluation on its efficiency, safety and other noteworthy issues.

    Release date:2017-04-01 08:56 Export PDF Favorites Scan
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