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[Treatment of thoracolumbar tuberculosis with robot-assisted and minimally invasive access via transforaminal expansion approach]. [通过机器人辅助和经椎间孔扩张微创入路治疗胸腰椎结核]。
Q3 Medicine Pub Date : 2024-08-15 DOI: 10.7507/1002-1892.202405079
Qunlong Pan, Haiming Yu, Yizhong Li, Xiaoyu He, Jinnan Shi

Objective: To investigate the feasibility and effectiveness of robot-assisted posterior minimally invasive access in treatment of thoracolumbar tuberculosis via transforaminal expansion approach.

Methods: A clinical data of 40 patients with thoracolumbar tuberculosis admitted between January 2017 and May 2022 and met the selection criteria was retrospectively analyzed. Among them, 15 cases were treated with robot-assisted and minimally invasive access via transforaminal expansion approach for lesion removal, bone graft, and internal fixation (robotic group), and 25 cases were treated with traditional transforaminal posterior approach for lesion removal and intervertebral bone grafting (traditional group). There was no significant difference in the baseline data between the two groups ( P>0.05) in terms of gender, age, lesion segment, and preoperative American Spinal Injury Association (ASIA) grading, Cobb angle, visual analogue scale (VAS) score, erythrocyte sedimentation rate (ESR), and C reactive protein (CRP). The outcome indicators were recorded and compared between the two groups, including operation time, intraoperative bleeding volume, hospital stay, postoperative bedtime, complications, ESR and CRP before operation and at 1 week after operation, the level of serum albumin at 3 days after operation, VAS score and ASIA grading of neurological function before operation and at 6 months after operation, the implant fusion, fusion time, Cobb angle of the lesion, and the loss of Cobb angle observed by X-ray films and CT. The differences of ESR, CRP, and VAS score (change values) between pre- and post-operation were calculated and compared.

Results: Compared with the traditional group, the operation time and intraoperative bleeding volume in the robotic group were significantly lower and the serum albumin level at 3 days after operation was significantly higher ( P<0.05); the postoperative bedtime and the length of hospital stay were also shorter, but the difference was not significant ( P>0.05). There were 2 cases of poor incision healing in the traditional group, but no complication occurred in the robotic group, and the difference in the incidence of complication between the two groups was not significant ( P>0.05). There were significant differences in the change values of ESR and CRP between the two groups ( P<0.05). All Patients were followed up, and the follow-up time was 12-18 months (mean, 13.0 months) in the traditional group and 12-16 months (mean, 13.0 months) in the robotic group. Imaging review showed that all bone grafts fused, and the difference in fusion time between the two groups was not significant ( P>0.05). The difference in Cobb angle between the pre- and post-operation in the two groups was significant ( P<0.05); and the Cobb angle loss was significant more in the traditional group than in the robotic group (

目的方法:回顾性分析2017年1月至2022年5月收治的40例符合入选标准的胸腰椎结核患者的临床资料:回顾性分析2017年1月至2022年5月期间收治的符合入选标准的40例胸腰椎结核患者的临床资料。其中,15例采用机器人辅助微创入路经椎间孔扩张入路进行病灶清除、植骨、内固定治疗(机器人组),25例采用传统经椎间孔后入路进行病灶清除、椎间植骨治疗(传统组)。两组患者在性别、年龄、病变节段、术前美国脊柱损伤协会(ASIA)分级、Cobb角、视觉模拟量表(VAS)评分、红细胞沉降率(ESR)和C反应蛋白(CRP)等基线数据方面无明显差异(P>0.05)。记录并比较两组患者的手术时间、术中出血量、住院时间、术后卧床时间、并发症、术前和术后1周的血沉和CRP、术后3天的血清白蛋白水平、术前和术后6个月的神经功能VAS评分和ASIA分级、植入物融合情况、融合时间、病灶的Cobb角、X光片和CT观察到的Cobb角消失情况等结果指标。计算并比较手术前后 ESR、CRP 和 VAS 评分(变化值)的差异:与传统组相比,机器人组的手术时间和术中出血量明显减少,术后 3 天的血清白蛋白水平明显升高(PP>0.05)。传统组有 2 例切口愈合不良,而机器人组未发生并发症,两组并发症发生率差异无学意义(P>0.05)。两组的血沉和 CRP 变化值差异有学意义(PP>0.05)。两组患者手术前后的 Cobb 角差异有学意义(PPPP>0.05)。两组患者术后均未出现或加重脊髓神经功能损伤。两组术后6个月的ASIA分级与术前相比差异有学意义(PP>0.05):与传统的后路开放手术相比,采用机器人辅助下经椎间孔微创入路进行病灶清除和植骨内固定治疗胸腰椎结核,可缩短手术时间,减少术中出血,最大限度地减少手术创伤,疗效确切。
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引用次数: 0
[Clinical analysis of breast reconstruction with endoscopic-assisted harvesting of latissimus dorsi muscle flap for breast cancer]. [乳腺癌背阔肌肌皮瓣内窥镜辅助采集乳房重建临床分析]。
Q3 Medicine Pub Date : 2024-07-15 DOI: 10.7507/1002-1892.202403136
Jiangtao Li, Chenlu Liu, Xinyu Ou, Yiwen Lu, Shicheng Su, Zhihan Liu

Objective: To investigate the benefits and drawbacks of breast reconstruction with endoscopic-assisted harvesting of the latissimus dorsi muscle flap for breast cancer and treatment experience of postoperative operation-related complications.

Methods: A retrospective analysis was performed on clinical data of 26 female patients with breast cancer who met the selection criteria between September 2021 and March 2023 aging 48.7 years (range, 26-69 years). All tumors were unilateral, with 17 on the left side and 9 on the right side. The tumor size ranged from 1.0 to 7.0 cm, with an average of 2.7 cm. The pathological staging included T 1 in 11 cases, T 2 in 14 cases, and T 3 in 1 case; N 0 in 10 cases, N 1 in 11 cases, N 2 in 2 cases, and N 3 in 3 cases; no distant metastasis (M 0) occurred when first diagnosed. Among them, 10 cases underwent breast conserving surgery, and 16 cases underwent nipple-sparing mastectomy. All patients underwent breast reconstruction with endoscopic-assisted harvesting of the latissimus dorsi muscle flap. The operation time, incision length, and postoperative drainage volume in 3 days were recorded. Breast-Q "Satisfaction with back" scale was conducted to evaluate patients' satisfaction with back at 6 months after operation.

Results: The operation time was 280-480 minutes (mean, 376.7 minutes), the incision length was 10-15 cm (mean, 12.2 cm), the postoperative drainage volume in 3 days was 500-1 600 mL (mean, 930.2 mL). There were 4 cases of postoperative seroma, 1 case of incision rupture, 1 case of paresthesia of the thoracic wall, and 1 case of edema of the ipsilateral upper limb. All patients were followed up 12-30 months (mean, 20.1 months). No latissimus dorsi muscle flap necrosis, latissimus dorsi muscle atrophy, or shoulder joint dysfunction occurred during follow-up; 2 patients had recurrence of lymph nodes in the ipsilateral axilla after operation, but no distant metastasis occurred. Breast-Q score at 6 months after operation was 64-100 (mean, 79.5). The average score was 78.6 (range, 64-100) in patients underwent nipple-sparing mastectomy and 81.0 (range, 78-100) in patients underwent breast conserving surgery.

Conclusion: Breast reconstruction with endoscopic-assisted harvesting of the latissimus dorsi muscle flap for breast cancer is proven to be a surgical approach with safety and cosmetic effects with mild postoperative operation-related complications and considerable patient satisfaction.

目的研究乳腺癌患者在内窥镜辅助下采集背阔肌肌皮瓣进行乳房重建的利弊,以及术后相关并发症的治疗经验:对2021年9月至2023年3月期间符合入选标准的26例女性乳腺癌患者的临床数据进行回顾性分析,患者年龄为48.7岁(26-69岁)。所有肿瘤均为单侧,其中左侧 17 例,右侧 9 例。肿瘤大小从1.0厘米到7.0厘米不等,平均为2.7厘米。病理分期为 T 1(11 例)、T 2(14 例)、T 3(1 例);N 0(10 例)、N 1(11 例)、N 2(2 例)、N 3(3 例);初诊时无远处转移(M 0)。其中,10 例接受了保乳手术,16 例接受了乳头保留乳房切除术。所有患者都接受了内窥镜辅助下的背阔肌肌皮瓣采集乳房重建术。记录了手术时间、切口长度和术后 3 天的引流量。采用乳房-Q "背部满意度 "量表评估患者术后 6 个月的背部满意度:手术时间为 280-480 分钟(平均 376.7 分钟),切口长度为 10-15 厘米(平均 12.2 厘米),术后三天引流量为 500-1600 毫升(平均 930.2 毫升)。术后血清肿 4 例,切口破裂 1 例,胸壁麻痹 1 例,同侧上肢水肿 1 例。所有患者均接受了 12-30 个月(平均 20.1 个月)的随访。随访期间未发生背阔肌皮瓣坏死、背阔肌萎缩或肩关节功能障碍;2 例患者术后同侧腋窝淋巴结复发,但未发生远处转移。术后 6 个月的乳房 Q 值为 64-100(平均 79.5)。接受乳头保留乳房切除术的患者平均得分为78.6(范围为64-100),接受保乳手术的患者平均得分为81.0(范围为78-100):结论:乳腺癌患者在内窥镜辅助下采集背阔肌肌皮瓣进行乳房再造被证明是一种安全且具有美容效果的手术方法,术后相关并发症较少,患者满意度较高。
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引用次数: 0
[Comparison of mid-term effectiveness between diabetic secondary stiff shoulder and primary frozen shoulder after arthroscopic shoulder capsular release combined with acromiohumeral distance restoration]. [肩关节镜下肩关节囊松解联合肩肱骨距离复位术后糖尿病继发性僵硬肩与原发性肩周炎的中期疗效比较]。
Q3 Medicine Pub Date : 2024-07-15 DOI: 10.7507/1002-1892.202403078
Zhou Zhou, Jun Wang, Huaisheng Li, Aining Yang, Kanglai Tang, You Zhou, Binghua Zhou

Objective: To compare the mid-term effectiveness of arthroscopic shoulder capsular release combined with acromiohumeral distance (AHD) restoration in the treatment of diabetic secondary stiff shoulder and primary frozen shoulder.

Methods: A retrospective analysis was conducted on clinical data of 22 patients with diabetic secondary stiff shoulder (group A) and 33 patients with primary frozen shoulder (group B), who underwent arthroscopic 270° capsular release combined with AHD restoration treatment. There was no significant difference between the two groups in gender, age, affected side, disease duration, and preoperative AHD, shoulder flexion range of motion, abduction range of motion, American Shoulder and Elbow Surgeons (ASES) score, visual analogue scale (VAS) score, and Constant score ( P>0.05). Only the difference in the internal rotation cone rank and external rotation range of motion between the two groups showed significant differences ( P<0.05). The improvement in shoulder pain and function was evaluated by using VAS score, ASES score, and Constant score before operation and at last follow-up. Active flexion, abduction, external rotation range of motion, and internal rotation cone rank were recorded and compared. AHD was measured on X-ray films.

Results: All patients were followed up 24-92 months (median, 57 months). There was no significant difference in follow-up time between group A and group B ( P>0.05). No fractures or glenoid labrum tears occurred during operation, all incisions healed by first intention, and no complication such as wound infection or nerve injury was observed during the follow-up. At last follow-up, there were significant improvements in active flexion, abduction, external rotation range of motion, internal rotation cone rank, AHD, VAS score, ASES score, and Constant score when compared with preoperative ones in both groups ( P<0.05). Except for the difference in change in external rotation range of motion, which had significant difference between the two groups ( P<0.05), there was no significant difference in other indicators between the two groups ( P>0.05).

Conclusion: Arthroscopic capsular release combined with AHD restoration can achieve good mid-term effectiveness in the treatment of diabetic secondary stiff shoulder and primary frozen shoulder. However, the improvement in external rotation range of motion is more significant in the patients with diabetic secondary stiff shoulder.

目的比较关节镜下肩关节囊松解联合肩肱距离(AHD)修复术治疗糖尿病继发性肩关节僵硬和原发性肩周炎的中期疗效:对22例糖尿病继发性肩关节僵硬患者(A组)和33例原发性肩周炎患者(B组)的临床数据进行了回顾性分析。两组患者在性别、年龄、患侧、病程、术前AHD、肩关节屈曲活动范围、外展活动范围、美国肩肘外科医生(ASES)评分、视觉模拟量表(VAS)评分和Constant评分方面均无明显差异(P>0.05)。只有内旋锥体等级和外旋活动范围在两组间存在显著差异(PResults:所有患者的随访时间为 24-92 个月(中位数为 57 个月)。A 组和 B 组的随访时间无明显差异(P>0.05)。手术过程中未发生骨折或盂唇撕裂,所有切口均第一意向愈合,随访期间未发现伤口感染或神经损伤等并发症。最后一次随访时,两组患者的主动屈曲、外展、外旋活动范围、内旋锥体等级、AHD、VAS评分、ASES评分和Constant评分与术前相比均有明显改善(PPP>0.05):结论:关节镜下肩关节囊松解联合AHD修复术在治疗糖尿病继发性肩关节僵硬和原发性肩周炎方面可取得良好的中期疗效。结论:关节镜下肩关节囊松解联合AHD修复术在治疗糖尿病继发性肩关节僵硬和原发性肩周炎方面可取得良好的中期疗效,但糖尿病继发性肩关节僵硬患者的外旋活动范围改善更为显著。
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引用次数: 0
[Analysis of kinematic changes of hip joint after total hip arthroplasty]. [全髋关节置换术后髋关节运动学变化分析]。
Q3 Medicine Pub Date : 2024-07-15 DOI: 10.7507/1002-1892.202403111
Duanyong Chen, Mengyuan Li, Yuhui Yang, Qiujian Zheng

Objective: To analyze the kinematic changes of the hip joint after total hip arthroplasty (THA) through three-dimensional gait analysis.

Methods: Patients with hip joint diseases admitted between October 2022 and June 2023 were selected as the subjects. The patients who met the selective criteria were finally included in the THA group. The healthy volunteers matched with the THA group in the same age were included as the control group. Baseline data including age, gender, body mass index (BMI), and laterality were compared between the two groups. The Harris hip score (HHS) and the Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) score were recorded preoperatively and at last follow-up in the THA group. Three-dimensional motion capture system was utilized to collect spatiotemporal parameters and kinematic data during walking, including stride length, cadence, and maximum/minimum values, range of motion (ROM) in hip joint abduction/adduction, external/internal rotation, and flexion/extension, as well as gait scores. Differences between the two groups were analyzed. Additionally, the correlation between gait scores and postoperative HHS and WOMAC scores were analyzed in the THA group. Finally, the kinematic data of each degree of freedom (DOF) were fitted into a gait diagram, and the dynamic changes of the 3-DOF of the hip joint during the gait cycle were quantitatively analyzed.

Results: There was no significant difference in gender, age, laterality, and BMI between the two groups ( n=20, P>0.05). The mean follow-up time in the THA group was 9.9 months (range, 6-12 months). The HHS and WOMAC scores at last follow-up in the THA group showed significant improvement when compared with preoperative scores ( P<0.05). Gait scores were positively correlated with postoperative HHS score ( r=0.585, P=0.007) and negatively correlated with WOMAC score ( r=-0.619, P=0.004). There was no significant difference in stride length and cadence between the THA and control groups ( P>0.05), but gait score was significantly lower in the THA group than in the control group ( P<0.05). There was no significant difference in maximum and minimum values of flexion/extension, external/internal rotation, and abduction/adduction between the two groups ( P>0.05); however, ROM in the THA group was significantly lower than that in the control group ( P<0.05). There were significant differences between the two groups of flexion/extension in multiple phases of the gait cycle ( P<0.05).

Conclusion: Early post-THA hip joint kinematics exhibit relative adduction, external rotation, and flexion during the gait cycle compared to normal individuals, with incomplete recovery of kinematic parameters in three degrees of freedom. Significant differences in flexion are observed at multiple phases of th

目的:通过三维步态分析通过三维步态分析,分析全髋关节置换术(THA)后髋关节的运动学变化:选取 2022 年 10 月至 2023 年 6 月期间收治的髋关节疾病患者作为研究对象。方法:选取 2022 年 10 月至 2023 年 6 月期间入院的髋关节疾病患者作为研究对象,最终将符合选择标准的患者纳入 THA 组。与 THA 组年龄相仿的健康志愿者作为对照组。比较两组患者的基线数据,包括年龄、性别、体重指数(BMI)和侧位。记录THA组患者术前和最后一次随访时的哈里斯髋关节评分(HHS)和西安大略与麦克马斯特大学骨关节炎指数(WOMAC)评分。利用三维运动捕捉系统收集行走时的时空参数和运动学数据,包括步长、步幅、最大/最小值、髋关节外展/内收、外旋/内旋、屈/伸的运动范围(ROM)以及步态评分。对两组之间的差异进行了分析。此外,还分析了 THA 组步态评分与术后 HHS 和 WOMAC 评分之间的相关性。最后,将每个自由度(DOF)的运动学数据拟合到步态图中,定量分析步态周期中髋关节 3-DOF 的动态变化:两组患者在性别、年龄、侧位和体重指数方面无明显差异(n=20,P>0.05)。THA组的平均随访时间为9.9个月(6-12个月)。THA组最后一次随访时的HHS和WOMAC评分与术前评分相比有显著改善(Pr=0.585,P=0.007),并与WOMAC评分呈负相关(r=-0.619,P=0.004)。THA组与对照组在步长和步频方面无明显差异(P>0.05),但THA组的步态评分明显低于对照组(PP>0.05);然而,THA组的ROM明显低于对照组(PPC结论:与正常人相比,THA术后早期髋关节运动学在步态周期中表现出相对内收、外旋和屈曲,三个自由度的运动学参数未完全恢复。在步态周期的多个阶段,与正常人相比,屈曲度存在显著差异。
{"title":"[Analysis of kinematic changes of hip joint after total hip arthroplasty].","authors":"Duanyong Chen, Mengyuan Li, Yuhui Yang, Qiujian Zheng","doi":"10.7507/1002-1892.202403111","DOIUrl":"10.7507/1002-1892.202403111","url":null,"abstract":"<p><strong>Objective: </strong>To analyze the kinematic changes of the hip joint after total hip arthroplasty (THA) through three-dimensional gait analysis.</p><p><strong>Methods: </strong>Patients with hip joint diseases admitted between October 2022 and June 2023 were selected as the subjects. The patients who met the selective criteria were finally included in the THA group. The healthy volunteers matched with the THA group in the same age were included as the control group. Baseline data including age, gender, body mass index (BMI), and laterality were compared between the two groups. The Harris hip score (HHS) and the Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) score were recorded preoperatively and at last follow-up in the THA group. Three-dimensional motion capture system was utilized to collect spatiotemporal parameters and kinematic data during walking, including stride length, cadence, and maximum/minimum values, range of motion (ROM) in hip joint abduction/adduction, external/internal rotation, and flexion/extension, as well as gait scores. Differences between the two groups were analyzed. Additionally, the correlation between gait scores and postoperative HHS and WOMAC scores were analyzed in the THA group. Finally, the kinematic data of each degree of freedom (DOF) were fitted into a gait diagram, and the dynamic changes of the 3-DOF of the hip joint during the gait cycle were quantitatively analyzed.</p><p><strong>Results: </strong>There was no significant difference in gender, age, laterality, and BMI between the two groups ( <i>n</i>=20, <i>P</i>>0.05). The mean follow-up time in the THA group was 9.9 months (range, 6-12 months). The HHS and WOMAC scores at last follow-up in the THA group showed significant improvement when compared with preoperative scores ( <i>P</i><0.05). Gait scores were positively correlated with postoperative HHS score ( <i>r</i>=0.585, <i>P</i>=0.007) and negatively correlated with WOMAC score ( <i>r</i>=-0.619, <i>P</i>=0.004). There was no significant difference in stride length and cadence between the THA and control groups ( <i>P</i>>0.05), but gait score was significantly lower in the THA group than in the control group ( <i>P</i><0.05). There was no significant difference in maximum and minimum values of flexion/extension, external/internal rotation, and abduction/adduction between the two groups ( <i>P</i>>0.05); however, ROM in the THA group was significantly lower than that in the control group ( <i>P</i><0.05). There were significant differences between the two groups of flexion/extension in multiple phases of the gait cycle ( <i>P</i><0.05).</p><p><strong>Conclusion: </strong>Early post-THA hip joint kinematics exhibit relative adduction, external rotation, and flexion during the gait cycle compared to normal individuals, with incomplete recovery of kinematic parameters in three degrees of freedom. Significant differences in flexion are observed at multiple phases of th","PeriodicalId":23979,"journal":{"name":"中国修复重建外科杂志","volume":"38 7","pages":"849-854"},"PeriodicalIF":0.0,"publicationDate":"2024-07-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11252683/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141627837","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
[Clinical application of endoscopic radical mastectomy for breast cancer combined with total pectoral muscle reconstruction with breast implants]. [内窥镜乳腺癌根治术联合全胸肌重建与乳房植入物的临床应用]。
Q3 Medicine Pub Date : 2024-07-15 DOI: 10.7507/1002-1892.202403102
Xiangmei He, Lan Hou, Donghui Wang, Liu Yang, Danxi Li, Yuan Qin, Mingkun Zhang, Ge Zhao, Huan Zhang, Juliang Zhang

Objective: To investigate the effectiveness of endoscopic radical mastectomy for breast cancer combined with total pectoral muscle reconstruction with breast implants.

Methods: The clinical data of 138 female patients with breast cancer who met the selection criteria between April 2019 and December 2023 were retrospectively analyzed. The mean age of the patients was 43.8 years (range, 27-61 years). The maximum diameter of the tumors ranged from 1.00 to 7.10 cm, with an average of 2.70 cm. Pathological examination showed that 108 cases were positive for both estrogen receptor and progesterone receptor, and 40 cases were positive for human epidermal growth factor receptor 2. All patients underwent endoscopic radical mastectomy for breast cancer combined with total pectoral muscle reconstruction with breast implants. The operation time, intraoperative blood loss, prosthesis size, and occurences of nipple-areola complex (NAC) ischemia, flap ischemia, infection, and capsular contracture were recorded. The Breast-Q2.0 score was used to evaluate breast aesthetics, patient satisfaction, and quality of life (including the social mental health score, breast satisfaction score, and chest pain score). Patients were divided into two groups based on the time of operation after the technique was implemented: group A (within 1 year, 25 cases) and group B (after 1 year, 113 cases). The above outcome indicators were compared between the two groups. Furthermore, based on the postoperative follow-up duration, patients were classified into a short-term group (follow-up time was less than 1 year) and a long-term group (follow-up time was more than 1 year). The baseline data and postoperative Breast-Q2.0 scores were compared between the two groups.

Results: The average operation time was 120.76 minutes, the average intraoperative blood loss was 23.77 mL, and the average prosthesis size was 218.37 mL. Postoperative NAC ischemia occurred in 21 cases (15.22%), flap ischemia in 30 cases (21.74%), infection in 23 cases (16.67%), capsular contracture in 33 cases (23.91%), and prosthesis removal in 2 cases (1.45%). The operation time of group A was significantly longer than that of group B ( P<0.05), and there was no significant difference in intraoperative blood loss, prosthesis size, and related complications between the two groups ( P>0.05). All patients were followed up 3-48 months (mean, 20 months). There were 33 cases in the short-term group and 105 cases in the long-term group. There was no significant difference in baseline data such as age, body mass index, number of menopause cases, number of neoadjuvant chemotherapy cases, number of axillary lymph node dissection cases, breast cup size, degree of breast ptosis, and postoperative radiotherapy constituent ratio between the two groups ( P>0.05). At last follow-up, the breast satisfaction score in the patients' Breast-Q2.0 score rang

目的研究内镜下乳腺癌根治性切除术联合全胸肌重建与乳房假体植入的有效性:回顾性分析2019年4月至2023年12月期间符合入选标准的138例女性乳腺癌患者的临床资料。患者的平均年龄为 43.8 岁(27-61 岁)。肿瘤的最大直径从 1.00 厘米到 7.10 厘米不等,平均为 2.70 厘米。病理检查显示,108 例患者的雌激素受体和孕激素受体均呈阳性,40 例患者的人表皮生长因子受体 2 呈阳性。所有患者均接受了内镜下乳腺癌根治性切除术,并用乳房假体进行了全胸肌重建。记录了手术时间、术中失血量、假体大小以及乳头乳晕复合体(NAC)缺血、皮瓣缺血、感染和包膜挛缩的发生率。乳房-Q2.0评分用于评估乳房美学、患者满意度和生活质量(包括社会心理健康评分、乳房满意度评分和胸痛评分)。根据技术实施后的手术时间将患者分为两组:A 组(1 年内,25 例)和 B 组(1 年后,113 例)。两组患者的上述结果指标进行了比较。此外,根据术后随访时间,将患者分为短期组(随访时间少于 1 年)和长期组(随访时间超过 1 年)。比较两组患者的基线数据和术后乳房-Q2.0评分:平均手术时间为 120.76 分钟,术中平均失血量为 23.77 mL,平均假体大小为 218.37 mL。术后NAC缺血21例(15.22%),皮瓣缺血30例(21.74%),感染23例(16.67%),包膜挛缩33例(23.91%),假体取出2例(1.45%)。A 组的手术时间明显长于 B 组(PP>0.05)。所有患者均接受了 3-48 个月(平均 20 个月)的随访。短期组有 33 例,长期组有 105 例。两组患者在年龄、体重指数、绝经例数、新辅助化疗例数、腋窝淋巴结清扫例数、乳房罩杯大小、乳房下垂程度、术后放疗成分比等基线数据上无明显差异(P>0.05)。最后一次随访时,患者的 Breast-Q2.0 评分中,乳房满意度评分从 33 分到 100 分不等,平均为 60.9 分;社会心理健康评分从 38 分到 100 分不等,平均为 71.3 分;胸痛评分从 20 分到 80 分不等,平均为 47.3 分。长期组的社会心理健康评分明显高于短期组(PP>0.05)。随访期间没有患者死亡,2 名患者分别在术后 649 天和 689 天复发。无复发生存率为98.62%:结论:内镜下乳腺癌根治性切除术联合全胸肌重建与乳房假体植入术并发症少、损伤小,重建乳房的美学效果更好。
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引用次数: 0
[Effect of different degrees of primary varus knee on short-term effectiveness of anterior cruciate ligament reconstruction]. [不同程度的原发性膝关节外翻对前交叉韧带重建术短期效果的影响]。
Q3 Medicine Pub Date : 2024-07-15 DOI: 10.7507/1002-1892.202403019
Fuji Ren, Jiang Wu, Dong Zhao, Rui Wang, Jingmin Huang

Objective: To investigate whether different degrees of primary varus knee affect joint function and stability in patients undergoing anterior cruciate ligament (ACL) reconstruction.

Methods: A clinical data of 160 patients with primary varus knee, who were admitted between January 2020 and December 2021 and met the selection criteria, was retrospectively analyzed. All patients underwent primary ACL reconstruction using autologous single-bundle hamstring tendon. Patients were divided into three groups based on the hip-knee-ankle angle (HKA): group A (64 patients with HKA 0°-3°), group B (55 patients with HKA 3°-6°), and group C (41 patients with HKA 6°-9°). Except for the significant difference in HKA among the three groups ( P<0.05), baseline data such as age, gender, affected side, body mass index, interval between injury and operation, Kellgren-Lawrence grading, posterior tibial slope, proportion of combined meniscal injuries, Tegner score, Lysholm score, and International Knee Documentation Committee (IKDC) objective score, anterior drawer test, Lachman test, pivot shift test, and the results of KT1000 (side-to-side difference, SSD) showed no significant difference ( P>0.05). At last follow-up, joint stability was assessed through the anterior drawer test, Lachman test, pivot shift test, and SSD; joint function was evaluated using the Tegner score, Lysholm score, and IKDC objective score.

Results: All incisions in the three groups healed by first intention after operation. All patients were followed up 24-31 months, with an average of 26 months; there was no significant difference in the follow-up time among the three groups ( Z=0.675, P=0.714). At last follow-up, the knee stability and functional assessment indicators in each group significantly improved when compared to preoperative ones ( P<0.05); there was no significant difference among the three groups ( P>0.05) in terms of the anterior drawer test, Lachman test, pivot shift test, IKDC objective scores, and the changes of the Lysholm scores and Tegner scores. The Kellgren-Lawrence grading and HKA at last follow-up were consistent with preoperative results in the three groups.

Conclusion: Varying degrees of primary varus knee do not affect early knee joint stability and functional recovery after ACL reconstruction, and there is no significant difference in effectiveness between different degrees of varus knee.

目的探讨不同程度的原发性膝关节内翻是否会影响前交叉韧带(ACL)重建术患者的关节功能和稳定性:方法:回顾性分析 2020 年 1 月至 2021 年 12 月期间收治的符合入选标准的 160 例原发性膝关节内翻患者的临床数据。所有患者均接受了使用自体单束腘绳肌腱的原发性前交叉韧带重建术。根据髋膝踝角度(HKA)将患者分为三组:A组(64例,HKA 0°-3°)、B组(55例,HKA 3°-6°)和C组(41例,HKA 6°-9°)。三组患者的 HKA 差异显著(PP>0.05)。最后一次随访时,通过前抽屉试验、Lachman试验、枢轴移位试验和SSD评估关节稳定性;通过Tegner评分、Lysholm评分和IKDC客观评分评估关节功能:结果:三组患者的切口均在术后第一意向愈合。所有患者均接受了 24-31 个月的随访,平均随访时间为 26 个月;三组患者的随访时间无显著差异(Z=0.675,P=0.714)。在最后一次随访中,各组患者的膝关节稳定性和功能评估指标与术前相比均有明显改善(PP>0.05),包括前抽屉试验、Lachman试验、枢轴移位试验、IKDC客观评分以及Lysholm评分和Tegner评分的变化。三组患者最后一次随访时的 Kellgren-Lawrence 分级和 HKA 与术前结果一致:结论:不同程度的原发性膝关节内翻不会影响前交叉韧带重建术后早期膝关节的稳定性和功能恢复,而且不同程度的膝关节内翻在效果上没有显著差异。
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引用次数: 0
[Implementation and development of endoscopic benign breast lump resection and breast-conserving surgery for cancer]. [内窥镜乳腺良性肿块切除术和癌症保乳手术的实施与发展]。
Q3 Medicine Pub Date : 2024-07-15 DOI: 10.7507/1002-1892.202403050
Xuliren Wang, Min Xiong, Zhibo Shao, Bingqiu Xiu, Jiong Wu, Benlong Yang

Objective: To review the development of endoscopic techniques in breast surgery, focusing on their use in benign breast lump resection and breast-conserving surgery for cancer, and also summarize the development and application of these techniques in China, highlighting promotion and homogenization challenges and future directions.

Methods: A systematic review of relevant literature was conducted to trace the historical evolution, clinical applications, and related research of endoscopic techniques in breast surgery, emphasizing their advantages and disadvantages of endoscopic benign breast lump resection and breast-conserving surgery for cancer.

Results: Endoscopic benign breast lump resection and breast-conserving surgery for cancer have improved patients' postoperative psychological health and quality of life, particularly in scar-free surgery. However, challenges such as limited intraoperative visibility and prolonged surgery time lead to controversy in clinical practice.

Conclusion: Despite significant advancements, endoscopic techniques in breast surgery also face challenges. Future efforts should focus on technological improvements and clinical research to address these issues, promoting widespread application and standardization. The key to future development lies in the promotion and homogenization of these technologies.

目的回顾内镜技术在乳腺外科中的发展,重点关注其在乳腺良性肿块切除和肿瘤保乳手术中的应用,同时总结这些技术在中国的发展和应用情况,强调推广和同质化的挑战以及未来的发展方向:方法:对相关文献进行系统综述,追溯乳腺外科内镜技术的历史演变、临床应用及相关研究,强调内镜下乳腺良性肿块切除术和肿瘤保乳手术的优缺点:结果:内窥镜乳腺良性肿块切除术和癌症保乳手术改善了患者的术后心理健康和生活质量,尤其是无疤痕手术。然而,术中可见度有限、手术时间延长等挑战导致临床实践中存在争议:结论:尽管内窥镜技术在乳腺手术中取得了重大进展,但也面临着挑战。结论:尽管内窥镜技术在乳腺手术中取得了重大进展,但也面临着挑战。未来的工作重点应放在技术改进和临床研究上,以解决这些问题,促进广泛应用和标准化。未来发展的关键在于这些技术的推广和同质化。
{"title":"[Implementation and development of endoscopic benign breast lump resection and breast-conserving surgery for cancer].","authors":"Xuliren Wang, Min Xiong, Zhibo Shao, Bingqiu Xiu, Jiong Wu, Benlong Yang","doi":"10.7507/1002-1892.202403050","DOIUrl":"10.7507/1002-1892.202403050","url":null,"abstract":"<p><strong>Objective: </strong>To review the development of endoscopic techniques in breast surgery, focusing on their use in benign breast lump resection and breast-conserving surgery for cancer, and also summarize the development and application of these techniques in China, highlighting promotion and homogenization challenges and future directions.</p><p><strong>Methods: </strong>A systematic review of relevant literature was conducted to trace the historical evolution, clinical applications, and related research of endoscopic techniques in breast surgery, emphasizing their advantages and disadvantages of endoscopic benign breast lump resection and breast-conserving surgery for cancer.</p><p><strong>Results: </strong>Endoscopic benign breast lump resection and breast-conserving surgery for cancer have improved patients' postoperative psychological health and quality of life, particularly in scar-free surgery. However, challenges such as limited intraoperative visibility and prolonged surgery time lead to controversy in clinical practice.</p><p><strong>Conclusion: </strong>Despite significant advancements, endoscopic techniques in breast surgery also face challenges. Future efforts should focus on technological improvements and clinical research to address these issues, promoting widespread application and standardization. The key to future development lies in the promotion and homogenization of these technologies.</p>","PeriodicalId":23979,"journal":{"name":"中国修复重建外科杂志","volume":"38 7","pages":"776-780"},"PeriodicalIF":0.0,"publicationDate":"2024-07-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11252680/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141627865","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
[Effectiveness comparison of endoscopic removal of injectable Amazingel with/without immediate prepectoral implant-based breast augmentation]. [内窥镜下取出注射用 Amazingel 和/或立即胸前植入假体隆胸的效果比较]。
Q3 Medicine Pub Date : 2024-07-15 DOI: 10.7507/1002-1892.202404032
Kawun Chung, Huanzuo Yang, Yanyan Xie, Faqing Liang, Yu Feng, Donglin Zhang, Zhenggui Du

Objective: To explore the surgical technique and preliminary safety and aesthetic results of endoscopic removal of injectable Amazingel with/without immediate prepectoral implant-based breast augmentation for patients.

Methods: The clinical data of 25 patients who underwent endoscopic removal of injectable Amazingel with/without immediate prepectoral implant-based breast augmentation between April 2020 and January 2024 and met the selection criteria was retrospective analysed. The patients' age ranged from 33 to 73 years, with a mean of 50.4 years, and the body mass index ranged from 16.8 to 26.6 kg/m 2, with a mean of 21.5 kg/m 2. They were all bilaterally injected with Amazingel, and the time between initial injections and surgery ranged from 17 to 26 years, with a mean of 21.4 years. Early safety was evaluated by the incidence of early postoperative complications, and early aesthetic results were evaluated using Harris scores (including breast shape satisfaction, sensation satisfaction, and elasticity satisfaction) at 3 months after operation.

Results: There were 9 cases underwent Amazingel removal (group A) and 16 cases underwent Amazingel removal with immediate prepectoral implant-based breast augmentation (group B). Intraoperative removal of Amazingel ranged from 808 to 1 285 mL, with a mean of 1 050.7 mL; the mass of the capsule removed ranged from 36 to 169 g, with a mean of 103.6 g; and a gross anatomical prosthesis was used with a median size of 345 mL (range, 315-355 mL). The operation time ranged from 95 to 395 minutes, with a mean of 194.2 minutes; and the cost of the procedure ranged from 8000to 91 000 yuan, with a mean of 33 000 yuan. Patients had a median follow-up time of 22.7 months (range, 3.0-48.1 months). There was 1 case of intraoperative skin burn due to the operation of the electric scalpel, which healed naturally after operation without flap necrosis. There was no adverse conditions such as prosthesis outline showing, ripple sign, and capsular contracture during follow-up; a small amount of Amazingel residue was found in 2 patients at 1 year after operation. The Harris score at 3 months after operation was used to evaluate the early aesthetic results, and the breast shape, elasticity, and sensation satisfaction of group A were lower than group B, but the differences between the two groups were not significant ( P>0.05).

Conclusion: Endoscopic removal of injectable Amazingel with/without immediate prepectoral implant-based breast augmentation is safe in the early stage with good aesthetic results, and it is also recommended that patients who had the indications for combined immediate breast augmentation after removal to rebuild the breast appearance.

目的探讨内窥镜下取出注射用Amazingel并/或不立即进行胸大肌前假体隆胸的手术技巧和初步的安全性及美学效果:回顾性分析2020年4月至2024年1月期间接受内窥镜下取出注射用Amazingel和/或不立即胸前植入假体隆胸术的25例符合选择标准的患者的临床资料。患者年龄从 33 岁到 73 岁不等,平均 50.4 岁,体重指数从 16.8 kg/m 2 到 26.6 kg/m 2 不等,平均 21.5 kg/m 2。他们都接受了阿马奇奈尔的双侧注射,初次注射与手术之间的间隔时间为17至26年,平均为21.4年。根据术后早期并发症的发生率评估早期安全性,根据术后3个月的Harris评分(包括乳房形态满意度、感觉满意度和弹性满意度)评估早期美学效果:共有9例患者进行了Amazingel移除术(A组),16例患者进行了Amazingel移除术并立即进行胸大肌前假体隆胸术(B组)。术中取出的Amazingel从808毫升到1 285毫升不等,平均为1 050.7毫升;取出的胶囊质量从36克到169克不等,平均为103.6克;使用的解剖假体中位数为345毫升(范围为315-355毫升)。手术时间从 95 分钟到 395 分钟不等,平均为 194.2 分钟;手术费用从 8000 元到 91000 元不等,平均为 33000 元。患者的中位随访时间为 22.7 个月(3.0-48.1 个月)。有 1 例患者术中因电刀操作导致皮肤灼伤,术后自然愈合,无皮瓣坏死。随访期间未发现假体轮廓显示、波纹征和包膜挛缩等不良情况;2 例患者在术后 1 年发现有少量 Amazingel 残留。用术后3个月的Harris评分来评价早期美学效果,A组的乳房形态、弹性和感觉满意度均低于B组,但两组间差异无学意义(P>0.05):结论:内窥镜下取出注射用Amazingel并/或不立即进行胸大肌前假体隆胸术在早期是安全的,具有良好的美学效果,同时建议有适应症的患者在取出后联合立即隆胸术重建乳房外观。
{"title":"[Effectiveness comparison of endoscopic removal of injectable Amazingel with/without immediate prepectoral implant-based breast augmentation].","authors":"Kawun Chung, Huanzuo Yang, Yanyan Xie, Faqing Liang, Yu Feng, Donglin Zhang, Zhenggui Du","doi":"10.7507/1002-1892.202404032","DOIUrl":"10.7507/1002-1892.202404032","url":null,"abstract":"<p><strong>Objective: </strong>To explore the surgical technique and preliminary safety and aesthetic results of endoscopic removal of injectable Amazingel with/without immediate prepectoral implant-based breast augmentation for patients.</p><p><strong>Methods: </strong>The clinical data of 25 patients who underwent endoscopic removal of injectable Amazingel with/without immediate prepectoral implant-based breast augmentation between April 2020 and January 2024 and met the selection criteria was retrospective analysed. The patients' age ranged from 33 to 73 years, with a mean of 50.4 years, and the body mass index ranged from 16.8 to 26.6 kg/m <sup>2</sup>, with a mean of 21.5 kg/m <sup>2</sup>. They were all bilaterally injected with Amazingel, and the time between initial injections and surgery ranged from 17 to 26 years, with a mean of 21.4 years. Early safety was evaluated by the incidence of early postoperative complications, and early aesthetic results were evaluated using Harris scores (including breast shape satisfaction, sensation satisfaction, and elasticity satisfaction) at 3 months after operation.</p><p><strong>Results: </strong>There were 9 cases underwent Amazingel removal (group A) and 16 cases underwent Amazingel removal with immediate prepectoral implant-based breast augmentation (group B). Intraoperative removal of Amazingel ranged from 808 to 1 285 mL, with a mean of 1 050.7 mL; the mass of the capsule removed ranged from 36 to 169 g, with a mean of 103.6 g; and a gross anatomical prosthesis was used with a median size of 345 mL (range, 315-355 mL). The operation time ranged from 95 to 395 minutes, with a mean of 194.2 minutes; and the cost of the procedure ranged from 8000to 91 000 yuan, with a mean of 33 000 yuan. Patients had a median follow-up time of 22.7 months (range, 3.0-48.1 months). There was 1 case of intraoperative skin burn due to the operation of the electric scalpel, which healed naturally after operation without flap necrosis. There was no adverse conditions such as prosthesis outline showing, ripple sign, and capsular contracture during follow-up; a small amount of Amazingel residue was found in 2 patients at 1 year after operation. The Harris score at 3 months after operation was used to evaluate the early aesthetic results, and the breast shape, elasticity, and sensation satisfaction of group A were lower than group B, but the differences between the two groups were not significant ( <i>P</i>>0.05).</p><p><strong>Conclusion: </strong>Endoscopic removal of injectable Amazingel with/without immediate prepectoral implant-based breast augmentation is safe in the early stage with good aesthetic results, and it is also recommended that patients who had the indications for combined immediate breast augmentation after removal to rebuild the breast appearance.</p>","PeriodicalId":23979,"journal":{"name":"中国修复重建外科杂志","volume":"38 7","pages":"807-812"},"PeriodicalIF":0.0,"publicationDate":"2024-07-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11252681/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141627845","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
[Past and present of endoscopic surgery and robotic surgery in treatment of breast diseases]. [内窥镜手术和机器人手术治疗乳腺疾病的过去和现在]。
Q3 Medicine Pub Date : 2024-07-15 DOI: 10.7507/1002-1892.202404034
Qing Zhang, Yanyan Xie, Faqing Liang, Yu Feng, Zhenggui Du

Objective: To review the research progress related to endoscopic surgery and robotic surgery for breast diseases, aiming to provide references for clinical practice.

Methods: The recent domestic and international literature on endoscopic surgery and robotic surgery for breast diseases was reviewed, then the challenges in their development, the innovative evolution of endoscopic surgery combined with clinical practice by our team, and its clinical applications were summarized.

Results: Traditional endoscopic surgery, despite its advantages such as minimal invasiveness, good cosmetic outcomes, and high patient's satisfaction, has been limited in its development due to specific difficulties in establishing the operative field. Our team innovatively proposed the "reverse sequence method" and the Huaxi Hole 1 theory and methods, cleverly altering the surgical procedure sequence, adding small operative orifices to transform single-port operations into multi-port ones, effectively overcoming the challenges restricting the advancement of endoscopic surgery in the field of breast diseases, thereby enabling further proliferation of endoscopic procedures. In terms of breast endoscopic reconstruction surgery, the parachute patch technique has broadened the indications for reconstruction surgery, benefiting patients with a certain degree of breast ptosis; and the postoperative adjustment concept, through early intervention in the post-reconstruction breast shape, has further refined the reconstruction procedure. Robot-assisted surgery derived from endoscopic surgery theory has further enhanced the precision and stability of surgeries, reducing surgical risks; however, excessive time and economic costs are urgent issues that must be addressed.

Conclusion: Through theoretical innovations, endoscopic surgery has been applied in the excision and reconstruction of breast lesions, while robotic surgery shows promising applications in autologous breast reconstruction, especially in the latissimus dorsi reconstruction field. Nevertheless, the lack of high-level large-sample, multi-center randomized controlled clinical trials to confirm its surgical safety, oncological safety, and postoperative cosmetic outcomes is an important direction for future research.

目的:综述乳腺疾病内窥镜手术和机器人手术的相关研究进展,旨在为临床实践提供参考:综述内窥镜手术和机器人手术治疗乳腺疾病的相关研究进展,旨在为临床实践提供参考:方法:综述近年来国内外关于乳腺疾病内镜手术和机器人手术的相关文献,总结其发展过程中面临的挑战、本团队将内镜手术与临床实践相结合的创新演进及其临床应用:结果:传统的内窥镜手术虽然具有微创、美容效果好、患者满意度高等优点,但由于在建立手术视野方面存在特殊困难,其发展受到了限制。我们的团队创新性地提出了 "逆序法 "和 "华西孔1号 "理论和方法,巧妙地改变了手术顺序,增加了小手术孔,将单孔手术转变为多孔手术,有效地克服了乳腺疾病领域制约内镜手术发展的难题,从而使内镜手术得到进一步推广。在乳房内窥镜重建手术方面,降落伞补片技术拓宽了重建手术的适应症,使有一定程度乳房下垂的患者受益;术后调整理念通过对重建后乳房形态的早期干预,进一步完善了重建手术。由内窥镜手术理论衍生的机器人辅助手术进一步提高了手术的精准性和稳定性,降低了手术风险,但时间过长、经济成本过高等问题亟待解决:通过理论创新,内窥镜手术已被应用于乳腺病变的切除和重建,而机器人手术在自体乳房重建,尤其是背阔肌重建领域的应用前景广阔。然而,目前还缺乏高水平的大样本、多中心随机对照临床试验来证实其手术安全性、肿瘤安全性和术后美容效果,这也是未来研究的一个重要方向。
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引用次数: 0
[Application of reverse traction device in preoperative treatment of high-energy tibial plateau fracture]. [反向牵引装置在高能量胫骨平台骨折术前治疗中的应用]。
Q3 Medicine Pub Date : 2024-07-15 DOI: 10.7507/1002-1892.202404004
Mingli Chen, Zonglin Chen, Honghan Li, Jinhong Chen, Hongpeng Gao, Miao Huang, Guanqi Xue, Zepeng Lin, Rongyuan Yang

Objective: To investigate the effectiveness of the reverse traction device in the preoperative treatment of high-energy tibial plateau fractures.

Methods: A retrospective study was conducted to analyze the clinical data of 33 patients with high-energy tibial plateau fractures who met the selection criteria between December 2020 and December 2023. All patients were treated by open reduction and internal fixation. According to the preoperative traction method, they were divided into the observation group (16 cases, treated with a reverse traction device on the day of admission) and the control group (17 cases, treated with heel traction on the day of admission). There was no significant difference in baseline data such as gender, age, body mass index, affected side, cause of injury, fracture Schatzker classification between the two groups ( P>0.05). Preoperative waiting time, preoperative related complications (nail channel loosening, nail channel oozing, nail channel infection, soft tissue necrosis, soft tissue infection, deep vein thrombosis of the lower extremity, etc.), operation time, and total hospitalization time were recorded and compared between the two groups. On the 4th day after traction, visual analogue scale (VAS) score was used to evaluate the pain relief of the patients, the swelling value of the affected limb was measured, and the Immobilization Comfort Questionnaire (ICQ) score was used to evaluate the perioperative hospital comfort of the patients.

Results: Both groups of patients completed the operation successfully, and the operation time, total hospitalization time, and preoperative waiting time of the observation group were significantly less than those of the control group ( P<0.05). There was no preoperative related complications in the observation group; in the control group, 3 patients had nail channel loosening and oozing, and 2 cases had the deep vein thrombosis of the lower extremity; the difference in the incidence of complication between the two groups was significant ( P<0.05). On the 4th day after traction, the ICQ score, VAS score, and limb swelling value of the observation group were significantly better than those of the control group ( P<0.05). X-ray films showed that the tibial plateau fracture separation and lower limb alignment recovered after calcaneal traction in the control group, but not as obvious as in the observation group. The fracture gap in the observation group significantly reduced, the tibial plateau alignment was good, and the lateral angulation deformity was corrected.

Conclusion: The use of reverse traction treatment in patients with high-energy tibial plateau fractures on admission can accelerate the swelling around the soft tissues to subside, reduce patients' pain, shorten the preoperative waiting time, improve the patients' preoperative quality of life, and contribut

目的:探讨反向牵引装置在术前治疗高能量胫骨平台骨折中的有效性:研究反向牵引装置在高能量胫骨平台骨折术前治疗中的有效性:回顾性研究分析了2020年12月至2023年12月期间符合筛选标准的33例高能量胫骨平台骨折患者的临床数据。所有患者均接受了切开复位和内固定治疗。根据术前牵引方法,将其分为观察组(16 例,入院当天使用反向牵引装置治疗)和对照组(17 例,入院当天使用足跟牵引治疗)。两组患者的性别、年龄、体重指数、患侧、受伤原因、骨折沙茨克分级等基线数据无明显差异(P>0.05)。记录并比较两组患者术前等待时间、术前相关并发症(钉道松动、钉道渗液、钉道感染、软组织坏死、软组织感染、下肢深静脉血栓等)、手术时间和总住院时间。牵引后第4天,采用视觉模拟量表(VAS)评分评估患者疼痛缓解情况,测量患肢肿胀值,采用固定舒适度问卷(ICQ)评分评估患者围手术期住院舒适度:结果:两组患者均顺利完成手术,观察组患者的手术时间、住院总时间、术前等待时间均明显少于对照组(PPP结论:对高能量胫骨平台骨折患者入院时采用反向牵引治疗,可加快软组织周围肿胀消退,减轻患者疼痛,缩短术前等待时间,提高患者术前生活质量,有利于缩短手术时间,效果良好。
{"title":"[Application of reverse traction device in preoperative treatment of high-energy tibial plateau fracture].","authors":"Mingli Chen, Zonglin Chen, Honghan Li, Jinhong Chen, Hongpeng Gao, Miao Huang, Guanqi Xue, Zepeng Lin, Rongyuan Yang","doi":"10.7507/1002-1892.202404004","DOIUrl":"10.7507/1002-1892.202404004","url":null,"abstract":"<p><strong>Objective: </strong>To investigate the effectiveness of the reverse traction device in the preoperative treatment of high-energy tibial plateau fractures.</p><p><strong>Methods: </strong>A retrospective study was conducted to analyze the clinical data of 33 patients with high-energy tibial plateau fractures who met the selection criteria between December 2020 and December 2023. All patients were treated by open reduction and internal fixation. According to the preoperative traction method, they were divided into the observation group (16 cases, treated with a reverse traction device on the day of admission) and the control group (17 cases, treated with heel traction on the day of admission). There was no significant difference in baseline data such as gender, age, body mass index, affected side, cause of injury, fracture Schatzker classification between the two groups ( <i>P</i>>0.05). Preoperative waiting time, preoperative related complications (nail channel loosening, nail channel oozing, nail channel infection, soft tissue necrosis, soft tissue infection, deep vein thrombosis of the lower extremity, <i>etc.</i>), operation time, and total hospitalization time were recorded and compared between the two groups. On the 4th day after traction, visual analogue scale (VAS) score was used to evaluate the pain relief of the patients, the swelling value of the affected limb was measured, and the Immobilization Comfort Questionnaire (ICQ) score was used to evaluate the perioperative hospital comfort of the patients.</p><p><strong>Results: </strong>Both groups of patients completed the operation successfully, and the operation time, total hospitalization time, and preoperative waiting time of the observation group were significantly less than those of the control group ( <i>P</i><0.05). There was no preoperative related complications in the observation group; in the control group, 3 patients had nail channel loosening and oozing, and 2 cases had the deep vein thrombosis of the lower extremity; the difference in the incidence of complication between the two groups was significant ( <i>P</i><0.05). On the 4th day after traction, the ICQ score, VAS score, and limb swelling value of the observation group were significantly better than those of the control group ( <i>P</i><0.05). X-ray films showed that the tibial plateau fracture separation and lower limb alignment recovered after calcaneal traction in the control group, but not as obvious as in the observation group. The fracture gap in the observation group significantly reduced, the tibial plateau alignment was good, and the lateral angulation deformity was corrected.</p><p><strong>Conclusion: </strong>The use of reverse traction treatment in patients with high-energy tibial plateau fractures on admission can accelerate the swelling around the soft tissues to subside, reduce patients' pain, shorten the preoperative waiting time, improve the patients' preoperative quality of life, and contribut","PeriodicalId":23979,"journal":{"name":"中国修复重建外科杂志","volume":"38 7","pages":"830-835"},"PeriodicalIF":0.0,"publicationDate":"2024-07-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11252696/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141627840","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
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中国修复重建外科杂志
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