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[Research status and progress of daytime total shoulder arthroplasty]. [日间全肩关节置换术的研究现状与进展]。
Q4 Medicine Pub Date : 2025-12-25 DOI: 10.12200/j.issn.1003-0034.20240804
Jun-Rong Chen, Long Chen, Sen-Lei Li, Li Sun

Total shoulder arthroplasty(TSA) is primarily used for treating severe shoulder injuries or diseases and has been shown to effectively improve shoulder function. With the expansion of TSA indications and an aging population, the demand for TSA continues to grow. To address this demand and alleviate the economic burden on patients, many countries have adopted the day surgery model for TSA, accompanied by extensive research and discussions on its safety and feasibility. This paper systematically reviews the safety, patient inclusion and exclusion criteria, implementation processes, and perioperative management strategies for TSA day surgery. Based on an analysis of relevant literature from domestic and international sources, the findings indicate that TSA day surgery, when preceded by appropriate patient screening, can safely replace traditional inpatient care. Furthermore, it could significantly reduce hospitalization durations, lower treatment costs, and optimize the utilization of medical resources. However, in clinical practice, there is still a lack of standardized protocols for patient selection criteria and perioperative management strategies. As China's aging population intensifies, TSA day surgery presents promising application prospects. Nevertheless, the development of day surgery in China lags behind that of other countries, and research on TSA day surgery remains in its early stages. Moving forward, research and clinical practices tailored to China's specific needs should be prioritized. Practical clinical operation guidelines must be established to facilitate the widespread adoption and standardized implementation of TSA day surgery, ultimately providing patients with higher-quality and safer medical care.

全肩关节置换术(TSA)主要用于治疗严重的肩关节损伤或疾病,并已被证明可以有效地改善肩关节功能。随着TSA适应症的扩大和人口老龄化,对TSA的需求持续增长。为了满足这一需求,减轻患者的经济负担,许多国家都采用了TSA的日间手术模式,并对其安全性和可行性进行了广泛的研究和讨论。本文系统地回顾了TSA日间手术的安全性、患者纳入和排除标准、实施过程和围手术期管理策略。通过对国内外相关文献的分析,研究结果表明,在术前进行适当的患者筛查后,TSA日间手术可以安全地取代传统的住院治疗。并可显著缩短住院时间,降低治疗费用,优化医疗资源利用。然而,在临床实践中,对于患者的选择标准和围手术期管理策略仍然缺乏标准化的方案。随着中国人口老龄化的加剧,TSA日间手术具有广阔的应用前景。然而,中国日间手术的发展相对滞后,TSA日间手术的研究还处于初级阶段。下一步,应优先开展适合中国具体需求的研究和临床实践。必须建立实用的临床操作指南,促进TSA日间手术的广泛采用和标准化实施,最终为患者提供更高质量和更安全的医疗服务。
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引用次数: 0
[Ultrasound-guided manual reduction combined with external fixation of small splints for the treatment of O'Brien type Ⅱ and Ⅲ radial neck fractures in children]. [超声引导下手动复位联合小夹板外固定治疗O'Brien型Ⅱ和Ⅲ儿童桡骨颈骨折]。
Q4 Medicine Pub Date : 2025-12-25 DOI: 10.12200/j.issn.1003-0034.20250517
Quan-Wei Ding, Jun Ying, Ying Zhao

Objective: To explore clinical efficacy of ultrasound-guided manual reduction combined with external fixation with small splints of fir bark in treating O'Brien typeⅡand Ⅲ radial neck fractures in children.

Methods: A retrospective analysis was conducted on clinical data of 21 children with type O'BrienⅡand Ⅲ radial neck fractures admitted from June 2023 to December 2024, including 11 boys and 10 girls; aged from 4 to 12 years old with an average of (8.43±1.60) years old;12 patients with O'Brien typeⅡand 9 patients with type Ⅲ. All treatments were carried out using ultrasound-guided manual reduction. Ultrasound examination was conducted again to check the quality of fracture reduction after reduction was completed. After the treatment, external fixation with small splints of fir bark was performed. The success rate of manual reduction and the incidence of complications during the process of manual reduction were observed. Postoperative images and post-operative functions were evaluated using Metaizeau standard.

Results: All the children were followed up, and the duration ranged from 3 to 12 months. Closed reduction was successful in 19 children, while 2 children had difficulty in reduction and were transferred to surgical treatment. No related complications such as neurovascular injury occurred. Closed reduction was successful in 19 patients. Postoperative X-ray films showed good alignment and alignment of fractures, and the fracture healing time ranged from 4 to 7 weeks. Metaizeau criteria at 3 months after treatment, 17 patients were excellent and 2 good. In the later functional evaluation, all 19 patients were rated as excellent, and no obvious elbow joint dysfunction or residual pain occurred.

Conclusion: Ultrasound-guided manual reduction could effectively increase success rate of manual reduction for O'Brien typeⅡand Ⅲ radial neck fractures in children, and reduce radiation and adverse outcomes.

目的:探讨超声引导下手工复位联合杉木皮小夹板外固定治疗儿童O'Brien型Ⅱ、Ⅲ桡颈骨折的临床疗效。方法:回顾性分析2023年6月至2024年12月收治的21例O'Brien型Ⅱ和Ⅲ型桡骨颈骨折患儿的临床资料,其中男11例,女10例;年龄4 ~ 12岁,平均(8.43±1.60)岁;O'Brien型Ⅱ12例,Ⅲ型9例。所有治疗均采用超声引导下的手动复位。复位完成后再次行超声检查骨折复位质量。治疗后,用杉木皮小夹板进行外固定。观察复位成功率及复位过程中并发症的发生情况。采用Metaizeau标准评价术后图像和术后功能。结果:所有患儿均获得随访,随访时间3 ~ 12个月。闭合复位19例成功,2例复位困难转手术治疗。未发生神经血管损伤等相关并发症。闭合复位19例成功。术后x线片显示骨折对齐、排列良好,骨折愈合时间4 ~ 7周。治疗后3个月Metaizeau标准,优17例,良2例。在后期功能评价中,19例患者均为优,未发生明显的肘关节功能障碍和残余疼痛。结论:超声引导下手动复位可有效提高小儿O'Brien型Ⅱ、Ⅲ桡骨颈骨折手动复位成功率,减少放射线和不良后果。
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引用次数: 0
[Observation on the clinical efficacy of Huazhuo Sanjie Chubi decoction() in the treatment of low-grade inflammation in chronic gouty arthritis]. [化浊散戒除痹汤治疗慢性痛风性关节炎低度炎症的临床疗效观察]。
Q4 Medicine Pub Date : 2025-12-25 DOI: 10.12200/j.issn.1003-0034.20250884
Si-Yuan Lin, Xiao-Hua Chen, Zhuo-Ming Zheng, Fan Yang, Zhu-Mou Zhang, Jun Liu, Jia-Li Luo, Yan Xiao, Jie-Mei Guo, You-Xin Su
<p><strong>Objective: </strong>To explore clinical efficacy of <i>Huazhuo Sanjie Chubi</i> decoction() in treating low-grade inflammation in chronic gouty arthritis (CGA).</p><p><strong>Methods: </strong>From May to December 2024, 68 male patients with CGA were admitted and divided into traditional Chinese medicine group and Western medicine group (1 patient dropped out and 4 patients excluded). There were 31 patients in traditional Chinese medicine group, aged from 21 to 63 years old with an average of (42.35±11.93) years old, body mass index (BMI) ranged from 21.0 to 37.5 kg·m<sup>-2</sup> with an average of (26.87±3.58) kg·m<sup>-2</sup>, and courses of disease raged from 3 to 30 years with an average of (9.55±6.25) years;treated with orally administered <i>Huazhuo Sanjie Chubi</i> decoction(). There were 32 patients in Western medicine group, aged from 21 to 65 years old with an average of (37.47±10.79) years old, BMI ranged from 19.5 to 30.7 kg·m<sup>-2</sup> with an average of (25.30±2.87) kg·m<sup>-2</sup>, and courses of disease ranged from 4 to 21 years with an average of (8.50±4.15) years;treated with oral allopurinol. TCM syndrome score, Likert score for joint swelling and pain, visual analogue scale (VAS) for pain, serum uric acid and serum low-grade inflammation-related indicators of patients before and after treatment, including tumornecrosis factor-α (tumornecrosis factor-α) TNF-α, interleukin-1β (IL-1β), interleukin-6(IL-6), chemokine 2 (c-c motif chemokine ligand 2), changes of CCL2) and S100 calcium binding protein A8/A9(S100 calcium binding protein A8/A9, S100A8/A9) were observed and compared. Spearman correlation analysis was used to analyze correlations between SUA and IL-1β, IL-6, TNF-α, CCL2, and S100A8/A9.</p><p><strong>Results: </strong>Sixty-three patients were followed up for two months, and no adverse reactions occurred in any of them. After 2 months of treatment, the scores of TCM syndrome, Likert score of joint swelling and pain, and VAS in traditional Chinese medicine group were 9.00(8.00, 11.00), 2.00 (1.00, 3.00), and 0.00 (0.00, 1.00) points respectively;which were lower than 16.00 (15.00, 18.00), 4.00 (4.00, 5.00), and 2.00 (1.00, 2.00) in Western medicine group, and the differences were statistically significant(<i>P</i><0.05). The serum uric acid level in Western medicine group was 465.68 (429.02, 500.94) μmol·L<sup>-1</sup>, which was lower than that in traditional Chinese medicine group 496.03 (484.90, 522.73) μmol·L<sup>-1</sup>, and the difference was statistically significant(<i>P</i><0.05). The levels of serum IL-1β, IL-6, TNF-α, CCL2 and S100A8/A9 in traditional Chinese medicine group were (25.01±8.18) pg·ml-1, (16.97±5.01) ng·L<sup>-1</sup>, (229.08±45.10) ng·L<sup>-1</sup> and (503.50±72.16) pg·ml<sup>-1</sup>, (13.35±2.80) pg·ml<sup>-1</sup>, respectively;which were lower than those of Western medicine group (35.51±6.35) pg·ml-1, (21.13±2.49) ng·L<sup>-1</sup>, (250.14±34.23) ng·L<sup>-1</sup>, (567.
目的:探讨化浊散戒除痹汤治疗慢性痛风性关节炎(CGA)低度炎症的临床疗效。方法:选取2024年5月~ 12月收治的68例男性CGA患者,分为中药组和西药组(退出1例,排除4例)。中药组31例,年龄21 ~ 63岁,平均(42.35±11.93)岁,体重指数(BMI) 21.0 ~ 37.5 kg·m-2,平均(26.87±3.58)kg·m-2,病程3 ~ 30年,平均(9.55±6.25)年;口服化浊三节除痹汤治疗()。西药组32例,年龄21 ~ 65岁,平均(37.47±10.79)岁,体重指数19.5 ~ 30.7 kg·m-2,平均(25.30±2.87)kg·m-2,病程4 ~ 21年,平均(8.50±4.15)年;口服别嘌呤醇治疗。观察并比较治疗前后患者中医证型评分、关节肿痛Likert评分、疼痛视觉模拟评分(VAS)、血清尿酸及血清低度炎症相关指标,包括肿瘤坏死因子-α (tumornecrosis factor-α) TNF-α、白细胞介素-1β (IL-1β)、白细胞介素-6(IL-6)、趋化因子2 (c-c基元趋化因子配体2)、CCL2、S100钙结合蛋白A8/A9(S100钙结合蛋白A8/A9、S100A8/A9)的变化。采用Spearman相关分析分析SUA与IL-1β、IL-6、TNF-α、CCL2、S100A8/A9的相关性。结果:63例患者随访2个月,无不良反应发生。治疗2个月后,中药组中医证候评分、关节肿痛Likert评分、VAS评分分别为9.00(8.00、11.00)、2.00(1.00、3.00)、0.00(0.00、1.00)分;均低于西药组16.00(15.00、18.00)、4.00(4.00、5.00)、2.00(1.00、2.00),差异均有统计学意义(P-1),低于中药组496.03(484.90、522.73)μmol·L-1,差异均有统计学意义(P-1,分别为(229.08±45.10)ng·L-1、(503.50±72.16)pg·ml-1、(13.35±2.80)pg·ml-1;低于西药组(35.51±6.35)pg·ml-1、(21.13±2.49)ng·L-1、(250.14±34.23)ng·L-1、(567.64±76.12)pg·ml-1、(19.36±4.24)pg·ml-1;两组间差异均有统计学意义(Pr=0.57)、IL-6 (r=0.43)、TNF-α (r=0.39)、CCL2 (r=0.27)、S100A8/A9 (r=0.36)。血清IL-1β、IL-6、TNF-α与CCL2、S100A8/A9水平呈正相关(p结论:化浊散结除痹汤()可改善CGA患者的临床症状、中医证候及低度炎症相关指标,具有降尿酸和抗低度炎症的双重作用。
{"title":"[Observation on the clinical efficacy of <i>Huazhuo Sanjie Chubi</i> decoction() in the treatment of low-grade inflammation in chronic gouty arthritis].","authors":"Si-Yuan Lin, Xiao-Hua Chen, Zhuo-Ming Zheng, Fan Yang, Zhu-Mou Zhang, Jun Liu, Jia-Li Luo, Yan Xiao, Jie-Mei Guo, You-Xin Su","doi":"10.12200/j.issn.1003-0034.20250884","DOIUrl":"https://doi.org/10.12200/j.issn.1003-0034.20250884","url":null,"abstract":"&lt;p&gt;&lt;strong&gt;Objective: &lt;/strong&gt;To explore clinical efficacy of &lt;i&gt;Huazhuo Sanjie Chubi&lt;/i&gt; decoction() in treating low-grade inflammation in chronic gouty arthritis (CGA).&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Methods: &lt;/strong&gt;From May to December 2024, 68 male patients with CGA were admitted and divided into traditional Chinese medicine group and Western medicine group (1 patient dropped out and 4 patients excluded). There were 31 patients in traditional Chinese medicine group, aged from 21 to 63 years old with an average of (42.35±11.93) years old, body mass index (BMI) ranged from 21.0 to 37.5 kg·m&lt;sup&gt;-2&lt;/sup&gt; with an average of (26.87±3.58) kg·m&lt;sup&gt;-2&lt;/sup&gt;, and courses of disease raged from 3 to 30 years with an average of (9.55±6.25) years;treated with orally administered &lt;i&gt;Huazhuo Sanjie Chubi&lt;/i&gt; decoction(). There were 32 patients in Western medicine group, aged from 21 to 65 years old with an average of (37.47±10.79) years old, BMI ranged from 19.5 to 30.7 kg·m&lt;sup&gt;-2&lt;/sup&gt; with an average of (25.30±2.87) kg·m&lt;sup&gt;-2&lt;/sup&gt;, and courses of disease ranged from 4 to 21 years with an average of (8.50±4.15) years;treated with oral allopurinol. TCM syndrome score, Likert score for joint swelling and pain, visual analogue scale (VAS) for pain, serum uric acid and serum low-grade inflammation-related indicators of patients before and after treatment, including tumornecrosis factor-α (tumornecrosis factor-α) TNF-α, interleukin-1β (IL-1β), interleukin-6(IL-6), chemokine 2 (c-c motif chemokine ligand 2), changes of CCL2) and S100 calcium binding protein A8/A9(S100 calcium binding protein A8/A9, S100A8/A9) were observed and compared. Spearman correlation analysis was used to analyze correlations between SUA and IL-1β, IL-6, TNF-α, CCL2, and S100A8/A9.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Results: &lt;/strong&gt;Sixty-three patients were followed up for two months, and no adverse reactions occurred in any of them. After 2 months of treatment, the scores of TCM syndrome, Likert score of joint swelling and pain, and VAS in traditional Chinese medicine group were 9.00(8.00, 11.00), 2.00 (1.00, 3.00), and 0.00 (0.00, 1.00) points respectively;which were lower than 16.00 (15.00, 18.00), 4.00 (4.00, 5.00), and 2.00 (1.00, 2.00) in Western medicine group, and the differences were statistically significant(&lt;i&gt;P&lt;/i&gt;&lt;0.05). The serum uric acid level in Western medicine group was 465.68 (429.02, 500.94) μmol·L&lt;sup&gt;-1&lt;/sup&gt;, which was lower than that in traditional Chinese medicine group 496.03 (484.90, 522.73) μmol·L&lt;sup&gt;-1&lt;/sup&gt;, and the difference was statistically significant(&lt;i&gt;P&lt;/i&gt;&lt;0.05). The levels of serum IL-1β, IL-6, TNF-α, CCL2 and S100A8/A9 in traditional Chinese medicine group were (25.01±8.18) pg·ml-1, (16.97±5.01) ng·L&lt;sup&gt;-1&lt;/sup&gt;, (229.08±45.10) ng·L&lt;sup&gt;-1&lt;/sup&gt; and (503.50±72.16) pg·ml&lt;sup&gt;-1&lt;/sup&gt;, (13.35±2.80) pg·ml&lt;sup&gt;-1&lt;/sup&gt;, respectively;which were lower than those of Western medicine group (35.51±6.35) pg·ml-1, (21.13±2.49) ng·L&lt;sup&gt;-1&lt;/sup&gt;, (250.14±34.23) ng·L&lt;sup&gt;-1&lt;/sup&gt;, (567.","PeriodicalId":23964,"journal":{"name":"Zhongguo gu shang = China journal of orthopaedics and traumatology","volume":"38 12","pages":"1201-9"},"PeriodicalIF":0.0,"publicationDate":"2025-12-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145935391","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
[Current status and prospects of traditional Chinese medicine in prevention and treatment of gouty arthritis]. 【中医药防治痛风性关节炎的现状及展望】。
Q4 Medicine Pub Date : 2025-12-25 DOI: 10.12200/j.issn.1003-0034.20251160
Xiao-Xu Li, Wei Cao, Guang-Cheng Wei, Jin-Jie Shi
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引用次数: 0
[Clinical efficacy of TightRope combined with threaded anchors in the treatment of acromioclavicular joint dislocation]. [钢丝联合螺纹锚钉治疗肩锁关节脱位的临床疗效]。
Q4 Medicine Pub Date : 2025-12-25 DOI: 10.12200/j.issn.1003-0034.20250008
Yi-Ke Qin, Jian-Ying Qin, Yi-Ming Luo
<p><strong>Objective: </strong>To compare short-term and long-term efficacy of TightRope combined with threaded anchor bolts and clavicular hook plate fixation in treating acromioclavicular joint dislocation.</p><p><strong>Methods: </strong>A retrospective analysis was conducted on clinical data of 90 patients with acromioclavicular joint dislocation admitted from March 2020 to March 2024. They were divided into anchor group and plate group according to surgical methods. There were 48 patients in anchor group, including 30 males and 18 females, aged from 18 to 65 years old with an average of (42.35±9.21) years old;20 patients caused by traffic accident injuries, 18 patients caused by sports injuries and 10 patients caused by falling;15 patients with type Ⅲ, 20 patients with type Ⅳ, and 13 patients with type Ⅴ according to Rockwood classification;26 patients on the left side and 22 patients on the right side;the time from injury to operation ranged from 2 to 7 days with an average of (4.62±1.13) days;TightRope combined with wire anchor technology was adopted. There were 42 patients in steel plate group, including 22 males and 20 females, aged from 20 to 64 years old with an average of (41.87±8.97) years old;18 patients caused by traffic accident injuries, 15 patients caused by sports injuries and 9 patients caused by falling; 14 patients with type Ⅲ, 17 patients with type Ⅳ, and 11 patients with type Ⅴ according to Rockwood classification;22 patients on the left side and 20 patients on the right side;the time from injury to operation ranged from 3 to 7 days with an average of (4.54±1.10) days;clavicular hook plates were used for fixation. The operation time, intraoperative blood loss, hospital stay and complications between two groups were compared. The changes of shoulder joint range of motion (flexion and elevation, abduction and elevation), visual analogue scale (VAS) for pain and Constant-Murley score were compared before operation, 3 months after operation respectively. At the latest follow-up, Karlsson score was used to compare its clinical efficacy.</p><p><strong>Results: </strong>Both groups of patients were successfully completed surgery and were followed up. The follow-up time of anchor group ranged from 8 to 33 months with an average of (16.22±5.09) months, and that of plate group ranged from 9 to 37 months with an average of (16.72±6.23) months. There was no statistically significant difference between two groups (<i>P</i>>0.05). There was no statistically significant difference in operation time between two groups (<i>P</i>>0.05). The intraoperative blood loss and postoperative hospital stay in anchor group were (50.26±14.82) ml and (5.21±1.29) d respectively, which were better than those in plate group (68.90±16.18) ml and (6.28±1.52) d, and the differences were statistically significant(<i>P</i><0.001). At 3 months after operation, the range of motion of forward flexion, upward lift and abduction and upward lift in anchor group were
目的:比较钢丝联合螺纹地脚螺栓与锁骨钩钢板固定治疗肩锁关节脱位的近期与长期疗效。方法:回顾性分析2020年3月至2024年3月收治的90例肩锁关节脱位患者的临床资料。根据手术方式分为锚钉组和钢板组。锚定组48例,男30例,女18例,年龄18 ~ 65岁,平均(42.35±9.21)岁;交通事故致伤20例,运动损伤18例,跌倒致伤10例;Rockwood分型:Ⅲ型15例,Ⅳ型20例,Ⅴ型13例;左侧26例,右侧22例;损伤至手术时间2 ~ 7 d,平均(4.62±1.13)d;采用钢丝绳结合钢丝锚固技术。钢板组42例,男22例,女20例,年龄20 ~ 64岁,平均(41.87±8.97)岁;交通事故致伤18例,运动损伤15例,坠落致伤9例;Rockwood分型:Ⅲ型14例,Ⅳ型17例,Ⅴ型11例;左侧22例,右侧20例;损伤至手术时间3 ~ 7 d,平均(4.54±1.10)d;采用锁骨钩钢板固定。比较两组手术时间、术中出血量、住院时间及并发症。比较术前、术后3个月肩关节活动范围(屈伸、外展、内抬)、疼痛视觉模拟评分(VAS)和Constant-Murley评分的变化。在最近一次随访时,采用Karlsson评分比较其临床疗效。结果:两组患者均顺利完成手术并随访。锚架组随访8 ~ 33个月,平均(16.22±5.09)个月;钢板组随访9 ~ 37个月,平均(16.72±6.23)个月。两组间比较差异无统计学意义(P < 0.05)。两组手术时间比较,差异无统计学意义(P < 0.05)。锚定组术中出血量(50.26±14.82)ml、术后住院时间(5.21±1.29)d,优于钢板组(68.90±16.18)ml、(6.28±1.52)d,差异均有统计学意义(PPPχ2=3.889, P=0.049)。锚定组术后感染1例,关节僵硬2例;钢板组2例发生感染,1例发生神经损伤,1例发生内固定松动移位,4例发生关节僵硬,2例发生反复脱位。结论:钢丝联合线锚技术治疗肩锁关节脱位可有效缓解术后疼痛,改善肩关节功能,减少并发症的发生,临床疗效良好,为治疗肩锁关节脱位提供了一种安全有效的选择。
{"title":"[Clinical efficacy of TightRope combined with threaded anchors in the treatment of acromioclavicular joint dislocation].","authors":"Yi-Ke Qin, Jian-Ying Qin, Yi-Ming Luo","doi":"10.12200/j.issn.1003-0034.20250008","DOIUrl":"https://doi.org/10.12200/j.issn.1003-0034.20250008","url":null,"abstract":"&lt;p&gt;&lt;strong&gt;Objective: &lt;/strong&gt;To compare short-term and long-term efficacy of TightRope combined with threaded anchor bolts and clavicular hook plate fixation in treating acromioclavicular joint dislocation.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Methods: &lt;/strong&gt;A retrospective analysis was conducted on clinical data of 90 patients with acromioclavicular joint dislocation admitted from March 2020 to March 2024. They were divided into anchor group and plate group according to surgical methods. There were 48 patients in anchor group, including 30 males and 18 females, aged from 18 to 65 years old with an average of (42.35±9.21) years old;20 patients caused by traffic accident injuries, 18 patients caused by sports injuries and 10 patients caused by falling;15 patients with type Ⅲ, 20 patients with type Ⅳ, and 13 patients with type Ⅴ according to Rockwood classification;26 patients on the left side and 22 patients on the right side;the time from injury to operation ranged from 2 to 7 days with an average of (4.62±1.13) days;TightRope combined with wire anchor technology was adopted. There were 42 patients in steel plate group, including 22 males and 20 females, aged from 20 to 64 years old with an average of (41.87±8.97) years old;18 patients caused by traffic accident injuries, 15 patients caused by sports injuries and 9 patients caused by falling; 14 patients with type Ⅲ, 17 patients with type Ⅳ, and 11 patients with type Ⅴ according to Rockwood classification;22 patients on the left side and 20 patients on the right side;the time from injury to operation ranged from 3 to 7 days with an average of (4.54±1.10) days;clavicular hook plates were used for fixation. The operation time, intraoperative blood loss, hospital stay and complications between two groups were compared. The changes of shoulder joint range of motion (flexion and elevation, abduction and elevation), visual analogue scale (VAS) for pain and Constant-Murley score were compared before operation, 3 months after operation respectively. At the latest follow-up, Karlsson score was used to compare its clinical efficacy.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Results: &lt;/strong&gt;Both groups of patients were successfully completed surgery and were followed up. The follow-up time of anchor group ranged from 8 to 33 months with an average of (16.22±5.09) months, and that of plate group ranged from 9 to 37 months with an average of (16.72±6.23) months. There was no statistically significant difference between two groups (&lt;i&gt;P&lt;/i&gt;&gt;0.05). There was no statistically significant difference in operation time between two groups (&lt;i&gt;P&lt;/i&gt;&gt;0.05). The intraoperative blood loss and postoperative hospital stay in anchor group were (50.26±14.82) ml and (5.21±1.29) d respectively, which were better than those in plate group (68.90±16.18) ml and (6.28±1.52) d, and the differences were statistically significant(&lt;i&gt;P&lt;/i&gt;&lt;0.001). At 3 months after operation, the range of motion of forward flexion, upward lift and abduction and upward lift in anchor group were","PeriodicalId":23964,"journal":{"name":"Zhongguo gu shang = China journal of orthopaedics and traumatology","volume":"38 12","pages":"1224-30"},"PeriodicalIF":0.0,"publicationDate":"2025-12-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145935106","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
[Effect of formononetin on endoplasmic reticulum stress and neuronal apoptosis in rats with chronic compressive cervical spinal cord injury]. [刺芒柄花素对慢性压迫性颈脊髓损伤大鼠内质网应激和神经元凋亡的影响]。
Q4 Medicine Pub Date : 2025-12-25 DOI: 10.12200/j.issn.1003-0034.20240199
Ya-Yun Zhang, Min Yao, Rui-Rui Xue, Xing Ding, Jin-Hai Xu, Xue-Jun Cui, Wen Mo

Objective: To explore effect and mechanism of formononetin on recovery of neurological function after chronic spinal cord injury (SCI) in rats.

Methods: Twenty-four SPF male SD rats, aged from 8 to 9 weeks old, weighted (327.29±15.19) g, were selected and randomly divided into sham operation group(Sham group), model group (Vehicle group), and formononetin group, with 8 rats in each group. Vehicle group and formononetin group were established chronic SCI models in rats by hydrogel compression. On the first day after modeling in formononetin group, formononetin officinalis solution was continuous administered orally (with a standard of 30 mg·kg-1) for 28 days, once a day. Basso-Beattie-Bresnahan (BBB) score, forelimb grip strength and rotating bar test of rats were performed in each group at 1, 7, 14, 21 and 28 days after modeling respectively to evaluate the limb motor function. Twenty-eight days after modeling, cardiac perfusion samples were collected to detect endoplasmic reticulum stress and neuronal apoptosis in spinal cord tissue. Hematoxylin-eosin staining was used to observe SCI, Nissl staining was used to observe number of surviving neurons, and Western blot (WB) was used to detect Bcl-2-associated X protein(Bax), B-cell lymphoma-2(Bcl-2) proteins and apoptosis-related proteins. The expression of endoplasmic reticulum stress pathway-related proteins was observed by immunofluorescence staining.

Results: Formononetin group were better than Vehicle group in BBB score on the 21st day after operation and grip test on the 3rd, 7th and 21st days, there were statistically differences(P<0.05). The results of HE and Nissl staining showed the number of surviving nerve cells in formononetin group were better than those in Vehicle group, and the difference were statistically significant(P<0.05). WB results showed the expression of Bcl-2 was upregulated, and protein expressions of Bax, C/EBP homologous protein(CHOP), phosphorylated protein kinase R-like endoplasmic reticulum kinase(p-PERK), and phosphorylated eukaryotic initiation factor 2α(p-eIF2α) in formononetin group were down regulated compared with Vehicle group, the differences were statistically significant(P<0.05). Immunofluorescence showed the protein expressions of p-PERK and activating transcription factor 6(ATF6) in neurons in formononetin group decreased compared with Vehicle group, and the differences were statistically significant (P<0.05).

Conclusion: Formononetin could alleviate pathological changes after chronic SCI in rats, improve behavioral scores, and promote the recovery of spinal cord nerve function. The specific mechanism may be related to the inhibition of necrotic apoptosis mediated by endoplasmic reticulum stress signaling pathway.

目的:探讨芒柄花素对大鼠慢性脊髓损伤(SCI)后神经功能恢复的影响及其机制。方法:选取8 ~ 9周龄SPF雄性SD大鼠24只,体重(327.29±15.19)g,随机分为假手术组(sham组)、模型组(Vehicle组)和刺芒柄花素组,每组8只。水凝胶加压法制备大鼠慢性脊髓损伤模型。刺芒柄花素组在造模后第1天,连续口服刺芒柄花素溶液(标准剂量为30 mg·kg-1),连续28 d,每天1次。各组大鼠分别于造模后第1、7、14、21和28天进行BBB评分、前肢握力和旋转杆试验,评价肢体运动功能。造模28天后,取心脏灌注标本,检测脊髓组织内质网应激和神经元凋亡情况。苏木精-伊红染色观察脊髓损伤,尼索染色观察存活神经元数量,Western blot (WB)检测Bcl-2相关X蛋白(Bax)、b细胞淋巴瘤-2(Bcl-2)蛋白和凋亡相关蛋白。免疫荧光染色观察内质网应激途径相关蛋白的表达。结果:芒柄花素组术后第21天BBB评分及第3、7、21天握力测试均优于Vehicle组,差异有统计学意义(ppppp)。结论:芒柄花素可减轻大鼠慢性脊髓损伤后的病理改变,改善行为评分,促进脊髓神经功能恢复。其具体机制可能与内质网应激信号通路对坏死细胞凋亡的抑制有关。
{"title":"[Effect of formononetin on endoplasmic reticulum stress and neuronal apoptosis in rats with chronic compressive cervical spinal cord injury].","authors":"Ya-Yun Zhang, Min Yao, Rui-Rui Xue, Xing Ding, Jin-Hai Xu, Xue-Jun Cui, Wen Mo","doi":"10.12200/j.issn.1003-0034.20240199","DOIUrl":"https://doi.org/10.12200/j.issn.1003-0034.20240199","url":null,"abstract":"<p><strong>Objective: </strong>To explore effect and mechanism of formononetin on recovery of neurological function after chronic spinal cord injury (SCI) in rats.</p><p><strong>Methods: </strong>Twenty-four SPF male SD rats, aged from 8 to 9 weeks old, weighted (327.29±15.19) g, were selected and randomly divided into sham operation group(Sham group), model group (Vehicle group), and formononetin group, with 8 rats in each group. Vehicle group and formononetin group were established chronic SCI models in rats by hydrogel compression. On the first day after modeling in formononetin group, formononetin officinalis solution was continuous administered orally (with a standard of 30 mg·kg<sup>-1</sup>) for 28 days, once a day. Basso-Beattie-Bresnahan (BBB) score, forelimb grip strength and rotating bar test of rats were performed in each group at 1, 7, 14, 21 and 28 days after modeling respectively to evaluate the limb motor function. Twenty-eight days after modeling, cardiac perfusion samples were collected to detect endoplasmic reticulum stress and neuronal apoptosis in spinal cord tissue. Hematoxylin-eosin staining was used to observe SCI, Nissl staining was used to observe number of surviving neurons, and Western blot (WB) was used to detect Bcl-2-associated X protein(Bax), B-cell lymphoma-2(Bcl-2) proteins and apoptosis-related proteins. The expression of endoplasmic reticulum stress pathway-related proteins was observed by immunofluorescence staining.</p><p><strong>Results: </strong>Formononetin group were better than Vehicle group in BBB score on the 21st day after operation and grip test on the 3rd, 7th and 21st days, there were statistically differences(<i>P</i><0.05). The results of HE and Nissl staining showed the number of surviving nerve cells in formononetin group were better than those in Vehicle group, and the difference were statistically significant(<i>P</i><0.05). WB results showed the expression of Bcl-2 was upregulated, and protein expressions of Bax, C/EBP homologous protein(CHOP), phosphorylated protein kinase R-like endoplasmic reticulum kinase(p-PERK), and phosphorylated eukaryotic initiation factor 2α(p-eIF2α) in formononetin group were down regulated compared with Vehicle group, the differences were statistically significant(<i>P</i><0.05). Immunofluorescence showed the protein expressions of p-PERK and activating transcription factor 6(ATF6) in neurons in formononetin group decreased compared with Vehicle group, and the differences were statistically significant (<i>P</i><0.05).</p><p><strong>Conclusion: </strong>Formononetin could alleviate pathological changes after chronic SCI in rats, improve behavioral scores, and promote the recovery of spinal cord nerve function. The specific mechanism may be related to the inhibition of necrotic apoptosis mediated by endoplasmic reticulum stress signaling pathway.</p>","PeriodicalId":23964,"journal":{"name":"Zhongguo gu shang = China journal of orthopaedics and traumatology","volume":"38 12","pages":"1241-8"},"PeriodicalIF":0.0,"publicationDate":"2025-12-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145935244","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
[A cohort study on treatment of intermission period of gout with Quzhuo Tongbi formula ()combined with febuxostat]. 【祛燥通痹方联合非布司他治疗间歇期痛风的队列研究】。
Q4 Medicine Pub Date : 2025-12-25 DOI: 10.12200/j.issn.1003-0034.20250554
Mei-Fei Li, Jing-Ya Zhang, Wei-Man Shi, Yi Zhang, Zhi-Jun Xie, Ji-Yong Huang, Cheng-Ping Wen, Dong-Hai Zhou, Qiao Wang
<p><strong>Objective: </strong>To explore efficacy and safety of <i>Quzhuo Tongbi</i> formula ()combined with febustat in treating interlude period of gout (spleen deficiency and dampness obstruction type).</p><p><strong>Methods: </strong>From July 2024 to April 2025, 102 patients with gout during intermission period were selected for a cohort study and divided into Western medicine group and Chinese and Western group. There were 51 male patients in Western medicine group, aged with an age of (43.59±12.18) years old and the average courses of disease was (91.04±82.26) months. There were 51 patients in Chinese and Western group, including 49 males and 2 females with an average age of (47.67±11.75) years old, and the average course of disease was (92.41±85.92) months. The Western medicine group was took febuxotropic orally, while Chinese and Western medicine group was took <i>Quzhuo Tongbi</i> formula() combined with febuxotropic orally, 12 weeks constituted as 1 course of treatment, and both groups were treated for 1 course in totally. The changes of serum uric acid (SUA), total cholesterol (TC), and triglycerides (TG), low-density lipoprotein (LDL), alanine aminotransferase (ALT), aspartate aminotransferase (AST), serum creatinine (Scr), and blood urea nitrogen (BUN) between two groups before and after treatment were detected and compared; numeric rating scale (NRS), patient global assessment (PGA), and TCM syndrome scores before and after treatment were compared;the number of gout attacks within 12 weeks and adverse reactions during treatment process were recorded.</p><p><strong>Results: </strong>Totally 99 patients were finally observed clinically, including 50 patients in Western group and 49 patients in Chinese and Western groups. After 12 weeks of treatment, the indicators such as SUA, Scr and BUN in Western medicine group were decreased compared with those of before treatment(<i>P</i><0.01), and the indicators such as SUA, TC, TG, LDL, ALT, AST, Scr and BUN in Chinese and Western medicine group were decreased significantly compared with those of before treatment (<i>P</i><0.05). Moreover, the improvement of indicators such as SUA, LDL, ALT, AST, and Scr in Chinese and Western medicine group were better than those of in Western medicine group(<i>P</i><0.05). During the treatment period, the frequency of gout attacks in Chinese and Western medicine group was lower than that in Western medicine group(<i>P</i><0.01). The NRS, PGA scores and TCM syndrome scores of both groups were decreased compared with those of before treatment (<i>P</i><0.01), and the improvement of NRS and PGA scores in Chinese and Western medicine group were better than those of in Western medicine group (<i>P</i><0.01). One patient developed liver function damage due to taking medicine in Western medicine group, while there were no adverse reactions in Chinese and Western medicine group.</p><p><strong>Conclusion: </strong><i>Quzhuo Tongbi</i> formula() combined with febuxo
目的:探讨祛燥通痹方联合非布斯他治疗痛风(脾虚湿阻型)间歇期的疗效和安全性。方法:选取2024年7月至2025年4月间间歇期痛风患者102例进行队列研究,分为西药组和中西医结合组。西药组男性51例,年龄(43.59±12.18)岁,平均病程(91.04±82.26)个月。中西组51例,男49例,女2例,平均年龄(47.67±11.75)岁,平均病程(92.41±85.92)个月。西药组口服非戊唑酮,中西医结合组口服祛瘀通痹方联合非戊唑酮,12周为1个疗程,两组共治疗1个疗程。检测两组患者治疗前后血清尿酸(SUA)、总胆固醇(TC)、甘油三酯(TG)、低密度脂蛋白(LDL)、丙氨酸转氨酶(ALT)、天冬氨酸转氨酶(AST)、血清肌酐(Scr)、血尿素氮(BUN)的变化并进行比较;比较治疗前后数值评定量表(NRS)、患者总体评估量表(PGA)和中医证候评分;记录12周内痛风发作次数及治疗过程中的不良反应。结果:最终临床观察99例患者,其中西医组50例,中西医结合组49例。治疗12周后,西药组患者SUA、Scr、BUN等指标较治疗前下降(ppppppp)。结论:祛瘀通痹方()联合非布司他治疗间隙期痛风临床疗效明确,安全性好,对预防复发有积极作用。
{"title":"[A cohort study on treatment of intermission period of gout with <i>Quzhuo Tongbi</i> formula ()combined with febuxostat].","authors":"Mei-Fei Li, Jing-Ya Zhang, Wei-Man Shi, Yi Zhang, Zhi-Jun Xie, Ji-Yong Huang, Cheng-Ping Wen, Dong-Hai Zhou, Qiao Wang","doi":"10.12200/j.issn.1003-0034.20250554","DOIUrl":"https://doi.org/10.12200/j.issn.1003-0034.20250554","url":null,"abstract":"&lt;p&gt;&lt;strong&gt;Objective: &lt;/strong&gt;To explore efficacy and safety of &lt;i&gt;Quzhuo Tongbi&lt;/i&gt; formula ()combined with febustat in treating interlude period of gout (spleen deficiency and dampness obstruction type).&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Methods: &lt;/strong&gt;From July 2024 to April 2025, 102 patients with gout during intermission period were selected for a cohort study and divided into Western medicine group and Chinese and Western group. There were 51 male patients in Western medicine group, aged with an age of (43.59±12.18) years old and the average courses of disease was (91.04±82.26) months. There were 51 patients in Chinese and Western group, including 49 males and 2 females with an average age of (47.67±11.75) years old, and the average course of disease was (92.41±85.92) months. The Western medicine group was took febuxotropic orally, while Chinese and Western medicine group was took &lt;i&gt;Quzhuo Tongbi&lt;/i&gt; formula() combined with febuxotropic orally, 12 weeks constituted as 1 course of treatment, and both groups were treated for 1 course in totally. The changes of serum uric acid (SUA), total cholesterol (TC), and triglycerides (TG), low-density lipoprotein (LDL), alanine aminotransferase (ALT), aspartate aminotransferase (AST), serum creatinine (Scr), and blood urea nitrogen (BUN) between two groups before and after treatment were detected and compared; numeric rating scale (NRS), patient global assessment (PGA), and TCM syndrome scores before and after treatment were compared;the number of gout attacks within 12 weeks and adverse reactions during treatment process were recorded.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Results: &lt;/strong&gt;Totally 99 patients were finally observed clinically, including 50 patients in Western group and 49 patients in Chinese and Western groups. After 12 weeks of treatment, the indicators such as SUA, Scr and BUN in Western medicine group were decreased compared with those of before treatment(&lt;i&gt;P&lt;/i&gt;&lt;0.01), and the indicators such as SUA, TC, TG, LDL, ALT, AST, Scr and BUN in Chinese and Western medicine group were decreased significantly compared with those of before treatment (&lt;i&gt;P&lt;/i&gt;&lt;0.05). Moreover, the improvement of indicators such as SUA, LDL, ALT, AST, and Scr in Chinese and Western medicine group were better than those of in Western medicine group(&lt;i&gt;P&lt;/i&gt;&lt;0.05). During the treatment period, the frequency of gout attacks in Chinese and Western medicine group was lower than that in Western medicine group(&lt;i&gt;P&lt;/i&gt;&lt;0.01). The NRS, PGA scores and TCM syndrome scores of both groups were decreased compared with those of before treatment (&lt;i&gt;P&lt;/i&gt;&lt;0.01), and the improvement of NRS and PGA scores in Chinese and Western medicine group were better than those of in Western medicine group (&lt;i&gt;P&lt;/i&gt;&lt;0.01). One patient developed liver function damage due to taking medicine in Western medicine group, while there were no adverse reactions in Chinese and Western medicine group.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Conclusion: &lt;/strong&gt;&lt;i&gt;Quzhuo Tongbi&lt;/i&gt; formula() combined with febuxo","PeriodicalId":23964,"journal":{"name":"Zhongguo gu shang = China journal of orthopaedics and traumatology","volume":"38 12","pages":"1194-200"},"PeriodicalIF":0.0,"publicationDate":"2025-12-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145935498","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
[Ilizarov technique combined with segmented removal of bone cement for the treatment of composite defects of tibia and soft tissues of skin]. [Ilizarov技术联合骨水泥分段去除治疗胫骨及皮肤软组织复合缺损]。
Q4 Medicine Pub Date : 2025-12-25 DOI: 10.12200/j.issn.1003-0034.20241027
Yun-Peng Zhang, Jiang-Hua Chen, Wei Qu, Xiu-Min Pi, Hong-Yu Hu, Tong Zhou, Shun-Hong Gao

Objective: To explore clinical efficacy of Ilizarov technique combined with the segmented removal of bone cement in treating tibial and skin-soft tissue composite defects.

Methods: From July 2018 to December 2021, 9 patients with composite defects of tibia and skin and soft tissue of the lower leg were treated by Ilizarov technique combined with segmented removal of bone cement, including 7 males and 2 females, aged from 38 to 52 years old, 4 patients on the left side and 5 patients on the right side;the length of bone defect ranged from 8.0 to 12.0 cm;the wound area ranged from 4.0 cm×5.0 cm to 6.0 cm×10.0 cm. After the infection lesion in the lower leg has been cleared and the infection has been controlled by bone cement filling for 6 to 8 weeks, the bone cement was removed after tibial osteotomy. Then, new bone cement was made and divided into several small sections to fill the bone defect area, leaving a sliding gap. Bone slippage began at 10 days after operation (1 mm/d, performed in 6 sessions). As the slippage progressed, the bone cement segments were removed successively until the connection points were successfully connected and the wound healed. The locking was completed, the mineralization of the sliding gap and bone healing at the docking point were evaluated based on X-ray films from 3 to 6(monthly), 9 and 12 months. The clinical efficacy was evaluated by Paley criteria at 2 years after operation.

Results: All 9 patients were followed up for 17 to 30 months. There were no soft tissue collapse or entrapment, and no complications such as infection recurrence occurred on the wound surface during bone segment sliding process. Eight patients achieved successful bony union at the junction, 1 patient achieved bony union after bone grafting at the junction, 6 patients had successful wound healing, and 3 patients underwent surgical adjustment due to indentations of skin margin at the junction, which affected the appearance. All the wounds achieved primary healing after operation. Two years after operation, the therapeutic effect was evaluated according to Paley standard, 7 patients got excellent results and 2 good.

Conclusion: Ilizarov technique combined with segmented removal of bone cement could simultaneously address composite defects of tibia and skin soft tissue of the lower leg, reducing flap surgery and avoiding complications such as soft tissue collapse and entrapation during bone segment sliding.

目的:探讨Ilizarov技术联合骨水泥分段去除治疗胫骨及皮肤软组织复合缺损的临床疗效。方法:2018年7月至2021年12月,采用Ilizarov技术联合骨水泥分段取出术治疗胫骨及小腿皮肤软组织复合缺损9例,男7例,女2例,年龄38 ~ 52岁,左侧4例,右侧5例;骨缺损长度为8.0 ~ 12.0 cm;创面面积4.0 cm×5.0 ~ 6.0 cm×10.0 cm。待下肢感染病灶清除,骨水泥充填控制感染6 ~ 8周后,行胫骨截骨术取出骨水泥。然后,制作新的骨水泥,并将其分成几小段填充骨缺损区域,留下滑动间隙。术后10天开始出现骨滑移(1 mm/d,共6次)。随着滑移的进展,骨水泥段被依次移除,直到连接点连接成功,创面愈合。完成锁定,根据3 - 6个月(每月)、9月和12个月的x线片评估滑动间隙的矿化和对接点的骨愈合情况。术后2年以Paley标准评价临床疗效。结果:9例患者均随访17 ~ 30个月。骨段滑动过程中无软组织塌陷、卡压,创面无感染复发等并发症发生。8例患者接口处骨愈合成功,1例患者接口处植骨后骨愈合,6例患者创面愈合成功,3例患者因接口处皮肤缘凹陷影响外观而行手术调整。术后创面均基本愈合。术后2年按Paley标准评价疗效,优7例,良2例。结论:Ilizarov技术联合骨水泥分段去除可同时修复胫骨和小腿皮肤软组织复合缺损,减少皮瓣手术,避免骨段滑动过程中软组织塌陷、夹闭等并发症。
{"title":"[Ilizarov technique combined with segmented removal of bone cement for the treatment of composite defects of tibia and soft tissues of skin].","authors":"Yun-Peng Zhang, Jiang-Hua Chen, Wei Qu, Xiu-Min Pi, Hong-Yu Hu, Tong Zhou, Shun-Hong Gao","doi":"10.12200/j.issn.1003-0034.20241027","DOIUrl":"https://doi.org/10.12200/j.issn.1003-0034.20241027","url":null,"abstract":"<p><strong>Objective: </strong>To explore clinical efficacy of Ilizarov technique combined with the segmented removal of bone cement in treating tibial and skin-soft tissue composite defects.</p><p><strong>Methods: </strong>From July 2018 to December 2021, 9 patients with composite defects of tibia and skin and soft tissue of the lower leg were treated by Ilizarov technique combined with segmented removal of bone cement, including 7 males and 2 females, aged from 38 to 52 years old, 4 patients on the left side and 5 patients on the right side;the length of bone defect ranged from 8.0 to 12.0 cm;the wound area ranged from 4.0 cm×5.0 cm to 6.0 cm×10.0 cm. After the infection lesion in the lower leg has been cleared and the infection has been controlled by bone cement filling for 6 to 8 weeks, the bone cement was removed after tibial osteotomy. Then, new bone cement was made and divided into several small sections to fill the bone defect area, leaving a sliding gap. Bone slippage began at 10 days after operation (1 mm/d, performed in 6 sessions). As the slippage progressed, the bone cement segments were removed successively until the connection points were successfully connected and the wound healed. The locking was completed, the mineralization of the sliding gap and bone healing at the docking point were evaluated based on X-ray films from 3 to 6(monthly), 9 and 12 months. The clinical efficacy was evaluated by Paley criteria at 2 years after operation.</p><p><strong>Results: </strong>All 9 patients were followed up for 17 to 30 months. There were no soft tissue collapse or entrapment, and no complications such as infection recurrence occurred on the wound surface during bone segment sliding process. Eight patients achieved successful bony union at the junction, 1 patient achieved bony union after bone grafting at the junction, 6 patients had successful wound healing, and 3 patients underwent surgical adjustment due to indentations of skin margin at the junction, which affected the appearance. All the wounds achieved primary healing after operation. Two years after operation, the therapeutic effect was evaluated according to Paley standard, 7 patients got excellent results and 2 good.</p><p><strong>Conclusion: </strong>Ilizarov technique combined with segmented removal of bone cement could simultaneously address composite defects of tibia and skin soft tissue of the lower leg, reducing flap surgery and avoiding complications such as soft tissue collapse and entrapation during bone segment sliding.</p>","PeriodicalId":23964,"journal":{"name":"Zhongguo gu shang = China journal of orthopaedics and traumatology","volume":"38 12","pages":"1276-81"},"PeriodicalIF":0.0,"publicationDate":"2025-12-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145935447","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
[Analysis of efficacy of high-frequency ultrasound and magnetic resonance imaging of shoulder joint in the diagnosis of rotator cuff tears]. 高频超声与肩关节磁共振成像诊断肩袖撕裂的疗效分析。
Q4 Medicine Pub Date : 2025-12-25 DOI: 10.12200/j.issn.1003-0034.20240285
Li-Qi Liu, Yuan Li, Cong-Cong Liu, Wen Lu, Qing-Jing Ma

Objective: To compare efficacy of high-frequency ultrasound(US) and MRI in detecting rotator cuff tears.

Methods: From June 2023 to January 2024, 104 patients with unilateral shoulder pain or dysfunction were selected, including 40 males and 64 females, aged from 29 to 87 years old with an average of (59.8±11.9) years old. Methods 7 patients caused by trauma and 97 patients caused by non-trauma. All patients were underwent US and MRI examinations, and taking results of arthroscopic surgery as gold standard; the accuracy rate, positive coincidence rate, negative coincidence rate and total coincidence rate of US and MRI in diagnosis of rotator cuff tears were compared, and the diagnostic efficacy between two methods were analyzed.

Results: Eighty-two patients was diagnosed as rotator cuff tears by arthroscopy(67 patients with partial tears and 15 patients with full-thickness tears), positive rate was 78.8%, accuracy rate of US in diagnosing rotator cuff tear was 29.3% (24/82), and that of MRI was 47.6%(39/82). Moreover, the diagnostic efficacy of MRI was significantly higher than that of US(χ2=5.799, P=0.061). According to analysis of tear depth, the accuracy rate of US in diagnosing full-thickness tears was 46.7% (7/15), and that of MRI was 53.3%(8/15), with no statistically significant difference (P=0.715). The accuracy rate of US in diagnosing partial tear was 25.3% (17/67), significantly lower than 46.2% (31/67) of MRI, and the difference was statistically significant (χ2=6.362, P=0.012). The total coincidence rates of US, MRI and the combined diagnosis of US+MRI for rotator cuff tear were 51.0%, 62.5% and 66.3% respectively.

Conclusion: MRI is superior to US in diagnosing rotator cuff tears, especially partial tears, and comparable in diagnosing full-thickness tears. When combined diagnosis of US and MRI could further improve diagnostic efficiency, it is recommended to apply it in combination in clinical practice.

目的:比较高频超声(US)与磁共振成像(MRI)检测肩袖撕裂的效果。方法:选取2023年6月~ 2024年1月单侧肩痛或功能障碍患者104例,其中男性40例,女性64例,年龄29 ~ 87岁,平均(59.8±11.9)岁。方法外伤致7例,非外伤致97例。所有患者均行US和MRI检查,以关节镜手术结果为金标准;比较US与MRI诊断肩袖撕裂的正确率、阳性符合率、阴性符合率及总符合率,并分析两种方法的诊断效果。结果:关节镜诊断肩袖撕裂82例(部分撕裂67例,全层撕裂15例),阳性率为78.8%,超声诊断肩袖撕裂准确率为29.3% (24/82),MRI诊断准确率为47.6%(39/82)。MRI的诊断效能显著高于US(χ2=5.799, P=0.061)。根据撕裂深度分析,US诊断全层撕裂的准确率为46.7% (7/15),MRI诊断全层撕裂的准确率为53.3%(8/15),差异无统计学意义(P=0.715)。超声诊断部分撕裂的准确率为25.3%(17/67),显著低于MRI的46.2%(31/67),差异有统计学意义(χ2=6.362, P=0.012)。US、MRI及US+MRI联合诊断肩袖撕裂的总符合率分别为51.0%、62.5%和66.3%。结论:MRI对肩袖撕裂尤其是局部撕裂的诊断优于超声,对全层撕裂的诊断与超声相当。当US与MRI联合诊断可进一步提高诊断效率时,建议在临床中联合应用。
{"title":"[Analysis of efficacy of high-frequency ultrasound and magnetic resonance imaging of shoulder joint in the diagnosis of rotator cuff tears].","authors":"Li-Qi Liu, Yuan Li, Cong-Cong Liu, Wen Lu, Qing-Jing Ma","doi":"10.12200/j.issn.1003-0034.20240285","DOIUrl":"https://doi.org/10.12200/j.issn.1003-0034.20240285","url":null,"abstract":"<p><strong>Objective: </strong>To compare efficacy of high-frequency ultrasound(US) and MRI in detecting rotator cuff tears.</p><p><strong>Methods: </strong>From June 2023 to January 2024, 104 patients with unilateral shoulder pain or dysfunction were selected, including 40 males and 64 females, aged from 29 to 87 years old with an average of (59.8±11.9) years old. Methods 7 patients caused by trauma and 97 patients caused by non-trauma. All patients were underwent US and MRI examinations, and taking results of arthroscopic surgery as gold standard; the accuracy rate, positive coincidence rate, negative coincidence rate and total coincidence rate of US and MRI in diagnosis of rotator cuff tears were compared, and the diagnostic efficacy between two methods were analyzed.</p><p><strong>Results: </strong>Eighty-two patients was diagnosed as rotator cuff tears by arthroscopy(67 patients with partial tears and 15 patients with full-thickness tears), positive rate was 78.8%, accuracy rate of US in diagnosing rotator cuff tear was 29.3% (24/82), and that of MRI was 47.6%(39/82). Moreover, the diagnostic efficacy of MRI was significantly higher than that of US(<i>χ</i><sup>2</sup>=5.799, <i>P</i>=0.061). According to analysis of tear depth, the accuracy rate of US in diagnosing full-thickness tears was 46.7% (7/15), and that of MRI was 53.3%(8/15), with no statistically significant difference (<i>P</i>=0.715). The accuracy rate of US in diagnosing partial tear was 25.3% (17/67), significantly lower than 46.2% (31/67) of MRI, and the difference was statistically significant (<i>χ</i><sup>2</sup>=6.362, <i>P</i>=0.012). The total coincidence rates of US, MRI and the combined diagnosis of US+MRI for rotator cuff tear were 51.0%, 62.5% and 66.3% respectively.</p><p><strong>Conclusion: </strong>MRI is superior to US in diagnosing rotator cuff tears, especially partial tears, and comparable in diagnosing full-thickness tears. When combined diagnosis of US and MRI could further improve diagnostic efficiency, it is recommended to apply it in combination in clinical practice.</p>","PeriodicalId":23964,"journal":{"name":"Zhongguo gu shang = China journal of orthopaedics and traumatology","volume":"38 12","pages":"1231-5"},"PeriodicalIF":0.0,"publicationDate":"2025-12-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145935503","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
[Calculation of personalized safety zone of hip joint prosthesis in patients with ankylosing spondylitis and analysis of influencing factors]. [强直性脊柱炎患者髋关节假体个性化安全区计算及影响因素分析]。
Q4 Medicine Pub Date : 2025-12-25 DOI: 10.12200/j.issn.1003-0034.20240374
Yin-Xi Chen, Geng Liu, Peng-Ge Fu, Qi-Zhong Wang, Yu-Xin Wang, Hui Li

Objective: To explore safe zones for acetabular prosthesis implantation in patients with ankylosing spondylitis (AS) at different anterior pelvic plane tilts (APPt), and to determine the optimal implantation angle of the prosthesis through the safe zones with different ranges of motion. To explore the influencing factors of size and scope of the safe zone.

Methods: CT data of pelvis before total hip arthroplasty (THA) in a 54-year-old male patient with Tonnis stage Ⅳ left hip arthritis, and virtual THA simulated by computer prosthesis with a femoral head diameter of 32 mm, a head-to-neck ratio of 2.67, and a cervical-shaft angle of 132° was selected and assembled by tilting forward by 15°. After defining the target range of motion of hip joint that could meet functions such as standing, sitting, and squatting, acetabular prosthesis implantation safety zones corresponding to bony impact and prosthesis impact when the anterior pelvic plane inclination angles are -10°, -5°, 0°, 5°, 10°, 15°, 20° and 25° respectively were calculated. A model to change the parameters of the femoral prosthesis was select and calculated the safety zone when different prostheses were implanted.

Results: When the range of motion of spine and pelvis disappeared, the safe zone for implant placement could meet the requirements of standing, sitting and squatting was extremely small. When the pelvis was tilted forward by 10° to backward by 25°, the abduction angle of acetabular implant could meet the daily range of motion decreased from 55.7° to 45.8°, and the forward inclination angle decreased from 29.9° to 7.4°. The diameter of femoral head was positively correlated with the size of safe zone. Within the range of 24 to 32 mm, for every 0.17 mm increased in the diameter of femoral head, the safe range of acetabular anterior inclination angle and abduction angle increased for 4° to 6°. For the ball head of the same diameter, the safety zone showed a trend of first increasing and then decreased with the increase of cervical shaft angle or anterior inclination angle of femur.

Conclusion: When AS patients undergo THA, precise implantation techniques are required to obtain a safe range of motion that could meet the requirements of standing, sitting and squatting. For patients with obvious anterior or posterior pelvic tilt, personalized prosthesis implantation should be carried out to reduce prosthesis suspension and impact on the iliopsoas muscle. Large-diameter femoral head prostheses are more sensitive to changes in the cervical shaft angle and anterior inclination angle, and the area of the implanted combined safety zone is larger.

目的:探讨强直性脊柱炎(AS)患者不同骨盆前平面倾斜度(APPt)下髋臼假体植入术的安全区域,通过不同活动范围的安全区域确定假体的最佳植入术角度。探讨影响安全区域大小和范围的因素。方法:54岁男性Tonnis期Ⅳ左髋关节关节炎患者全髋关节置换术前骨盆CT资料,选择股骨头直径32 mm、头颈比2.67、颈轴角132°的计算机模拟虚拟髋关节,前倾15°组装。在确定髋关节能满足站、坐、蹲等功能的目标活动范围后,计算骨盆前平面倾角分别为-10°、-5°、0°、5°、10°、15°、20°和25°时骨冲击和假体冲击对应的髋臼假体植入安全区域。选择改变股骨假体参数的模型,计算不同假体植入时的安全范围。结果:当脊柱和骨盆的活动范围消失时,能够满足站立、坐姿和下蹲要求的植入物安全范围极小。当骨盆前倾10°至后倾25°时,髋臼假体可满足日常活动范围的外展角由55.7°降至45.8°,前倾角由29.9°降至7.4°。股骨头直径与安全区域的大小呈正相关。在24 ~ 32 mm范围内,股骨头直径每增加0.17 mm,髋臼前倾角和外展角的安全范围增加4°~ 6°。对于相同直径的球头,随着颈轴角或股骨前倾角的增大,安全区域呈现先增大后减小的趋势。结论:AS患者行全髋关节置换术时,需要精确的植入技术,以获得可满足站、坐、蹲要求的安全活动范围。对于骨盆前后倾斜明显的患者,应进行个体化假体植入,以减少假体悬吊及对髂腰肌的影响。大直径股骨头假体对颈椎轴角和前倾角的变化更敏感,植入联合安全区面积更大。
{"title":"[Calculation of personalized safety zone of hip joint prosthesis in patients with ankylosing spondylitis and analysis of influencing factors].","authors":"Yin-Xi Chen, Geng Liu, Peng-Ge Fu, Qi-Zhong Wang, Yu-Xin Wang, Hui Li","doi":"10.12200/j.issn.1003-0034.20240374","DOIUrl":"https://doi.org/10.12200/j.issn.1003-0034.20240374","url":null,"abstract":"<p><strong>Objective: </strong>To explore safe zones for acetabular prosthesis implantation in patients with ankylosing spondylitis (AS) at different anterior pelvic plane tilts (APPt), and to determine the optimal implantation angle of the prosthesis through the safe zones with different ranges of motion. To explore the influencing factors of size and scope of the safe zone.</p><p><strong>Methods: </strong>CT data of pelvis before total hip arthroplasty (THA) in a 54-year-old male patient with Tonnis stage Ⅳ left hip arthritis, and virtual THA simulated by computer prosthesis with a femoral head diameter of 32 mm, a head-to-neck ratio of 2.67, and a cervical-shaft angle of 132° was selected and assembled by tilting forward by 15°. After defining the target range of motion of hip joint that could meet functions such as standing, sitting, and squatting, acetabular prosthesis implantation safety zones corresponding to bony impact and prosthesis impact when the anterior pelvic plane inclination angles are -10°, -5°, 0°, 5°, 10°, 15°, 20° and 25° respectively were calculated. A model to change the parameters of the femoral prosthesis was select and calculated the safety zone when different prostheses were implanted.</p><p><strong>Results: </strong>When the range of motion of spine and pelvis disappeared, the safe zone for implant placement could meet the requirements of standing, sitting and squatting was extremely small. When the pelvis was tilted forward by 10° to backward by 25°, the abduction angle of acetabular implant could meet the daily range of motion decreased from 55.7° to 45.8°, and the forward inclination angle decreased from 29.9° to 7.4°. The diameter of femoral head was positively correlated with the size of safe zone. Within the range of 24 to 32 mm, for every 0.17 mm increased in the diameter of femoral head, the safe range of acetabular anterior inclination angle and abduction angle increased for 4° to 6°. For the ball head of the same diameter, the safety zone showed a trend of first increasing and then decreased with the increase of cervical shaft angle or anterior inclination angle of femur.</p><p><strong>Conclusion: </strong>When AS patients undergo THA, precise implantation techniques are required to obtain a safe range of motion that could meet the requirements of standing, sitting and squatting. For patients with obvious anterior or posterior pelvic tilt, personalized prosthesis implantation should be carried out to reduce prosthesis suspension and impact on the iliopsoas muscle. Large-diameter femoral head prostheses are more sensitive to changes in the cervical shaft angle and anterior inclination angle, and the area of the implanted combined safety zone is larger.</p>","PeriodicalId":23964,"journal":{"name":"Zhongguo gu shang = China journal of orthopaedics and traumatology","volume":"38 12","pages":"1249-55"},"PeriodicalIF":0.0,"publicationDate":"2025-12-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145934976","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
期刊
Zhongguo gu shang = China journal of orthopaedics and traumatology
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