Pub Date : 2025-12-25DOI: 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.
{"title":"[Research status and progress of daytime total shoulder arthroplasty].","authors":"Jun-Rong Chen, Long Chen, Sen-Lei Li, Li Sun","doi":"10.12200/j.issn.1003-0034.20240804","DOIUrl":"https://doi.org/10.12200/j.issn.1003-0034.20240804","url":null,"abstract":"<p><p>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.</p>","PeriodicalId":23964,"journal":{"name":"Zhongguo gu shang = China journal of orthopaedics and traumatology","volume":"38 12","pages":"1282-8"},"PeriodicalIF":0.0,"publicationDate":"2025-12-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145935439","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}
Pub Date : 2025-12-25DOI: 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.
{"title":"[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].","authors":"Quan-Wei Ding, Jun Ying, Ying Zhao","doi":"10.12200/j.issn.1003-0034.20250517","DOIUrl":"https://doi.org/10.12200/j.issn.1003-0034.20250517","url":null,"abstract":"<p><strong>Objective: </strong>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.</p><p><strong>Methods: </strong>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.</p><p><strong>Results: </strong>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.</p><p><strong>Conclusion: </strong>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.</p>","PeriodicalId":23964,"journal":{"name":"Zhongguo gu shang = China journal of orthopaedics and traumatology","volume":"38 12","pages":"1255-9"},"PeriodicalIF":0.0,"publicationDate":"2025-12-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145935426","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}
Pub Date : 2025-12-25DOI: 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.
{"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":"<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.","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}
Pub Date : 2025-12-25DOI: 10.12200/j.issn.1003-0034.20251160
Xiao-Xu Li, Wei Cao, Guang-Cheng Wei, Jin-Jie Shi
{"title":"[Current status and prospects of traditional Chinese medicine in prevention and treatment of gouty arthritis].","authors":"Xiao-Xu Li, Wei Cao, Guang-Cheng Wei, Jin-Jie Shi","doi":"10.12200/j.issn.1003-0034.20251160","DOIUrl":"https://doi.org/10.12200/j.issn.1003-0034.20251160","url":null,"abstract":"","PeriodicalId":23964,"journal":{"name":"Zhongguo gu shang = China journal of orthopaedics and traumatology","volume":"38 12","pages":"1189-93"},"PeriodicalIF":0.0,"publicationDate":"2025-12-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145935066","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}
Pub Date : 2025-12-25DOI: 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
{"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":"<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","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}
Pub Date : 2025-12-25DOI: 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}
Pub Date : 2025-12-25DOI: 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
{"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":"<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","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}
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.
{"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}
Pub Date : 2025-12-25DOI: 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.
{"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}
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.
{"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}