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[Comparison of two transforaminal endoscopic techniques for recurrent L5S1 lumbar disc herniation with high iliac crest]. [两种经椎间孔内窥镜技术治疗复发性L5S1高髂嵴腰椎间盘突出症的比较]。
Q4 Medicine Pub Date : 2025-11-25 DOI: 10.12200/j.issn.1003-0034.20240747
Yue-Hong Guan, Jian Wu, Li-Jun Wang, Bin Xu, Jian Tang, Ying Zhang, Ying-Qi He
<p><strong>Objective: </strong>To explore the clinical efficacy of conventional transforaminal endoscopic technique and I See transforaminal endoscopic technique in the treatment of recurrent L<sub>5</sub>S<sub>1</sub> lumbar disc herniation with high iliac crest.</p><p><strong>Methods: </strong>A total of 36 patients with recurrent L5S1 lumbar disc herniation with high iliac crest after posterior small-incision discectomy, admitted from May 2016 to May 2023, were selected. They were divided into the conventional transforaminal endoscopy group and the I See transforaminal endoscopy group according to the different transforaminal endoscopic techniques adopted, and all patients in both groups underwent lateral transforaminal spinal canal decompression and discectomy. There were 18 patients in the conventional transforaminal endoscopy group, including 11 males and 7 females, with an age of (52.24±6.68) years;the I See transforaminal endoscopy group also had 18 patients, including 12 males and 6 females, with an age of (50.75±7.79) years. The perioperative indicators (operation time, number of intraoperative radiographs, and length of hospital stay) were compared between two groups. The clinical efficacy was evaluated using the visual analogue scale(VAS) for pain, the Japanese Orthopaedic Association(JOA) low back pain score, and the modified MacNab criteria before and after surgery.</p><p><strong>Results: </strong>All patients achieved gradeⅠincision healing, with no infection cases. The operation time of the I See group was (64.25±16.67) minutes, which was significantly shorter than that of the conventional transforaminal endoscopy group (89.11±17.24) minutes, and the difference was statistically significant(<i>P</i><0.05). The number of intraoperative radiographs in the I See group was (5.20±2.29) times, which was significantly less than that in the conventional transforaminal endoscopy group(19.16±3.68) times, and the difference was statistically significant(<i>P</i><0.05). The VAS and total JOA scores of both groups at the 3rd day, the 3rd month after surgery, and the last follow-up were significantly lower than those before surgery, with statistically significant differences(<i>P</i><0.05);however, there were no statistically significant differences in VAS and total JOA scores between two groups at the 3rd day, the 3rd month after surgery, and the last follow-up (<i>P</i>>0.05). According to the modified MacNab criteria for efficacy evaluation:in the conventional transforaminal endoscopy group, 14 cases were excellent and 4 cases were good;in the I See transforaminal endoscopy group, 15 cases were excellent and 3 cases were good;there was no statistically significant difference in efficacy between two groups(<i>Z</i>=0.177, <i>P</i>=0.674).</p><p><strong>Conclusion: </strong>Both transforaminal endoscopic techniques have good clinical effects in the treatment of recurrent L<sub>5</sub>S<sub>1</sub> lumbar disc herniation with high iliac crest,
目的:探讨常规经椎间孔内窥镜技术与I - See经椎间孔内窥镜技术治疗复发性高髂嵴L5S1腰椎间盘突出症的临床疗效。方法:选取2016年5月至2023年5月收治的36例后路小切口椎间盘切除术后复发性L5S1高髂嵴腰椎间盘突出症患者。根据采用的内镜技术不同分为常规经椎间孔内窥镜组和I See经椎间孔内窥镜组,两组患者均行经椎间孔外侧椎管减压和椎间盘切除术。常规经椎间孔内窥镜组18例,其中男性11例,女性7例,年龄(52.24±6.68)岁;I See经椎间孔内窥镜组18例,男12例,女6例,年龄(50.75±7.79)岁。比较两组围手术期指标(手术时间、术中x线片次数、住院时间)。采用视觉模拟疼痛量表(VAS)、日本骨科协会(JOA)腰痛评分、术前术后改良MacNab标准评估临床疗效。结果:所有患者均达到Ⅰ级切口愈合,无感染病例。I See组手术时间为(64.25±16.67)min,明显短于常规经椎间孔内窥镜组(89.11±17.24)min,差异有统计学意义(PPPP>0.05)。根据改良MacNab疗效评价标准:常规经椎间孔内窥镜组优14例,良4例;I See经椎间孔内窥镜组,优15例,良3例;两组疗效比较,差异无统计学意义(Z=0.177, P=0.674)。结论:两种经椎间孔内镜技术治疗复发性高髂嵴L5S1腰椎间盘突出症临床效果良好,术后症状明显改善,是安全、可靠、微创的手术方法。与传统的经椎间孔内窥镜相比,I See经椎间孔内窥镜技术操作时间更短,术中x线片较少,因此通常是首选。
{"title":"[Comparison of two transforaminal endoscopic techniques for recurrent L5S1 lumbar disc herniation with high iliac crest].","authors":"Yue-Hong Guan, Jian Wu, Li-Jun Wang, Bin Xu, Jian Tang, Ying Zhang, Ying-Qi He","doi":"10.12200/j.issn.1003-0034.20240747","DOIUrl":"https://doi.org/10.12200/j.issn.1003-0034.20240747","url":null,"abstract":"&lt;p&gt;&lt;strong&gt;Objective: &lt;/strong&gt;To explore the clinical efficacy of conventional transforaminal endoscopic technique and I See transforaminal endoscopic technique in the treatment of recurrent L&lt;sub&gt;5&lt;/sub&gt;S&lt;sub&gt;1&lt;/sub&gt; lumbar disc herniation with high iliac crest.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Methods: &lt;/strong&gt;A total of 36 patients with recurrent L5S1 lumbar disc herniation with high iliac crest after posterior small-incision discectomy, admitted from May 2016 to May 2023, were selected. They were divided into the conventional transforaminal endoscopy group and the I See transforaminal endoscopy group according to the different transforaminal endoscopic techniques adopted, and all patients in both groups underwent lateral transforaminal spinal canal decompression and discectomy. There were 18 patients in the conventional transforaminal endoscopy group, including 11 males and 7 females, with an age of (52.24±6.68) years;the I See transforaminal endoscopy group also had 18 patients, including 12 males and 6 females, with an age of (50.75±7.79) years. The perioperative indicators (operation time, number of intraoperative radiographs, and length of hospital stay) were compared between two groups. The clinical efficacy was evaluated using the visual analogue scale(VAS) for pain, the Japanese Orthopaedic Association(JOA) low back pain score, and the modified MacNab criteria before and after surgery.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Results: &lt;/strong&gt;All patients achieved gradeⅠincision healing, with no infection cases. The operation time of the I See group was (64.25±16.67) minutes, which was significantly shorter than that of the conventional transforaminal endoscopy group (89.11±17.24) minutes, and the difference was statistically significant(&lt;i&gt;P&lt;/i&gt;&lt;0.05). The number of intraoperative radiographs in the I See group was (5.20±2.29) times, which was significantly less than that in the conventional transforaminal endoscopy group(19.16±3.68) times, and the difference was statistically significant(&lt;i&gt;P&lt;/i&gt;&lt;0.05). The VAS and total JOA scores of both groups at the 3rd day, the 3rd month after surgery, and the last follow-up were significantly lower than those before surgery, with statistically significant differences(&lt;i&gt;P&lt;/i&gt;&lt;0.05);however, there were no statistically significant differences in VAS and total JOA scores between two groups at the 3rd day, the 3rd month after surgery, and the last follow-up (&lt;i&gt;P&lt;/i&gt;&gt;0.05). According to the modified MacNab criteria for efficacy evaluation:in the conventional transforaminal endoscopy group, 14 cases were excellent and 4 cases were good;in the I See transforaminal endoscopy group, 15 cases were excellent and 3 cases were good;there was no statistically significant difference in efficacy between two groups(&lt;i&gt;Z&lt;/i&gt;=0.177, &lt;i&gt;P&lt;/i&gt;=0.674).&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Conclusion: &lt;/strong&gt;Both transforaminal endoscopic techniques have good clinical effects in the treatment of recurrent L&lt;sub&gt;5&lt;/sub&gt;S&lt;sub&gt;1&lt;/sub&gt; lumbar disc herniation with high iliac crest, ","PeriodicalId":23964,"journal":{"name":"Zhongguo gu shang = China journal of orthopaedics and traumatology","volume":"38 11","pages":"1100-5"},"PeriodicalIF":0.0,"publicationDate":"2025-11-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145669875","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
[Application of 3D-printed auxiliary guides in adolescent scoliosis surgery]. 【3d打印辅助导具在青少年脊柱侧凸手术中的应用】。
Q4 Medicine Pub Date : 2025-11-25 DOI: 10.12200/j.issn.1003-0034.20240850
Dong Hou, Jian-Tao Wen, Chen Zhang, Jin Huang, Chang-Quan Dai, Kai Li, Han Leng, Jing Zhang, Shao-Bo Yang, Xiao-Juan Cui, Juan Wang, Xiao-Yun Yuan

Objective: To investigate the accuracy and safety of pedicle screw placement using 3D-printed auxiliary guides in scoliosis correction surgery for adolescents.

Methods: A retrospective analysis was conducted on the clinical data of 51 patients who underwent posterior scoliosis correction surgery from January 2020 to March 2023. Among them, there were 35 cases of adolescent idiopathic scoliosis and 16 cases of congenital scoliosis. The patients were divided into two groups based on the auxiliary tool used:the 3D-printed auxiliary guide screw placement group (3D printing group) and the free-hand screw placement group (free-hand group, without auxiliary tools). The 3D printing group included 32 patients (12 males and 20 females) with an average age of (12.59±2.60) years;the free-hand group included 19 patients (7 males and 12 females) with an average age of (14.58±3.53) years. The two groups were compared in terms of screw placement accuracy and safety, spinal correction rate, intraoperative blood loss, number of intraoperative fluoroscopies, operation time, hospital stay, and preoperative and last follow-up scores of the Scoliosis Research Society-22 (SRS-22) questionnaire.

Results: A total of 707 pedicle screws were placed in the two groups, with 441 screws in the 3D printing group and 266 screws in the free-hand group. All patients in both groups successfully completed the surgery. There was a statistically significant difference in operation time between the two groups (P<0.05). The screw placement accuracy rate of the 3D printing group was 95.46% (421/441), among which the Grade A placement rate was 89.34% (394/441);the screw placement accuracy rate of the free-hand group was 86.47% (230/266), with a Grade A placement rate of 73.31% (195/266). There were statistically significant differences in the accuracy of Grade A, B, and C screw placements between the two groups (P<0.05), while no statistically significant differences were observed in intraoperative blood loss, number of fluoroscopies, correction rate, or hospital stay (P>0.05). In the SRS-22 questionnaire scores, the scores of functional status and activity ability, self-image, mental status, and pain of patients in each group at the last follow-up were significantly improved compared with those before surgery (P<0.05), but there were no statistically significant differences in all scores between the two groups (P>0.05).

Conclusion: In scoliosis correction surgery, compared with traditional free-hand screw placement, the use of 3D-printed auxiliary guides for screw placement significantly improves the accuracy and safety of screw placement and shortens the operation time.

目的:探讨3d打印辅助导具在青少年脊柱侧凸矫正手术中置入椎弓根螺钉的准确性和安全性。方法:回顾性分析2020年1月至2023年3月行后路脊柱侧凸矫正手术的51例患者的临床资料。其中青少年特发性脊柱侧凸35例,先天性脊柱侧凸16例。根据使用的辅助工具将患者分为两组:3D打印辅助导钉放置组(3D打印组)和徒手放置组(徒手组,无辅助工具)。3D打印组32例,男12例,女20例,平均年龄(12.59±2.60)岁;徒手组19例,男7例,女12例,平均年龄(14.58±3.53)岁。比较两组置入螺钉的准确性和安全性、脊柱矫正率、术中出血量、术中透视次数、手术时间、住院时间、脊柱侧凸研究学会-22 (SRS-22)问卷术前和末次随访评分。结果:两组共置入椎弓根螺钉707枚,其中3D打印组置入441枚,徒手组置入266枚。两组患者均成功完成手术。两组手术时间比较,差异有统计学意义(p < 0.05)。在SRS-22问卷评分中,末次随访时各组患者的功能状态与活动能力、自我形象、精神状态、疼痛等得分均较术前有显著改善(p < 0.05)。结论:在脊柱侧弯矫正手术中,与传统徒手置入螺钉相比,使用3d打印辅助导钉置入螺钉的准确性和安全性显著提高,缩短了手术时间。
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引用次数: 0
[Posterior medial branch block for persistent pain after percutaneous vertebral augmentation in osteoporotic vertebral fractures]. [后内侧支阻滞治疗骨质疏松性椎体骨折经皮椎体增强术后持续疼痛]。
Q4 Medicine Pub Date : 2025-11-25 DOI: 10.12200/j.issn.1003-0034.20250335
Zhe-Ren Wang, Ren Yu, Chun-de Lu, Zhi-Yuan Xu, Bin Wu, Cheng Ni

Objective: To evaluate the short-and medium-term efficacy of posterior medial branch block in the treatment of persistent pain after percutaneous vertebral augmentation.

Methods: From January 2018 to January 2023, a total of 1, 062 patients with osteoporotic vertebral compression fractures underwent percutaneous vertebral augmentation. Among them, 32 elderly patients who experienced persistent low back pain after surgery and subsequently received posterior medial branch block and cryoablation were included. Six patients died during follow-up, leaving 26 patients for final analysis (1 male, 25 females). The mean age was (82.96±5.66) years (ranged, 76 to 94 years). The mean body mass index was (23.76±3.08) kg·m-2(ranged 18.1 to 27.2 kg·m-2). The bone mineral density T-value ranged from -2.5 to -4.3 with a mean of (-3.09±0.56). The mean volume of bone cement injected was 6.00 (5.38, 7.00) ml. Fracture locations were T11 (2 cases), T12 (7 cases), L1 (10 cases), L2 (6 cases), and L3 (1 case). The mean interval from vertebral augmentation to block treatment was (7.12±2.22) months (rangd 6 to 12 months). The vertebral augmentation procedures were percutaneous kyphoplasty(PKP) in 12 cases and percutaneous vertebroplasty (PVP) in 14 cases. At the 2nd week, 3rd month, and 6th month after the block, the numerical rating scale(NRS), Oswestry disability index(ODI), patient satisfaction, and pain relief rate at the 6th month were evaluated. Relationships between pain relief rate at the 6th month after the last treatment and possible influencing factors were analyzed.

Results: Compared with X-ray films after percutaneous vertebral augmentation, the X-ray films before block showed an increase in kyphotic angle and vertebral compression rate, with statistically significant differences(P<0.05). At the 2nd week, 3rd month, and 6th month after posterior medial branch block and cryoablation, NRS and ODI scores were significantly lower than before the block(P<0.05). Among the 26 patients, 5 received additional cryoablation. At the 6th month after the last treatment, 19 patients reported excellent or good satisfaction. Univariate binary Logistic analysis showed all P>0.05, and no independent factor affecting final satisfaction or pain relief at 6 months after the last treatment was identified.

Conclusion: Posterior medial branch block(with cryoablation) can effectively improve short-and medium-term symptoms and function in patients with persistent axial low back pain after percutaneous vertebral augmentation for osteoporotic vertebral fractures.

目的:评价后内侧支阻滞治疗经皮椎体隆胸术后持续性疼痛的中短期疗效。方法:2018年1月至2023年1月,对1062例骨质疏松性椎体压缩性骨折患者行经皮椎体隆胸术。其中包括32例术后持续腰痛并接受后内侧支阻滞和冷冻消融的老年患者。随访期间死亡6例,最终分析26例(男1例,女25例)。平均年龄(82.96±5.66)岁,年龄范围76 ~ 94岁。平均体重指数为(23.76±3.08)kg·m-2(18.1 ~ 27.2 kg·m-2)。骨密度t值范围为-2.5 ~ -4.3,平均值为(-3.09±0.56)。骨水泥注射体积平均为6.00(5.38、7.00)ml,骨折部位分别为T11(2例)、T12(7例)、L1(10例)、L2(6例)、L3(1例)。从椎体增强到阻滞治疗的平均间隔时间为(7.12±2.22)个月(范围6至12个月)。经皮椎体成形术(PKP) 12例,经皮椎体成形术(PVP) 14例。分别于阻滞后第2周、第3个月和第6个月,评估数值评定量表(NRS)、Oswestry残疾指数(ODI)、患者满意度和第6个月疼痛缓解率。分析末次治疗后6个月疼痛缓解率与可能的影响因素的关系。结果:与经皮椎体增强术后x线片比较,阻滞前x线片显示后凸角度和椎体压缩率增加,差异有统计学意义(PPP>0.05),未发现影响末次治疗后6个月最终满意度和疼痛缓解的独立因素。结论:经皮椎体增强术治疗骨质疏松性椎体骨折后持续性轴性腰痛患者后内侧支阻滞(联合冷冻消融)可有效改善中短期症状和功能。
{"title":"[Posterior medial branch block for persistent pain after percutaneous vertebral augmentation in osteoporotic vertebral fractures].","authors":"Zhe-Ren Wang, Ren Yu, Chun-de Lu, Zhi-Yuan Xu, Bin Wu, Cheng Ni","doi":"10.12200/j.issn.1003-0034.20250335","DOIUrl":"https://doi.org/10.12200/j.issn.1003-0034.20250335","url":null,"abstract":"<p><strong>Objective: </strong>To evaluate the short-and medium-term efficacy of posterior medial branch block in the treatment of persistent pain after percutaneous vertebral augmentation.</p><p><strong>Methods: </strong>From January 2018 to January 2023, a total of 1, 062 patients with osteoporotic vertebral compression fractures underwent percutaneous vertebral augmentation. Among them, 32 elderly patients who experienced persistent low back pain after surgery and subsequently received posterior medial branch block and cryoablation were included. Six patients died during follow-up, leaving 26 patients for final analysis (1 male, 25 females). The mean age was (82.96±5.66) years (ranged, 76 to 94 years). The mean body mass index was (23.76±3.08) kg·m<sup>-2</sup>(ranged 18.1 to 27.2 kg·m<sup>-2</sup>). The bone mineral density T-value ranged from -2.5 to -4.3 with a mean of (-3.09±0.56). The mean volume of bone cement injected was 6.00 (5.38, 7.00) ml. Fracture locations were T<sub>11</sub> (2 cases), T<sub>12</sub> (7 cases), L<sub>1</sub> (10 cases), L<sub>2</sub> (6 cases), and L<sub>3</sub> (1 case). The mean interval from vertebral augmentation to block treatment was (7.12±2.22) months (rangd 6 to 12 months). The vertebral augmentation procedures were percutaneous kyphoplasty(PKP) in 12 cases and percutaneous vertebroplasty (PVP) in 14 cases. At the 2nd week, 3rd month, and 6th month after the block, the numerical rating scale(NRS), Oswestry disability index(ODI), patient satisfaction, and pain relief rate at the 6th month were evaluated. Relationships between pain relief rate at the 6th month after the last treatment and possible influencing factors were analyzed.</p><p><strong>Results: </strong>Compared with X-ray films after percutaneous vertebral augmentation, the X-ray films before block showed an increase in kyphotic angle and vertebral compression rate, with statistically significant differences(<i>P</i><0.05). At the 2nd week, 3rd month, and 6th month after posterior medial branch block and cryoablation, NRS and ODI scores were significantly lower than before the block(<i>P</i><0.05). Among the 26 patients, 5 received additional cryoablation. At the 6th month after the last treatment, 19 patients reported excellent or good satisfaction. Univariate binary Logistic analysis showed all <i>P</i>>0.05, and no independent factor affecting final satisfaction or pain relief at 6 months after the last treatment was identified.</p><p><strong>Conclusion: </strong>Posterior medial branch block(with cryoablation) can effectively improve short-and medium-term symptoms and function in patients with persistent axial low back pain after percutaneous vertebral augmentation for osteoporotic vertebral fractures.</p>","PeriodicalId":23964,"journal":{"name":"Zhongguo gu shang = China journal of orthopaedics and traumatology","volume":"38 11","pages":"1145-50"},"PeriodicalIF":0.0,"publicationDate":"2025-11-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145669982","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
[Ipsilateral femoral neck fracture after InterTan internal fixation for intertrochanteric femoral fracture:a case report]. 【InterTan内固定治疗股骨粗隆间骨折致同侧股骨颈骨折1例】。
Q4 Medicine Pub Date : 2025-11-25 DOI: 10.12200/j.issn.1003-0034.20250049
Rong-Xuan Liu, Qiang Li, Rong Chen, Yong-Ping Wang
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引用次数: 0
[One-hole split endoscope-assisted transforaminal lumbar interbody fusion for the treatment of lumbar degenerative diseases:an early efficacy observation]. [单孔分裂内窥镜辅助经椎间孔腰椎椎体间融合术治疗腰椎退行性疾病的早期疗效观察]。
Q4 Medicine Pub Date : 2025-11-25 DOI: 10.12200/j.issn.1003-0034.20250208
You Lyu, Gui-Guang Liu, Fu-Li Li
<p><strong>Objective: </strong>To investigate the early clinical efficacy, safety, and application value of one-hole split endoscopy (OSE)-assisted transforaminal lumbar interbody fusion(TLIF) in the treatment of lumbar degenerative diseases.</p><p><strong>Methods: </strong>A retrospective analysis was conducted on 17 patients with lumbar degenerative diseases who underwent OSE-assisted TLIF between June 2023 and June 2024. There were 10 males and 7 females, with a mean of (55.30±6.52) years old ranging 43 to 65 years. The disease duration ranged from 3 to 36 months with a mean of(12.4±13.3) months. The disease distribution was as follows:lumbar disc herniation (7 cases), lumbar spinal stenosis (5 cases), and lumbar spondylolisthesis (2 cases). Operative time, incision length, intraoperative blood loss, number of intraoperative fluoroscopic exposures, time to ambulation, postoperative hospital stay, and complications were recorded. The dural sac area at the affected segment, visual analogue scale (VAS) for low back pain and leg pain, and Oswestry disability index (ODI) were recorded preoperatively and postoperatively. The modified MacNab criteria were used to evaluate the surgical outcome at the final follow-up.</p><p><strong>Results: </strong>All 17 patients successfully underwent surgery and were followed up for 3 to 15 months with a mean of (8.4±3.3) months. The operative time was 120 to 200 minutes with a mean of (143.2±22.0) minutes, the incision length on the decompression side was 1.80 to 4.00 cm with a mean of (2.56±0.65) cm, intraoperative blood loss was 50 to 300 ml with a mean of (161.2±72.5) ml, the number of fluoroscopic exposures was 15 to 38 with a mean of (23.4±6.5), time to ambulation was 24 to 72 hours with a mean of (49.2±11.9) hours, and postoperative hospital stay was 3 to 9 days with a mean of (4.9±1.5) days. Two patients developed transient lower limb pain and numbness, which completely resolved with conservative treatment. The postoperative dural sac area was (121.47±14.90) mm<sup>2</sup>, which was significantly larger than the preoperative area (51.47±7.69) mm<sup>2</sup>(<i>P</i><0.001). The VAS for low back pain were (6.23±1.64), (2.94±1.43), and (1.94±0.75) at preoperation, 3 days postoperation, and final follow-up, respectively;the VAS for leg pain were (7.06±1.43), (2.35±1.17), and (2.06±0.90) at the same time points. The VAS at all postoperative time points were significantly lower than preoperative scores (<i>P</i><0.001). The ODI at final follow-up was (25.29±8.15)%, which was significantly better than the preoperative ODI of(82.35±5.16)%(<i>P</i><0.001). At the final follow-up, the MacNab surgical outcome was excellent in 11 cases, good in 4 cases, and fair in 2 cases.</p><p><strong>Conclusion: </strong>OSE-assisted TLIF is an effective, safe, and minimally invasive technique with a gentle learning curve for the treatment of lumbar degenerative diseases, capable of effectively relieving symptoms and improving fu
目的:探讨一孔分裂内镜(OSE)辅助经椎间孔腰椎椎体间融合术(TLIF)治疗腰椎退行性疾病的早期临床疗效、安全性及应用价值。方法:回顾性分析2023年6月至2024年6月期间17例腰椎退行性疾病患者行ose辅助TLIF。男性10例,女性7例,平均(55.30±6.52)岁,年龄43 ~ 65岁。病程3 ~ 36个月,平均(12.4±13.3)个月。疾病分布如下:腰椎间盘突出7例,腰椎管狭窄5例,腰椎滑脱2例。记录手术时间、切口长度、术中出血量、术中透视次数、下床时间、术后住院时间和并发症。术前、术后分别记录患段硬膜囊面积、腰痛、腿痛视觉模拟评分(VAS)和Oswestry失能指数(ODI)。在最后随访时,采用改良的MacNab标准评估手术结果。结果:17例患者均顺利完成手术,随访3 ~ 15个月,平均(8.4±3.3)个月。手术时间是120到200分钟的意思(143.2±22.0)分钟,减压侧切口的长度是1.80到4.00厘米的意思(2.56±0.65)厘米,术中失血是50到300毫升(161.2±72.5)的意思是ml,荧光镜的曝光的数量是15到38平均(23.4±6.5),步行时间是24到72小时平均值为(49.2±11.9)小时,和术后住院时间与平均3至9天(4.9±1.5)天。2例患者出现一过性下肢疼痛和麻木,经保守治疗后完全缓解。术后硬膜囊面积为(121.47±14.90)mm2,明显大于术前面积(51.47±7.69)mm2(ppp)。结论:osse辅助下的TLIF治疗腰椎退行性疾病是一种有效、安全、微创的技术,学习曲线平缓,能有效缓解症状,改善功能。
{"title":"[One-hole split endoscope-assisted transforaminal lumbar interbody fusion for the treatment of lumbar degenerative diseases:an early efficacy observation].","authors":"You Lyu, Gui-Guang Liu, Fu-Li Li","doi":"10.12200/j.issn.1003-0034.20250208","DOIUrl":"https://doi.org/10.12200/j.issn.1003-0034.20250208","url":null,"abstract":"&lt;p&gt;&lt;strong&gt;Objective: &lt;/strong&gt;To investigate the early clinical efficacy, safety, and application value of one-hole split endoscopy (OSE)-assisted transforaminal lumbar interbody fusion(TLIF) in the treatment of lumbar degenerative diseases.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Methods: &lt;/strong&gt;A retrospective analysis was conducted on 17 patients with lumbar degenerative diseases who underwent OSE-assisted TLIF between June 2023 and June 2024. There were 10 males and 7 females, with a mean of (55.30±6.52) years old ranging 43 to 65 years. The disease duration ranged from 3 to 36 months with a mean of(12.4±13.3) months. The disease distribution was as follows:lumbar disc herniation (7 cases), lumbar spinal stenosis (5 cases), and lumbar spondylolisthesis (2 cases). Operative time, incision length, intraoperative blood loss, number of intraoperative fluoroscopic exposures, time to ambulation, postoperative hospital stay, and complications were recorded. The dural sac area at the affected segment, visual analogue scale (VAS) for low back pain and leg pain, and Oswestry disability index (ODI) were recorded preoperatively and postoperatively. The modified MacNab criteria were used to evaluate the surgical outcome at the final follow-up.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Results: &lt;/strong&gt;All 17 patients successfully underwent surgery and were followed up for 3 to 15 months with a mean of (8.4±3.3) months. The operative time was 120 to 200 minutes with a mean of (143.2±22.0) minutes, the incision length on the decompression side was 1.80 to 4.00 cm with a mean of (2.56±0.65) cm, intraoperative blood loss was 50 to 300 ml with a mean of (161.2±72.5) ml, the number of fluoroscopic exposures was 15 to 38 with a mean of (23.4±6.5), time to ambulation was 24 to 72 hours with a mean of (49.2±11.9) hours, and postoperative hospital stay was 3 to 9 days with a mean of (4.9±1.5) days. Two patients developed transient lower limb pain and numbness, which completely resolved with conservative treatment. The postoperative dural sac area was (121.47±14.90) mm&lt;sup&gt;2&lt;/sup&gt;, which was significantly larger than the preoperative area (51.47±7.69) mm&lt;sup&gt;2&lt;/sup&gt;(&lt;i&gt;P&lt;/i&gt;&lt;0.001). The VAS for low back pain were (6.23±1.64), (2.94±1.43), and (1.94±0.75) at preoperation, 3 days postoperation, and final follow-up, respectively;the VAS for leg pain were (7.06±1.43), (2.35±1.17), and (2.06±0.90) at the same time points. The VAS at all postoperative time points were significantly lower than preoperative scores (&lt;i&gt;P&lt;/i&gt;&lt;0.001). The ODI at final follow-up was (25.29±8.15)%, which was significantly better than the preoperative ODI of(82.35±5.16)%(&lt;i&gt;P&lt;/i&gt;&lt;0.001). At the final follow-up, the MacNab surgical outcome was excellent in 11 cases, good in 4 cases, and fair in 2 cases.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Conclusion: &lt;/strong&gt;OSE-assisted TLIF is an effective, safe, and minimally invasive technique with a gentle learning curve for the treatment of lumbar degenerative diseases, capable of effectively relieving symptoms and improving fu","PeriodicalId":23964,"journal":{"name":"Zhongguo gu shang = China journal of orthopaedics and traumatology","volume":"38 11","pages":"1106-11"},"PeriodicalIF":0.0,"publicationDate":"2025-11-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145669901","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
[Short-to-medium-term clinical efficacy of total hip arthroplasty with Pinnacle ES constrained liner in the treatment of femoral neck fractures associated with lower limb neuromuscular disorders]. 【Pinnacle ES约束衬套全髋关节置换术治疗股骨颈骨折合并下肢神经肌肉疾病的中短期临床疗效观察】。
Q4 Medicine Pub Date : 2025-11-25 DOI: 10.12200/j.issn.1003-0034.20250712
Can-Feng Wang, Xiao-Qing Wang, Lei Han, Yun-Gen Hu, Tuo Wang

Objective: To investigate the short-to-medium-term clinical efficacy of total hip arthroplasty(THA) with Pinnacle ES constrained liner in the treatment of femoral neck fractures(FNF) associated with lower limb neuromuscular disorders.

Methods: A retrospective analysis was conducted on 16 patients who underwent primary THA using Pinnacle ES constrained liner for FNF with lower limb neuromuscular disorders and had complete follow-up data, treated between January 2020 and January 2023. There were 7 males and 9 females, with a mean age of (68.42±3.58) years old ranging from 61 to 75 years old. Among them, 10 cases had left-sided fractures and 6 had right-sided fractures;based on the Garden classification, 11 cases were type Ⅲ and 5 cases were type Ⅳ. The affected limbs were complicated with sequelae of poliomyelitis (2 cases), Parkinson's disease (2 cases), and sequelae of cerebral infarction (12 cases). All operations were performed via a posterolateral approach. Prosthesis position was evaluated using imaging data. Hip function was assessed by the Harris hip score(HHS) and Merle D'Aubigne hip score. During the follow-up period, the occurrence of complications such as prosthetic dislocation, loosening, and infection was recorded.

Results: One patient died of advanced tumor 2 years after surgery, and the remaining 15 patients were followed up for 24 to 64 months with a mean of (34.8±5.5) months. The operation time ranged from 50 to 90 minutes with a mean of (75.56±8.15) minutes, and the blood loss ranged from 150 to 200 ml with a mean of (170.32±12.56) ml. All patients achieved primary wound healing after surgery. Intraoperatively, femoral calcar splitting occurred in 2 cases, which were treated with titanium cable binding;no neurovascular injuries were observed in any case. The mean HHS increased from (18.95±2.25) preoperatively to (88.02±2.42) at the last follow-up, and the mean Merle D'Aubigne Score increased from (3.05±0.06) preoperatively to (16.65±0.93) at the last follow-up. Postoperative follow-up X-rays showed good prosthetic position, and no complications such as dislocation, prosthetic loosening, periprosthetic fracture, or deep infection occurred during the follow-up period.

Conclusion: Total hip arthroplasty with Pinnacle ES constrained liner is effective in the treatment of femoral neck fractures associated with lower limb neuromuscular disorders. It can significantly improve hip function, reduce the postoperative prosthetic dislocation rate, provide good initial stability, and achieve satisfactory short-to-medium-term clinical efficacy.

目的:探讨全髋关节置换术联合Pinnacle ES约束衬线治疗股骨颈骨折合并下肢神经肌肉疾病的中短期临床疗效。方法:回顾性分析2020年1月至2023年1月期间,使用Pinnacle ES约束线性治疗伴有下肢神经肌肉疾病的FNF的16例患者,并有完整的随访数据。男性7例,女性9例,平均年龄(68.42±3.58)岁,年龄61 ~ 75岁。其中左侧骨折10例,右侧骨折6例;根据Garden分类,Ⅲ型11例,Ⅳ型5例。患肢合并脊髓灰质炎后遗症2例,帕金森病后遗症2例,脑梗死后遗症12例。所有手术均经后外侧入路进行。利用影像学资料评估假体位置。采用Harris髋关节评分(HHS)和Merle D'Aubigne髋关节评分评估髋关节功能。随访期间记录假体脱位、松动、感染等并发症的发生情况。结果:1例患者术后2年因肿瘤晚期死亡,其余15例患者随访24 ~ 64个月,平均(34.8±5.5)个月。手术时间50 ~ 90分钟,平均(75.56±8.15)分钟,出血量150 ~ 200 ml,平均(170.32±12.56)ml。所有患者术后创面基本愈合。术中发生股骨跟骨劈裂2例,采用钛缆绑扎处理;未见神经血管损伤。平均HHS由术前的(18.95±2.25)分上升至末次随访时的(88.02±2.42)分;平均Merle D’aubigne评分由术前的(3.05±0.06)分上升至末次随访时的(16.65±0.93)分。术后随访x线片显示假体位置良好,随访期间无脱位、假体松动、假体周围骨折、深部感染等并发症发生。结论:Pinnacle ES约束衬垫全髋关节置换术是治疗股骨颈骨折合并下肢神经肌肉疾病的有效方法。可显著改善髋关节功能,降低术后假体脱位率,提供良好的初期稳定性,取得满意的中短期临床疗效。
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引用次数: 0
[Intraspinal canal chondromyxoid fibroma of the spine:a case report]. 脊柱椎管内软骨粘液样纤维瘤1例。
Q4 Medicine Pub Date : 2025-11-25 DOI: 10.12200/j.issn.1003-0034.20240900
Tong Yu, You Zhou, Zhi-Hai Zhang, Yu-Bin Li
{"title":"[Intraspinal canal chondromyxoid fibroma of the spine:a case report].","authors":"Tong Yu, You Zhou, Zhi-Hai Zhang, Yu-Bin Li","doi":"10.12200/j.issn.1003-0034.20240900","DOIUrl":"https://doi.org/10.12200/j.issn.1003-0034.20240900","url":null,"abstract":"","PeriodicalId":23964,"journal":{"name":"Zhongguo gu shang = China journal of orthopaedics and traumatology","volume":"38 11","pages":"1170-3"},"PeriodicalIF":0.0,"publicationDate":"2025-11-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145669880","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
[Study on the efficacy of automatic-controlled pressure cupping for lumbar disc herniation]. [自动控制压力罐治疗腰椎间盘突出症疗效研究]。
Q4 Medicine Pub Date : 2025-11-25 DOI: 10.12200/j.issn.1003-0034.20250599
Bo-Chen Peng, Min-Shan Feng, Li Li, Gui-Ju Ren, Yi-Zhen Yuan, Li-Jie Chang, Shu-Ying Ren, Liu Zeng, Guang-Wei Liu, Li-Guo Zhu, Na Yuan
<p><strong>Objective: </strong>To observe the clinical efficacy and safety of automatic pressure-controlled pressure cupping in patients with lumbar disc herniation, and compare it with traditional cupping.</p><p><strong>Methods: </strong>A total of 100 patients diagnosed with lumbar disc herniation from January 2022 to August 2024 were selected and divided into two groups:the automatic pressure-controlled pressure cupping group (controlled pressure cupping group) and the traditional cupping group (control group), 50 cases in each group. In the controlled pressure cupping group, there were 18 males and 32 females, with an age of (51.98±12.69) years;in the control group, there were 16 males and 34 females, with an age of (51.32±12.05) years. The visual analogue scale(VAS), comfort score, and lumbar range of motion were observed before treatment and after the 1st, 3rd, and 7th treatments to evaluate the efficacy and safety.</p><p><strong>Results: </strong>All patients completed the treatment intervention, with complete follow-up data collected. No adverse reactions or complications occurred during treatment and follow-up. After the 3rd treatment, the VAS score of the controlled pressure cupping group was (2.38±0.49), which was lower than that of the control group (2.94±0.68), with a statistically significant difference (<i>P</i><0.001). In the controlled pressure cupping group, the VAS scores after the 1st, 3rd, and 7th treatments were significantly better than those before treatment (<i>P</i>=0.026);in the control group, the VAS scores after the 3rd and 7th treatments were better than those before treatment, but the difference was not statistically significant(<i>P</i>=0.182). Repeated-measures analysis of variance (ANOVA) on VAS scores at different time points in both groups showed that there were statistically significant differences in inter-group, time, and interaction effects (<i>P</i><0.05). After the 1st treatment, in the controlled pressure cupping group, 0 patients felt comfortable, 42 patients (84%) felt mild discomfort, and 8 patients (16%) felt moderate discomfort;in the control group, 0 patients felt comfortable, 28 patients (56%) felt mild discomfort, and 22 patients(44%) felt moderate discomfort;the difference between the two groups was statistically significant(<i>P</i>=0.005). After the 3rd treatment, in the controlled pressure cupping group, 30 patients(60%) felt comfortable, 20 patients (40%) felt mild discomfort, and 0 patients felt moderate discomfort; in the control group, 9 patients (18%) felt comfortable, 41 patients (82%) felt mild discomfort, and 0 patients felt moderate discomfort;the difference between the two groups was statistically significant(<i>P</i><0.001). There was no statistically significant difference in comfort between the two groups after the 7th treatment(<i>P</i>>0.001). There was no statistically significant difference in lumbar range of motion between the two groups before and after treatment(<i>P</i>>0
目的:观察自动控压拔罐治疗腰椎间盘突出症的临床疗效和安全性,并与传统拔罐进行比较。方法:选择2022年1月至2024年8月诊断为腰椎间盘突出症的患者100例,分为自动控压拔罐组(对照压力拔罐组)和传统拔罐组(对照组),每组50例。对照组压力拔罐患者男性18例,女性32例,年龄(51.98±12.69)岁;对照组男性16例,女性34例,年龄(51.32±12.05)岁。观察治疗前及第1、3、7次治疗后视觉模拟评分(VAS)、舒适度评分、腰椎活动度,评价治疗前后疗效和安全性。结果:所有患者均完成治疗干预,随访资料完整。治疗及随访期间无不良反应及并发症发生。第3次治疗后,对照组压力拔罐VAS评分为(2.38±0.49)分,低于对照组(2.94±0.68)分,差异有统计学意义(PP=0.026);对照组患者第3、7次治疗后VAS评分均优于治疗前,但差异无统计学意义(P=0.182)。两组患者不同时间点VAS评分的重复测量方差分析(ANOVA)显示,组间、时间、交互效应差异均有统计学意义(PP=0.005)。第3次治疗后,对照组压力拔罐30例(60%)感觉舒适,20例(40%)感觉轻度不适,0例(0)感觉中度不适;对照组9例(18%)患者感觉舒适,41例(82%)患者感觉轻度不适,0例患者感觉中度不适;两组间差异有统计学意义(p < 0.001)。治疗前后两组腰椎活动度比较,差异无统计学意义(P < 0.05);与治疗前比较,两组治疗后腰椎活动度均有明显改善,差异有统计学意义(p)结论:自动控压拔罐可有效缓解腰椎间盘突出症患者的症状,安全性极好。
{"title":"[Study on the efficacy of automatic-controlled pressure cupping for lumbar disc herniation].","authors":"Bo-Chen Peng, Min-Shan Feng, Li Li, Gui-Ju Ren, Yi-Zhen Yuan, Li-Jie Chang, Shu-Ying Ren, Liu Zeng, Guang-Wei Liu, Li-Guo Zhu, Na Yuan","doi":"10.12200/j.issn.1003-0034.20250599","DOIUrl":"https://doi.org/10.12200/j.issn.1003-0034.20250599","url":null,"abstract":"&lt;p&gt;&lt;strong&gt;Objective: &lt;/strong&gt;To observe the clinical efficacy and safety of automatic pressure-controlled pressure cupping in patients with lumbar disc herniation, and compare it with traditional cupping.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Methods: &lt;/strong&gt;A total of 100 patients diagnosed with lumbar disc herniation from January 2022 to August 2024 were selected and divided into two groups:the automatic pressure-controlled pressure cupping group (controlled pressure cupping group) and the traditional cupping group (control group), 50 cases in each group. In the controlled pressure cupping group, there were 18 males and 32 females, with an age of (51.98±12.69) years;in the control group, there were 16 males and 34 females, with an age of (51.32±12.05) years. The visual analogue scale(VAS), comfort score, and lumbar range of motion were observed before treatment and after the 1st, 3rd, and 7th treatments to evaluate the efficacy and safety.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Results: &lt;/strong&gt;All patients completed the treatment intervention, with complete follow-up data collected. No adverse reactions or complications occurred during treatment and follow-up. After the 3rd treatment, the VAS score of the controlled pressure cupping group was (2.38±0.49), which was lower than that of the control group (2.94±0.68), with a statistically significant difference (&lt;i&gt;P&lt;/i&gt;&lt;0.001). In the controlled pressure cupping group, the VAS scores after the 1st, 3rd, and 7th treatments were significantly better than those before treatment (&lt;i&gt;P&lt;/i&gt;=0.026);in the control group, the VAS scores after the 3rd and 7th treatments were better than those before treatment, but the difference was not statistically significant(&lt;i&gt;P&lt;/i&gt;=0.182). Repeated-measures analysis of variance (ANOVA) on VAS scores at different time points in both groups showed that there were statistically significant differences in inter-group, time, and interaction effects (&lt;i&gt;P&lt;/i&gt;&lt;0.05). After the 1st treatment, in the controlled pressure cupping group, 0 patients felt comfortable, 42 patients (84%) felt mild discomfort, and 8 patients (16%) felt moderate discomfort;in the control group, 0 patients felt comfortable, 28 patients (56%) felt mild discomfort, and 22 patients(44%) felt moderate discomfort;the difference between the two groups was statistically significant(&lt;i&gt;P&lt;/i&gt;=0.005). After the 3rd treatment, in the controlled pressure cupping group, 30 patients(60%) felt comfortable, 20 patients (40%) felt mild discomfort, and 0 patients felt moderate discomfort; in the control group, 9 patients (18%) felt comfortable, 41 patients (82%) felt mild discomfort, and 0 patients felt moderate discomfort;the difference between the two groups was statistically significant(&lt;i&gt;P&lt;/i&gt;&lt;0.001). There was no statistically significant difference in comfort between the two groups after the 7th treatment(&lt;i&gt;P&lt;/i&gt;&gt;0.001). There was no statistically significant difference in lumbar range of motion between the two groups before and after treatment(&lt;i&gt;P&lt;/i&gt;&gt;0","PeriodicalId":23964,"journal":{"name":"Zhongguo gu shang = China journal of orthopaedics and traumatology","volume":"38 11","pages":"1133-8"},"PeriodicalIF":0.0,"publicationDate":"2025-11-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145669943","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
[Multicenter randomized controlled trial of Yiqi Huoxue formula() for the treatment of ruptured lumbar disc herniation]. 【益气活血方()治疗腰椎间盘突出症破裂的多中心随机对照试验】。
Q4 Medicine Pub Date : 2025-11-25 DOI: 10.12200/j.issn.1003-0034.20240543
Yu Zhu, Zhi-Qiang Wang, Shun Lin, Ying-Ying Yao, Xue-Qiang Shen, Xiao-Chun Li, Feng Yu, Xiao-Yang Xiong, Yi Song, Meng-Fei Chen, Peng-Fei Yu, Hong Jiang, Jin-Tao Liu
<p><strong>Objective: </strong>To observe the clinical symptoms and MRI outcomes of patients with ruptured lumbar disc herniation(LDH) through a multicenter randomized controlled study, and to evaluate the clinical efficacy and safety of <i>Yiqi Huoxue</i> formula() in the treatment of this disease.</p><p><strong>Methods: </strong>A total of 160 outpatients and inpatients with ruptured LDH admitted to 4 medical centers from January 2023 to June 2023 were selected and randomly divided into the <i>Yiqi Huoxue</i> formula group and the control group, with 80 patients in each group. In the <i>Yiqi Huoxue</i> formula group, there were 43 males and 37 females, with an age of (41.03±9.56) years and a disease duration of (10.45±25.37) days, and the patients were treated with <i>Yiqi Huoxue</i> formula. In the control group, there were 34 males and 46 females, with an age of (42.14±8.73) years and a disease duration of (11.31±21.14) days;during the acute phase, patients in this group could take celecoxib capsules orally, and methylcobalamin orally at the same time. The Japanese Orthopaedic Association (JOA) score, Oswestry disability index (ODI), changes in the volume of herniated disc tissue on MRI, herniation rate, and absorption rate were recorded at the time of enrollment and during follow-ups at the 3rd, 6th, and 12th month after treatment.</p><p><strong>Results: </strong>A total of 156 patients completed the clinical follow-up, and 4 patients withdrew midway. The clinical symptoms of all patients who completed the study were relieved to varying degrees, and reabsorption of herniated disc tissue was observed in all patients in the <i>Yiqi Huoxue</i> formula group after treatment. For the JOA score:in the <i>Yiqi Huoxue</i> formula group, it was (10.73±2.76) points before treatment and (24.65±2.19) points at the 12th month after treatment;in the control group, it was (11.01±1.20) points before treatment and (17.07±3.26) points at the 12th month after treatment. For the ODI score:in the <i>Yiqi Huoxue</i> formula group, it was (26.21±3.55) points before treatment and (5.65±2.19) points at the 12th month after treatment;in the control group, it was (27.92±2.51) points before treatment and (9.09±2.15) points at the 12th month after treatment. At the 12th month after treatment, the JOA and ODI scores of both groups were better than those before treatment, and the scores of the <i>Yiqi Huoxue</i> formula group were better than those of the control group, with statistically significant differences (<i>P</i><0.05). In terms of the herniated disc volume and herniation rate on MRI, the <i>Yiqi Huoxue</i> formula group was superior to the control group, with statistically significant differences(<i>P</i><0.05). Reabsorption occurred in 56.96%(45/79) of patients in the <i>Yiqi Huoxue</i> formula group, which was significantly higher than the 37.66%(29/77) in the control group.</p><p><strong>Conclusion: </strong>After treatment with <i>Yiqi Huoxue</i> formula, pa
目的:通过多中心随机对照研究,观察腰椎间盘突出症(LDH)患者的临床症状及MRI结果,评价益气活血方()治疗该疾病的临床疗效及安全性。方法:选择2023年1月至2023年6月在4个医疗中心收治的160例门诊和住院的LDH破裂患者,随机分为益气活血方组和对照组,每组80例。益气活血方组男性43例,女性37例,年龄(41.03±9.56)岁,病程(10.45±25.37)天,均予益气活血方治疗。对照组男性34例,女性46例,年龄(42.14±8.73)岁,病程(11.31±21.14)d;本组患者急性期可口服塞来昔布胶囊,同时口服甲钴胺素。记录入组时及治疗后第3、6、12个月随访时的JOA评分、Oswestry失能指数(ODI)、椎间盘突出组织MRI体积变化、突出率、吸收率。结果:156例患者完成临床随访,4例中途退出。所有完成研究的患者临床症状均有不同程度缓解,益气活血方组治疗后均观察到椎间盘突出组织重吸收。JOA评分:益气活血方组治疗前为(10.73±2.76)分,治疗后12个月为(24.65±2.19)分;对照组治疗前为(11.01±1.20)分,治疗后12个月为(17.07±3.26)分。ODI评分:益气活血方组治疗前为(26.21±3.55)分,治疗后12个月为(5.65±2.19)分;对照组治疗前为(27.92±2.51)分,治疗后12个月为(9.09±2.15)分。治疗后12个月,两组患者JOA、ODI评分均优于治疗前,且益气活血方组评分优于对照组,差异有统计学意义(益气活血方组优于对照组),差异有统计学意义(益气活血方组优于对照组),差异有统计学意义(益气活血方组优于对照组,差异有统计学意义,显著高于对照组的37.66%(29/77)。结论:LDH破裂患者经益气活血方治疗后,临床症状明显改善,椎间盘突出体积明显减小。随访期间未见患者出现明显药物不良反应,末次随访未见症状复发,说明该配方疗效安全可靠。
{"title":"[Multicenter randomized controlled trial of <i>Yiqi Huoxue</i> formula() for the treatment of ruptured lumbar disc herniation].","authors":"Yu Zhu, Zhi-Qiang Wang, Shun Lin, Ying-Ying Yao, Xue-Qiang Shen, Xiao-Chun Li, Feng Yu, Xiao-Yang Xiong, Yi Song, Meng-Fei Chen, Peng-Fei Yu, Hong Jiang, Jin-Tao Liu","doi":"10.12200/j.issn.1003-0034.20240543","DOIUrl":"10.12200/j.issn.1003-0034.20240543","url":null,"abstract":"&lt;p&gt;&lt;strong&gt;Objective: &lt;/strong&gt;To observe the clinical symptoms and MRI outcomes of patients with ruptured lumbar disc herniation(LDH) through a multicenter randomized controlled study, and to evaluate the clinical efficacy and safety of &lt;i&gt;Yiqi Huoxue&lt;/i&gt; formula() in the treatment of this disease.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Methods: &lt;/strong&gt;A total of 160 outpatients and inpatients with ruptured LDH admitted to 4 medical centers from January 2023 to June 2023 were selected and randomly divided into the &lt;i&gt;Yiqi Huoxue&lt;/i&gt; formula group and the control group, with 80 patients in each group. In the &lt;i&gt;Yiqi Huoxue&lt;/i&gt; formula group, there were 43 males and 37 females, with an age of (41.03±9.56) years and a disease duration of (10.45±25.37) days, and the patients were treated with &lt;i&gt;Yiqi Huoxue&lt;/i&gt; formula. In the control group, there were 34 males and 46 females, with an age of (42.14±8.73) years and a disease duration of (11.31±21.14) days;during the acute phase, patients in this group could take celecoxib capsules orally, and methylcobalamin orally at the same time. The Japanese Orthopaedic Association (JOA) score, Oswestry disability index (ODI), changes in the volume of herniated disc tissue on MRI, herniation rate, and absorption rate were recorded at the time of enrollment and during follow-ups at the 3rd, 6th, and 12th month after treatment.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Results: &lt;/strong&gt;A total of 156 patients completed the clinical follow-up, and 4 patients withdrew midway. The clinical symptoms of all patients who completed the study were relieved to varying degrees, and reabsorption of herniated disc tissue was observed in all patients in the &lt;i&gt;Yiqi Huoxue&lt;/i&gt; formula group after treatment. For the JOA score:in the &lt;i&gt;Yiqi Huoxue&lt;/i&gt; formula group, it was (10.73±2.76) points before treatment and (24.65±2.19) points at the 12th month after treatment;in the control group, it was (11.01±1.20) points before treatment and (17.07±3.26) points at the 12th month after treatment. For the ODI score:in the &lt;i&gt;Yiqi Huoxue&lt;/i&gt; formula group, it was (26.21±3.55) points before treatment and (5.65±2.19) points at the 12th month after treatment;in the control group, it was (27.92±2.51) points before treatment and (9.09±2.15) points at the 12th month after treatment. At the 12th month after treatment, the JOA and ODI scores of both groups were better than those before treatment, and the scores of the &lt;i&gt;Yiqi Huoxue&lt;/i&gt; formula group were better than those of the control group, with statistically significant differences (&lt;i&gt;P&lt;/i&gt;&lt;0.05). In terms of the herniated disc volume and herniation rate on MRI, the &lt;i&gt;Yiqi Huoxue&lt;/i&gt; formula group was superior to the control group, with statistically significant differences(&lt;i&gt;P&lt;/i&gt;&lt;0.05). Reabsorption occurred in 56.96%(45/79) of patients in the &lt;i&gt;Yiqi Huoxue&lt;/i&gt; formula group, which was significantly higher than the 37.66%(29/77) in the control group.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Conclusion: &lt;/strong&gt;After treatment with &lt;i&gt;Yiqi Huoxue&lt;/i&gt; formula, pa","PeriodicalId":23964,"journal":{"name":"Zhongguo gu shang = China journal of orthopaedics and traumatology","volume":"38 11","pages":"1112-8"},"PeriodicalIF":0.0,"publicationDate":"2025-11-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145669893","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
[Imaging analysis of the posterior occipital muscles in cervical vertigo based on shear wave elastography]. 基于横波弹性成像的颈性眩晕枕后肌成像分析。
Q4 Medicine Pub Date : 2025-11-25 DOI: 10.12200/j.issn.1003-0034.20240987
Ying-Sen Pan, Yi Shen, Fei-Peng Qin, Hao-Yang Zhang, Nao Liu, Yan-Jun Xu, Xiao-Ming Ying

Objective: To evaluate the partial biomechanical properties of the posterior occipital muscles (rectus capitis posterior major, rectus capitis posterior minor, and obliquus capitis inferior) in patients with cervical vertigo.

Methods: A total of 30 patients with cervical vertigo admitted from April 2024 to September 2024 were included in the vertigo group, and 30 age-and gender-matched healthy subjects were recruited as the normal group. In the vertigo group, there were 21 females and 9 males, with an average age of (24.00±2.25) years;in the normal group, there were 22 females and 8 males, with an average age of (23.00±3.00) years. Shear wave elastography was used to measure the thickness and stiffness of the posterior occipital muscles in both groups.

Results: In the vertigo group, there were no statistically significant differences in the Young's modulus values (E) of stiffness of the posterior occipital muscles (rectus capitis posterior major, rectus capitis posterior minor, obliquus capitis inferior) between the left and right sides(P>0.05). The Young's modulus values(E) of stiffness of the right posterior occipital muscles (rectus capitis posterior major, rectus capitis posterior minor, obliquus capitis inferior) in the cervical vertigo group were (39.66±8.21) kPa, (45.61±5.85) kPa, and (43.73±5.22) kPa, respectively, which were significantly higher than those in the normal group 33.97(17.76) kPa, 41.38(8.99) kPa, 38.27(12.58) kPa, with statistically significant differences (P<0.05). In the vertigo group, the Young's modulus values(E) of stiffness of the left rectus capitis posterior major and left obliquus capitis inferior were (40.41±9.13) kPa and (42.11±6.20) kPa, respectively, which were significantly greater than those in the normal group (33.30±11.31) kPa, 38.94(14.62) kPa, with statistically significant differences(P<0.05);however, there was no statistically significant difference in the left rectus capitis posterior minor between the two groups(P>0.05). In the vertigo group, there were no statistically significant differences in the stiffness of the posterior occipital muscles (rectus capitis posterior major, rectus capitis posterior minor, obliquus capitis inferior) between the left and right sides(P>0.05). Additionally, there were no statistically significant differences in the thickness of the bilateral posterior occipital muscles between the vertigo group and the normal group (P>0.05).

Conclusion: The posterior occipital muscles of patients with cervical vertigo are stiffer than those of healthy individuals, while there is no significant difference in muscle thickness between the two groups.

目的:评价颈性眩晕患者枕后肌(头后大直肌、头后小直肌和头下斜肌)的部分生物力学特性。方法:选取2024年4月~ 2024年9月收治的颈性眩晕患者30例作为眩晕组,选取年龄、性别匹配的健康受试者30例作为正常组。眩晕组女性21例,男性9例,平均年龄(24.00±2.25)岁;正常组女性22例,男性8例,平均年龄(23.00±3.00)岁。采用横波弹性成像测量两组患者枕后肌的厚度和刚度。结果:眩晕组患者左右侧枕后肌(后大直肌、后小直肌、下斜肌)刚度的杨氏模值(E)比较,差异均无统计学意义(P < 0.05)。颈性眩晕组右侧枕后肌(后大头直肌、后小头直肌、下头斜肌)刚度的杨氏模量值(E)分别为(39.66±8.21)kPa、(45.61±5.85)kPa、(43.73±5.22)kPa,显著高于正常组33.97(17.76)kPa、41.38(8.99)kPa、38.27(12.58)kPa,差异有统计学意义(PPP>0.05)。眩晕组左右侧枕后肌(后大头直肌、后小头直肌、下头斜肌)僵硬度差异无统计学意义(P < 0.05)。眩晕组与正常组双侧枕后肌厚度比较,差异无统计学意义(P < 0.05)。结论:颈性眩晕患者枕后肌较正常人僵硬,但两组间枕后肌厚度差异无统计学意义。
{"title":"[Imaging analysis of the posterior occipital muscles in cervical vertigo based on shear wave elastography].","authors":"Ying-Sen Pan, Yi Shen, Fei-Peng Qin, Hao-Yang Zhang, Nao Liu, Yan-Jun Xu, Xiao-Ming Ying","doi":"10.12200/j.issn.1003-0034.20240987","DOIUrl":"https://doi.org/10.12200/j.issn.1003-0034.20240987","url":null,"abstract":"<p><strong>Objective: </strong>To evaluate the partial biomechanical properties of the posterior occipital muscles (rectus capitis posterior major, rectus capitis posterior minor, and obliquus capitis inferior) in patients with cervical vertigo.</p><p><strong>Methods: </strong>A total of 30 patients with cervical vertigo admitted from April 2024 to September 2024 were included in the vertigo group, and 30 age-and gender-matched healthy subjects were recruited as the normal group. In the vertigo group, there were 21 females and 9 males, with an average age of (24.00±2.25) years;in the normal group, there were 22 females and 8 males, with an average age of (23.00±3.00) years. Shear wave elastography was used to measure the thickness and stiffness of the posterior occipital muscles in both groups.</p><p><strong>Results: </strong>In the vertigo group, there were no statistically significant differences in the Young's modulus values (E) of stiffness of the posterior occipital muscles (rectus capitis posterior major, rectus capitis posterior minor, obliquus capitis inferior) between the left and right sides(<i>P</i>>0.05). The Young's modulus values(E) of stiffness of the right posterior occipital muscles (rectus capitis posterior major, rectus capitis posterior minor, obliquus capitis inferior) in the cervical vertigo group were (39.66±8.21) kPa, (45.61±5.85) kPa, and (43.73±5.22) kPa, respectively, which were significantly higher than those in the normal group 33.97(17.76) kPa, 41.38(8.99) kPa, 38.27(12.58) kPa, with statistically significant differences (<i>P</i><0.05). In the vertigo group, the Young's modulus values(E) of stiffness of the left rectus capitis posterior major and left obliquus capitis inferior were (40.41±9.13) kPa and (42.11±6.20) kPa, respectively, which were significantly greater than those in the normal group (33.30±11.31) kPa, 38.94(14.62) kPa, with statistically significant differences(<i>P</i><0.05);however, there was no statistically significant difference in the left rectus capitis posterior minor between the two groups(<i>P</i>>0.05). In the vertigo group, there were no statistically significant differences in the stiffness of the posterior occipital muscles (rectus capitis posterior major, rectus capitis posterior minor, obliquus capitis inferior) between the left and right sides(<i>P</i>>0.05). Additionally, there were no statistically significant differences in the thickness of the bilateral posterior occipital muscles between the vertigo group and the normal group (<i>P</i>>0.05).</p><p><strong>Conclusion: </strong>The posterior occipital muscles of patients with cervical vertigo are stiffer than those of healthy individuals, while there is no significant difference in muscle thickness between the two groups.</p>","PeriodicalId":23964,"journal":{"name":"Zhongguo gu shang = China journal of orthopaedics and traumatology","volume":"38 11","pages":"1126-32"},"PeriodicalIF":0.0,"publicationDate":"2025-11-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145669834","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}
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Zhongguo gu shang = China journal of orthopaedics and traumatology
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