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前路微创钳夹技术联合下肢轴向骨牵引装置在不可复位型转子间骨折中的应用

Application of anterior minimally invasive clamping technique combined with lower extremity axial bone traction device in irreducible intertrochanteric fractures.

作者信息

Zhu Yunliang, Lu Baoliang, Ouyang Changwu, Gu Sichao

机构信息

Department of Orthopedics, Gaoyou People's Hospital, The Third Clinical Medical College of Yangzhou University, Yangzhou, Jiangsu, China.

Department of Orthopedics, The First Affiliated Hospital of USTC, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, Anhui, China.

出版信息

Front Surg. 2025 Sep 3;12:1584651. doi: 10.3389/fsurg.2025.1584651. eCollection 2025.

DOI:10.3389/fsurg.2025.1584651
PMID:40969307
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12441023/
Abstract

OBJECTIVE

This study aims to evaluate the effectiveness of the anterior minimally invasive clamping technique in conjunction with a lower extremity axial bone traction device for treating irreducible intertrochanteric fractures.

METHODS

We conducted a retrospective analysis of data from 69 patients with irreducible intertrochanteric fractures who underwent limited open reduction and intramedullary nail fixation at our hospital between January 2022 and October 2023. All patients had subtrochanteric fractures of the femur. Patients received treatment using the anterior minimally invasive clamping technique combined with a lower extremity axial bone traction device for reduction (clamping + bone traction device group). The cohort included 27 males and 42 females with a mean age of (71.32 ± 5.11) years (range, 60-83 years). Sixty-nine patients with irreducible intertrochanteric fractures were matched for gender and age in a 1:1 ratio. The 1:1 matching process was performed using a propensity score matching method to ensure comparability between the two groups. Key matching variables included comorbidities (hypertension, diabetes mellitus, coronary heart disease, and cerebrovascular disease), with a maximum allowable difference of one comorbidity between matched pairs. Treatment schedules were strictly aligned, meaning patients in both groups received surgery within 72 h of admission, and preoperative management (including anti-coagulation and pain control) followed the same protocol. For fracture patterns, the AO/OTA classification was used as a critical matching criterion: each patient in the clamping + bone traction device group was matched with a patient in the clamping + traction bed group with the same AO/OTA subtype (31-A1, 31-A2, or 31-A3). The matching tolerance for fracture displacement (assessed by preoperative x-ray) was set at <2 mm to ensure similar fracture severity. A caliper width of 0.2 standard deviations of the propensity score was used to minimize selection bias, and the balance of baseline characteristics after matching was verified using standardized mean differences (all <0.1, indicating good balance). The control group (clamping + traction bed group) consisted of patients treated during the same period using limited open reduction and intramedullary nailing with an anterior minimally invasive clamping technique combined with a traction bed. This group included 30 males and 39 females with a mean age of (69.49 ± 6.59) years (range, 54-86 years). We compared the two groups regarding surgical indicators, postoperative recovery, and the quality of fracture reduction. The Harris functional score was used to assess hip joint function at baseline, as well as 6 and 12 months post-surgery. Record and compare the levels of mMPTA and mLDFA between two groups before surgery, 1 month after surgery, and 3 months after surgery. We also recorded the occurrence of postoperative complications in both groups.

RESULTS

In the clamping + bone traction device group, the operation time, intraoperative blood loss, and number of fluoroscopic images were (78.49 ± 15.29) minutes, (242.25 ± 15.65) ml, and (15.52 ± 3.12) times, respectively. These values were significantly lower than those in the clamping + traction bed group, which were (85.57 ± 12.18) minutes, (251.20 ± 19.45) ml, and (17.14 ± 2.95) times ( < 0.05). The length of hospital stay, time to assist in ambulation, and fracture healing time for the clamping + bone traction device group were 13.00 (12.00, 13.00) days, (15.84 ± 3.10) hours, and (15.38 ± 2.35) weeks, respectively, which were shorter compared to the clamping + traction bed group: 15.00 (13.00, 16.00) days, (19.75 ± 4.28) hours, and (16.77 ± 2.41) weeks, with significant differences ( < 0.05). The quality of fracture reduction was better in the clamping + bone traction device group than in the clamping + traction bed group, with significant differences ( < 0.05). The Harris functional scores for the clamping + bone traction device group were (53.29 ± 3.08), (60.84 ± 5.06), (72.33 ± 4.21), and (88.29 ± 6.78) at 1, 3, 6, and 12 months post-surgery, respectively. These scores were higher than those of the clamping + traction bed group, which were (50.86 ± 4.18), (56.23 ± 4.24), (68.52 ± 3.46), and (85.33 ± 5.56) ( < 0.05). The mMPTA, mLDFA levels for the clamping + bone traction device group were (87.63 ± 4.41)°, (90.82 ± 5.53)°, (88.92 ± 7.44)°, (91.62 ± 7.73)°at 1, 3 months post-surgery, respectively. These scores were higher than those of the clamping + traction bed group, which were (85.55 ± 5.57)°, (88.40 ± 4.12)°, (85.51 ± 8.05)°, (88.34 ± 7.25)° ( < 0.05). The incidence of postoperative complications in the clamping + bone traction device group was 4.35%, significantly lower than the 14.49% in the clamping + traction bed group ( < 0.05).

CONCLUSION

The anterior minimally invasive clamping technique combined with a lower limb axial bone distraction device in patients with irreducible intertrochanteric fractures can reduce operation time, minimize intraoperative blood loss and fluoroscopy usage, enhance fracture reduction quality, lower the occurrence of postoperative complications, and promote fracture healing and recovery of hip joint function.

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/90f7/12441023/c0b9e1a2f01d/fsurg-12-1584651-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/90f7/12441023/ee09abab49fc/fsurg-12-1584651-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/90f7/12441023/c0b9e1a2f01d/fsurg-12-1584651-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/90f7/12441023/ee09abab49fc/fsurg-12-1584651-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/90f7/12441023/c0b9e1a2f01d/fsurg-12-1584651-g002.jpg
摘要

目的

本研究旨在评估前路微创钳夹技术联合下肢轴向骨牵引装置治疗难复性股骨粗隆间骨折的有效性。

方法

我们对2022年1月至2023年10月在我院接受有限切开复位髓内钉固定的69例难复性股骨粗隆间骨折患者的数据进行了回顾性分析。所有患者均为股骨转子下骨折。患者采用前路微创钳夹技术联合下肢轴向骨牵引装置进行复位治疗(钳夹+骨牵引装置组)。该队列包括27例男性和42例女性,平均年龄为(71.32±5.11)岁(范围60-83岁)。69例难复性股骨粗隆间骨折患者按1:1的性别和年龄比例进行匹配。采用倾向评分匹配法进行1:1匹配过程,以确保两组之间具有可比性。关键匹配变量包括合并症(高血压、糖尿病、冠心病和脑血管疾病),匹配对之间合并症的最大允许差异为一种。治疗方案严格一致,即两组患者均在入院后72小时内接受手术,术前管理(包括抗凝和疼痛控制)遵循相同的方案。对于骨折类型,采用AO/OTA分类作为关键匹配标准:钳夹+骨牵引装置组的每例患者与钳夹+牵引床组中具有相同AO/OTA亚型(31-A1、31-A2或31-A3)的患者进行匹配。骨折移位(通过术前X线评估)的匹配容忍度设定为<2mm,以确保骨折严重程度相似。使用倾向评分的卡尺宽度为0.2个标准差,以尽量减少选择偏倚,并使用标准化均数差异验证匹配后基线特征的平衡(均<0.1,表明平衡良好)。对照组(钳夹+牵引床组)包括同期采用有限切开复位髓内钉结合前路微创钳夹技术和牵引床治疗的患者。该组包括30例男性和39例女性,平均年龄为(69.49±6.59)岁(范围54-86岁)。我们比较了两组的手术指标、术后恢复情况和骨折复位质量。采用Harris功能评分在基线以及术后6个月和12个月评估髋关节功能。记录并比较两组术前、术后1个月和术后3个月的mMPTA和mLDFA水平。我们还记录了两组术后并发症的发生情况。

结果

钳夹+骨牵引装置组的手术时间、术中出血量和透视图像数量分别为(78.49±15.29)分钟、(242.25±15.65)ml和(15.52±3.12)次。这些值显著低于钳夹+牵引床组,分别为(85.57±12.18)分钟、(251.20±19.4)ml和(17.14±2.95)次(P<0.)。钳夹+骨牵引装置组的住院时间、辅助行走时间和骨折愈合时间分别为13.00(12.00,13.00)天、(15.84±3.10)小时和(15.38±2.35)周,与钳夹+牵引床组相比更短:15.00(13.00,16.00)天、(19.75±4.28)小时和(16.77±2.41)周,差异有统计学意义(P<0.05)。钳夹+骨牵引装置组的骨折复位质量优于钳夹+牵引床组,差异有统计学意义(P<0.05)。钳夹+骨牵引装置组术后1、3、6和12个月的Harris功能评分分别为(53.29±3.08)、(60.84±5.06)、(72.33±4.21)和(88.29±6.78)。这些评分高于钳夹+牵引床组,分别为(50.86±4.18)、(56.23±4.24)、(68.52±3.46)和(85.33±5.56)(P<0.05)。钳夹+骨牵引装置组术后1、3个月的mMPTA、mLDFA水平分别为(87.63±4.41)°、(90.82±5.53)°、(88.92±7.44)°、(91.62±7.73)°。这些评分高于钳夹+牵引床组,分别为(85.55±5.57)°、(88.40±4.12)°、(85.51±8.05)°、(88.34±7.25)°(P<0.05)。钳夹+骨牵引装置组术后并发症发生率为4.35%,显著低于钳夹+牵引床组的14.49%(P<0.05)。

结论

前路微创钳夹技术联合下肢轴向骨牵引装置治疗难复性股骨粗隆间骨折,可减少手术时间,减少术中出血量和透视使用次数,提高骨折复位质量,降低术后并发症发生率,促进骨折愈合和髋关节功能恢复。

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