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Correct positioning of the calcar screw leads to superior results in proximal humerus fractures treated with carbon-fibre-reinforced polyetheretherketone plate osteosynthesis with polyaxial locking screws. 在使用碳纤维增强聚醚醚酮接骨板和多轴锁定螺钉治疗肱骨近端骨折时,跟骨螺钉的正确定位可带来优越的效果。
IF 2.8 2区 医学 Q1 Medicine Pub Date : 2023-10-10 DOI: 10.1186/s10195-023-00733-3
Michael Kimmeyer, Jonas Schmalzl, Verena Rentschler, Christian Schieffer, Arno Macken, Christian Gerhardt, Lars-Johannes Lehmann

Background: Plate osteosynthesis with implants made of carbon-fibre-reinforced polyetheretherketone (CFR-PEEK) has recently been introduced for the treatment of fractures of the proximal humerus (PHFs). The advantages of the CFR-PEEK plate are considered to be its radiolucency, its favourable modulus of elasticity, and the polyaxial placement of the screws with high variability of the angle. The primary aim of this study is to investigate the influence of calcar screw positioning on the complication and revision rates after CFR-PEEK plating of PHFs. The secondary aim is to assess its influence on functional outcome.

Material and methods: Patients were identified retrospectively. Minimum follow-up was 12 months. The cohort was divided into two groups depending on the distance of the calcar screw to the calcar (group I: < 12 mm, group II: ≥ 12 mm). The range of motion (ROM), Subjective Shoulder Value Score (SSV) and Constant-Murley Score (CS) were analysed at follow-up examination. Subjective complaints, complications (e.g. humeral head necrosis, varus dislocation) and the revision rate were evaluated.

Results: 51 patients (33 female, 18 male) with an average age of 68.6 years were included after a period of 26.6 months (group I: 32 patients, group II: 19 patients). Apart from the gender distribution, no significant differences were seen in the patient characteristics. The outcome scores showed significantly better clinical results in group I: SSV 83.4 vs 71.2, p = 0.007; CS 79.1 vs 67.8, p = 0.013. Complications were seen less frequently in group I (18.8 % vs 47.4 %, p = 0.030).

Conclusion: This study shows that the positioning of the calcar screw is relevant for CFR-PEEK plate osteosynthesis in PHFs with a good reduction of the fracture. Optimal positioning of the calcar screw close to the calcar (< 12 mm) is associated with a lower rate of complications, resulting in significantly superior functional outcomes.

Level of evidence: III, retrospective cohort study.

背景:碳纤维增强聚醚醚酮(CFR-PEEK)植入物的钢板接骨术最近被引入治疗肱骨近端骨折(PHF)。CFR-PEEK板的优点被认为是其射线透过性、良好的弹性模量以及螺钉的多轴放置,角度变化很大。本研究的主要目的是研究股骨距螺钉定位对PHF CFR-PEEK钢板术后并发症和翻修率的影响。次要目的是评估其对功能结果的影响。材料和方法:对患者进行回顾性鉴定。最低随访时间为12个月。根据股骨距螺钉到股骨距的距离,将队列分为两组(第一组:<12mm,第二组:≥12mm)。在随访检查中分析运动范围(ROM)、主观肩部价值评分(SSV)和恒定Murley评分(CS)。评估主观主诉、并发症(如肱骨头坏死、内翻脱位)和翻修率。结果:在26.6个月后纳入了51名患者(33名女性,18名男性),平均年龄68.6岁(第一组:32名患者,第二组:19名患者)。除了性别分布外,患者特征没有显著差异。结果评分显示I组的临床结果明显更好:SSV 83.4 vs 71.2,p=0.007;CS 79.1 vs 67.8,p=0.013。I组并发症发生率较低(18.8%vs 47.4%,p=0.030)。结论:本研究表明,股骨距螺钉的定位与CFR-PEEK钢板在PHFs中的接骨相关,骨折复位良好。股骨距螺钉靠近股骨距(<12mm)的最佳位置与较低的并发症发生率相关,从而产生显著优越的功能结果。证据水平:III,回顾性队列研究。
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引用次数: 0
LARAI portal provides a safe method for lateral meniscus repair: three-dimensional computed tomography and cadaveric assessment. LARAI门提供了一种安全的外侧半月板修复方法:三维计算机断层扫描和尸体评估。
IF 2.8 2区 医学 Q1 Medicine Pub Date : 2023-09-29 DOI: 10.1186/s10195-023-00727-1
Yi Long, Zhengzheng Zhang, Min Zhou, Jingyi Hou, Yunfeng Zhou, Liang Jiang, Xiaoding Xu, Rui Yang

Background: Lateral, All-Round and All-Inside (LARAI) portal is a viewing or working portal for observing and repairing the lesions of the lateral meniscus. However, there are safety concerns about popliteal artery (PA) injuries during the procedure. This study aimed to assess the safe distance between the trajectory of the LARAI portal and PA.

Materials and methods: Both three-dimensional computed tomography (3D-CT) and cadavers were used to simulate the LARAI portal trajectory. In the 3D-CT study, between January 2020 and September 2020, 45 participants who underwent computed tomography angiography were included in the study. The shortest distance from the PA to the simulated trajectory needle (PS) was measured using 3D-CT. Mean -3SD -2 was calculated to assess the safety of the LARAI portal trajectory. If this value was more than zero, the trajectory was considered "safe." In the cadaveric study, lower limbs from seven fresh-frozen cadavers were used to establish the "safe" trajectories of the LARAI portal, and the PS was measured.

Results: In the 3D-CT study, the longest PS (P < 0.001) was found 20 mm lateral to the edge of the patellar tendon trajectory at 0 mm from the posterior cruciate ligament (PCL). Safe trajectories were also found 10 mm, 15 mm, and 20 mm lateral to the edge of the patellar tendon at 0 mm from the PCL, as well as the 20 mm lateral to the edge of the patellar tendon at 3 mm from the PCL. The cadaveric study showed that the average PS of all safe trajectories closely adjoined to PCL was greater than 14 mm.

Conclusions: The LARAI portal trajectory in the "figure of four" is safe, and the optimal insertion point is 10-20 mm lateral to the edge of the patellar tendon and closely adjoined to the posterolateral margin of the PCL at knee joint line level.

Level of evidence: Level IV.

背景:外侧、全周、全内(LARAI)门是观察和修复外侧半月板损伤的一种观察或工作门。然而,手术过程中腘动脉(PA)损伤存在安全隐患。本研究旨在评估LARAI门脉与PA之间的安全距离。材料和方法:使用三维计算机断层扫描(3D-CT)和尸体模拟LARAI的门脉轨迹。在2020年1月至2020年9月的3D-CT研究中,45名接受计算机断层扫描血管造影术的参与者被纳入研究。使用3D-CT测量从PA到模拟轨迹针(PS)的最短距离。意思是 -3SD -2,以评估LARAI门脉轨迹的安全性。如果这个值大于零,则轨迹被认为是“安全的”。在尸体研究中,使用七具新鲜冷冻尸体的下肢来建立LARAI门的“安全”轨迹,并测量PS。结果:在3D-CT研究中,最长PS(P 结论:“四图”中的LARAI门静脉轨迹是安全的,最佳插入点位于髌腱边缘外侧10-20mm,并在膝关节线水平上紧贴PCL后外侧边缘。证据级别:四级。
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引用次数: 0
Higher pelvic incidence values are a risk factor for trans-iliac trans-sacral screw malposition in sacroiliac complex fracture treatment. 较高的骨盆发生率是骶髂复合体骨折治疗中经髂-骶椎螺钉错位的危险因素。
IF 2.8 2区 医学 Q1 Medicine Pub Date : 2023-09-21 DOI: 10.1186/s10195-023-00728-0
An-Jhih Luo, Angela Wang, Chih-Yang Lai, Yi-Hsun Yu, Yung-Heng Hsu, Ying-Chao Chou, I-Jung Chen

Background: Percutaneous iliosacral (IS) screw fixation and trans-iliac trans-sacral (TITS) screw fixation are clinically effective treatments of posterior pelvic sacroiliac fractures. In order to accurately assess the sacrum position relative to the pelvis, pelvic incidence (PI) is a commonly utilized radiographic parameter in sagittal view. This study aimed to investigate and compare the surgical outcomes and radiographic parameters of IS or TITS screw fixations for the treatment of posterior sacroiliac complex fractures with different PI values.

Materials and methods: The data on patients with posterior pelvic sacroiliac fractures who underwent percutaneous IS or TITS screw fixations, or both, at a single level I trauma center between January 2017 and June 2020 were reviewed. We documented the patient characteristics and fracture types, reviewed surgical records, and measured the radiographic parameters via plain films and multi-planar computed tomography (mpCT) images. Radiographic variations in PI, sacral slope, pelvic tilt, sacral dysmorphism, pelvic ring reduction quality, screw deviation angles, screw malposition grading, and iatrogenic complications were documented and analyzed.

Results: A total of 85 patients were included, and 65 IS and 70 TITS screws were accounted for. Patients were divided into two groups according to screw fixation method and further divided into four sub-groups based on baseline PI values. The PI cutoff values were 49.85° and 48.05° in the IS and TITS screw groups, respectively, according to receiver operating characteristic analysis and Youden's J statistic. Smaller PI values were significantly correlated with sacral dysmorphism (p = 0.027 and 0.003 in the IS and TITS screw groups, respectively). Patients with larger PI values were at a significantly increased risk of screw malposition in the TITS screw group (p = 0.049), with no association in the IS screw group. Logistic regression confirmed that a larger PI value was a significant risk factor for screw malposition in the TITS screw group (p = 0.010). The post-operative outcomes improved from poor/fair (at 6 months) to good/average (at 12 months) based on the Postel Merle d'Aubigné and Majeed scores, with no significant differences between subgroups.

Conclusions: Both percutaneous IS and TITS screw fixations are safe and effective treatments for posterior pelvic sacroiliac fractures. Due to the higher risk of screw malposition in patients with larger PI values, it is crucial to identify potential patients at risk when performing TITS screw fixation surgery.

Level of evidence: Level III.

背景:经皮骶髂螺钉内固定和经髂骶髂螺钉固定是治疗骶髂后骨折的有效方法。为了准确评估骶骨相对于骨盆的位置,骨盆发生率(PI)是矢状面视图中常用的放射学参数。本研究旨在研究和比较IS或TITS螺钉固定治疗不同PI值的骶髂后复合体骨折的手术结果和放射学参数。材料和方法:回顾2017年1月至2020年6月期间在一级创伤中心接受经皮IS或TITS螺钉固定或两者兼有的骨盆骶髂后骨折患者的数据。我们记录了患者的特征和骨折类型,回顾了手术记录,并通过平片和多平面计算机断层扫描(mpCT)图像测量了放射学参数。记录并分析了PI、骶骨倾斜度、骨盆倾斜、骶骨畸形、骨盆环复位质量、螺钉偏转角、螺钉错位分级和医源性并发症的放射学变化。结果:共纳入85例患者,其中65例为IS螺钉,70例为TITS螺钉。根据螺钉固定方法将患者分为两组,并根据基线PI值进一步分为四个子组。根据受试者操作特征分析和Youden’s J统计,IS和TITS螺钉组的PI截止值分别为49.85°和48.05°。较小的PI值与骶骨畸形显著相关(p = 在IS和TITS螺钉组中分别为0.027和0.003)。在TITS螺钉组中,PI值较大的患者发生螺钉错位的风险显著增加(p = 0.049),在IS螺钉组中没有关联。Logistic回归证实,较大的PI值是TITS螺钉组螺钉错位的重要危险因素(p = 0.010)。根据Postel Merle d’Aubigné和Majeed评分,术后结果从差/一般(6个月时)改善为好/平均(12个月时时),各亚组之间没有显著差异。结论:经皮IS和TITS螺钉固定治疗骶髂后骨折安全有效。由于PI值较大的患者发生螺钉错位的风险较高,因此在进行TITS螺钉固定手术时,识别潜在的风险患者至关重要。证据级别:三级。
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引用次数: 0
Functional leg performance 2 years after ACL surgery: a comparison between InternalBrace™-augmented repair versus reconstruction versus healthy controls. ACL手术后2年的功能性腿部表现:两种内支架的比较™-增强修复与重建与健康对照。
IF 2.8 2区 医学 Q1 Medicine Pub Date : 2023-09-21 DOI: 10.1186/s10195-023-00723-5
Linda Bühl, Sebastian Müller, Corina Nüesch, Geert Pagenstert, Annegret Mündermann, Christian Egloff

Background: While clinical and patient-reported outcomes have been investigated in patients after InternalBrace™-augmented anterior cruciate ligament repair (ACL-IB), less is known regarding restoration of functional performance. We aimed to determine differences in functional performance within and between patients 2 years after ACL-IB, patients 2 years after ACL reconstruction (ACL-R), and healthy controls.

Materials and methods: A total of 29 ACL-IB, 27 ACL-R (hamstring autograft), and 29 controls performed single-leg hop (maximum forward distance hop, SLH; side hop > 40 cm in 30 s, SH), proprioception (knee joint position sense at 30° and 60° flexion), and dynamic postural balance (Y Balance) tests. Differences were calculated within groups (side-to-side difference) and between the involved leg of patients and the non-dominant leg of controls, and were evaluated to predefined statistical (P < 0.05), clinically relevant, and methodological (smallest detectable change) thresholds. The number of exceeded thresholds represented no (0), small (1), moderate (2), or strong (3) differences. In addition, the relative number of participants achieving leg symmetry (≥ 90%) and normal performance (≥ 90% of the average performance of the non-dominant leg of controls) were compared between groups (chi-squared tests, P < 0.05).

Results: We observed no-to-moderate leg differences within ACL-IB (moderate difference in hops) and within ACL-R (moderate difference in knee proprioception), no leg differences between patient groups, no-to-small leg differences between ACL-IB and controls, and no leg differences between ACL-R and controls in functional performance. However, two patients in ACL-IB and ACL-R, respectively, passed the hop pretest only with their uninvolved leg, and fewer patients after ACL-IB and ACL-R than controls reached a leg symmetry and normal leg performance of controls in SLH (P < 0.001).

Conclusions: Functional performance seems to be comparable 2 years postoperatively between ACL-IB and ACL-R for a specific subgroup of patients (i.e., proximal ACL tears, moderate activity level). However, the presumed advantage of comparable functional outcome with preserved knee structures after augmented ACL repair compared with ACL-R, and the tendency of both patient groups toward leg asymmetry and compromised single-leg hop performance in the involved legs, warrants further investigation. Level of Evidence Level III, case-control study. Trial registration clinicaltrials.gov, NCT04429165 (12/09/2020). Prospectively registered, https://clinicaltrials.gov/ct2/show/NCT04429165 .

背景:虽然已经对内支架术后患者的临床和患者报告结果进行了调查™-增强型前交叉韧带修复(ACL-IB),关于功能表现的恢复知之甚少。我们旨在确定ACL-IB后2年患者、ACL重建后2年(ACL-R)患者和健康对照组之间功能表现的差异。材料和方法:共有29个ACL-IB、27个ACL-R(自体腘绳肌移植)和29个对照组进行单腿跳跃(最大向前距离跳跃,SLH;侧跳 > 30秒内40 cm,SH)、本体感觉(30°和60°屈曲时的膝关节位置感)和动态姿势平衡(Y平衡)测试。计算各组之间的差异(侧对侧差异)以及患者受累腿和对照组非优势腿之间的差异,并根据预定义的统计学方法进行评估(P 结果:我们观察到ACL-IB(跳跃的中度差异)和ACL-R(膝盖本体感觉的中度差异。然而,分别在ACL-IB和ACL-R中的两名患者仅在其未受累的腿上通过跳跃预测试,并且在ACL-IB/AL-R后,在SLH中达到腿对称性和正常腿表现的患者比对照组少(P 结论:对于特定的亚组患者(即近端ACL撕裂、中等活动水平),术后2年ACL-IB和ACL-R的功能表现似乎相当。然而,与ACL-R相比,增强ACL修复后保留膝关节结构的功能结果具有可比优势,并且两个患者组都有腿部不对称和受累腿部单腿跳跃性能受损的趋势,值得进一步研究。证据水平III级,病例对照研究。试验注册clinicaltrials.gov,NCT04429165(2020年9月12日)。前瞻性地注册,https://clinicaltrials.gov/ct2/show/NCT04429165。
{"title":"Functional leg performance 2 years after ACL surgery: a comparison between InternalBrace™-augmented repair versus reconstruction versus healthy controls.","authors":"Linda Bühl, Sebastian Müller, Corina Nüesch, Geert Pagenstert, Annegret Mündermann, Christian Egloff","doi":"10.1186/s10195-023-00723-5","DOIUrl":"10.1186/s10195-023-00723-5","url":null,"abstract":"<p><strong>Background: </strong>While clinical and patient-reported outcomes have been investigated in patients after InternalBrace™-augmented anterior cruciate ligament repair (ACL-IB), less is known regarding restoration of functional performance. We aimed to determine differences in functional performance within and between patients 2 years after ACL-IB, patients 2 years after ACL reconstruction (ACL-R), and healthy controls.</p><p><strong>Materials and methods: </strong>A total of 29 ACL-IB, 27 ACL-R (hamstring autograft), and 29 controls performed single-leg hop (maximum forward distance hop, SLH; side hop > 40 cm in 30 s, SH), proprioception (knee joint position sense at 30° and 60° flexion), and dynamic postural balance (Y Balance) tests. Differences were calculated within groups (side-to-side difference) and between the involved leg of patients and the non-dominant leg of controls, and were evaluated to predefined statistical (P < 0.05), clinically relevant, and methodological (smallest detectable change) thresholds. The number of exceeded thresholds represented no (0), small (1), moderate (2), or strong (3) differences. In addition, the relative number of participants achieving leg symmetry (≥ 90%) and normal performance (≥ 90% of the average performance of the non-dominant leg of controls) were compared between groups (chi-squared tests, P < 0.05).</p><p><strong>Results: </strong>We observed no-to-moderate leg differences within ACL-IB (moderate difference in hops) and within ACL-R (moderate difference in knee proprioception), no leg differences between patient groups, no-to-small leg differences between ACL-IB and controls, and no leg differences between ACL-R and controls in functional performance. However, two patients in ACL-IB and ACL-R, respectively, passed the hop pretest only with their uninvolved leg, and fewer patients after ACL-IB and ACL-R than controls reached a leg symmetry and normal leg performance of controls in SLH (P < 0.001).</p><p><strong>Conclusions: </strong>Functional performance seems to be comparable 2 years postoperatively between ACL-IB and ACL-R for a specific subgroup of patients (i.e., proximal ACL tears, moderate activity level). However, the presumed advantage of comparable functional outcome with preserved knee structures after augmented ACL repair compared with ACL-R, and the tendency of both patient groups toward leg asymmetry and compromised single-leg hop performance in the involved legs, warrants further investigation. Level of Evidence Level III, case-control study. Trial registration clinicaltrials.gov, NCT04429165 (12/09/2020). Prospectively registered, https://clinicaltrials.gov/ct2/show/NCT04429165 .</p>","PeriodicalId":48603,"journal":{"name":"Journal of Orthopaedics and Traumatology","volume":null,"pages":null},"PeriodicalIF":2.8,"publicationDate":"2023-09-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10513977/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"41173075","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Efficacy and safety of modular versus monoblock stems in revision total hip arthroplasty: a systematic review and meta-analysis. 模块化与单块假体在翻修全髋关节置换术中的有效性和安全性:一项系统回顾和荟萃分析。
IF 2.8 2区 医学 Q1 Medicine Pub Date : 2023-09-16 DOI: 10.1186/s10195-023-00731-5
Daofeng Wang, Hua Li, Wupeng Zhang, Huanyu Li, Cheng Xu, Wanheng Liu, Jiantao Li

Background: Both modular and monoblock tapered fluted titanium (TFT) stems are increasingly being used for revision total hip arthroplasty (rTHA). However, the differences between the two designs in clinical outcomes and complications are not yet clear. Here, we intend to compare the efficacy and safety of modular versus monoblock TFT stems in rTHA.

Methods: PubMed, Embase, Web of Science, and Cochrane Library databases were searched to include studies comparing modular and monoblock implants in rTHA. Data on the survivorship of stems, postoperative hip function, and complications were extracted following inclusion criteria. Inverse variance and Mantel-Haenszel methods in Review Manager (version 5.3 from Cochrane Collaboration) were used to evaluate differences between the two groups.

Results: Ten studies with a total of 2188 hips (1430 modular and 758 monoblock stems) were finally included. The main reason for the revision was aseptic loosening. Paprosky type III was the most common type in both groups. Both stems showed similar re-revision rates (modular vs monoblock: 10.3% vs 9.5%, P = 0.80) and Harris Hip Scores (WMD = 0.43, P = 0.46) for hip function. The intraoperative fracture rate was 11.6% and 5.0% (P = 0.0004) for modular and monoblock stems, respectively. The rate of subsidence > 10 mm was significantly higher in the monoblock group (4.5% vs 1.0%, P = 0.003). The application of extended trochanteric osteotomy was more popular in monoblock stems (22.7% vs 17.5%, P = 0.003). The incidence of postoperative complications such as periprosthetic femoral fracture and dislocation was similar between both stems.

Conclusions: No significant difference was found between modular and monoblock tapered stems as regards postoperative hip function, re-revision rates, and complications. Severe subsidence was more frequent in monoblock stems while modular ones were at higher risk of intraoperative fracture.

Level of evidence: Level III, systematic review of randomized control and non-randomized studies.

Trial registration: We registered our study in the international prospective register of systematic reviews (PROSPERO) (CRD42020213642).

背景:模块化和单块锥形凹槽钛(TFT)柄越来越多地用于翻修全髋关节置换术(rTHA)。然而,两种设计在临床结果和并发症方面的差异尚不清楚。在这里,我们打算比较模块化与单块TFT系统在rTHA中的有效性和安全性。方法:检索PubMed、Embase、Web of Science和Cochrane Library数据库,包括比较rTHA中模块化植入物和单块植入物的研究。根据纳入标准提取茎的存活率、术后髋关节功能和并发症的数据。使用Review Manager (Cochrane Collaboration版本5.3)中的逆方差和Mantel-Haenszel方法来评估两组之间的差异。结果:最终纳入了10项研究,共2188个髋关节(1430个模块和758个单块茎)。修改的主要原因是无菌性松动。两组患者中最常见的是papprosky III型。两种支架在髋关节功能方面显示相似的再翻修率(模块化vs单块:10.3% vs 9.5%, P = 0.80)和Harris髋关节评分(WMD = 0.43, P = 0.46)。模组骨折率为11.6%,单块骨折率为5.0% (P = 0.0004)。单块组沉降bbb10 mm的速率显著高于对照组(4.5% vs 1.0%, P = 0.003)。扩展粗隆截骨术在单块骨柄中应用更为普遍(22.7% vs 17.5%, P = 0.003)。术后并发症如假体周围股骨骨折和脱位的发生率在两茎之间相似。结论:在术后髋关节功能、再翻修率和并发症方面,模块化和单块锥形柄无显著差异。严重的下陷在单块柄中更常见,而模块化柄在术中骨折的风险更高。证据等级:III级,随机对照和非随机研究的系统评价。试验注册:我们在国际前瞻性系统评价注册(PROSPERO) (CRD42020213642)中注册了我们的研究。
{"title":"Efficacy and safety of modular versus monoblock stems in revision total hip arthroplasty: a systematic review and meta-analysis.","authors":"Daofeng Wang, Hua Li, Wupeng Zhang, Huanyu Li, Cheng Xu, Wanheng Liu, Jiantao Li","doi":"10.1186/s10195-023-00731-5","DOIUrl":"10.1186/s10195-023-00731-5","url":null,"abstract":"<p><strong>Background: </strong>Both modular and monoblock tapered fluted titanium (TFT) stems are increasingly being used for revision total hip arthroplasty (rTHA). However, the differences between the two designs in clinical outcomes and complications are not yet clear. Here, we intend to compare the efficacy and safety of modular versus monoblock TFT stems in rTHA.</p><p><strong>Methods: </strong>PubMed, Embase, Web of Science, and Cochrane Library databases were searched to include studies comparing modular and monoblock implants in rTHA. Data on the survivorship of stems, postoperative hip function, and complications were extracted following inclusion criteria. Inverse variance and Mantel-Haenszel methods in Review Manager (version 5.3 from Cochrane Collaboration) were used to evaluate differences between the two groups.</p><p><strong>Results: </strong>Ten studies with a total of 2188 hips (1430 modular and 758 monoblock stems) were finally included. The main reason for the revision was aseptic loosening. Paprosky type III was the most common type in both groups. Both stems showed similar re-revision rates (modular vs monoblock: 10.3% vs 9.5%, P = 0.80) and Harris Hip Scores (WMD = 0.43, P = 0.46) for hip function. The intraoperative fracture rate was 11.6% and 5.0% (P = 0.0004) for modular and monoblock stems, respectively. The rate of subsidence > 10 mm was significantly higher in the monoblock group (4.5% vs 1.0%, P = 0.003). The application of extended trochanteric osteotomy was more popular in monoblock stems (22.7% vs 17.5%, P = 0.003). The incidence of postoperative complications such as periprosthetic femoral fracture and dislocation was similar between both stems.</p><p><strong>Conclusions: </strong>No significant difference was found between modular and monoblock tapered stems as regards postoperative hip function, re-revision rates, and complications. Severe subsidence was more frequent in monoblock stems while modular ones were at higher risk of intraoperative fracture.</p><p><strong>Level of evidence: </strong>Level III, systematic review of randomized control and non-randomized studies.</p><p><strong>Trial registration: </strong>We registered our study in the international prospective register of systematic reviews (PROSPERO) (CRD42020213642).</p>","PeriodicalId":48603,"journal":{"name":"Journal of Orthopaedics and Traumatology","volume":null,"pages":null},"PeriodicalIF":2.8,"publicationDate":"2023-09-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10505121/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10654436","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
National spine surgery registries' characteristics and aims: globally accepted standards have yet to be met. Results of a scoping review and a complementary survey. 国家脊柱外科登记的特点和目标:全球公认的标准尚未达到。范围审查和补充调查的结果。
IF 2.8 2区 医学 Q1 Medicine Pub Date : 2023-09-16 DOI: 10.1186/s10195-023-00732-4
Simona Pascucci, Francesco Langella, Michela Franzò, Marco Giovanni Tesse, Enrico Ciminello, Alessia Biondi, Eugenio Carrani, Letizia Sampaolo, Gustavo Zanoli, Pedro Berjano, Marina Torre

Background: Surgery involving implantable devices is widely used to solve several health issues. National registries are essential tools for implantable device surveillance and vigilance. In 2017, the European Union encouraged Member States to establish "registries and databanks for specific types of devices" to evaluate device safety and performance and ensure their traceability. Spine-implantable devices significantly impact patient safety and public health; spine registries might help improve surgical outcomes. This study aimed to map existing national spine surgery registries and highlight their features and organisational standards to provide an essential reference for establishing other national registries.

Methods: A scoping search was performed using the Embase, PubMed/Medline, Scopus, and Web of Science databases for the terms "registry", "register", "implantable", and all terms and synonyms related to spinal diseases and national registries in publications from January 2000 to December 2020. This search was later updated and finalised through a web search and an ad hoc survey to collect further detailed information.

Results: Sixty-two peer-reviewed articles were included, which were related to seven national spine registries, six of which were currently active. Three additional active national registries were found through the web search. The nine selected national registries were set up between 1998 and 2021. They collect data on the procedure and use patient-reported outcome measures (PROMs) for the follow-up.

Conclusion: Our study identified nine currently active national spine surgery registries. However, globally accepted standards for developing a national registry of spine surgery are yet to be established. Therefore, an international effort to increase result comparability across registries is highly advisable. We hope the recent initiative from the Orthopaedic Data Evaluation Panel (ODEP) to establish an international collaboration will meet these needs.

背景:植入式手术被广泛用于解决一些健康问题。国家登记处是植入式装置监测和警戒的重要工具。2017年,欧盟鼓励成员国建立“特定类型器械的注册和数据库”,以评估器械的安全性和性能,并确保其可追溯性。脊柱植入装置显著影响患者安全和公众健康;脊柱登记可能有助于改善手术结果。本研究旨在绘制现有国家脊柱外科登记系统的分布图,突出其特点和组织标准,为建立其他国家脊柱外科登记系统提供重要参考。方法:使用Embase、PubMed/Medline、Scopus和Web of Science数据库对2000年1月至2020年12月出版物中的术语“registry”、“register”、“implantable”以及与脊柱疾病和国家注册相关的所有术语和同义词进行范围搜索。后来通过网络搜索和收集进一步详细信息的特别调查更新并最终确定了这一搜索。结果:纳入了62篇同行评议的文章,这些文章与7个国家脊柱登记处有关,其中6个目前是活跃的。通过网络搜索发现了另外三个活跃的国家登记处。9个选定的国家登记处是在1998年至2021年之间建立的。他们收集手术过程的数据,并使用患者报告的结果测量(PROMs)进行随访。结论:我们的研究确定了9个目前活跃的国家脊柱外科登记处。然而,全球公认的脊柱手术登记标准尚未建立。因此,在国际上努力提高注册中心之间的结果可比性是非常可取的。我们希望骨科数据评估小组(ODEP)最近发起的建立国际合作的倡议能够满足这些需求。
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引用次数: 0
Anterior debridement combined with autogenous iliac bone graft fusion for the treatment of lower cervical tuberculosis: a multicenter retrospective study. 前路清创联合自体髂骨融合治疗下颈结核:一项多中心回顾性研究。
IF 2.8 2区 医学 Q1 Medicine Pub Date : 2023-09-14 DOI: 10.1186/s10195-023-00730-6
Ping Xia, Pengfei Tao, Xiaolong Zhao, Xianglin Peng, Songfeng Chen, Xiucai Ma, Lei Fan, Jing Feng, Feifei Pu

Background: This study aimed to analyze the clinical efficacy of one-stage anterior debridement of lower cervical tuberculosis using iliac crest bone graft fusion and internal fixation.

Materials and methods: A retrospective analysis was performed on 48 patients with lower cervical tuberculosis admitted to multiple medical centers from June 2018 to June 2021. Among them, 36 patients had lesions involving two vertebrae and 12 patients had lesions involving more than three vertebrae. All patients were treated with quadruple antituberculosis drugs for more than 2 weeks before the operation, and then treated with one-stage anterior debridement and autogenous iliac bone graft fusion combined with titanium plate internal fixation. After the operation, antituberculosis drugs were continued for 12-18 months. The patients were followed-up to observe the improvement in clinical symptoms, bone graft fusion, Cobb angle, visual analog score (VAS), erythrocyte sedimentation rate (ESR), C-reactive protein (CRP), wound healing, and neurological function.

Results: The patients were followed-up for 13-43 months, with an average of 21.46 ± 1.52 months. The clinical symptoms significantly improved after the operation. The bone graft was completely fused in all patients, and the bone fusion time was 3-6 months, with an average of 4.16 ± 0.47 months. At the last follow-up, the Cobb angle, VAS, ESR, and CRP level were significantly lower than those before surgery (P < 0.05). None of the patients had loosening, detachment, or rupture of the internal fixation, and no recurrence occurred. All surgical incisions healed in one stage without infection or sinus formation. The preoperative Frankel neurological function classification was grade B in 7 cases, grade C in 13, grade D in 18, and grade E in 10. At the last follow-up, 8 cases recovered to grade D and 40 recovered to grade E.

Conclusions: For patients with lower cervical tuberculosis, based on oral treatment with quadruple antituberculosis drugs, direct decompression through anterior debridement, followed by autologous iliac bone graft fusion combined with internal fixation can completely remove tuberculosis foci, rebuild the stability of the cervical spine, and obtain good clinical efficacy. Level of evidence Level 3.

背景:本研究旨在分析髂嵴植骨融合内固定一期前路清创治疗下颈结核的临床疗效。材料与方法:对2018年6月至2021年6月在多家医疗中心收治的48例下宫颈结核患者进行回顾性分析。其中累及2节椎骨病变36例,累及3节以上病变12例。所有患者术前均给予四联抗结核药物治疗2周以上,术后行一期前路清创、自体髂骨融合联合钛板内固定。术后继续使用抗结核药物12-18个月。随访观察患者临床症状、植骨融合、Cobb角、视觉模拟评分(VAS)、红细胞沉降率(ESR)、c反应蛋白(CRP)、创面愈合及神经功能改善情况。结果:患者随访13 ~ 43个月,平均21.46±1.52个月。术后临床症状明显改善。所有患者植骨完全融合,骨融合时间3-6个月,平均4.16±0.47个月。末次随访时,Cobb角、VAS、ESR、CRP水平均明显低于术前(P)。结论:对于下颈结核患者,在口服四联抗结核药物治疗的基础上,经前路清创直接减压,再行自体髂骨植骨融合联合内固定,可完全切除结核病灶,重建颈椎的稳定性,取得较好的临床疗效。证据等级三级。
{"title":"Anterior debridement combined with autogenous iliac bone graft fusion for the treatment of lower cervical tuberculosis: a multicenter retrospective study.","authors":"Ping Xia, Pengfei Tao, Xiaolong Zhao, Xianglin Peng, Songfeng Chen, Xiucai Ma, Lei Fan, Jing Feng, Feifei Pu","doi":"10.1186/s10195-023-00730-6","DOIUrl":"10.1186/s10195-023-00730-6","url":null,"abstract":"<p><strong>Background: </strong>This study aimed to analyze the clinical efficacy of one-stage anterior debridement of lower cervical tuberculosis using iliac crest bone graft fusion and internal fixation.</p><p><strong>Materials and methods: </strong>A retrospective analysis was performed on 48 patients with lower cervical tuberculosis admitted to multiple medical centers from June 2018 to June 2021. Among them, 36 patients had lesions involving two vertebrae and 12 patients had lesions involving more than three vertebrae. All patients were treated with quadruple antituberculosis drugs for more than 2 weeks before the operation, and then treated with one-stage anterior debridement and autogenous iliac bone graft fusion combined with titanium plate internal fixation. After the operation, antituberculosis drugs were continued for 12-18 months. The patients were followed-up to observe the improvement in clinical symptoms, bone graft fusion, Cobb angle, visual analog score (VAS), erythrocyte sedimentation rate (ESR), C-reactive protein (CRP), wound healing, and neurological function.</p><p><strong>Results: </strong>The patients were followed-up for 13-43 months, with an average of 21.46 ± 1.52 months. The clinical symptoms significantly improved after the operation. The bone graft was completely fused in all patients, and the bone fusion time was 3-6 months, with an average of 4.16 ± 0.47 months. At the last follow-up, the Cobb angle, VAS, ESR, and CRP level were significantly lower than those before surgery (P < 0.05). None of the patients had loosening, detachment, or rupture of the internal fixation, and no recurrence occurred. All surgical incisions healed in one stage without infection or sinus formation. The preoperative Frankel neurological function classification was grade B in 7 cases, grade C in 13, grade D in 18, and grade E in 10. At the last follow-up, 8 cases recovered to grade D and 40 recovered to grade E.</p><p><strong>Conclusions: </strong>For patients with lower cervical tuberculosis, based on oral treatment with quadruple antituberculosis drugs, direct decompression through anterior debridement, followed by autologous iliac bone graft fusion combined with internal fixation can completely remove tuberculosis foci, rebuild the stability of the cervical spine, and obtain good clinical efficacy. Level of evidence Level 3.</p>","PeriodicalId":48603,"journal":{"name":"Journal of Orthopaedics and Traumatology","volume":null,"pages":null},"PeriodicalIF":2.8,"publicationDate":"2023-09-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10501986/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10287216","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Italian Orthopaedic and Traumatology Society (SIOT) position statement on the non-surgical management of knee osteoarthritis. 意大利骨科和创伤学会(SIOT)关于膝关节骨关节炎非手术治疗的立场声明。
IF 2.8 2区 医学 Q1 Medicine Pub Date : 2023-09-07 DOI: 10.1186/s10195-023-00729-z
Elisa Pesare, Giovanni Vicenti, Elisaveta Kon, Massimo Berruto, Roberto Caporali, Biagio Moretti, Pietro S Randelli

Background: Knee osteoarthritis (OA) is a chronic disease associated with a severe impact on quality of life. However, unfortunately, there are no evidence-based guidelines for the non-surgical management of this disease. While recognising the gap between scientific evidence and clinical practice, this position statement aims to present recommendations for the non-surgical management of knee OA, considering the available evidence and the clinical knowledge of experienced surgeons. The overall goal is to offer an evidenced-based expert opinion, aiding clinicians in the management of knee OA while considering the condition, values, needs and preferences of individual patients.

Methods: The study design for this position statement involved a preliminary search of PubMed, Google Scholar, Medline and Cochrane databases for literature spanning the period between January 2021 and April 2023, followed by screening of relevant articles (systematic reviews and meta-analyses). A Società Italiana Ortopedia e Traumatologia (SIOT) multidisciplinary task force (composed of four orthopaedic surgeons and a rheumatologist) subsequently formulated the recommendations.

Results: Evidence-based recommendations for the non-surgical management of knee OA were developed, covering assessment, general approach, patient information and education, lifestyle changes and physical therapy, walking aids, balneotherapy, transcutaneous electrical nerve stimulation, pulsed electromagnetic field therapy, pharmacological interventions and injections.

Conclusions: For non-surgical management of knee OA, the recommended first step is to bring about lifestyle changes, particularly management of body weight combined with physical exercise and/or hydrotherapy. For acute symptoms, non-steroidal anti-inflammatory drugs (NSAIDs), topic or oral, can be used. Opioids can only be used as third-line pharmacological treatment. Glucosamine and chondroitin are also suggested as chronic pharmacological treatment. Regarding intra-articular infiltrative therapy, the use of hyaluronic acid is recommended in cases of chronic knee OA [platelet-rich plasma (PRP) as second line), in the absence of active acute disease, while the use of intra-articular injections of cortisone is effective and preferred for severe acute symptoms.

背景:膝骨关节炎(OA)是一种严重影响生活质量的慢性疾病。然而,不幸的是,对于这种疾病的非手术治疗尚无循证指南。虽然认识到科学证据和临床实践之间的差距,但考虑到现有证据和经验丰富的外科医生的临床知识,本立场声明旨在为膝关节OA的非手术治疗提供建议。总体目标是提供以证据为基础的专家意见,帮助临床医生在考虑个体患者的病情、价值、需求和偏好的同时管理膝关节OA。方法:本立场声明的研究设计包括对PubMed、谷歌Scholar、Medline和Cochrane数据库进行初步检索,检索时间跨度为2021年1月至2023年4月的文献,然后筛选相关文章(系统综述和荟萃分析)。意大利骨科创伤学会(SIOT)多学科工作组(由四名骨科医生和一名风湿病学家组成)随后制定了这些建议。结果:对膝关节OA的非手术治疗提出了循证建议,包括评估、一般方法、患者信息和教育、生活方式改变和物理治疗、助行器、按摩疗法、经皮神经电刺激、脉冲电磁场治疗、药物干预和注射。结论:对于膝关节OA的非手术治疗,建议的第一步是改变生活方式,特别是控制体重,结合体育锻炼和/或水疗。对于急性症状,可以使用非甾体抗炎药(NSAIDs),局部或口服。阿片类药物只能作为三线药物治疗。氨基葡萄糖和软骨素也建议作为慢性药物治疗。关于关节内浸润治疗,在没有活动性急性疾病的情况下,建议使用透明质酸(富血小板血浆(PRP)作为二线),而使用关节内注射可的松是有效的,对于严重的急性症状是首选。
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引用次数: 1
Consensus for management of sacral fractures: from the diagnosis to the treatment, with a focus on the role of decompression in sacral fractures. 骶骨骨折的治疗共识:从诊断到治疗,重点是减压在骶骨骨折中的作用。
IF 2.8 2区 医学 Q1 Medicine Pub Date : 2023-09-04 DOI: 10.1186/s10195-023-00726-2
Alessandro Aprato, Luigi Branca Vergano, Alessandro Casiraghi, Francesco Liuzza, Umberto Mezzadri, Alberto Balagna, Lorenzo Prandoni, Mohamed Rohayem, Lorenzo Sacchi, Amarildo Smakaj, Mario Arduini, Alessandro Are, Concetto Battiato, Marco Berlusconi, Federico Bove, Stefano Cattaneo, Matteo Cavanna, Federico Chiodini, Matteo Commessatti, Francesco Addevico, Rocco Erasmo, Alberto Ferreli, Claudio Galante, Pietro Domenico Giorgi, Federico Lamponi, Alessandro Moghnie, Michel Oransky, Antonio Panella, Raffaele Pascarella, Federico Santolini, Giuseppe Rosario Schiro, Marco Stella, Kristijan Zoccola, Alessandro Massé

Background: There is no evidence in the current literature about the best treatment option in sacral fracture with or without neurological impairment.

Materials and methods: The Italian Pelvic Trauma Association (A.I.P.) decided to organize a consensus to define the best treatment for traumatic and insufficiency fractures according to neurological impairment.

Results: Consensus has been reached for the following statements: When complete neurological examination cannot be performed, pelvic X-rays, CT scan, hip and pelvis MRI, lumbosacral MRI, and lower extremities evoked potentials are useful. Lower extremities EMG should not be used in an acute setting; a patient with cauda equina syndrome associated with a sacral fracture represents an absolute indication for sacral reduction and the correct timing for reduction is "as early as possible". An isolated and incomplete radicular neurological deficit of the lower limbs does not represent an indication for laminectomy after reduction in the case of a displaced sacral fracture in a high-energy trauma, while a worsening and progressive radicular neurological deficit represents an indication. In the case of a displaced sacral fracture and neurological deficit with imaging showing no evidence of nerve root compression, a laminectomy after reduction is not indicated. In a patient who was not initially investigated from a neurological point of view, if a clinical investigation conducted after 72 h identifies a neurological deficit in the presence of a displaced sacral fracture with nerve compression on MRI, a laminectomy after reduction may be indicated. In the case of an indication to perform a sacral decompression, a first attempt with closed reduction through external manoeuvres is not mandatory. Transcondylar traction does not represent a valid method for performing a closed decompression. Following a sacral decompression, a sacral fixation (e.g. sacroiliac screw, triangular osteosynthesis, lumbopelvic fixation) should be performed. An isolated and complete radicular neurological deficit of the lower limbs represents an indication for laminectomy after reduction in the case of a displaced sacral fracture in a low-energy trauma associated with imaging suggestive of root compression. An isolated and incomplete radicular neurological deficit of the lower limbs does not represent an absolute indication. A worsening and progressive radicular neurological deficit of the lower limbs represents an indication for laminectomy after reduction in the case of a displaced sacral fracture in a low-energy trauma associated with imaging suggestive of root compression. In the case of a displaced sacral fracture and neurological deficit in a low-energy trauma, sacral decompression followed by surgical fixation is indicated.

Conclusions: This consensus collects expert opinion about this topic and may guide the surgeon in choosing the

背景:目前文献中没有证据表明骶骨骨折伴或不伴神经损伤的最佳治疗方案。材料和方法:意大利骨盆创伤协会(A.I.P.)决定组织一致意见,根据神经损伤确定创伤性和不全性骨折的最佳治疗方法。结果:以下观点已达成共识:当不能进行完整的神经学检查时,盆腔x光片,CT扫描,髋关节和骨盆MRI,腰骶MRI和下肢诱发电位是有用的。下肢肌电图不应用于急症;马尾综合征合并骶骨骨折的患者是骶骨复位的绝对指征,正确的复位时机是“尽早”。在高能创伤中移位性骶骨骨折复位后,下肢孤立和不完整的神经根缺损不能作为椎板切除术的指征,而恶化和进行性神经根缺损则是指征。对于移位性骶骨骨折和影像学未显示神经根受压证据的神经功能缺损患者,不建议在复位后行椎板切除术。对于最初未从神经学角度进行调查的患者,如果72小时后进行的临床调查在MRI上发现移位性骶骨骨折伴神经压迫的神经功能缺损,则可能需要复位后的椎板切除术。在有骶椎减压指征的情况下,通过外旋闭式复位的首次尝试并不是强制性的。经髁牵引不是进行闭合性减压的有效方法。骶骨减压后,应进行骶骨固定(如骶髂螺钉、三角骨固定、腰骨盆固定)。下肢孤立的完全性神经根神经缺损是低能创伤伴影像学提示椎根受压的骶骨移位骨折复位后椎板切除术的指征。孤立的和不完全的下肢神经根性缺损并不代表绝对的指征。下肢神经根神经缺损的恶化和进行性表现为骶骨移位骨折复位后伴有影像学提示椎根受压的低能量创伤患者椎板切除术的指征。在低能量创伤中发生移位性骶骨骨折和神经功能缺损的病例中,建议骶骨减压后进行手术固定。结论:这一共识收集了关于这一主题的专家意见,可以指导外科医生为这些患者选择最佳的治疗方法。证据等级:iv .试验注册:不适用(共识文件)。
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引用次数: 0
Intramedullary nailing versus cemented plate for treating metastatic pathological fracture of the proximal humerus: a comparison study and literature review. 髓内钉与骨水泥钢板治疗肱骨近端转移性病理性骨折的比较研究及文献综述。
IF 2.8 2区 医学 Q1 Medicine Pub Date : 2023-08-24 DOI: 10.1186/s10195-023-00721-7
Karl Wu, Ting Lin, Cheng-Han Lee

Background: Pathological fracture of the humerus causes severe pain, limited use of the hand, and decreased quality of life. This study aimed to compare the outcomes of intramedullary nailing and locking plate in treating metastatic pathological fractures of the proximal humerus.

Methods: This retrospective comparison study included 45 patients (22 male, 23 female) with proximal humerus metastatic pathological fractures who underwent surgical treatment between 2011 and 2022. All data were collected from medical records and were analyzed retrospectively. Seventeen cases underwent intramedullary nailing plus cement augmentation, and 28 cases underwent locking plate plus cement augmentation. The main outcomes were pain relief, function scores, and complications.

Results: Among 45 patients with mean age 61.7 ± 9.7 years, 23 (51.1%) had multiple bone metastases, and 28 (62.2%) were diagnosed with impending fractures. The nailing group had significantly lower blood loss [100 (60-200) versus 500 (350-600) ml, p < 0.001] and shorter hospital stay (8.4 ± 2.6 versus 12.3 ± 4.3 days, p < 0.001) than the plating group. Average follow-up time of the nailing group was 12 months and 16.5 months for the plating group. The nailing group had higher visual analog scale (VAS) scores than the plating group, indicating greater pain relief with nailing [7 (6-8) versus 6 (5-7), p = 0.01]. Musculoskeletal Tumor Society functional scores [28 (27-29) versus 27 (26.5-28.5), p = 0.23] were comparable between groups. No complications, local recurrence, or revision surgery were reported until the last follow-up in either group. However, one case in the plating group had a humeral head collapse and fragmentation without needing revision surgery.

Conclusions: Intramedullary nailing with cement augmentation is a viable option for treating proximal humerus metastatic pathological fracture, providing rigid fixation and better pain relief resulting in earlier mobility to optimize functional outcomes. Less invasive procedure with less blood loss and shorter hospital stay also benefits patients. Level of evidence Level II. Trial registration statement Not applicable.

背景:病理性肱骨骨折导致剧烈疼痛,手部活动受限,生活质量下降。本研究旨在比较髓内钉和锁定钢板治疗肱骨近端转移性病理性骨折的疗效。方法:本回顾性比较研究纳入了2011年至2022年间接受手术治疗的45例肱骨近端转移性病理性骨折患者(男22例,女23例)。所有数据均来自医疗记录,并进行回顾性分析。髓内钉+骨水泥加固17例,锁定钢板+骨水泥加固28例。主要结果为疼痛缓解、功能评分和并发症。结果:45例患者平均年龄(61.7±9.7岁)中,23例(51.1%)发生多发骨转移,28例(62.2%)诊断为即将发生骨折。髓内钉组的失血量明显低于500 (350-600)ml [100 (60-200) ml]。结论:骨水泥增强髓内钉是治疗肱骨近端转移性病理性骨折的可行选择,它提供了刚性固定和更好的疼痛缓解,导致早期活动,从而优化功能预后。微创手术、出血量少、住院时间短也有利于患者。证据等级二级。试验注册声明不适用。
{"title":"Intramedullary nailing versus cemented plate for treating metastatic pathological fracture of the proximal humerus: a comparison study and literature review.","authors":"Karl Wu, Ting Lin, Cheng-Han Lee","doi":"10.1186/s10195-023-00721-7","DOIUrl":"10.1186/s10195-023-00721-7","url":null,"abstract":"<p><strong>Background: </strong>Pathological fracture of the humerus causes severe pain, limited use of the hand, and decreased quality of life. This study aimed to compare the outcomes of intramedullary nailing and locking plate in treating metastatic pathological fractures of the proximal humerus.</p><p><strong>Methods: </strong>This retrospective comparison study included 45 patients (22 male, 23 female) with proximal humerus metastatic pathological fractures who underwent surgical treatment between 2011 and 2022. All data were collected from medical records and were analyzed retrospectively. Seventeen cases underwent intramedullary nailing plus cement augmentation, and 28 cases underwent locking plate plus cement augmentation. The main outcomes were pain relief, function scores, and complications.</p><p><strong>Results: </strong>Among 45 patients with mean age 61.7 ± 9.7 years, 23 (51.1%) had multiple bone metastases, and 28 (62.2%) were diagnosed with impending fractures. The nailing group had significantly lower blood loss [100 (60-200) versus 500 (350-600) ml, p < 0.001] and shorter hospital stay (8.4 ± 2.6 versus 12.3 ± 4.3 days, p < 0.001) than the plating group. Average follow-up time of the nailing group was 12 months and 16.5 months for the plating group. The nailing group had higher visual analog scale (VAS) scores than the plating group, indicating greater pain relief with nailing [7 (6-8) versus 6 (5-7), p = 0.01]. Musculoskeletal Tumor Society functional scores [28 (27-29) versus 27 (26.5-28.5), p = 0.23] were comparable between groups. No complications, local recurrence, or revision surgery were reported until the last follow-up in either group. However, one case in the plating group had a humeral head collapse and fragmentation without needing revision surgery.</p><p><strong>Conclusions: </strong>Intramedullary nailing with cement augmentation is a viable option for treating proximal humerus metastatic pathological fracture, providing rigid fixation and better pain relief resulting in earlier mobility to optimize functional outcomes. Less invasive procedure with less blood loss and shorter hospital stay also benefits patients. Level of evidence Level II. Trial registration statement Not applicable.</p>","PeriodicalId":48603,"journal":{"name":"Journal of Orthopaedics and Traumatology","volume":null,"pages":null},"PeriodicalIF":2.8,"publicationDate":"2023-08-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10449752/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10435035","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
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Journal of Orthopaedics and Traumatology
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