Hip revision arthroplasty

髋关节翻修术
  • 文章类型: Journal Article
    髋关节置换术翻修手术中的股骨骨缺损是一个复杂的问题,对于整形外科医生来说,治疗是一个挑战,他们需要评估解剖结构改变后的残余骨量,并获得新植入物的稳定性。可用的分类系统主要基于X射线二维图像,缺乏准确性和可重复性以及全面的治疗算法。然而,没有基于计算机断层扫描(CT)扫描图像或三维(3D)建模现代技术的任何分类记录。我们旨在回顾目前有关股骨缺损分类(FDC)的文献,分析其不同的理论基础,可靠性和准确性,以及它们在临床实践中的益处。此外,我们强调了基于CT扫描的3D建模技术在股骨骨缺损设置和髋关节翻修术中的作用.
    进行了叙述性审查。文章选自更新至2023年3月的PubMed和Scopus医学数据库。所有英语I至IV级研究都被考虑纳入。研究使用相关搜索词项目进行:“股骨缺损”,\"分类\",\"射线照相\",“修正髋关节置换术”,“CT扫描”和“3D”,我们仅包括评估不同股骨骨缺损分类系统的准确性或可靠性(或两者)的文章。
    我们的搜索产生了408个结果,其中17个被认为是高度相关的。我们发现了七个基于X射线的分类系统,这些系统已尝试以低至好的可重复性量化骨丢失的程度。最常用的股骨骨缺损分类系统是AAOS和Peprosk分类,它还提供了一种临床治疗算法。2021年,FDC有趣地展示了一种新的简单分类系统,具有次优的可重复性和实用的治疗算法。尽管股骨缺损的分类系统众多,他们都不了解CT扫描和3D成像技术的使用。
    如果观察者内部和观察者之间的可靠性次优,则传统的基于X射线的分类系统仍然是广泛使用的事件。3D建模技术是一种重要的诊断工具,可以提高对骨缺损和残余骨支持结构的理解。允许阐述新的,更精确,分类系统。
    UNASSIGNED: Femoral bone defect in hip arthroplasty revision surgery represents a complex problem, and the treatment is a challenge for orthopedic surgeons called to assess the residual bone stock in an altered anatomy and obtain stability for the new implant. Classification systems available are mostly based on X-rays two-dimensional images and lack of accuracy and reproducibility and comprehensive therapeutic algorithms. However, there is no record of any classification based on computed tomography (CT)-scan images or three-dimensional (3D) modeling modern techniques. We aimed to review the current literature around femoral defect classifications (FDCs) analyzing their different rationale basis, reliability and accuracy, and their benefit in clinical practice. Moreover, we highlighted the role of CT scan-based 3D modeling techniques in the setting of femoral bone defects and revision hip arthroplasty.
    UNASSIGNED: A narrative review was conducted. The articles were selected from the PubMed and Scopus medical database updated to March 2023. All Level-I to IV studies in the English language were considered for inclusion. The research was performed using relevant search term items: \"femoral defects\", \"classification\", \"radiographic\", \"revision hip arthroplasty\", \"CT scan\" and \"3D\" and we included only articles that evaluated the accuracy or reliability (or both) of the different femoral bone defects classification system.
    UNASSIGNED: Our search yielded 408 results, of which 17 were deemed highly relevant. We found seven X-ray-based classification systems which have been attempted to quantify the degree of bone loss with low to good reproducibility. The most used classification system for femoral bone defects were the AAOS and Paprosky classification, which also offers a clinical therapeutic algorithm. In 2021, the FDC interestingly showed a new simple classification system with sub-optimal reproducibility and a practical therapeutic algorithm. Despite the numerous classification system of femoral defects, none of them comprehends the use of CT scan and 3D imaging technologies.
    UNASSIGNED: Traditional X-rays-based classification system are still widely used event if their intra-observer and inter-observer reliability is sub-optimal. 3D modeling techniques represent an important diagnostic tool that could improve the understanding of bone defects and residual bone supportive structures, allowing to elaborate new, more precise, classification systems.
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  • 文章类型: Journal Article
    在年轻的时候,越来越多的髋关节置换会使患者多年来植入物失败的风险增加。如果失败,翻修特异性茎旨在克服骨丢失。这些装置的模块化是外科医生的重要资源,因为它们允许新的植入物更好地适应患者的解剖结构。本系统评价的目的是提供有关长期随访(>8年)髋关节模块化翻修股骨干的结果的数据。
    本系统评价和荟萃分析遵循PRISMA(系统评价和荟萃分析的首选报告项目)声明指南进行。对PubMed和GoogleScholar数据库进行了系统和独立的搜索,根据纳入和排除标准。两名审阅者独立执行数据提取。如果有分歧,资深作者被寻求解决分歧。根据美国国家卫生与护理卓越研究所(NICE)指南(八项清单)和纽卡斯尔-渥太华量表(NOS)评估了所涉及研究的质量。评估主要和次要结果。使用MicrosoftExcel和STATA软件对该荟萃分析进行统计分析。
    主要结果是长期随访时模块化修订茎的重新修订率。范围从1.4%到45.6%:随机效应汇总估计为5.5%[95%置信区间(CI):4%到7%],I2为12.3%(P=0.332)。平均Harris髋关节评分(HHS)为83[min:79;max:87.6;标准偏差(SD):3.55]。次要评估结果是:沉降>5毫米,假体周围感染或骨折(术中和术后)和脱位的发生率。NICE工具的平均值为5.5(SD:1.13)和NOS工具的7.3(SD:0.79)。长期随访生存率>90%(min:60%;max:97%)。
    模块化股骨翻修茎已显示出良好的长期可靠性和有效性。这项荟萃分析表明,随访8年后的重新修订率很低,90%的植入物没有失败。
    UNASSIGNED: Increasingly hip replacements at young age exposes the patient to an increased risk of failure of the implant over the years. In case of failure, revision specific stems were designed to overcome bone loss. Modularity of these devices is an important resource for the surgeon as they allow the new implant to be better adapted to the patient\'s anatomy. The purpose of this systematic review is to provide data about the outcome at long-term follow-up (>8 years) of hip modular revision femoral stems.
    UNASSIGNED: This systematic review and meta-analysis were conducted following the PRISMA (Preferred Reporting Items for Systematic Reviews and Meta-Analyses) statement guidelines. PubMed and Google Scholar databases were systematically and independently searched, according to the inclusion and exclusion criteria. Two reviewers performed the data extraction independently. In case of disagreement, the senior authors were sought to resolve the divergences. Quality of the involved studies was evaluated with National Institute for Health and Care Excellence (NICE) guidelines (eight-item list) and the Newcastle-Ottawa scale (NOS). Primary and secondary outcomes were evaluated. The statistical analysis of this meta-analysis was performed by using Excel Microsoft and the software STATA.
    UNASSIGNED: The primary outcome was the re-revision rate of modular revision stems at long-term follow-up. It ranged from 1.4% to 45.6%: random effect pooled estimate was 5.5% [95% confidence interval (CI): 4% to 7%], with a I2 of 12.3% (P=0.332). Mean Harris Hip Score (HHS) was 83 [min: 79; max: 87.6; standard deviation (SD): 3.55]. Secondary evaluated outcomes were: subsidence >5 mm, rate of periprosthetic infection or fractures (intra- and post-operative) and dislocations. The mean value for the NICE tool was 5.5 (SD: 1.13) and 7.3 (SD: 0.79) for the NOS tool. The survival rate was >90% at long-term follow-up (min: 60%; max: 97%).
    UNASSIGNED: The modular femoral revision stems have demonstrated good long-term reliability and efficacy. This meta-analysis demonstrates that the re-revision rate after 8 years of follow-up is low and 90% of the implants did not fail.
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  • 文章类型: Journal Article
    模块化颈部适配器允许不同的长度和偏移变化,以达到稳定的全髋关节置换术(THA),并允许在不移除现有组件的情况下进行快速的部分髋关节翻修手术。关于这个问题和长期相关结果的文献很少。这篇叙述性综述总结了有关这些装置作为部分全髋关节置换术翻修术(THAr)手术治疗选择的最新文献,重点是适应症。临床和放射学结果,和相关并发症。
    对当前可用文献的叙述性审查是在2022年12月通过电子数据库进行的。使用的术语是:“头颈部锥度”或“MeretteBioBall”和“修订全髋关节置换术(MeSH术语)”。时间限制在2000年1月1日至2022年1月12日之间。包括有关MeretteBioBall®系统在髋关节翻修手术中的临床应用的研究,而所有关于模块化柄假体的论文都被排除在外。
    外科手术是安全的,快速并允许外科医生纠正固定好的茎版本,长度和偏移量,除了重新拉紧软组织。临床和放射学结果良好,并发症发生率低。
    模块化颈部适配器系统似乎是THA复发性脱位的良好外科手术,特别是在第二次TAr手术的情况下。然而,适配器使用的主要适应症仍然是孤立的髋臼杯翻修。相关的并发症很少见:最糟糕的是由于茎版本和长度校正不足而导致的再脱位。文献中报道的再位错率从5.2%到15%不等。文献中未报道模块化系统的腐蚀或微动。
    UNASSIGNED: Modular neck adapters allow different length and offset changes to reach a stable total hip arthroplasty (THA) and permit a quick partial hip revision procedure without removing the existing components. The literature is poor on this matter and about the long-term related outcomes. This narrative review summarizes the most recent literature about these devices as an option of surgical treatment in partial total hip arthroplasty revision (THAr) focusing on indications, clinical and radiological outcomes, and related complications.
    UNASSIGNED: The narrative review of the current available literature was conducted in December 2022 through electronic database. The terms used were: \"Head neck taper\" OR \"Merete BioBall\" AND \"revision Total Hip Arthroplasty (MeSH Terms)\". The timeframe was limited between 01/01/2000 and 01/12/2022. The studies regarding the clinical use of the Merete BioBall® system in hip revision surgery were included, while all the papers concerning modular stem prosthesis were excluded.
    UNASSIGNED: The surgical procedure is safe, quick and allows the surgeon to correct a well-fixed stem version, length and offset, besides retensioning soft tissues. Clinical and radiological outcomes are good with low complications rates.
    UNASSIGNED: The modular neck adapter system seems to be a good surgical procedure for recurrent dislocation of THA, especially in case of a second THAr surgery. However, the main indication of adapter use remains the isolated acetabular cup revision. The related complications are rare: the worst is the re-dislocation due to an insufficient stem version and length correction. Re-dislocation rates reported in literature vary from 5.2% to 15%. Corrosion or fretting of the modular system are not reported in literature.
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  • 文章类型: Journal Article
    背景:模块化股骨组件允许在翻修全髋关节置换术(THA)中针对患者进行髋关节几何形状的恢复和广泛的骨缺损的重建;但是,模块化植入物的潜在问题,如锥形腐蚀和植入物骨折的风险继续受到关注。本研究的目的是评估由于无菌性松动和假体周围骨折而进行的翻修手术后的无骨水泥模块化翻修茎的临床和放射学结果,并在中期评估这些患者的患者报告结果指标(PROM)随访。
    方法:在本研究中,在平均7.7年的随访时间内,对我们机构采用模块化无骨水泥茎设计(MRP-TITAN茎)进行初次翻修THA的75例患者进行了回顾性评估.进行Kaplan-Meier生存分析,以任何原因翻修股骨组件为终点。哈里斯-臀部得分,加州大学洛杉矶分校活动得分,使用遗忘关节评分和SF-12评分进行临床评估.我们使用Wilcoxon符号秩检验比较术前和术后临床评分。
    结果:在平均7.7年(范围2.4-14年)的随访中,以任何原因重新修订终点茎的总生存率为85.4%。无菌性松动组的茎存活率为89.5%,假体周围骨折组为78.3%,两组之间无统计学差异(p=0.107)。由于锥形骨折,一名患者必须进行修正。PROM在最新的后续行动中得到了显着改善,和影像学评估显示该队列中所有茎的全骨整合。
    结论:使用模块化无骨水泥钛修订茎的修订THA在该队列中的中长期随访中显示出足够的临床和放射学结果。无水泥翻修茎是一个有用的治疗选择,以恢复解剖,特别是在畸形的髋关节和复杂的翻修髋关节置换术中。然而,存在一些与机械故障风险增加相关的显著缺点,例如腐蚀/微动损伤和植入物断裂。未来有必要进行高质量的前瞻性研究,并进行更长的随访,以确认假定的优势。
    BACKGROUND: Modular femoral components allow for patient-specific restoration of hip joint geometry and the reconstruction of extensive bone defects in revision total hip arthroplasty (THA); however, potential problems of modular implants such as taper corrosion and the risk of implant fracture continue to be of concern. The aim of the present study was to evaluate the clinical and radiological results of a cementless modular revision stem following revision surgery due to aseptic loosening and periprosthetic fracture and to assess patient-reported outcome measures (PROMs) in these patients at mid-term follow-up.
    METHODS: In this study, a consecutive cohort of 75 patients who underwent primary revision THA at our institution using a modular cementless stem design (MRP-TITAN stem) was retrospectively evaluated at a mean follow-up of 7.7 years. Kaplan-Meier survivorship analyses were performed with revision of the femoral component for any reason as the end point. The Harris-Hip Score, the UCLA Activity Score, the Forgotten Joint Score and the SF-12 Score were used for clinical assessment. We used the Wilcoxon signed rank test to compare pre- and postoperative clinical scores.
    RESULTS: Overall stem survival with the endpoint stem re-revision for any reason was 85.4% at a mean follow-up of 7.7 years (range 2.4-14 years). Stem survival was 89.5% in the aseptic loosening group and 78.3% in the periprosthetic fracture group with no statistically significant difference between both groups (p = 0.107). One patient had to be revised due to taper fracture. PROMs improved significantly up to the latest follow-up, and radiographic evaluation showed full osseointegration of all stems in this cohort.
    CONCLUSIONS: Revision THA using a modular cementless titanium revision stem demonstrated adequate clinical and radiological results at mid- to long-term follow-up in this cohort. Cementless revision stems are a useful treatment option to restore the anatomy, especially in deformed hips and in complex revision hip arthroplasty. However, there are some significant disadvantages related to an increased risk of mechanical failure such as corrosion/fretting damage and implant fracture. Future high-quality prospective studies with longer follow-up are necessary to confirm the supposed advantages.
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  • 文章类型: Comparative Study
    目的:评价预防性闭合切口负压伤口治疗(ciNPWT)与常规敷料相比,预防髋膝关节翻修术后假体周围感染(PJI)的有效性。
    方法:五个数据库(MEDLINE,Embase.,Emcare,CINAHL和Scopus)进行了搜索,没有日期或语言限制。两名独立审稿人根据纳入的3项研究的纳入标准和方法学质量对文章进行了评估。使用定制的数据工具提取数据,并包括干预措施,研究方法和感兴趣的结果。进行了荟萃分析,结果以森林地块的叙事形式呈现。
    结果:三项研究,一项随机对照试验和两项准实验研究,包括136名干预参与者和228名对照参与者(样本364)。与保守敷料组相比,ciNPWT组的PJI率降低(2[1.47%]vs27[11.84%])。ciNPWT队列的再手术率低于常规队列(4[2.94%]vs35[15.35%])。与常规敷料组相比,ciNPWT组的伤口并发症发生率显着降低(14[10.29%]v85[37.28),p=<0.001)。
    结论:预防性应用cINPWT可有效减少伤口并发症,髋关节和膝关节置换术后的PJI和再次手术。ciNPWT的增加成本在减少伤口并发症方面可能是合理的,PJI和再手术。正在进行的试验确定在髋关节和膝关节置换术后预防性应用ciNPWT是否有利于预防PJI,特别是在具有其他合并症的高风险患者中。
    OBJECTIVE: To evaluate the effectiveness of prophylactic closed incision negative pressure wound therapy (ciNPWT) compared to conventional dressings in the prevention of periprosthetic joint infection (PJI) post hip and knee revision arthroplasty surgery.
    METHODS: Five databases (MEDLINE, Embase., Emcare, CINAHL and Scopus) were searched with no date or language limits. Two independent reviewers assessed articles against the inclusion criteria and methodological quality of the 3 included studies. Data was extracted using a customised data tool and included the intervention, study methods and outcomes of interest. A meta-analysis was performed, and results presented in narrative form with forest plots.
    RESULTS: The three studies, one randomized control trial and two quasi-experimental studies, included 136 intervention and 228 control participants (Sample 364). The PJI rate decreased in the ciNPWT cohort compared to the conservative dressing cohort (2 [1.47%] vs 27 [11.84%]). The reoperation rate was lower in the ciNPWT cohort versus the conventional cohort (4 [2.94%] vs 35 [15.35%]). The rate of wound complications was significantly decreased in the ciNPWT cohort compared to the conventional dressing cohort (14 [10.29%] v 85 [37.28), p=<0.001).
    CONCLUSIONS: Prophylactic application of ciNPWT may be effective in reducing wound complications, PJI and reoperation post hip and knee revision arthroplasty surgery. The added cost of ciNPWT may be justified in the reduction of wound complications, PJI and reoperation. Ongoing trials determining if the prophylactic application of ciNPWT post hip and knee revision arthroplasty surgery is beneficial in preventing PJI particularly in high risk patients with additional comorbidities are warranted.
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  • 文章类型: Journal Article
    目的:未能恢复天然髋关节的股骨偏移是髋关节置换术功能失调的潜在原因。这项研究的目的是报告我们在修订THA中使用模块化头颈适配器的经验,具体分析其作为纠正股骨偏移略微减少的工具的有用性。
    方法:这是一项回顾性单中心研究,包括2017年1月至2022年3月在我们机构进行的所有髋关节翻修,其中使用了BioBallTM头颈金属适配器。术前和一年随访改良Merled\'Aubigné髋关节评分用于评估功能结局。
    结果:共纳入34例供修订的病例,头颈适配器系统专门用于六名患者(17.6%),以增加股骨偏移,保留髋臼和股骨组件。在这个亚组患者中,初次THA后的平均偏移减少为6.6mm(4.0-9.1),相当于平均16.3%的股骨偏移减少。中位改良Merled'Aubigné评分从术前的13.3升至一年随访时的16.2。
    结论:使用头颈适配器是一种安全可靠的手术,可以使外科医生在功能失调的THA中容易地纠正股骨偏移略微减小,而无需修改固定良好的假体组件。
    Failure to restore the femoral offset of the native hip is a potential cause of dysfunctional hip arthroplasty. The aim of this study was to report our experience of using a modular head-neck adapter in revision THA, specifically analyzing its usefulness as a tool to correct a slightly diminished femoral offset.
    This was a retrospective single-center study including all hip revisions performed at our institution from January 2017 to March 2022 where the BioBallTM head-neck metal adapter was used. The preoperative and one year follow-up modified Merle d\'Aubigné hip score was used to evaluate functional outcomes.
    Of a total of 34 cases included for revision, the head-neck adapter system was used specifically in six patients (17.6%) to increase femoral offset, retaining both the acetabular and femoral components. In this subgroup of patients, mean offset decrease after primary THA was 6.6 mm (4.0-9.1), equivalent to a mean 16.3% femoral offset reduction. The median modified Merle d\'Aubigné score went from 13.3 preoperatively to 16.2 at one year follow-up.
    The use of a head-neck adapter is a safe and reliable procedure that may allow the surgeon to easily correct a slightly diminished femoral offset in a dysfunctional THA without the need to revise well-fixed prosthetic components.
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  • 文章类型: Observational Study
    背景:在三级医院的质量管理项目中,在使用单中心的髋关节翻修术中实施使用晶体的目标导向液体治疗(GDFT)方案,前瞻性观察性研究。
    方法:选择择期髋关节翻修术的成年患者纳入本前瞻性研究。使用未校准的脉冲轮廓分析和平衡晶体,在先前发布的协议中优化了术中搏动量(SV)。围手术期GDFT的质量通过方案依从性进行评估,SV增加以及围手术期并发症的发生率。然后将结果与先前试验的两个不同的历史组进行比较:一个在整个手术中接受GDFT与胶体(前瞻性胶体组)和一个标准液体治疗(回顾性对照组)。统计分析构成探索性数据分析,结果以第25和第75百分位数的中位数表示,绝对和相对频率,并发症发生率使用无连续性校正的正态逼近法,进一步给出比例的95%置信区间.
    结果:66例患者接受了使用平衡晶体液的GDFT,并与130例使用平衡胶体的GDFT患者和130例未接受GDFT液体复苏的对照进行了比较。SV的增加相当(晶体:65(54-74ml;胶体:67.5(60-75.25ml)和注入的总体积(晶体:2575(2000-4210)ml;胶体:2435(1760-3480)ml;对照:2210(1658-3000)ml)。总体围手术期并发症发生率相似(晶体为42.4%(95CI30.3-55.2%),胶体为49.2%(95CI40.4-58.1%),与对照组相比更低:66.9%(95CI58.1-74.9))。有趣的是,在晶体内观察到出血并发症数量减少:30%(95CI19.6~42.9);胶体:43%(95CI34.4~52.0);对照组:62%(95CI52.6~69.9).麻醉后监护病房或重症监护病房的入院率以及住院时间没有差异。
    结论:在每天的临床常规中,使用GDFT方案和晶体在髋关节翻修术中的围手术期液体管理已成功实施。与以前没有GDFT的管理相比,围手术期并发症发生率降低,并且在使用胶体时具有可比性。
    背景:ClinicalTrials.gov标识符:NCT01753050。
    BACKGROUND: To implement a goal-directed fluid therapy (GDFT) protocol using crystalloids in hip revision arthroplasty surgery within a quality management project at a tertiary hospital using a monocentric, prospective observational study.
    METHODS: Adult patients scheduled for elective hip revision arthroplasty surgery were screened for inclusion in this prospective study. Intraoperatively stroke volume (SV) was optimized within a previously published protocol using uncalibrated pulse contour analysis and balanced crystalloids. Quality of perioperative GDFT was assessed by protocol adherence, SV increase as well as the rate of perioperative complications. Findings were then compared to two different historical groups of a former trial: one receiving GDFT with colloids (prospective colloid group) and one standard fluid therapy (retrospective control group) throughout surgery. Statistical analysis constitutes exploratory data analyses and results are expressed as median with 25th and 75th percentiles, absolute and relative frequencies, and complication rates are further given with 95% confidence intervals for proportions using the normal approximation without continuity correction.
    RESULTS: Sixty-six patients underwent GDFT using balanced crystalloids and were compared to 130 patients with GDFT using balanced colloids and 130 controls without GDFT fluid resuscitation. There was a comparable increase in SV (crystalloids: 65 (54-74 ml; colloids: 67.5 (60-75.25 ml) and total volume infused (crystalloids: 2575 (2000-4210) ml; colloids: 2435 (1760-3480) ml; and controls: 2210 (1658-3000) ml). Overall perioperative complications rates were similar (42.4% (95%CI 30.3-55.2%) for crystalloids and 49.2% (95%CI 40.4-58.1%) for colloids and lower compared to controls: 66.9% (95%CI 58.1-74.9)). Interestingly, a reduced number of hemorrhagic complications was observed within crystalloids: 30% (95%CI 19.6-42.9); colloids: 43% (95%CI 34.4-52.0); and controls: 62% (95%CI 52.6-69.9). There were no differences in the rate of admission to the post-anesthesia care unit or intensive care unit as well as the length of stay.
    CONCLUSIONS: Perioperative fluid management using a GDFT protocol with crystalloids in hip revision arthroplasty surgery was successfully implemented in daily clinical routine. Perioperative complications rates were reduced compared to a previous management without GDFT and comparable when using colloids.
    BACKGROUND: ClinicalTrials.gov identifier: NCT01753050.
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  • 文章类型: English Abstract
    Significant key points for a successful revision surgery in hip arthroplasty are as follows: identification of the implants, preoperative clinical diagnoses, planning (including alternatives) as well as establishing a surgical strategy, selection of revision implants and provision with special tools, secure fixation of acetabular and femoral components and the reconstruction of a stable joint without risk of dislocation or impingement. It seems to be obvious that most problems can be avoided by clear and concise decision-making. Some tips and tricks are also presented.
    UNASSIGNED: Die Eckpunkte für eine erfolgreiche Revisionsendoprothetik sind Identifikation der Implantate, präoperative klinische Diagnostik, Planung (einschließlich Alternativen) und Strategie, Weichteilmanagement, Auswahl der Revisionsimplantate und Bereitstellung von speziellen Instrumentarien, die sichere Fixation der azetabulären und femoralen Komponenten sowie abschließend die Herstellung stabiler Gelenkverhältnisse ohne Risiko für Luxation oder Impingement. Bei der Analyse von Komplikationen fällt immer wieder auf, wie sehr Probleme bei richtiger perioperativer Entscheidungsfindung vermeidbar gewesen wären. Tipps und Tricks für die Revisionsendoprothetik werden im nachfolgend dargestellt.
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  • 文章类型: Journal Article
    背景:准确评估髋臼缺损并设计精确可行的手术计划对于髋关节翻修术的积极结果至关重要。增材制造(AM)是一种打印物理对象模型的新技术。我们提出了一种基于AM模型的三维髋臼骨缺损分类系统,并进一步评估其在盲法条件下的信度和效度。
    方法:我们回顾了2014年1月至2019年12月在我们部门接受髋关节翻修术的104例连续患者,其中45例具有AM模型,并被纳入信度和效度测试。三位骨科医生根据我们提出的分类回顾性评估了这45例患者的骨缺损,制定了手术计划,并在2周后重复该过程。采用类内相关系数或kappa相关系数对分类结果和相应手术方案的信度和效度进行评估。
    结果:分类结果的信度和效度非常好。观察者间可靠性的平均初始类内相关系数为0.947,第二次测试时增加到0.972。观察者内部的可靠性范围为0.958至0.980。分类结果的有效性还显示0.951-0.967的高κ相关系数。在考虑相应的手术计划时,信度和效度也很好,类内相关系数和κ相关系数均超过0.9。
    结论:这种三维髋臼缺损分类具有良好的信度和效度。使用此分类系统和AM模型,骨缺损的准确评估和可靠的手术方案。AM辅助的这种分类是外科医生术前评估的有前途的工具。
    BACKGROUND: Accurate assessment of acetabular defects and designing precise and feasible surgical plans are essential for positive outcomes of hip revision arthroplasty. Additive manufacturing (AM) is a novel technique to print physical object models. We propose a three-dimensional acetabular bone defect classification system aided with AM model, and further assess its reliability and validity under blinded conditions.
    METHODS: We reviewed 104 consecutive patients who underwent hip revision arthroplasty at our department between January 2014 and December 2019, of whom 45 had AM models and were included in the reliability and validity tests. Three orthopedic surgeons retrospectively evaluated the bone defects of these 45 patients with our proposed classification, made surgical plans, and repeated the process after 2 weeks. The reliability and validity of the classification results and corresponding surgical plans were assessed using the intra-class correlation coefficient or kappa correlation coefficient.
    RESULTS: The reliability and validity of the classification results were excellent. The mean initial intra-class correlation coefficient for inter-observer reliability was 0.947, which increased to 0.972 when tested a second time. The intra-observer reliability ranged from 0.958 to 0.980. Validity of the classification results also showed a high kappa correlation coefficient of 0.951-0.967. When considering corresponding surgical plans, the reliability and validity were also excellent, with intra-class correlation coefficients and kappa correlation coefficients measuring all over 0.9.
    CONCLUSIONS: This three-dimensional acetabular defect classification has excellent reliability and validity. Using this classification system and AM models, accurate assessment of bone defect and reliable surgical plans could be achieved. This classification aided with AM is a promising tool for surgeons for preoperative evaluation.
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  • 文章类型: Journal Article
    目的是检验以下假设:在经股动脉植入锥形翻修茎的过程中,杆在远端尖端的固定导致假体周围骨折的发生率低。
    在PoproskyII型和IIIA型缺损(具有足够的峡部)的情况下,通过经股动脉入路对二百八十二个茎进行了修正,并在手术期间和影像学上进行了分析。截骨下方的意外假体周围骨折。
    在所有情况下,固定总是在股骨峡部远端部件的尖端实现。未观察到假体周围骨折。
    当股骨峡部完好无损时,在远端经股骨植入锥形翻修杆,可防止用杆绕过峡部,从而降低假体周围骨折的风险.知道公称直径和锥形区的远端开始处的直径之间的差异可以帮助创建这种固定技术,从而导致短的翻修茎。
    UNASSIGNED: The aim was to test the hypothesis that during transfemoral implantation of a conical revision stem, the fixation of the stem at the distal tip leads to a low rate of periprosthetic fractures.
    UNASSIGNED: Two hundred eighty-two stem revisions by a transfemoral approach in cases of Paprosky Type II and IIIA-defects (with a sufficient isthmus) were carried out and analyzed during and radiographically after the surgery for unintentional periprosthetic fractures below the osteotomy.
    UNASSIGNED: In all cases, fixation was always achieved at the tip of the distal component in the isthmus of the femur. No periprosthetic fractures were observed.
    UNASSIGNED: When the isthmus of the femur is intact, a transfemoral implantation of a tapered revision stem at the distal end reduces the risk of periprosthetic fractures by preventing bypassing the isthmus with the stem. Knowing the difference between the nominal diameter and the diameter at the distal start of the conical zone can help to create this fixation technique resulting in short revision stems.
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