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Benchmarking THA Implant Combinations Using Data From a US Total Joint Replacement Registry. 使用美国全关节置换术注册中心的数据对THA植入物组合进行基准测试。
IF 4.2 2区 医学 Q1 ORTHOPEDICS Pub Date : 2025-12-18 DOI: 10.1097/corr.0000000000003799
Tanmaya D Sambare,Sung Jun Son,Hong Sun,Brian H Fasig,Elizabeth W Paxton,Nithin C Reddy,Matthew P Kelly,Heather A Prentice
BACKGROUNDBenchmarking is a surveillance methodology used to evaluate implants against predetermined standards at select time points after surgery. Receiving a benchmark indicates that an implant has acceptable revision-free survivorship based on a predefined set of standards. Assessing implant performance against benchmarks offers valuable insights for surgeons, industry, and regulatory bodies, and also serves as a foundation for future evidence-based research.QUESTIONS/PURPOSESWe sought to apply the benchmarking standards proposed by the International Society of Arthroplasty Registries (ISAR) International Prosthesis Benchmarking Working Group to our US-based healthcare system's total joint replacement registry and determine and identify THA implant constructs, as well as individual femoral stem and acetabular cup components, that received benchmarks at (1) early 2- and 5-year time points, (2) the midpoint 10-year time point, and (3) the late 15-year time point. As a secondary aim, (4) we sought to evaluate the consistency of these benchmarks when stratified by gender and age.METHODSData from our US-based healthcare system's total joint replacement registry was used to conduct a cohort study. The registry is a surveillance tool that collects a predefined set of information, including implants used, for all THAs performed within the healthcare system. Surgeons complete interoperative registry forms via the electronic health record (EHR) for all THAs. This information is cross-checked with implant information, including manufacturer, implant, and catalog number, that is recorded into the EHR via barcode scan and then extracted into the registry. Patients are longitudinally followed for outcomes, including revision surgery, after their THA until they either leave the healthcare plan or they die, and identified revisions were manually validated through chart review. Primary THAs with highly crosslinked polyethylene acetabular liners for osteoarthritis were identified (2001 to 2024). The final eligible sample included 155,123 primary THAs performed by 509 surgeons at 67 hospitals. The mean ± SD patient age and BMI were 67 ± 10 years and 29 ± 5 kg/m2, respectively. More patients were women (57% [89,092 of 155,123]), White (79% [121,913 of 155,123]), and had an American Society of Anesthesiologists classification of 1 or 2 (64% [98,913 of 155,123]). The proportions of the cohort lost to follow-up through membership termination were 4%, 9%, 16%, and 22% at 2, 5, 10, and 15 years, respectively. The all-cause cumulative percent revision (CPR) and 95% confidence intervals (CIs) during follow-up were calculated using 1 - the Kaplan-Meier estimate. Standards proposed by the International Prosthesis Benchmarking Working Group to identify benchmarks were used; at each time point of interest, there needed to be at least 250 THAs still at risk at that time of follow-up to be considered for benchmarking, and 95% CIs rather than the CPR were compared with the ben
基准测试是一种监测方法,用于在手术后的选定时间点根据预定标准评估植入物。接受基准测试表明,基于预定义的一组标准,植入物具有可接受的无修订存活。根据基准评估植入物的性能为外科医生、行业和监管机构提供了有价值的见解,也为未来的循证研究奠定了基础。问题/目的我们试图将国际关节置换术注册协会(ISAR)国际假体基准工作组提出的基准标准应用于我们美国医疗保健系统的全关节置换术注册,并确定和识别THA植入物结构,以及单个股骨干和髋臼杯组件,这些组件在(1)早期2年和5年时间点,(2)中期10年时间点接受基准。(3) 15年后期的时间点。作为次要目标,(4)我们试图评估这些基准在按性别和年龄分层时的一致性。方法采用美国医疗保健系统的全关节置换术登记数据进行队列研究。注册中心是一种监视工具,用于收集医疗保健系统内执行的所有tha的预定义信息集,包括使用的植入物。外科医生通过电子健康记录(EHR)完成所有tha的手术登记表格。该信息与植入物信息交叉核对,包括制造商、植入物和目录号,这些信息通过条形码扫描记录在EHR中,然后提取到注册表中。患者在THA后进行纵向随访,包括翻修手术,直到他们离开医疗保健计划或死亡,并通过图表审查手动验证已确定的翻修。原发性tha与高度交联聚乙烯髋臼衬垫一起用于治疗骨关节炎(2001年至2024年)。最终合格样本包括67家医院509名外科医生进行的155,123例初级tha手术。平均±SD患者年龄为67±10岁,BMI为29±5 kg/m2。更多的患者是女性(57%[89,092 / 155,123]),白人(79%[121,913 / 155,123]),并且美国麻醉医师学会分级为1或2(64%[98,913 / 155,123])。在第2年、第5年、第10年和第15年,因会员终止而失去随访的队列比例分别为4%、9%、16%和22%。随访期间的全因累积百分比修正(CPR)和95%置信区间(ci)采用1 - Kaplan-Meier估计计算。采用了国际假肢基准工作组提出的确定基准的标准;在每个感兴趣的时间点,随访时至少需要250例仍有风险的tha被考虑作为基准,95%的ci而不是CPR与基准标准进行比较。对于早期的基准,如果95% CI的下限小于或等于2年的2%修订率标准,且小于或等于5年的3%标准,则构建体获得基准。对于10年的中点基准,5%的修订率为基准标准,并考虑相对于标准的优劣性。如果95% CI的上界≤5%,则接受较好的基准。对于非劣效性,边际设定为比标准高20%的相对修订率。因此,如果上界≤6%(高于5%标准20%,或非劣效边际1%),则接受非劣效基准;如果上界高于6%的非劣效性阈值,则植入物未接受基准测试。在15年的后期基准中,以6.5%的修订率基准标准也考虑了优劣性。上界≤6.5%为优标杆,上界≤7.8%为不优标杆,上界为> 7.8%为不优标杆。结果:我们考虑的大多数(86% [35 / 30])THA结构接受了2年的基准,这意味着95% CI的下限小于或等于2%修订率的基准标准,占87% (152,799 / 132,195)THA。五个植入系统不接受2年基准Zimmer-Biomet M / L锥形®/连续®(n = 9903风险仍在2年随访,CPR 3.1 (95% CI 2.8 - 3.5)), Zimmer-Biomet小梁金属®/连续(n = 2939, CPR 3.2 (95% CI 2.6 - 3.8)), Zimmer-Biomet Kinectiv®/连续(n = 2467, CPR 2.7 (95% CI 2.1 - 3.3)), Zimmer-Biomet M / L锥/小梁金属®(n = 2375, CPR 2.7 (95% CI 2.1 - 3.4)),和Zimmer-Biomet VerSys®/连续(n = 772, CPR 3.3 (95% CI 2.3 - 4.8))。 在5年时间点的30个构建中,90%(27个)获得了基准,这意味着95% CI的下限小于或等于3%的基准标准,在考虑的90%(146,465个中的131,904个)的tha中使用。M/L锥度/连续油管、Kinectiv/连续油管和VerSys/连续油管均未能获得2年和5年的基准测试。在10年中点评估了20个构式,其中13个构式获得了上界小于或等于5%基准标准的优质基准(80%[83,134 / 103,919]),另外5个构式获得了上界≤6%的非劣质基准(15%[15,528 / 103,919])。M/L锥度/小梁金属和Kinectiv/Continuum没有得到中点基准;这些构造也未能在较早的时间点接受基准测试。在15年后的时间点评估了8个构建体,其中7个获得了更好的基准,95% CI上限小于或等于6.5%的基准标准(评估的THAs中有97%[74,613 / 77,204])。M/L锥度/小梁金属再次未能获得基准,与之前的时间点一致。未能在性别和分层分析中获得基准的结构与已经在总体分析中确定的结构一致。建议的ISAR国际假体基准工作组基准方法被应用于美国的注册中心,并确定了不同的假体组合为优越或适当的表现,以及那些未能达到基准的修改率在预定义范围内。外科医生和卫生系统在为原发性THA选择植入物时应考虑到这些发现。未接受基准测试的植入物应仔细检查失败模式或进行直接比较研究。基准测试方法应纳入美国的注册管理机构。证据等级:III级,治疗性研究。
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引用次数: 0
Letter to the Editor: Editorial: AI-assisted Letters to the Editor-Scope of a Growing Ethical and Practical Concern, and CORR 's Approach to Managing It. 给编辑的信:社论:人工智能辅助给编辑的信——日益增长的伦理和实践关注的范围,以及CORR的管理方法。
IF 4.2 2区 医学 Q1 ORTHOPEDICS Pub Date : 2025-12-18 DOI: 10.1097/corr.0000000000003809
Timothy Daly,Jaime A Teixeira da Silva
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引用次数: 0
A Conversation With … Peter Singer PhD, Ethicist, Philosopher, and Author of Animal Liberation Now. 彼得·辛格博士,伦理学家,哲学家,《动物解放》的作者。
IF 4.2 2区 医学 Q1 ORTHOPEDICS Pub Date : 2025-12-16 DOI: 10.1097/corr.0000000000003802
Seth S Leopold
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引用次数: 0
CORR Insights®: What Patient Factors Are Associated With Clinician Likelihood to Order a Test in a Setting of Low Pretest Odds of Important Pathophysiology. CORR Insights®:哪些患者因素与临床医生在重要病理生理学低预测几率的情况下订购检测的可能性相关。
IF 4.4 2区 医学 Q1 ORTHOPEDICS Pub Date : 2025-12-15 DOI: 10.1097/CORR.0000000000003807
Alicia R Jacobson
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引用次数: 0
Reply to the Letter to the Editor: Factors That Increase the Risk of Prosthetic Joint Infection Within 90 Days After THA and TKA: A Nationwide Population-based Study. 致编辑的回复:THA和TKA术后90天内增加假体关节感染风险的因素:一项基于全国人群的研究。
IF 4.4 2区 医学 Q1 ORTHOPEDICS Pub Date : 2025-12-15 DOI: 10.1097/CORR.0000000000003804
Cheng-Ming Chou, Tsung-Che Chuang, Chen-Hao Chiang
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引用次数: 0
CORR Insights®: What Factors and Patient-reported Outcome Measures Are Associated With Stress Fracture After Periacetabular Osteotomy? CORR Insights®:髋臼周围截骨术后应力性骨折与哪些因素和患者报告的预后指标相关?
IF 4.2 2区 医学 Q1 ORTHOPEDICS Pub Date : 2025-12-15 DOI: 10.1097/corr.0000000000003806
Bridget K Ellsworth
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引用次数: 0
CORR Insights®: Posterior Tibial Slope Is Associated With the Chondral Wear Pattern of the Medial Tibial Plateau. CORR Insights®:胫骨后坡与胫骨内侧平台的软骨磨损模式有关。
IF 4.2 2区 医学 Q1 ORTHOPEDICS Pub Date : 2025-12-10 DOI: 10.1097/corr.0000000000003803
Charles N Cornell
{"title":"CORR Insights®: Posterior Tibial Slope Is Associated With the Chondral Wear Pattern of the Medial Tibial Plateau.","authors":"Charles N Cornell","doi":"10.1097/corr.0000000000003803","DOIUrl":"https://doi.org/10.1097/corr.0000000000003803","url":null,"abstract":"","PeriodicalId":10404,"journal":{"name":"Clinical Orthopaedics and Related Research®","volume":"13 1","pages":""},"PeriodicalIF":4.2,"publicationDate":"2025-12-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145711018","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Behind the Mask: My First Case-Not a Chip Shot. 面具背后:我的第一个案例——不是一个芯片射击。
IF 4.2 2区 医学 Q1 ORTHOPEDICS Pub Date : 2025-12-10 DOI: 10.1097/corr.0000000000003795
Steven E Zhang
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引用次数: 0
Is RAGE Expression in Flexor Tendon Synovium Associated With Carpal Tunnel Syndrome in Patients With Diabetes? 糖尿病患者屈肌腱滑膜RAGE表达与腕管综合征相关吗?
IF 4.2 2区 医学 Q1 ORTHOPEDICS Pub Date : 2025-12-10 DOI: 10.1097/corr.0000000000003800
Dong Uk Jin,Ji Sup Hwang,Hyun Sik Gong
BACKGROUNDCarpal tunnel syndrome (CTS) is the most common entrapment neuropathy and is more prevalent in patients with diabetes. However, the underlying mechanisms linking diabetes and CTS have not been fully elucidated. The advanced glycation end products (AGEs) and the receptor for AGEs (RAGE) are involved in chronic inflammation and diabetic complications, suggesting that this pathway may be relevant to the pathogenesis of CTS in patients with diabetes.QUESTIONS/PURPOSES(1) Is RAGE expressed in the flexor tendon synovium in patients with CTS, and if so, is it expressed more in patients with diabetes? (2) Is RAGE expression in the flexor tendon synovium associated with CTS severity?METHODSBetween February 2020 and March 2023, a total of 130 patients underwent open carpal tunnel release performed by a single highly experienced hand surgeon. Patients with peripheral neuropathies, cervical radiculopathy, diabetic polyneuropathy, systemic inflammatory diseases such as gout or rheumatoid arthritis, a history of wrist fracture, or previous wrist surgery were excluded. Patients who did not consent to tissue storage or whose consent was not documented were also excluded. As a result, flexor tendon synovium samples were available in the biobank for 72% (93 patients) of the initial cohort. Among these, 8% (7 of 93) of samples were excluded because of poor immunohistochemical staining quality, leaving 66% (86 patients) of the initial cohort for the final analysis. The mean ± SD age of the patients was 60 ± 12 years. Of the 86 patients, 81% (70) were female. CTS severity was classified according to the Bland scale as mild to moderate (Grades 1 to 3) or severe (Grades 4 to 6) based on electrophysiologic findings. In this cohort, 45% (39) had severe CTS and 21% (18) had diabetes. RAGE expression in the flexor tendon synovium was measured semiquantitatively by immunohistochemistry. The scoring method showed excellent interobserver reliability (intraclass correlation coefficient 0.92). RAGE expression was compared between patients with and without diabetes. Multivariable logistic regression analysis was performed to identify factors that were independently related to CTS severity.RESULTSHistopathologic analysis revealed that RAGE expression was predominantly observed in the vascular endothelial cells of the subsynovial connective tissue. Patients with diabetes had a greater RAGE staining index expression than those without diabetes (median [IQR] 8.5 [6.0 to 9.0] versus 8.0 [6.0 to 8.0], difference of medians 0.5; p = 0.03). For all patients, those with and without diabetes, RAGE staining index expression was not associated with CTS severity (OR 1.17 [95% confidence interval (CI) 0.94 to 1.44]; p = 0.16), BMI was not associated (OR 1.12 [95% CI 0.98 to 1.29]; p = 0.10), and only age was associated (OR 1.10 [95% CI 1.05 to 1.17]; p < 0.001). When stratified to only those patients with diabetes, after controlling for potentially confounding variables such as age
背景:腕管综合征(carpal tunnel syndrome, CTS)是最常见的压迫性神经病变,在糖尿病患者中更为常见。然而,将糖尿病和CTS联系起来的潜在机制尚未完全阐明。晚期糖基化终产物(AGEs)和AGEs受体(RAGE)参与慢性炎症和糖尿病并发症,提示该途径可能与糖尿病患者CTS的发病机制有关。(1) RAGE是否在CTS患者的屈肌腱滑膜中表达,如果有,是否在糖尿病患者中表达更多?(2)屈肌腱滑膜RAGE表达是否与CTS严重程度相关?方法:在2020年2月至2023年3月期间,共有130例患者接受了由一位经验丰富的手外科医生实施的开放式腕管松解术。排除有周围神经病变、颈神经根病、糖尿病多发性神经病变、全身炎性疾病如痛风或类风湿关节炎、腕部骨折史或既往腕部手术的患者。不同意组织储存或没有书面同意的患者也被排除在外。结果,初始队列中72%(93例)的屈肌腱滑膜样本在生物库中可用。其中,由于免疫组化染色质量差,有8%(93例中的7例)的样本被排除,留下66%(86例)的初始队列进行最终分析。患者平均±SD年龄为60±12岁。86例患者中,81%(70例)为女性。根据电生理结果,CTS的严重程度根据Bland量表分为轻度至中度(1至3级)或重度(4至6级)。在该队列中,45%(39人)患有严重CTS, 21%(18人)患有糖尿病。采用免疫组化半定量法检测RAGE在屈肌腱滑膜中的表达。评分方法具有良好的观察者间信度(类内相关系数0.92)。比较糖尿病患者和非糖尿病患者的RAGE表达。进行多变量logistic回归分析,以确定与CTS严重程度独立相关的因素。结果组织病理学分析显示RAGE主要表达于滑膜下结缔组织血管内皮细胞。糖尿病患者RAGE染色指数表达高于无糖尿病患者(中位数[IQR] 8.5[6.0 ~ 9.0]对8.0[6.0 ~ 8.0],中位数差异0.5;p = 0.03)。对于所有患者,无论是否患有糖尿病,RAGE染色指数的表达与CTS严重程度无关(OR 1.17[95%可信区间(CI) 0.94至1.44];p = 0.16), BMI无关(OR 1.12 [95% CI 0.98 ~ 1.29]; p = 0.10),只有年龄相关(OR 1.10 [95% CI 1.05 ~ 1.17]; p < 0.001)。当只对糖尿病患者进行分层时,在控制了年龄、BMI等潜在的混杂变量后,在我们研究的变量中,只有RAGE染色指数表达与CTS相关(OR 3.40 [95% CI 1.10 ~ 10.53]; p = 0.03),这是本研究的关键发现。结论rage介导的机制可能参与糖尿病相关CTS的病理生理机制。需要进一步的研究来阐明RAGE相关的分子通路,并确定靶向RAGE是否可能成为影响疾病进展或手术结果的潜在治疗策略。证据等级:诊断性研究III级。
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引用次数: 0
Preliminary Surgical Findings and Complications After National Centralization of Pediatric Bone Sarcoma Resections in the Netherlands: A Benchmarking Study. 荷兰儿童骨肉瘤全国集中切除后的初步手术结果和并发症:一项基准研究。
IF 4.2 2区 医学 Q1 ORTHOPEDICS Pub Date : 2025-12-10 DOI: 10.1097/corr.0000000000003782
Lorenz H M van Schalkwijk,Jasper M van der Zee,Roelof van Ewijk,Johannes H M Merks,Jos A M Bramer,Hendrik W B Schreuder,Lianne M Haveman,Michiel A J van de Sande,Lizz van der Heijden
BACKGROUNDPediatric bone sarcomas are rare malignancies that are usually treated with specialized multimodal care to allow specialized oncologists to gain experience and provide expertise in treatment. In the Netherlands, oncologic care for all pediatric cancers, including pediatric bone sarcoma, has been centralized in one tertiary referral center for pediatric oncology since 2018. Surgical decision-making is not solely driven by whether limb salvage is oncologically feasible, but rather by a comprehensive shared decision-making process in which all surgical options are carefully weighed against one another. This includes not only oncologic safety, but also expected functional outcomes such as sports participation, the risk of complications, and the burden of additional surgeries that may be performed over time. By openly discussing these trade-offs with patients and families, we aim to reach a decision that best aligns with the family's values and expectations, and thereby with the child's long-term well-being and priorities. The objective of this study was to provide benchmark values for future comparisons of short-term perioperative and postoperative outcomes.QUESTIONS/PURPOSESWe evaluated results following the national centralization of pediatric bone sarcoma care in the Netherlands to determine: (1) What were the intraoperative complications and blood loss? (2) What was the proportion of patients who achieved R0 margins? (3) What were the 30- and 90-day complications after surgical treatment, and what proportion had a delay in resuming chemotherapy?METHODSBetween 2018 and 2024, a total of 157 children age 0 to 18 years underwent surgical resection for primary malignant bone sarcoma. We excluded 42 patients who had centralized systemic treatment but underwent surgery at referring adult sarcoma centers and 16 patients who had an axial localization. We included 99 patients who underwent surgery at the national pediatric oncology center for osteosarcoma (n = 69), Ewing sarcoma (n = 25), or other (n = 5); the extremities were involved in most patients (91% [90]). Of these, none were lost to follow-up; 1% (1) died within the first year from other causes. Seventy percent (69 of 99) had ≥ 1 year of follow-up. Ninety-day postoperative outcomes were evaluated to capture clinically relevant short-term treatment morbidity and care continuity. Tumor and treatment characteristics were retrospectively analyzed. The median (IQR) age was 13 years (9 to 15); 36% (36) were female. The median (IQR) follow-up time was 18 months (8 to 43). Among the 99 included patients, surgical procedures included limb-sparing surgery (68% [67]), amputation (15% [15]), rotationplasty (17% [17]), and other (1% [1]). Medical charts were reviewed for blood loss and surgical margins. Postoperative complications (using the Clavien-Dindo and the Henderson classifications) are reported from short-term (< 30 days) to midterm (< 90 days).RESULTSThree percent (3 of 99) of patients had s
背景:儿童骨肉瘤是一种罕见的恶性肿瘤,通常采用专业的多模式治疗,以使专业的肿瘤学家获得治疗经验并提供专业知识。在荷兰,自2018年以来,包括小儿骨肉瘤在内的所有儿科癌症的肿瘤治疗都集中在一个儿科肿瘤三级转诊中心。手术决策不仅仅是由肢体保留在肿瘤上是否可行驱动的,而是由一个全面的共同决策过程驱动的,在这个过程中,所有的手术选择都是仔细权衡的。这不仅包括肿瘤安全性,还包括预期的功能结果,如运动参与,并发症的风险,以及随着时间的推移可能进行的额外手术的负担。通过与患者和家属公开讨论这些权衡,我们的目标是达成一个最符合家庭价值观和期望的决定,从而符合孩子的长期福祉和优先事项。本研究的目的是为将来短期围手术期和术后结果的比较提供基准值。问题/目的:我们评估了荷兰儿童骨肉瘤全国集中治疗后的结果,以确定:(1)术中并发症和出血量是什么?(2)达到R0边际的患者比例是多少?(3)手术治疗后30天和90天的并发症是什么,延迟恢复化疗的比例是多少?方法:2018年至2024年间,共有157名0至18岁的儿童接受了原发性恶性骨肉瘤手术切除。我们排除了42例接受集中全身治疗但在转诊成人肉瘤中心接受手术的患者和16例轴向定位的患者。我们纳入了99例在国家儿童肿瘤中心因骨肉瘤(n = 69)、尤文氏肉瘤(n = 25)或其他(n = 5)而接受手术的患者;大多数患者(91%[90])累及四肢。其中,没有人因随访而丢失;1%(1)在第一年内死于其他原因。70%(69 / 99)患者随访≥1年。对术后90天的结果进行评估,以获取临床相关的短期治疗发病率和护理连续性。回顾性分析肿瘤及治疗特点。中位(IQR)年龄为13岁(9 ~ 15岁);36%(36例)为女性。中位(IQR)随访时间为18个月(8 ~ 43)。在纳入的99例患者中,手术方式包括保肢手术(68%[67])、截肢(15%[15])、旋转成形术(17%[15])和其他(1%[1])。我们回顾了失血和手术边缘的病历。术后并发症(使用Clavien-Dindo和Henderson分类)从短期(< 30天)到中期(< 90天)报道。结果99例患者中有3例(3%)出现严重的术中并发症,出血量中位数(范围)为100 mL(50 ~ 4000)。94%(93)的患者实现了R0边缘。22%(22)的患者在术后30天内出现任何并发症(感染、伤口裂开、压疮、骨折、神经血管),11%(11)的患者因并发症再次手术。最常见的并发症是感染和/或伤口裂开(11%);发生一例骨折。术后化疗的中位(IQR)时间为18天(16 ~ 22天)。7%(7)的患者因并发症在术后28天内开始化疗。在第90天,假体关节感染(Henderson 4a型)通过清创、抗生素和种植体保留(DAIR)(4%[2])或两阶段翻修(2%[2])进行治疗。结论虽然并发症较多,但很少延误术后化疗。尽量减少术后并发症可能有助于改善治疗的连续性和效果。在国家集中护理之后,这一初步基准为未来研究中评估手术效果提供了有临床意义的围手术期和术后结果指标;术后晚期并发症和肿瘤预后将在随访时间延长后报告。证据等级:III级,治疗性研究。
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