金属全髋关节置换术患者假瘤与感染并发症之间的关系。

IF 4.9 1区 医学 Q1 ORTHOPEDICS
Justin Leal, Christopher T Holland, Niall H Cochrane, Thorsten M Seyler, William A Jiranek, Samuel S Wellman, Michael P Bolognesi, Sean P Ryan
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引用次数: 0

摘要

目的:本研究旨在评估继发于金属对金属(MoM)植入物的假性瘤形成史与假体周围关节感染(PJI)率之间的关系,并确定提示这些患者感染的血沉和CRP阈值。我们假设假瘤患者的感染风险会增加:我们回顾性地确定了2000年8月至2014年3月期间1171例MoM关节的全髋关节置换术(THA)患者。其中,328 名患者接受了金属伪影减少序列磁共振成像检查,并接受了至少两年的临床随访,符合我们的纳入标准。收集的数据包括详细的人口统计学资料、手术指征、侧位、使用的植入物、假性肿瘤病史以及相应的术前血沉(mm/hr)和CRP(mg/dl)水平。采用多变量逻辑回归模型评估 PJI 和假瘤病史,并绘制接收器操作特征曲线评估 ESR 和 CRP 的诊断能力,以确定接受翻修手术的患者是否存在感染:所有已确定的MoM THAs的PJI发生率为3.5%(41/1,171),平均随访时间为10.9年(2.0至20.4年)。在纳入最终队列的患者中,8.2%(27/328)患有 PJI,平均随访时间为 12.2 年(2.3 至 20.4 年)。在这批患者中,31.1%(102/328)有假瘤病史。这些患者的 PJI 发生率为 14.7%(15/102),高于无假瘤患者的 5.3%(12/226)(P = 0.008)。此外,逻辑回归分析显示假瘤病史与 PJI 之间存在关联(几率比 4.36(95% 置信区间 1.77 至 11.3);P = 0.002)。有假瘤病史与无假瘤病史患者的最佳 PJI 诊断临界值分别为:ESR 为 33.1 mm/hr 和 24.5 mm/hr;CRP 为 7.37 mg/dl 和 1.88 mg/dl:有MoM THA继发假瘤病史的患者比没有假瘤病史的患者感染的可能性更高。虽然这些患者应高度怀疑感染,但欧洲骨与关节感染学会公布的 ESR 和 CRP 临界值可能并不适合有假瘤病史的患者,因为提示 PJI 的 ESR 和 CRP 水平可能高于没有假瘤的患者。除非临床怀疑和实验室指标较低,否则强烈建议对这些患者进行抽吸等其他检查。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The relationship between pseudotumours and infected complications in patients who have undergone metal-on-metal total hip arthroplasty.

Aims: This study aims to assess the relationship between history of pseudotumour formation secondary to metal-on-metal (MoM) implants and periprosthetic joint infection (PJI) rate, as well as establish ESR and CRP thresholds that are suggestive of infection in these patients. We hypothesized that patients with a pseudotumour were at increased risk of infection.

Methods: A total of 1,171 total hip arthroplasty (THA) patients with MoM articulations from August 2000 to March 2014 were retrospectively identified. Of those, 328 patients underwent metal artefact reduction sequence MRI and had minimum two years' clinical follow-up, and met our inclusion criteria. Data collected included demographic details, surgical indication, laterality, implants used, history of pseudotumour, and their corresponding preoperative ESR (mm/hr) and CRP (mg/dl) levels. Multivariate logistic regression modelling was used to evaluate PJI and history of pseudotumour, and receiver operating characteristic curves were created to assess the diagnostic capabilities of ESR and CRP to determine the presence of infection in patients undergoing revision surgery.

Results: The rate of PJI for all identified MoM THAs was 3.5% (41/1,171), with a mean follow-up of 10.9 years (2.0 to 20.4). Of the patients included in the final cohort, 8.2% (27/328) had PJI, with a mean follow-up of 12.2 years (2.3 to 20.4). Among this cohort, 31.1% (102/328) had a history of pseudotumour. The rate of PJI in these patients was 14.7% (15/102), which was greater than those without pseudotumour, 5.3% (12/226) (p = 0.008). Additionally, logistic regression analysis showed an association between history of pseudotumour and PJI (odds ratio 4.36 (95% confidence interval 1.77 to 11.3); p = 0.002). Optimal diagnostic cutoffs for PJI in patients with history of pseudotumour versus those without were 33.1 mm/hr and 24.5 mm/hr for ESR and 7.37 mg/dl and 1.88 mg/dl for CRP, respectively.

Conclusion: Patients with history of pseudotumour secondary to MoM THA had a higher likelihood of infection than those without. While suspicion of infection should be high for these patients, ESR and CRP cutoffs published by the European Bone and Joint Infection Society may not be appropriate for patients with a history of pseudotumour, as ESR and CRP levels suggestive of PJI are likely to be higher than for those without a pseudotumour. Additional investigation, such as aspiration, is highly recommended for these patients unless clinical suspicion and laboratory markers are low.

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来源期刊
Bone & Joint Journal
Bone & Joint Journal ORTHOPEDICS-SURGERY
CiteScore
9.40
自引率
10.90%
发文量
318
期刊介绍: We welcome original articles from any part of the world. The papers are assessed by members of the Editorial Board and our international panel of expert reviewers, then either accepted for publication or rejected by the Editor. We receive over 2000 submissions each year and accept about 250 for publication, many after revisions recommended by the reviewers, editors or statistical advisers. A decision usually takes between six and eight weeks. Each paper is assessed by two reviewers with a special interest in the subject covered by the paper, and also by members of the editorial team. Controversial papers will be discussed at a full meeting of the Editorial Board. Publication is between four and six months after acceptance.
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