Does three-dimensional planning of anterior acetabular component overhang affect short-term functional outcomes after robotic-assisted total hip arthroplasty?

IF 2.6 3区 医学 Q2 ORTHOPEDICS
Pascal Kouyoumdjian, Rémy Lavigne, Youssef Jamaleddine, Thomas Grosso, Rémy Coulomb
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引用次数: 0

Abstract

Purpose: Three-dimensional robotic planning may oblige the surgeon to accept an anterior overhang of the acetabular cup. Whether this planned overhang compromises short-term outcomes is unknown.

Methods: We retrospectively reviewed 437 consecutive robotic total hip arthroplasties (THA) performed between November 2018 and March 2022; 192 hips with complete 3-D screenshots and 12-month follow-up formed the study cohort. Anterior overhang on the definitive plan was graded minor (≤ 2 mm), moderate (between 2 and 4 mm), or major (≥ 4 mm). Primary outcome was psoas pain at one year, defined by pain on resisted-hip-flexion testing; psoas impingement was confirmed if infiltration or tenotomy was performed. Secondary endpoints were Harris Hip Score (HHS), Oxford Hip Score (OHS) and Forgotten Joint Score (FJS-12).

Results: Planned overhang occurred in 52 of 192 hips (27%): 33 minor, 18 moderate and one major. Psoas pain was more frequent with overhang (16% vs. 3.8%; p = 0.008); no differences were recorded for confirmed psoas impingement, groin pain, re-operation or revision of implants. Differences of mean HHS, OHS and FJS-12 at three and twelve months were non-significant between groups. Anterior wall index < 0.33, lateral center-edge angle < 25° and female sex are associated with overhang.

Conclusions: Minor anterior cup overhang is common in robotic THA. It increases the likelihood of clinical psoas impingement but does not impair early hip function or raise revision risk. Accepting minor overhang is clinically acceptable when necessary, provided patients are counselled about increased psoas pain risk and high-risk anatomies are monitored.

髋臼前构件悬垂的三维规划是否影响机器人辅助全髋关节置换术后的短期功能结局?
目的:三维机器人规划可能迫使外科医生接受髋臼杯前悬垂。目前尚不清楚这种计划中的过剩是否会危及短期结果。方法:回顾性分析2018年11月至2022年3月期间进行的437例连续机器人全髋关节置换术(THA);192个髋部有完整的3d截图和12个月的随访。确定平面上的前悬垂分为轻度(≤2mm)、中度(2 - 4mm)和重度(≥4mm)。主要终点是一年后的腰肌疼痛,由抗髋屈曲试验的疼痛来定义;如果进行浸润或肌腱切开术,则确认腰肌撞击。次要终点是哈里斯髋关节评分(HHS)、牛津髋关节评分(OHS)和遗忘关节评分(FJS-12)。结果:192例髋关节中52例(27%)发生计划性悬垂,其中轻度33例,中度18例,重度1例。腰大肌疼痛与悬垂更常见(16%比3.8%;p = 0.008);在确认的腰肌撞击、腹股沟疼痛、再手术或植入物翻修方面没有记录差异。3、12个月时HHS、OHS、FJS-12平均值组间差异无统计学意义。结论:轻度前杯悬垂在机器人THA中很常见。它增加了临床发生腰肌撞击的可能性,但不会损害早期髋关节功能或增加翻修风险。必要时接受轻微的悬垂在临床上是可以接受的,前提是告知患者腰肌疼痛风险增加,并监测高危解剖结构。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
International Orthopaedics
International Orthopaedics 医学-整形外科
CiteScore
5.50
自引率
7.40%
发文量
360
审稿时长
1 months
期刊介绍: International Orthopaedics, the Official Journal of the Société Internationale de Chirurgie Orthopédique et de Traumatologie (SICOT) , publishes original papers from all over the world. The articles deal with clinical orthopaedic surgery or basic research directly connected with orthopaedic surgery. International Orthopaedics will also link all the members of SICOT by means of an insert that will be concerned with SICOT matters. Finally, it is expected that news and information regarding all aspects of orthopaedic surgery, including meetings, panels, instructional courses, etc. will be brought to the attention of the readers. Manuscripts submitted for publication must contain a statement to the effect that all human studies have been approved by the appropriate ethics committee and have therefore been performed in accordance with the ethical standards laid down in the 1964 Declaration of Helsinki. It should also be stated clearly in the text that all persons gave their informed consent prior to their inclusion in the study. Details that might disclose the identity of the subjects under study should be omitted. Reports of animal experiments must state that the "Principles of laboratory animal care" (NIH publication No. 85-23, revised 1985) were followed, as well as specific national laws (e.g. the current version of the German Law on the Protection of Animals) where applicable. The editors reserve the right to reject manuscripts that do not comply with the above-mentioned requirements. The author will be held responsible for false statements or for failure to fulfil the above-mentioned requirements.
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