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直接前方入路联合传统器械与机器人后外侧入路在原发性骨关节炎初次全髋关节置换术中的应用:一项病例对照研究。

Direct anterior approach with conventional instruments versus robotic posterolateral approach in elective total hip replacement for primary osteoarthritis: a case-control study.

机构信息

Unità di Ortopedia e Traumatologia, IRCCS Ospedale San Raffaele, Via Olgettina 60, 20132, Milan, Italy.

Università Vita-Salute San Raffaele, Via Olgettina 58, 20132, Milan, Italy.

出版信息

J Orthop Traumatol. 2024 Feb 21;25(1):9. doi: 10.1186/s10195-024-00753-7.

Abstract

BACKGROUND

The purpose of this study is to compare peri-operative and short-term outcomes in patients who underwent elective total hip replacement (THA) for primary osteoarthritis (OA) with direct anterior approach (DAA) versus a pair-matched cohort of patients who underwent robotic-assisted THA with posterolateral approach.

MATERIALS AND METHODS

Data from consecutive patients who underwent elective hip replacement from 2021 to 2023 for primary OA were retrospectively retrieved and divided into two groups: the DAA group, who underwent THA with the DAA approach using conventional instruments, and the robotic posterolateral (R-PL group), who underwent robot arm-assisted THA with the posterolateral approach. Comparative assessed outcomes were: operative time, radiographical implant positioning, intake of rescue analgesics, blood loss, transfusion rate, leg length discrepancy and functional outcomes (Harris hip score and forgotten joint score).

RESULTS

A total of 100 pair-matched patients were retrieved with a mean age of 66.7 ± 10.7 (range: 32-85) years and a mean follow-up of 12.8 ± 3.6 (range: 7-24) months. No differences in patients' characteristics were detected. Patients in the R-PL group required less rescue tramadol (p > 0.001), ketorolac (p = 0.028) and acetaminophen (p < 0.001). There was no significant difference in the operative time between (MD = 5.0 min; p = 0.071). Patients in the DAA group had significantly lower Hb levels at day 1 (p = 0.002) without significant differences in transfusion rate (p = 0.283). Patients in the R-PL group had shorter length of stay (LOS) with a mean difference of 1.8 days [p < 0.001; 95% confidence interval (CI) 1.4-2.3]. No difference in clinical outcomes was found [leg length discrepancy (LLD), p = 0.572; HHS, p = 0.558; forgotten joint score (FJS), p = 0.629]. No radiographical differences were measured in cup inclination (MD = 2.0°, p = 0.069), malpositioning [odd ratio (OR) = 0.2; p = 0.141], stem alignment (OR = 0.3; p = 0.485) and stem sizing (OR = 1.5; p = 1.000). There was no difference in complication rate except for lateral femoral cutaneous nerve damage, which was higher in DAA group (p < 0.001).

CONCLUSIONS

R-PL and DAA THA had comparable short-term clinical and radiological outcomes along with similar complication rates. The R-PL group showed significantly lower Hb drop, rescue analgesic consumption and shorter LOS. This is a preliminary study and no strong recommendation can be provided. Further prospective randomized trials are requested to further investigate the cost-effectiveness of robotic surgery in THA.

LEVEL OF EVIDENCE

Level IV, case-control study.

摘要

背景

本研究旨在比较行初次全髋关节置换术(THA)治疗原发性骨关节炎(OA)的患者中,直接前侧入路(DAA)组与机器人辅助后侧入路(R-PL 组)配对队列患者的围手术期和短期结果。

材料与方法

回顾性检索了 2021 年至 2023 年间连续行择期髋关节置换术治疗原发性 OA 的患者数据,并将其分为两组:DAA 组采用传统器械行 DAA 入路 THA,R-PL 组采用机器人辅助后侧入路行机器人辅助 THA。比较评估的结果包括:手术时间、影像学植入物定位、补救性镇痛药的摄入、失血量、输血率、下肢长度差异和功能结果(Harris 髋关节评分和遗忘关节评分)。

结果

共检索到 100 对匹配患者,平均年龄为 66.7±10.7(范围:32-85)岁,平均随访 12.8±3.6(范围:7-24)个月。未发现患者特征存在差异。R-PL 组患者需要更少的曲马多(p>0.001)、酮咯酸(p=0.028)和对乙酰氨基酚(p<0.001)来缓解疼痛。手术时间无显著差异(MD=5.0 分钟;p=0.071)。DAA 组患者在术后第 1 天的血红蛋白水平显著降低(p=0.002),但输血率无显著差异(p=0.283)。R-PL 组患者的住院时间更短,平均差异为 1.8 天[ p<0.001;95%置信区间(CI)1.4-2.3]。在临床结果方面未发现差异[下肢长度差异(LLD),p=0.572;Harris 髋关节评分(HHS),p=0.558;遗忘关节评分(FJS),p=0.629]。影像学上测量的杯倾斜度(MD=2.0°,p=0.069)、错位情况[比值比(OR)=0.2;p=0.141]、柄对准情况(OR=0.3;p=0.485)和柄尺寸(OR=1.5;p=1.000)无差异。除股外侧皮神经损伤外,两组并发症发生率无差异(p<0.001)。

结论

R-PL 和 DAA THA 具有相似的短期临床和影像学结果,并发症发生率相似。R-PL 组血红蛋白下降、补救性镇痛药使用量和住院时间更短。这是一项初步研究,不能提供强烈的推荐。需要进一步的前瞻性随机试验来进一步研究机器人手术在 THA 中的成本效益。

证据水平

IV 级,病例对照研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b033/10881946/11bcdb7301ce/10195_2024_753_Fig1_HTML.jpg

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