常规和机器人膝关节置换术结果的比较:一项回顾性观察研究。

Mehmet Anıl Süzer, Erdem Şahin, Mehmet Özgür Özhan, Umut Kara
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引用次数: 0

摘要

目的:本研究旨在确定由腰麻-硬膜外联合麻醉(CSEA)和控制性降压麻醉(CHA)组成的标准麻醉方案是否适用于常规全膝关节置换术(cTKA),可以为机器人全膝关节置换术(rTKA)提供同样有效的麻醉条件。方法:从2021年至2023年接受选择性单侧cTKA(n=52)或rTKA(n=61)但不使用止血带的113名患者(中位年龄=67岁;年龄范围=55-84)的医疗记录中收集数据。主要的结果指标是在手术过程中,麻醉方法没有提供足够的运动和感觉阻滞,不得不转为全身麻醉的患者的比率。次要的结果指标是比较围手术期的变量,包括疼痛评分、镇痛药消耗、失血、输血和并发症。结果:rTKA组有6名患者(11.5%)在160-180分钟因手术膝盖疼痛和/或手术腿在手术过程中的运动而需要将CSEA转换为全身麻醉,而cTKA组则没有/没有(P=0.008)。这些患者的运动和感觉阻滞早于总手术时间终止。rTKA组的平均总手术时间显著高于cTKA组(151.25±24.51(120-240)分钟vs.116.72±4.99(105-125)分钟,P<.001)。第11例病例发生后,rTKA的总手术时间趋于逐渐减少,这表明手术性能呈学习曲线。与之前的5名患者相比,第11例患者后仅1名患者需要转为全身麻醉。rTKA组在术后0小时和0至4小时的平均疼痛评分和抢救性镇痛药消耗较高(P<0.05),但在以下时间点相似(P>0.05),并且并发症发生率相似(P>0.05)。rTKA组的出院时间更高(P<0.05)。结论:尽管我们的标准CSEA方案在11.5%的rTKA患者中由于手术过程中运动和感觉障碍的消退而失败,CSEA技术结合控制性降压麻醉在rTKA组的其余患者中提供了与cTKA组相似的麻醉条件。如果对这种新型外科技术进行干预以延长CSEA的持续时间,CSEA可能被认为是治疗rTKA的有效和安全的麻醉方法。证据级别:三级,治疗性研究。
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Comparison of conventional and robotic knee arthroplasty results: A retrospective observational study.

Objective: This study aimed to determine whether a standard anesthetic protocol consisting of combined spinal epidural anesthesia (CSEA) in conjunction with controlled hypotensive anesthesia (CHA), which was used for conventional total knee arthroplasty (cTKA), could provide equally effective anesthetic conditions for robotic total knee arthroplasty (rTKA).

Methods: Data were collected from the medical records of 113 patients (median age=67 years; age range=55-84) who underwent elective unilateral cTKA (n=52) or rTKA (n=61) without a tourniquet from 2021 to 2023. The primary outcome measure was the rate of patients whose anesthetic method did not provide adequate motor and sensory block during the surgery and had to be converted to general anesthesia. The secondary outcome measure was to compare perioperative variables, including pain scores, analgesic consumption, blood loss, transfusions, and complications.

Results: In 6 patients (11.5%) in group rTKA, it was required to convert CSEA to general anesthesia at 160-180 minutes due to the pain at the operative knee and/or to the movement of the operative leg during surgery compared to none / zero in group cTKA (P=.008). Motor and sensory blocks terminated earlier than the total surgery time in those patients. Mean total surgery time was significantly higher in group rTKA than in group cTKA (151.25 ± 24.51 (120-240) minutes vs. 116.72 ± 4.99 (105-125) minutes, P < .001). Total surgery times tended to decrease gradually in group rTKA after the 11th case, indicating a learning curve for surgical performance. Conversion to general anesthesia was required only in 1 patient after the 11th case compared to the previous 5 patients. Mean pain scores and rescue analgesic consumption were higher in group rTKA at postoperative 0 hour and between 0 and 4 hours (P < .05) but similar at the following time points (P > .05). Blood loss, transfusion, and complication rates were similar (P > .05). Hospital discharge times were higher in group rTKA (P < .05).

Conclusion: Although our standard CSEA protocol failed due to the regression of motor and sensory block during surgery in 11.5% of patients in rTKA, the CSEA technique combined with controlled hypotensive anesthesia provided similar anesthetic conditions in the remaining patients in group rTKA as in group cTKA. The CSEA may be considered an effective and safe anesthetic method for rTKA if interventions are applied to extend the duration of the CSEA for this novel surgical technique.

Level of evidence: Level III, Therapeutic Study.

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