Bhatt Fenil R, Orosz Lindsay D, Tewari Anant, Boyd David, Roy Rita, Good Christopher R, Schuler Thomas C, Haines Colin M, Jazini Ehsan
Virginia Spine Institute, Reston, VA, USA.
National Spine Health Foundation, Reston, VA, USA.
Global Spine J. 2023 Sep;13(7):2047-2052. doi: 10.1177/21925682211069321. Epub 2022 Jan 10.
Prospective cohort study.
In spine surgery, accurate screw guidance is critical to achieving satisfactory fixation. Augmented reality (AR) is a novel technology to assist in screw placement and has shown promising results in early studies. This study aims to provide our early experience evaluating safety and efficacy with an Food and Drug Administration-approved head-mounted (head-mounted device augmented reality (HMD-AR)) device.
Consecutive adult patients undergoing AR-assisted thoracolumbar fusion between October 2020 and August 2021 with 2 -week follow-up were included. Preoperative, intraoperative, and postoperative data were collected to include demographics, complications, revision surgeries, and AR performance. Intraoperative 3D imaging was used to assess screw accuracy using the Gertzbein-Robbins (G-R) grading scale.
Thirty-two patients (40.6% male) were included with a total of 222 screws executed using HMD-AR. Intraoperatively, 4 (1.8%) were deemed misplaced and revised using AR or freehand. The remaining 218 (98.2%) screws were placed accurately. There were no intraoperative adverse events or complications, and AR was not abandoned in any case. Of the 208 AR-placed screws with 3D imaging confirmation, 97.1% were considered clinically accurate (91.8% Grade A, 5.3% Grade B). There were no early postoperative surgical complications or revision surgeries during the 2 -week follow-up.
This early experience study reports an overall G-R accuracy of 97.1% across 218 AR-guided screws with no intra or early postoperative complications. This shows that HMD-AR-assisted spine surgery is a safe and accurate tool for pedicle, cortical, and pelvic fixation. Larger studies are needed to continue to support this compelling evolution in spine surgery.
前瞻性队列研究。
在脊柱手术中,精确的螺钉引导对于实现满意的固定至关重要。增强现实(AR)是一种辅助螺钉置入的新技术,早期研究已显示出有前景的结果。本研究旨在提供我们使用美国食品药品监督管理局批准的头戴式(头戴式设备增强现实(HMD-AR))设备评估安全性和有效性的早期经验。
纳入2020年10月至2021年8月期间接受AR辅助胸腰椎融合术且随访2周的连续成年患者。收集术前、术中和术后数据,包括人口统计学信息、并发症、翻修手术和AR性能。术中使用3D成像,采用Gertzbein-Robbins(G-R)分级量表评估螺钉准确性。
纳入32例患者(男性占40.6%),共使用HMD-AR置入222枚螺钉。术中,4枚(1.8%)被判定位置不当,通过AR或徒手操作进行了修正。其余218枚(98.2%)螺钉置入准确。术中无不良事件或并发症发生,且在任何情况下均未放弃AR技术。在208枚经3D成像确认由AR置入的螺钉中,97.1%被认为临床准确(A级占91.8%,B级占5.3%)。在2周的随访期间,无早期术后手术并发症或翻修手术。
这项早期经验研究报告了218枚AR引导螺钉的总体G-R准确性为97.1%,术中及术后早期均无并发症。这表明HMD-AR辅助脊柱手术是一种用于椎弓根、皮质和骨盆固定的安全且准确的工具。需要更大规模的研究来继续支持脊柱手术中的这一引人注目的进展。