Urakawa Hikari, Sivaganesan Ahilan, Vaishnav Avani S, Sheha Evan, Qureshi Sheeraz A
25062Hospital for Special Surgery, New York, NY, USA.
Weill Cornell Medical College, New York, NY, USA.
Global Spine J. 2023 Apr;13(3):737-744. doi: 10.1177/21925682211006700. Epub 2021 Apr 28.
Retrospective cohort study.
To evaluate perioperative outcomes, accuracy of cage placement and radiation exposure in lateral lumbar interbody fusion (LLIF) using 3D intraoperative navigation (ION), compared to conventional 2D fluoroscopy only.
The perioperative outcomes and accuracy of cage placement were examined in all patients who underwent LLIF using ION (ION group) or fluoroscopy only (non-ION group) by a single surgeon. The radiation exposure was examined in patients who underwent stand-alone LLIF.
A total of 87 patients with 154 levels (ION 49 patients with 79 levels/ non-ION 38 patients with 75 levels) were included. There were no significant differences in operative time (ION 143.5 min vs. non-ION 126.0 min, = .406), time from induction end to surgery start (ION 31.0 min vs. non-ION 31.0 min, = .761), estimated blood loss (ION 37.5 ml vs. non-ION 50.0 ml, = .351), perioperative complications (ION 16.3% vs. non-ION 7.9%, = .335) and length of stay (ION 50.6 hours vs. non-ION 41.7 hours, = .841). No significant difference was found in the accuracy of cage placement ( = .279). ION did not significantly increase total radiation dose (ION 51.0 mGy vs. non-ION 47.4 mGy, = .237) and tended to reduce radiation dose during the procedure (ION 32.2 mGy vs. non-ION 47.4 mGy, = .932).
The perioperative outcomes, accuracy of cage placement and radiation exposure in LLIF using ION were comparable to those using fluoroscopy only. The use of ION in LLIF was feasible, safe and accurate and may reduce radiation dose to the surgeon and surgical team.
回顾性队列研究。
与仅使用传统二维荧光透视法相比,评估使用三维术中导航(ION)进行腰椎侧方椎间融合术(LLIF)的围手术期结果、椎间融合器放置的准确性以及辐射暴露情况。
由一名外科医生对所有接受使用ION的LLIF(ION组)或仅接受荧光透视法的患者(非ION组)进行围手术期结果和椎间融合器放置准确性的检查。对接受单纯LLIF的患者进行辐射暴露检查。
共纳入87例患者,154个节段(ION组49例患者79个节段/非ION组38例患者75个节段)。手术时间(ION组143.5分钟 vs. 非ION组126.0分钟,P = 0.406)、诱导结束至手术开始的时间(ION组31.0分钟 vs. 非ION组31.0分钟,P = 0.761)所、估计失血量(ION组37.5毫升 vs. 非ION组50.0毫升,P = 0.351)、围手术期并发症(ION组16.3% vs. 非ION组7.9%,P = 0.335)和住院时间(ION组50.6小时 vs. 非ION组41.7小时,P = 0.841)方面均无显著差异。椎间融合器放置的准确性方面未发现显著差异(P = 0.279)。ION并未显著增加总辐射剂量(ION组51.0毫戈瑞 vs. 非ION组47.4毫戈瑞,P = 0.237),且在手术过程中倾向于降低辐射剂量(ION组32.2毫戈瑞 vs. 非ION组47.4毫戈瑞,P = 0.932)。
使用ION进行LLIF的围手术期结果、椎间融合器放置的准确性和辐射暴露情况与仅使用荧光透视法相当。在LLIF中使用ION是可行、安全且准确的,并且可能减少对外科医生和手术团队的辐射剂量。