Bagan Bradley, Patel Nimesh, Deutsch Harel, Harrop James, Sharan Ashwini, Vaccaro Alexander R, Ratliff John K
Department of Neurosurgery, Rush University Medical Center, Chicago, Illinois, USA.
Surg Technol Int. 2008;17:281-6.
The risk of perioperative complications while adopting minimally invasive spine surgery techniques may slow the acceptance of this technology. We assess the perioperative complication rate with minimally invasive single- and two-level interbody fusions and compare this incidence with a contemporaneous cohort of open single- and two-level open interbody fusions, with all procedures completed by a single surgeon in a single practice group. We compiled all open and MIS interbody fusion cases completed during the study period. Sofamor-Danek X-Tube and Stryker Luxor minimally invasive systems were used on all patients. Medical records were reviewed to assess any adverse events occurring in the perioperative period. Care was taken to include all medical and surgical adverse events and complications occurring within 30 days of surgery. Over the study period, 28 minimally invasive lumbar fusions were identified: 24 single- and 4 two-level cases. Both TLIF and PLIF techniques were used. This cohort was compared with a group of 19 single- and two-level open interbody fusion cases completed over the same period. The complication rate for the MIS cohort was 18%, with 7 complications occurring in 5 patients. In the open group, 8 complications occurred in 7 patients, an incidence of 37%. A standard distribution of complications occurred, and the difference between the two groups was not statistically significant. Limiting our analysis to severe complications yielded rates of 7% and 21% for the two groups, also not significantly divergent. Perioperative complications are not more common in well-selected MIS patients. Allowing for proper patient selection, MIS techniques have a favorable complication profile.
采用微创脊柱手术技术时围手术期并发症的风险可能会延缓这项技术的推广。我们评估了微创单节段和双节段椎间融合术的围手术期并发症发生率,并将这一发生率与同期一组开放性单节段和双节段椎间融合术的发生率进行比较,所有手术均由单一外科医生在单一医疗组完成。我们汇总了研究期间完成的所有开放性和微创椎间融合病例。所有患者均使用了Sofamor-Danek X-Tube和Stryker Luxor微创系统。回顾医疗记录以评估围手术期发生的任何不良事件。我们注意纳入了手术30天内发生的所有医疗和手术不良事件及并发症。在研究期间,共确定了28例微创腰椎融合术:24例单节段和4例双节段病例。同时使用了经椎间孔腰椎椎体间融合术(TLIF)和后路腰椎椎体间融合术(PLIF)技术。将该队列与同期完成的一组19例单节段和双节段开放性椎间融合病例进行比较。微创队列的并发症发生率为18%,5例患者出现7例并发症。在开放组中,7例患者出现8例并发症,发生率为37%。并发症的分布符合标准,两组之间的差异无统计学意义。将分析局限于严重并发症时,两组的发生率分别为7%和21%,差异也无显著性。在精心挑选的微创患者中,围手术期并发症并不更常见。在进行适当的患者选择后,微创技术具有良好的并发症情况。