Rohan Michael X, Ohnmeiss Donna D, Guyer Richard D, Zigler Jack E, Blumenthal Scott L, Hochschuler Stephen H, Sachs Barton L, Rashbaum Ralph F
Texas Back Institute Research Foundation, 6020 West Parker Road, No. 200, Plano, TX 75093, USA.
Spine J. 2009 May;9(5):360-5. doi: 10.1016/j.spinee.2008.07.004. Epub 2008 Sep 21.
A recent study involving interbody fusion patients found that preoperative work status was significantly related to clinical outcome. In another study comparing the best and worst outcomes of total disc replacement, among a battery of variables analyzed, the only one that differentiated the best and worst outcome groups was the length of time off work before total disc replacement.
The purpose of this study was to determine if there was a relationship between the length of time off work and treatment outcome at 24-month follow-up. If such a relationship existed, a secondary study objective would be to determine if a duration of work could be identified beyond which would be associated with compromised clinical outcome.
Data were collected prospectively from randomized clinical trials comparing total disc replacement with lumbar fusion conducted at a single site.
A database of 232 patients enrolled in one of two Food and Drug Administration-regulated trials comparing total disc replacement with fusion for the treatment of symptomatic disc degeneration was the basis of the study group. Only patients who had reached 24-month follow-up were included. The 28 patients who were not employed by choice preoperatively were not included in the analysis.
Primary outcome measures used were visual analog scales (VAS) assessing pain and Oswestry disability index.
The length of time off work before surgery was recorded in weeks. The mean percentage improvement between preoperative and 24-month follow-up scores were analyzed.
There was a significant relationship between duration off work preoperatively and clinical outcome (p<.05). The length of time off work preoperatively was more strongly related to outcome than was surgery type, insurance type, job demand, or preoperative VAS and Oswestry scores. Further analysis of the data identified a window of approximately 0 to 13 weeks off work preoperatively that was related to significantly greater improvements on visual analog scales (VAS) and Oswestry scores after surgery compared with patients who were off work for more than 13 weeks preoperatively. Although the subgroup off work for more than 13 weeks improved significantly from their preoperative status, the improvement was not as great as in the subgroup off work for a shorter duration.
The results of this study found that patients off work for a longer duration before surgery improved significantly postoperatively, but had less favorable clinical outcomes than patients off work for a lesser duration. This study suggests a window of approximately 13 weeks off work before surgery after which clinical improvement is reduced. Implications of this finding may be that once a patient becomes unable to work for an extended period, more rigorous psychological screening may be in order as well as perhaps engaging in more rigorous rehabilitation after surgery. Further investigation is needed to determine if the 13 weeks identified in this study is applicable to other populations.
最近一项针对椎间融合术患者的研究发现,术前工作状态与临床结果显著相关。在另一项比较全椎间盘置换最佳和最差结果的研究中,在分析的一系列变量中,唯一能区分最佳和最差结果组的变量是全椎间盘置换术前的休假时间。
本研究的目的是确定休假时间与24个月随访时的治疗结果之间是否存在关联。如果存在这种关联,次要研究目标将是确定是否能确定一个休假时长,超过该时长会与临床结果受损相关。
数据前瞻性地收集自一项在单一地点进行的比较全椎间盘置换与腰椎融合术的随机临床试验。
研究组的基础是一个包含232名患者的数据库,这些患者参与了两项由美国食品药品监督管理局监管的试验之一,该试验比较了全椎间盘置换与融合术治疗有症状椎间盘退变的效果。仅纳入达到24个月随访的患者。术前选择不工作的28名患者未纳入分析。
使用的主要结局指标是评估疼痛的视觉模拟量表(VAS)和奥斯威斯利功能障碍指数。
记录术前休假的周数。分析术前和24个月随访评分之间的平均改善百分比。
术前休假时长与临床结果之间存在显著关联(p<0.05)。术前休假时长与结果的相关性比手术类型、保险类型、工作需求或术前VAS和奥斯威斯利评分更强。对数据的进一步分析确定了术前约0至13周的休假窗口,与术前休假超过13周的患者相比,该窗口内的患者术后视觉模拟量表(VAS)和奥斯威斯利评分有显著更大的改善。虽然术前休假超过13周的亚组与术前状态相比有显著改善,但改善程度不如休假时长较短的亚组。
本研究结果发现,术前休假时间较长的患者术后有显著改善,但临床结果不如休假时间较短的患者。本研究表明术前约13周的休假窗口,超过该窗口临床改善会降低。这一发现的意义可能是,一旦患者长期无法工作,可能需要进行更严格的心理筛查,并可能在术后进行更严格的康复治疗。需要进一步研究以确定本研究中确定的13周是否适用于其他人群。