LOW BACK PAIN--A MULTICENTER RANDOMIZED TRIAL

腰痛被认为是美国和世界上最常见的健康问题之一。这种情况仅次于普通感冒，是患者最常去看医生或失去工作时间的情况。据估计，那些因下腰痛而严重残疾的人每年的成本在300亿至700亿美元之间。随着时间的推移，美国脊柱手术的比率急剧上升，这些手术的比率在地理上的差异已被记录下来15倍。在许多情况下，手术率似乎取决于一个人的居住地和见过的人。尽管有这些趋势，但几乎没有证据证明这些治疗方法的有效性/疗效优于非手术治疗。这项研究将利用国家脊柱网络的独特资源，对脊柱手术中最常见的三个诊断组进行多中心、随机、对照试验：腰椎间盘突出症(IDH)、椎管狭窄症(SPS)和继发于退行性腰椎滑脱(DS)的椎管狭窄症。这些试验将比较最常用的标准手术治疗和最常用的标准非手术治疗。这项研究将在全美16个地点进行。这项研究的主要终点将是由SF-36健康状况问卷衡量的与健康相关的一般生活质量的变化，以及由OSwestry下腰痛问卷衡量的与脊柱相关的残疾。次要终点将包括患者对治疗的满意度、用于估计成本的资源利用以及用于估计质量调整寿命年(QALY)的当前健康效用。后两个终点将用于完成正式的成本效益评价。患者将被跟踪至少24个月，并计划在3、6、12和24个月进行访问。所有终端的数据将在每次研究访问时收集。如果可能，将在36个月和48个月期间安排延长的后续访问。我们预计将有1450个科目报名和随机分配。将跟踪另一个观察队列，以评估健康和资源结果。来自随机对照试验和观察队列的数据将被整合，以正式评估IDH、SPS和DS的手术干预与非手术干预的成本效益。在这项试验的基础上，我们将第一次获得关于手术和非手术治疗这三种常见腰椎疾病的相对有效性/有效性的科学证据。

Low back pain is considered one of the most widely experienced health problems in the U.S. and the world. This condition is second only to the common cold as the condition for which patients most frequently see a physician or suffer days lost from work. Estimated costs to those who are severely disabled from low back pain range from 30-70 billion dollars annually. Rates of spinal surgery in the U.S. have increased sharply over time, and 15-fold geographic variation in rates of these surgeries has been documented. In many cases the rates of surgery appear to be determined by where one lives and who one sees. Despite these trends, there is little evidence proving the effectiveness/efficacy of these therapies over non-operative management. This study will use the unique resource of the National Spine Network to conduct multicentered, randomized, controlled trials for the three most common diagnostic groups for which spine surgery is performed: lumbar intervertebral disc herniation (IDH), spinal stenosis (SpS) and spinal stenosis secondary to degenerative spondylolithesis (DS). The trials will compare the most commonly used standard surgical treatments to the most commonly used standard non-operative treatments. The study will be conducted at 16 sites throughout the United States. The primary endpoints of the study will be changes in general health-related quality of life as measured by the SF-36 health status questionnaire and spine-related disability as measured by the Oswestry Low Back Pain questionnaire. Secondary endpoints will include patient satisfaction with treatment, resource utilization for estimation of cost, and utility for current health for estimation of quality-adjusted life years (QALYs). The latter two endpoints will be used to complete a formal cost-effectiveness evaluation. Patients will be followed a minimum of 24 months with visits scheduled at 3, 6, 12, and 24 months. Data on all endpoints will be collected at each study visit. If possible, extended follow-up visits will be scheduled at 36 and 48 months. We anticipate that a total of 1450 subjects will be enrolled and randomly allocated. An additional observational cohort will be tracked to assess health and resource outcomes. Data from the RCT and observational cohorts will be integrated to formally estimate the cost-effectiveness of operative versus non-operative interventions for IDH, SpS, and DS. Based on this trial we will, for the first time, have scientific evidence as to the relative effectiveness/efficacy of surgical versus non-surgical treatment for these three common lumbar spine conditions.