Wilby Martin John, Best Ashley, Wood Eifiona, Burnside Girvan, Bedson Emma, Short Hannah, Wheatley Dianne, Hill-McManus Daniel, Sharma Manohar, Clark Simon, Baranidharan Ganesan, Price Cathy, Mannion Richard, Hutchinson Peter J, Hughes Dyfrig A, Marson Anthony, Williamson Paula R
Department of Neurosurgery, The Walton Centre NHS Foundation Trust, Liverpool, UK.
Liverpool Clinical Trials Centre, University of Liverpool, Liverpool, UK.
Lancet Rheumatol. 2021 Mar 18;3(5):e347-e356. doi: 10.1016/S2665-9913(21)00036-9. eCollection 2021 May.
The optimal invasive treatment for sciatica secondary to herniated lumbar disc remains controversial, with a paucity of evidence for use of non-surgical treatments such as transforaminal epidural steroid injection (TFESI) over surgical microdiscectomy. We aimed to investigate the clinical and cost-effectiveness of these options for management of radicular pain secondary to herniated lumbar disc.
We did a pragmatic, multicentre, phase 3, open-label, randomised controlled trial at 11 spinal units across the UK. Eligible patients were aged 16-65 years, had MRI-confirmed non-emergency sciatica secondary to herniated lumbar disc with symptom duration between 6 weeks and 12 months, and had leg pain that was not responsive to non-invasive management. Participants were randomly assigned (1:1) to receive either TFESI or surgical microdiscectomy by an online randomisation system that was stratified by centre with random permuted blocks. The primary outcome was Oswestry Disability Questionnaire (ODQ) score at 18 weeks. All randomly assigned participants who completed a valid ODQ at baseline and at 18 weeks were included in the analysis. Safety analysis included all treated participants. Cost-effectiveness was estimated from the EuroQol-5D-5L, Hospital Episode Statistics, medication usage, and self-reported resource-use data. This trial was registered with ISRCTN, number ISRCTN04820368, and EudraCT, number 2014-002751-25.
Between March 6, 2015, and Dec 21, 2017, 163 (15%) of 1055 screened patients were enrolled, with 80 participants (49%) randomly assigned to the TFESI group and 83 participants (51%) to the surgery group. At week 18, ODQ scores were 30·02 (SD 24·38) for 63 assessed patients in the TFESI group and 22·30 (19·83) for 61 assessed patients in the surgery group. Mean improvement was 24·52 points (18·89) for the TFESI group and 26·74 points (21·35) for the surgery group, with an estimated treatment difference of -4·25 (95% CI -11·09 to 2·59; p=0·22). There were four serious adverse events in four participants associated with surgery, and none with TFESI. Compared with TFESI, surgery had an incremental cost-effectiveness ratio of £38 737 per quality-adjusted life-year gained, and a 0·17 probability of being cost-effective at a willingness-to-pay threshold of £20 000 per quality-adjusted life-year.
For patients with sciatica secondary to herniated lumbar disc, with symptom duration of up to 12 months, TFESI should be considered as a first invasive treatment option. Surgery is unlikely to be a cost-effective alternative to TFESI.
Health Technology Assessment programme of the National Institute for Health Research (NIHR), UK.
腰椎间盘突出继发坐骨神经痛的最佳侵入性治疗仍存在争议,缺乏证据表明经椎间孔硬膜外类固醇注射(TFESI)等非手术治疗优于手术显微椎间盘切除术。我们旨在研究这些方法治疗腰椎间盘突出继发神经根性疼痛的临床效果和成本效益。
我们在英国11个脊柱治疗单位进行了一项实用、多中心、3期、开放标签、随机对照试验。符合条件的患者年龄在16 - 65岁之间,经MRI证实为腰椎间盘突出继发非紧急性坐骨神经痛,症状持续时间在6周和12个月之间,且腿痛对非侵入性治疗无反应。参与者通过在线随机系统(按中心分层并采用随机排列的区组)随机分配(1:1)接受TFESI或手术显微椎间盘切除术。主要结局是18周时的Oswestry功能障碍问卷(ODQ)评分。所有在基线和18周时完成有效ODQ的随机分配参与者都纳入分析。安全性分析包括所有接受治疗的参与者。成本效益根据欧洲五维健康量表-5L(EuroQol-5D-5L)、医院事件统计、药物使用情况和自我报告的资源使用数据进行估计。本试验在国际标准随机对照试验编号注册库(ISRCTN)注册,编号为ISRCTN04820368,在欧盟临床试验注册库(EudraCT)注册,编号为2014 - 002751 - 25。
在2015年3月6日至2017年12月21日期间,1055名筛查患者中有163名(15%)入组,80名参与者(49%)随机分配到TFESI组,83名参与者(51%)分配到手术组。在第18周时,TFESI组63名评估患者的ODQ评分为30.02(标准差24.38),手术组61名评估患者的评分为22.30(19.83)。TFESI组平均改善24.52分(18.89),手术组平均改善26.74分(21.35),估计治疗差异为 -4.25(95%置信区间 -11.09至2.59;p = 0.22)。有4名参与者发生了与手术相关的4起严重不良事件,TFESI组无严重不良事件。与TFESI相比,手术每获得一个质量调整生命年的增量成本效益比为38737英镑,在每质量调整生命年支付意愿阈值为20000英镑时具有成本效益的概率为0.17。
对于腰椎间盘突出继发坐骨神经痛、症状持续时间长达12个月的患者,应将TFESI视为首选的侵入性治疗选择。手术不太可能是TFESI具有成本效益的替代方案。
英国国家卫生研究院(NIHR)卫生技术评估项目。