45. Return to work activities of daily living and disability improvement of an FDA IDE trial of decompression and dynamic sagittal tether stabilization versus decompression and transforaminal lumbar interbody fusion
William F. Lavelle MD, MBA , Rick C. Sasso MD , Hyun W. Bae MD , Jeffrey L. Gum MD , Alan T. Villavicencio MD , Mick J Perez-Cruet MD , S. Tim Yoon MD, PhD , W. Jacob Lavelle , Kee D. Kim MD , Michael Y. Wang MD, MBA , Ravi S. Bains MD , Michael Stauff MD , Sigurd H. Berven MD , Harel Deutsch MD , Jeffrey S. Fischgrund MD , Adam L. Shimer MD , Reginald J. Davis MD, FACS , Elizabeth Yu MD , Todd F. Alamin MD , Louis C Fielding MS , William C Welch MD, FACS, FICS
{"title":"45. Return to work activities of daily living and disability improvement of an FDA IDE trial of decompression and dynamic sagittal tether stabilization versus decompression and transforaminal lumbar interbody fusion","authors":"William F. Lavelle MD, MBA , Rick C. Sasso MD , Hyun W. Bae MD , Jeffrey L. Gum MD , Alan T. Villavicencio MD , Mick J Perez-Cruet MD , S. Tim Yoon MD, PhD , W. Jacob Lavelle , Kee D. Kim MD , Michael Y. Wang MD, MBA , Ravi S. Bains MD , Michael Stauff MD , Sigurd H. Berven MD , Harel Deutsch MD , Jeffrey S. Fischgrund MD , Adam L. Shimer MD , Reginald J. Davis MD, FACS , Elizabeth Yu MD , Todd F. Alamin MD , Louis C Fielding MS , William C Welch MD, FACS, FICS","doi":"10.1016/j.spinee.2025.08.227","DOIUrl":null,"url":null,"abstract":"<div><h3>BACKGROUND CONTEXT</h3><div>Degenerative spondylolisthesis (DS) with lumbar spinal stenosis (LSS) is commonly treated with decompression and fusion. An investigational procedure, Spondyloplasty, incorporates direct surgical decompression and stabilization with a dynamic sagittal tether (DST). The primary objective of surgery is resolution of symptoms so patients can return to work and their normal activities of daily living.</div></div><div><h3>PURPOSE</h3><div>Assess return to work (RTW) and activities of daily living (ADL) receiving either decompression and DST stabilization (Spondyloplasty) compared to decompression and transforaminal lumbar interbody fusion (D+TLIF) at 24 months.</div></div><div><h3>STUDY DESIGN/SETTING</h3><div>Interim analysis from a multicenter, concurrently controlled study.</div></div><div><h3>PATIENT SAMPLE</h3><div>Patients undergoing treatment (Spondyloplasty or D+TLIF) of Grade I Meyerding lumbar DS and LSS. Propensity score (PS) selected patients with 24-month follow-up were included.</div></div><div><h3>OUTCOME MEASURES</h3><div>Time to return to work and activities of daily living, Oswestry disability index (ODI), VAS Back Pain and VAS Leg/Hip Pain (Worst Side).</div></div><div><h3>METHODS</h3><div>PS-selected FDA IDE study subjects (NCT03115983) with 24-months follow-up were included in this analysis. Study records queried for work status preoperatively and various time points up to 24 months, as well as time to ADL and RTW, and change in disability (ODI, VAS Back and VAS Leg/Hip [Worst Side]) at 24 months vs preoperatively.</div></div><div><h3>RESULTS</h3><div>Of 299 enrolled subjects, 287 were PS-selected (140= Spondyloplasty and 147= D+TLIF). Both groups demonstrated significant durable improvements in pain and disability. The Spondylopasty group had significantly lower ODI at 6-week and 3-month follow-ups (p<0.05). At 24 months, there were no statistical differences seen between groups in ODI, VAS Back Pain or VAS Lip/Hip (Worst Side), although the Spondyloplasty group demonstrated larger improvement effect sizes in all measures. The patient-reported outcomes showed the return to ADL and RTW (among patients working preoperatively) for the Spondyloplasty group was greater at every postoperative time point compared to the D+TLIF group. At 24 months, return to ADL was >95% for Spondyloplasty versus <80% for D+TLIF; and the RTW was >90% for Spondyloplasty versus < 75% D+TLIF.</div></div><div><h3>CONCLUSIONS</h3><div>The primary objective of surgery for symptomatic DS is resolution of symptoms so patients can return to their normal ADL and work. Both Spondyloplasty and D+TLIF treated patients demonstrated significant reductions in disability at 24-month follow-up. The Spondyloplasty group had quicker recovery, including lower disability at immediate postoperative intervals and significantly faster RTW and ADL. Decompression and stabilization with DST procedure (Spondyloplasty) may be a minimally invasive alternative to lumbar fusion for patients with symptomatic DS. Longer-term follow-up assessment with propensity score-adjusted outcomes will demonstrate whether this advantage and long-term outcomes are durable and generalizable.</div></div><div><h3>FDA Device/Drug Status</h3><div>LimiFlex Dynamic Sagittal Tether (Investigational/Not Approved)</div></div>","PeriodicalId":49484,"journal":{"name":"Spine Journal","volume":"25 11","pages":"Pages S24-S25"},"PeriodicalIF":4.7000,"publicationDate":"2025-10-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Spine Journal","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1529943025006072","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CLINICAL NEUROLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
BACKGROUND CONTEXT
Degenerative spondylolisthesis (DS) with lumbar spinal stenosis (LSS) is commonly treated with decompression and fusion. An investigational procedure, Spondyloplasty, incorporates direct surgical decompression and stabilization with a dynamic sagittal tether (DST). The primary objective of surgery is resolution of symptoms so patients can return to work and their normal activities of daily living.
PURPOSE
Assess return to work (RTW) and activities of daily living (ADL) receiving either decompression and DST stabilization (Spondyloplasty) compared to decompression and transforaminal lumbar interbody fusion (D+TLIF) at 24 months.
STUDY DESIGN/SETTING
Interim analysis from a multicenter, concurrently controlled study.
PATIENT SAMPLE
Patients undergoing treatment (Spondyloplasty or D+TLIF) of Grade I Meyerding lumbar DS and LSS. Propensity score (PS) selected patients with 24-month follow-up were included.
OUTCOME MEASURES
Time to return to work and activities of daily living, Oswestry disability index (ODI), VAS Back Pain and VAS Leg/Hip Pain (Worst Side).
METHODS
PS-selected FDA IDE study subjects (NCT03115983) with 24-months follow-up were included in this analysis. Study records queried for work status preoperatively and various time points up to 24 months, as well as time to ADL and RTW, and change in disability (ODI, VAS Back and VAS Leg/Hip [Worst Side]) at 24 months vs preoperatively.
RESULTS
Of 299 enrolled subjects, 287 were PS-selected (140= Spondyloplasty and 147= D+TLIF). Both groups demonstrated significant durable improvements in pain and disability. The Spondylopasty group had significantly lower ODI at 6-week and 3-month follow-ups (p<0.05). At 24 months, there were no statistical differences seen between groups in ODI, VAS Back Pain or VAS Lip/Hip (Worst Side), although the Spondyloplasty group demonstrated larger improvement effect sizes in all measures. The patient-reported outcomes showed the return to ADL and RTW (among patients working preoperatively) for the Spondyloplasty group was greater at every postoperative time point compared to the D+TLIF group. At 24 months, return to ADL was >95% for Spondyloplasty versus <80% for D+TLIF; and the RTW was >90% for Spondyloplasty versus < 75% D+TLIF.
CONCLUSIONS
The primary objective of surgery for symptomatic DS is resolution of symptoms so patients can return to their normal ADL and work. Both Spondyloplasty and D+TLIF treated patients demonstrated significant reductions in disability at 24-month follow-up. The Spondyloplasty group had quicker recovery, including lower disability at immediate postoperative intervals and significantly faster RTW and ADL. Decompression and stabilization with DST procedure (Spondyloplasty) may be a minimally invasive alternative to lumbar fusion for patients with symptomatic DS. Longer-term follow-up assessment with propensity score-adjusted outcomes will demonstrate whether this advantage and long-term outcomes are durable and generalizable.
期刊介绍:
The Spine Journal, the official journal of the North American Spine Society, is an international and multidisciplinary journal that publishes original, peer-reviewed articles on research and treatment related to the spine and spine care, including basic science and clinical investigations. It is a condition of publication that manuscripts submitted to The Spine Journal have not been published, and will not be simultaneously submitted or published elsewhere. The Spine Journal also publishes major reviews of specific topics by acknowledged authorities, technical notes, teaching editorials, and other special features, Letters to the Editor-in-Chief are encouraged.