Stylianos Kapetanakis, Benjamin Cappin, Mikail Chatzivasiliadis
{"title":"Outcomes of Percutaneous Laser Disc Decompression for Lumbar Disc Herniation: A Systematic Review and Meta-Analysis.","authors":"Stylianos Kapetanakis, Benjamin Cappin, Mikail Chatzivasiliadis","doi":"10.22603/ssrr.2025-0401","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Percutaneous laser disc decompression (PLDD) is a minimally invasive treatment option for carefully selected patients with lumbar disc herniations (LDH) whose condition does not respond to conservative therapy but who may not require surgical decompression. Although PLDD has been increasingly adopted, reported outcomes vary widely across studies. This systematic review and meta-analysis aimed to evaluate the effectiveness and safety of PLDD in adults with LDH.</p><p><strong>Methods: </strong>A systematic search of PubMed, Scopus, and Web of Science was conducted through November 2025. Adult PLDD studies reporting clinical outcomes were included. Random-effects models pooled continuous and binary outcomes. Primary outcomes were visual analog scale (VAS) improvement and clinical success. Secondary outcomes were Oswestry Disability Index (ODI) change, reoperation rates, and complications. Heterogeneity was assessed with I<sup>2</sup>, and risk of bias with the Risk of Bias in Non-randomized Studies of Interventions.</p><p><strong>Results: </strong>Fifteen publications reporting 14 unique PLDD cohorts were included. Eight studies (n=506) reported VAS outcomes, showing a pooled pain reduction of 4.33 points on a 0-10 scale (95% confidence interval [CI] 3.03-5.64; I<sup>2</sup>=98.8%). Three studies (n=128) reported ODI outcomes, with a pooled improvement of 20.1 points, but with substantial uncertainty (95% CI -21.7 to 61.9; I<sup>2</sup>=99.6%). Five studies (n=298) reported clinical success, yielding a pooled success rate of 73.8% (95% CI 55.9%-86.2%; I<sup>2</sup>=91.0%). The pooled reoperation rate across eight cohorts (n=650) was 10.3% (95% CI 6.3%-16.5%; I<sup>2</sup>=65.8%), and the pooled complication rate across ten studies (n=750) was 1.3% (95% CI 0.4%-3.9%; I<sup>2</sup>=1.0%). Most studies had moderate risk of bias due to non-randomized, single-arm designs.</p><p><strong>Conclusions: </strong>PLDD is associated with meaningful pain reduction and moderate clinical success with a very low complication rate in selected patients with LDH. Functional outcomes and reoperation rates varied across studies. Further high-quality comparative research is needed to better define long-term results and optimal patient selection.</p>","PeriodicalId":22253,"journal":{"name":"Spine Surgery and Related Research","volume":"10 3","pages":"366-375"},"PeriodicalIF":1.6000,"publicationDate":"2026-04-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13255130/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Spine Surgery and Related Research","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.22603/ssrr.2025-0401","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/5/27 0:00:00","PubModel":"eCollection","JCR":"Q3","JCRName":"SURGERY","Score":null,"Total":0}
引用次数: 0
Abstract
Background: Percutaneous laser disc decompression (PLDD) is a minimally invasive treatment option for carefully selected patients with lumbar disc herniations (LDH) whose condition does not respond to conservative therapy but who may not require surgical decompression. Although PLDD has been increasingly adopted, reported outcomes vary widely across studies. This systematic review and meta-analysis aimed to evaluate the effectiveness and safety of PLDD in adults with LDH.
Methods: A systematic search of PubMed, Scopus, and Web of Science was conducted through November 2025. Adult PLDD studies reporting clinical outcomes were included. Random-effects models pooled continuous and binary outcomes. Primary outcomes were visual analog scale (VAS) improvement and clinical success. Secondary outcomes were Oswestry Disability Index (ODI) change, reoperation rates, and complications. Heterogeneity was assessed with I2, and risk of bias with the Risk of Bias in Non-randomized Studies of Interventions.
Results: Fifteen publications reporting 14 unique PLDD cohorts were included. Eight studies (n=506) reported VAS outcomes, showing a pooled pain reduction of 4.33 points on a 0-10 scale (95% confidence interval [CI] 3.03-5.64; I2=98.8%). Three studies (n=128) reported ODI outcomes, with a pooled improvement of 20.1 points, but with substantial uncertainty (95% CI -21.7 to 61.9; I2=99.6%). Five studies (n=298) reported clinical success, yielding a pooled success rate of 73.8% (95% CI 55.9%-86.2%; I2=91.0%). The pooled reoperation rate across eight cohorts (n=650) was 10.3% (95% CI 6.3%-16.5%; I2=65.8%), and the pooled complication rate across ten studies (n=750) was 1.3% (95% CI 0.4%-3.9%; I2=1.0%). Most studies had moderate risk of bias due to non-randomized, single-arm designs.
Conclusions: PLDD is associated with meaningful pain reduction and moderate clinical success with a very low complication rate in selected patients with LDH. Functional outcomes and reoperation rates varied across studies. Further high-quality comparative research is needed to better define long-term results and optimal patient selection.
背景:经皮激光椎间盘减压术(PLDD)是一种微创治疗选择,用于精心挑选的腰椎间盘突出症(LDH)患者,这些患者的病情对保守治疗没有反应,但可能不需要手术减压。尽管PLDD已被越来越多地采用,但各研究报告的结果差异很大。本系统综述和荟萃分析旨在评估PLDD治疗LDH成人患者的有效性和安全性。方法:系统检索PubMed、Scopus和Web of Science,检索时间截止到2025年11月。纳入了报告临床结果的成人PLDD研究。随机效应模型汇集了连续和二元结果。主要结果为视觉模拟评分(VAS)改善和临床成功。次要结果为Oswestry残疾指数(ODI)变化、再手术率和并发症。异质性评估采用I2,偏倚风险评估采用非随机干预研究的偏倚风险。结果:纳入了15篇报道14个独特PLDD队列的出版物。8项研究(n=506)报告了VAS结果,在0-10级评分中,疼痛减轻总分为4.33分(95%可信区间[CI] 3.03-5.64; I2=98.8%)。三项研究(n=128)报告了ODI结果,共改善20.1点,但存在很大的不确定性(95% CI -21.7 ~ 61.9; I2=99.6%)。5项研究(n=298)报告了临床成功,总成功率为73.8% (95% CI 55.9%-86.2%; I2=91.0%)。8个队列(n=650)的合并再手术率为10.3% (95% CI 6.3%-16.5%; I2=65.8%), 10个研究(n=750)的合并并发症率为1.3% (95% CI 0.4%-3.9%; I2=1.0%)。由于采用非随机、单臂设计,大多数研究具有中等偏倚风险。结论:在选定的LDH患者中,PLDD与有意义的疼痛减轻和中等临床成功率以及非常低的并发症发生率相关。不同研究的功能结局和再手术率各不相同。需要进一步的高质量比较研究来更好地确定长期结果和最佳患者选择。