Perioperative outcomes after minimally invasive and open surgery for treatment of spine metastases: a systematic review and meta-analysis.

IF 2.9 2区 医学 Q2 CLINICAL NEUROLOGY
Husain Shakil, Ahmad Essa, Armaan K Malhotra, Alex Kiss, Christopher D Witiw, Donald A Redelmeier, Jefferson R Wilson
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引用次数: 0

Abstract

Objective: This systematic review and meta-analysis compared minimally invasive surgery (MIS) to open surgery for treatment of spinal metastases with respect to perioperative outcomes. Few studies have systemically assessed the body of evidence on this topic.

Methods: A systematic review of EMBASE and PubMed from database inception to December 2023 was performed to identify studies comparing MIS with open surgery for the treatment of spine metastases. Nine outcomes were collected: estimated blood loss (EBL), operative time, hospital length of stay (LOS), risk of revision, risk of neurological deterioration, likelihood of receiving postoperative radiation therapy, time to radiation therapy, time to chemotherapy, and treatment of pain measured through patient-reported visual analog scale (VAS) scores. Meta regression was used to estimate adjusted mean differences (aMDs) and adjusted odds ratios (aORs) for outcomes. Certainty of evidence was appraised using the Grading of Recommendations, Assessment, Development and Evaluations approach.

Results: There were 34 eligible studies including 1656 patients with spinal metastases; 904 (54.6%) patients were treated with MIS and 752 (45.4%) were treated with open surgery. MIS was associated with significantly less blood loss (aMD -602 mL, 95% CI -1204 to -0.2 mL; I2 = 97%) with a moderate certainty of evidence. MIS was found to be noninferior with respect to operative time (aMD -2.6 minutes, 95% CI -53.3 to 48.1 minutes; I2 = 88%), risk of revision (aOR 0.9, 95% CI 0.8-1.1; I2 < 0.01), risk of neurological deterioration (aOR 0.9, 95% CI 0.8-1.0; I2 < 0.01), likelihood of postoperative radiation therapy (aOR 0.9, 95% CI 0.7-1.4; I2 < 0.01), and postoperative VAS score (aMD -0.6, 95% CI -1.5 to 0.4; I2 = 52%) with low certainty of evidence. MIS was associated with significantly shorter time to chemotherapy (MD -0.9 weeks, 95% CI -1.9 to -0.01 weeks; I2 = 22%), with very low certainty of evidence. Inferences for LOS and time to radiation were indeterminate; however, we found a trend toward earlier radiation therapy with MIS that was significant in the subgroup of patients treated with decompression and fusion.

Conclusions: Treatment with MIS compared with open surgery was associated with reduced EBL, shorter time to chemotherapy, similar operative time, and similar reductions in postoperative pain. Limitations were largely due to heterogeneity across studies. Future research among subgroups is very likely to improve certainty in the comparative effect estimates.

微创和开放手术治疗脊柱转移的围手术期结果:系统回顾和荟萃分析。
目的:本系统综述和荟萃分析比较了微创手术(MIS)和开放手术治疗脊柱转移的围手术期预后。很少有研究系统地评估了关于这一主题的大量证据。方法:从数据库建立到2023年12月,对EMBASE和PubMed进行系统回顾,以确定比较MIS与开放手术治疗脊柱转移的研究。收集了9个结果:估计失血量(EBL)、手术时间、住院时间(LOS)、翻修风险、神经功能恶化风险、接受术后放射治疗的可能性、放射治疗时间、化疗时间以及通过患者报告的视觉模拟量表(VAS)评分测量的疼痛治疗。Meta回归用于估计结果的调整平均差异(aMDs)和调整优势比(aORs)。采用建议、评估、发展和评估分级方法评价证据的确定性。结果:34项符合条件的研究包括1656例脊柱转移患者;904例(54.6%)患者接受MIS治疗,752例(45.4%)患者接受开放手术。MIS与出血量显著减少相关(aMD -602 mL, 95% CI -1204至-0.2 mL;I2 = 97%),证据确定性中等。MIS与手术时间无关(aMD -2.6分钟,95% CI -53.3 ~ 48.1分钟;I2 = 88%),修订风险(aOR 0.9, 95% CI 0.8-1.1;I2 < 0.01),神经功能恶化的风险(aOR 0.9, 95% CI 0.8-1.0;I2 < 0.01),术后放射治疗的可能性(aOR 0.9, 95% CI 0.7-1.4;I2 < 0.01),术后VAS评分(aMD -0.6, 95% CI -1.5 ~ 0.4;I2 = 52%),证据确定性较低。MIS与化疗时间显著缩短相关(MD -0.9周,95% CI -1.9至-0.01周;I2 = 22%),证据的确定性非常低。对LOS和辐射时间的推断是不确定的;然而,我们发现在接受减压融合治疗的患者亚组中,早期MIS放射治疗的趋势是显著的。结论:与开放手术相比,MIS治疗与EBL减少、化疗时间缩短、手术时间相似、术后疼痛减轻相似相关。局限性主要是由于研究的异质性。未来对亚组的研究很可能提高比较效应估计的确定性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of neurosurgery. Spine
Journal of neurosurgery. Spine 医学-临床神经学
CiteScore
5.10
自引率
10.70%
发文量
396
审稿时长
6 months
期刊介绍: Primarily publish original works in neurosurgery but also include studies in clinical neurophysiology, organic neurology, ophthalmology, radiology, pathology, and molecular biology.
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