Posterior allograft sacroiliac joint fusion with pre-operative mapping

Chris Bovinet , Robert Moghim , Max Y. Jin , Alaa Abd-Elsayed
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Abstract

Background

Low back pain is a highly prevalent and disabling condition. Sacroiliac joint dysfunction is prevalent in up to 62 % of some populations and is a common origin of low back pain. The posterior approach for minimally invasive sacroiliac joint fusion with an allograft is still relatively novel, with limited studies examining its safety and efficacy.

Objective

The objective of our study was to analyze changes in pain and opioid usage for patients who underwent this procedure with pre-operative mapping after exhausting conservative treatment methods.

Methods

This was a single-center, retrospective study with all cases completed by a single interventional pain physician. Outcomes regarding pain and opioid usage were extracted from electronic medical records, Georgia Prescription Drug Monitoring Program reports, and all other available state databases for 208 consecutive patients who underwent the minimally invasive sacroiliac joint fusion procedure with the LinQ Fusion Implant (PainTeq, Tampa, FL) after pre-operative mapping between August 2019 and October 2022. Pain was assessed using the Numerical Rating Scale (NRS), and opioid consumption was measured using Morphine Milligram Equivalents (MME).

Results

NRS scores decreased from 7.23 ± 1.82 at baseline to 1.16 ± 1.35 at the final available follow-up (p < 0.001). Pain improvements ranged from 40 to 100 %, and all patients reported at least some improvement post-intervention. 205 of the 208 patients reported an improvement in pain of at least 50 %. MME reduced from 20.74 ± 26.33 mg to 10.00 ± 18.69 mg (p < 0.001).

Conclusion

Posterior allograft sacroiliac joint fusion significantly reduces pain and opioid consumption. Pre-operative mapping is beneficial but requires more evidence to elucidate its role in optimizing implant placement.
后路同种异体骶髂关节融合术术前定位
背景:腰痛是一种非常普遍和致残的疾病。骶髂关节功能障碍在某些人群中普遍存在,高达62%,是腰痛的常见原因。后路微创同种异体骶髂关节融合术仍然是一种相对新颖的方法,对其安全性和有效性的研究有限。目的本研究的目的是分析在用尽保守治疗方法后进行该手术的患者的疼痛和阿片类药物使用的变化。方法本研究为单中心回顾性研究,所有病例均由一名介入性疼痛医师完成。在2019年8月至2022年10月进行术前绘图后,从电子病历、乔治亚州处方药监测项目报告和所有其他可用的州数据库中提取了208名连续接受LinQ融合植入物(PainTeq, Tampa, FL)微创骶髂关节融合手术的患者的疼痛和阿片类药物使用结果。使用数值评定量表(NRS)评估疼痛,使用吗啡毫克当量(MME)测量阿片类药物消耗。结果snrs评分从基线时的7.23±1.82降至最终随访时的1.16±1.35 (p <;0.001)。疼痛改善从40%到100%不等,所有患者在干预后都报告了至少一些改善。208例患者中有205例报告疼痛改善至少50%。MME由20.74±26.33 mg降至10.00±18.69 mg (p <;0.001)。结论同种异体骶髂关节后路融合术能明显减轻疼痛和阿片类药物的消耗。术前定位是有益的,但需要更多的证据来阐明其在优化种植体放置中的作用。
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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