Canada East Spine Centre and Horizon Health Network, Saint John, NB, Canada.
Clinic for Neurosurgery, Medical Center, Faculty of Medicine, University of Freiburg, Freiburg, Germany.
Clin Spine Surg. 2020 Aug;33(7):284-291. doi: 10.1097/BSD.0000000000001019.
A retrospective subgroup analysis of a prospective observational study was carried out.
Patients' baseline characteristics may influence the clinical outcomes after minimally invasive lumbar interbody fusion (MILIF).
This study aimed to investigate the influence of patient's age and body mass index (BMI) on the clinical outcomes of MILIF for degenerative lumbar disorder.
A total of 252 patients underwent MILIF. The clinical outcomes, including time to first ambulation, time to postsurgical recovery, back/leg pain in visual analog scale, Oswestry Disability Index, and EuroQol-5 Dimension, were collected at baseline, 4 weeks, 6, and 12 months. Patients were subgrouped by age (50 y and below: N=102; 51-64 y: N=102; 65 y and above: N=48) and BMI (≤25.0: N=79; 25.1-29.9: N=104; ≥30.0: N=69). Data from baseline to 12 months were compared for all clinical outcomes within age/BMI subgroups. Adverse events (AEs) and serious adverse events (SAEs) were summarized by age and BMI subgroups.
All age and BMI subgroups showed significant improvements in clinical outcomes at 12 months compared with the baseline. The median time to first ambulation was similar for all subgroups (age groups: P=0.8707; BMI: P=0.1013); older people show a trend of having longer time to postsurgical recovery (age groups: P=0.0662; BMI: P=0.1591). Oswestry Disability Index, back, and leg pain visual analog scale, and EuroQol-5 Dimension were similar in all subgroups at every timepoint. A total of 50 AEs (N=39) were reported, 9 of which were SAEs; 3 AEs and 1 SAE were considered to be related to surgical procedure. No differences were observed in safety by age groups and BMI groups.
MILIF appears to be safe and effective, independent of age or weight in the treatment of degenerative lumbar disorder.
Level II.
对一项前瞻性观察研究进行了回顾性亚组分析。
患者的基线特征可能会影响微创腰椎体间融合术(MILIF)后的临床结果。
本研究旨在探讨患者年龄和体重指数(BMI)对退行性腰椎疾病 MILIF 临床结果的影响。
共 252 例患者接受 MILIF 治疗。收集基线时、4 周、6 个月和 12 个月时的临床结果,包括首次下床时间、术后恢复时间、腰背/腿痛视觉模拟评分、Oswestry 功能障碍指数和 EuroQol-5 维度。根据年龄(50 岁及以下:N=102;51-64 岁:N=102;65 岁及以上:N=48)和 BMI(≤25.0:N=79;25.1-29.9:N=104;≥30.0:N=69)将患者分为亚组。对各年龄/BMI 亚组的所有临床结局进行基线至 12 个月的比较。根据年龄和 BMI 亚组总结不良事件(AE)和严重不良事件(SAE)。
与基线相比,所有年龄和 BMI 亚组在 12 个月时的临床结局均有显著改善。各亚组首次下床时间中位数相似(年龄组:P=0.8707;BMI:P=0.1013);老年人术后恢复时间较长(年龄组:P=0.0662;BMI:P=0.1591)。各亚组在各个时间点的 Oswestry 功能障碍指数、腰背/腿痛视觉模拟评分和 EuroQol-5 维度均相似。共报告 50 例 AE(N=39),其中 9 例为 SAE;3 例 AE 和 1 例 SAE 被认为与手术过程相关。各年龄组和 BMI 组之间在安全性方面无差异。
在治疗退行性腰椎疾病方面,MILIF 似乎是安全有效的,与年龄或体重无关。
II 级。