Passias Peter G, Bortz Cole A, Pierce Katherine E, Alas Haddy, Brown Avery, Vasquez-Montes Dennis, Naessig Sara, Ahmad Waleed, Diebo Bassel G, Raman Tina, Protopsaltis Themistocles S, Buckland Aaron J, Gerling Michael C, Lafage Renaud, Lafage Virginie
Department of Orthopedics, NYU Langone Orthopedic Hospital, New York, New York.
Department of Orthopedics, SUNY Downstate Medical Center, Brooklyn, New York.
Int J Spine Surg. 2020 Dec;14(6):1031-1036. doi: 10.14444/7154.
The Miller et al adult spinal deformity frailty index (ASD-FI) correlates with complication risk; however, its development was not rooted in clinical outcomes, and the 40 factors needed for its calculation limit the index's clinical utility. The present study aimed to develop a simplified, weighted frailty index for ASD patients METHODS: This study is a retrospective review of a single-center database. Component ASD-FI parameters contributing to overall ASD-FI score were assessed via Pearson correlation. Top significant, clinically relevant factors were regressed against ASD-FI score to generate the modified ASD-FI (mASD-FI). Component mASD-FI factors were regressed against incidence of medical complications, and factor weights were calculated from regression of these coefficients. Total mASD-FI score ranged from 0 to 21, and was calculated by summing weights of expressed parameters. Linear regression and published ASD-FI cutoffs generated corresponding mASD-FI frailty cutoffs: not frail (NF, <7), frail (7-12), severely frail (SF, >12). Analysis of variance assessed the relationship between frailty category and validated baseline measures of pain and disability at baseline.
The study included 50 ASD patients. Eight factors were included in the mASD-FI. Overall mean mASD-FI score was 5.7 ± 5.2. Combined, factors comprising the mASD-FI showed a trend of predicting the incidence of medical complications (Nagelkerke = 0.558; Cox & Snell = 0.399; = .065). Breakdown by frailty category is NF (70%), frail (12%), and SF (18%). Increasing frailty category was associated with significant impairments in measures of pain and disability: Oswestry Disability Index (NF: 23.4; frail: 45.0; SF: 49.3; < .001), SRS-22r (NF: 3.5; frail: 2.6; SF: 2.4; = .001), Pain Catastrophizing Scale (NF: 41.9; frail: 32.4; SF: 27.6; < .001), and NRS Leg Pain (NF: 2.3; frail: 7.2; SF: 5.6; = .001).
This study modifies an existing ASD frailty index and proposes a weighted, shorter mASD-FI. The mASD-FI relies less on patient-reported variables, and it weights component factors by their contribution to adverse outcomes. Because increasing mASD-FI score is associated with inferior clinical measures of pain and disability, the mASD-FI may serve as a valuable tool for preoperative risk assessment.
米勒等人的成人脊柱畸形虚弱指数(ASD - FI)与并发症风险相关;然而,其制定并非基于临床结果,且计算所需的40个因素限制了该指数的临床实用性。本研究旨在为ASD患者开发一种简化的加权虚弱指数。
本研究是对单中心数据库的回顾性分析。通过Pearson相关性评估对整体ASD - FI评分有贡献的ASD - FI组成参数。将最显著的、临床相关因素与ASD - FI评分进行回归分析,以生成改良的ASD - FI(mASD - FI)。将mASD - FI组成因素与医疗并发症发生率进行回归分析,并根据这些系数的回归计算因素权重。mASD - FI总分范围为0至21,通过对表达参数的权重求和来计算。线性回归和已发表的ASD - FI临界值生成相应的mASD - FI虚弱临界值:非虚弱(NF,<7);虚弱(7 - 12);严重虚弱(SF,>12)。方差分析评估了虚弱类别与基线时经验证的疼痛和残疾基线测量值之间的关系。
该研究纳入了50例ASD患者。mASD - FI包含8个因素。mASD - FI总体平均评分为5.7±5.2。综合来看,构成mASD - FI的因素显示出预测医疗并发症发生率的趋势(Nagelkerke = 0.558;Cox & Snell = 0.399;P = 0.065)。按虚弱类别划分:非虚弱(70%)、虚弱(12%)和严重虚弱(18%)。虚弱类别增加与疼痛和残疾测量值的显著损害相关:Oswestry残疾指数(非虚弱:23.4;虚弱:45.0;严重虚弱:49.3;P < 0.001)、SRS - 22r(非虚弱:3.5;虚弱:2.6;严重虚弱:2.4;P = 0.001)、疼痛灾难化量表(非虚弱:41.9;虚弱:32.4;严重虚弱:27.6;P < 0.001)和NRS腿痛(非虚弱:2.3;虚弱:7.2;严重虚弱:5.6;P = 0.001)。
本研究对现有的ASD虚弱指数进行了改良,并提出了一种加权的、更简短的mASD - FI。mASD - FI较少依赖患者报告的变量,并根据各组成因素对不良结局的贡献对其进行加权。由于mASD - FI评分增加与疼痛和残疾的较差临床测量值相关,mASD - FI可作为术前风险评估的有价值工具。