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患者分析可识别出患有成人脊柱畸形(ASD)且有从非手术治疗转为手术治疗风险的患者:减少无效 ASD 管理的初始步骤。

Patient profiling can identify patients with adult spinal deformity (ASD) at risk for conversion from nonoperative to surgical treatment: initial steps to reduce ineffective ASD management.

机构信息

Department of Orthopaedic Surgery, Hospital for Joint Diseases, NYU Langone Medical Center, 301 E 17th St, New York, NY 10003, USA.

Department of Orthopaedic Surgery, Hospital for Joint Diseases, NYU Langone Medical Center, 301 E 17th St, New York, NY 10003, USA.

出版信息

Spine J. 2018 Feb;18(2):234-244. doi: 10.1016/j.spinee.2017.06.044. Epub 2017 Jul 5.

DOI:10.1016/j.spinee.2017.06.044
PMID:28688984
Abstract

BACKGROUND CONTEXT

Non-operative management is a common initial treatment for patients with adult spinal deformity (ASD) despite reported superiority of surgery with regard to outcomes. Ineffective medical care is a large source of resource drain on the health system. Characterization of patients with ASD likely to elect for operative treatment from non-operative management may allow for more efficient patient counseling and cost savings.

PURPOSE

This study aimed to identify deformity and disability characteristics of patients with ASD who ultimately convert to operative treatment compared with those who remain non-operative and those who initially choose surgery.

STUDY DESIGN/SETTING: A retrospective review was carried out.

PATIENT SAMPLE

A total of 510 patients with ASD (189 non-operative, 321 operative) with minimum 2-year follow-up comprised the patient sample.

OUTCOME MEASURES

Oswestry Disability Index (ODI), Short-Form 36 Health Assessment (SF-36), Scoliosis Research Society questionnaire (SRS-22r), and spinopelvic radiographic alignment were the outcome measures.

METHODS

Demographic, radiographic, and patient-reported outcome measures (PROMs) from a cohort of patients with ASD prospectively enrolled into a multicenter database were evaluated. Patients were divided into three treatment cohorts: Non-operative (NON=initial non-operative treatment and remained non-operative), Operative (OP=initial operative treatment), and Crossover (CROSS=initial non-operative treatment with subsequent conversion to operative treatment). NON and OP groups were propensity score-matched (PSM) to CROSS for baseline demographics (age, body mass index, Charlson Comorbidity Index). Time to crossover was divided into early (<1 year) and late (>1 year). Outcome measures were compared across and within treatment groups at four time points (baseline, 6 weeks, 1 year, and 2 years).

RESULTS

Following PSM, 118 patients were included (NON=39, OP=38, CROSS=41). Crossover rate was 21.7% (41/189). Mean time to crossover was 394 days. All groups had similar baseline sagittal alignment, but CROSS had larger pelvic incidence and lumbar lordosis (PI-LL) mismatch than NON (11.9° vs. 3.1°, p=.032). CROSS and OP had similar baseline PROM scores; however, CROSS had worse baseline ODI, PCS, SRS-22r (p<.05). At time of crossover, CROSS had worse ODI (35.7 vs. 27.8) and SRS Satisfaction (2.6 vs. 3.3) compared with NON (p<.05). Alignment remained similar for CROSS from baseline to conversion; however, PROMs (ODI, PCS, SRS Activity/Pain/Total) worsened (p<.05). Early and late crossover evaluation demonstrated CROSS-early (n=25) had worsening ODI, SRS Activity/Pain at time of crossover (p<.05). From time of crossover to 2-year follow-up, CROSS-early had less SRS Appearance/Mental improvement compared with OP. Both CROSS-early/late had worse baseline, but greater improvements, in ODI, PCS, SRS Pain/Total compared with NON (p<.05). Baseline alignment and disability parameters increased crossover odds-Non with Schwab T/L/D curves and ODI≥40 (odds ratio [OR]: 3.05, p=.031), and Non with high PI-LL modifier grades ("+"/'++') and ODI≥40 (OR: 5.57, p=.007) were at increased crossover risk.

CONCLUSIONS

High baseline and increasing disability over time drives conversion from non-operative to operative ASD care. CROSS patients had similar spinal deformity but worse PROMs than NON. CROSS achieved similar 2-year outcome scores as OP. Profiling at first visit for patients at risk of crossover may optimize physician counseling and cost savings.

摘要

背景情况

尽管手术在结果方面优于非手术治疗,但对于成人脊柱畸形(ASD)患者,非手术治疗仍是常见的初始治疗方法。无效的医疗护理是医疗系统资源消耗的主要来源。对可能选择手术治疗的 ASD 患者进行特征描述,可能有助于更有效地对患者进行咨询并节省成本。

目的

本研究旨在确定与非手术治疗相比,最终转为手术治疗的 ASD 患者的畸形和残疾特征,以及与那些仍接受非手术治疗和最初选择手术治疗的患者相比。

研究设计/设置:回顾性研究。

患者样本

共有 510 例 ASD 患者(189 例非手术治疗,321 例手术治疗),随访时间至少 2 年,构成患者样本。

评估结果

Oswestry 残疾指数(ODI)、SF-36 健康评估量表(SF-36)、脊柱侧凸研究协会问卷(SRS-22r)和脊柱骨盆放射影像学排列是评估结果。

方法

评估了前瞻性纳入多中心数据库的 ASD 患者队列的人口统计学、放射影像学和患者报告的结果测量(PROMs)数据。患者分为三组治疗:非手术治疗(NON=初始非手术治疗且仍为非手术治疗)、手术治疗(OP=初始手术治疗)和交叉治疗(CROSS=初始非手术治疗后转为手术治疗)。NON 和 OP 组通过倾向评分匹配(PSM)与 CROSS 匹配,以匹配基线人口统计学数据(年龄、体重指数、Charlson 合并症指数)。交叉时间分为早期(<1 年)和晚期(>1 年)。在四个时间点(基线、6 周、1 年和 2 年)比较各组之间和各组内的结果测量。

结果

经过 PSM,共纳入 118 例患者(NON=39 例,OP=38 例,CROSS=41 例)。交叉率为 21.7%(41/189)。平均交叉时间为 394 天。所有组的基线矢状面排列相似,但 CROSS 的骨盆入射角和腰椎前凸(PI-LL)不匹配大于 NON(11.9°比 3.1°,p=.032)。CROSS 和 OP 的基线 PROM 评分相似,但 CROSS 的基线 ODI、PCS、SRS-22r 较差(p<.05)。在交叉时,CROSS 的 ODI(35.7 比 27.8)和 SRS 满意度(2.6 比 3.3)比 NON 更差(p<.05)。从基线到转换时,CROSS 的排列保持相似;然而,PROMs(ODI、PCS、SRS 活动/疼痛/总分)恶化(p<.05)。早期和晚期交叉评估表明,CROSS-早期(n=25)在交叉时 ODI 和 SRS 活动/疼痛恶化(p<.05)。从交叉时间到 2 年随访,CROSS-早期与 OP 相比,SRS 外观/精神改善较少。CROSS-早期和晚期都有较差的基线,但与 NON 相比,ODI、PCS、SRS 疼痛/总分的改善更大(p<.05)。基线排列和残疾参数增加了交叉的可能性-非 Schwab T/L/D 曲线和 ODI≥40(比值比[OR]:3.05,p=.031),非高 PI-LL 修正等级(“+”/“++”)和 ODI≥40(OR:5.57,p=.007)的患者有更高的交叉风险。

结论

基线高和随时间推移的残疾增加导致非手术治疗向手术治疗 ASD 治疗的转变。CROSS 患者的脊柱畸形相似,但 PROMs 较差。CROSS 实现了与 OP 相似的 2 年结局评分。在初次就诊时对可能发生交叉的患者进行风险评估,可能有助于优化医生咨询和节省成本。

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