早期再手术对成人畸形患者的长期疼痛和活动评分没有不利影响。

IF 1.6 Q3 CLINICAL NEUROLOGY
Erik Lewerenz, Sarthak Mohanty, Fthimnir M Hassan, Nathan J Lee, Justin K Scheer, Chun Wai Hung, Steven G Roth, Joseph M Lombardi, Zeeshan M Sardar, Ronald A Lehman, Lawrence G Lenke
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引用次数: 0

摘要

目的:比较成人脊柱畸形(ASD)患者在首次手术后6个月内再次手术与未再入院/再手术的患者报告的结果(PROs),并注意活动和疼痛结果的相似/不同之处。方法:纳入在单一机构接受脊柱融合术至少2年随访的ASD患者。没有再入院/再手术的患者(No Reops)与那些需要在指数后6个月解决的早期再手术的患者(early Reop)进行比较。结果包括2Y PROs、改善和MCID的实现。SRS-22r中的问题22,评估选择相同治疗的可能性,被单独评估。结果:238例患者[211例(89%)无手术;包括27例(11%)早期Reop。早期再手术与PJK/DJK (29.63%, n = 8)、种植体脱位(18.52%,n = 5)和椎弓根/椎体骨折(14.81%,n = 4)相关。在人口统计学、手术特征、基线对齐和术前PROs方面没有差异。在SRS活动(p = 0.392)、疼痛(p = 0.291)、外观(p = 0.179)、心理健康(p = 0.840)、满意度(p = 0.098)、总分(p = 0.152)和ODI (p = 0.564)方面,PRO的改善无显著差异。MCID成绩在SRS活动(p = 0.536)、疼痛(p = 0.115)、外观(p = 0.269)、心理健康(p = 0.99)、满意度(p = 0.149)和ODI (p = 0.403)方面具有可比性。无Reops队列的SRS总分MCID达到率更高(82% vs 70%, p = 0.048)。此外,如果必须再次选择,更大比例的No Reop患者表示他们会选择相同的手术管理(86% vs 70%, p = 0.046)。结论:ASD术后6个月内的早期再手术解决了翻修手术的原因,不会对2年的功能和疼痛结果产生不利影响。然而,在没有Reop的队列中,只有70%的人会再次选择相同的治疗,而86%的人没有接受再手术,SRS22r总分MCID达到更高。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Early reoperations do not adversely affect long-term pain and activity scores in adult deformity patients.

Purpose: To compare patient-reported outcomes (PROs) in adult spinal deformity (ASD) patients reoperated within six months of their index surgery to patients without readmissions/reoperations and note any similarities/dissimilarities in activity and pain outcomes.

Methods: ASD patients who underwent spinal fusion at a single institution with minimum two years follow-up were included. Patients without readmissions/reoperations (No Reops) were compared to those requiring early reoperation resolved by six months post-index procedure (Early Reop) cohort. Outcomes included 2Y PROs, improvement, and MCID attainment. Question 22 from the SRS-22r, assessing likelihood of choosing the same treatment, was separately evaluated.

Results: 238 patients [211(89%) No Reops; 27(11%) Early Reop] were included. Early reoperations were associated with PJK/DJK (29.63%, n = 8), implant dislodgement (18.52%, n = 5), and pedicle/vertebral fracture (14.81%, n = 4). There was no difference in demographics, operative characteristics, baseline alignment, and preoperative PROs. PRO improvement was not significantly different for SRS Activity (p = 0.392), Pain (p = 0.291), Appearance (p = 0.179), Mental Health (p = 0.840), Satisfaction (p = 0.098), Total score (p = 0.152), and ODI (p = 0.564). MCID achievement was comparable for SRS Activity (p = 0.536), Pain (p = 0.115), Appearance (p = 0.269), Mental Health (p > 0.999), Satisfaction (p = 0.149), and ODI (p = 0.403). SRS total score MCID attainment was greater for No Reops Cohort (82% vs 70%, p = 0.048). In addition, a greater proportion of No Reop patients endorsed that they would choose the same operative management (86% vs 70%, p = 0.046) if they had to choose again.

Conclusion: Early reoperations within 6 months after ASD surgery that addresses the reason for the revision surgery do not adversely affect two-year functional and pain outcomes. However, only 70% would choose the same treatment again vs 86% of those who didn't undergo a reoperation with greater SRS22r total score MCID attainment among the No Reop cohort.

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来源期刊
CiteScore
3.20
自引率
18.80%
发文量
167
期刊介绍: Spine Deformity the official journal of the?Scoliosis Research Society is a peer-refereed publication to disseminate knowledge on basic science and clinical research into the?etiology?biomechanics?treatment?methods and outcomes of all types of?spinal deformities. The international members of the Editorial Board provide a worldwide perspective for the journal's area of interest.The?journal?will enhance the mission of the Society which is to foster the optimal care of all patients with?spine?deformities worldwide. Articles published in?Spine Deformity?are Medline indexed in PubMed.? The journal publishes original articles in the form of clinical and basic research. Spine Deformity will only publish studies that have institutional review board (IRB) or similar ethics committee approval for human and animal studies and have strictly observed these guidelines. The minimum follow-up period for follow-up clinical studies is 24 months.
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