How will early onset scoliosis surgery affect my child's future as a young adult? A follow-up study using patient-reported outcome measures.

IF 1.6 Q3 CLINICAL NEUROLOGY Spine deformity Pub Date : 2024-11-01 Epub Date: 2024-06-10 DOI:10.1007/s43390-024-00910-2
Dmitri A Falkner, Kyle J Miller, John B Emans, George H Thompson, John T Smith, Jack M Flynn, Jeffrey R Sawyer
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Abstract

Purpose: Using patient-reported outcome measures (PROMs), this study was undertaken to determine how well patients with early onset scoliosis (EOS) fare in adulthood.

Methods: Among eight healthcare centers, 272 patients (≥ 18 years) surgically managed for EOS (≥ 5 years) completed the Scoliosis Research Society (SRS)-22r, Functional Assessment of Chronic Illness Therapy-10 (FACIT-Dyspnea-10), and Short Form (SF)-12. Functional and demographic data were collected.

Results: The response rate was 40% (108/272). EOS etiologies were congenital (45%), neuromuscular (20%), idiopathic (20%) syndromic (11%), and unknown (4%). All patients scored within normal limits on the FACIT-Dyspnea-10 pulmonary (no breathing aids, 78%; no oxygen, 92%). SF-12 physical health scores and most SRS-22r domains were significantly decreased (p < 0.05 and p < 0.001, respectively) compared with normative values. SF-12 and SRS-22r mental health scores (MHS) were lower than normative values (p < 0.05 and p < 0.02, respectively). Physical health PROMs varied between etiologies. Treatment varied by etiology. Patients with congenital EOS were half as likely to undergo definitive fusion. There was no difference between EOS etiologies in SF-12 MHS, with t scores being slightly lower than normative peers.

Conclusion: Good long-term physical and social function and patient-reported quality of life were noted in surgically managed patients. Patients with idiopathic EOS physically outperformed those with other etiologies in objective and PROM categories but had similar MHS PROMs. Compared to normative values, EOS patients demonstrated decreased long-term physical capacity, slightly lower MHS, and preserved cardiopulmonary function.

Level of evidence: Level IV Case Series.

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早发脊柱侧弯手术会如何影响我孩子的未来?使用患者报告结果的跟踪研究。
目的:本研究采用患者报告的结果测量(PROMs)来确定早发性脊柱侧弯症(EOS)患者成年后的状况:在八个医疗中心中,272 名接受过 EOS(≥ 5 年)手术治疗的患者(≥ 18 岁)完成了脊柱侧凸研究学会(SRS)-22r、慢性疾病治疗功能评估-10(FACIT-呼吸困难-10)和短表格(SF)-12 的填写。收集了功能和人口统计学数据:结果:应答率为 40%(108/272)。EOS病因包括先天性(45%)、神经肌肉性(20%)、特发性(20%)、综合征(11%)和不明原因(4%)。所有患者的 FACIT-Dyspnea-10 肺部评分均在正常范围内(无呼吸辅助设备,78%;无氧气,92%)。SF-12 身体健康评分和大多数 SRS-22r 领域评分均显著下降(P经手术治疗的患者具有良好的长期身体和社会功能以及患者报告的生活质量。特发性 EOS 患者在客观和 PROM 方面优于其他病因的患者,但他们的 MHS PROMs 相似。与常模值相比,EOS患者的长期体能下降,MHS略低,心肺功能保持不变:证据等级:IV 级
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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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