肋骨-骨盆畸形:导致脑瘫患者疼痛和健康相关生活质量低下的可调节因素。

IF 1.6 Q3 CLINICAL NEUROLOGY
Vineet M Desai, Margaret Bowen, Jason B Anari, John M Flynn, Burt Yaszay, Paul Sponseller, Mark Abel, Joshua Pahys, Patrick J Cahill
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引用次数: 0

摘要

目的:脑性瘫痪(CP)通常表现为胸腰椎侧弯和骨盆倾斜。骨盆严重倾斜时,肋骨会接触到倾斜骨盆的高侧,称为肋骨骨盆畸形(ROP)。肋骨骨盆畸形会导致肋髂关节撞击或与肋骨骨盆畸形相关的疼痛,还会对呼吸和坐姿平衡产生不利影响。本研究的目的是评估患有 ROP 的 CP 患者在手术前的健康相关生活质量(HRQOL)是否较差,以及手术后的 HRQOL 是否有较大改善:对所有接受脊柱融合术治疗且至少随访两年的非行动不便的 CP 患者进行了回顾性分析。HRQOL通过照顾者优先权和儿童残疾生活健康指数(CPCHILD)问卷的各领域进行测量(0 = 最严重残疾,100 = 最轻微残疾)。在术前直立位X光片上,肋骨远端位于髂嵴上部即为ROP。将 ROP 组与无 ROP 的对照组在 CPCHILD 的六个领域得分和总分方面进行比较。采用多元线性回归控制曲线顶点位置、主要冠状面 Cobb 角、音调类型和骨盆倾斜度:340名患者符合纳入标准(52%为女性,平均年龄14.0岁)。主要冠状面 Cobb 角的平均值为 81 度,骨盆倾斜的平均值为 22 度。176名患者(51.8%)患有视网膜病变,164名患者(48.2%)没有视网膜病变。ROP 与术前体位/转移/活动度 (PTM)、舒适度和情绪 (C&E) 以及 CPCHILD 问卷中的 CPCHILD 总分较差独立相关(P 结论:ROP 和 CPCHILD 总分较低的患者术前体位/转移/活动度较差:与无肋骨-骨盆畸形的患者相比,有肋骨-骨盆畸形的 CP 患者会经历更多的疼痛和更差的 HRQOL。脊柱融合术后,通过 CPCHILD 问卷测量,这些患者的 HRQOL 有了更大的改善。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Rib-on-pelvis deformity: a modifiable driver of pain and poor health-related quality of life in cerebral palsy.

Purpose: Cerebral Palsy (CP) often presents with a sweeping thoracolumbar scoliosis and pelvic obliquity. With severe pelvic obliquity, the ribs come into contact with the high side of the oblique pelvis, termed rib-on-pelvis deformity (ROP). ROP can result in costo-iliac impingement, or pain associated with ROP, and can also adversely affect breathing and sitting balance. The goal of this study was to evaluate whether CP patients with ROP have worse health-related quality of life (HRQOL) before surgery and a greater improvement in HRQOL after surgery.

Methods: A retrospective analysis of a prospectively collected, multicenter, international registry was performed for all nonambulatory patients with CP treated with spinal fusion with at least two-year follow-up. HRQOL was measured via the Caregiver Priorities & Child Health Index of Life with Disabilities (CPCHILD) questionnaire domains (0 = most disability, 100 = least disability). ROP was defined as having a rib distal to the superior portion of the iliac crest on preop upright radiographs. The ROP group and control group without ROP were compared regarding six domain scores and total score of CPCHILD. Multiple linear regression was used to control for curve apex location, major coronal Cobb angle, type of tone, and pelvic obliquity.

Results: 340 patients met inclusion criteria (52% female, mean age 14.0 years). The mean major coronal Cobb angle was 81 degrees and mean pelvic obliquity was 22 degrees. 176 patients (51.8%) had ROP while 164 patients (48.2%) did not. ROP was independently associated with worse preoperative Positioning/Transfers/Mobility (PTM), Comfort & Emotions (C&E), and total CPCHILD score via the CPCHILD questionnaire (p < 0.05). Patients with preoperative ROP experienced a greater improvement in the C&E and PTM domains as well as total CPCHILD score than patients without ROP (p < 0.05).

Conclusion: CP patients with rib-on-pelvis deformity experience more pain and worse HRQOL than patients without this deformity. These patients experienced a greater improvement in HRQOL after spinal fusion measured via the CPCHILD questionnaire.

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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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