Outcome Assessment in Neuromuscular Spinal Deformity

被引:15
作者
Bowen, Richard E. [1 ]
Abel, Mark F. [1 ]
Arlet, Vincent [1 ]
Brown, Desmond [1 ]
Burton, Douglas C. [1 ]
D'Ambra, Phyllis [1 ]
Gill, Laura [1 ]
Hoekstra, Dale V. [1 ]
Karlin, Lawrence I. [1 ]
Raso, James [1 ]
Sanders, James O. [1 ]
Schwab, Frank J. [1 ]
机构
[1] Univ Calif Los Angeles, David Geffen Sch Med, Dept Orthopaed Surg, Los Angeles, CA 90095 USA
关键词
neuromuscular scoliosis; outcome assessment; myelodysplasia; cerebral palsy; muscular dystrophy; SPASTIC CEREBRAL-PALSY; MUSCULAR-DYSTROPHY; NATURAL-HISTORY; SCOLIOSIS; CHILDREN; SURGERY; MYELOMENINGOCELE; QUESTIONNAIRE; MANAGEMENT; FUSION;
D O I
10.1097/BPO.0b013e318273ab5a
中图分类号
R826.8 [整形外科学]; R782.2 [口腔颌面部整形外科学]; R726.2 [小儿整形外科学]; R62 [整形外科学(修复外科学)];
学科分类号
摘要
Patient-based outcome measures are important tools quantifying the disease-specific and/or global quality of life (QOL) effects of spinal deformity treatment. In patients with neuromuscular disorders such as cerebral palsy, muscular dystrophy, and myelomeningocele, treatment effects must be differentiated from underlying disease functional impairments. In general, the goals of spinal surgery in these patients are to improve QOL by enhancing sitting balance and posture, improving lung and gastrointestinal function, and reducing pain and deformity. In selected patients, improving ambulation and hand function may also be realistic surgical goals. QOL measures specific to both the neuromuscular diagnosis and spinal deformity provide higher quality information on treatment outcomes for a particular patient than standard radiographic measures. This article reviews patient-based outcome measures in spinal deformity patients with neuromuscular disorders, including their development and use in comparative outcome studies in the recent literature.
引用
收藏
页码:792 / 798
页数:7
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