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宫椎间盘关节整形:随机对照试验的推理,设计和结果
Djani M Robertson1, Andy Ton2, Michael Brown3
1Department of Orthopedic Surgery, NYU Langone Medical Center, New York, NY, USA.
International journal of spine surgery
|February 27, 2024
概括
本评论总结了FDA批准的宫椎间盘置换 (CDR) 植入物,表明证据支持它们在宫椎间盘疾病的传统融合上使用. 外科医生可以使用这些数据进行知情的手术前规划.
科学领域:
- 脊柱外科手术 脊柱外科手术
- 生物材料是一种生物材料.
- 整形外科植入物 整形外科植入物
背景情况:
- 目前食品和药物管理局 (FDA) 批准的宫椎间盘置换/宫椎间盘关节整形 (CDR/CDA) 植入物的概述.
- 脊椎外科医生对CDR/CDA临床数据和特征的集中资源.
研究的目的:
- 概述FDA批准的CDR/CDA植入物的临床数据和特征.
- 为脊椎外科医生提供一个全面的资源,用于术前规划.
主要方法:
- 2010年至2020年期间发表的CDR/CDA随机对照试验 (RCT) 的系统审查.
- 搜索了PubMed,科学网和谷歌学者数据库,包括34项符合条件的研究.
- 由两位作者进行独立审查,仲裁员参与,以解决差异.
主要成果:
- 将这些发现综合成一个表格,详细说明FDA批准的CDR/CDA植入物的特征和临床结果.
- 结果表明,CDR/CDA的适用范围正在扩大,使用率也在增加.
- 关于每个植入物的关键特征和临床结果的全面数据.
结论:
- 随机试验提供了大量证据支持CDR/CDA对单级和2级宫退行性磁盘疾病.
- CDR/CDA作为前椎间盘切除和融合的可行替代方案.
- 这一审查有助于脊椎外科医生做出关于CDR/CDA的术前规划的明智决定.
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