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关节镜手术与假手术治疗股骨髋臼撞击症和/或盂唇撕裂患者的随机对照试验研究方案(HIPARTI)和前瞻性队列研究(HARP)。

Arthroscopic Surgical Procedures Versus Sham Surgery for Patients With Femoroacetabular Impingement and/or Labral Tears: Study Protocol for a Randomized Controlled Trial (HIPARTI) and a Prospective Cohort Study (HARP).

出版信息

J Orthop Sports Phys Ther. 2018 Apr;48(4):325-335. doi: 10.2519/jospt.2018.7931.

Abstract

Study Design Study protocol for a randomized controlled trial and a prospective cohort. Background The number of arthroscopic surgical procedures for patients with femoroacetabular impingement syndrome (FAIS) has significantly increased worldwide, but high-quality evidence of the effect of such interventions is lacking. Objectives The primary objective will be to determine the efficacy of hip arthroscopic procedures compared to sham surgery on patient-reported outcomes for patients with FAIS (HIP ARThroscopy International [HIPARTI] Study). The secondary objective will be to evaluate prognostic factors for long-term outcome after arthroscopic surgical interventions in patients with FAIS (Hip ARthroscopy Prospective [HARP] Study). Methods The HIPARTI Study will include 140 patients and the HARP Study will include 100 patients. The international Hip Outcome Tool-33 will be the primary outcome measure at 1 year. Secondary outcome measures will be the Hip disability and Osteoarthritis Outcome Score, Arthritis Self-Efficacy Scale, fear of movement (Tampa Scale of Kinesiophobia), Patient-Specific Functional Scale, global rating of change score, and expectations. Other outcomes will include active hip range of motion, hip muscle strength tests, functional performance tests, as well as radiological assessments using radiographs and magnetic resonance imaging. Conclusion To determine the true effect of surgery, beyond that of placebo, double-blinded placebo-controlled trials including sham surgery are needed. The HIPARTI Study will direct future evidence-based treatment of FAIS. Predictors for long-term development and progression of degenerative changes in the hip are also needed for this young patient group with FAIS; hence, responders and nonresponders to treatment could be determined. J Orthop Sports Phys Ther 2018;48(4):325-335. doi:10.2519/jospt.2018.7931.

摘要

研究设计 一项随机对照试验和前瞻性队列研究的研究方案。 背景 全世界接受髋关节镜手术治疗股骨髋臼撞击综合征(FAIS)的患者数量显著增加,但此类干预措施效果的高质量证据仍然缺乏。 目的 主要目的将确定髋关节镜手术与假手术相比,对 FAIS 患者的患者报告结局的疗效(髋关节镜国际研究 [HIPARTI])。次要目的将评估 FAIS 患者关节镜手术后长期结局的预测因素(髋关节镜前瞻性研究 [HARP])。 方法 HIPARTI 研究将纳入 140 例患者,HARP 研究将纳入 100 例患者。国际髋关节结局工具-33 将是 1 年时的主要结局测量指标。次要结局测量指标将包括髋关节残疾和骨关节炎结局评分、关节炎自我效能量表、运动恐惧(坦帕运动恐惧量表)、患者特定功能量表、总体变化评分和期望。其他结局包括主动髋关节活动范围、髋关节肌肉力量测试、功能表现测试以及使用 X 线和磁共振成像的影像学评估。 结论 为了确定手术的真实效果,而不仅仅是安慰剂的效果,需要进行包括假手术的双盲安慰剂对照试验。HIPARTI 研究将指导 FAIS 的未来循证治疗。对于 FAIS 这一年轻患者群体,还需要确定髋关节退行性变化的长期发展和进展的预测因素,从而确定治疗的反应者和无反应者。 骨科与运动物理治疗杂志 2018;48(4):325-335.doi:10.2519/jospt.2018.7931.

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