Efficacy and safety of balloon kyphoplasty compared with non-surgical care for vertebral compression fracture (FREE): a randomised controlled trial

被引:607
作者
Wardlaw, Douglas [1 ]
Cummings, Steven R. [2 ,3 ]
Van Meirhaeghe, Jan [4 ]
Bastian, Leonard [5 ]
Tillman, John B. [6 ]
Ranstam, Jonas [7 ]
Eastell, Richard [8 ]
Shabe, Peter [9 ]
Talmadge, Karen [6 ]
Boonen, Steven [10 ]
机构
[1] Woodend Gen Hosp, Dept Orthopaed, NHS Grampian, Aberdeen AB15 6ZQ, Scotland
[2] Univ Calif San Francisco, Dept Epidemiol & Biostat, San Francisco, CA 94143 USA
[3] Calif Pacific Med Ctr, Res Inst, San Francisco Coordinating Ctr, San Francisco, CA USA
[4] Algemeen Ziekenhuis St Jan, Dienst Orthopedie & Traumatol, Brugge, Belgium
[5] Klinikum Leverkusen, Leverkusen, Germany
[6] Medtron Spine LLC, Sunnyvale, CA USA
[7] Univ Lund Hosp, Swedish Natl Competence Ctr Musculoskeletal Disor, S-22185 Lund, Sweden
[8] Univ Sheffield, Acad Unit Bone Metab, Sheffield, S Yorkshire, England
[9] Adv Res Associates Inc, Mountain View, CA USA
[10] Katholieke Univ Leuven, Div Geriatr Med, Louvain, Belgium
关键词
QUALITY-OF-LIFE; OSTEOPOROTIC FRACTURES; IMPORTANT DIFFERENCE; BACK-PAIN; OUTCOMES; QUESTIONNAIRE; ASSOCIATION; PREVALENT; SPINE;
D O I
10.1016/S0140-6736(09)60010-6
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Balloon kyphoplasty is a minimally invasive procedure for the treatment of painful vertebral fractures, which is intended to reduce pain and improve quality of life. We assessed the efficacy and safety of the procedure. Methods Adults with one to three acute vertebral fractures were eligible for enrolment in this randomised controlled trial at 21 sites in eight countries. We randomly assigned 300 patients by a computer-generated sequence to receive kyphoplasty treatment (n=149) or non-surgical care (n=151). The primary outcome was the difference in change from baseline to 1 month in the short-form (SF)-36 physical component summary (PCS) score (scale 0-100) between the kyphoplasty and control groups. Quality of life and other efficacy measurements and safety were assessed up to 12 months. Analysis was by intention to treat. This trial is registered with ClinicalTrials.gov, number NCT00211211. Findings 138 participants in the kyphoplasty group and 128 controls completed follow-up at 1 month. By use of repeated measures mixed effects modelling, all 300 randomised participants were included in the analysis. Mean SF-36 PCS score improved by 7.2 points (95% CI 5.7-8.8), from 26.0 at baseline to 33.4 at 1 month, in the kyphoplasty group, and by 2.0 points (0.4-3.6), from 25.5 to 27.4, in the non-surgical group (difference between groups 5.2 points, 2.9-7.4; p<0.0001). The frequency of adverse events did not differ between groups. There were two serious adverse events related to kyphoplasty (haematoma and urinary tract infection); other serious adverse events (such as myocardial infarction and pulmonary embolism) did not occur perioperatively and were not related to procedure. Interpretation Our findings suggest that balloon Icyphoplasty is an effective and safe procedure for patients with acute vertebral fractures and will help to inform decisions regarding its use as an early treatment option. Funding Medtronic Spine LLC.
引用
收藏
页码:1016 / 1024
页数:9
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