A Randomized Trial of Vertebroplasty for Painful Osteoporotic Vertebral Fractures

被引:970
作者
Buchbinder, Rachelle [1 ,2 ]
Osborne, Richard H. [3 ]
Ebeling, Peter R. [4 ]
Wark, John D. [5 ,6 ]
Mitchell, Peter [5 ,6 ]
Wriedt, Chris [7 ]
Graves, Stephen [8 ]
Staples, Margaret P. [1 ,2 ]
Murphy, Bridie [1 ,2 ]
机构
[1] Monash Univ, Cabrini Hosp, Monash Dept Clin Epidemiol, Malvern, Vic, Australia
[2] Monash Univ, Dept Epidemiol & Prevent Med, Malvern, Vic, Australia
[3] Deakin Univ, Melbourne, Vic, Australia
[4] Univ Melbourne, Western Hosp, Royal Melbourne Hosp, Dept Med, Footscray, Vic, Australia
[5] Univ Melbourne, Dept Med, Royal Melbourne Hosp, Western Hosp, Parkville, Vic 3052, Australia
[6] Univ Melbourne, Dept Radiol, Royal Melbourne Hosp, Parkville, Vic 3052, Australia
[7] Cabrini Hlth, Cabrini Med Imaging, Malvern, Vic, Australia
[8] Univ Adelaide, Data Management & Anal Ctr, Australian Orthopaed Assoc, Natl Joint Replacement Register, Adelaide, SA, Australia
基金
英国医学研究理事会;
关键词
QUALITY-OF-LIFE; PERCUTANEOUS VERTEBROPLASTY; COMPRESSION FRACTURES; AUGMENTATION; EFFICACY; SAFETY; RISK; MEN;
D O I
10.1056/NEJMoa0900429
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND Vertebroplasty has become a common treatment for painful osteoporotic vertebral fractures, but there is limited evidence to support its use. METHODS We performed a multicenter, randomized, double-blind, placebo-controlled trial in which participants with one or two painful osteoporotic vertebral fractures that were of less than 12 months' duration and unhealed, as confirmed by magnetic resonance imaging, were randomly assigned to undergo vertebroplasty or a sham procedure. Participants were stratified according to treatment center, sex, and duration of symptoms (<6 weeks or >= 6 weeks). Outcomes were assessed at 1 week and at 1, 3, and 6 months. The primary outcome was overall pain (on a scale of 0 to 10, with 10 being the maximum imaginable pain) at 3 months. RESULTS A total of 78 participants were enrolled, and 71 (35 of 38 in the vertebroplasty group and 36 of 40 in the placebo group) completed the 6-month follow-up (91%). Vertebroplasty did not result in a significant advantage in any measured outcome at any time point. There were significant reductions in overall pain in both study groups at each follow-up assessment. At 3 months, the mean (+/- SD) reductions in the score for pain in the vertebroplasty and control groups were 2.6 +/- 2.9 and 1.9 +/- 3.3, respectively (adjusted between-group difference, 0.6; 95% confidence interval, -0.7 to 1.8). Similar improvements were seen in both groups with respect to pain at night and at rest, physical functioning, quality of life, and perceived improvement. Seven incident vertebral fractures (three in the vertebroplasty group and four in the placebo group) occurred during the 6-month follow-up period. CONCLUSIONS We found no beneficial effect of vertebroplasty as compared with a sham procedure in patients with painful osteoporotic vertebral fractures, at 1 week or at 1, 3, or 6 months after treatment. (Australian New Zealand Clinical Trials Registry number, ACTRN012605000079640.)
引用
收藏
页码:557 / 568
页数:12
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