Twenty-four month follow-up for reporting results of spinal implant studies: Is this guideline supported by the literature?

Donna D. Ohnmeiss Dr.Med, Richard D. Guyer MD
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引用次数: 6

Abstract

Background

Traditionally, spine societies and journals have set guidelines requiring a minimum 24-month follow-up for reporting results of surgical implant studies. However, the basis for this particular time period is not clear. The purpose of this study was to analyze prospective spinal implant studies reporting data at multiple specific follow-up periods to determine if there were significant changes in the clinical outcome throughout the 24-month follow-up period.

Methods

A comprehensive literature search was conducted using PubMed as well as searching the FDA web page. Studies were evaluated to identify those meeting the inclusion criteria: involved at least 100 patients receiving a spinal implant with data reported at multiple pre-defined time periods post-operatively for at least 24-months. Data recorded from each study included, number of patients, diagnoses, implant used, outcome measures used, and the results reported. The primary outcome data were analyzed in the current study to determine the amount of change in scores, with particular focus on the six and 24-month follow-up periods.

Results

Only 7 studies met the inclusion criteria. All seven studies were FDA-regulated trials published since 1997. Six addressed the treatment of symptomatic disc degeneration and 1 involved patients with neurogenic claudication due to stenosis. The outcome measures in the studies varied but pain and function were frequently assessed. In none of the studies was there a significant deterioration in results between the 6 and 24-month follow-up periods. In fact, the only changes during the follow-up periods were slight, not statistically significant, improvements, with the exception of 1 scale in 1 study where a slight, not statistically significant, decrease in the extent of improvement on a physical function assessment was noted between 6 and 24 months. These results suggest a great deal of stability in the mean scores for various outcome measures between the 6 and 24 months in patients receiving spinal implants.

Conclusions

Although long-term follow-up is certainly desirable for any clinical outcome study, there appears to be no significant change in outcome measures between the 6-month and 24-month follow-ups. These results support that earlier dissemination of results may be appropriate without producing overly-optimistic reports.

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对脊柱植入研究结果的24个月随访:该指南是否有文献支持?
传统上,脊柱学会和期刊已经制定了指南,要求至少24个月的随访报告手术植入研究的结果。然而,这一特定时期的基础并不清楚。本研究的目的是分析在多个特定随访期间的前瞻性脊柱植入研究报告数据,以确定在24个月的随访期间临床结果是否有显著变化。方法利用PubMed进行文献检索,同时检索FDA相关网页。评估研究以确定符合纳入标准的研究:涉及至少100例接受脊柱植入的患者,并在术后至少24个月的多个预定时间段报告数据。每项研究记录的数据包括患者数量、诊断、使用的植入物、使用的结果测量和报告的结果。本研究对主要结果数据进行了分析,以确定评分的变化量,特别关注6个月和24个月的随访期。结果仅有7项研究符合纳入标准。所有七项研究都是1997年以来由fda监管的试验。6例涉及症状性椎间盘退变的治疗,1例涉及狭窄导致的神经源性跛行患者。研究的结果测量各不相同,但疼痛和功能经常被评估。在6至24个月的随访期间,没有一项研究的结果出现明显恶化。事实上,在随访期间,唯一的变化是轻微的,没有统计学意义的改善,除了1个研究中的1个量表,在6到24个月期间,身体功能评估的改善程度略有下降,没有统计学意义。这些结果表明,在接受脊柱植入物的患者6至24个月期间,各种结果测量的平均得分具有很大的稳定性。结论:虽然长期随访对于任何临床结果研究都是可取的,但在6个月和24个月的随访中,结果测量似乎没有显著变化。这些结果支持,尽早传播结果可能是适当的,而不必产生过于乐观的报告。
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