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脊柱植入物研究报告结果的24个月随访:该指南是否有文献支持?

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

作者信息

Ohnmeiss Donna D, Guyer Richard D

机构信息

Texas Back Institute Research Foundation, Plano, Texas.

出版信息

SAS J. 2009 Sep 1;3(3):100-7. doi: 10.1016/j.esas.2009.09.003. eCollection 2009.

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.

摘要

背景

传统上,脊柱协会和期刊制定了指南,要求对手术植入物研究的结果进行至少24个月的随访。然而,这个特定时间段的依据尚不清楚。本研究的目的是分析前瞻性脊柱植入物研究在多个特定随访期报告的数据,以确定在24个月的随访期内临床结果是否有显著变化。

方法

使用PubMed进行了全面的文献检索,并搜索了FDA网页。对研究进行评估,以确定符合纳入标准的研究:涉及至少100例接受脊柱植入物的患者,术后在多个预先定义的时间段报告数据,至少持续24个月。从每项研究中记录的数据包括患者数量、诊断、使用的植入物、使用的结果测量指标以及报告的结果。在本研究中对主要结果数据进行分析,以确定评分变化量,特别关注6个月和24个月的随访期。

结果

只有7项研究符合纳入标准。所有7项研究均为1997年以来发表的受FDA监管的试验。6项研究涉及有症状椎间盘退变的治疗,1项研究涉及因狭窄导致神经源性间歇性跛行的患者。研究中的结果测量指标各不相同,但疼痛和功能经常被评估。在所有研究中,6个月和24个月随访期之间的结果均无显著恶化。事实上,随访期间唯一的变化是轻微的、无统计学意义的改善,但有一项研究中的一个量表除外,在该量表中,6个月至24个月期间身体功能评估的改善程度略有下降,但无统计学意义。这些结果表明,接受脊柱植入物的患者在6个月至24个月期间,各种结果测量指标的平均评分具有很大的稳定性。

结论

虽然任何临床结果研究都确实需要长期随访,但6个月和24个月随访之间的结果测量指标似乎没有显著变化。这些结果支持在不产生过度乐观报告的情况下,可能适合更早地传播结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c49c/4365596/e572c4536be7/SAS-3-2009-09-003-g001.jpg

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