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危重病大临床试验中引文影响力的决定因素:以研究者为主体的临床试验组的作用。

Determinants of Citation Impact in Large Clinical Trials in Critical Care: The Role of Investigator-Led Clinical Trials Groups.

机构信息

1Keenan Research Centre at the Li Ka Shing Knowledge Institute and the Department of Critical Care Medicine, St. Michael's Hospital, and the Interdepartmental Division of Critical Care, University of Toronto, Toronto, ON, Canada. 2Faculty of Medicine, Queen's University, Kingston, ON, Canada.

出版信息

Crit Care Med. 2016 Apr;44(4):663-70. doi: 10.1097/CCM.0000000000001466.

Abstract

OBJECTIVES

Randomized clinical trials provide the best evidence of treatment effectiveness; factors determining their impact are unknown. We sought to determine the influence of funding (industry vs nonindustry), research (comparative effectiveness vs technology evaluation), and organizational models (investigator-led trials group vs others) on the impact of large trials in critical care medicine.

DATA SOURCES

We searched MEDLINE for randomized clinical trials published between 1990 and 2012 in five critical care, five general interest, and one pediatrics journal. Impact was evaluated as annual citation rates measured using the ISI Web of Knowledge database.

STUDY SELECTION

Eligible trials enrolled at least 100 critically ill adults, children, or neonates, evaluated an intervention that was applied during the ICU stay, and reported mortality and/or length of ICU or hospital stay.

DATA EXTRACTION

Two reviewers identified eligible studies, and two separate reviewers extracted data.

DATA SYNTHESIS

We identified 391 randomized clinical trials, recruiting 208,154 subjects. Funding source--industry versus peer review versus mixed--did not impact citation rates. Comparative effectiveness studies made up 52.5% of the reports and were cited more frequently than studies evaluating novel technologies (median, 15.6 vs 10.3 citations/yr; p = 0.002). Trials conducted by investigator-led trials groups (n = 45) were cited a median of 45.7 (interquartile range [IQR], 17.3-86.2) times per year, significantly more often (p < 0.0001) than multicenter trials conducted by ad hoc groups (n = 89; median, 19 [IQR, 8.7-30.4]) or industry (n = 85; median, 12.3 [IQR, 5.4-24.1]), and more than single-center trials (n = 116; median, 6.8 [IQR, 3.5-12.8]) or small ad hoc trials involving two to five centers (n = 59; median, 11.0 [IQR, 4.5-22.4]). Although only 11.5% of all trials included, randomized clinical trials from investigator-led research consortia accounted for nine of the 16 studies cited more than 100 times per year and 23.4% of all citations; their costs were substantially less than the typical costs of industry-run trials..

CONCLUSIONS

Clinical trials conducted by investigator-led research groups are significantly more frequently cited than industry-led trials in critical care medicine. In addition, costs appear to be substantially lower with investigator-led trials. Support for and expansion of this model of research can ensure that critical care research is clinically relevant and practice changing.

摘要

目的

随机临床试验提供了治疗效果的最佳证据;但决定其影响的因素尚不清楚。我们旨在确定资金(行业与非行业)、研究(有效性比较与技术评估)和组织模式(研究者主导的试验组与其他模式)对重症监护医学中大型试验的影响。

数据来源

我们在五个重症监护、五个一般兴趣和一个儿科期刊中,检索了 1990 年至 2012 年间发表的随机临床试验。使用 ISI Web of Knowledge 数据库评估影响,评估指标为每年的引用率。

研究选择

符合条件的试验至少招募了 100 名重症成人、儿童或新生儿,评估了 ICU 期间应用的干预措施,并报告了死亡率和/或 ICU 或住院时间。

数据提取

两名评审员确定了符合条件的研究,两名独立评审员提取了数据。

数据综合

我们确定了 391 项随机临床试验,共招募了 208154 名受试者。资金来源(行业、同行评议、混合)并未影响引用率。比较有效性研究占报告的 52.5%,比评估新技术的研究更常被引用(中位数,15.6 比 10.3 次/年;p = 0.002)。由研究者主导的试验组(n = 45)进行的试验每年平均被引用 45.7(四分位间距 [IQR],17.3-86.2)次,明显高于多中心试验(n = 89;中位数,19 [IQR,8.7-30.4])或行业资助的试验(n = 85;中位数,12.3 [IQR,5.4-24.1]),也高于单中心试验(n = 116;中位数,6.8 [IQR,3.5-12.8])或涉及 2-5 个中心的小型临时试验(n = 59;中位数,11.0 [IQR,4.5-22.4])。尽管只占所有试验的 11.5%,但由研究者主导的研究联盟进行的随机临床试验占每年被引用超过 100 次的 16 项研究中的 9 项,占所有引用的 23.4%;其成本明显低于典型的行业主导试验。

结论

在重症监护医学中,由研究者主导的研究组进行的临床试验比行业主导的试验更常被引用。此外,研究者主导的试验成本明显更低。支持和扩展这种研究模式可以确保重症监护研究具有临床相关性和实践改变性。

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