Cochrane Collaboration


Cochrane Collaboration
The Cochrane Collaboration
Motto Working together to provide the best evidence for health care
Formation 1993 (1993)
Type International NPO
Purpose/focus Health care information
Headquarters Oxford, England
Region served Worldwide
Official languages English
Steering Group Co-Chairs Jeremy Grimshaw,
Jonathan Craig[1]
Volunteers Over 28,000 as of 2011[2]
Website www.cochrane.org

The Cochrane Collaboration is a group of over 28,000 volunteers in more than 100 countries who review the effects of health care interventions tested in biomedical randomized controlled trials.[3] A few more recent reviews have also studied the results of non-randomized, observational studies. The results of these systematic reviews are published as "Cochrane Reviews" in the Cochrane Library.

Contents

The logo of Cochrane Collaboration illustrates a meta analysis of data from seven randomized controlled trials (RCTs), comparing one health care treatment with a placebo in a forest plot. The diagram shows the results of a systematic review and meta analysis on inexpensive course of corticosteroid given to women about to give birth too early – the evidence on effectiveness that would have been revealed had the available RCTs been reviewed systematically a decade later. This treatment reduces the odds of the babies of such women dying from the complications of immaturity by 30–50%. Because no systematic review of these trials had been published until 1989, most obstetricians had not realised that the treatment was so effective and therefore many premature babies have probably suffered or died unnecessarily.[4]

History

The Cochrane Collaboration was founded in 1993 under the leadership of Iain Chalmers. It was developed in response to Archie Cochrane's call for up-to-date, systematic reviews of all relevant randomized controlled trials of health care.

Cochrane's suggestion that the methods used to prepare and maintain reviews of controlled trials in pregnancy and childbirth should be applied more widely was taken up by the Research and Development Programme, initiated to support the United Kingdom's National Health Service. Through the NHS R&D programme, led by the first Director of Research and Development Professor Michael Peckham,[5] funds were provided to establish a 'Cochrane Centre', to collaborate with others, in the UK and elsewhere, to facilitate systematic reviews of randomized controlled trials across all areas of health care.[6].

In October 1995, The Collaboration formed the Cochrane Consumer Network[7] to incorporate patient perspectives into the review process. Shortly thereafter, new 'plain language summaries' provided users with a jargon-free synopsis of each systematic review.[8]

Goal and principles

The goal of the collaboration is to help people make well informed decisions about health care by preparing, maintaining and ensuring the accessibility of systematic reviews of the effects of health care interventions. The principles of the Cochrane Collaboration are:

  • collaboration
  • "building on the enthusiasm of individuals"[9]
  • avoiding duplication
  • minimizing bias
  • keeping up to date
  • striving for relevance
  • promoting access
  • ensuring quality
  • continuity
  • enabling wide participation

Criticism

A 2011 study done to disclose possible conflicts of interests in underlying research studies used for medical meta-analyses reviewed 29 meta-analyses and found that conflicts of interests in the studies underlying the meta-analyses were rarely disclosed. The 29 meta-analyses included 11 from general medicine journals; 15 from specialty medicine journals, and 3 from the Cochrane Database of Systematic Reviews. The 29 meta-analyses reviewed an aggregate of 509 randomized controlled trials (RCTs). Of these, 318 RCTs reported funding sources with 219 (69%) industry funded. 132 of the 509 RCTs reported author conflict of interest [COI] disclosures, with 91 studies (69%) disclosing industry financial ties with one or more authors. The information was, however, seldom reflected in the meta-analyses. Only two (7%) reported RCT funding sources and none reported RCT author-industry ties. The authors concluded “without acknowledgement of COI due to industry funding or author industry financial ties from RCTs included in meta-analyses, readers’ understanding and appraisal of the evidence from the meta-analysis may be compromised.” Noting that most assessment tools for meta-analysis do not include a domain for study funding source the authors state: “Currently, The Cochrane Collaboration’s Risk of Bias tool includes an optional 'other sources of bias' domain, which meta-analysts could use to include information on COIs. We recommend that The Cochrane Collaboration consider formalizing the requirement to assess potential bias from COIs.”[10]

See also

References

External links


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  • Cochrane Library — Die Cochrane Library ist ein die evidenzbasierte Medizin unterstützendes Informationsportal für Ärzte, Patienten und Wissenschaftler. Als Einrichtung der Cochrane Collaboration bietet sie ihren Lesern in insgesamt sechs Datenbanken Informationen… …   Deutsch Wikipedia

  • Cochrane Library — The Cochrane Library (named after Archie Cochrane) is a collection of databases in medicine and other healthcare specialties provided by the Cochrane Collaboration and other organisations. At its core is the collection of Cochrane Reviews, a… …   Wikipedia

  • Cochrane-Zentrum — Die Cochrane Collaboration (Aussprache: kokrən) ist ein weltweites Netz von Wissenschaftlern und Ärzten. Ziel ist, systematische Übersichtsarbeiten (systematic reviews) zur Bewertung von medizinischen Therapien zu erstellen, aktuell zu halten und …   Deutsch Wikipedia

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  • Cochrane (surname) — For places and entities named Cochrane, see Cochrane. Cochrane Family name Pronunciation /ˈkɒkrən/ Spelled Pronunciation kok ruhn Meaning Derives Cochrane in Scotland, meaning red brook (residential); Anglicisation of corcair, meaning crimson …   Wikipedia