I am a medical epidemiologist with a long-standing interest in the
mechanisms of publishing, the quality of international biomedical
literature and editorial peer review. I will limit my comments to the
biomedical field.
One of the best ways of assessing the status of each of the three
interlinked areas is to base one’s observations and predictions on the
totality of available evidence. In biomedicine this is summed-up in
systematic reviews which are sometimes also incorrectly known as meta-
analyses (this is more properly the name a statistical technique to
pool data, but is of little relevance to my comments).
Biomedical publishing is a huge global business producing a plethora
of information of all kinds. In the last few years there has been a
growing body of evidence showing some fundamental problems with
contemporary literature. These problems are due to partial and biased
publication of data, fraud (which is probably rare) research
misconduct in its many forms (which is more common), redundant
publication (in which the same set of data are published more than
once without cross referencing), poor study design, optimistic
conclusions favouring new and expensive treatments, media buzz for new
(and more expensive) treatments which years later are shown not to be
so effective, ghost writing of studies and (more recently) prestigious
journals preferentially publishing studies with rich backers,
regardless of their quality or size.
These problems would not really matter, were it not for the fact that
ultimately people’s health and health care delivery are affected.
Ethically to me as a physician this situation is intolerable.
However, the problems are of difficult resolution without a
fundamental paradigm shift which requires two linked interventions to
address the causes of this situation.
First the publishing of biomedical should not be a business. Research
conducted on human beings should be freely available in public
archives and (as your project aims to achieve) freely available. There
is no scientifically tenable reason for the so-called Inglefinger rule
(the right to publish only what has not been published before), nor
for the very existence of journals. There is little evidence that
journal rituals such as peer review add anything. Even less is there a
requirement to transfer copyright of a research paper to one of the
big publishing houses.
Second, the assessment of research quality and researchers’ careers
should not be based on the number of publications nor on their quality
as judged indirectly by bibliometric indicators such as the impact
factor (IF). The IF is a measure of journal citation and is not linked
to methodological quality of what is published in it. Academic
pressures to publish in journals with a high journal impact factor are
distorting and corrupting biomedical research, as both authors,
sponsors and journals are in fierce competition for ever higher factor
scores and the perverse incentives of the current system are beginning
to be clearly visible.
Projects such as yours are desperately needed to provide incentives
for honest biomedical research conduct and reporting. However: beware
of substituting the IF with endorsements. There is no point in getting
rid of one totem and providing another incentive for points
collection. Research should be judged on its capacity to improve
health and that takes time and an open debate.
Tom Jefferson
Jeffer...@gmail.com