Misinformation in the medical literature: what role do error and fraud play?

R Grant Steen1

  • 1Medical Communications Consultants, LLC, 103 Van Doren Place, Chapel Hill, NC 27517, USA. g_steen_medicc@yahoo.com

Journal of Medical Ethics
|February 24, 2011
PubMed

Insights

Retracted research highlights medical misinformation, often stemming from errors rather than fraud. Improving data integrity and transparency in clinical trials can minimize future inaccuracies in scientific literature.

Area of Science:

  • Medical research integrity
  • Scientific communication
  • Research ethics

Background:

  • Media focus on retracted research often overstates the prevalence of deliberate misinformation.
  • All scientific papers contain some level of misinformation; the key is the balance of correct versus incorrect information.
  • Retracted papers offer insights into medical misinformation but are not representative of all incorrect publications.

Purpose of the Study:

  • To analyze retracted research papers to understand the sources and nature of medical misinformation.
  • To differentiate between misinformation arising from error versus fraud.
  • To propose measures for minimizing misinformation in the medical literature.

Main Methods:

  • Analysis of retracted research papers to identify common causes of retraction and misinformation.
  • Categorization of misinformation sources into error and fraud.
  • Review of scientific impropriety in experimental design, data collection, analysis, and presentation.

Main Results:

  • Error is the most frequent reason for research retraction and a primary source of misinformation.
  • Fraud accounts for approximately one-quarter of retracted papers, also contributing to misinformation.
  • Scientific impropriety leading to bias can stem from unintentional errors or statistical naiveté, not exclusively fraud.

Conclusions:

  • Error and fraud are the principal sources of medical misinformation, with error being more prevalent.
  • Bias represents non-retracted misinformation resulting from scientific impropriety.
  • Recommendations include enhanced clinical trial registries, clear statistical criteria, author accountability, financial transparency, and clearer retraction reasons to reduce misinformation.

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