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Improving bioscience research reporting: The ARRIVE guidelines for reporting animal research

Carol Kilkenny, William J. Browne, Innes C. Cuthill and 2 more

Journal of Pharmacology and Pharmacotherapeutics · 2010 · Review

doi:10.4103/0976-500x.72351

Abstract

This FAIRsharing record describes: The ARRIVE (Animal Research: Reporting In Vivo Experiments) guidelines are intended to improve the reporting of research using animals - maximising information published and minimising unnecessary studies. The ARRIVE guidelines were developed in consultation with the scientific community as part of an NC3Rs initiative to improve the standard of reporting of research using animals. They are available in Chinese (Mandarin), French, Italian, Japanese, Korean, Portuguese (including Brazilian Portuguese) and Spanish as well as the original English.

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Full text

From PubMed Central, U.S. National Library of Medicine, as current on Oct 17, 2026. Paragraph numbers are ours, so an answer can point at one.

In the last decade the number of bioscience journals has increased enormously, with many filling specialised niches reflecting new disciplines and technologies. The emergence of open-access journals has revolutionised the publication process, maximising the availability of research data. Nevertheless, a wealth of evidence shows that across many areas, the reporting of biomedical research is often inadequate, leading to the view that even if the science is sound, in many cases the publications themselves are not “fit for purpose,” meaning that incomplete reporting of relevant information effectively renders many publications of limited value as instruments to inform policy or clinical and scientific practice. A recent review of clinical research showed that there is considerable cumulative waste of financial resources at all stages of the research process, including as a result of publications that are unusable due to poor reporting. It is unlikely that this issue is confined to clinical research.

Failure to describe research methods and to report results appropriately therefore has potential scientific, ethical and economic implications for the entire research process and the reputation of those involved in it. This is particularly true for animal research, one of the most controversial areas of science. The largest and most comprehensive review of published animal research undertaken to date, to our knowledge, has highlighted serious omissions in the way research using animals is reported. The survey, commissioned by the National Centre for the Replacement, Refinement and Reduction of Animals in Research (NC3Rs), a UK Government-sponsored scientific organisation, found that only 59% of the 271 randomly chosen articles assessed stated the hypothesis or objective of the study and the number and characteristics of the animals used (i.e., species/strain, sex and age/weight). Most of the papers surveyed did not report using randomisation (87%) or blinding (86%) to reduce bias in animal selection and outcome assessment. Only 70% of the publications that used statistical methods fully described them and presented the results with a measure of precision or variability. These findings are a cause for concern and are consistent with reviews of many research areas, including clinical studies, published in recent years.

GOOD REPORTING IS ESSENTIAL FOR PEER REVIEW AND TO INFORM FUTURE RESEARCH

Scrutiny by scientific peers has long been the mainstay of “quality control” for the publication process. The way that experiments are reported, in terms of the level of detail of methods and the presentation of key results, is crucial to the peer review process and, indeed, the subsequent utility and validity of the knowledge base that is used to inform future research. The onus is therefore on the research community to ensure that their research articles include all relevant information to allow in-depth critique and to avoiding duplicating studies and performing redundant experiments. Ideally scientific publications should present sufficient information to allow a knowledgeable reader to understand what was done, why and how and to assess the biological relevance of the study and the reliability and validity of the findings. There should also be enough information to allow the experiment to be repeated. The problem therefore is how to ensure that all relevant information is included in research publications.

USING REPORTING GUIDELINES MEASURABLY IMPROVES THE QUALITY OF REPORTING

Evidence provided by reviews of published research suggests that many researchers and peer reviewers would benefit from guidance about what information should be provided in a research article. The CONSORT Statement for randomised controlled clinical trials was one of the first guidelines developed in response to this need. Since publication, an increasing number of leading journals have supported CONSORT as part of their instructions to authors. As a result, convincing evidence is emerging that CONSORT improves the quality and transparency of reports of clinical trials.

Following CONSORT, many other guidelines have been developed—there are currently more than 90 available for reporting different types of health research, most of which have been published in the last ten years (see http://www.equator-network.org and references). Guidelines have also been developed to improve the reporting of other specific bioscience research areas including metabolomics and gene expression studies. Several organisations support the case for improved reporting and recommend the use of reporting guidelines, including the International Committee of Medical Journal Editors, the Council of Science Editors, the Committee on Publication Ethics and the Nuffield Council for Bioethics.

IMPROVING THE REPORTING OF ANIMAL EXPERIMENTS—THE ARRIVE GUIDELINES

Most bioscience journals currently provide little or no guidance on what information to report when describing animal research. Our review found that 4% of the 271 journal articles assessed did not report the number of animals used anywhere in the methods or the results sections. Reporting animal numbers is essential so that the biological and statistical significance of the experimental results can be assessed or the data reanalysed and is also necessary if the experimental methods are to be repeated. Improved reporting of these and other details will maximise the availability and utility of the information gained from every animal and every experiment, preventing unnecessary animal use in the future. To address this, we led an initiative to produce guidelines for reporting animal research. The guidelines, referred to as ARRIVE (Animals in Research: Reporting In vivo Experiments), have been developed using the CONSORT Statement as their foundation.

The ARRIVE guidelines consist of a checklist of 20 items describing the minimum information that all scientific publications reporting research using animals should include, such as the number and specific characteristics of animals used (including species, strain, sex and genetic background); details of housing and husbandry; and the experimental, statistical and analytical methods (including details of methods used to reduce bias such as randomisation and blinding). All the items in the checklist have been included to promote high-quality, comprehensive reporting to allow an accurate critical review of what was done and what was found.

Consensus and consultation are the corner-stones of the guideline development process. To maximise their utility, the ARRIVE guidelines have been prepared in consultation with scientists, statisticians, journal editors and research funders. We convened an expert working group, comprising researchers and statisticians from a range of disciplines and journal editors from Nature Cell Biology, Science, Laboratory Animals and the British Journal of Pharmacology (see Acknowledgments). At a one-day meeting in June 2009, the working group agreed the scope and broad content of a draft set of guidelines that were then used as the basis for a wider consultation with the scientific community, involving researchers and grant holders and representatives of the major bioscience funding bodies including the Medical Research Council, Wellcome Trust, Biotechnology and Biological Sciences Research Council and The Royal Society [Tables 1 and 2]. Feedback on the content and wording of the items was incorporated into the final version of the checklist. Further feedback on the content utility of the guidelines is encouraged and sought.

IMPROVED REPORTING WILL MAXIMISE THE OUTPUT OF PUBLISHED RESEARCH

These guidelines were developed to maximise the output from research using animals by optimising the information that is provided in publications on the design, conduct and analysis of the experiments. The need for such guidelines is further illustrated by the systematic reviews of animal research that have been carried out to assess the efficacy of various drugs and interventions in animal models. Well-designed and -reported animal studies are the essential building blocks from which such a systematic review is constructed. The reviews have found that, in many cases, reporting omissions, in addition to the limitations of the animal models used in the individual studies assessed in the review, are a barrier to reaching any useful conclusion about the efficacy of the drugs and interventions being compared.

Driving improvements in reporting research using animals will require the collective efforts of authors, journal editors, peer reviewers and funding bodies. There is no single simple or rapid solution, but the ARRIVE guidelines provide a practical resource to aid these improvements. The guidelines will be published in several leading bioscience research journals simultaneously, and publishers have already endorsed the guidelines by including them in their journal Instructions to Authors subsequent to publication. The NC3Rs will continue to work with journal editors to extend the range of journals adopting the guidelines and with the scientific community to disseminate the guidelines as widely as possible (http://www.nc3rs.org.uk/ARRIVE).

References 60

  1. 1.

    Simera I, Altman DG. Writing a research article that is “fit for purpose”: EQUATOR network and reporting guidelines. Evid Based Med. 2009;14:132-4.

    Not in our library10.1136/ebm.14.5.132

  2. 2.
  3. 3.
  4. 4.

    Sargeant JM, Thompson A, Valcour J, Elgie R, Saint-Onge J, Marcynuk P, et al. Quality of reporting of clinical trials of dogs and cats and associations with treatment effects. J Vet Intern Med. 2010;24:44-50.

    Not in our library10.1111/j.1939-1676.2009.0386.x

  5. 5.
  6. 6.

    Sargeant JM, Elgie R, Valcour J, Saint-Onge J, Thompson A, Marcynuk P, et al. Methodological quality and completeness of reporting in clinical trials conducted in livestock species. Prev Vet Med. 2009;91:107-15.

    Not in our library10.1016/j.prevetmed.2009.06.002

  7. 7.

    Macleod MR, Fisher M, O’Collins V, Sena ES, Dirnagl U, Bath PM, et al. Good laboratory practice. Preventing introduction of bias at the bench. Stroke. 2009;40:e50-2.

    Not in our library10.1161/strokeaha.108.525386

  8. 8.

    Hainsworth AH, Markus HS. Do in vivo experimental models reflect human cerebral small vessel disease? A systematic review. J Cereb Blood Flow Metab. 2008;28:1877-91.

    Not in our library10.1038/jcbfm.2008.91

  9. 9.

    Rice AS, Cimino-Brown D, Eisenach JC, Kontinen VK, Lacroix-Fralish ML, Machin I, et al. Animal models and the prediction of efficacy in clinical trials of analgesic drugs: A critical appraisal and call for uniform reporting standards. Pain. 2008;139:243-7.

    Not in our library10.1016/j.pain.2008.08.017

  10. 10.

    Sherwin CM. Animal welfare: Reporting details is good science. Nature. 2007;448:251.

    Not in our library10.1038/448251b

  11. 11.

    Jafari P, Azuaje F. An assessment of recently published gene expression analyses: Reporting experimental design and statistics. BMC Med Inform Decis Mak. 2006;6:27.

    Not in our library10.1186/1472-6947-6-27

  12. 12.

    Hackam DG, Redelmeier DA. Translation of research evidence from animals to humans. JAMA. 2006;296:1731-2.

    Not in our library10.1001/jama.296.14.1731

  13. 13.

    Perel P, Roberts I, Sena E, Wheble P, Briscoe C, Sandercock P, et al. Comparison of treatment effects between animal experiments and clinical trials: Systematic review. BMJ. 2006;334:197.

    Not in our library10.1136/bmj.39048.407928.be

  14. 14.

    Macleod M. What can systematic review and meta-analysis tell us about the experimental data supporting stroke drug development? Int J Neuroprot Neuroregener. 2005;1:201.

    Not in our library

  15. 15.

    Tooth L, Ware R, Bain C, Purdie DM, Dobson A. Quality of reporting of observational longitudinal research. Am J Epidemiol. 2005;161:280-8.

    Not in our library10.1093/aje/kwi042

  16. 16.

    Pound P, Ebrahim S, Sandercock P, Bracken MB, Roberts I. Where is the evidence that animal research benefits humans? BMJ. 2004;328:514-7.

    Not in our library10.1136/bmj.328.7438.514

  17. 17.

    Bennett LT, Adams MA. Assessment of ecological effects due to forest harvesting: Approaches and statistical issues. J Appl Ecol. 2004;41:585-98.

    Not in our library

  18. 18.

    Morris CE, Bardin M, Berge O, Frey-Klett P, Fromin N. Microbial biodiversity: Approaches to experimental design and hypothesis testing in primary scientific literature from 1975 to 1999. Microbiol Mol Biol Rev. 2002;66:592-616.

    Not in our library10.1128/mmbr.66.4.592-616.2002

  19. 19.

    Smith JA, Birke L, Sadler D. Reporting animal use in scientific papers. Lab Anim. 1997;31:312-7.

    Not in our library10.1258/002367797780596176

  20. 20.

    McCance I. Assessment of statistical procedures used in papers in the Australian Veterinary Journal. Aust Vet J. 1995;72:322-8.

    Not in our library10.1111/j.1751-0813.1995.tb07534.x

  21. 21.

    Pocock SJ, Hughes MD, Lee RJ. Statistical problems in the reporting of clinical trials. A survey of three medical journals. N Engl J Med. 1987;317:426-32.

    Not in our library10.1056/nejm198708133170706

  22. 22.

    Chalmers I, Glasziou P. Avoidable waste in the production and reporting of research evidence. Lancet. 2009;374:86-9.

    Not in our library10.1016/s0140-6736(09)60329-9

  23. 23.

    Festing MF, Altman DG. Guidelines for the design and statistical analysis of experiments using laboratory animals. ILAR J. 2002;43:244-58.

    Not in our library10.1093/ilar.43.4.244

  24. 24.

    Schulz KF, Altman DG, Moher D; CONSORT Group. CONSORT 2010 Statement: Updated guidelines for reporting parallel group randomised trials. BMJ. 2010;340:c332.

    Not in our library10.1136/bmj.c332

  25. 25.

    Moher D, Schulz KF, Altman DG. The CONSORT statement: Revised recommendations for improving the quality of reports of parallel-group randomised trials. Lancet. 2001;357:1191-4.

    Not in our library

  26. 26.

    Altman DG. Endorsement of the CONSORT statement by high impact medical journals: Survey of instructions for authors. BMJ. 2005;330:1056-7.

    Not in our library10.1136/bmj.330.7499.1056

  27. 27.
  28. 28.

    Plint AC, Moher D, Morrison A, Schulz K, Altman DG, Hill C, et al. Does the CONSORT checklist improve the quality of reports of randomised controlled trials? A systematic review. Med J Aust. 2006;185:263-7.

    Not in our library10.5694/j.1326-5377.2006.tb00557.x

  29. 29.

    Kane RL, Wang J, Garrard J. Reporting in randomized clinical trials improved after adoption of the CONSORT statement. J Clin Epidemiol. 2007;60:241-9.

    Not in our library10.1016/j.jclinepi.2006.06.016

  30. 30.

    Altman DG, Simera I, Hoey J, Moher D, Schulz K. EQUATOR: Reporting guidelines for health research. Lancet. 2008;371:1149-50.

    Not in our library10.1016/s0140-6736(08)60505-x

  31. 31.

    Simera I, Moher D, Hoey J, Schulz K, Altman DG. A catalogue of reporting guidelines for health research. Eur J Clin Invest. 2010;40:35-53.

    Not in our library10.1111/j.1365-2362.2009.02234.x

  32. 32.

    Wager E, Field EA, Grossman L. Good publication practice for pharmaceutical companies. Curr Med Res Opin. 2003;19:149-54.

    Not in our library10.1185/030079903125001767

  33. 33.

    Brazma A, Hingamp P, Quackenbush J, Sherlock G, Spellman P, Stoeckert C, et al. Minimum information about a microarray experiment (MIAME)-toward standards for microarray data. Nat Genet. 2001;29:365-71.

    Not in our library10.1038/ng1201-365

  34. 34.

    Goodacre R, Broadhurst D, Smilde AK, Kristal BS, Baker DJ. Proposed minimum reporting standards for data analysis in metabolomics. Metabolomics. 2007;3:231-41.

    Not in our library

  35. 35.

    Stone SP, Cooper BS, Kibbler CC, Cookson BD, Roberts JA. The ORION statement: Guidelines for transparent reporting of outbreak reports and intervention studies of nosocomial infection. J Antimicrob Chemother. 2007;59:833-40.

    Not in our library10.1093/jac/dkm055

  36. 36.

    Peters JL, Sutton AJ, Jones DR, Rushton L, Abrams KR. A systematic review of systematic reviews and meta-analyses of animal experiments with guidelines for reporting. J Environ Sci Health B. 2006;41:1245-58.

    Not in our library10.1080/03601230600857130

  37. 37.

    O’Connor AM, Sargeant JM, Gardner IA, Dickson JS, Torrence ME, Dewey CE, et al. The REFLECT statement: Methods and processes of creating reporting guidelines for randomised controlled trials for livestock and food safety. Prev Vet Med. 2010;93:11-8.

    Not in our library10.1016/j.prevetmed.2009.10.008

  38. 38.

    International Committee of Medical Journal EditorsUniform Requirements for Manuscripts Submitted to Biomedical Journals.

    Not in our library

  39. 39.

    Council of Science Editors – Editorial Policy Committee (2008–2009) CSE’s White Paper on promoting integrity in scientific journal publications. [last updated on 2009].

    Not in our library

  40. 40.

    Committee on publication ethics (COPE)COPE best practice guidelines for journal editors.

    Not in our library

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