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Taking advantage of unexpected WebCONSORT results
BMC Medicine volume 14, Article number: 204 (2016)
To estimate treatment effects, trials are initiated by randomising patients to the interventions under study and finish by comparing patient evolution. In order to improve the trial report, the CONSORT statement provides authors and peer reviewers with a guide of the essential items that would allow research replication. Additionally, WebCONSORT aims to facilitate author reporting by providing the items from the different CONSORT extensions that are relevant to the trial being reported. WebCONSORT has been estimated to improve the proportion of reported items by 0.04 (95% CI, –0.02 to 0.10), interpreted as “no important difference”, in accordance with the scheduled desired scenario of a 0.15 effect size improvement. However, in a non-scheduled analysis, it was found that, despite clear instructions, around a third of manuscripts selected for trials by the editorial staff were not actually randomised trials. We argue that surprises benefit science, and that further research should be conducted in order to improve the performance of editorial staff.
Please see related research: http://bmcmedicine.biomedcentral.com/articles/10.1186/s12916-016-0736-x
Research should welcome and capitalise on surprises. A classic example of this occurred when Barry Marshall and Robin Warren found Helicobacter pylori in a person with chronic gastritis and gastric ulcers, conditions that were previously attributed to stress or spicy food . When serendipity helped Alexander Fleming discover penicillin, his achievement was not in staining a lab plate, but in reproducing the results and advancing the possibilities.
There is a continuous research path from the discovery to the implementation of new interventions. At the beginning, researchers such as Fleming have ‘an idea’. At the end, they measure the intervention effect. In other words, they ask themselves: What would the evolution be for some patients if, instead of the standard intervention, we provide them the updated one. Since researchers are unable to observe both evolutions in the same patient, a fairly simple (at least, conceptually) process is chosen: randomly allocate both treatments to patients and compare their evolution. This, and nothing else, is a randomised clinical trial.
Unfortunately, things can go wrong – protocol deviations, unmasked evaluation and sample attrition have been proven to bias the results , and poor methodological background  and conflict of interests  may further misguide authors. Therefore, in order to facilitate reproducibility, the CONSORT statement  has been developed to guide them in the reporting of essential items. However, as trials with different objectives, methodologies or types of interventions may need different essential items, new extensions have been added and gathered into the EQUATOR website . To facilitate manuscript preparation, WebCONSORT provides all the items that apply to the reported trial. In order to estimate the effect of WebCONSORT on manuscript completeness, Hopewell et al.  conducted a randomised trial in which experimental units were themselves manuscripts of randomised clinical trials, and reported that WebCONSORT improves the proportion of reported items by 0.04, although random allocation makes this result compatible (95% CI) with any true value between a decrease of 0.02 and an improvement of 0.10. The authors interpret those values as “no important difference” , in accordance with the scheduled scenario of a 0.15 effect size improvement.
Unexpected findings – editors under the magnifying glass
Looking at additional results, Hopewell et al.  showed no surprise when they found “that in a quarter (23%) of manuscripts, authors either selected an inappropriate CONSORT extension or failed to select the right extension applicable to their trial”. As this agreed with their prior thoughts, it reinforced their aim to enhance authors’ reporting of randomised trials. However, if there is no surprise, one may feel that this is a boring result.
Nevertheless, Hopewell et al.  “did not anticipate that journals would enroll manuscripts that were not in fact reports of randomised trials”. In the Discussion, they state that: “More than one third (39%) of registered manuscripts were excluded from the analysis as they were not reports of randomised trials. This was despite clear instructions provided to journal editorial staff, and included in the revision letter to authors, that only manuscripts reporting the results of randomised trials were eligible for inclusion. Clearly, the editorial staff at some journals were unable to correctly identify a randomised trial based on what was reported in the submitted manuscript”. Further, in their Results section, they describe the recruitment process: “Between 25 March 2013 and 22 September 2015, 357 manuscripts were registered on the WebCONSORT study site from 46 general medical and specialty journals with an impact factor ranging from 11.34 to 0.65 as of 2014. […] The percentage of eligible manuscripts varied considerably across journals (median 73%; IQR 27% to 100%).” Thus, randomised trials constitute the methodological gold standard for assessing treatment effects, but the editorial staff of medical journals were unable to correctly classify their own manuscripts as randomised trials. Aha!
In their Discussion, Hopewell et al.  state: “Better education is needed […] for both authors and journal editorial staff”. This is of no surprise with regards to the authors; however, in terms of the editorial staff, it initially seems surprising, yet further consideration reveals that it may not be so. In order to assess what goes wrong along the research pipeline, the clinical scientific community, led by JAMA and BMJ, organises the quadrennial Congress on Peer Review in Biomedical Publication, which is devoted to improving the quality of biomedical literature [8, 9]. In its inception, the congress initially concentrated mainly on the peer review process – hence its name. However, the meeting now includes “featured research describing poor practices on the parts of authors, reviewers, editors, and journals” . Thus, as editors and journals are already under the magnifying glass of investigation, this is of no surprise at all.
Unfortunately, this unanticipated, poor selection made it impossible to perform the designed intervention on misclassified manuscripts. Therefore, the WebCONSORT authors had to leave out a substantial proportion of papers, thereby losing the scheduled study power and thus making interpretation difficult. Nevertheless, the non-significance of their results should at least be interpreted carefully .
Surprising unexpected results: what can we learn?
When anyone agrees to participate in clinical research – whether they be patients, recruiters, interventionists or raters – they are generously volunteering their time, efforts and data. At every stage of the pipeline, transparency implies that the scientific community has to be able to assess what went wrong. Inevitably, researchers must be unpleasant to these volunteers by asking important questions, including, Have patients followed the recommendations? Have recruiters adequately explained to them how important it is to adhere to the agreed protocol? Have interventionists applied it carefully? Have monitors made any effort to complete patient follow-up? Indeed, clinical science may never have progressed without the noble-mindedness of volunteers.
Along similar lines, while keeping in mind the generosity of everyone involved in peer review research, we should ponder the questions that the unexpected results of WebCONSORT have provided: Is there any characteristic among editors or journals that predicts the proportion of correctly classified manuscripts? For example, is impact factor involved? What is the manuscript process flow? What are the responsibilities shared by different staff members? What was their selection process? Are they professional or academic editors? What scientific and methodological background do they have? Are different scientific communities represented in their editorial staff? The answers will, ideally, lead to more ambitious research questions about the assumed causal factors: Would the modification of any of them result in the desired improvement. Obviously, this process would imply further generosity from researchers, editors and journals.
The WebCONSORT randomised trial was designed to test an intervention for improving the transparent reporting of methods and results by authors. The main analysis of this objective was performed by following the most exigent experimental conditions, with the exception of the already mentioned unexpected loss of power. However, they also observed that the journal gatekeepers classified too many manuscripts as randomised trials when they were not, in fact, so. Shocking? Perhaps. Nevertheless, this post-hoc data is certainly informative and deserves further study by either the authors of the WebCONSORT study or the very same editors.
Christopher Columbus was looking for a new path to Asia. However, to the world’s surprise, he came upon America. Then, to complete the path from discovery to innovation, Columbus travelled several other times. Now, the scientific community must unravel how to improve editors’ performance.
Pincock S. Nobel Prize winners Robin Warren and Barry Marshall. Lancet. 2005;366(9495):1429.
Liberati A, Altman DG, Tetzlaff J, Mulrow C, Gøtzsche PC, et al. The PRISMA statement for reporting systematic reviews and meta-analyses of studies that evaluate health care interventions: explanation and elaboration. PLoS Med. 2009;6(7):e1000100. doi:10.1371/journal.pmed.1000100.
Collins FS, Tabak LA. Policy: NIH plans to enhance reproducibility. Nature. 2014;505:612–3.
Mandrioli D, Kearns CE, Bero LA. Relationship between research outcomes and risk of bias, study sponsorship, and author financial conflicts of interest in reviews of the effects of artificially sweetened beverages on weight outcomes: a systematic review of reviews. PLoS One. 2016;11(9):e0162198.
Schulz KF, Altman DG, Moher D, for the CONSORT Group. CONSORT 2010 Statement: updated guidelines for reporting parallel group randomised trials. BMC Med. 2010;8:18.
EQUATOR site. 2016. http://www.equator-network.org/. Accessed 18 Nov 2016.
Hopewell S, Boutron I, Altman DG, Ravaud P, on behalf of the WebCONSORT Study Group. Impact of a web-based tool (WebCONSORT) to improve the reporting of randomised trials: results of a randomised controlled trial. BMC Med. 2016;14:199.
Rennie D, Flanagin A, Godlee F, Bloom T. Eighth international congress on peer review in biomedical publication. BMJ. 2015;350:h2411.
Rennie D. Let’s make peer review scientific. Nature. 2016;535:31–3.
Pocock S, Stone G. The primary outcome fails. What next? N Engl J Med. 2016;375:861–70.
EC drafted a first version, but the final report has benefited from the nearly equal contributions of both authors. Both authors read and approved the final manuscript.
Both authors are Associate Professors at the Department of Statistics and Operations Research of Barcelona-Tech. Both belong to MiRoR (Methods in Research on Research), which has received funding from the European Union’s Horizon 2020 research and innovation programme under the Marie Skłodowska-Curie grant agreement No. 676207. EC is partially funded by the Research Group in Biostatistics and Bioinformatics GRBIO (2014 SGR 464), and JAG by Project MTM2015-65362-R, Spanish Ministry of Economy and Competitiveness.
The authors declare that, although they have no direct financial competing interests, their academic prestige is related to the research success of reporting guidelines initiatives. Furthermore, as researchers on this topic, they share some funded initiatives with some of the authors of the referenced WebCONSORT trial.
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Cobo, E., González, J.A. Taking advantage of unexpected WebCONSORT results. BMC Med 14, 204 (2016). https://doi.org/10.1186/s12916-016-0758-4
- Clinical trials
- Peer review
- Reporting guidelines