Yearly Archives: 2016

A call for cluster randomized cross-over trial reporting guidelines

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When asking a research question, you need to ensure the trial design you choose is the most appropriate for that particular question. All have particular benefits and pitfalls that need to be considered and addressed when it comes to reporting. The cluster randomized cross-over trial is one of these potential choices and here, Sarah Arnup and Joanne McKenzie discuss their research into the reporting of this trial design, published today in Trials, and highlight the need for a CONSORT extension.

Medical Evidence Medicine

Wise to go nuts?

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A systematic review and meta-analysis published today in BMC Medicine reports that higher nut consumption is associated with lower risk of cardiovascular disease, all-cause mortality and mortality from cancer, respiratory disease, diabetes, and infections. Here, Agneta Åkesson and Carolina Donat-Vargas discuss the broader context of these results. Please be aware that some of the references in this blog require a subscription to read the full text.

Medicine

Post-marketing withdrawal of anti-obesity medicinal products: benefits versus harms, profits versus losses

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A research article published in BMC Medicine investigates the withdrawal of anti-obesity drugs from the market because of serious adverse reactions. In this guest blog, authors Igho Onakpoya, Carl Heneghan, and Jeffrey Aronson, from the University of Oxford, discuss the poor benefit to harm balance of many anti-obesity drugs and conclude that drug companies have profited while patients who have suffered adverse reactions have lost.

Medicine

Large underreporting of network meta-analyses conducted by contracting companies commissioned by industry

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Network meta-analyses are extremely useful if you want to compare the effectiveness of three or more interventions by collating both the direct and indirect evidence on a clinical question. It’s known that contracting companies often conduct network meta-analyses for the biotech and the pharmaceutical industry but until now no one has looked into what extent that this is happening and whether they are being published. Here, Ewoud Schuit and John Ioannidis discuss their research looking into this, published in Systematic Reviews, and discuss the implications of the huge underreporting that they found.

Medical Evidence Medicine

Useful data: developing standards for describing clinical research data across repositories

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Movements towards increased transparency have resulted in more and more documents, journal publications and original datasets relating to specific clinical trials being included in a wide range of repositories. This is a great direction for the field but if we are to use these ‘data objects’ in the most effective manner, we need to establish consistency in the way they are described (and therefore searchable) across these repositories. Steve Canham and Christian Ohmann from the European Clinical Research Infrastructure Network have recently published a Methodology in Trials proposing standards for consistent descriptions of these data objects and here, both authors highlight its importance for the field and summarize their proposal.

Health Medical Evidence Medicine

Pulmonary hypertension in the eyes of a clinician and a patient

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This week (19th-27th November) in the UK is Pulmonary Hypertension awareness week. The theme for this year is “Let’s talk about PH” so we thought we’d do just that by inviting Dr. Stylianos E. Orfanos, Professor of Critical Care and Medicine at National and Kapodistrian University of Athens, to give us a comprehensive overview of the disease as well the current treatments available and the barriers that can prevent patients form being effectively treated.

Health Medicine