Oversimplified efforts to counter health misinformation are missing the mark
BMJ 2025; 388 doi: https://doi.org/10.1136/bmj.r393 (Published 27 February 2025) Cite this as: BMJ 2025;388:r393Health misinformation and harmful online narratives are a major threat to public health and security. Driving low confidence in vaccines and medicines, denial of pandemic risk, or use of unproven health treatments, inaccurate information can create confusion, sow mistrust, harm health, and undermine public health efforts. In 2020, the wave of accurate and inaccurate information on covid-19 was declared an infodemic by the World Health Organization (WHO).12 Additionally, misinformation and disinformation was recently named as one of the greatest threats to global security at the World Economic Forum.3 Our current approach to health misinformation is limited and we need to progress our understanding of the information ecosystems4 and drivers of online health narratives.
The challenges of health misinformation go beyond countering false claims. People increasingly go online to answer questions and explore concerns they may have about their health, treatments, or healthcare. Digital access, commercial internet platforms, and artificial intelligence are supercharging the spread of misinformation. Meanwhile, online users scroll through feeds filled with outdated, false or poorly sourced information, amplified by algorithms, adverts, and the information sharing behaviours of friends and family.
Science driven health guidance is outpaced by rapidly evolving online conversations and often falls short of people’s information needs. Recently, the Canadian Medical Association reported a dramatic increase in the proportion of Canadians (35%) who avoided effective health treatments because of false information,5 a trend echoed in other nations. In response, WHO, the European Centre for Disease Prevention and Control, and national medical associations worldwide have issued guidance on how to tackle health misinformation.67891011
However, we identify three outstanding concerns that limit an effective response to the complex problem of health misinformation.
A cacophony of definitions
Firstly, we need more clarity and consistency in definitions to assess and foster a healthier information environment. Many words describe the quality of information: untrustworthy, low quality, unverified, unbalanced, contradictory, deceptive, or sensationalised, among others. But each conveys a different value judgment and thus frames the problem differently. Misinformation is false or inaccurate information. Disinformation is deliberately false information, spread for political or monetary gain.
The terms misinformation and disinformation are often conflated in research and policy, failing to recognise that the definition of the problem influences how it is tackled. Labelling something as misinformation is a value judgment on its accuracy. Disinformation is a value judgment on intent for distribution of inaccurate content. Each requires a different solution.
Medicalising a systemic challenge to health
Secondly, we should not individualise a problem that is structural, as has been done with many issues in public health. This can lead to individualised solutions, ignoring the complex dynamics at play. It is important to focus on the root causes of the problem, not simply treat how it manifests on an individual level that is easier to observe.
Popular covid-19 pandemic era strategies often focused on the individual, such as expecting doctors to debunk misinformation patients shared,8 or building resilience to health misinformation through social inoculation.12 These tactics shift the focus and burden of confronting a systematic problem onto the individual, who has little control over the digital onslaught of information they receive. We need to consider how consumer protection laws and regulatory mechanisms can improve the general availability and quality of health information on websites, internet platforms, and apps.
More complex than communications alone
Thirdly, the covid-19 pandemic demonstrated the limited success of trying to communicate our way out of mis- and disinformation,1314 showing how complex and contextualised the problem is. Persistent focus on factual public health information and “better comms” alone will set us up to fail.
For example, journalists and health organisations tried fact checking health claims online, but these did not always reach the intended audiences.1516 We should be holding internet platforms to account for weakening design and moderation policies that were meant to protect users from harmful narratives and harassment.17 Unfortunately, accurate, reliable information does not compete well against emotionally manipulative anecdotes, especially if amplified by cultural influencers.18
Well intended efforts by public health organisations to promote better moderation of health misinformation, including deleting content and banning users,19 can lead to a backlash from people claiming government over-reach or censorship.18
Similarly limited were the attempts by health workers who went online to challenge health misinformation directly, only to experience harassment and doxing.2021
Ineffective counter measures can have dire consequences: misinformation and reframed facts became embedded into policies and guidance. For example, in the US, state legislation echoed language of abortion misinformation that was amplified online and then promulgated non-evidence based policies.22
Contextualised approaches to current and future challenges
Users curate and shape their online experiences by training their personal feeds for information they want. Advertisers happily take advantage of detailed user analytics to advertise products and ideas to consumers, regardless of accuracy.
Public health and medical professionals can no longer assume that more communication or stronger social media campaigns will be sufficient in reaching their intended audiences or informing their health decisions. Instead, we must understand how users seek health information and services online, engage them there, and respond to their concerns and information needs, but recognise we have an audience watching.23
If we do not recognise the drivers of health narratives online and how users are influenced by the information environment broadly, we are concerned that public health research and practice will develop and mobilise solutions that will continue to fail.
Footnotes
Competing interests: TDP and JC developed this article as 2024 Salzburg Global fellows of the equitable health knowledge production systems programme.
Provenance and peer review: Not commissioned, not externally peer reviewed.
We thank Salzburg Global and other fellows for their inputs and support.