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DOI 10.1080/10826084.2021.2019777

Медицинская библиотека · Substance use & misuse · 2022

Social Media Discussions on the FDA's Modified Risk Tobacco Product Authorization of IQOS.

Jun Jungmi, Zhang Nanlan, Zain Ali, Mohammadi Ehsan

СтатьяПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

Background

The U.S. Food and Drug Administration (FDA) authorized the marketing of the IQOS tobacco heating system as a modified risk tobacco product (MRTP) in July 2020, permitting its 'reduced exposure' marketing. This decision is accompanied by much controversy among the global health community. We provide a preliminary analysis of Twitter conversations regarding the MRTP authorization of IQOS by identifying the authors, valence towards the policy decision, source of cited link, and focused topic.

Methods

We analyzed 548 tweets mentioning MRTP posted between July 2016 (when PMI submitted the proposal) and October 2020.

Results

We found a higher proportion of pro-MRTP valence (25.4%) than anti-MRTP (16.2%). Nearly half of the tweets (47.2%) expressing personal opinions presented pro-MRTP valence (vs. anti-MRTP = 23.9%). The FDA website was more frequently cited in pro-MRTP tweets (30.8% vs. anti = 4.8%), while tobacco control advocates' websites were cited only in anti-MRTP tweets (77.4% vs. pro = 0). Pro-MRTP valence appeared more frequently in tweets mentioning health (53.1% vs. anti =38.5%) and cessation (100% vs. anti = 0). Nearly 42% of tweets showed a bot score greater than .43, indicating a possibility of automation.

Conclusion

Continuous efforts are needed to surveil the industry's attempts to create a climate of false consensus and circulate misinformation regarding MRTP on social media, as well as to assist non-scientific audiences' understanding of MRTP.

Для цитирования: Jun Jungmi, Zhang Nanlan, Zain Ali, Mohammadi Ehsan. Social Media Discussions on the FDA's Modified Risk Tobacco Product Authorization of IQOS.. Substance use & misuse. 2022. DOI: 10.1080/10826084.2021.2019777.

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