Evidence map›Paper›PMID 29398886›Full record

ArticleFood and drug law journal2017

Communicating Tobacco Product Information to the Public.

Micah L Berman, M Justin Byron, Natalie Hemmerich, Eric N Lindblom, Allison J Lazard, Ellen Peters, Noel T Brewer

Abstract read
In one paragraph

Article in Food and drug law journal, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

10 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Trial
  3. Trial
  4. Article
  5. Does smoking affect your skin?Postepy dermatologii i alergologii · 2021
    Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Micah L BermanAssociate professor at Ohio State University's College of Public Health and Moritz College of Law.
M Justin ByronResearch scientist at the University of North Carolina's Lineberger Comprehensive Cancer Center.
Natalie HemmerichPostdoctoral fellow at Ohio State University's College of Public Health.
Eric N LindblomDirector for Tobacco Control and Food and Drug Law at Georgetown University Law Center's O'Neill Institute for National and Global Health Law.
Allison J LazardAssistant professor at the University of North Carolina's School of Media and Journalism.
Ellen PetersProfessor at Ohio State University's Department of Psychology.
Noel T BrewerProfessor at the University of North Carolina's Gillings School of Global Public Health.

Funding

Training & Education Program p294-308P50CA180907 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI RIBISL, KURT M. · 2013 to 2017
$20.2M
Project 4: Comprehension of Health Risks in More and Less Arousing Affe p240-275P50CA180908 · NCI · OHIO STATE UNIVERSITY · PI SHIELDS, PETER G., WEWERS, MARY ELLEN · 2013 to 2017
$18.9M
Designing a Comprehensive Framework for the Evaluation of Tobacco Product RisksK07CA197221 · NCI · OHIO STATE UNIVERSITY · PI BERMAN, MICAH L. · 2016 to 2020
$820k
NCI NIH HHS K07 CA197221NCI NIH HHS P50 CA180907NCI NIH HHS P50 CA180908
6 · The paper itself

Abstract

The 2009 Family Smoking Prevention and Tobacco Control Act (TCA) requires tobacco companies to disclose information about the harmful chemicals in their products to the U.S. Food and Drug Administration (FDA). The law requires the FDA, in turn, to communicate this information to the public "in a format that is understandable and not misleading to a lay person." But how should the FDA comply with this requirement? What does it mean for information about complex chemicals to be "understandable and not misleading to a lay person"? These questions are not easy ones to answer. Disclosures about the amount of harmful chemicals (constituents) in different tobacco products may help to inform consumers, but may also conversely prompt consumers to reach incorrect or unsupported conclusions about products' relative health risks. This paper first analyzes the FDA's legal obligation to publish tobacco constituent information so that it is "understandable and not misleading to a layperson." Second, it discusses how that legal analysis has guided scientific research examining how members of the public interpret messages regarding tobacco constituents. Lastly, this paper concludes with policy recommendations for the FDA as it considers how to comply with the law's constituent disclosure requirement while still furthering its overall objective of promoting public health.

Indexed as

Smoking PreventionTobacco ProductsUnited States Food and Drug AdministrationCommunicationPatient Education as TopicRiskSmokingTobacco IndustryUnited States

Identifiers

PMID29398886
PMCPMC5794026

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.