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3.
Lancet ; 388(10056): 2109, 2016 10 29.
Article in English | MEDLINE | ID: mdl-27968743
5.
Milbank Q ; 94(1): 126-62, 2016 Mar.
Article in English | MEDLINE | ID: mdl-26994712

ABSTRACT

POLICY POINTS: In situations of scientific uncertainty, public health interventions, such as counseling for HIV infection, sometimes must be implemented before obtaining evidence of efficacy. The history of HIV counseling and testing, which served as the cornerstone of HIV prevention efforts at the US Centers for Disease Control and Prevention (CDC) for a quarter of a century, illustrates the influence of institutional resistance on public health decision making and the challenge of de-implementing well-established programs. CONTEXT: In 1985, amid uncertainty about the accuracy of the new test for HIV, public health officials at the Centers for Disease Control and Prevention (CDC) and AIDS activists agreed that counseling should always be provided both before and after testing to ensure that patients were tested voluntarily and understood the meaning of their results. As the "exceptionalist" perspective that framed HIV in the early years began to recede, the purpose of HIV test counseling shifted over the next 30 years from emphasizing consent, to providing information, to encouraging behavioral change. With this increasing emphasis on prevention, HIV test counseling faced mounting doubts about whether it "worked." The CDC finally discontinued its preferred test counseling approach in October 2014. METHODS: Drawing on key informant interviews with current and former CDC officials, behavioral scientists, AIDS activists, and others, along with archival material, news reports, and scientific and governmental publications, we examined the origins, development, and decline of the CDC's "counseling and testing" paradigm for HIV prevention. FINDINGS: Disagreements within the CDC emerged by the 1990s over whether test counseling could be justified on the basis of efficacy and cost. Resistance to the prospect of policy change by supporters of test counseling in the CDC, gay activists for whom counseling carried important ethical and symbolic meanings, and community organizations dependent on federal funding made it difficult for the CDC to de-implement the practice. CONCLUSIONS: Analyses of changes in public health policy that emphasize the impact of research evidence produced in experimental or epidemiological inquiries may overlook key social and political factors involving resistance to deimplementation that powerfully shape the relationship between science and policy.


Subject(s)
AIDS Serodiagnosis , Blood Safety/standards , Centers for Disease Control and Prevention, U.S./standards , Counseling/standards , HIV Infections/prevention & control , Homosexuality, Male/psychology , Public Health Practice/standards , Social Stigma , Attitude of Health Personnel , Blood Safety/methods , Counseling/methods , Counseling/trends , HIV Infections/diagnosis , HIV Infections/psychology , HIV Infections/transmission , Harm Reduction , Humans , Interviews as Topic , Male , Politics , United States
6.
Int J Epidemiol ; 45(1): 251-60, 2016 Feb.
Article in English | MEDLINE | ID: mdl-26888870

ABSTRACT

BACKGROUND: Although several public health organizations have recommended population-wide reduction in salt intake, the evidence on the population benefits remains unclear. We conducted a metaknowledge analysis of the literature on salt intake and health outcomes. METHODS: We identified reports--primary studies, systematic reviews, guidelines and comments, letters or reviews--addressing the effect of sodium intake on cerebro-cardiovascular disease or mortality. We classified reports as supportive or contradictory of the hypothesis that salt reduction leads to population benefits, and constructed a network of citations connecting these reports. We tested for citation bias using an exponential random graph model. We also assessed the inclusion of primary studies in systematic reviews on the topic. RESULTS: We identified 269 reports (25% primary studies, 5% systematic reviews, 4% guidelines and 66% comments, letters, or reviews) from between 1978 and 2014. Of these, 54% were supportive of the hypothesis, 33% were contradictory and 13% were inconclusive. Reports were 1.51 [95% confidence interval (CI) 1.38 to 1.65] times more likely to cite reports that drew a similar conclusion, than to cite reports drawing a different conclusion. In all, 48 primary studies were selected for inclusion across 10 systematic reviews. If any given primary study was selected by a review, the probability that a further review would also have selected it was 27.0% (95% CI 20.3% to 33.7%). CONCLUSIONS: We documented a strong polarization of scientific reports on the link between sodium intake and health outcomes, and a pattern of uncertainty in systematic reviews about what should count as evidence.


Subject(s)
Bias , Bibliometrics , Sodium Chloride, Dietary/standards , Humans
8.
Health Aff (Millwood) ; 31(12): 2738-46, 2012 Dec.
Article in English | MEDLINE | ID: mdl-23213158

ABSTRACT

For more than four decades, starting in the late 1960s, a sometimes furious battle has raged among scientists over the extent to which elevated salt consumption has adverse implications for population health and contributes to deaths from stroke and cardiovascular disease. Various studies and trials have produced conflicting results. Despite this scientific controversy over the quality of the evidence implicating dietary salt in disease, public health leaders at local, national, and international levels have pressed the case for salt reduction at the population level. This article explores the development of this controversy. It concludes that the concealment of scientific uncertainty in this case has been a mistake that has served neither the ends of science nor good policy. The article poses questions that arise from this debate and frames the challenges of formulating evidence-based public health practice and policy, particularly when the evidence is contested.


Subject(s)
Decision Making , Health Promotion/organization & administration , Nutrition Policy , Public Health , Sodium Chloride, Dietary/adverse effects , Evidence-Based Medicine , Female , Humans , Male , Policy Making , Science , United States
9.
Am J Public Health ; 102(8): 1447-50, 2012 Aug.
Article in English | MEDLINE | ID: mdl-22698051

ABSTRACT

In the wake of scandal over troubling research abuses, the 1970s witnessed the birth of a new system of ethical oversight. The bioethics framework, with its emphasis on autonomy, assumed a commanding role in debates regarding how to weigh the needs of society against the rights of individuals. Yet the history of resistance to oversight underscores that some domains of science hewed to a different paradigm of accountability--one that elevated the common good over individual rights. Federal officials have now proposed to dramatically limit the reach of ethical oversight. The Institute of Medicine has called for a rollback of the federal privacy rule. The changing emphasis makes it imperative to grapple with the history of the public interest paradigm.


Subject(s)
Bioethics , Biomedical Research/ethics , Ethical Review/standards , Public Health , Biomedical Research/legislation & jurisprudence , Ethical Review/legislation & jurisprudence , Government Regulation , Health Insurance Portability and Accountability Act , History, 20th Century , History, 21st Century , Humans , Privacy , Social Responsibility , United States , United States Dept. of Health and Human Services
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