28 research outputs found
Using Nominal Group Technique to Identify Key Attributes of Oncology Treatments for a Discrete Choice Experiment.
Background. Responding to rising oncology therapy costs, multiple value frameworks are emerging. However, input from economists in their design and conceptualization has been limited, and no existing framework has been developed using preference weightings as legitimate indicators of value. This article outlines use of the nominal group technique to identify valued treatment attributes (such as treatment inconvenience) and contextual considerations (such as current life expectancy) to inform the design of a discrete choice experiment to develop a preference weighted value framework for future decision makers. Methods. Three focus groups were conducted in 2017 with cancer patients, oncology physicians, and nurses. Using the nominal group technique, participants identified and prioritized cancer therapy treatment and delivery attributes as well as contextual issues considered when choosing treatment options. Results. Focus groups with patients (n = 8), physicians (n = 6), and nurses (n = 10) identified 30 treatment attributes and contextual considerations. Therapy health gains was the first priority across all groups. Treatment burden/inconvenience to patients and their families and quality of evidence were prioritized treatment attributes alongside preferences for resource use and cost (to patients and society) attributes. The groups also demonstrated that contextual considerations when choosing treatment varied across the stakeholders. Patients prioritized existence of alternative treatments and oncologist/center reputation while nurses focused on administration harms, communication, and treatment innovation. The physicians did not prioritize any contextual issues in their top rankings. Conclusions. The study demonstrates that beyond health gains, there are treatment attributes and contextual considerations that are highly prioritized across stakeholder groups. These represent important candidates for inclusion in a discrete choice experiment seeking to provide weighted preferences for a value framework for oncology treatment that goes beyond health outcomes
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Association of Medical Students' Reports of Interactions with the Pharmaceutical and Medical Device Industries and Medical School Policies and Characteristics: A Cross-Sectional Study
Background: Professional societies use metrics to evaluate medical schools' policies regarding interactions of students and faculty with the pharmaceutical and medical device industries. We compared these metrics and determined which US medical schools' industry interaction policies were associated with student behaviors. Methods and Findings: Using survey responses from a national sample of 1,610 US medical students, we compared their reported industry interactions with their schools' American Medical Student Association (AMSA) PharmFree Scorecard and average Institute on Medicine as a Profession (IMAP) Conflicts of Interest Policy Database score. We used hierarchical logistic regression models to determine the association between policies and students' gift acceptance, interactions with marketing representatives, and perceived adequacy of facultyâindustry separation. We adjusted for year in training, medical school size, and level of US National Institutes of Health (NIH) funding. We used LASSO regression models to identify specific policies associated with the outcomes. We found that IMAP and AMSA scores had similar median values (1.75 [interquartile range 1.50â2.00] versus 1.77 [1.50â2.18], adjusted to compare scores on the same scale). Scores on AMSA and IMAP shared policy dimensions were not closely correlated (gift policies, r = 0.28, 95% CI 0.11â0.44; marketing representative access policies, r = 0.51, 95% CI 0.36â0.63). Students from schools with the most stringent industry interaction policies were less likely to report receiving gifts (AMSA score, odds ratio [OR]: 0.37, 95% CI 0.19â0.72; IMAP score, OR 0.45, 95% CI 0.19â1.04) and less likely to interact with marketing representatives (AMSA score, OR 0.33, 95% CI 0.15â0.69; IMAP score, OR 0.37, 95% CI 0.14â0.95) than students from schools with the lowest ranked policy scores. The association became nonsignificant when fully adjusted for NIH funding level, whereas adjusting for year of education, size of school, and publicly versus privately funded school did not alter the association. Policies limiting gifts, meals, and speaking bureaus were associated with students reporting having not received gifts and having not interacted with marketing representatives. Policy dimensions reflecting the regulation of industry involvement in educational activities (e.g., continuing medical education, travel compensation, and scholarships) were associated with perceived separation between faculty and industry. The study is limited by potential for recall bias and the cross-sectional nature of the survey, as school curricula and industry interaction policies may have changed since the time of the survey administration and study analysis. Conclusions: As medical schools review policies regulating medical students' industry interactions, limitations on receipt of gifts and meals and participation of faculty in speaking bureaus should be emphasized, and policy makers should pay greater attention to less research-intensive institutions. Please see later in the article for the Editors' Summar
SPECIAL COMMUNICATION Health Industry Practices That Create Conflicts of Interest A Policy Proposal for Academic Medical Centers
market incentives in the United States is posing extraordinary challenges to the principles of medical professionalism. Physiciansâ commitment to altruism, putting the interests of the patients first, scientific integrity, and an absence of bias in medical decision making now regularly come up against financial conflicts of interest. Arguably, the most challenging and extensive of these conflicts emanate from relationships between physicians and pharmaceutical companies and medical device manufacturers. 1 As part of the health care industry
Physicians and Drug Representatives: Exploring the Dynamics of the Relationship
BACKGROUND: Interactions between physicians and drug representatives are common, even though research shows that physicians understand the conflict of interest between marketing and patient care. Little is known about how physicians resolve this contradiction. OBJECTIVE: To determine physiciansâ techniques for managing cognitive inconsistencies within their relationships with drug representatives. DESIGN, SETTING, AND PARTICIPANTS: Six focus groups were conducted with 32 academic and community physicians in San Diego, Atlanta, and Chicago. MEASUREMENTS: Qualitative analysis of focus group transcripts to determine physiciansâ attitudes towards conflict of interest and detailing, their beliefs about the quality of information conveyed and the impact on prescribing, and their resolution of the conflict between detailersâ desire to sell product and patient care. RESULTS: Physicians understood the concept of conflict of interest and applied it to relationships with detailers. However, they maintained favorable views of physicianâdetailer exchanges. Holding these mutually contradictory attitudes, physicians were in a position of cognitive dissonance. To resolve the dissonance, they used a variety of denials and rationalizations: They avoided thinking about the conflict of interest, they disagreed that industry relationships affected physician behavior, they denied responsibility for the problem, they enumerated techniques for remaining impartial, and they reasoned that meetings with detailers were educational and benefited patients. CONCLUSIONS: Although physicians understood the concept of conflict of interest, relationships with detailers set up psychological dynamics that influenced their reasoning. Our findings suggest that voluntary guidelines, like those proposed by most major medical societies, are inadequate. It may be that only the prohibition of physicianâdetailer interactions will be effective
No More Free Drug Samples?
Susan Chimonas and Jerome Kassirer argue that giving out âfreeâ drug samples is not effective in improving drug access for the indigent, does not promote rational drug use, and raises the cost of care
Moral panics: Towards a new model.
This dissertation reworks sociological theories of the causes, processes, and consequences of moral panics. Sociologists who study panics see material life as real and ideologies as false. In this view, moral panics deflect attention away from real problems. However, sociologists cannot explain why panics focus particular subjects. Nor do these theorists identify how panics develop or how they leave a lasting imprint on society. To investigate these processes, I study the panic over day care in the 1980s. The panic was triggered by the 1983 McMartin Preschool case in Los Angeles. After McMartin, media attention to day care skyrocketed, and the claims of danger proliferated to include socio-emotional damage, disease spread, and moral decay. In all cases, however, prescriptions of full-time motherhood exempted women on welfare, who require day care to become economically independent. Rather than dismiss the panic as false, my dissertation argues that ideology makes material life possible by constructing meanings that guide human behavior. Thus, the moral panic over day care gave urgent meanings to mothers' rising employment and use of day care, expressing deep-seated, race- and class-bound anxieties about changing gender roles and family arrangements. Far from concealing its causes, the panic over day care openly expressed the cultural beliefs out of which it grew. To study the processes by which panics develop and spread, I borrow Foucault's genealogy. This method attends to three levels of discursive and material processes: inter-discursive (the discourse on child care since the early 1900s), intra-discursive (between the discourses of child care, Satanism, mother-child attachment and conservative morality), and extra-discursive (the context of changing family and gender roles, the ascent of the New Right, and the competitive public arenas in which problems are constructed). Finally, I examine the effects of moral panics. Rather than assume panics, as smokescreens, deny and repress truth, I examine how panics produce truth regimes. These regimes control the production of truth by circulating some claims and silencing others. The day-care panic, for instance, elevated certain truths about day care, pedophilia, and welfare dependency and excluded competing interpretations.Ph.D.Social SciencesSociologyUniversity of Michigan, Horace H. Rackham School of Graduate Studieshttp://deepblue.lib.umich.edu/bitstream/2027.42/132757/2/9990865.pd
Factors driving growth in drug spending, 1993â2003.
<p>Factors driving growth in drug spending, 1993â2003.</p
Electronic consent in clinical care: an international scoping review
Objective Digital technologies create opportunities for improvement of consenting processes in clinical care. Yet little is known about the prevalence, characteristics or outcomes of shifting from paper to electronic consenting, or e-consent, in clinical settings. Thus questions remain around e-consentâs impact on efficiency, data integrity, user experience, care access, equity and quality. Our objective was to scope all known findings on this critical topic.Materials and methods Through an international, systematic scoping review, we identified and assessed all published findings on clinical e-consent in the scholarly and grey literatures, including consents for telehealth encounters, procedures and health information exchanges. From each relevant publication, we abstracted data on study design, measures, findings and other study features.Main outcome measures Metrics describing or evaluating clinical e-consent, including preferences for paper versus e-consenting; efficiency (eg, time, workload) and effectiveness (eg, data integrity, care quality). User characteristics were captured where available.Results A total of 25 articles published since 2005, most from North America or Europe, report on the deployment of e-consent in surgery, oncology and other clinical settings. Experimental designs and other study characteristics vary, but nearly all focus on procedural e-consents. Synthesis reveals relatively consistent findings around improved efficiency and data integrity with, and user preferences for, e-consent. Care access and quality issues are less frequently explored, with disparate findings.Discussion and conclusion The literature is nascent and largely focused on issues that are immediate and straightforward to measure. As virtual care pathways expand, more research is urgently needed to ensure that care quality and access are advanced, not compromised, by e-consent
Retail value of US samples, in billions of dollars.
<p>Retail value of US samples, in billions of dollars.</p