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Knowledge and values for cancer screening decisions: Results from a national survey.
Hoffman, Richard M; Elmore, Joann G; Pignone, Michael P; Gerstein, Bethany S; Levin, Carrie A; Fairfield, Kathleen M.
Afiliação
  • Hoffman RM; Department of Medicine, University of Iowa Carver College of Medicine, Iowa City, IA, United States; Medicine Service, Iowa City VA Medical Center, Iowa City, IA, United States.
  • Elmore JG; Department of Medicine, University of Washington School of Medicine, Seattle, WA, United States.
  • Pignone MP; University of North Carolina Division of General Internal Medicine, Chapel Hill, NC, United States; University of North Carolina Institute for Healthcare Quality Improvement, Chapel Hill, NC, United States.
  • Gerstein BS; Informed Medical Decisions Foundation, Division of Healthwise, Inc. Boston, MA, United States.
  • Levin CA; Informed Medical Decisions Foundation, Division of Healthwise, Inc. Boston, MA, United States.
  • Fairfield KM; Department of Medicine and Center for Outcomes Research and Evaluation, Maine Medical Center Research Institute, Portland, ME, United States. Electronic address: fairfk@mmc.org.
Patient Educ Couns ; 99(4): 624-630, 2016 Apr.
Article em En | MEDLINE | ID: mdl-26603446
ABSTRACT

BACKGROUND:

Guidelines recommend shared decision making (SDM) for cancer screening decisions. SDM requires providers to ensure that patients are informed about screening issues and to support decisions that are concordant with patient values. We evaluated decision-quality factors for breast, colorectal, and prostate cancer screening decisions.

METHODS:

We conducted a national, population-based Internet survey of adults aged 40+ to characterize perceptions about about cancer screening, the importance of information sources, cancer screening knowledge, values and preferences for screening, and the most influential drivers of decisions.

RESULTS:

Among 1452 participants who completed the survey, the mean age was 60, and 94% were insured. Most participants reported feeling well informed about cancer screening, though only 21% reported feeling extremely well informed. Most participants correctly answered about 50% of the knowledge questions, with the majority markedly overestimating lifetime risk of cancer diagnoses and mortality. Participants rated health care providers as the most important source of information.

CONCLUSION:

Although respondents considered themselves well informed about cancer they performed poorly on knowledge questions. This discordance suggests the potential for poor-quality decision making. PRACTICE IMPLICATIONS To improve the quality of decision making, providers need training to utilize decision support tools and time to carry out SDM.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Participação do Paciente / Conhecimentos, Atitudes e Prática em Saúde / Programas de Rastreamento / Internet / Tomada de Decisões / Neoplasias Tipo de estudo: Diagnostic_studies / Guideline / Prognostic_studies / Qualitative_research / Screening_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Participação do Paciente / Conhecimentos, Atitudes e Prática em Saúde / Programas de Rastreamento / Internet / Tomada de Decisões / Neoplasias Tipo de estudo: Diagnostic_studies / Guideline / Prognostic_studies / Qualitative_research / Screening_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2016 Tipo de documento: Article