Translating medical evidence to promote informed health care decisions

Health Services Research

Volumn 46, Issue 4, 2011, Pages 1200-1223

  McCormack, Lauren ^a   Treiman, Katherine ^a   Bann, Carla ^a   Williams Piehota, Pamela ^a   Driscoll, David ^b   Poehlman, Jon ^a   Soloe, Cindy ^a   Lohr, Kathleen ^a   Sheridan, Stacey ^c   Golin, Carol ^c   Cykert, Samuel ^d   Harris, Russell ^c  

^a RTI INTERNATIONAL   (United States)

^b UNIVERSITY OF ALASKA ANCHORAGE   (United States)

^c UNIVERSITY OF NORTH CAROLINA   (United States)

^d MOSES H CONE MEMORIAL HOSPITAL   (United States)

Author keywords

Decision making; level of involvement; patient provider communication; prostate cancer screening

Indexed keywords

PROSTATE SPECIFIC ANTIGEN;

ADULT; AGED; ARTICLE; HEALTH CARE; HUMAN; INFORMED CONSENT; KNOWLEDGE; MALE; MEDICAL DECISION MAKING; ORGANIZATION; PROSTATE BIOPSY; PROSTATE CANCER; SCREENING;

ADULT; AGED; AGED, 80 AND OVER; COMMUNITY-BASED PARTICIPATORY RESEARCH; DECISION MAKING; HEALTH KNOWLEDGE, ATTITUDES, PRACTICE; HUMANS; MALE; MASS SCREENING; MEN'S HEALTH; MIDDLE AGED; OUTCOME AND PROCESS ASSESSMENT (HEALTH CARE); PATIENT PARTICIPATION; PROSTATE-SPECIFIC ANTIGEN; SELF EFFICACY; SOCIOECONOMIC FACTORS;

EID: 79960096794     PISSN: 00179124     EISSN: 14756773     Source Type: Journal    
DOI: 10.1111/j.1475-6773.2011.01248.x     Document Type: Article

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