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Views of treatment decision making from adolescents with chronic illnesses and their parents: a pilot study
Authors:Jennifer M. Knopf MA  Richard W. Hornung Dr PH  Gail B. Slap MD MS  Robert F. DeVellis PhD  Maria T. Britto MD MPH
Affiliation:1. Project Specialist, Division of Adolescent Medicine, Center for Innovation in Chronic Disease Care, Cincinnati Children’s Hospital Medical Center, Cincinnati, OH;2. Professor of Environmental Health, Division of General and Community Pediatrics, Cincinnati Children’s Hospital Medical Center and the University of Cincinnati School of Medicine, Cincinnati, OH;3. Professor of Pediatrics and Internal Medicine, Office of Fellowship Programs, Children’s Hospital of Philadelphia and the University of Pennsylvania School of Medicine, Philadelphia, PA;4. Research Professor, Department of Health Behavior and Health Education, School of Public Health, Thurston Arthritis Research Center, University of North Carolina at Chapel Hill, Chapel Hill, NC;5. Professor of Pediatrics, Division of Adolescent Medicine, Center for Innovation in Chronic Disease Care, Cincinnati Children’s Hospital Medical Center and the University of Cincinnati School of Medicine, Cincinnati, OH, USA
Abstract:Objective Shared decision making may increase satisfaction with health care and improve outcomes, but little is known about adolescents’ decision‐making preferences. The primary purpose of this study is to describe the decision‐making preferences of adolescents with chronic illnesses and their parents, and the extent to which they agree. Design Survey. Setting and participants Participants were 82 adolescents seen at one of four paediatric chronic illness subspecialty clinics and 62 of their parents. Main variables Predictor variables include sociodemographics, health parameters, risk behaviour, and physical and cognitive development. The main outcome variable is preferences for decision‐making style. Results and conclusions When collapsed into three response categories, nearly equal percentages of adolescents (37%) and parents (36%) preferred shared decision making. Overall, the largest proportion of adolescents (46%) and parents (53%) preferred passive decision making compared to active or shared decision making. Across five response choices, 33% of pairs agreed. Agreement was slight and not significant. Improved general health perceptions (OR = 0.76, 95% CI = 0.59–0.99) and improved behaviour (OR = 0.75, 95% CI = 0.56–0.99) were significantly associated with parents’ preferences for less active decision making. Older age was significantly associated with agreement (OR 1.58, 95% CI = 1.09–2.30) between parents and adolescents. The paucity of significant predictor variables may indicate physicians need to inquire directly about patient and parent preferences.
Keywords:adolescents  chronic illness  decision making  patient participation  patient preferences
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