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Parent Perspectives in Shared Decision-Making for Children With Medical Complexity
Jody L Lin1, Catherine L Clark2, Bonnie Halpern-Felsher3
1Division of Pediatric Hospital Medicine, Department of Pediatrics, Stanford University School of Medicine (JL Lin), Stanford, Calif; Division of Pediatric Hospital Medicine, Department of Pediatrics, University of Utah (JL Lin), Salt Lake City, Utah.
Insights
Parents of children with medical complexity (CMC) desire improved shared decision-making (SDM). Key opportunities include clear timelines, integrating patient values, and addressing uncertainty to enhance SDM for CMC.
Area of Science:
- Pediatric healthcare
- Patient-centered care
- Health outcomes research
Background:
- Shared decision-making (SDM) is crucial for improving outcomes in children with medical complexity (CMC).
- Children with medical complexity experience lower rates of SDM compared to other pediatric populations.
- Effective strategies to enhance SDM for CMC remain underexplored.
Purpose of the Study:
- To explore parent perspectives on shared decision-making (SDM) for children with medical complexity (CMC).
- To identify specific opportunities for improving SDM tailored to the unique needs of CMC and their families.
Main Methods:
- Qualitative study involving interviews with 32 parents of children with medical complexity (CMC).
- Interviews explored parents' experiences and preferences regarding SDM.
- Data analyzed using modified grounded theory to identify emergent themes.
Main Results:
- Three overarching themes emerged: participant, knowledge, and context.
- Parents highlighted the need for a defined shared decision timeline.
- Integrating patient/family values and addressing decision-related uncertainty are key areas for SDM improvement.
Conclusions:
- Parent insights offer valuable perspectives on SDM for children with medical complexity (CMC).
- Identified opportunities can guide future interventions and research to enhance SDM for this population.
Objective:
Shared decision-making (SDM) may improve outcomes for children with medical complexity (CMC). CMC have lower rates of SDM than other children, but little is known about how to improve SDM for CMC. The objective of this study is to describe parent perspectives of SDM for CMC and identify opportunities to improve elements of SDM specific to this vulnerable population.
Methods:
Interviews with parents of CMC explored SDM preferences and experiences. Eligible parents were ≥18 years old, English- or Spanish-speaking, with a CMC <12 years old. Interviews were recorded, transcribed, and analyzed by independent coders for shared themes using modified grounded theory. Codes were developed using an iterative process, beginning with open-coding of a subset of transcripts followed by discussion with all team members, and distillation into preliminary codes. Subsequent coding reviews were conducted until no new themes emerged and existing themes were fully explored.
Results:
We conducted interviews with 32 parents (27 in English, mean parent age 34 years, standard deviation = 7; mean child age 4 years, standard deviation = 4; 50% with household income <$50,000, 47% with low health literacy) in inpatient and outpatient settings. Three categories of themes emerged: participant, knowledge, and context. Key opportunities to improve SDM included: providing a shared decision timeline, purposefully integrating patient preferences and values, and addressing uncertainty in decisions.
Conclusion:
Our results provide insight into parent experiences with SDM for CMC. We identified unique opportunities to improve SDM for CMC that will inform future research and interventions to improve SDM for CMC.
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