Adults with cerebral palsy rank factors associated with quality of life and perceived impact of childhood surgery on adult outcomes

Abstract

Background

Person-centered care concerns the values and perceptions of the patient in assessment of outcomes. Little is known about perceptions of adults with cerebral palsy (CP) concerning: the most important factors associated with quality of life, definitions of success, short- and long-term outcomes of childhood orthopedic care, and current needs for information surrounding childhood orthopedic care.

Methods

An online survey gathered information using structured and semi-structured questions. Descriptive statistics and content analysis summarized findings of structured questions and comments.

Results

A total of 71 adults with CP (44 women, median age range 30–39 years), with a variety of functional abilities, participated in the study. Priorities for a good life were clustered. There existed two groups: achievement orientation and relationship orientation. Good health and interpersonal relationships were priorities for both groups. Definitions of success included happiness, independence, meaningful relationships/activities, and mindfulness/lifelong-learning. Fifty-eight percent perceived a positive impact of childhood orthopedic care on current function. A positive perception was associated with being included in the decision making process (chi-square 25, p < .001). Suggestions to improve childhood orthopedic care included: more information about long-term outcomes, surgical timing, and alternatives to surgery, and improved service delivery models to prevent gaps in care across the lifespan.

Conclusion

Ongoing conversations about how improvements from orthopedic surgery in childhood may not last through adolescence or adulthood are needed. The importance of impairment-based interventions should be contextualized within needs for health promotion and social engagement long-term. More research is needed on cost-benefit of childhood orthopedic surgery.

Implications for Rehabilitation

• Perceptions of being included in decisions about surgery as a child was associated with long term satisfaction.

• Consumer education is needed about how improvements gained in childhood may not persist through adolescence or into adulthood.

• Individual priorities for quality of life vary; and these priorities should be considered when weighing the cost benefit ratio of interventions.

• Clinicians should broaden the conversation to include how orthopedic surgery and rehabilitation afterwards could potentially impact health and well being in the future.

Keywords:

• Cerebral palsy
• long-term outcomes
• quality of life
• orthopedic care
• person centered care

Disclosure statement

No potential conflict of interest was reported by the authors.

Additional information

Funding

This work was supported by Kosair Charities, Inc.