Table 3.
Proposed interventions to decrease disparities in DBS
Level of intervention | Proposed interventions |
---|---|
Provider level | Implement provider and leadership training to increase awareness of implicit and explicit biases |
Specialized training in cultural competency and DEI | |
Diverse representation among healthcare providers caring for PD patients | |
Increase provider awareness of existing disparities to increase referral rates | |
Introducing DBS treatment to all patients early in the decision-making process | |
DBS education and structured referral guidelines for primary care providers and neurologists | |
Patient level | Accessible educational materials |
Individualized patient education | |
Specialized digital educational materials | |
Increase education among minority communities about PD and treatment options | |
Increase understanding of differences in Parkinson’s symptom expression and experience | |
Community level | Improve access to preventive care in minority communities |
Implement community-based social or physical health programs | |
Increase access to movement disorder neurologists in minority communities, ex through mobile clinics | |
Implementation of community partnerships (i.e., with religious groups or barbershops) | |
National-level interventions | Increase research into causes of and solutions for disparities in DBS access |
Inclusion of a greater diversity of individuals in leadership of national organizations, as well as healthcare providers | |
Development of official guidelines for reducing disparities in DBS access | |
Increase telemedicine opportunities to those in underserved locations | |
Streamlined referral process | |
Increased diversity in targeted advertising | |
Change reimbursement policies |