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 |