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Adoption of Subcutaneous Infusion Systems in Clinical Practice for Parkinson Disease

Panelists discuss how medical professionals have incorporated continuous subcutaneous infusion systems into their clinical practice.

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Adoption of Subcutaneous Infusion Systems in Clinical Practice for Parkinson Disease

Overview

This summary provides key information on the implementation and clinical adoption of subcutaneous infusion systems for the management of advanced Parkinson's disease (PD). Continuous subcutaneous medication delivery represents an important therapeutic option for patients experiencing motor fluctuations and dyskinesias despite optimized oral therapy.

Clinical Indications

  • Advanced Parkinson's disease with motor fluctuations not adequately controlled by oral medications
  • Patients experiencing significant "off" periods or troublesome dyskinesias
  • Candidates who would benefit from continuous dopaminergic stimulation
  • Patients with preserved levodopa response but struggling with oral medication regimens

Available Medication Options

  • Apomorphine: Potent non-ergoline dopamine agonist delivered via subcutaneous infusion
  • Levodopa-carbidopa intestinal gel (LCIG): While technically not subcutaneous, provides an alternative continuous infusion approach
  • Foslevodopa/foscarbidopa suspension: Recently approved subcutaneous formulation of levodopa/carbidopa

Patient Selection Considerations

  • Preserved levodopa responsiveness
  • Adequate cognitive function to manage the device (or reliable caregiver support)
  • Absence of contraindications to specific medications (cardiac issues for apomorphine)
  • Patient/caregiver willingness and ability to maintain infusion system
  • Assessment of skin integrity for infusion site management

Implementation Steps

  • Patient assessment and selection: Comprehensive evaluation by movement disorder specialist
  • Medication trial: Initial test dose under medical supervision
  • Education and training: Patient and caregiver instruction on device operation and maintenance
  • Initiation of therapy: Typically begins in inpatient or closely supervised outpatient setting
  • Titration phase: Gradual adjustment of infusion rate to optimize symptom control
  • Regular follow-up: Monitoring for efficacy, side effects, and infusion site management

Clinical Benefits

  • Reduction in "off" time and dyskinesias
  • More consistent motor symptom control
  • Potential reduction in oral medication burden
  • Improved quality of life metrics
  • Enhanced ability to perform activities of daily living

Common Challenges and Management

  • Infusion site reactions: Proper site rotation and hygiene protocols
  • Technical difficulties: Troubleshooting device issues and proper maintenance
  • Medication side effects: Monitoring for nausea, orthostatic hypotension, impulse control disorders
  • Patient adherence: Regular reinforcement of proper technique and schedule

Practical Considerations

  • Insurance coverage and prior authorization requirements
  • Coordination with specialty pharmacy for medication supply
  • Multidisciplinary team approach (neurologist, nurse, pharmacist)
  • Regular assessment of continued appropriateness of therapy

Follow-up Schedule

  • Initial weekly assessments during titration phase
  • Monthly visits for first 3 months
  • Quarterly follow-up once stable

24/7 access to clinical support for urgent issues

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Brad Kamitaki, MD
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