Adopting a palliative care mindset is an unmet need in Parkinson’s disease

Abstract

Introduction

Parkinson’s disease (PD) affects multiple facets of patients’ lives, many of which may not be recognized or addressed by their healthcare team. A growing body of evidence has shown that palliative care improves patients’ quality of life with PD; however, little is currently known about how patients with PD perceive palliative care.

Methods

An 8-question multiple choice survey was created and given to patients with established care for PD at a movement disorders clinic in a quaternary care center. Patients with less than two years of follow-up or that had atypical features of PD were excluded from the survey.

Results

There were 106 respondents to the survey. A third of patients reported having never heard of palliative care and an additional 25% had heard of it but did not know what it was. Eighty-eight percent reported being familiar with or very knowledgeable about hospice, though 50% of respondents did not know the difference between hospice and palliative care. 93% had never been offered either service. 37.7% thought their neurologist should discuss advance care planning early in the course of their disease.

Conclusion

Even among established patients with Parkinson’s disease in a quaternary center, over half were not familiar with palliative care, and the majority had never been offered palliative or hospice services despite growing evidence that it could improve their quality of life. Additionally, patients would like to be introduced to advanced care planning early in the course of their disease.