Objective: To assess deficiencies in patient care for individuals with Parkinson’s disease in neurology clinics, with a particular focus on nonmotor symptoms.
Background: While motor symptoms are the hallmark of Parkinson’s disease (PD), non-motor symptoms (NMS) significantly impact patients’ quality of life, but are often underrecognized and inadequately addressed in clinical practice. These symptoms include neuropsychiatric disturbances, sleep disorders, autonomic dysfunction, and sensory abnormalities. This study aims to assess patients’ perspectives on the prevalence, severity, and clinical management of NMS at a tertiary neurology center.
Method: A quality improvement (QI) initiative was conducted at the University of Utah Department of Neurology to evaluate patient-reported experiences with NMS. A survey was disseminated via the Parkinson’s Center of Excellence listserv, collecting data on symptom prevalence, impact, and the frequency with which these concerns were addressed during neurology visits.
Results: Sixty-two patients (mean age = 71.3, SD = 7.9 years) completed the pre-intervention survey. The most frequently reported NMS were fatigue (83.9%), gastrointestinal dysfunction (72.6%), sleep disturbances (66.1%), anxiety (61.3%), and depression (56.5%). Approximately 22.6% of patients reported that NMS always affected daily life, and 46.8% stated they often had an impact. While 71% of patients reported being screened for NMS at least often, 29% indicated inconsistent screening. Similarly, while 66.2% of patients felt their symptoms were often or always addressed, 33.8% expressed that their concerns were only sometimes or rarely acknowledged. Qualitative responses highlighted a desire for structured symptom screening, improved provider awareness, and comprehensive symptom management strategies.
Conclusion: Patients with PD frequently experience NMS, which are not consistently addressed in clinical encounters. Implementing structured pre-visit symptom screening tools may enhance provider-patient communication, increase symptom recognition, and improve management. In the next phase of this project, we will implement an in-clinic screening survey to enhance provider awareness and guide discussions during consultations. Ongoing analysis of post-intervention data will assess the effectiveness of this initiative in optimizing the care of PD patients and ensuring a more comprehensive approach to their treatment.
NMS Response Rate
NMS Screening Results
NMS Addressed in Clinic
Proposed survey of NMS in Clinic
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To cite this abstract in AMA style:
C. Flavin, G. Lamotte, P. Moretti. Patients’ Perspective on Screening for Non-Motor Symptoms in Parkinson’s Disease, A QI Project [abstract]. Mov Disord. 2025; 40 (suppl 1). https://www.mdsabstracts.org/abstract/patients-perspective-on-screening-for-non-motor-symptoms-in-parkinsons-disease-a-qi-project/. Accessed October 5, 2025.« Back to 2025 International Congress
MDS Abstracts - https://www.mdsabstracts.org/abstract/patients-perspective-on-screening-for-non-motor-symptoms-in-parkinsons-disease-a-qi-project/