Loading…
Dopamine agonist withdrawal syndrome associated factors: A retrospective chart review
•DAWS is a condition that results from reduction or suspension of dopamine agonist medications.•Identification of patients at risk is fundamental to mitigate DAWS occurrence.•DA dose ≥150 LEDD, ICD and history of DBS, are significant associated factors with DAWS development. Dopamine agonist withdra...
Saved in:
Published in: | Clinical parkinsonism & related disorders 2022-01, Vol.7, p.100153-100153, Article 100153 |
---|---|
Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Summary: | •DAWS is a condition that results from reduction or suspension of dopamine agonist medications.•Identification of patients at risk is fundamental to mitigate DAWS occurrence.•DA dose ≥150 LEDD, ICD and history of DBS, are significant associated factors with DAWS development.
Dopamine agonist withdrawal syndrome (DAWS) has been introduced to describe the constellation of symptoms resulting from reduction or suspension of dopamine agonist medications. In patients with Parkinson’s disease (PD) the impact of DAWS can be significant in terms of distress and disability. Unfortunately, no standard treatment exists other than reintroduce the dopamine agonist even in the presence of adverse effects. Therefore, identification of vulnerable patients would be beneficial. Previous studies have linked DAWS with impulse control disorder behavior (ICD), higher dopamine agonist doses, and milder motor impairment in PD patients.
We conducted a retrospective chart reviewof PD patients treated with dopamine agonist. A total of 313 charts from January 2011 to December 2013 were reviewed, showing 126 patients who were discontinued from dopamine agonist. Twenty-one patients (16.8 %) fulfilled the diagnostic criteria for DAWS. Factors associated with the occurrence of DAWS were: (1) dose of dopamine agonist ≥150 mg expressed in levodopa equivalents daily dose (LEDD) (p = 0.018), (2) impulse control disorder as an adverse effect to dopamine agonist (p = 0.002), and (3) prior deep brain stimulation (DBS) (p = 0.049). The probability of developing DAWS in the presence of all 3 identified factors was 92 %; presence of 2 factors raised the probability up to 70 %; the presence of one factor increased the probability up to 30 %. In the absence of these 3 factors the probability of developing DAWS was 3 %. Prospective studies are warranted to confirm these findings. |
---|---|
ISSN: | 2590-1125 2590-1125 |
DOI: | 10.1016/j.prdoa.2022.100153 |