This risk calculator is intended for estimating the likelihood of developing dyskinesia in patients who are initiating their levodopa treatment. The calculator is based on the STRIDE-PD study and therefore the risk is calculated for the next approximately 3 years following the start of levodopa. Dyskinesia risk cannot be calculated for patients, whose characteristics (age, weight or UPDRS II score) are outside those seen in STRIDE-PD population.
This calculator is not to be used as the only tool to decide how to treat patients with levodopa and it should not replace clinical judgment on any treatment decisions.
Gender | xx |
Age | xx |
Weight | xx |
UPDRS II | xx |
Daily dose of levodopa (mg)
Levodopa is the most effective agent for the symptomatic treatment of Parkinson’s disease (PD). However, long-term use of levodopa is associated with the development of motor complications such as wearing-off and dyskinesia.
This dyskinesia risk calculator is intended for estimating the probability of developing dyskinesia in PD patients who are initiating their levodopa treatment. The calculator is based on the STRIDE-PD ¹ study and therefore the risk is calculated for the next 169 weeks (approximately 3 years) following the initiation of levodopa treatment. Dyskinesia risk cannot be estimated for patients, whose characteristics (age, weight or UPDRS II score) are outside those seen in STRIDE-PD population.
In order to use the risk calculator, first select the gender of the patient and then input patient’s age, weight in kg and UDPRS part II score before the initiation of levodopa treatment using the sliders. When the Calculate button is clicked, a graph is created indicating the probability of developing dyskinesia within 169 weeks at different daily levodopa dose levels.
This calculator is intended for use by healthcare professionals. However, it is not to be used as the only tool to decide how to treat patients with levodopa and it should not replace clinical judgment on any treatment decisions. The calculator can also be used for example for educational purposes.
The risk cannot be estimated for doses lower than 150 mg or higher than 800 mg because this kind of combination of dose and predictive factors was not present in the STRIDE-PD study.
The probability of developing dyskinesia is calculated based on risk factors identified from the STRIDE-PD study ¹. The model was developed using both statistical and clinical considerations. An initial model was created by screening the potential predictive factors for development of dyskinesia from the STRIDE-PD data using a Cox proportional hazard model. The factors to be used in the model were selected on the basis that they were statistically significant predictive factors, easy to assess in routine clinical practice and did not directly correlate with another variable being used in the model. The discriminative properties of the set of the predictive factors were assessed using the Concordance-Index (C-Index). In addition to the criteria listed above, the selected model was not to decrease the C-Index value significantly compared with the initial model.
The following factors were selected for the model estimating the risk of dyskinesia at 169 weeks − age, weight, UPDRS part II score and gender ².
Functionality of this tool has been tested with the following minimum browser versions: Internet Explorer 8, Firefox 10, Chrome 15 or Safari 5
¹ Stocchi F, Rascol O, Kieburtz K, Poewe W, Jankovic J, Tolosa E, Barone P, Lang AE, Olanow CW. Initiating levodopa/carbidopa therapy with and without entacapone in early Parkinson disease: the STRIDE-PD study. Ann Neurol 2010;68(1):18–27
² Schapira AH, Poewe W, Kieburtz K, Rascol O, Stocchi F, Nissinen H, Leinonen M, Olanow CW for the STRIDE-PD Investigators. Development of a risk calculator for prediction of dyskinesia for patients with Parkinson’s disease based on the STRIDE-PD study. Mov Disord 2012; 27 (Suppl S1): 429.
Please, assess the scores based on the patient’s functioning during the past one week.