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VALIdation of models for assessing eligibility for referral for Device-Aided Treatment in Parkinson’s disease (VALIDATE)

H. Moes, E. Buskens, A. Portman, B. van Harten, M. van Kesteren, T. Mondria, L. Teune, E. van Wensen, M. van Onna, M. Schilperoord, A. Wertenbroek, M. Tjepkema-Cloostermans, L. Dorresteijn, T. van Laar (Groningen, Netherlands)

Meeting: 2023 International Congress

Abstract Number: 1413

Keywords: Apomorphine, Deep brain stimulation (DBS), Levodopa(L-dopa)

Category: Parkinson’s Disease: Pharmacology and Therapy

Objective: To externally validate the Dutch Device-Aided Therapy Screening tool (D-DATS) and to compare it with the 5-2-1 criteria.

Background: Timely identification of patients with Parkinson’s disease (PD) who may be eligible for device-aided therapy (DAT) is important but challenging for general neurologists. To this end several screening tools have been proposed, such as the 5-2-1 criteria, and more recently the easy-to-use D-DATS (Moes et al. 2023). The latter is based on the presence of response fluctuations and troublesome dyskinesias, and the levodopa equivalent daily dose. The 5-2-1 criteria are met if a patient has at least one of the following three clinical indicators: ≥5 doses of oral levodopa per day, OR ≥2 hours of “off” time per day, OR ≥1 hour of troublesome dyskinesia per day. Meanwhile, after rigorous development, the D-DATS is awaiting external validation and comparison with other screening tools.

Method: We performed a multicenter prospective, cross-sectional diagnostic study in DAT-naive PD patients attending a routine visit in a secondary care setting in the northeastern part of the Netherlands. Clinical characteristics of consecutive patients were collected by the attending physician. Anonymized patient vignettes were assessed by a panel of 5 movement disorder experts with expertise in DAT. The outcome (reference test) was eligibility for referral for DAT as assessed by the expert panel. The diagnostic accuracy of the D-DATS and 5-2-1 criteria was compared with the reference test.

Results: The cohort of 250 patients included 32 patients eligible for DAT referral (12.4%). The D-DATS had excellent discrimination in assessing eligibility for DAT referral (ROC AUC = 0.95; 95% CI: 0.91-0.98), while the 5-2-1 criteria had acceptable discrimination (ROC AUC = 0.79; 95% CI: 0.73-0.82). The diagnostic accuracy of the D-DATS (cut-off value 5.8) compared to the 5-2-1 criteria was 81% vs 92% for sensitivity, and 92% vs 59% for specificity respectively. The positive predictive value was 59% for D-DATS and 26% for the 5-2-1 criteria.

Conclusion: The results of this external validation study confirm the validity of the D-DATS in identifying PD patients eligible for referral for DAT. Compared with the 5-2-1 criteria, the D-DATS appears to be slightly less sensitive but more specific, resulting in a superior positive predictive value.

References: Moes, Harmen R., et al. “Timely referral for device-aided therapy in Parkinson’s disease. Development of a screening tool.” Parkinsonism & Related Disorders (2023): 105359.

To cite this abstract in AMA style:

H. Moes, E. Buskens, A. Portman, B. van Harten, M. van Kesteren, T. Mondria, L. Teune, E. van Wensen, M. van Onna, M. Schilperoord, A. Wertenbroek, M. Tjepkema-Cloostermans, L. Dorresteijn, T. van Laar. VALIdation of models for assessing eligibility for referral for Device-Aided Treatment in Parkinson’s disease (VALIDATE) [abstract]. Mov Disord. 2023; 38 (suppl 1). https://www.mdsabstracts.org/abstract/validation-of-models-for-assessing-eligibility-for-referral-for-device-aided-treatment-in-parkinsons-disease-validate/. Accessed June 15, 2025.
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