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. 2022 Apr 1;18(4):1135-1143.
doi: 10.5664/jcsm.9830.

Validation of the Dutch translation of the Paris Arousal Disorders Severity Scale for non-REM parasomnias in a 1-year and 1-month version

Affiliations

Validation of the Dutch translation of the Paris Arousal Disorders Severity Scale for non-REM parasomnias in a 1-year and 1-month version

Petra van Mierlo et al. J Clin Sleep Med. .

Abstract

Study objectives: We created a Dutch version of the Paris Arousal Disorders Severity Scale (PADSS), which assesses non-rapid eye movement (NREM) parasomnia symptoms over the past year (PADSS-year). This questionnaire was previously validated in patients with sleep walking and/or sleep terrors (SW/ST). We validated the questionnaire in SW/ST patients, and in a broader population, including patients with confusional arousals, comorbidities, and medication users ("other NREM parasomnias"). Furthermore, we introduced a version covering the past month (PADSS-month), with the potential purpose of evaluating symptom evolution and treatment response.

Methods: We compared PADSS scores among 54 SW/ST patients, 34 age-matched controls, and 23 patients with other NREM parasomnias. We evaluated discriminative capacity, internal consistency, and construct validity. Furthermore, we assessed the test-retest reliability and treatment response of PADSS-month.

Results: Healthy controls scored significantly lower than both patient groups. We found an excellent diagnostic accuracy (area under the curve PADSS-year 0.990, PADSS-month 0.987) and an acceptable internal consistency. Exploratory factor analysis identified 3 components: "behaviors outside the bed," "behaviors in/around the bed," and "violent behaviors," with the former 2 factors reflecting the distinction between SW and ST. PADSS-month showed an acceptable test-retest reliability (0.75). Additionally, PADSS-month significantly decreased after pharmaceutical and/or behavioral treatment. This change was correlated with the clinical impression of the caregiver, implying that PADSS-month is sensitive to treatment effects.

Conclusions: The Dutch PADSS questionnaire can be used as a screening tool in a broad population of patients with NREM parasomnia, not only SW/ST. Furthermore, we validated a PADSS-month version to assess the evolution of symptoms and treatment effect.

Citation: van Mierlo P, Hermans L, Arnulf I, Pijpers A, Overeem S, van Gilst M. Validation of the Dutch translation of the Paris Arousal Disorders Severity Scale for non-REM parasomnias in a 1-year and 1-month version. J Clin Sleep Med. 2022;18(4):1135-1143.

Keywords: NREM parasomnia; sleep terror; sleepwalking.

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Conflict of interest statement

All authors have seen and approved the manuscript. S. Overeem consulted for Bioprojet, Jazz Pharmaceuticals, UCB Pharma, and Takeda, all paid to the institution, and not related to the present work. The other authors report no conflicts of interest.

Figures

Figure 1
Figure 1. Schematic representation of the study procedures.
Blue rectangles represent procedures that were part of clinical treatment; white rectangles represent time instances during which data were collected for the study. GGI-C = treatment evaluation question (reflecting change between before and after treatment) of the Clinical Global Impression Scale, PADSS = Paris Arousal Disorders Severity Scale, PSG = polysomnography,
Figure 2
Figure 2. Total scores for first-visit PADSS questionnaires for SW/ST patients, healthy controls, and other parasomnia patients.
NREM = non–rapid eye movement, PADSS = Paris Arousal Disorders Severity Scale, SW/ST = sleep walking/sleep terrors.
Figure 3
Figure 3. ROC curve for discriminating between SW/ST patients and age-matched healthy participants.
The red diagonal lines are reference lines; the blue lines represent the ROC curves. PADSS = Paris Arousal Disorders Severity Scale, ROC = receiver operating characteristic, SW/ST = sleep walking/sleep terrors.
Figure 4
Figure 4. Total scores for PADSS-month-1 (before treatment) and PADSS-month-3 (after treatment) for subgroups of participants stratified for type of treatment.
The 2 participants who received various other types of treatment and the 2 participants for whom the treatment was not known are not shown in this graph. CBT-p = standard lifestyle advice + cognitive behavioral therapy (n = 21), Comb = standard lifestyle advice + cognitive behavioral therapy + medication (n = 5), Lifest = only standard lifestyle advice (n = 8), Med = standard lifestyle advice + medication (n = 9), PADSS = Paris Arousal Disorders Severity Scale.

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