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SIPS – Screening-Instrument für prämenstruelle Symptome*

Die deutsche Version des Premenstrual Symptoms Screening Tool zur Erfassung klinisch relevanter Beschwerden

SIPS – screening instrument for premenstrual symptoms*

The German version of Premenstrual Symptoms Screening Tool to assess clinically relevant disturbances

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Zusammenfassung

Hintergrund

Prämenstruelle dysphorische Störungen (PMDS) und schwere prämenstruelle Syndrome (PMS) treten häufig auf, bleiben jedoch oft unerkannt und unbehandelt. Begünstigt wird dies durch das Fehlen eines entsprechenden deutschsprachigen Screening-Instruments. Ziel dieser Studie war es, das englischsprachige Premenstrual Symptoms Screening Tool (PSST) ins Deutsche zu übertragen und seine Anwendung zu prüfen.

Material und Methoden

Die deutschsprachige Version des PSST wurde als „Screening-Instrument für prämenstruelle Symptome“ (SIPS) erstellt und ihre Güte an 47 Frauen mit und ohne PMDS/schwerem PMS internetbasiert mittels täglichen Symptomeinschätzungen bestimmt.

Ergebnisse

Die Retest-Reliabilität des SIPS betrug r=0,69, das Cronbachs α 0,924. Als Validitätsmaß des SIPS zeigten sich signifikante Unterschiede zwischen Frauen mit und ohne PMDS/schwerem PMS, bestimmt durch das SIPS, bezüglich prospektiv erfasster prämenstrueller Symptomatik (F[2,44]=4,52, p<0,001) und Symptomveränderung (F[2,44]=25,23, p<0,001).

Schlussfolgerung

Das SIPS ist reliabel und valide und kann helfen, Frauen mit behandlungsbedürftigen prämenstruellen Beschwerden zu identifizieren.

Summary

Background

Premenstrual dysphoric disorder (PMDD) and severe premenstrual syndrome (PMS) are common, yet often remain unrecognized and not adequately treated. One reason for this is the lack of a valid German screening instrument. The aim of the present study was to create a German version of the English“Premenstrual Symptoms Screening Tool (PSST)” and to verify its applicability.

Material and methods

The German version of the PSST was created as“Screening-Instrument für prämenstruelle Symptome (SIPS)” and its reliability and validity determined based on data from 47 women with and without PMDD/severe PMS using Internet-based daily symptom ratings.

Results

The retest reliability of the SIPS was r=0.69, and Cronbach’s alpha was 0.924. As an indicator of the convergent validity of the SIPS, there were significant differences between women with and without PMDD/severe PMS as identified by the SIPS with regard to prospectively assessed premenstrual symptomatology (F[2,44]=4.52, p<0.001) and symptom change (F[2,44]=25.23, p<0.001).

Conclusions

The SIPS is reliable and valid and may help to improve the identification of women who require treatment for their premenstrual symptoms.

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Interessenkonflikte

Der korrespondierende Autor weist auf folgende Beziehungen hin:

Meir Steiner: Consultant: Wyeth Pharmaceuticals, Bayer Shering Pharmaceuticals, Astra-Zeneca, Azevan Pharmaceuticals, Servier. Grants: Canadian Institutes of Health Research, Physicians Services Inc. Research Support: Wyeth Pharmaceuticals, Astra-Zeneca, Lundbeck. Honorarium: Azevan Pharmaceuticals, Ortho-McNeil.

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Correspondence to G. Meinlschmidt.

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*© McMaster University

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Bentz, D., Steiner , M. & Meinlschmidt, G. SIPS – Screening-Instrument für prämenstruelle Symptome*. Nervenarzt 83, 33–39 (2012). https://doi.org/10.1007/s00115-010-3210-6

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  • DOI: https://doi.org/10.1007/s00115-010-3210-6

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