The prevalence of major abnormalities of the levator ani in urogynaecological patients

Objectives  While morphological abnormalities of the pubovisceral muscle have been described on magnetic resonance imaging (MRI), their relevance remains unclear. This study was designed to define prevalence and clinical significance of such abnormalities in urogynaecological patients. Design  Prosp...

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Veröffentlicht in:BJOG : an international journal of obstetrics and gynaecology 2006-02, Vol.113 (2), p.225-230
Hauptverfasser: Dietz, HP, Steensma, AB
Format: Artikel
Sprache:eng
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Zusammenfassung:Objectives  While morphological abnormalities of the pubovisceral muscle have been described on magnetic resonance imaging (MRI), their relevance remains unclear. This study was designed to define prevalence and clinical significance of such abnormalities in urogynaecological patients. Design  Prospective observational study. Setting  Tertiary urogynaecological clinic. Population  Three hundred and thirty‐eight consecutive women referred for urodynamic assessment. Methods  Participants underwent a clinical assessment, multichannel urodynamics and imaging with 3D translabial ultrasound. Blinded offline analysis was performed with the software 4D View (GE Kretztechnik, Zipf, Austria). Main outcome measures  Major morphological abnormalities of the pubovisceral muscle. Results  Defects of the pubovisceral muscle were found in 15.4% of parous women. They were exclusively anteromedial (uni‐ or bilateral), only occurred among women who had delivered vaginally and were associated with anterior and central compartment prolapse (all P < 0.001). There was no association with symptoms of bladder dysfunction or urodynamic findings. Conclusions  Major morphological abnormalities of the pubovisceral muscle are common in parous urogynaecological patients. They are associated with prolapse of the anterior and central compartment, but not with symptoms of bladder dysfunction or urodynamic findings.
ISSN:1470-0328
1471-0528
DOI:10.1111/j.1471-0528.2006.00819.x