Cross-sectional Area of Pubovisceral Muscle in Nulliparous and Primiparous Women

Sponsor
Institute for the Care of Mother and Child, Prague, Czech Republic (Other)
Overall Status
Completed
CT.gov ID
NCT05800678
Collaborator
(none)
80
1
23.7
3.4

Study Details

Study Description

Brief Summary

Pelvic-floor disorders (PFD), including pelvic organ prolapse, urinary and fecal incontinence, decrease quality of life of every fourth women. 1 The main known risk factor for PFD is vaginal delivery 2,3 causing pelvic floor muscle avulsion, ischemia or denervation.4 Ultrasound (US) and magnetic resonance imaging (MRI) are frequently used to investigate structural changes in pelvic floor muscles. We aimed to focus on structural changes (atrophy) caused by muscle denervation. 5 The pubovisceral muscle (PVM) is the part of the levator ani muscle (LAM) which is most frequently injured and it is thought to be possibly denervated by overstretching 6 Recently, the most precise measurement of PVM cross-sectional area was performed by the group of DeLancey. 7 In our study, we aimed to describe which are the normal values of PVM volume in nulliparous women. We performed a measurement of PVM volume in women after the first vaginal delivery.

We hypothesized that there will be a decrease of the cross-sectional area of the PVM developed after denervation trauma.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    Two groups of women were recruited. First, the nulliparous group served as a control. The second group will be women after their first vaginal delivery. Personal characteristics, anamnestic and delivery data were collected, and clinical examination, US and MRI were performed. The number of women to reach significance in the study is 40/per group. We did not expect transfer of patients between the two groups. Volunteers were recruited from general gynecological outpatient clinic.

    They were thoroughly informed and informed consent was provided. Inclusion criteria: women of reproductive age, nulliparous or primiparous, delivering vaginally, contraction of LAM (Oxford scale 0-3:where 0=no contraction in primiparous; 1-5 in nulliparous).

    Exclusion criteria: anamnesis of pelvic floor surgery, US detection of LAM avulsion. In nulliparous women, all examinations (clinical, US, MRI) were performed only once. In women after vaginal delivery first US was performed within 72h after childbirth, in order to detect LAM avulsion and exclude these women. In women without avulsion, 6 weeks after delivery, during general postpartum checkup, the clinical evaluation of pelvic floor muscle contraction was performed. In those where the score is 0-3 the 3D US was performed to confirm no change of hiatal area during contraction. Those scans were recorded as investigated data. Those women underwent MRI within 4 months US images were obtained with a GE Voluson E10 system (General Electric Healthcare, Chicago, IL) by one investigator (SO).

    US data acquisition was performed translabial as already described.9 Volumes were acquired at rest, during Valsalva and contraction. From acquired volume was assessed PVM avulsion, size of urogenital hiatus. Decrease of hiatal area at contraction proves muscle function. The assessment of US scans was performed off-line at axial plane using the 4D View v 2.1-5.0 software (GE Medical Systems) by two investigators blinded against all clinical data (AD,AS).

    MRI images were obtained with a 3-T scanner (AchievaTM, Philips Healthcare). MRI included coronal, axial, and sagittal proton density-weighted sequences performed at rest, Valsalva and contraction. Primary outcome evaluated by MRI will be the cross-sectional area of the PVM. The precise MRI technique was already defined by the group of DeLancey and is in detail described in recent publication.7 Evaluation will be performed off-line by two investigators blinded against all clinical data ( AD, KZ) using ImageJ software. Intra- and interobserver variability will be calculated.

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    80 participants
    Observational Model:
    Cohort
    Time Perspective:
    Prospective
    Official Title:
    Comparison of Cross-sectional Area of Pubovisceral Muscle in Nulliparous and Primiparous Women
    Actual Study Start Date :
    Apr 1, 2021
    Actual Primary Completion Date :
    Mar 23, 2023
    Actual Study Completion Date :
    Mar 23, 2023

    Arms and Interventions

    Arm Intervention/Treatment
    nulliparous

    inclusion: reproductive age exclusion: history of gynecological surgery or disorder with possible impact on pelvic floor

    primiparous

    Inclusion: reproductive age, vaginal birth exclusion: history of gynecological surgery or disorder with possible impact on pelvic floor assisted vaginal delivery (forceps, vaccumextraction) labour induction pregnancy-related disorders perineal tear grade III-IV (women with episiotomy were included) suspicion of LAM avulsion by ultrasound or palpation Oxford score 4 or 5 after delivery

    Outcome Measures

    Primary Outcome Measures

    1. cross-sectional area of pubovisceral muscle [in nulliparous group measurements performed imediately after MRI. In primiparous group the MRI was performed within 3-6 months after delivery]

      The PVM CSA was measured as previously described by Masteling et al.. Briefly, the MR images were imported into 3D Slicer, where slices containing the volume of interest were identified in a plane perpendicular to the muscle direction. To identify a plane perpendicular to the PVM, the PVM fibres direction was first established between origin and insertion, namely the inner surface of the pubic bone and its insertion into the perineal structures. In the coronal plane perpendicular to the muscle direction, the boundaries of the PVM were identified and images of this region were taken. The captured images were then exported into ImageJ for measurement of CSA.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    N/A and Older
    Sexes Eligible for Study:
    Female
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • reproductive age

    • vaginal birth

    Exclusion Criteria:
    • history of gynecological surgery or disorder with possible impact on pelvic floor

    • forceps, vaccumextraction)

    • labour induction

    • pregnancy-related disorders

    • perineal tear grade III-IV (women with episiotomy were included)

    • suspicion of LAM avulsion by ultrasound or palpation

    • Oxford score 4 or 5 after delivery

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Institute for mother and child care Prague Czechia 147 00

    Sponsors and Collaborators

    • Institute for the Care of Mother and Child, Prague, Czech Republic

    Investigators

    • Principal Investigator: Lucie Hájková Hympánová, PhD, Ústav pro péči o matku a dítě, Praha, CZ

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Katarina Ivankova, Katarina Ivankova, Institute for the Care of Mother and Child, Prague, Czech Republic
    ClinicalTrials.gov Identifier:
    NCT05800678
    Other Study ID Numbers:
    • UPMDPrague2021/28_1/2
    First Posted:
    Apr 5, 2023
    Last Update Posted:
    Apr 5, 2023
    Last Verified:
    Mar 1, 2023
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Katarina Ivankova, Katarina Ivankova, Institute for the Care of Mother and Child, Prague, Czech Republic
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Apr 5, 2023