Does cystocele type vary between vaginally parous and nulliparous women?

Vereeck S1, Pacquee S2, Weeg N2, Dietz H2

Research Type

Clinical

Abstract Category

Pelvic Organ Prolapse

Abstract 67
Prolapse
Scientific Podium Short Oral Session 6
On-Demand
Imaging Pelvic Organ Prolapse Retrospective Study
1. Department of Gynecology, Antwerp University Hospital UZA, ASTARC Antwerp University UA, Belgium, 2. Sydney Medical School Nepean, University of Sydney, Australia
Presenter
S

Sascha Vereeck

Links

Abstract

Hypothesis / aims of study
The aim of our observational study was to determine whether cystocele type varies between vaginally parous and vaginally nulliparous women in order to gain insights into the etiology of cystocele.
Study design, materials and methods
This is a retrospective analysis of 464 vaginally nulliparous women seen routinely at two tertiary urogynecology centers between November 2006 and November 2019. Our control group consisted of 872 vaginally parous women who had visited our unit between July 2017 and November 2019. All patients underwent a standardized interview, clinical examination, uroflowmetry, multichannel urodynamic testing and 3D/4D translabial ultrasound. On imaging, a significant cystocele was defined as a bladder descent to 10mm or more below the symphysis pubis. Volume datasets were retrieved and analyzed offline by the first author, blinded against all clinical data. Statistical analysis was carried out with SAS version 9.4 (Cary, USA).
Results
Of 5266 women seen during the inclusion period, 464 were vaginally nulliparous. Three datasets were excluded because of missing volumes. Out of 872 vaginally parous women, one patient was excluded due to missing volumes. Compared to vaginally parous women, vaginally nulliparous women presented at a younger age, 58 compared to 49 years respectively (p < 0.0001). 104 vaginally nulliparous (22.4%) and 489 vaginally parous women (56.1%) presented with symptoms of prolapse (p < 0.0001). 306 vaginally nulliparous (66.1%) and 648 parous women (74.3%) presented with symptoms of urinary stress incontinence (SUI) (p < 0.002). Mean bladder descent on ultrasound was significantly different between vaginally nulliparous and parous women with 11mm above and 8mm below symphysis pubis, respectively (p < 0.0001). Of 461 vaginally nulliparous women, 43 (9.3%) had a significant cystocele on ultrasound, with 23 (53.5%) being of Green type II and 20 (46.5%) Green type III. Out of 871 vaginally parous women, 418 (48.0%) had a significant cystocele on ultrasound, of whom 145 (34.7%) were Green type II and 273 (65.3%) Green type III cystocele (p < 0.0001). This significant difference was confirmed after excluding women with previous anterior repair and/or incontinence surgery.
Interpretation of results
Cystoceles were much more prevalent in vaginally parous women, but they do also occur in nulliparae. There are two distinct types of cystocele, classified on the basis of retrovesical angle (RVA) and the degree of urethral rotation (1). Cystourethrocele or Green type II cystocele has in the past been considered to be due to a lateral fascial defect, while Green type III cystocele was thought to be due to a central fascial defect. However, sonographic studies have not provided any support for this thesis. On the contrary, it has been demonstrated that Green type III cystocele is associated with avulsion injury of the levator ani muscle and hence more likely to be caused by birth-related trauma (2, 3). In vaginally nulliparous women, a Green type II cystocele was more prevalent while Green type III cystocele was more common in women who had given birth vaginally (p < 0.015). On testing for multiple confounders (age, BMI, asthma, smoking, heavy lifting and familial history of prolapse) on multivariate analysis, the difference in proportions of cystocele Green type II and III in vaginally nulliparous versus parous women remained significant (p < 0.0001).
Concluding message
Nulliparity was associated with a higher proportion of Green type II cystoceles. Green type III cystocele was more common in vaginally parous women. This suggest that Green type III cystocele may be more likely to be due to birth-related trauma to pelvic floor structures.
Figure 1 The distinction between Type II (A) and Type III (B) cystocele as seen on translabial ultrasound in the midsagittal plane. The left image in both panels is at rest, the right image is at maximal Valsalva.
References
  1. Green, T.H., Jr., Urinary stress incontinence: differential diagnosis, pathophysiology, and management. Am J Obstet Gynecol, 1975. 122(3): p. 368-400.
  2. Eisenberg, V.H., et al., Does levator ani injury affect cystocele type? Ultrasound Obstet Gynecol, 2010. 36(5): p. 618-23.
  3. Chantarasorn, V. and H.P. Dietz, Diagnosis of cystocele type by clinical examination and pelvic floor ultrasound. Ultrasound Obstet Gynecol, 2012. 39(6): p. 710-4.
Disclosures
Funding HP Dietz has received lecture honoraria and travel assistance from GE Medical. The other authors have no conflicts of interest to declare. Clinical Trial No Subjects Human Ethics Committee Nepean Blue Mountains Local Health District Human Research Ethics Helsinki Yes Informed Consent No
30/04/2024 03:29:24