A 3D finite element model of anterior vaginal wall support to evaluate mechanisms underlying cystocele formation.

OBJECTIVES To develop a 3D computer model of the anterior vaginal wall and its supports, validate that model, and then use it to determine the combinations of muscle and connective tissue impairments that result in cystocele formation, as observed on dynamic magnetic resonance imaging (MRI). METHODS A subject-specific 3D model of the anterior vaginal wall and its supports were developed based on MRI geometry from a healthy nulliparous woman. It included simplified representations of the anterior vaginal wall, levator muscle, cardinal and uterosacral ligaments, arcus tendineus fascia pelvis and levator ani, paravaginal attachments, and the posterior compartment. This model was then imported into ABAQUS and tissue properties were assigned from the literature. An iterative process was used to refine anatomical assumptions until convergence was obtained between model behavior under increases of abdominal pressure up to 168 cm H(2)O and deformations observed on dynamic MRI. RESULTS Cystocele size was sensitive to abdominal pressure and impairment of connective tissue and muscle. Larger cystocele formed in the presence of impairments in muscular and apical connective tissue support compared to either support element alone. Apical impairment resulted in a larger cystocele than paravaginal impairment. Levator ani muscle impairment caused a larger urogenital hiatus size, longer length of the distal vagina exposed to a pressure differential, larger apical descent, and resulted in a larger cystocele size. CONCLUSIONS Development of a cystocele requires a levator muscle impairment, an increase in abdominal pressure, and apical and paravaginal support defects.

[1]  A. McTiernan,et al.  Pelvic organ prolapse in the Women's Health Initiative: gravity and gravidity. , 2002, American journal of obstetrics and gynecology.

[2]  A. C. Richardson,et al.  A new look at pelvic relaxation. , 1976, American journal of obstetrics and gynecology.

[3]  J. Ashton-Miller,et al.  Anterior vaginal wall length and degree of anterior compartment prolapse seen on dynamic MRI , 2007, International Urogynecology Journal.

[4]  J R Fielding,et al.  Two- and 3-dimensional MRI comparison of levator ani structure, volume, and integrity in women with stress incontinence and prolapse. , 2001, American journal of obstetrics and gynecology.

[5]  J. Delancey,et al.  A structured system to evaluate urethral support anatomy in magnetic resonance images. , 2001, American journal of obstetrics and gynecology.

[6]  J. Delancey,et al.  Structural support of the urethra as it relates to stress urinary incontinence: the hammock hypothesis. , 1994, American journal of obstetrics and gynecology.

[7]  F. G. Evans,et al.  Strength of biological materials , 1970 .

[8]  B. Hamm,et al.  Static magnetic resonance imaging of the pelvic floor muscle morphology in women with stress urinary incontinence and pelvic prolapse , 1998, Neurourology and urodynamics.

[9]  Marianna Jakab,et al.  Levator ani thickness variations in symptomatic and asymptomatic women using magnetic resonance-based 3-dimensional color mapping. , 2004, American journal of obstetrics and gynecology.

[10]  James A Ashton-Miller,et al.  Comparison of Levator Ani Muscle Defects and Function in Women With and Without Pelvic Organ Prolapse , 2007, Obstetrics and gynecology.

[11]  H. Hussain,et al.  The relationship between anterior and apical compartment support. , 2006, American journal of obstetrics and gynecology.

[12]  J. Ellis,et al.  Magnetic Resonance Imaging of the Levator Ani With Anatomic Correlation , 1996, Obstetrics and gynecology.

[13]  J. Delancey,et al.  A technique to study the passive supports of the uterus. , 1988, Obstetrics and gynecology.

[14]  R. H. J. Brown Strength of Biological Materials. Hiroshi Yamada , 1971 .

[15]  T. Kuehl,et al.  A transvaginal approach to repair of apical and other associated sites of pelvic organ prolapse with uterosacral ligaments. , 2000, American journal of obstetrics and gynecology.

[16]  Marianna Jakab,et al.  Three-dimensional magnetic resonance imaging assessment of levator ani morphologic features in different grades of prolapse. , 2003, American journal of obstetrics and gynecology.

[17]  James A. Ashton-Miller,et al.  Levator Ani Muscle Stretch Induced by Simulated Vaginal Birth , 2004, Obstetrics and gynecology.

[18]  H. Hussain,et al.  Levator plate angle in women with pelvic organ prolapse compared to women with normal support using dynamic MR imaging. , 2006, American journal of obstetrics and gynecology.

[19]  Marianna Jakab,et al.  Racial differences in pelvic morphology among asymptomatic nulliparous women as seen on three-dimensional magnetic resonance images. , 2005, American journal of obstetrics and gynecology.

[20]  J. Delancey Fascial and muscular abnormalities in women with urethral hypermobility and anterior vaginal wall prolapse , 2002 .

[21]  G. Smidt,et al.  The difference in stiffness of the active plantarflexors between young and elderly human females. , 1993, Journal of gerontology.

[22]  J. Delancey Anatomic aspects of vaginal eversion after hysterectomy. , 1992, American journal of obstetrics and gynecology.

[23]  J. Ashton-Miller,et al.  Vaginal Thickness, Cross-Sectional Area, and Perimeter in Women With and Those Without Prolapse , 2005, Obstetrics and gynecology.

[24]  J A Ashton-Miller,et al.  Measurement of the pubic portion of the levator ani muscle in women with unilateral defects in 3‐D models from MR images , 2006, International journal of gynaecology and obstetrics: the official organ of the International Federation of Gynaecology and Obstetrics.