CC BY 4.0 · Rev Bras Ginecol Obstet 2021; 43(01): 046-053
DOI: 10.1055/s-0040-1718441
Original Article
Surgery

Mid- to Long-Term Magnetic Resonance Imaging Results of Two Prolapse Surgeries for Apical Defect: A Secondary Analysis of a Randomized Controlled Trial

Resultados de ressonância magnética de médio a longo prazos de duas cirurgias de prolapso por defeito apical: Uma análise secundária de um ensaio clínico randomizado
1   Department of Obstetrics and Gynecology, Pelvic Floor Dysfunction Division, Faculdade de Ciências Médicas, Universidade Estadual de Campinas, Campinas, SP, Brazil
,
1   Department of Obstetrics and Gynecology, Pelvic Floor Dysfunction Division, Faculdade de Ciências Médicas, Universidade Estadual de Campinas, Campinas, SP, Brazil
,
1   Department of Obstetrics and Gynecology, Pelvic Floor Dysfunction Division, Faculdade de Ciências Médicas, Universidade Estadual de Campinas, Campinas, SP, Brazil
,
1   Department of Obstetrics and Gynecology, Pelvic Floor Dysfunction Division, Faculdade de Ciências Médicas, Universidade Estadual de Campinas, Campinas, SP, Brazil
,
1   Department of Obstetrics and Gynecology, Pelvic Floor Dysfunction Division, Faculdade de Ciências Médicas, Universidade Estadual de Campinas, Campinas, SP, Brazil
› Institutsangaben
 

Abstract

Objective Magnetic resonance imaging (MRI) has been considered another tool for use during the pre- and postoperative periods of the management of pelvic-organ prolapse (POP). However, there is little consensus regarding its practical use for POP and the association between MRI lines of reference and physical examination. We aimed to evaluate the mid- to long-term results of two surgical techniques for apical prolapse.

Methods In total, 40 women with apical POP randomized from 2014 to 2016 underwent abdominal sacrocolpopexy (ASC group; n = 20) or bilateral vaginal sacrospinous fixation with an anterior mesh (VSF-AM group; n = 20). A physical examination using the POP Quantification System (POP-Q) for staging (objective cure) and the International Consultation on Incontinence Questionnaire-Vaginal Symptoms (ICIQ-VS: subjective cure), were applied and analyzed before and one year after surgery respectively. All MRI variables (pubococcigeous line [PCL], bladder base [BB], anorectal junction [ARJ], and the estimated levator ani subtended volume [eLASV]) were investigated one year after surgery. Significance was established at p < 0.05.

Results After a mean 27-month follow-up, according to the MRI criteria, 60% of the women were cured in the VSF-AM group versus 45% in ASC group (p = 0.52). The POP-Q and objective cure rates by MRI were correlated in the anterior vaginal wall (p = 0.007), but no correlation was found with the subjective cure. The eLASV was larger among the patients with surgical failure, and a cutoff of ≥ 33.5 mm3 was associated with postoperative failure (area under the receiver operating characteristic curve [ROC]: 0.813; p = 0.002).

Conclusion Both surgeries for prolapse were similar regarding the objective variables (POP-Q measurements and MRI cure rates). Larger eLASV areas were associated with surgical failure.


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Resumo

Objetivo A ressonância magnética (RM) tem sido considerada uma outra ferramenta para uso pré e pós-operatório em casos de prolapso de órgãos pélvicos. Contudo, pouco consenso existe sobre a sua prática para prolapso e a associação entre as linhas de referência da RM e o exame físico. Nós objetivamos avaliar resultados de médio a longo prazo de duas técnicas cirúrgicas para prolapso apical.

Métodos Um total de 40 mulheres com prolapso apical foram submetidas entre 2014 a 2016 a sacrocolpopexia abdominal (grupo SCA; n = 20) ou fixação bilateral vaginal no ligamento sacroespinhoso com tela anterior (grupo FVLS-TA; n = 20). Os exames físicos com estadiamento usando o Pelvic Organ Prolapse Quantification System (POP-Q: cura objetiva), e o International Consultation on Incontinence Questionnaire-Vaginal Symptoms (ICIQ-VS: cura subjetiva) foram analisados antes e depois de um ano da cirurgia, respectivamente. O exame de RM (linha pubococcígea [LPC], base vesical [BV], junção anorretal [JAR] e o volume subtendido estimado do levantador do ânus [VSELA]) foi realizado um ano antes da cirurgia. Estabeleceu-se o nível de significância em 5%.

Resultados Depois de uma média de 27 meses de seguimento, de acordo com a RM, 60% das mulheres foram curadas no grupo FVLS-TA versus 45% no grupo SCA (p = 0.52). As curas objetivas associadas ao POP-Q e à RM foram correlacionadas na parede vaginal anterior (p = 0.007), mas nenhuma correlação foi encontrada com a cura subjetiva. O VSELA foi maior entre as pacientes com fracasso da cirurgia, e um ponto de corte de ≥ 33.5 mm3 esteve associado ao fracasso da cirurgia (area sob a curva característica de operação do receptor [COR]: 0.813; p = 0.002).

Conclusão Ambas as cirurgias para o prolapso foram similares nas curas objetivas tanto pelo POP-Q quanto pela RM. Áreas maiores de VSELA estiveram associadas com o fracasso das cirurgias.


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Introduction

Pelvic organ prolapse (POP) is a major health issue worldwide, and treatment is often surgical. However, reoperation rates may vary from 5% to 40%; up to 30% of the patients undergo more than 1 surgery throughout their lives.[1] The symptoms of POP are not always associated with physical examination findings, and the role of magnetic resonance imaging (MRI) in cases of POP has been investigated in recent years.[2] [3] [4]

Many lines of reference and different protocols are used for the evaluation, and the most frequently used is the pubococcygeal line (PCL).[5] This line appears to have the best interobserver correlation and accordance with POP quantification systems (such as the Pelvic Organ Prolapse Quantification System, POP-Q), especially in the vaginal anterior wall.[4] In 2017, the European Society of Urogenital Radiology (ESUR) and the European Society of Gastrointestinal and Abdominal Radiology (ESGAR) released a joint recommendation guideline for MRI in POP, also recommending the PCL as the line of reference.[6]

The role of the levator ani muscle (LAM) complex in pelvic support has been thoroughly described in the literature, as LAM alterations occur in women with POP, and are described on both ultrasound and MRI.[7] Rodrigues Junior et al.[8] have recently described the estimated levator ani subtended volume (eLASV) through MRI, and have showed significant posterior enlargement in patients with surgical failure following reconstructive prolapse surgery.[8] [9]

Apical defects (uterine prolapse, vault prolapse) are usually corrected by abdominal sacrocolpopexy (ASC) or vaginal sacrospinous fixation (VSF). In a previous study (Juliato et al.[10]), our group showed that using an anterior mesh (VSF-AM) in the anterior compartment, the vaginal axis is deviated in both surgeries, however with no difference between them.[10] Nonetheless, we still have little data about the behavior of the MRI lines of reference for patients operated for POP and their association with physical examination findings and subjective cure using standardized questionnaires. Thus, we aimed to study these postoperative findings. Moreover, a receiver operating characteristic (ROC) curve was built for eLASV to look for a cutoff point as a failure of the surgical treatment.


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Methods

Study Design

A secondary analysis of a prospective, randomized, single-blinded, two-arm, parallel study was performed from 2016 to 2017 in the Pelvic Floor Dysfunction Division, Department of Obstetrics and Gynecology, Faculdade de Ciências Médicas, Universidade Estadual de Campinas (FCM/UNICAMP). The present study was approved by the institutional Review Board (CAAE 64652217.0.0000.5404), and this trial was registered at the Clinical Trials Registry (http://www.ensaiosclinicos.gov.br, code RBR-7t6rg2). The present study followed the Consolidated Standards of Reporting Trials (CONSORT) guidelines.


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Inclusion Criteria

The randomized controlled trial (RCT) included postmenopausal women aged 55 to 75 years with advanced POP (stage 3 or 4 according to the POP-Q) with no current hormone replacement therapy, and no previous gynecological surgery or malignancy.[11] These women were randomized by a computer-generated sequence. The attending physicians in the postoperative period were blinded to the surgery performed. All surgeries were performed from 2014 to 2016 in the Women's Hospital at UNICAMP, and all women were revaluated at least one year postoperatively.


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Exclusion Criteria

The exclusion criteria were the use of metallic implants (intrauterine devices, cardiac valves or stents, aneurism clips, orthopedic implants, or piercings), use of electronic implants (cardiac pacemakers, cochlear implants), claustrophobia, or recent tattoos.


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Interventions

The women were randomized into two groups ([Fig. 1]). The first group underwent surgery with hysterectomy and bilateral vaginal sacrospinous fixation with an anterior mesh (VSF-AM group). To correct the anterior vaginal wall, a polyvinylidene fluoride mesh (DynaMesh, FEG Textiltechnik, Aachen, North Rhine-Westphalia, Germany) was used in this group. The second group underwent abdominal supracervical hysterectomy with abdominal sacralcolpopexy (ASC group). Details of both intervention arms were published elsewhere.[11] If the patients presented concomitant stress urinary incontinence, they did not receive treatment for incontinence.

Zoom Image
Fig. 1 Flowchart depicting the recruitment process of the patients.

After at least one year of follow-up, the women underwent a physical examination performed by only one trained urogynecologist with at least five years of experience with the POP-Q who was blinded to the surgery performed.[12] During this visit, all women were instructed to answer a questionnaire regarding vaginal symptoms (International Consultation on Incontinence Questionnaire-Vaginal Symptoms, ICIQ-VS).[13] The MRI was scheduled no more than two weeks after the physical examination.


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MRI Protocol

Thei MRI was performed postoperatively. The women were instructed to empty their bladder within 2 hours before the MRI, and were taught the Valsalva maneuver for at least 20 seconds by a senior urogynecologist. Images were acquired in the supine position at rest and at maximum Valsalva using a 1.5-Tesla Philips Achieva Scanner v3.2 (Philips Medical Systems, Best, The Netherlands) with a 4-channel phased-array coil. At rest, T1-weighted sequences were obtained in the sagittal, coronal, and axial planes for the estimation of the pelvic anatomical structure and image planning. After vaginal introduction of 30 mL of ultrasound gel for better evaluation of the contours, T2-weighted single-shot fast spin-echo dynamic rest and Valsalva images were obtained through the midsagittal and parasagittal pelvic planes using the following parameters: repetition time, 1,300 milliseconds; echo time, 60 milliseconds; slice thickness, 6 mm; field of view, 36 cm; matrix size, 256 × 160. The description of this technique did not include one step of the ESUR/ESGAR guidelines with regard to the use of ultrasound gel in the rectal canal; we have had limitations regarding the use of this material in the steps to analyze rectal function (rest, straining, squeezing and evacuation). The images were interpreted with the aid of the MicroDicom software (Medical Imaging & Technology Alliance, Arlington, VA, US), using the PCL as references.[6] All images were analyzed independently by two professionals: a radiologist (SSD) with 18 years of experience in pelvic floor imaging, and a urogynecologist (LCSJ) with 5 years of experience in pelvic imaging. Both physicians were blinded to the surgery performed in each patient.


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Outcomes

The primary endpoint was the postoperative mid- and long-term MRI findings for both surgical techniques. The anatomical MRI references followed the ESUR/ESGAR recommendations ([Fig. 2]).[6]

Zoom Image
Fig. 2 MRI in sagittal view depicting anatomical points and lines of reference (static and dynamic). Upper left (static); abbreviations: ARJ, anorectal junction; BB, bladder base; PCL, pubococcygeal line; VV, vaginal vault. Upper right (dynamic): rectocele pouch measure. Bottom left (static); red: H-line; light blue: M-line; yellow: pubococcygeal line. Bottom right (static); abbreviations: PCL, pubococcygeal line; PICS, pelvic inclination correction system line; SCIPP, sacrococcygeal inferior pubic point line.

The staging of the POP followed the ESUR/ESGAR recommendations. Regarding the PCL, the “rule of three” was used for the anterior and apical walls, and the POP was considered pathological starting at grade 2.[14] The anorectal junction (ARJ) has a different staging system; an ARJ descent > 5 cm is defined as grade II.[15] Measurement of the rectocele followed the “rule of two,” with grade II (> 4 cm) considered pathological.[7] [16]

Failure of the MRI was defined as bladder base stage ≥ 2, vaginal vault stage ≥ 2, or rectocele pouch stage ≥ 2.[6] Objective failure was defined as any point of prolapse beyond the hymen in the POP-Q (Points Ba [point B in the anterior vaginal wall, in centimeters]; Bp [point B in the posterior wall, in centimeters]; or C [point C in the apical wall] > 0).[17] Subjective cure was considered when ICIQ-VS questions 5a and 6a were equal to zero.

The H line (anteroposterior width of the levator hiatus), M-line (represent distance of its descent) and the width of the levator hiatus were also measured in millimeters in static MRI to calculate the eLASV: eLASV in mm3 = −72.838 + 0.598 (H-line) + 1.217 (M-line) + 1.136 (width of levator hiatus).[9]

The variables of the physical examination were basically defined by POP-Q measurements.[12] Sociodemographic characteristics were also recorded.


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Statistical Analysis

Objective measures, subjective measures, and cure rates are expressed as means or percentages, and the groups were compared using the Chi-squared test and the Fisher exact test. The Fisher exact test was used to compare the objective cure rate by physical examination, subjective cure rate, and MRI-based cure. The MRI and POP-Q were compared using the PCL as a line of reference. We also calculated the eLASV for each patient and compared it with surgical failure. A ROC curve was calculated to look for a cut-off point so that the eLASV could predict worse surgical outcomes. Correlations between the different methods (MRI versus POP-Q) were calculated using the Spearman correlation index. Values of p < 0.05 were considered statistically significant. The data were analyzed using the Statistical Analysis System (SAS, SAS Institute, Cary, NC, US) software for Windows, version 9.2.


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Results

MRI and Physical Examination Results

[Fig. 1] shows the flowchart of the studied patients, and [Table 1] displays their sociodemographic characteristics. Out of 71 women from the original RCT who were screened for the present study, 12 could not be reached (lost to follow-up), and another 19 patients dropped out because of: refusal to participate (n = 3), moved to other states (n = 3), health restrictions (n = 2), MRI restrictions (cardiac pacemaker; n = 1), and absence from 2 scheduled MRI examinations (n = 10) ([Fig. 1]). The final sample comprised 40 women. The mean follow-up was of 27 months. [Table 1] shows the baseline characteristics and both groups are similar, except for a higher mean age of menopause for the ASC group (p = 0.009).

Table 1

Sample demographics and preoperative status

Variables

ASC (n = 20)

VSF-AM (n = 20)

p-value

Age (years) – mean (±SD)

67.9 (4.9)

67.1 (4.82)

0.75

 < 60 years

1

2

 60–69 years

12

10

 > 70 years

7

8

Pregnancies – mean (±SD)

4.85 (3.7)

5.4 (3)

0.28

Vaginal delivery – mean (±SD)

4.15 (3.39)

4.35 (3.08)

0.74

Body mass index (kg/m2) – mean (±SD)

27.06 (3.72)

25.79 (4.84)

0.26

Tobacco use (current or previous)

3

4

0.66

Menopause (years of age) – mean (±SD)

51.85 (3.67)

48.4 (4.25)

0.009

Preoperative POP-Q

Anterior

1.0

stages → 2

1

0

 3

10

10

 4

9

10

Apical

0.75

stages → 3

11

10

4

9

10

Posterior

0.79

stages → 0

1

2

 1

31

2

 2

6

3

 3

3

3

 4

9

10

GH – mean, in centimeters (±SD)

3.5 (1.08)

3.37 (1.72)

0.06

PB – mean, in centimeters (±SD)

2.15 (0.72)

2.05 (0.77)

0.77

Abbreviations: ASC, abdominal sacrocolpopexy; GH, genital hiatus; PB, perineal body; POP, Pelvic Organ Prolapse; POP-Q, Pelvic Organ Prolapse Quantification System; SD, standard deviation; VSF-AM, vaginal sacrospinous fixation with an anterior mesh.


Regarding the MRI results, the mean kappa coefficient between the two professionals presented good reliability (0.7). The measurements of the vaginal vault were larger for the VSF-AM group than for the ASC group (−0.08 ± 1.84 cm versus −1.43 ± 1.07 cm respectively; p = 0.007). The mean rectocele pouch was significantly larger in the ASC than in the VSF-AM group (3.91 ± 0.98 cm versus 3.38 ± 0.66 cm respectively; p = 0.033). The MRI staging showed no significant difference between the groups with regard to the anterior wall (p = 0.73), the apical segment (p = 1.0), or the posterior wall (ARJ) (p = 1.0); however, the rectocele staging revealed significantly more stage-2 diagnoses in the ASC group (p = 0.013) ([Table 2]).

Table 2

MRI and POP-Q measurements of the operated patients

Variables

VSF-M (n = 20)

ASC (n = 20)

p-value

Objective cure

13

15

0.49

Subjective cure

17

17

1.0

MRI measures

Bladder base – mean (±SD)

1.6 (1.8)

1.1 (1.6)

0.51

Vaginal vault – mean (±SD)

-0.08 (1.8)

-1.4 (1.0)

0.007

Anorectal junction – mean (±SD)

2.4 (0.9)

2.5 (1.0)

0.93

Rectocele – mean (±SD)

3.3 (0.6)

3.9 (0.9)

0.033

Bladder base MRI stage

 Stages 0 and 1

13

14

0.73

 Stage ≥2

7

6

0.73

Vaginal vault MRI stage

 Stages 0 and 1

16

17

1.0

 Stage ≥2

4

3

1.0

Anorectal junction MRI stage

 Stage 0

14

14

1.0

 Stage 1 or 2

6

6

1.0

Rectocele MRI stage

 Stage 0 or 1

18

11

 Stage 2

2

9

0.0013

MRI cure

12

9

0.52

Apical POP-Q

 stage 0

12

14

0.74

 stage 1

7

6

 stage 2

1

0

Anterior (bladder)

 stage 0

7

8

0.27

 stage 1

2

2

 stage 2

7

10

 stage 3

4

0

Posterior (rectal)

 stage 0

19

11

0.013

 stage 1

0

4

 stage 2

1

4

 stage 3

0

1

Abbreviations: ASC, abdominal sacrocolpopexy; MRI, Magnetic resonance imaging; POP-Q, pelvic organ prolapse quantification; SD, standard deviation; VSF-AM, vaginal sacrospinous fixation with an anterior mesh.


When the physical examination using the POP-Q was performed, more patients in the ASC group had stage 2 and 3 posterior prolapses than those in the VSF-AM group (5 versus 1 respectively; p = 0.013). The rate of objective cure was of 65% (n = 13) and 75% (n = 15) in the VSF-AM and ASC groups respectively (p = 0.49) ([Table 2]). The rate of subjective cure did not present any difference between the groups; in total 85% of the women were cured according the ICIQ-VS (p = 1.0) ([Table 2]).


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MRI versus Physical Examination – POP-Q

When comparing failure rates between both methods (MRI and physical examination), there was a significant correlation with anterior wall failure: 13 patients had MRI-based failures, and 11 had POP-Q failures (p = 0.002) and general failures (p = 0.007). The MRI detected more apical failures than physical examination (7 versus 0). In the posterior segment, there were only 2 POP-Q failures versus 12 MRI-based failures with regard to the ARJ (p = 0.08), and 11 failures after rectocele pouch MRI-staging (p = 0.47). Using subjective failure as a reference, we found no association between the POP-Q findings and the rate of subjective cure (p = 0.55); we have also found no association between POP-Q measurements and MRI-based cure in general (p = 0.6), in the anterior wall (bladder base; p = 1.0), in the apical wall (vaginal vault; p = 1.0), or in the posterior wall (rectocele; p = 0.12) ([Table 3]).

Table 3

Comparison among MRI, physical examination (POP-Q) and subjective cure rates

Vaginal wall - n (%)

MRI failure

POP-Q Failure

p-value

Subjective failure

p-value

General

19 (47.5)

12 (30)

0.007[a]

6 (15)

0.6[e]

0.055[f]

Anterior

13 (32.5)

11 (27.5)

0.02[b]

6 (15)

0.31[g]

1.0[h]

Apical

7 (17.5)

0

[*]

6 (15)

[*]

Posterior

ARJ

12 (30)

2 (5)

0.08[c]

6 (15)

0.6[i]

Rectocele

11 (2.5)

2 (5)

0.47[d]

0.12[j]

Abbreviations: ARJ, anorectal junction; MRI, magnetic resonance imaging; POP-Q, Pelvic Organ Prolapse Quantification System.


Notes:


a MRI general failure versus POP-Q general failure (Fisher exact test).


b Bladder base to PCL in the MRI (grade ≥ 2) versus POP-Q Ba > 0 (Fisher exact test).


c Anorectal junction to PCL in the MRI (grade ≥ 1) versus POP-Q Bp > 0.


d Rectocele measure in the MRI (grade ≥ 2) versus POP-Q Bp > 0.


e Subjective cure in the ICIQ-VS versus general MRI cure.


f Subjective cure in the ICIQ-VS versus POP-Q general failure.


g Subjective cure in the ICIQ-VS versus POP-Q Ba > 0 (grade ≥ 2).


h Subjective cure in the ICIQ-VS versus BB to PCL in the MRI.


i Subjective cure in the ICIQ-VS versus ARJ to PCL in the MRI (grade ≥ 1).


j Subjective cure in the ICIQ-VS versus rectocele pouch stage in the MRI (grade ≥ 2).


* Vaginal vault to PCL in the MRI (stage ≥ 2) versus POP-Q C > 0 and subjective cure (ICIQ-VS questions 5a and 6a equal to zero) – homogenous sample, no test was made.


Abbreviations: ARJ, anorectal juntion; Ba, point B in the anterior vaginal wall, in centimeters;BB, bladder base; Bp, point B in the posterior wall, in centimeters; C, point C in the apical wall, in centimeters; ICIQ-VS, international consultation on incontinence questionnaire - vaginal symptoms; MRI, Magnetic resonance imaging; PCL, pubococcygeal line; POP-Q, pelvic organ prolapse quantification.



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Levator Ani Subtended Volume (LASV)

The width of the levator hiatus and the length of the H- and M-lines were measured in static MRI for eLASV calculation, and the numbers were compared by dividing the sample according to POP-Q success. The H- and M-lines were significantly longer among the patients who presented POP-Q failure than among those who achieved objective success (69.6 ± 5.6 mm versus 62.2 ± 7.8 mm respectively; p = 0.004; and 23.5 ± 7.8 mm versus 16.7 ± 6.9 mm respectively; p = 0.004). The width of the levator hiatus was similar: 38.5 ± 8.1 mm for the patients with failure versus 34.6 ± 5.5 mm for those with success (p = 0.08).

The eLASV was calculated for each patient, and it was larger among those with failure than among those with success (41.1 ± 16.5 mm3 versus 24.1 ± 13.6 mm3 respectively; p = 0.002). The area under the ROC curve was of 0.813 (p = 0.002; confidence interval [CI] = 0.672–0.953), and the optimal cutoff was of 33.5 mm3, with specificity of 89.2% (70.6% to 97.1%), sensitivity of 66.6% (35.4% to 88.7%), and accuracy of 83.5% (66.4% to 92.1%). Among the patients who experienced surgical failure, 66.6% had an eLASV of ≥ 33.5 mm3 versus 10.7% among those who experienced surgical success (p < 0.001) ([Fig. 3]).

Zoom Image
Fig. 3 eLASV measurement (ROC curve). Area under the curve: 0.813; p = 0.002; 95%CI: 0.672–0.953; cutoff point: eLASV ≥ 33.5 mm3.

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Discussion

The present study showed good results for both vaginal and abdominal surgeries, especially regarding subjective outcomes at the mean 27-month follow-up. The MRI staging showed greater failures compared with the POP-Q, and neither correlated well with the symptomatology.

In their nonrandomized study, Ginath et al.[18] compared two surgical approaches (ASC versus Prolift vaginal mesh) and showed equally good postoperative results for both techniques in the POP-Q, but not in the MRI, which revealed no difference between the preoperative and postoperative anatomical positions and angles relative to the PCL. Van der Weiden et al.[19] evaluated 43 women at 6 months after laparoscopic ASC, and found great improvement in prolapse measures for all compartments, but only for the apex in the MRI assessment, resulting in a poor correlation with the POP-Q.[19] Conversely, Brocker et al.[20] studied 69 patients who underwent vaginal mesh repair for POP; during the one-year follow-up, both the dynamic MRI and the clinical examination showed good results, but the MRI showed more prolapse.

The correlation between the POP-Q and the symptoms is frequently poor because the symptoms do not necessarily correlate with the severity of the POP.[21] The MRI assessment seems to be even more dissociated from the symptomatology – MRI scans often describe a great number of prolapses in asymptomatic women.[22] We also found no significant correlation between subjective cure or quality of life questionnaire scores and MRI-based prolapse staging and failure definitions.

Several studies[4] [23] have compared physical examination findings with different lines of reference and points of anatomical interest in the MRI, mainly with poor results. The anterior wall seems to show good accordance.[2] Our results were also better for the anterior compartment in terms of a significant association between MRI-based pathological POP and a Ba point > 0 in the POP-Q. We found a rate of 70% of objective cure, a rate of 85% of subjective cure, and a rate of 52.5% of MRI-based cure for the whole sample, without a significant association among symptomatology, POP-Q, and MRI. The MRI staging system showed a greater number of pathological prolapses than the POP-Q and the symptoms in our sample.

The MRI has become an important asset in the evaluation of pelvic-floor dysfunction.[24] The most commonly used line of reference, the PCL, is also the one with the greatest interobserver correlation indexes.[7] This line unites the pubic bone and coccyx, but precise definitions vary among studies. We used the PCL as described by El Sayed et al.[6] in 2017,; that is, a line from the inferior tip of the pubic bone to the anterior aspect of the last visible coccygeal joint.

Another important contribution of the MRI is the proper evaluation of the eLASV and its role in pelvic support. We intended to do a study similar to the research by Wyman et al.[9]; they found a cutoff in the eLASV that correlated with surgical failure: they retrospectively analyzed a cohort of 66 women who underwent laparoscopic uterosacral ligament suspension, and found a significant association between the eLASV and surgical failure at the one-year follow-up, with a cutoff value of 38.5 mm3. In our study, an eLASV ≥ 33.5 mm3 was associated with surgical failure, with good accuracy. However, as this parameter was analyzed postoperatively, we cannot say that this would be a predictor of surgical failure, but as a diagnosis and/or audit of the surgery performed. Our sample might have comprised women with worse preoperative prolapses, and a smaller eLASV could be associated with failure, given that other important factors such as age or parity also play important roles in surgical outcomes. Apart from that, we evaluated a different surgical modality.

Our study has many strengths. We studied a homogeneous group of women without previous surgical treatment who were randomized according to two surgical POP correction techniques for a mean follow-up  > 2 years. We have followed the latest recommendations regarding MRIs for prolapse. Our limitations are: we did not use rectal gel or perform MRI defecography, and this might have impaired our evaluation of the posterior wall. Additionally, almost all operations were performed for advanced cases of prolapse, which affected the preoperative MRI examinations of these patients for purposes of comparison. The assessment of the eLASV by postoperative MRI could have produced some bias, and the fact that the ARJ was not adequately visualized may have impaired the measurement of the H-line; this can alter the eLASV assessment as well. However, we do not believe that our surgical techniques directly affected the measurements used for this calculation (that is, the length of the H- and M-lines and the width of the levator hiatus). Finally, we included a limited number of patients, and further studies with larger samples are necessary.


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Conclusion

The MRI and POP-Q cure rates were associated, but only in the anterior wall. The MRI staging showed greater failures compared with the POP-Q, and neither correlated well with the symptomatology. Both surgical techniques for advanced prolapse were similar in terms of the objective POP-Q and MRI cure rates. The objective results were poorer in the posterior compartment in the ASC group. The eLASV was larger among the patients whho experienced surgical failure, and when this value was ≥ 33.5 mm3, there was a significant increase in the chance of postoperative failure, but with the limitation that it was only analyzed postoperatively.


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Conflict of Interests

The authors have no conflict of onterests to declare.

Acknowledgments

The present study was supported by Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) under number 2016/24065–2. We would like to thank Helymar da Costa Machado, the statistician who performed all of the statistical analysis for the present study.

Contributions

All authors of the present study made substantial contributions to conception and design, data collection or analysis, and interpretation of data; participated in the writing of the article or critical review of the intellectual content, and provided final approval of the version to be published.


  • References

  • 1 Nygaard I, Barber MD, Burgio KL, Kenton K, Meikle S, Schaffer J. et al; Pelvic Floor Disorders Network. Prevalence of symptomatic pelvic floor disorders in US women. JAMA 2008; 300 (11) 1311-1316
  • 2 Gousse AE, Barbaric ZL, Safir MH, Madjar S, Marumoto AK, Raz S. Dynamic half Fourier acquisition, single shot turbo spin-echo magnetic resonance imaging for evaluating the female pelvis. J Urol 2000; 164 (05) 1606-1613
  • 3 Comiter CV, Vasavada SP, Barbaric ZL, Gousse AE, Raz S. Grading pelvic prolapse and pelvic floor relaxation using dynamic magnetic resonance imaging. Urology 1999; 54 (03) 454-457
  • 4 Pizzoferrato AC, Nyangoh Timoh K, Fritel X, Zareski E, Bader G, Fauconnier A. Dynamic Magnetic Resonance Imaging and pelvic floor disorders: how and when?. Eur J Obstet Gynecol Reprod Biol 2014; 181: 259-266
  • 5 Yang A, Mostwin JL, Rosenshein NB, Zerhouni EA. Pelvic floor descent in women: dynamic evaluation with fast MR imaging and cinematic display. Radiology 1991; 179 (01) 25-33
  • 6 El Sayed RF, Alt CD, Maccioni F, Meissnitzer M, Masselli G, Manganaro L. et al; ESUR and ESGAR Pelvic Floor Working Group. Magnetic resonance imaging of pelvic floor dysfunction - joint recommendations of the ESUR and ESGAR Pelvic Floor Working Group. Eur Radiol 2017; 27 (05) 2067-2085
  • 7 DeLancey JO, Morgan DM, Fenner DE, Kearney R, Guire K, Miller JM. et al. Comparison of levator ani muscle defects and function in women with and without pelvic organ prolapse. Obstet Gynecol 2007; 109 (2 Pt 1): 295-302
  • 8 Rodrigues Junior AA, Herrera-Hernadez MC, Bassalydo R, McCullough M, Terwilliger HL, Downes K, Hoyte L. et al. Estimates of the levator ani subtended volume based on magnetic resonance linear measurements. Neurourol Urodyn 2016; 35 (02) 199-205
  • 9 Wyman AM, Rodrigues Jr AA, Hahn L, Greene KA, Bassaly R, Hart S. et al. Estimated levator ani subtended volume: a novel assay for predicting surgical failure after uterosacral ligament suspension. Am J Obstet Gynecol 2016; 214 (05) 611.e1-611.e6
  • 10 Juliato CRT, Santos-Junior LC, de Castro EB, Dertkigil SS, Brito LGO. Vaginal axis after abdominal sacrocolpopexy versus vaginal sacrospinous fixation-a randomized trial. Neurourol Urodyn 2019; 38 (04) 1142-1151
  • 11 de Castro EB, Brito LGO, Juliato CRT. Vaginal hysterectomy with bilateral sacrospinous fixation plus an anterior mesh versus abdominal sacrocervicopexy for the treatment of primary apical prolapse in postmenopausal women: a randomized controlled study. Int Urogynecol J Pelvic Floor Dysfunct 2020; 31 (02) 365-372
  • 12 Bump RC, Mattiasson A, Bø K, Brubaker LP, DeLancey JO, Klarsko P. et al. The standardization of terminology of female pelvic organ prolapse and pelvic floor dysfunction. Am J Obstet Gynecol 1996; 175 (01) 10-17
  • 13 Tamanini JT, Almeida FG, Girotti ME, Riccetto CL, Palma PC, Rios LA. The Portuguese validation of the International Consultation on Incontinence Questionnaire-Vaginal Symptoms (ICIQ-VS) for Brazilian women with pelvic organ prolapse. Int Urogynecol J Pelvic Floor Dysfunct 2008; 19 (10) 1385-1391
  • 14 Woodfield CA, Hampton BS, Sung V, Brody JM. Magnetic resonance imaging of pelvic organ prolapse: comparing pubococcygeal and midpubic lines with clinical staging. Int Urogynecol J Pelvic Floor Dysfunct 2009; 20 (06) 695-701
  • 15 Halligan S, Spence-Jones C, Kamm MA, Bartram CI. Dynamic cystoproctography and physiological testing in women with urinary stress incontinence and urogenital prolapse. Clin Radiol 1996; 51 (11) 785-790
  • 16 Hecht EM, Lee VS, Tanpitukpongse TP, Babb JS, Taouli B, Wong S. et al. MRI of pelvic floor dysfunction: dynamic true fast imaging with steady-state precession versus HASTE. AJR Am J Roentgenol 2008; 191 (02) 352-358
  • 17 Nygaard I, Brubaker L, Zyczynski HM, Cundiff G, Richter H, Gantz M. et al. Long-term outcomes following abdominal sacrocolpopexy for pelvic organ prolapse. JAMA 2013; 309 (19) 2016-2024
  • 18 Ginath S, Garely AD, Luchs JS, Shahryarinejad A, Olivera CK, Zhou S. et al. Magnetic resonance imaging of abdominal versus vaginal prolapse surgery with mesh. Int Urogynecol J Pelvic Floor Dysfunct 2012; 23 (11) 1569-1576
  • 19 van der Weiden RM, Rociu E, Mannaerts GH, van Hooff MH, Vierhout ME, Withagen MI. Dynamic magnetic resonance imaging before and 6 months after laparoscopic sacrocolpopexy. Int Urogynecol J Pelvic Floor Dysfunct 2014; 25 (04) 507-515
  • 20 Brocker KA, Alt CD, Rzepka J, Sohn C, Hallscheidt P. One-year dynamic MRI follow-up after vaginal mesh repair: evaluation of clinical, radiological, and quality-of-life results. Acta Radiol 2015; 56 (08) 1002-1008
  • 21 Ellerkmann RM, Cundiff GW, Melick CF, Nihira MA, Leffler K, Bent AE. Correlation of symptoms with location and severity of pelvic organ prolapse. Am J Obstet Gynecol 2001; 185 (06) 1332-1337 , discussion 1337–1338
  • 22 Cimsit C, Yoldemir T, Akpinar IN. Prevalence of dynamic magnetic resonance imaging-identified pelvic organ prolapse in pre- and postmenopausal women without clinically evident pelvic organ descent. Acta Radiol 2016; 57 (11) 1418-1424
  • 23 Broekhuis SR, Fütterer JJ, Barentsz JO, Vierhout ME, Kluivers KB. A systematic review of clinical studies on dynamic magnetic resonance imaging of pelvic organ prolapse: the use of reference lines and anatomical landmarks. Int Urogynecol J Pelvic Floor Dysfunct 2009; 20 (06) 721-729
  • 24 Attenberger UI, Morelli JN, Budjan J, Herold A, Kienle P, Kleine W. et al. The value of dynamic magnetic resonance imaging in interdisciplinary treatment of pelvic floor dysfunction. Abdom Imaging 2015; 40 (07) 2242-2247

Address for correspondence

Cássia Raquel Teatin Juliato, MD, PhD
Universidade Estadual de Campinas
Rua Alexander Fleming 101, Cidade Universitária Zeferino Vaz, Campinas, SP, 13083-881
Brazil   

Publikationsverlauf

Eingereicht: 14. April 2020

Angenommen: 10. August 2020

Artikel online veröffentlicht:
29. Januar 2021

© 2021. Federação Brasileira de Ginecologia e Obstetrícia. This is an open access article published by Thieme under the terms of the Creative Commons Attribution License, permitting unrestricted use, distribution, and reproduction so long as the original work is properly cited. (https://creativecommons.org/licenses/by/4.0/)

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  • References

  • 1 Nygaard I, Barber MD, Burgio KL, Kenton K, Meikle S, Schaffer J. et al; Pelvic Floor Disorders Network. Prevalence of symptomatic pelvic floor disorders in US women. JAMA 2008; 300 (11) 1311-1316
  • 2 Gousse AE, Barbaric ZL, Safir MH, Madjar S, Marumoto AK, Raz S. Dynamic half Fourier acquisition, single shot turbo spin-echo magnetic resonance imaging for evaluating the female pelvis. J Urol 2000; 164 (05) 1606-1613
  • 3 Comiter CV, Vasavada SP, Barbaric ZL, Gousse AE, Raz S. Grading pelvic prolapse and pelvic floor relaxation using dynamic magnetic resonance imaging. Urology 1999; 54 (03) 454-457
  • 4 Pizzoferrato AC, Nyangoh Timoh K, Fritel X, Zareski E, Bader G, Fauconnier A. Dynamic Magnetic Resonance Imaging and pelvic floor disorders: how and when?. Eur J Obstet Gynecol Reprod Biol 2014; 181: 259-266
  • 5 Yang A, Mostwin JL, Rosenshein NB, Zerhouni EA. Pelvic floor descent in women: dynamic evaluation with fast MR imaging and cinematic display. Radiology 1991; 179 (01) 25-33
  • 6 El Sayed RF, Alt CD, Maccioni F, Meissnitzer M, Masselli G, Manganaro L. et al; ESUR and ESGAR Pelvic Floor Working Group. Magnetic resonance imaging of pelvic floor dysfunction - joint recommendations of the ESUR and ESGAR Pelvic Floor Working Group. Eur Radiol 2017; 27 (05) 2067-2085
  • 7 DeLancey JO, Morgan DM, Fenner DE, Kearney R, Guire K, Miller JM. et al. Comparison of levator ani muscle defects and function in women with and without pelvic organ prolapse. Obstet Gynecol 2007; 109 (2 Pt 1): 295-302
  • 8 Rodrigues Junior AA, Herrera-Hernadez MC, Bassalydo R, McCullough M, Terwilliger HL, Downes K, Hoyte L. et al. Estimates of the levator ani subtended volume based on magnetic resonance linear measurements. Neurourol Urodyn 2016; 35 (02) 199-205
  • 9 Wyman AM, Rodrigues Jr AA, Hahn L, Greene KA, Bassaly R, Hart S. et al. Estimated levator ani subtended volume: a novel assay for predicting surgical failure after uterosacral ligament suspension. Am J Obstet Gynecol 2016; 214 (05) 611.e1-611.e6
  • 10 Juliato CRT, Santos-Junior LC, de Castro EB, Dertkigil SS, Brito LGO. Vaginal axis after abdominal sacrocolpopexy versus vaginal sacrospinous fixation-a randomized trial. Neurourol Urodyn 2019; 38 (04) 1142-1151
  • 11 de Castro EB, Brito LGO, Juliato CRT. Vaginal hysterectomy with bilateral sacrospinous fixation plus an anterior mesh versus abdominal sacrocervicopexy for the treatment of primary apical prolapse in postmenopausal women: a randomized controlled study. Int Urogynecol J Pelvic Floor Dysfunct 2020; 31 (02) 365-372
  • 12 Bump RC, Mattiasson A, Bø K, Brubaker LP, DeLancey JO, Klarsko P. et al. The standardization of terminology of female pelvic organ prolapse and pelvic floor dysfunction. Am J Obstet Gynecol 1996; 175 (01) 10-17
  • 13 Tamanini JT, Almeida FG, Girotti ME, Riccetto CL, Palma PC, Rios LA. The Portuguese validation of the International Consultation on Incontinence Questionnaire-Vaginal Symptoms (ICIQ-VS) for Brazilian women with pelvic organ prolapse. Int Urogynecol J Pelvic Floor Dysfunct 2008; 19 (10) 1385-1391
  • 14 Woodfield CA, Hampton BS, Sung V, Brody JM. Magnetic resonance imaging of pelvic organ prolapse: comparing pubococcygeal and midpubic lines with clinical staging. Int Urogynecol J Pelvic Floor Dysfunct 2009; 20 (06) 695-701
  • 15 Halligan S, Spence-Jones C, Kamm MA, Bartram CI. Dynamic cystoproctography and physiological testing in women with urinary stress incontinence and urogenital prolapse. Clin Radiol 1996; 51 (11) 785-790
  • 16 Hecht EM, Lee VS, Tanpitukpongse TP, Babb JS, Taouli B, Wong S. et al. MRI of pelvic floor dysfunction: dynamic true fast imaging with steady-state precession versus HASTE. AJR Am J Roentgenol 2008; 191 (02) 352-358
  • 17 Nygaard I, Brubaker L, Zyczynski HM, Cundiff G, Richter H, Gantz M. et al. Long-term outcomes following abdominal sacrocolpopexy for pelvic organ prolapse. JAMA 2013; 309 (19) 2016-2024
  • 18 Ginath S, Garely AD, Luchs JS, Shahryarinejad A, Olivera CK, Zhou S. et al. Magnetic resonance imaging of abdominal versus vaginal prolapse surgery with mesh. Int Urogynecol J Pelvic Floor Dysfunct 2012; 23 (11) 1569-1576
  • 19 van der Weiden RM, Rociu E, Mannaerts GH, van Hooff MH, Vierhout ME, Withagen MI. Dynamic magnetic resonance imaging before and 6 months after laparoscopic sacrocolpopexy. Int Urogynecol J Pelvic Floor Dysfunct 2014; 25 (04) 507-515
  • 20 Brocker KA, Alt CD, Rzepka J, Sohn C, Hallscheidt P. One-year dynamic MRI follow-up after vaginal mesh repair: evaluation of clinical, radiological, and quality-of-life results. Acta Radiol 2015; 56 (08) 1002-1008
  • 21 Ellerkmann RM, Cundiff GW, Melick CF, Nihira MA, Leffler K, Bent AE. Correlation of symptoms with location and severity of pelvic organ prolapse. Am J Obstet Gynecol 2001; 185 (06) 1332-1337 , discussion 1337–1338
  • 22 Cimsit C, Yoldemir T, Akpinar IN. Prevalence of dynamic magnetic resonance imaging-identified pelvic organ prolapse in pre- and postmenopausal women without clinically evident pelvic organ descent. Acta Radiol 2016; 57 (11) 1418-1424
  • 23 Broekhuis SR, Fütterer JJ, Barentsz JO, Vierhout ME, Kluivers KB. A systematic review of clinical studies on dynamic magnetic resonance imaging of pelvic organ prolapse: the use of reference lines and anatomical landmarks. Int Urogynecol J Pelvic Floor Dysfunct 2009; 20 (06) 721-729
  • 24 Attenberger UI, Morelli JN, Budjan J, Herold A, Kienle P, Kleine W. et al. The value of dynamic magnetic resonance imaging in interdisciplinary treatment of pelvic floor dysfunction. Abdom Imaging 2015; 40 (07) 2242-2247

Zoom Image
Fig. 1 Flowchart depicting the recruitment process of the patients.
Zoom Image
Fig. 2 MRI in sagittal view depicting anatomical points and lines of reference (static and dynamic). Upper left (static); abbreviations: ARJ, anorectal junction; BB, bladder base; PCL, pubococcygeal line; VV, vaginal vault. Upper right (dynamic): rectocele pouch measure. Bottom left (static); red: H-line; light blue: M-line; yellow: pubococcygeal line. Bottom right (static); abbreviations: PCL, pubococcygeal line; PICS, pelvic inclination correction system line; SCIPP, sacrococcygeal inferior pubic point line.
Zoom Image
Fig. 3 eLASV measurement (ROC curve). Area under the curve: 0.813; p = 0.002; 95%CI: 0.672–0.953; cutoff point: eLASV ≥ 33.5 mm3.