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Presurgical bladder wall thickness is a useful marker to predict the postsurgical improvement of symptoms in patients with pelvic organ prolapse-related overactive bladder.

Otsubo, A ; Matsuo, T ; et al.
In: Lower urinary tract symptoms, Jg. 13 (2021-07-01), Heft 3, S. 347-355
Online academicJournal

Presurgical bladder wall thickness is a useful marker to predict the postsurgical improvement of symptoms in patients with pelvic organ prolapse‐related overactive bladder 

Objectives: Pelvic organ prolapse (POP) is a cause of overactive bladder (OAB), and transvaginal mesh (TVM) surgery can improve the symptoms. Bladder wall thickness (BWT) is a useful and safe marker to evaluate bladder function in urinary disorders. The main purpose of this study is to clarify the relationship between BWT and changes in the OAB symptom score (OABSS) after TVM operation in patients with POP. Methods: BWT was measured by ultrasonography before and 6 months after surgery at three sites in the bladder: the anterior wall, trigone, and dome. Similarly, the OABSS was evaluated at the time of BWT measurement. Changes induced in BWT at each site and the mean BWT at all sites after TVM surgery were analyzed. Similarly, the relationship between presurgical BWT and the decrease in OABSS was investigated. Results: TVM surgery improved OABSS in 30 patients (responders; 73.2%), while 11 patients were judged as nonresponders (26.8%). BWT at the anterior bladder wall and dome as well as the mean BWT at all three sites were significantly decreased by TVM surgery (P <.001). Similar trends were identified in OABSS responders; however, all markers showed no significant changes in OABSS nonresponders. All the BWT‐related markers before surgery were significantly lower in OABSS responders than in OABSS nonresponders. Conclusions: BWT at the bladder anterior wall and dome, but not the trigone, were decreased by TVM surgery. We conclude that presurgical BWT may be a useful marker to predict the improvement in OAB symptoms by TVM surgery in patients with POP‐related OAB.

Keywords: bladder wall thickness; overactive bladder symptom score; pelvic organ prolapse; transvaginal mesh surgery

INTRODUCTION

Overactive bladder (OAB) is defined as urinary urgency, usually with daytime frequency and nocturia, with or without urgency urinary incontinence, in the absence of urinary tract infection or other obvious pathologies.1 Pelvic organ prolapse (POP) is a major health‐care problem that impairs the quality of life in women, and many urologists support the opinion that patients with POP often experience OAB symptoms.2–4 Several reports revealed that transvaginal POP repairs, such as transvaginal mesh (TVM) surgery, are effective treatment tools, and they lead to the disappearance or improvement in OAB symptoms.2,3,5,6

However, only approximately 75% to 79% of patients experience such clinical effects of TVM surgery for OAB symptoms; conversely, >20% of patients experience worsening or no changes in symptoms after TVM surgery.3,4 Therefore, many investigators attempted to define predictive markers for the improvement in urinary conditions, including OAB symptoms, after surgery.2–4,7 Previous studies used the severities of preoperative subjective symptoms, including International Prostate Symptom Score, overactive bladder symptom score (OABSS), and urodynamic examination data, as useful preoperative predictors.2–4,7 However, since the examination exclusively based on subjective symptoms cannot evaluate objective findings, such as detrusor overactivity and bladder outlet obstruction, and urodynamic tests are invasive and carry the risk of urinary tract infections, noninvasive and effective predictors of surgery outcomes are needed.2,8

The measurement of bladder wall thickness (BWT) is supposedly a useful noninvasive parameter to evaluate the lower urinary tract function.9,10 In fact, BWT was significantly correlated with clinical parameters, symptom scores, and uroflowmetry results under obstructive bladder conditions.11,12 In addition to bladder outlet obstruction, BWT in women with OAB was greater than that in women with stress incontinence or normal urinary function.13–17 Thus, BWT has been hypothesized to reflect the bladder activity and urinary symptoms in various urinary disorders. Additionally, in recent years, sonographic parameters, including BWT, were reported to be useful predictors of outcomes in patients with lower urinary tract symptoms treated with an alpha‐1 adrenoceptor antagonist.18 Similarly, BWT is considered a potentially useful parameter for monitoring the response to antimuscarinic treatment in patients with OAB.19,20 However, the predictive value of BWT for OAB symptoms in POP patients treated with TVM has not been studied. Therefore, this study mainly aimed to determine the usefulness of BWT as a predictive marker for the improvement in OAB symptoms after TVM surgery in POP patients.

METHODS

Patients

The study group consisted of 41 women who underwent TVM surgery for POP and who met the diagnostic criteria for OAB using OABSS (urgency ≥2, total score ≥3)21 at Nagasaki University Hospital. Patients who underwent a sling procedure for stress incontinence at the time of the TVM surgery were excluded from the study. In addition, bladder or rectal cancers, urinary tract infection, additional perioperative treatment, including antimuscarinic drugs, or uncontrollable systemic disorder were the major exclusion criteria (Figure 1). We used a soft polypropylene mesh (Gynemesh PS; Ethicon, Somerville, New Jersey, or Polyform; Boston Scientific, Tokyo, Japan), and the surgical technique was similar to that of the French TVM group.22 Patients with anterior vaginal wall prolapse underwent the anterior TVM (A‐TVM) procedure. The A‐TVM procedure starts with anterior colpotomy after local infiltration. Repair of a cystocele required two arms of the transobturator mesh to be passed on both sides to suspend the cystocele. On either side, both arms of the mesh were passed into the paravesical region using a modified Emmet needle. The anterior subvesical strap was inserted into the tendinous arch of the pelvic fascia. Patients with both anterior and posterior vaginal wall prolapse underwent an anterior‐posterior TVM (AP‐TVM) procedure. The posterior subvesical strap was inserted into the tendinous arch 1 cm from the ischial spine using a gently curved needle. In the posterior TVM (P‐TVM) procedure, posterior colpotomy was performed longitudinally, and the mesh was placed under the vaginal wall. On each side, one strap of the mesh was passed into the pararectal space through the sacrospinous ligament and exteriorized via incisions located outside and below the anus. Furthermore, patients without a uterus underwent total TVM (T‐TVM), wherein one piece of a prosthetic mesh, consisting of two connected parts, is inserted into the anterior and posterior walls.22–24 All patients underwent the same surgical procedure using TVM by an expert surgeon (T.M.). Finally, 41 patients treated with TVM (anterior 24, posterior 0, anterior and posterior 12, and total 5) were enrolled in this study. Table 1 shows the baseline characteristics of the patients and the surgical procedures this study. This study was approved by the Nagasaki University Hospital Ethical Committee and was performed in accordance with the principles of the Declaration of Helsinki. All patients provided written informed consent.

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1 TABLEPatients' characteristics at the presurgical stage

EntireOABSS responderOABSS nonresponderP value
Number of patients413011
Age, y68.0 ± 7.369.0 ± 4.769.3 ± 8.1.539
POP‐Q stage (%).545
00 (0)00
10 (0)00
24 (9.8)22
333 (80.5)258
44 (9.8)31
Postmenopausal status39 (95.1)2910.448
Hormone replacement therapy (%)0 (0)0 (0)0 (0)
Parity2.1 ± 0.91.9 ± 0.82.2 ± 0.8.889
Previous surgery (%)
Hysterectomy4 (9.8)3 (10.0)1 (9.1).931
Reconstructive surgery8 (19.5)7 (23.3)1 (9.1).308
Others0 (0)0 (0)0 (0)1.000
Surgical procedure (%).566
Anterior24 (58.5)19 (63.3)5 (45.5)
Posterior0 (0)0 (0)0 (0)
Anterior and posterior12 (29.3)8 (26.7)4 (36.4)
Total5 (12.2)3 (10.0)2 (13.6)
OABSS
Q1 Daytime frequency0.9 ± 0.71.1 ± 0.60.6 ± 0.7.048
Q2 Nighttime frequency1.3 ± 0.81.3 ± 0.81.3 ± 0.9.915
Q3 Urgency2.0 ± 1.62.8 ± 1.12.3 ± 0.9.136
Q4 Urgency incontinence1.0 ± 1.51.2 ± 1.70.4 ± 0.7.243
Total score5.1 ± 3.36.3 ± 3.14.6 ± 2.1.071
Voided volume (mL)199.6 ± 154.5167.5 ± 118.5289.3 ± 209.4.097
Qmax (mL/s)16.7 ± 11.414.8 ± 9.821.9 ± 14.3.066
PVR (mL)65.4 ± 78.068.5 ± 80.956.9 ± 72.6.751

1 Note: Data are presented as mean ± SD.

2 Abbreviations: OABSS, overactive bladder symptom score; POP‐Q, Pelvic Organ Prolapse‐Quantification; PVR, postvoid residual urine volume; Qmax, maximum urinary flow rate.

Evaluation of BWT and urinary conditions

BWT was evaluated by ultrasonographic examination before and 6 months after the surgery at three sites in the bladder: the anterior wall, trigone, and dome, as reported earlier.25,26 All patients were examined by one urologist (T.M.). Ultrasonography was performed by a transvaginal approach using a conbex probe (HI VISION Avius, 7.5 MHz B mode; Hitachi‐Aloka Medical, Ltd, Tokyo, Japan). When the examination was performed, <50 mL of urine pooled in the bladder (Figure 2). All patients simultaneously filled in the self‐reporting questionnaire for evaluating the OABSS. The validated Japanese language questionnaire was completed by patients in a separate and secluded space. Patients with lower OABSS after surgery than before operation were considered responders, while those with worsening or unchanged OABSS after operation were considered nonresponders. Briefly, OABSS responders in this study were defined as individuals with a decrease in the total score of OABSS by 1 point or more. In addition, the maximum urinary flow rate (Qmax) and voided volume (VV) were determined using free uroflowmetry, and postvoid residual urine volume (PVR) was measured using suprapubic ultrasonography.

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Statistical analysis

Data are presented as the number of patients (percentage, %) or mean ± SD. All statistical analyses were performed using the JMP14 software (SAS Institute Inc, Cary, North Carolina). Differences in the changes in parameters from baseline to 6 months in patients were examined using the paired Student's t or Wilcoxon signed rank tests. Values of P < .05 were considered statistically significant.

RESULTS

Changes in urinary symptoms after surgery

Among the 41 patients evaluated, TVM surgery improved urinary condition in 30 patients,

as evaluated by the OABSS (73.2%). However, the score deteriorated in 6 patients (14.6%) and was unchanged in 5 patients (12.2%). There was no case of POP recurrence, especially during the follow‐up period regarding surgery. Table 2 shows the changes observed in the OABSS and objective findings, including uroflowmetry, after TVM surgery. After the operation, the total OABSS of all patients decreased significantly (5.1 ± 3.3 to 2.9 ± 2.9; P < .001). In OABSS responders, the total score improved from 6.3 ± 3.1 to 2.0 ± 2.0 (P < .001). The individual questionnaires showed that the Q1 (Daytime frequency) and Q3 (Urgency) scores were significantly decreased by TVM surgery (0.9 ± 0.7 to 0.3 ± 0.5 and 2.0 ± 1.6 to 1.0 ± 1.6, respectively), whereas the changes in Q2 (Nighttime frequency) and Q4 (Urgency incontinence) were not significant (1.3 ± 0.8 to 1.1 ± 0.9 and 1.0 ± 1.5 to 0.5 ± 1.1, respectively) in patients overall. In OABSS nonresponders, total OABSS and all items in the OABSS did not improve after TVM operation. Finally, among the 41 patients, 30 and 11 were found to be OABSS responders and OABSS nonresponders, respectively (73.2% and 26.8%, respectively). In objective findings, the PVR of patients overall and OABSS responders improved after operation (overall, 65.4 ± 78.0 mL to 19.7 ± 33.7 mL, P < .001; OABSS responders, 68.5 ± 80.9 mL to 19.6 ± 35.8 mL, P < .001). However, not all objective findings significantly improved after operation in OABSS nonresponders (Table 2).

2 TABLEChanges in OABSS and urological parameters by surgery

OverallOABSS responderOABSS nonresponder
VariablesPresurgeryPostsurgeryP valuePresurgeryPostsurgeryP valuePresurgeryPostsurgeryP value
OABSS
Q1 Daytime frequency0.9 (0.7)0.3 (0.5)<.0011.1 (0.6)0.2 (0.4)<.0010.6 (0.7)0.5 (0.7)1.000
Q2 Nighttime frequency1.3 (0.8)1.1 (0.9).3321.3 (0.8)1.1 (0.9).3501.3 (0.9)1.4 (1.0)1.000
Q3 Urgency2.0 (1.6)1.0 (1.6).0012.8 (1.1)0.6 (1.1)<.0012.3 (0.9)2.2 (2.0).914
Q4 Urgency incontinence1.0 (1.5)0.5 (1.1).0701.2 (1.7)0.2 (0.7)<.0010.4 (0.7)1.3 (1.7).125
Total score5.1 (3.3)2.9 (2.9)<.0016.3 (3.1)2.0 (2.0)<.0014.6 (2.1)5.4 (3.7).406
Voided volume (mL)199.6 (154.5)220.9 (157.0).649167.5 (118.5)217.2 (145.0).262289.3 (209.0)231.3 (195.3).375
Qmax (mL/s)16.7 (11.4)20.1 (12.0).08014.8 (9.8)18.8 (10.2).13921.9 (14.3)23.8 (16.1).426
PVR (mL)65.4 (78.0)19.7 (33.7)<.00168.5 (80.9)19.6 (35.8).00156.9 (72.6)20.0 (28.5).078

  • 3 Note: Data are expressed as mean (SD).
  • 4 Abbreviations: OABSS, overactive bladder symptom score; PVR, postvoid residual urine volume; Qmax, maximum urinary flow rate.
Changes in BWT after surgery

Table 3 shows the measurements of BWT at three different sites and their mean values before and after TVM surgery. No significant differences in BWT were observed among the three sites before surgery. Postsurgical BWT levels at the anterior and dome regions were altered significantly, along with the mean levels at all three sites (P < .001). However, BWT at the trigone region was not altered significantly (P = .741).

3 TABLEChanges in urinary bladder wall thickness in all patients

Bladder wall thickness (mm)Transvaginal mesh surgeryP value
BeforeAfter
Anterior5.73 ± 1.254.75 ± 1.37<.001
Trigone6.09 ± 1.286.26 ± 2.18.741
Dome5.82 ± 1.094.98 ± 1.34<.001
Mean of the three sites5.88 ± 1.175.33 ± 1.53<.001

Correlation between BWT and urinary symptoms after surgery

Figure 3 shows the correlation between the changes observed in BWT and OABSS after surgery. In OABSS responders, BWT at the anterior wall and dome was significantly decreased after TVM surgery (5.46 ± 1.32 mm to 4.47 ± 1.20 mm and 5.56 ± 1.06 mm to 4.65 ± 1.20 mm, respectively). In contrast, in OABSS nonresponders, these two parameters exhibited a decreasing trend but did not reach significance (6.56 ± 1.02 mm to 5.89 ± 1.53 mm and 6.62 ± 1.02 mm to 5.88 ± 1.55 mm, respectively; P = .126 and P = .093, respectively). BWT at the trigone region was unchanged after surgery in both responders and nonresponders (5.69 ± 1.27 mm to 5.69 ± 2.08 mm, P = .501, and 7.04 ± 0.89 mm to 7.53 ± 2.13 mm, P = .169, respectively). The mean BWT at all three sites before and after TVM surgery was significantly different among OABSS responders (5.57 ± 1.21 mm and 4.94 ± 1.63 mm, P < .001), unlike among nonresponders (6.74 ± 0.92 mm to 6.43 ± 1.84 mm, P = .254).

luts12374-fig-0003.jpg

Prognostic roles of BWT for the efficacy of the surgery

Table 4 shows the relationship between lower OABSS and BWT before surgery. All measurements of BWT at the three sites in OABSS responders were significantly lower than those in OABSS nonresponders. In addition, the mean BWT at all three sites was also significantly different among the responders, and it showed the most significant difference among the parameters evaluated. In addition, when the postoperative BWT change between OAB responders and OAB nonresponders was examined, BWT decreased postoperatively in the OAB responder group at all sites. However, no statistically significant difference was observed (Table 5). Furthermore, we examined the correlation between the changes in bladder capacity (VV + PVR) and BWT before and after operation. Consequently, the increase in postoperative bladder capacity was statistically significantly inversely correlated with BWT (r = −0.4541, P = .005). In contrast, improvement in OAB symptoms and BWT with receiver operating characteristic (ROC) curve showed an area under the curve (AUC) of 0.858 (95% CI, 0.713‐1.003) and 0.868 (95% CI, 0.743‐0.993) for anterior wall and dome, respectively. When the cutoff values for BWT were defined as 6.72 mm and 6.41 mm for the anterior wall and dome, the sensitivities were 77.8% and 77.8%, and the specificities were 79.3% and 75.9%, respectively, for the predicted improvement in OAB symptoms after TVM surgery (Figure 4A,B).

4 TABLEBladder wall thickness before surgery and improvement in overactive bladder symptoms by surgery

Bladder wall thickness, presurgery (mm)OABSS responderOABSS nonresponderP value
Anterior; mm, mean ± SD5.46 ± 1.326.56 ± 1.02.017
Trigone5.69 ± 1.277.04 ± 0.89.003
Dome5.56 ± 1.066.62 ± 1.02.008
Mean of the three sites5.57 ± 1.126.77 ± 0.92<.001

  • 5 Abbreviation: OABSS, overactive bladder symptom score.
  • 5 TABLEChanges in bladder wall thickness by operation between improvements in overactive bladder symptom scores

Changes in BWT by operation (mm)OABSS responderOABSS nonresponderP value
Anterior; mm, mean ± SD−1.03 ± 1.22−0.82 ± 1.54.676
Trigone−0.01 ± 1.860.61 ± 1.60.207
Dome−0.91 ± 1.32−0.82 ± 1.31.765
Mean of the three sites−0.62 ± 1.18−0.32 ± 1.37.507

6 Abbreviations: BWT, bladder wall thickness; OABSS, overactive bladder symptom score.

luts12374-fig-0004.jpg

In addition, the unfit rate for the diagnosis of OAB was 61.0% (25/41). Furthermore, the deviation from diagnostic criteria for OAB and BWT with ROC showed an AUC of 0.698 (95% CI, 0.531‐0.864) and 0.703 (95% CI, 0.510‐0.895) for the anterior wall and dome, respectively. When the cutoff values for BWT were defined as 6.43 mm and 6.74 mm for the anterior wall and dome, the sensitivities were 80.0% and 84.0%, and the specificities were 56.3% and 50.0%, respectively, for predicting the deviation of the diagnosis for OAB after TVM surgery (Figure 5A,B).

luts12374-fig-0005.jpg

DISCUSSION

This study shows that presurgical measurement of BWT using ultrasound may be a useful predictor of lower OABSS after TVM surgery in patients with POP. In general, the most useful method to evaluate bladder activity is supposedly a conventional urodynamic test. In fact, in previous studies, urodynamic tests revealed useful predictive factors for improving OAB symptoms in POP after TVM surgery.3,4 However, this test is invasive, time‐consuming, and presents various types of risks.8 Clinical parameters, such as age, body mass index, postmenopausal status, and smoking, have similarly been investigated as potential predictive factors for improved OAB symptoms after TVM repair, and some of them were identified as useful predictors.3 In this study, we focused on the measurement of BWT due to its noninvasive nature.

One of our interesting results is that all BWT parameters were significantly thinner in OABSS responders than in OABSS nonresponders. Based on our results regarding changes in BWT at individual sites, the findings that BWT at the anterior wall and dome regions can predict the improvement in OABSS after TVM surgery are expected. Similarly, the finding that the mean BWT of all three sites before surgery was associated with improvement in the OABSS is logically expected. However, surprisingly, presurgical BWT at the trigone region in OABSS responders was significantly lower than that in OABSS nonresponders, despite remaining unchanged before and after TVM surgery. Unfortunately, our study design cannot provide an answer to this phenomenon. However, we speculate that the higher BWT is attributable to the development of connective tissue and/or fibrosis of the bladder, resulting from mesh insertion, because the thickness was unchanged despite improvement in OABSS symptoms. Therefore, the increase observed in BWT at the trigone region in patients with POP may be irreversible.

Several investigators have proposed that BWT may be a useful diagnostic tool for OAB.15,16,25,26 In addition, change in BWT was suggested to be a potential marker to predict the success of treatments in patients with OAB.20,27 On the other hand, Robinson et al17 reported no significant change in BWT after 12 weeks of administering solifenacin to female patients for OAB. However, we strongly emphasize that standardized methods and convincing criteria to measure BWT according to pathological conditions remain unestablished. Hence, we considered the following arguments to design our study and discuss the clinical significance of BWT based on previous reports.

First, we measured BWT at three different anatomical points of the bladder: the trigone, dome, and anterior wall, and calculated their mean. Previous reports used the mean values of measurements at these three sites as BWT for statistical analyses in women with OAB symptoms.17,20 In addition, there is the opinion that the average of results at more than a single site is better for the measurement of BWT.28 Our results show that the mean BWT at the three sites and the anterior wall and dome of the bladder were altered by TVM surgery, while BWT at the trigone region was not altered. In addition, interestingly, similar changes in BWT were observed in OABSS responders, unlike in nonresponders. Hence, we support the opinion that measurements at multiple sites are essential to accurately calculate BWT. Furthermore, we would like to emphasize that the measurement of BWT at the trigone region alone may lead to an erroneous evaluation of bladder function and understanding of the pathological role of BWT.

Second, in addition to the transvaginal approach, the transrectal or suprapubic approach has been used to measure BWT.12,29 However, several investigators reported that transvaginal ultrasound was the best method for measuring BWT in women regarding intra‐observer and inter‐observer reliability compared with the others.30,31 Therefore, we used a transvaginal probe in this study. Although we were uncertain initially about the suitability of a transvaginal approach for patients with POP, BWT could be measured easily in all patients. Similarly, we suggest that the transvaginal method is useful in patients with POP.

Subsequently, we evaluated the OABSS and BWT at 6 months after TVM surgery. However, consensus about the optimal post‐TVM surgery duration to evaluate the subjective and objective parameters does not exist. Previous studies ranged from 1 month,32 3 months,4 6 months,3 to 12 months.33 In reality, although we performed the examinations 6 months post surgery due to past experience and the patients' requests; it is not supported by medical rationale. Therefore, further studies are necessary to determine the optimal schedule for the evaluation of BWT. In addition, the optimal cutoff value to diagnose OAB and criteria to reflect the accurate pathological significance still need to be established.15,16,25

The major limitation of our study is the relatively small number of patients. Although we defined the optimal cutoff value of BWT to predict the improvement in OAB symptoms by TVM surgery in this study, the accuracy of these indicators remains questionable. In addition, because the number of cases was small and many of the included patients had mild to moderate OAB based on the OABSS, it was impossible to conduct a comparative study based on the severity of the OAB symptoms. In particular, in this study, we did not conduct a pressure flow study and could not examine the relationship between BWT and detrusor pressure in detail. However, we highlight that BWT is a noninvasive parameter that can directly evaluate the bladder wall condition. Presently, we agree that BWT cannot replace urodynamic tests.15,26 In addition, we similarly agree that the standardization of BWT measurements, such as the types of transducer, frequency of the ultrasonic waves, and zooming power, is essential for widespread adoption.9,10 However, this is the first report evaluating the relationship between the changes in OAB symptoms and BWT in POP patients before and after transvaginal operation. More standardized clinical trials using larger study populations are required to clarify the "real power" of BWT as a predictive marker for the improvement in symptoms after TVM surgery in patients with POP.

In conclusion, our results demonstrate that BWT at the anterior wall and dome and the mean BWT at all three sites were significantly lower after TVM surgery than before surgery in OABSS responders, unlike in OABSS nonresponders. On the other hand, all BWT‐related parameters before the surgery were significantly associated with the improvement in OABSS by the surgery. Based on these results, we suggest that presurgical measurement of BWT may be a useful marker to predict the therapeutic effects evaluated by OAB symptoms after TVM surgery in patients with POP‐related OAB.

ACKNOWLEDGMENTS

This work was not funded by any foundation or company.

CONFLICT OF INTEREST

The authors declare no conflict of interest.

AUTHOR CONTRIBUTIONS

Tomohiro Matsuo and Yasuyoshi Miyata were responsible for the design and the conceptualization of this study. Data acquisition was performed by Tomohiro Matsuo. The clinical studies were conducted by Asato Otsubo, Yuta Mukae, and Kojiro Ohba. Data analyses were performed by Tomohiro Matsuo, Yasuyoshi Miyata, and Kensuke Mitsunari. The draft manuscript was written by Asato Otsubo and Tomohiro Matsuo, and Yasuyoshi Miyata and Hideki Sakai edited the manuscript.

DATA AVAILABILITY STATEMENT

The data that support the findings of this study are available from the corresponding author upon reasonable request.

REFFERENCES 1 Haylen BT, De Ridder D, Freeman RM et al. International Urogynecological association; international continence society. An international Urogynecological association (IUGA)/international continence society (ICS) joint report on the terminology for female pelvic floor dysfunction. Neurourol Urodyn 2020 ; 29 : 4 – 20. 2 Otsuka A, Watanabe K, Matsushita Y et al. Predictive factors for persistence of preoperative overactive bladder symptoms after transvaginal mesh surgery in women with pelvic organ prolapse. Lower Urinary Tract Symptoms 2020 ; 12 : 167 – 72. 3 Long CY, Hsu CS, Wu MP, Liu CM, Chiang PH, Juan YS, Tsai EM. Predictors of improvement overactive bladder symptoms after transvaginal mesh repair for treatment of pelvic organ relapse. Int Urogynecol J 2011 ; 22 : 535 – 42. 4 Tomoe H. Improvement of overactive bladder symptoms after tension‐free virginal mesh operation in women with pelvic organ prolapse: correlation with preoperative urodynamic findings. Int J Urol 2015 ; 22 : 577 – 80. 5 Nguyen J, Bhatia NN. Resolution of motor urge incontinence after surgical repair of pelvic organ relapse. J Urol 2001 ; 166 : 2263 – 6. 6 Heinonen P, Aaltonen R, Joronen K, Ala‐Nissilä S. Long‐term outcome after transvaginal mesh repair of pelvic organ prolapse. Int Urogynecol J 2016 ; 27 : 1069 – 74. 7 Huang L, He L, Wu SL, Sun RY, Lu D. Impact of preoperative urodynamic testing for urinary incontinence and pelvic organ prolapse on clinical management in Chinese women. J Obstet Gynaecol Res 2016 ; 42 : 72 – 6. 8 Antunes‐Lopes T, Carvalho‐Barros S, Cruz CD, Cruz F, Martins‐Silva C. Biomarkers in overactive bladder: a new onjective and noninvasive tool? Ther Adv Urol 2011 ; 2011 : 382431. 9 De Nunzio C, Autorino R, Bachmann A et al. The diagnosis of benign prostatic obstraction: development of a clinical nomogram. Neurourol Urodyn 2016 ; 35 : 235 – 40. Farag FF, Heesakkers J. Imaging assessments of lower urinary tract dysfunctions: future steps. Turk J Urol 2014 ; 40 : 78 – 81. Oelke M, Höfner K, Jonas U, de la Rosette JJ, Ubbink DT, Wijkstra H. Diagnostic accuracy of noninvasive tests to evaluate bladder outlet obstruction in men: detrusor wall thickness, uroflowmetry, postvoidual urine, and prostate volume. Eur Urol 2007 ; 52 : 827 – 34. Güzel Ö, Aslan Y, Balci M et al. Can bladder wall thichness measuring be used for detecting bladder outlet obstruction? Urology 2015 ; 86 : 439 – 44. Khullar V, Salvatore S, Uccella S et al. A novel technique for measuring bladder wall thickness in women using transvaginal ultrasound. Ultrasound Obstet Gynecol 1994 ; 4 : 220 – 423. Khullar V, Cardozo LD, Salvatore S, Hill S. Ultrasound: a novel invasive screening test for detrusor instability. Br J Obstet Gynaecol 1996 ; 103 : 904 – 8. Serati M, Salvatore S, Cattoni E, Soligo M, Cromi A, Ghezzi F. Ultrasound measurement of bladder wall thickness in different forms of detrusor overactivity. Int J Urogynecol 2010 ; 21 : 1405 – 11. Kuhn A, Genoud S, Robinson D, Herrmann G, Günthert A, Brandner S, Raio L. Sonographic transvaginal bladder wall thickness: does the measurement discriminate between urodynamic diagnoses? Neurourol Urodyn 2011 ; 30 : 325 – 8. Robinson D, Oelke M, Khullar V et al. Bladder wall thickness in women with symptoms of overactive bladder and detrusor overactivity: results from the randomised, placebo‐controlled shrink study. Neurourol Urodyn 2016 ; 35 : 819 – 25. Ahmed AF. Sonographic parameters predicting the outcome of patients with lower urinary tract symptoms/benign prostatic hyperplasia treated with alpha1‐ adrenoreceptor antagonist. Urology 2016 ; 88 : 143 – 8. Panayi DC, Tekkis P, Fernando R, Khullar V. Is the beneficial effect of antimuscarinics related motor or sensory changes in the bladder? Int Urogynecol J 2010 ; 21 : 841 – 5. Oelke M, Bachmann A, Descazeaud A et al. EAU guidelines on the treatment and follow‐up of non‐neurogenic male lower urinary tract symptoms including benign prostatic obstruction. Eur Urol 2013 ; 64 : 118 – 40. Homma Y, Yoshida M, Seki N et al. Symptom assessment tool for overactive bladder syndrome–overactive bladder symptom score. Urology 2006 ; 68 : 318 – 23. Debodinance P, Berrocal J, Clave H et al. Changing attitudes on the surgical treatment of urogenital prolapse: birth of the tension‐free vaginal mesh. J Gynecol Obstet Biol Reprod (Paris) 2004 ; 33 : 577 – 88. Oride A, Kanasaki H, Hara T, Kyo S. Postoperative outcomes following tension‐free vaginal mesh surgery for pelvic organ prolapse: a retrospective study. Urol J 2019 ; 16 : 581 – 5. Kanasaki H, Oride A, Hara T, Kyo S. Comparison of Postoperative Short‐Term Outcomes between Tension‐Free Vaginal Mesh Surgery Using the Capio SLIM Suture Capturing Device and Conventional TVM Surgery for Pelvic Organ Prolapse. Obstet Gynecol Int 2018 ; 2018 : 7918071. https://doi.org/10.1155/2018/7918071, 1, 5. Robinson D, Snders K, Cardozo L et al. Can ultrasound replace ambulatory urodynamics when investigating women with irritative urinary symptoms? BJOG 2002 ; 109 : 145 – 8. Otsuki EN, Júnior EA, Oliveira E et al. Ultrasound thickness of bladder wall in continent and incontinent women and its correlation with cystometry. Sci World J 2014 ; 2014 : 684671 1, 5. Irwin DE, Milsom I, Hunskaar S et al. Population‐based survey of urinary incontinence, overactive bladder, and other lower urinary tract symptoms in five countries: results of the EPIC study. Eur Urol 2006 ; 50 : 1306 – 14. Singh K, Goel A, Sankhwar S, Kumar M, Gupta A. Can bladder wall thickness measurement be used for detecting bladder outlet obstruction? Urology 2016 ; 88 : 228. Park JS, Lee HW, Lee SW, Moon HS, Park HY, Kim YT. Bladder wall thickness is associated with responsiveness of storage symptoms to alpha‐blockers in men with lower urinary tract symptoms. Korean J Urol 2012 ; 53 : 487 – 91. Panayi DC, Khullar V, Fernando R, Tekkis P. Transvaginal ultrasound measurement of bladder wall thickness: a more reliable approach than transperineal and transabdominal approaches. BJU Int 2010 ; 106 : 1519 – 22. Farag FF, Heesakkers JP. Non‐invasive techniques in the diagnosis of the bladder strange disorders. Neurourol Urodyn 2011 ; 30 : 1422 – 8. Kuribayashi M, Kitagawa Y, Narimoto K et al. Postoperative voiding function in patients undergoing tension‐free vaginal mesh procedure for pelvic organ prolapse. Int J Urogynecol J 2011 ; 22 : 1299 – 303. Takahashi S, Obinata D, Sakuma T et al. Tension‐free vaginal mesh procedure for pelvic organ prolapse: a single‐center experience of 310 cases with 1‐year follow up. Int J Urol 2010 ; 17 : 353 – 8.

By Asato Otsubo; Tomohiro Matsuo; Yasuyoshi Miyata; Yuta Mukae; Kensuke Mitsunari; Kojiro Ohba and Hideki Sakai

Reported by Author; Author; Author; Author; Author; Author; Author

Titel:
Presurgical bladder wall thickness is a useful marker to predict the postsurgical improvement of symptoms in patients with pelvic organ prolapse-related overactive bladder.
Autor/in / Beteiligte Person: Otsubo, A ; Matsuo, T ; Miyata, Y ; Mukae, Y ; Mitsunari, K ; Ohba, K ; Sakai, H
Link:
Zeitschrift: Lower urinary tract symptoms, Jg. 13 (2021-07-01), Heft 3, S. 347-355
Veröffentlichung: Richmond, Vic. : Blackwell Publishing Asia, 2009-, 2021
Medientyp: academicJournal
ISSN: 1757-5672 (electronic)
DOI: 10.1111/luts.12374
Schlagwort:
  • Humans
  • Surgical Mesh
  • Ultrasonography
  • Pelvic Organ Prolapse surgery
  • Urinary Bladder, Overactive etiology
  • Urinary Bladder, Overactive surgery
Sonstiges:
  • Nachgewiesen in: MEDLINE
  • Sprachen: English
  • Publication Type: Journal Article
  • Language: English
  • [Low Urin Tract Symptoms] 2021 Jul; Vol. 13 (3), pp. 347-355. <i>Date of Electronic Publication: </i>2021 Feb 12.
  • MeSH Terms: Pelvic Organ Prolapse* / surgery ; Urinary Bladder, Overactive* / etiology ; Urinary Bladder, Overactive* / surgery ; Humans ; Surgical Mesh ; Ultrasonography
  • References: Urol J. 2019 Dec 24;16(6):581-585. (PMID: 31630387) ; J Obstet Gynaecol Res. 2016 Jan;42(1):72-6. (PMID: 26530321) ; Int Urogynecol J. 2016 Jul;27(7):1069-74. (PMID: 26837782) ; Adv Urol. 2011;2011:382431. (PMID: 21687625) ; Eur Urol. 2013 Jul;64(1):118-40. (PMID: 23541338) ; Int Urogynecol J. 2011 May;22(5):535-42. (PMID: 21079919) ; Low Urin Tract Symptoms. 2021 Jul;13(3):347-355. (PMID: 33580634) ; Low Urin Tract Symptoms. 2020 May;12(2):167-172. (PMID: 31837207) ; Neurourol Urodyn. 2016 Feb;35(2):235-40. (PMID: 25524269) ; BJOG. 2002 Feb;109(2):145-8. (PMID: 11888096) ; Int Urogynecol J. 2011 Oct;22(10):1299-303. (PMID: 21547603) ; BJU Int. 2010 Nov;106(10):1519-22. (PMID: 20438565) ; Urology. 2015 Sep;86(3):439-44. (PMID: 26142716) ; Urology. 2016 Feb;88:143-8. (PMID: 26607685) ; Br J Obstet Gynaecol. 1996 Sep;103(9):904-8. (PMID: 8813311) ; Neurourol Urodyn. 2011 Nov;30(8):1422-8. (PMID: 21780168) ; Neurourol Urodyn. 2011 Mar;30(3):325-8. (PMID: 20949598) ; Turk J Urol. 2014 Jun;40(2):78-81. (PMID: 26328155) ; J Urol. 2001 Dec;166(6):2263-6. (PMID: 11696748) ; Neurourol Urodyn. 2016 Sep;35(7):819-25. (PMID: 26199198) ; Int Urogynecol J. 2010 Jul;21(7):841-5. (PMID: 20349178) ; Urology. 2016 Feb;88:228. (PMID: 26546810) ; Neurourol Urodyn. 2010;29(1):4-20. (PMID: 19941278) ; ScientificWorldJournal. 2014;2014:684671. (PMID: 25538959) ; Korean J Urol. 2012 Jul;53(7):487-91. (PMID: 22866221) ; Urology. 2006 Aug;68(2):318-23. (PMID: 16904444) ; Ultrasound Obstet Gynecol. 1994 May 1;4(3):220-3. (PMID: 12797185) ; Eur Urol. 2006 Dec;50(6):1306-14; discussion 1314-5. (PMID: 17049716) ; Int Urogynecol J. 2010 Nov;21(11):1405-11. (PMID: 20535449) ; Int J Urol. 2015 Jun;22(6):577-80. (PMID: 25754989) ; Int J Urol. 2010 Apr;17(4):353-8. (PMID: 20202001) ; J Gynecol Obstet Biol Reprod (Paris). 2004 Nov;33(7):577-88. (PMID: 15550876) ; Eur Urol. 2007 Sep;52(3):827-34. (PMID: 17207910) ; Obstet Gynecol Int. 2018 Apr 1;2018:7918071. (PMID: 29805449)
  • Contributed Indexing: Keywords: bladder wall thickness; overactive bladder symptom score; pelvic organ prolapse; transvaginal mesh surgery
  • Entry Date(s): Date Created: 20210213 Date Completed: 20211028 Latest Revision: 20211028
  • Update Code: 20240513
  • PubMed Central ID: PMC8359317

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