Abstract
Objective
Stress urinary incontinence (SUI) is a common problem in women that affects their quality of life. According to the current evidence, 15%–50% of severe pelvic organ prolapse (POP) surgeries lead to de novo urinary incontinence (UI). This study aimed at determining the risk factors and characteristics of de novo SUI after POP surgeries in a systematic review.
Material and methods
We conducted a systematic search of articles in English related to the risk of UI after POP surgery published until December 2019 in the selected bibliographic databases, including PubMed, EMBASE, Scopus, Cochrane Library, and ProQuest.
Results
The initial search resulted in 2,363 studies, and after reviewing the titles and abstracts, 146 studies were identified. Moreover, 2 independent reviewers, using the Joanna Briggs Institute checklists, evaluated the risk of biases in the selected studies. Finally, 40 studies met the inclusion criteria. The most important predictors of UI after POP surgery were positive pessary testing, age >50 years, and maximum urethral closure pressure (MUCP) <60 cmH2O.
Conclusion
Positive pessary testing, older age, and low MUCP were the most important risk factors for de novo incontinence after POP surgeries.
Keywords: Pelvic organ prolapse, risk factors, operative surgical procedures, stress urinary incontinence
Introduction
Pelvic floor disorders (PFDs) are common urological disorders in women that can result in sexual and social problems and affect the overall quality of life (QoL).[1–3] Various risk factors trigger pelvic organ prolapse (POP) and cause stress urinary incontinence (SUI). Accurate recognition of the relevant risk factors could be effective in preventing PFDs and improving patients’ QoL.[4]
The risk of surgery for prolapse in a woman’s lifetime is 7%–11%.[5] Several factors such as aging, obesity, childbirth, previous hysterectomy, constipation, estrogen deficiency, and smoking increase the risk of POP.[6] POP surgery can result in de novo urinary incontinence (UI),[7] but some factors may increase the risk of SUI in general, such as race, obesity, vaginal delivery, age, parity, genetics, and chronic obstructive pulmonary disease.[2,4,8–11] It is obvious that for patients with severe POP, surgery can be the best therapeutic approach.[12] In a study by van der Ploeg et al. [9] the incidence of postoperative UI was reported to be 11%–44%. According to recent studies, 36%–80% of women with severe prolapse may develop UI after surgery,[13] and 29% of women need surgery for UI.[14] In addition to the high costs of reconstructive or recurrent surgeries, de novo incontinence can impair daily functioning and can cause sexual and mental health problems.[2] Many diagnostic tests such as urodynamic tests, stress tests, and pessary tests can help to detect post-POP disorders, but none of these tests can assure the accuracy of diagnosis because the sensitivity of these tests in predicting UI is very low (17%–39%).[15] On the other hand, although ultrasound has high sensitivity for diagnose of stress urinary incontinence, it is not sensitive for diagnosis of prolapse.[16] Adding a preoperative urodynamic test can partially help predict the risk of UI.[9] Although any of the factors mentioned earlier may individually increase the risk of de novo incontinence, we need to quantify the number of multiple risks for presenting this condition. Preoperative risk prediction is also known as one of the best strategies to manage and reduce the risk factors for SUI after POP surgeries.[4] This study aimed at identifying the risk factors for de novo SUI after surgery for moderate to severe POP.
Material and methods
Review question
The Patient Intervention Comparison Outcome (PICO) schema includes: Patients: female candidate for POP surgeries; Intervention/Exposure: POP surgery; Comparison: no treatment or exposure; Outcome: de novo SUI.
This systematic review is based on the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) statement.[17] According the PICO schema, the question of the review was: What are the risk factors that cause de novo SUI in patients after POP surgeries?
Search strategy
A systematic search was conducted in databases, including PubMed, EMBASE, Scopus, Cochrane Library, and ProQuest (thesis & dissertation), for articles published until December 2019. Google Scholar was also used to search for more relevant studies. Reference lists and citations of the included articles were correspondingly tracked. Hand searching was further performed for relevant studies. Both free-text and controlled vocabularies were searched accordingly using the keywords extracted from the PICO schema, including “de novo stress urinary incontinence,” “post-operative stress urinary incontinence,” “postsurgical stress urinary incontinence,” and “pelvic organ prolapse.” The full search strategy in EMBASE is shown in Appendix 1.
Appendix 1.
Search Strategy Embase Database Results (Updated in September 2019)
| No. | Query |
|---|---|
| #1. | pelvic AND organ AND prolapse:ab,ti |
| #2. | ‘pelvic organ prolapse’/exp |
| #3 | #1 OR #2 |
| #4. | post*operat* AND stress AND urinary AND incontinence:ab,ti |
| #5. | ‘de novo’ AND stress AND urinary AND incontinence:ab,ti |
| #6. | post*surg* AND stress AND urinary AND incontinence:ab,ti |
| #7. | #4 OR #5 OR #6 |
| #8. | #3 AND #7 |
Eligibility criteria
The studies with women of any age who underwent POP surgery and had no early symptoms of SUI but had moderate to severe POP were included in the review. We included randomized controlled trials, quasi-experimental trials, and cohort, case-control, and case series studies. All women with preoperative SUI, urinary tract infection, and bladder disorders were excluded. Letters, commentaries, editorial notes, conference proceedings, and review articles were excluded.
Study selection and data extraction
Two independent reviewers screened and selected the retrieved articles. In the first phase, the articles were screened by titles and abstracts according to the inclusion and exclusion criteria. The articles were then screened on the basis of full texts, and finally, the selected studies were included in the quality assessment. In case of disagreements, a third reviewer rechecked the studies. If the full text of the article was not available, the relevant authors were contacted to send the full text. All the eligible risk factors and their odds ratio (OR) were extracted from the selected papers. If the OR was not reported, it was calculated. We defined the eligibility as statistical significance (p<0.05) of the risk factor. It should be noted that in this study, we considered only OR with positive confidence interval (CI), except[18] that the pessary test was considered with a negative CI (Table 1).
Table 1.
Extracted risk factors and attributes
| # | Study | Risk factor & attributes | N/n | Adjusted OR (95% CI) | p |
|---|---|---|---|---|---|
| 1 | Lo et al.[6] | TVM type | |||
| Prolift T | 71/20 | 3.50 (1.88–5.91) | <0.001 | ||
| Elevate A | 71/18 | 3.48 (1.90–6.10) | <0.001 | ||
| Diabetes | 71/28 | 2.18 (1.631–4.21) | <0.002 | ||
| Age | |||||
| ≥66 years | 71/45 | 2.86 (1.01–2.53) | <0.014 | ||
| FUL | 71/33 | 3.48 (2.13–5.83) | <0.001 | ||
| MUCP | 71/33 | 4.65 (2.87–8.64) | <0.001 | ||
|
| |||||
| 2 | Haverkorn et al.[10] | BMI | 297/na** | <0.001 | |
| BMI>30 | |||||
|
| |||||
| 3 | Reena et al.[13] | Menopause | 47/38 | 2.60 (0.54–12.50) | <0.003 |
| Age | 40/33 | 2.07 (0.41–10.41) | <0.005 | ||
| ≥50 years | |||||
| Pessary test (300 mL) | 34/53 | RR 0.35 (0.25–0.51) | <0.001 | ||
|
| |||||
| 4 | Engh et al.[18] | Speculum | 100/74 | 42.9 (12.0–76.9) | *** |
| Pessary tests | 33.3 (−4.4 to +71.5) | *** | |||
|
| |||||
| 5 | Weil et al.[20] | MUCP | 6/na** | * | |
| PTR | 6/na** | * | |||
| Previous pelvic surgery | 6/na** | 15.56 (0.82–28.73) | <0.06 | ||
|
| |||||
| 6 | Borstad an Rud[21] | Age | 15/16 | 0.024 (0.001–0.416) | 0.01 |
| >60 years | |||||
| Uterine prolapse | 16/3 | 0.13 (0.0–0.3) | <0.05 | ||
| Previous pelvic surgery | 16/73 | 0.12 (0.025–0.588) | <0.001 | ||
| CP | 73/17 | 0.22 (0.083–0.616) | <0.05 | ||
|
| |||||
| 7 | Svenningsen et al.[22] | Pessary | |||
| Test 3 Pessary (300 mL) | 107/10 | 6.5 (1.6–25.4) | <0.012 | ||
| Test 4 Pessary continuous use | 79/15 | 6.5 (1.6–25.4) | <0.004 | ||
|
| |||||
| 8 | Liang et al.[24] | Patients with a positive stress test (Pessary test) | 79/49 | 0.056 (0.012–0.266) | <0.001 |
|
| |||||
| 9 | Davenport et al.[27] | SUI with prolapse reduction | 164 | 2.39 (1.10–5.21) | 0.03 |
| Point Ba (per cm) | 1.16 (1.01–1.34) | 0.04 | |||
| Cystocele severity | 1.17 | 0.02 | |||
|
| |||||
| 10 | Ugianskiene et al.[29] | Parity | 299/678 | 0.03 | |
|
| |||||
| 11 | Wang et al.[30] | LUTO | 75/300 | 2.3 (1.2–4.6) | 0.013 |
|
| |||||
| 12 | Kuribayashi et al.[31] | Urethral obstruction moderate or more | 24/65 | 12.616 (1.580–268.731) | 0.033 |
High risk according to the study (the significant P-value was not mentioned). n: number of patients with postoperative SUI and significant risk factor.
NA /na: not available; N: the number of patients with postoperative SUI; BMI: body mass index; FUL: functional urethral length; MUCP: maximum urethral closure pressure; PTR: pressure transmission ratio; LUTO: lower urinary tract obstruction; SUI: stress urinary incontinence; TVM: transvaginal mesh
This study reported PPV and NPV without range of statistical significance.
Methodological quality assessment
The quality of the selected studies was evaluated using the Joanna Briggs Institute critical appraisal tools (appropriate tool was used, based on the study design, for every article).[19] Two authors independently assessed the quality of the studies, and in case of disagreement, a third reviewer assessed the study for confirmation. The qualitative evaluation of the results is summarized in Table 2–6.
Table 2.
Evaluation of included quasi-experimental studies
| # | Study | Year of publication | Q 1 | Q 2 | Q 3 | Q 4 | Q 5 | Q 6 | Q 7 | Q 8 | Q 9 | Quality of study |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 1 | Weil et al.[20] | 1993 | Y | Y | Y | Y | U | Y | Y | Y | Y | low risk |
Table 3.
Evaluation of included case-series studies
| # | Study | Year of publication | Q 1 | Q 2 | Q 3 | Q 4 | Q 5 | Q 6 | Q 7 | Q 8 | Q 9 | Q 10 | Quality of study |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 1 | Borstad and Rud[21] | 1989 | U | Y | Y | Y | Y | U | Y | Y | U | Y | low risk |
Table 4.
Evaluation of included case-control studies
| # | Study | Year of publication | Q 1 | Q 2 | Q 3 | Q 4 | Q 5 | Q 6 | Q 7 | Q 8 | Q 9 | Q 10 | Quality of study |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 1 | Wang et al.[30] | 2017 | Y | Y | Y | Y | Y | Y | U | Y | Y | Y | low risk |
Table 5.
Evaluation of included cohort studies
| # | Study | Year of publication | Q 1 | Q 2 | Q 3 | Q 4 | Q 5 | Q 6 | Q 7 | Q 8 | Q 9 | Q 10 | Q 11 | Quality of study |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 1 | Liang et al.[1] | 2015 | Y | Y | Y | Y | U | Y | Y | Y | Y | Y | U | low risk |
| 2 | Lo et al.[6] | 2019 | Y | Y | Y | Y | Y | Y | Y | Y | Y | U | Y | low risk |
| 3 | van der Ploeg et al.[9] | 2018 | Y | Y | Y | Y | U | Y | Y | Y | Y | U | Y | low risk |
| 4 | Haverkorn et al.[10] | 2011 | Y | Y | Y | Y | U | Y | Y | Y | Y | U | U | low risk |
| 5 | Reena et al.[13] | 2007 | Y | Y | U | Y | Y | Y | U | N | U | U | N | moderate risk |
| 6 | Engh et al.[18] | 2011 | Y | Y | Y | Y | U | Y | Y | Y | Y | U | Y | low risk |
| 7 | Svenningsen et al.[22] | 2012 | Y | Y | Y | Y | U | Y | Y | U | N | N | Y | moderate risk |
| 8 | Song et al.[23] | 2016 | Y | Y | Y | Y | U | Y | Y | Y | Y | U | Y | low risk |
| 9 | Liang et al.[24] | 2004 | Y | Y | Y | Y | U | Y | U | Y | Y | U | U | moderate risk |
| 10 | Duecy et al.[25] | 2010 | Y | Y | U | Y | U | Y | U | Y | Y | U | U | moderate risk |
| 11 | Sierra et al.[26] | 2019 | Y | Y | Y | Y | Y | U | Y | N | Y | U | U | moderate risk |
| 12 | Jelovsek[28] | 2013 | Y | Y | Y | Y | U | Y | Y | Y | Y | U | Y | low risk |
| 13 | Ugianskiene et al.[29] | 2017 | Y | Y | Y | Y | U | Y | Y | N | Y | U | Y | low risk |
| 14 | Kuribayashi et al.[31] | 2013 | Y | Y | Y | Y | U | Y | Y | Y | Y | U | Y | low risk |
| 15 | Klutke and Ramos[32] | 2000 | Y | Y | U | Y | Y | Y | U | Y | N | U | N | moderate risk |
| 16 | Groutz et al.[33] | 2004 | Y | Y | U | Y | U | Y | Y | Y | Y | U | U | moderate risk |
| 17 | Ek et al.[34] | 2010 | Y | Y | Y | Y | U | Y | Y | Y | Y | Y | U | low risk |
| 18 | Liapis et al.[35] | 2011 | Y | Y | Y | Y | U | Y | Y | Y | Y | U | Y | low risk |
| 19 | Ennemoser et al.[36] | 2012 | Y | Y | Y | U | U | Y | Y | Y | Y | U | U | moderate risk |
| 20 | Lensen et al.[37] | 2013 | Y | Y | Y | Y | U | Y | Y | Y | Y | U | Y | low risk |
| 21 | Hafidh, et al.[38] | 2013 | Y | Y | U | Y | U | Y | Y | Y | N | Y | N | moderate risk |
| 22 | LeClaire et al.[39] | 2014 | Y | Y | Y | Y | Y | Y | Y | Y | Y | U | Y | low risk |
| 23 | Lo et al.[40] | 2015 | Y | Y | Y | Y | Y | Y | Y | N | Y | U | Y | low risk |
| 24 | El Hamamsy and Fayyad[41] | 2015 | Y | Y | Y | Y | U | U | Y | Y | Y | U | U | moderate risk |
| 25 | Inan et al.[42] | 2016 | Y | Y | Y | Y | U | Y | Y | Y | U | N | Y | low risk |
| 26 | Manodoro et al.[43] | 2016 | Y | Y | Y | Y | Y | Y | Y | Y | U | U | Y | low risk |
| 27 | Huang and Yang[44] | 2017 | Y | Y | Y | U | U | Y | U | Y | Y | U | Y | moderate risk |
| 28 | Requena et al.[45] | 2018 | Y | Y | Y | Y | U | Y | Y | Y | U | U | U | moderate risk |
| 29 | Sabadell et al.[46] | 2018 | Y | Y | Y | Y | U | Y | Y | Y | N | U | Y | low risk |
| 30 | Goessens et al.[47] | 2019 | Y | Y | U | N | U | Y | Y | N | Y | U | N | moderate risk |
| 31 | Kurdoglu et al.[48] | 2019 | Y | Y | Y | Y | U | Y | Y | N | Y | U | Y | moderate risk |
Table 6.
Evaluation of included randomized control trial studies
| # | Study | Year of publication | Q 1 | Q 2 | Q 3 | Q 4 | Q 5 | Q 6 | Q 7 | Q 8 | Q 9 | Q 10 | Q 11 | Q 12 | Q 13 | Quality of study |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 1 | Schierlitz et al.[3] | 2014 | Y | N | U | N | N | U | Y | Y | Y | Y | Y | Y | Y | moderate risk |
| 2 | Costantin et al.[5] | 2011 | Y | Y | U | U | N | Y | Y | U | Y | Y | Y | Y | Y | moderate risk |
| 3 | Davenport et al.[27] | 2018 | Y | U | Y | U | U | U | Y | Y | Y | Y | Y | Y | Y | moderate risk |
| 4 | Brubaker et al.[49] | 2006 | Y | Y | Y | Y | U | Y | Y | Y | Y | Y | Y | Y | Y | low risk |
| 5 | Wei et al.[50] | 2009 | Y | U | Y | U | N | N | Y | Y | Y | Y | Y | Y | Y | moderate risk |
| 6 | Wei et al.[51] | 2012 | Y | Y | Y | N | U | Y | Y | U | Y | Y | Y | Y | Y | low risk |
Results
Of the 2,363 studies retrieved from the bibliographic databases and other relevant resources, duplicated studies were eliminated, and 146 articles were screened on the basis of title and abstract. Furthermore, 40 studies were potentially eligible for inclusion in the review. After the assessment of full texts and considering the inclusion and exclusion criteria, 24 studies were excluded from the review (Appendix 2), and 40 studies were selected for quality assessment. Figure 1 illustrates the flow diagram of study selection. The list of excluded studies and the reasons for exclusion are listed in Appendix 2.
Appendix 2.
List of excluded articles and exclusion reasons
| Author names | Publish | Study type | N* | Inclusion criteria | Exclusion criteria | |
|---|---|---|---|---|---|---|
| 1 | C. Graham & V. Mallett1 | 2001 | Cohort | 324 | The women with SUI, pop | Inclusion criteria did not match the main criterion of the study. |
| 2 | D. Altman & et al 2 | 2008 | Cohort | 3376 | Women who underwent POP surgery | Only the genetic effect on urinary incontinence was considered and these patients did not undergo surgery and did not meet the inclusion criteria. |
| 3 | R. E. Gutman & et al3 | 2008 | Cross-sectional | 296 | Women who underwent POP surgery | There was no associated risk factor and Inclusion criteria |
| 4 | P. Dällenbach & et al4 | 2012 | Case-control | 1811 | Women who underwent POP surgery | In this paper, condition SUI Inclusion criteria is not considered |
| 5 | J. Leruth & et al5 | 2013 | Cohort | 106 | The women with SUI | Inclusion criteria did not match the main criterion of the study |
| 6 | J. Marinus van der Ploeg & et al 6 | 2018 | RCT | 173 | The women who had SUI | Inclusion criteria did not match the main criterion of the study. |
| 7 | A G. Visco & et al7 | 2008 | RCT | 322 | The women with SUI, underwent POP surgery | Inclusion criteria did not match the main criterion of the study. |
| 8 | E. Borstad, et al8 | 2010 | RCT | 194 | The women who had symptoms of SUI, underwent POP surgery | Inclusion criteria did not match the main criterion of the study. |
| 9 | M. L. Gallentine & R. D. Cespedes9 | 2001 | Cohort | 24 | The women with or without symptoms of SUI, underwent POP surgery | Inclusion criteria did not match the main criterion of the study. |
| 10 | K. J. van Rensburg& J. A. van Rensburg6 | 2014 | Cohort | 131 | The women with SUI underwent POP surgery | Inclusion criteria did not match the main criterion of the study. |
| 11 | J. E. Jelovsek10 | 2019 | Original | 239 | The women with SUI | In this paper, condition SUI Inclusion criteria is not considered. |
| 12 | J. E. Jelovsek, et al11 | 2018 | RCT | 374 | The women with SUI underwent POP surgery | The inclusion criteria and the history of people with urinary incontinence |
| 13 | A. Ugianskiene, et al12 | 2019 | Cohort | 678 | The women with SUI underwent POP surgery | The inclusion criteria and the history of people with urinary incontinence. |
| 14 | V. leanza, et al13 | 2001 | Cohort | 85 | The women with symptoms of SUI | The inclusion criteria and the history of people with urinary incontinence. |
| 15 | S. C. R. Panicker & S. Srinivas14 | 2009 | Cohort | 50 | The women who underwent POP surgery | Inclusion criteria did not match the main criterion of the study. |
| 16 | J. M. van derPloeg, et al15 | 2019 | RCT | 255 | The women who underwent POP surgery | Inclusion criteria did not match the main criterion of the study. |
| 17 | E. Borstad, et al 16 | 1991 | Cohort | 73 | The women with SUI, underwent POP surgery | Inclusion criteria did not match the main criterion of the study. |
| 18 | Y. Khayyami, et al17 | 2019 | Cohort | 1198 | The women with SUI, underwent POP surgery | Inclusion criteria did not match the main criterion of the study |
| 19 | J. Marinus van der Ploeg, et al18 | 2016 | RCT | 231 | The women with SUI, underwent POP surgery | Inclusion criteria did not match the main criterion of the study |
| 20 | M. M. E. Lakeman, et al19 | 2011 | RCT | 234 | The women who underwent POP surgery | Inclusion criteria did not match the main criterion of the study |
| 21 | E. Costantin, et al20 | 2007 | RCT | 66 | The women who underwent POP surgery | Inclusion criteria did not match the main criterion of the study |
| 22 | M. Frigerio, et al21 | 2018 | Cohort | 417 | The women who underwent POP surgery | Inclusion criteria did not match the main criterion of the study |
| 23 | John E. Jelovsek22 | 2016 | Model | The women who underwent POP surgery | Review | |
| 24 | J. Eric Jelovsek23 | 2018 | Combined cohort: 3 randomized trials and 2 prospective cohort | 1,301 | The women who underwent POP surgery | The output criteria was not corresponded |
Graham CA, Mallett VT. Race as a predictor of urinary incontinence and pelvic organ prolapse. American journal of obstetrics and gynecology. 2001;185:116–20.
Altman D, Forsman M, Falconer C, Lichtenstein P. Genetic influence on stress urinary incontinence and pelvic organ prolapse. European urology. 2008;54:918–23.
Gutman RE, Ford DE, Quiroz LH, Shippey SH, Handa VL. Is there a pelvic organ prolapse threshold that predicts pelvic floor symptoms? American journal of obstetrics and gynecology. 2008;199:683. e1–. e7.
Dällenbach P, Nancoz CJ, Eperon I, Dubuisson J-B, Boulvain M. Incidence and risk factors for reoperation of surgically treated pelvic organ prolapse. International urogynecology journal. 2012;23:35–41.
Leruth J, Fillet M, Waltregny D. Incidence and risk factors of postoperative stress urinary incontinence following laparoscopic sacrocolpopexy in patients with negative preoperative prolapse reduction stress testing. International urogynecology journal. 2013;24:485–91.
van der Ploeg JM, Zwolsman SE, Posthuma S, Wiarda HS, van der Vaart CH, Roovers JPW. The predictive value of demonstrable stress incontinence during basic office evaluation and urodynamics in women without symptomatic urinary incontinence undergoing vaginal prolapse surgery. Neurourology and urodynamics. 2018;37:1011–8.
Visco AG, Brubaker L, Nygaard I, et al. The role of preoperative urodynamic testing in stress-continent women undergoing sacrocolpopexy: the Colpopexy and Urinary Reduction Efforts (CARE) randomized surgical trial. International Urogynecology Journal. 2008;19:607.
Borstad E, Abdelnoor M, Staff AC, Kulseng-Hanssen S. Surgical strategies for women with pelvic organ prolapse and urinary stress incontinence. International urogynecology journal. 2010;21:179–86.
Gallentine ML, Cespedes RD. Occult stress urinary incontinence and the effect of vaginal vault prolapse on abdominal leak point pressures. Urology. 2001;57:40–4.
Jelovsek JE, van der Ploeg JM, Roovers J-P, Barber MD. Validation of a Model Predicting De Novo Stress Urinary Incontinence in Women Undergoing Pelvic Organ Prolapse Surgery. Obstetrics & Gynecology. 2019;133:683–90.
Jelovsek JE, Barber MD, Brubaker L, et al. Effect of uterosacral ligament suspension vs sacrospinous ligament fixation with or without perioperative behavioral therapy for pelvic organ vaginal prolapse on surgical outcomes and prolapse symptoms at 5 years in the OPTIMAL randomized clinical trial. Jama. 2018;319:1554–65.
Ugianskiene A, Kjærgaard N, Larsen T, Glavind K. What happens to urinary incontinence after pelvic organ prolapse surgery? International urogynecology journal. 2019;30:1147–52.
Leanza V, Gasbarro N, Caschetto S. New Technique for Correcting Both Incontinence and Cystocele: TICT (Tension-Free Incontinence Cystocele Treatment). Urogynaecologia. 2001;15:133–40.
Panicker R, Srinivas S. Urodynamic changes in pelvic organ prolapse and the role of surgery. Medical Journal Armed Forces India. 2009;65:221–4.
van der Ploeg JM, Steyerberg EW, Zwolsman SE, van der Vaart CH, Roovers JPW. Stress urinary incontinence after vaginal prolapse repair: development and internal validation of a prediction model with and without the stress test. Neurourology and urodynamics. 2019;38:1086–92.
Borstad E, Skrede M, Rud T. Failure to predict and attempts to explain urinary stress incontinence following vaginal repair in continent women by using a modified lateral urethrocystography. Acta obstetricia et gynecologica Scandinavica. 1991;70:501–6.
Khayyami Y, Elmelund M, Lose G, Klarskov N. De novo urinary incontinence after pelvic organ prolapse surgery—a national database study. International urogynecology journal. 2020;31:305–8.
van der Ploeg JM, Rengerink KO, van der Steen A, et al. Vaginal prolapse repair with or without a midurethral sling in women with genital prolapse and occult stress urinary incontinence: a randomized trial. International urogynecology journal. 2016;27:1029–38.
Lakeman MM, Van Der Vaart CH, Van Der Steeg JW, Roovers J-PW, group Hs. Predicting the development of stress urinary incontinence 3 years after hysterectomy. International urogynecology journal. 2011;22:1179–84.
Costantini E, Zucchi A, Giannantoni A, Mearini L, Bini V, Porena M. Must colposuspension be associated with sacropexy to prevent postoperative urinary incontinence? European urology. 2007;51:788–94.
Frigerio M, Manodoro S, Palmieri S, Spelzini F, Milani R. Risk factors for stress urinary incontinence after native-tissue vaginal repair of pelvic organ prolapse. International Journal of Gynecology & Obstetrics. 2018;141:349–53.
Jelovsek JE. Predicting urinary incontinence after surgery for pelvic organ prolapse. Current opinion in obstetrics & gynecology. 2016;28:399.
Jelovsek JE, Chagin K, Lukacz ES, et al. Models for Predicting Recurrence, Complications, and Health Status in Women After Pelvic Organ Prolapse Surgery. Obstetrics and gynecology. 2018;132:298.
Figure 1.

The PRISMA flow diagram of study selection
The final list of selected articles (n=40) included 31 cohort studies, 6 randomized control trials, 1 case-control study, 1 case series, and 1 quasi-experimental study.[1,3,5,6,9,10,13,18,20–51]
The studies were categorized according to quality as low, moderate, and high groups (Table 2–6). We considered 3 levels of risk for the assessment of each article, 0%–35% (low risk), 35%–70% (moderate risk), and 70%–100% (high risk). Of the 40 studies that were included, 22 studies (55%) had low and 18 had moderate risk of bias (45%), but all 40 studies were included. No low-quality (high risk) studies were obtained. The study was approved by the Ethics Committee of Tabriz University of Medical Sciences and Iranian Registry of Clinical Trials.
Study characteristics
We retrieved any significant OR from the selected articles. If OR was not reported in a study, we calculated the OR using available data if possible. Appendix 3 describes the characteristics of selected studies. In 28 studies, the measurable risk factors were not reported (Appendix 3). In the included studies, the follow-up period was 3–12 months or more than 1 year, neither could be categorized as a long-term follow-up period. The major diagnostic tests used in the studies that reported measurable risk factors were urodynamic test (40%), pessary test (25%), and stress test (27.5%). In most of these studies, urodynamic variables were used for risk identification (5 of 12). In 15% (6 of 40) of the studies, the type of previously performed surgery was vaginal hysterectomy, and in 17.5% (7 of 40) of them, it was abdominal surgery. Owing to the high levels of heterogeneity, meta-analysis was not possible.
Appendix 3.
List of included articles and characteristics of selected articles
| # | Authors | Publication Year | Study type | Population | Inclusion criteria | Risk factors | Type of examination | Following | Type of surgery |
|---|---|---|---|---|---|---|---|---|---|
| 1 | E. Borstad & T. Rud1 | 1989 | Case-series | 102 | Women with POP surgeries without SUI | Urodynamic variables | The urodynamic examinations | 3 months | Manchester operation |
| 2 | A. Weil, et al2 | 1993 | Cohort | 40 | Women with POP surgeries without SUI | Urodynamic variables | Pessary test, Urodynamic test | 3–6 months | Vaginal surgery for genital prolapse |
| 3 | J. J. Klutke& S. Ramos3 | 2000 | Cohort | 125 | Women with POP surgeries without SUI | No risk factor | Pessary test, urodynamic evaluation | 3.5 year | Vaginal hysterectomy |
| 4 | C-C Liang, et al4 | 2004 | Cohort | 79 | Women with POP surgeries without SUI | Urodynamic variables | Pessary test | 1 month, 3 6 months, 1 year | Vaginal hysterectomy |
| 5 | A. Groutz, et al5 | 2004 | Cohort | 100 | Women with POP surgeries without SUI | No risk factor | Stress test, pad test | 27 month | Transvaginal prolapse repair and prophylactic TVT procedure |
| 6 | L. Brubaker, et al6 | 2006 | RCT | 322 | Women with POP surgeries without SUI | No risk factor | Stress test | 10 year | Abdominal Sacrocolpopexy with Burch Colposuspension |
| 7 | C. Reena, et al7 | 2007 | Cohort | 78 | Women with POP surgeries without SUI | Pessary test/Age, Menopausal | Pessary test | 6 weeks | Vaginal hysterectomy and pelvic floor repair |
| 8 | G. Wei, et al8 | 2009 | RCT | 337 | Women with POP surgeries without SUI | No risk factor | Cough test, stress test | 12 months | Vaginal prolapse surgery |
| 9 | M. Ek, et al9 | 2010 | Cohort | 121 | Women with POP surgeries without SUI | No risk factor | No test | 12 months | Trans vaginal mesh Surgery (TVM) |
| 10 | E. E. Duecy, et al10 | 2010 | Cohort | 41 | Women with POP surgeries without SUI | No risk factor | Cough stress test, urodynamic | 6 months | Vaginal surgery |
| 11 | R. M. Haverkorn, et al11 | 2011 | Cohort | 412 | Women with POP surgeries without SUI | BMI>30 | Cough stress test | Minimum of 12 months | Rectus fascia, porcine dermis and polypropylene sling procedures |
| 12 | A. M. E. Engh, et al12 | 2011 | Cohort | 100 | Women with POP surgeries without SUI | Pessary test, Speculum | Cough test, speculum test standardized quantification test and a 48-hour pad test, pessary test | 12 months | Vaginal surgery |
| 13 | E. Costantin, et al13 | 2011 | RCT | 66 | Women with POP surgeries without SUI | No risk factor | Urodynamic test, UDI-6 and IIQ-7 | 97 months | Abdominal pelvic organ prolapse repair |
| 14 | A. Liapis, et al14 | 2011 | Cohort | 82 | Women with POP surgeries without SUI | No risk factor | Pessary test, cough test | 24 month | TVT-O surgery |
| 15 | R. Svenningsen, et al15 | 2012 | Cohort | 204 | Women with POP surgeries without SUI | Pessary Test | Manual (100 ml), Pessary (100 ml), Pessary (300 ml), Pessary | Minimum of 3 months | POP repair (Manchester, vaginal hysterectomy Bio mesh, one or two compartments) |
| 16 | S. Ennemoser, et al16 | 2012 | Cohort | 491 | The women without SUI, underwent POP surgery | No risk factor | A stress test, a pad test and urodynamics test | 2–8 years | Vaginal prolapse surgery |
| 17 | J. T. Wei, et al17 | 2012 | RCT | 337 | Women with POP surgeries without SUI | No risk factor | Cough test, stress test | 12 month | Vaginal prolapse surgery |
| 18 | J. E. Jelovsek18 | 2013 | Cohort | 465 | Women with POP surgeries without SUI | No risk factor | Stress test, cough stress test | 12 month | Vaginal Prolapse, Midurethral Sling |
| 19 | B. A. Hafidh, et al19 | 2013 | Cohort | 64 | Women with POP surgeries without SUI | No risk factor | Urodynamics test, cough stress test | 12 month | Vaginal surgery |
| 20 | M. Kuribayashi, et al20 | 2013 | Cohort | 65 | Women with POP surgeries without SUI | Urethral obstruction moderate or more | Stress test | 6 month | Tension-free vaginal mesh procedure (TVM) |
| 21 | E. J. M. Lensen, et al21 | 2013 | Cohort | 907 | Women with POP surgeries without SUI | No risk factor | Preoperative tests | 12 months | POP surgery without concomitant UI surgery |
| 22 | L. Schierlitz, et al22 | 2014 | RCT | 845 | Women with POP surgeries without SUI | No risk factor | Urodynamic test, cough test | 6 month | Tension-free vaginal tape (TVT) |
| 23 | E. L. LeClaire, et al23 | 2014 | Cohort | 795 | Women with POP surgeries without SUI | No risk factor | Cough stress test | 15 weeks | Sacrocolpopexy (SCP) |
| 24 | D. El. Hamamsy& A. M. Fayyad 24 | 2015 | Cohort | 220 | Women with POP surgeries without SUI | No risk factor | Cough stress test, urodynamic test, POP-Q system | 12 months | Laparoscopic sacrocolpopexy |
| 25 | C-C Liang, et al25 | 2015 | Cohort | 183 | Women with POP surgeries without SUI | No risk factor | Urogynecological questionnaire, POP-quantitation system, urodynamic | 6 months and 12 months | Trans vaginal mesh (TVM) |
| 26 | T. Lo, et al26 | 2015 | Cohort | 637 | Women with POP surgeries without SUI | Urodynamic variables | Cough stress test, urodynamic test | 1 week, 6 months, annually | Pelvic reconstructive surgery (PRS) |
| 27 | S. Manodoro, et al27 | 2016 | Cohort | 150 | Women with POP surgeries without SUI | No risk factor | Urodynamic test, pessary test | 18.4 ± 9.0 month | Vaginal hysterectomy |
| 28 | X. Song, et al28 | 2016 | Cohort | 224 | Women with POP surgeries without SUI | No risk factor | Stress test, POP-Q system, 1-h pad test | 31 month | Vaginal prolapse surgery |
| 29 | A. H. Inan, et al29 | 2016 | Cohort | 145 | Women with POP surgeries without SUI | No risk factor | Cough test, validated Urinary Distress | 24 months | Abdominal sacrocolpopexy (ASC) |
| 30 | W. C. Huang& J. M. Yang30 | 2017 | Cohort | 102 | Women with POP surgeries without SUI | Mesh location (Straining) | Son graphic | 12 month | Pelvic reconstructive surgery |
| 31 | A. Ugianskiene, et al31 | 2017 | Cohort | 768 | Women with POP surgery, without SUI | Parity | Pessary test, stress test, incontinence-Vaginal Symptoms (ICIQ-VS) | 3 month | Cervix amputation/vaginal hysterectomy/vaginal vault suspension |
| 32 | S. Y. Wang, et al32 | 2017 | Case - control | 533 | The women who had no symptoms of SUI, underwent POP surgery | LUTO (lower urinary tract obstruction) | Cough leakage postoperatively, had positive 1-h pad test, urodynamics | 24 months | Pelvic reconstruction surgery. |
| 33 | J. F. C. Requena, et al33 | 2018 | Cohort | 39 | Women with symptomatic grade ≥ 2 POP and had no symptoms of SUI | No risk factor | Cough stress test, Ultrasound measurement of bladder volume, Urodynamic | 12 months | Vaginal surgery |
| 34 | J. M. van der Ploeg, et al34 | 2018 | Cohort | 362 | Women undergoing prolapse without a SUI | No risk factor | Stress tests | 12 months | Vaginal prolapse surgery |
| 35 | M. T. Davenport, et al35 | 2018 | RCT | 164 | Women undergoing prolapse repair without a SUI | Method of prolapse repair | Cough and Valsalva test, urodynamic test | 3 months | Prolapse surgery, (abdominal sacrocolpopexy) |
| 36 | J. Sabadell, et al36 | 2019 | Cohort | 169 | Women who underwent POP surgical correction, without a SUI | No risk factor | Cough stress test, diagnostic test | 10 month | Vaginal mesh repair |
| 37 | E. Goessens, et al37 | 2019 | Cohort | 220 | Women with symptomatic POP, but without bothersome SUI | No risk factor | Pessary test | 2 month | Vaginal prolapse repair |
| 38 | T. Lo, et al | 2019 | Cohort | 40 | Patients underwent mesh surgery and had no symptoms of SUI | No risk factor | Cough stress test, urodynamic test, 2D introital ultrasonography | 1 week, 6 months, and annually | Midurethral sling (MUS), vaginal pelvic reconstructive surgery (PRS) |
| 39 | T. Sierra, et al39 | 2019 | Cohort | 223 | Women without symptoms of SUI. | No risk factor | Stress test | 6 month | POP repair UDS and subsequent prolapse surgery. |
| 40 | M. Kurdoglu, et al40 | 2019 | Cohort | 48 | Patients underwent RALUSLS and RALSC, and had no symptoms of SUI | No risk factor | POP Quantification system (POP-Q), urodynamic | 3 month | RALUSLS and RALSC procedures |
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Risk factors for SUI
The results showed that 3 studies suggested age >60, ≥50, and ≥66 years (OR, 0.024 [95% CI, 0.001–0.416], OR, 2.07 [95% CI, 0.41–10.41], and OR, 2.86 [95% CI, 1.01–2.53], respectively) as the most prevalent risk or predictive factor for de novo SUI occurrence. In contrast, 2 studies suggested positive pessary testing (300 mL) (OR, 6.5 [95% CI, 1.6–25.4] and RR, 0.35 [95% CI, 0.25–0.51], respectively) as the most prevalent risk or predictive factor. Table 1 shows the extracted risk factors and their characteristics, and Table 7 shows the definitions of risk factors and characteristics of de novo SUI. For urodynamic characteristics, only 1 study mentioned abdominal leak point pressures (ALPPs) as a risk without any objective measurement or statistical analysis. They demonstrated the ALPP reduction range after correction and reposition of prolapse as a risk for de novo incontinence; however, the study had a small sample size and low-quality method. Low maximum urethral closure pressure (MUCP) (OR, 4.65 [95% CI, 2.87–8.64]) was the most prevalent variable (Table 1).
Table 7.
Definition of risks and characteristics of de novo SUI
| # | Risks and characteristics | Definition | Frequency of statistical significance |
|---|---|---|---|
| 1 | Age | 60–70 years=high risk | 3 |
| 2 | Pessary test (300 mL) | “A positive pessary test could predict postsurgical stress urinary incontinence in women with severe pelvic organ prolapse. Pessaries are widely considered to be a safe and effective management option for women with pelvic organ prolapse.” Positive test=high risk | 3 |
| 3 | History of pelvic surgery | Previous pelvic=high risk | 2 |
| 4 | MUCP | “MUCP is the maximum difference between the urethral pressure and the intravesical pressure.” MUCP <60 cmH2O=high risk | 2 |
| 5 | FUL, mm | “FUL is the length of the urethra along which the urethral pressure exceeds intravesical pressure in women.” FUL <2 mm (high risk) | 1 |
| 6 | PTR | PTR is the increment in urethral pressure on stress as a percentage §of the simultaneously recorded increment in intravesical pressure. PTR <100% (high risk) | 1 |
| 7 | TVM | TVM, type (Prolift T, Elevate A)=high risk | 1 |
| 8 | LUTO LUTO detected by UDS (Q max ≤12 mL/s and PdetQ max ≥25 cmH2O or residual urine ≥100 mL)=high risk | 1 | |
| 9 | Parity | Parity >4=high risk | 1 |
| 10 | Diabetes | Diabetes positive=high risk | 1 |
| 11 | Menopause | Menopause positive=high risk | 1 |
| 12 | Urethral obstruction moderate or more | Urethral obstruction moderate or more=high risk | 1 |
| 13 | BMI | BMI ≥30=high risk | 1 |
MUCP: maximum urethral closure pressure; FUL: functional urethral length; PTR: pressure transmission ratio; TVM: transvaginal mesh surgery; LUTO: lower urinary tract obstruction; BMI: body mass index; UDS: Urodynamic study; PdetQ: detrusor pressure at maximal flow
Discussion
This systematic review was an overview of the risk factors for de novo SUI in women undergoing POP surgery. Moreover, 50%–80% of patients with POP have UI simultaneously,[20] and women with severe prolapse complain of SUI 10%–30% more than those with mild to moderate prolapse.[21] According to the results of this review, the main risk factors for de novo UI after prolapse surgery in women were older age (>50 years), positive pessary testing, previous pelvic surgery, obesity, menopause, moderate or severe urethral obstruction/compression, and diabetes. Low MUCP, ALPPs, functional urethral length (FUL), and lower urinary tract obstruction were the most important urodynamic variables in the incidence of UI. Genetic factors could also play an important role in UI and POP, but the effects of environmental factors cannot be underestimated.[9] Although risk factors such as smoking, age, diabetes, obesity, pregnancy, and childbirth are presumed to increase the risk of de novo UI after POP surgery, we did not find strong evidence regarding the effect of smoking and parity on SUI. In our study, positive pessary testing was a strong predictive factor. This was in line with several studies that reported pessary testing as a strong predictor of de novo UI.[13,22,23]
ALPPs can be considered a risk factor for de novo SUI. ALPPs are defined as the amount of abdominal pressure needed to produce a urine leak from the urethra. In fact, if there is a leak of urine during an abdominal pressure-boosting maneuver, such as a cough or a Valsalva maneuver, nonhypertensive blood pressure causes weight gain. If ALPP is measured as standard, it has the ability to validate duct sphincter resistance. ALPP is also useful in determining the type of cause of incontinence as well as the type of surgery for stress incontinence. Occasionally, in patients with stress urinary incontinence, an ALPP of less than 60 cmH2O is observed.
The ALPP measurement method is not standardized yet, we do not yet have any specific factors for standard ALPP factors, and no specific standards have been used in the studies.
Positive pessary testing results usually occur in women with severe POP before surgery. There are individuals who do not have SUI and suffer from severe POP with a positive pessary testing result. This can be considered as a potential postsurgical risk for SUI.[24] Urodynamic testing also plays a major role in predicting de novo SUI after surgery.[25,26] In this study, we evaluated the urodynamic variables and showed that these variables are important in predicting de novo SUI. However, these tests are costly for the patients.[52] If after POP surgery, urodynamic tests show certain values (i.e., CP [cmH2O] and pressure transmission ratio <100), there is a chance that one can predict the occurrence of SUI. Urodynamic test alone cannot predict the severity of incontinence,[20] but adding a urodynamic test may predict the risk of UI after surgery[9]. Age can also play an important role in increasing the risk of UI because that has been shown in several studies.[19,20] Combined POP surgery and prophylactic surgeries for SUI may prevent occult incontinence that occurs after POP surgery in such cases.[22] Although the tests can be used to predict the risk of UI before the surgery, studies indicated that it could help the surgeons in only 17%–39% of the cases. In the predictive model provided by Jelovsek et al., [28] risk factors, such as age, diabetes, smoking, parity, and body mass index, were similarly identified as candidates for de novo UI risk assessment. It seems that age and obesity have a greater impact on the incidence of UI.
To the best of our knowledge, most of the previous studies reported the risks of UI after surgery individually. In contrast, this is the first study to simultaneously study several risk factors, which can provide a clearer vision on the impact of risk factors in developing SUI after POP surgery. As a work in progress, this team is designing and developing a predictor system for the risk of using the extracted risk factors in this review. One of the limitations of this study was the lack of access to the raw data of all selected studies; thus, we obtained the risk on the basis of the data reported in the articles. In one of the studies, parity was considered a risk for developing de novo UI by including SUI as a subtype of incontinence; however, parity was not specifically identified as a risk for SUI.[29] Moreover, OR was not calculated for this risk factor because of inssufficient raw data. Furthermore, we did not consider abdominal sacrocolpopexy as a risk because of the low number of cases.[53]
In summary, several factors are recognized as risk factors for UI. However, there are no strong evidences to categorize the risk factors based on importance. This can be achieved in a well-designed original study.
Main Points.
According to our study, a positive pessary test had the highest risk or predictor compared with other diagnostic tests.
In this study, low maximum urethral closure pressure (MUCP), functional urethral length, and lower urinary tract obstruction were the most important urodynamic variables in the incidence of urinary incontinence, and MUCP was the most common among them.
In total, 3 studies suggested that the most important predictors of urinary incontinence after pelvic organ prolapse surgery were positive pessary testing, age >50 years, and MUCP <60 cmH2O.
Acknowledgements
We hereby gratefully acknowledge the Research Center for Evidence-Based Medicine, Tabriz University of Medical Sciences.
Footnotes
Ethics Committee Approval: Ethics committee approval was received for this study from the ethics committee of IR.TBZMED.REC (1398200).
Informed Consent: N/A.
Peer-review: Externally peer-reviewed.
Author Contributions: Concept – S.Y.M., S.H.; Design – S.H., T.S.S.; Supervision – S.H.; Resources – S.Y.M., S.H., F.S.G.; Materials – S.Y.M., S.H., T.S.S.; Data Collection and/or Processing – S.Y.M., F.S.G.; Analysis and/or Interpretation – S.Y.M., S.H., F.S.G.; Literature Search – S.H., F.P.; Writing Manuscript – S.Y.M., S.H., T.S.S., F.S.G.; Critical Review – S.Y.M., S.H., N.A.
Conflict of Interest: The authors have no conflicts of interest to declare.
Financial Disclosure: This study was supported by Tabriz University of Medical Sciences under Grant No. 62520.
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