Pub Date : 2026-01-01DOI: 10.1097/SPV.0000000000001660
Uduak U Andy, Benjamin Carper, Halina Zyczynski, Abhishek Sripad, Keisha Y Dyer, Joseph Schaffer, Donna Mazloomdoost, Marie G Gantz
Objective: This study aimed to determine the effect of a run-in period on fecal incontinence (FI) symptom severity.
Study design: This study conducted a planned secondary analysis of the run-in period to a study evaluating the effect of 12-week treatment with percutaneous tibial nerve stimulation versus sham in reducing FI severity in women. All participants completed a 4-week run-in period designed to exclude from randomization women whose symptoms reduced below the eligibility threshold after receiving education on FI and completing bowel diaries. Change in St Mark's (Vaizey) score and weekly FI episodes during the run-in period (week 1 vs week 4) was assessed.
Results: One hundred and eighty-five women completed the run-in period. The mean St Mark's (Vaizey) score was 17.8 ± 2.6 and 16.9 ± 3.5 at week 1 and week 4, respectively. There was no significant change in the St Mark's (Vaizey) score from week 1 to week 4 (mean change, -0.93 [95% CI, -1.56 to -0.31]). The average number of FI episodes per week did not change significantly between week 1 and week 4, nor did other bowel diary measures. Only 11 (6%) women became ineligible for the trial following the run-in period, all of whom had baseline St Mark's (Vaizey) scores of 18 or lower.
Conclusions: Completion of a bowel diary and receiving education on FI during the 4-week run-in period did not significantly affect symptom severity in women with FI. Only 6% of women became ineligible for participation following the run-in period, suggesting that, in a refractory population, a run-in period may have minimal effect.
{"title":"Impact of Bowel Diary Completion and Education on Fecal Incontinence Severity.","authors":"Uduak U Andy, Benjamin Carper, Halina Zyczynski, Abhishek Sripad, Keisha Y Dyer, Joseph Schaffer, Donna Mazloomdoost, Marie G Gantz","doi":"10.1097/SPV.0000000000001660","DOIUrl":"10.1097/SPV.0000000000001660","url":null,"abstract":"<p><strong>Objective: </strong>This study aimed to determine the effect of a run-in period on fecal incontinence (FI) symptom severity.</p><p><strong>Study design: </strong>This study conducted a planned secondary analysis of the run-in period to a study evaluating the effect of 12-week treatment with percutaneous tibial nerve stimulation versus sham in reducing FI severity in women. All participants completed a 4-week run-in period designed to exclude from randomization women whose symptoms reduced below the eligibility threshold after receiving education on FI and completing bowel diaries. Change in St Mark's (Vaizey) score and weekly FI episodes during the run-in period (week 1 vs week 4) was assessed.</p><p><strong>Results: </strong>One hundred and eighty-five women completed the run-in period. The mean St Mark's (Vaizey) score was 17.8 ± 2.6 and 16.9 ± 3.5 at week 1 and week 4, respectively. There was no significant change in the St Mark's (Vaizey) score from week 1 to week 4 (mean change, -0.93 [95% CI, -1.56 to -0.31]). The average number of FI episodes per week did not change significantly between week 1 and week 4, nor did other bowel diary measures. Only 11 (6%) women became ineligible for the trial following the run-in period, all of whom had baseline St Mark's (Vaizey) scores of 18 or lower.</p><p><strong>Conclusions: </strong>Completion of a bowel diary and receiving education on FI during the 4-week run-in period did not significantly affect symptom severity in women with FI. Only 6% of women became ineligible for participation following the run-in period, suggesting that, in a refractory population, a run-in period may have minimal effect.</p>","PeriodicalId":75288,"journal":{"name":"Urogynecology (Hagerstown, Md.)","volume":" ","pages":"3-8"},"PeriodicalIF":1.2,"publicationDate":"2026-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12353015/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143517443","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-01DOI: 10.1097/SPV.0000000000001679
Pedro Alvarez, Cem Demirkiran, Leslie Rickey, Lisbet Lundsberg, Oz Harmanli
Importance: Postoperative activity restrictions can affect patient satisfaction after midurethral sling (MUS) surgery.
Objective: The aim of the study was to assess the effect of a duration of postoperative activity restrictions on patient satisfaction and surgical outcomes after MUS surgery for stress urinary incontinence.
Study design: Women undergoing MUS surgery alone for stress urinary incontinence were enrolled in this provider-blinded, randomized clinical trial. Randomization to either 3- or 6-weeks' duration of activity restrictions was assigned. Restrictions included abstaining from lifting greater than 20 pounds, high-impact activity, or strenuous exercise. Primary outcome was patient satisfaction with surgery, using a 5-point Likert patient satisfaction scale. Satisfaction scores were analyzed in a "complete satisfaction" ("completely" satisfied only) and a "higher satisfaction" approach (both "completely" and "mostly" satisfied). Secondary outcomes included objective and subjective assessment of incontinence symptoms and activity assessment.
Results: Ninety-eight women underwent MUS surgery between July 2021 and September 2022, and 88 were randomized. Of them, 41 and 43 women with 3- and 6-week restrictions had patient satisfaction data, respectively. Baseline characteristics did not differ between groups. At the 6-month postoperative visit, overall patient satisfaction ("completely" and "mostly" satisfied) was very high at 92%. Complete satisfaction was significantly higher in the 3-week (73.2%) versus the 6-week restriction group (51.2%) ( P = 0.04). "Higher satisfaction" did not reach a statically significant difference between groups ( P = 0.11). Subjective urinary incontinence indices did not differ between groups.
Conclusions: Return to normal activities 3 weeks after MUS surgery resulted in significantly higher satisfaction scores at 6 months compared to a 6-week restriction without compromising subjective and objective surgical success.
{"title":"Activity Restrictions After Midurethral Sling: A Randomized Controlled Trial.","authors":"Pedro Alvarez, Cem Demirkiran, Leslie Rickey, Lisbet Lundsberg, Oz Harmanli","doi":"10.1097/SPV.0000000000001679","DOIUrl":"10.1097/SPV.0000000000001679","url":null,"abstract":"<p><strong>Importance: </strong>Postoperative activity restrictions can affect patient satisfaction after midurethral sling (MUS) surgery.</p><p><strong>Objective: </strong>The aim of the study was to assess the effect of a duration of postoperative activity restrictions on patient satisfaction and surgical outcomes after MUS surgery for stress urinary incontinence.</p><p><strong>Study design: </strong>Women undergoing MUS surgery alone for stress urinary incontinence were enrolled in this provider-blinded, randomized clinical trial. Randomization to either 3- or 6-weeks' duration of activity restrictions was assigned. Restrictions included abstaining from lifting greater than 20 pounds, high-impact activity, or strenuous exercise. Primary outcome was patient satisfaction with surgery, using a 5-point Likert patient satisfaction scale. Satisfaction scores were analyzed in a \"complete satisfaction\" (\"completely\" satisfied only) and a \"higher satisfaction\" approach (both \"completely\" and \"mostly\" satisfied). Secondary outcomes included objective and subjective assessment of incontinence symptoms and activity assessment.</p><p><strong>Results: </strong>Ninety-eight women underwent MUS surgery between July 2021 and September 2022, and 88 were randomized. Of them, 41 and 43 women with 3- and 6-week restrictions had patient satisfaction data, respectively. Baseline characteristics did not differ between groups. At the 6-month postoperative visit, overall patient satisfaction (\"completely\" and \"mostly\" satisfied) was very high at 92%. Complete satisfaction was significantly higher in the 3-week (73.2%) versus the 6-week restriction group (51.2%) ( P = 0.04). \"Higher satisfaction\" did not reach a statically significant difference between groups ( P = 0.11). Subjective urinary incontinence indices did not differ between groups.</p><p><strong>Conclusions: </strong>Return to normal activities 3 weeks after MUS surgery resulted in significantly higher satisfaction scores at 6 months compared to a 6-week restriction without compromising subjective and objective surgical success.</p>","PeriodicalId":75288,"journal":{"name":"Urogynecology (Hagerstown, Md.)","volume":" ","pages":"58-64"},"PeriodicalIF":1.2,"publicationDate":"2026-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12708032/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143659982","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-12-31DOI: 10.1097/SPV.0000000000001783
Lauren Simms, Cynthia Hall, Katherine Leung, Emily Wu, Charlotte Cipparone, Kunal Patel, Michael Flynn
Importance: Constipation is a common and bothersome problem for many patients with prolapse. This study attempts to understand rates of constipation following abdominal and vaginal prolapse surgical procedures.
Objective: The objective of this study was to evaluate whether sacral colpopexy increases postoperative constipation compared with vaginal prolapse surgery.
Study design: This was a prospective cohort study of participants undergoing surgery for apical prolapse at a single academic urogynecology practice. Preoperative, intraoperative, and 6-week and 6-month postoperative data were collected. The Patient Assessment of Constipation Symptoms (PAC-SYM) questionnaire was utilized to assess for constipation preoperatively and postoperatively. The primary outcome measure was the difference in PAC-SYM scores from preoperative evaluation to 6 weeks postoperatively between those who underwent sacral colpopexy (abdominal group) and those who underwent vaginal prolapse surgery (vaginal group). Unadjusted and adjusted linear regression were used to evaluate the change in PAC-SYM.
Results: Ninety-seven participants were enrolled in the study, and 6-week postoperative data were available for 91 participants (50 participants in the abdominal group and 41 participants in the vaginal group). Forty-three percent of participants had preoperative constipation. There were no statistically significant changes in total or subscale PAC-SYM scores at 6 weeks or 6 months postoperatively. At 6 weeks, more participants in the abdominal group had changes in the number of weekly bowel movements than the vaginal group.
Conclusions: Constipation is common among women with pelvic organ prolapse. Symptoms of constipation do not significantly change after prolapse surgery. Sacral colpopexy does not appear to worsen constipation postoperatively compared with vaginal prolapse surgery.
{"title":"Does Sacral Colpopexy Increase Constipation Compared With Vaginal Prolapse Surgery?","authors":"Lauren Simms, Cynthia Hall, Katherine Leung, Emily Wu, Charlotte Cipparone, Kunal Patel, Michael Flynn","doi":"10.1097/SPV.0000000000001783","DOIUrl":"https://doi.org/10.1097/SPV.0000000000001783","url":null,"abstract":"<p><strong>Importance: </strong>Constipation is a common and bothersome problem for many patients with prolapse. This study attempts to understand rates of constipation following abdominal and vaginal prolapse surgical procedures.</p><p><strong>Objective: </strong>The objective of this study was to evaluate whether sacral colpopexy increases postoperative constipation compared with vaginal prolapse surgery.</p><p><strong>Study design: </strong>This was a prospective cohort study of participants undergoing surgery for apical prolapse at a single academic urogynecology practice. Preoperative, intraoperative, and 6-week and 6-month postoperative data were collected. The Patient Assessment of Constipation Symptoms (PAC-SYM) questionnaire was utilized to assess for constipation preoperatively and postoperatively. The primary outcome measure was the difference in PAC-SYM scores from preoperative evaluation to 6 weeks postoperatively between those who underwent sacral colpopexy (abdominal group) and those who underwent vaginal prolapse surgery (vaginal group). Unadjusted and adjusted linear regression were used to evaluate the change in PAC-SYM.</p><p><strong>Results: </strong>Ninety-seven participants were enrolled in the study, and 6-week postoperative data were available for 91 participants (50 participants in the abdominal group and 41 participants in the vaginal group). Forty-three percent of participants had preoperative constipation. There were no statistically significant changes in total or subscale PAC-SYM scores at 6 weeks or 6 months postoperatively. At 6 weeks, more participants in the abdominal group had changes in the number of weekly bowel movements than the vaginal group.</p><p><strong>Conclusions: </strong>Constipation is common among women with pelvic organ prolapse. Symptoms of constipation do not significantly change after prolapse surgery. Sacral colpopexy does not appear to worsen constipation postoperatively compared with vaginal prolapse surgery.</p>","PeriodicalId":75288,"journal":{"name":"Urogynecology (Hagerstown, Md.)","volume":" ","pages":""},"PeriodicalIF":1.2,"publicationDate":"2025-12-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145936560","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Importance: Social and structural barriers affect access to urogynecologic care for underserved patients, but few studies explore patient experiences at federally qualified health centers (FQHCs).
Objective: The objective of this study was to identify barriers to accessing urogynecologic care from the patient perspective at an FQHC affiliated with an academic medical center.
Study design: Female-identifying patients ages 18-100 years who were referred for and subsequently missed their new urogynecology appointment from October 1, 2022, through February 28, 2023, were recruited for participation in qualitative interviews. A semi-structured interview guide was used for telephone interviews. Transcripts were coded thematically using grounded theory until theoretical saturation was reached.
Results: Thematic saturation occurred with 17 participants. Participants were predominantly Hispanic, the mean age was 55 years, and most were insured by Medicaid or self-pay. The most common referral diagnosis was urinary incontinence (n=13). Major themes regarding barriers included scheduling issues, transportation, language barriers, and perceived costs. All participants identified at least 1 barrier to accessing urogynecologic care, with scheduling challenges related to poor communication from clinic staff as the most common reason. Transportation was the second most cited barrier.
Conclusions: Barriers to accessing urogynecology care are prevalent, even at FQHCs with dedicated subspecialists on site. Poor communication and transportation were the most cited barriers. These findings can inform quality improvement projects to increase access to urogynecologic care in these settings. It is imperative that women's health providers advocate for expanded access and implement changes to address these inequalities in urogynecologic care.
{"title":"Barriers to Accessing Urogynecologic Care in a Federally Qualified Health Center.","authors":"Xiomara Brioso, Rebecca Borneman, Liz Yanes, Ayomipo Madein, Abigail Davenport, Nancy Ringel","doi":"10.1097/SPV.0000000000001782","DOIUrl":"10.1097/SPV.0000000000001782","url":null,"abstract":"<p><strong>Importance: </strong>Social and structural barriers affect access to urogynecologic care for underserved patients, but few studies explore patient experiences at federally qualified health centers (FQHCs).</p><p><strong>Objective: </strong>The objective of this study was to identify barriers to accessing urogynecologic care from the patient perspective at an FQHC affiliated with an academic medical center.</p><p><strong>Study design: </strong>Female-identifying patients ages 18-100 years who were referred for and subsequently missed their new urogynecology appointment from October 1, 2022, through February 28, 2023, were recruited for participation in qualitative interviews. A semi-structured interview guide was used for telephone interviews. Transcripts were coded thematically using grounded theory until theoretical saturation was reached.</p><p><strong>Results: </strong>Thematic saturation occurred with 17 participants. Participants were predominantly Hispanic, the mean age was 55 years, and most were insured by Medicaid or self-pay. The most common referral diagnosis was urinary incontinence (n=13). Major themes regarding barriers included scheduling issues, transportation, language barriers, and perceived costs. All participants identified at least 1 barrier to accessing urogynecologic care, with scheduling challenges related to poor communication from clinic staff as the most common reason. Transportation was the second most cited barrier.</p><p><strong>Conclusions: </strong>Barriers to accessing urogynecology care are prevalent, even at FQHCs with dedicated subspecialists on site. Poor communication and transportation were the most cited barriers. These findings can inform quality improvement projects to increase access to urogynecologic care in these settings. It is imperative that women's health providers advocate for expanded access and implement changes to address these inequalities in urogynecologic care.</p>","PeriodicalId":75288,"journal":{"name":"Urogynecology (Hagerstown, Md.)","volume":" ","pages":""},"PeriodicalIF":1.2,"publicationDate":"2025-12-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12885760/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145812348","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-12-01DOI: 10.1097/SPV.0000000000001734
Omar Mesina, Emily S Lukacz
Importance: Single-incision slings (SIS) offer a minimally invasive option for treating stress urinary incontinence (SUI), aiming to reduce operative time, postoperative pain, and recovery compared to traditional slings. Their growing use underscores the importance of understanding their effectiveness, safety profile, and long-term outcomes to ensure optimal patient care.
Objective: The objective was to update current evidence on the safety, efficacy, and economic impact of SISs for the treatment of SUI in women.
Study design: A structured literature review was conducted using PubMed, Cochrane Library, and the U.S. Food and Drug Administration (FDA) 522 Postmarket Surveillance Studies Database up to December 2024. Inclusion criteria were randomized controlled trials, prospective observational studies, meta-analyses and the FDA summary addressing SIS outcomes. Key metrics included objective and subjective cure rates, complications, and economic evaluations.
Results: A total of 28 publications were reviewed since the most recent Cochrane review in 2023. Overall, high subjective (73.3% to 94.2%) and objective cure rates (61.5% to 94%) continue to be reported for SISs with operative times of 10.7 to 20.4 min and low adverse events of mesh complications (0% to 14.2%), reintervention procedures (0% to 16.3%) and de novo urgency urinary incontinence (0% to 15%) up to 36 months. Economic analyses revealed short-term cost savings for SISs, particularly in outpatient settings under local anesthesia, though cost-effectiveness over longer periods remains uncertain due to potential retreatment and/or complications.
Conclusions: Single-incision slings offer a minimally invasive option for SUI with comparable efficacy to full-length midurethral slings, with rare perioperative complications and short operative times. Long-term outcomes on complications and durability are needed. Future studies are needed to guide clinical decision making, particularly regarding longer-term complications and cost-effectiveness.
{"title":"Update on Single-Incision Slings.","authors":"Omar Mesina, Emily S Lukacz","doi":"10.1097/SPV.0000000000001734","DOIUrl":"10.1097/SPV.0000000000001734","url":null,"abstract":"<p><strong>Importance: </strong>Single-incision slings (SIS) offer a minimally invasive option for treating stress urinary incontinence (SUI), aiming to reduce operative time, postoperative pain, and recovery compared to traditional slings. Their growing use underscores the importance of understanding their effectiveness, safety profile, and long-term outcomes to ensure optimal patient care.</p><p><strong>Objective: </strong>The objective was to update current evidence on the safety, efficacy, and economic impact of SISs for the treatment of SUI in women.</p><p><strong>Study design: </strong>A structured literature review was conducted using PubMed, Cochrane Library, and the U.S. Food and Drug Administration (FDA) 522 Postmarket Surveillance Studies Database up to December 2024. Inclusion criteria were randomized controlled trials, prospective observational studies, meta-analyses and the FDA summary addressing SIS outcomes. Key metrics included objective and subjective cure rates, complications, and economic evaluations.</p><p><strong>Results: </strong>A total of 28 publications were reviewed since the most recent Cochrane review in 2023. Overall, high subjective (73.3% to 94.2%) and objective cure rates (61.5% to 94%) continue to be reported for SISs with operative times of 10.7 to 20.4 min and low adverse events of mesh complications (0% to 14.2%), reintervention procedures (0% to 16.3%) and de novo urgency urinary incontinence (0% to 15%) up to 36 months. Economic analyses revealed short-term cost savings for SISs, particularly in outpatient settings under local anesthesia, though cost-effectiveness over longer periods remains uncertain due to potential retreatment and/or complications.</p><p><strong>Conclusions: </strong>Single-incision slings offer a minimally invasive option for SUI with comparable efficacy to full-length midurethral slings, with rare perioperative complications and short operative times. Long-term outcomes on complications and durability are needed. Future studies are needed to guide clinical decision making, particularly regarding longer-term complications and cost-effectiveness.</p>","PeriodicalId":75288,"journal":{"name":"Urogynecology (Hagerstown, Md.)","volume":" ","pages":"1090-1100"},"PeriodicalIF":1.2,"publicationDate":"2025-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145202408","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-11-25DOI: 10.1097/SPV.0000000000001708
Caitlyn E Painter, Douglas Stram, Victor S Velasco, Wenjin Cheng, Abner Korn, Olga Ramm
Importance: Antimuscarinic medications are widely used for overactive bladder (OAB). Recent studies linking antimuscarinics to dementia and cognitive impairment (DCI) have raised concerns about long-term antimuscarinic use for OAB management.
Objectives: We sought to investigate the incidence of DCI among patients with OAB and whether DCI incidence is associated with antimuscarinic use.
Study design: We conducted a retrospective cohort study of women aged 55 years or older with OAB, without a preexisting DCI diagnosis, within a managed health care system with at least 10 years of follow-up. Participants were divided into 2 groups: antimuscarinic users and nonusers for OAB. We calculated each participant's total antimuscarinic burden and identified incident DCI using International Classification of Diseases codes. We used bivariate analysis to identify factors associated with DCI and multivariate logistic regression to assess the association between antimuscarinic use and DCI.
Results: Of the 16,249 women included, 7,141 (44%) received antimuscarinics for OAB and 1,200 (7.4%) were diagnosed with DCI. Compared with those without DCI, women with DCI were older, less likely to be white, had more comorbidities, were more likely to use antimuscarinics, and had higher mean anticholinergic burden scores. Age at OAB diagnosis (OR: 1.13, CI: 1.12-1.14, P <0.001), diabetes (OR: 1.43, CI: 1.22-1.68, P <0.001), and bladder antimuscarinic use (OR: 1.27, CI: 1.12-1.44, P <0.001) were associated with incident DCI using multivariate analysis.
Conclusions: Among women with OAB, DCI is associated with bladder antimuscarinic use and with higher cumulative exposure to antimuscarinics. This association persists after controlling for age and comorbidities.
{"title":"Antimuscarinic Use and Dementia Incidence in Women With Overactive Bladder.","authors":"Caitlyn E Painter, Douglas Stram, Victor S Velasco, Wenjin Cheng, Abner Korn, Olga Ramm","doi":"10.1097/SPV.0000000000001708","DOIUrl":"10.1097/SPV.0000000000001708","url":null,"abstract":"<p><strong>Importance: </strong>Antimuscarinic medications are widely used for overactive bladder (OAB). Recent studies linking antimuscarinics to dementia and cognitive impairment (DCI) have raised concerns about long-term antimuscarinic use for OAB management.</p><p><strong>Objectives: </strong>We sought to investigate the incidence of DCI among patients with OAB and whether DCI incidence is associated with antimuscarinic use.</p><p><strong>Study design: </strong>We conducted a retrospective cohort study of women aged 55 years or older with OAB, without a preexisting DCI diagnosis, within a managed health care system with at least 10 years of follow-up. Participants were divided into 2 groups: antimuscarinic users and nonusers for OAB. We calculated each participant's total antimuscarinic burden and identified incident DCI using International Classification of Diseases codes. We used bivariate analysis to identify factors associated with DCI and multivariate logistic regression to assess the association between antimuscarinic use and DCI.</p><p><strong>Results: </strong>Of the 16,249 women included, 7,141 (44%) received antimuscarinics for OAB and 1,200 (7.4%) were diagnosed with DCI. Compared with those without DCI, women with DCI were older, less likely to be white, had more comorbidities, were more likely to use antimuscarinics, and had higher mean anticholinergic burden scores. Age at OAB diagnosis (OR: 1.13, CI: 1.12-1.14, P <0.001), diabetes (OR: 1.43, CI: 1.22-1.68, P <0.001), and bladder antimuscarinic use (OR: 1.27, CI: 1.12-1.44, P <0.001) were associated with incident DCI using multivariate analysis.</p><p><strong>Conclusions: </strong>Among women with OAB, DCI is associated with bladder antimuscarinic use and with higher cumulative exposure to antimuscarinics. This association persists after controlling for age and comorbidities.</p>","PeriodicalId":75288,"journal":{"name":"Urogynecology (Hagerstown, Md.)","volume":" ","pages":""},"PeriodicalIF":1.2,"publicationDate":"2025-11-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145662884","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-11-24DOI: 10.1097/SPV.0000000000001765
Rodger W Rothenberger, Jeremy T Gaskins, Laurel Carbone, Kathryn Seymour, Stacy M Lenger, Sean Francis, Ankita Gupta
Importance: When treating pelvic organ prolapse (POP) through surgery, age may factor into joint decision making for surgeons and patients.
Objective: The objective of this study was to determine if 30-day perioperative outcomes after POP surgery vary by age.
Study design: This was a retrospective cohort study of women who underwent surgery for POP using the 2011-2022 American College of Surgeons National Surgical Quality Improvement Program database. Composite rates of adverse events were categorized as major complications (deep/organ space surgical site infection [SSI], reintubation, renal failure, wound dehiscence, pulmonary embolism, cardiac arrest, myocardial infarction, deep vein thrombosis, sepsis, septic shock, return to operating room, stroke, and death) or minor complications (pneumonia, blood transfusion, superficial SSI, or urinary tract infection). Multivariate logistic regression models were used to assess the association between patient age and perioperative complications after adjusting for relevant variables. Interaction models were created to determine if age modulates the effect of procedure type (apical, nonapical, obliterative prolapse surgery) or concomitant hysterectomy on risk of complications.
Results: We included 133,058 women (aged 18-59 years, n=60,659, 45.6%; aged 60-69 years, n=37,818, 28.4%; aged 70-79 years, n=27,598, 20.7%; aged 80 years and older, n=6,983, 5.2%) who underwent POP surgical procedures. On multivariate logistic regression, relative to patients younger than 60 years, age groups 60-69 years and 70-79 years had significantly lower rates of major complications (60-69 years: adjusted odds ratio [aOR]=0.68 [0.62-0.74]; 70-79 years: aOR=0.71 [0.64-0.78]) and patients older than 80 years had similar rates of major complications (aOR=0.98 [0.86-1.12]). In the patients younger than 60 years, the addition of a hysterectomy to a prolapse procedure carried a slightly increased risk of major complications (aOR=1.19, 95% CI=1.06-1.32). No other group carried an increased risk of major complications when adding a hysterectomy or performing an apical or obliterative repair.
Conclusion: This study shows a low risk of complications after POP procedures, even in patients older than 80 years.
{"title":"Association of Age With Adverse Events After Pelvic Organ Prolapse Surgery.","authors":"Rodger W Rothenberger, Jeremy T Gaskins, Laurel Carbone, Kathryn Seymour, Stacy M Lenger, Sean Francis, Ankita Gupta","doi":"10.1097/SPV.0000000000001765","DOIUrl":"https://doi.org/10.1097/SPV.0000000000001765","url":null,"abstract":"<p><strong>Importance: </strong>When treating pelvic organ prolapse (POP) through surgery, age may factor into joint decision making for surgeons and patients.</p><p><strong>Objective: </strong>The objective of this study was to determine if 30-day perioperative outcomes after POP surgery vary by age.</p><p><strong>Study design: </strong>This was a retrospective cohort study of women who underwent surgery for POP using the 2011-2022 American College of Surgeons National Surgical Quality Improvement Program database. Composite rates of adverse events were categorized as major complications (deep/organ space surgical site infection [SSI], reintubation, renal failure, wound dehiscence, pulmonary embolism, cardiac arrest, myocardial infarction, deep vein thrombosis, sepsis, septic shock, return to operating room, stroke, and death) or minor complications (pneumonia, blood transfusion, superficial SSI, or urinary tract infection). Multivariate logistic regression models were used to assess the association between patient age and perioperative complications after adjusting for relevant variables. Interaction models were created to determine if age modulates the effect of procedure type (apical, nonapical, obliterative prolapse surgery) or concomitant hysterectomy on risk of complications.</p><p><strong>Results: </strong>We included 133,058 women (aged 18-59 years, n=60,659, 45.6%; aged 60-69 years, n=37,818, 28.4%; aged 70-79 years, n=27,598, 20.7%; aged 80 years and older, n=6,983, 5.2%) who underwent POP surgical procedures. On multivariate logistic regression, relative to patients younger than 60 years, age groups 60-69 years and 70-79 years had significantly lower rates of major complications (60-69 years: adjusted odds ratio [aOR]=0.68 [0.62-0.74]; 70-79 years: aOR=0.71 [0.64-0.78]) and patients older than 80 years had similar rates of major complications (aOR=0.98 [0.86-1.12]). In the patients younger than 60 years, the addition of a hysterectomy to a prolapse procedure carried a slightly increased risk of major complications (aOR=1.19, 95% CI=1.06-1.32). No other group carried an increased risk of major complications when adding a hysterectomy or performing an apical or obliterative repair.</p><p><strong>Conclusion: </strong>This study shows a low risk of complications after POP procedures, even in patients older than 80 years.</p>","PeriodicalId":75288,"journal":{"name":"Urogynecology (Hagerstown, Md.)","volume":" ","pages":""},"PeriodicalIF":1.2,"publicationDate":"2025-11-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145662814","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-11-21DOI: 10.1097/SPV.0000000000001772
Hisham Arafa, Waleed Mousa, Mahmoud Hossam, Mohammed Yassin, Ahmed Farouk
Importance: Due to the lack of data comparing transvesical (TV) and extravesical (EV) techniques for uterovesical fistulas (UVFs), specifically comparing surgical success rates, intraoperative complications, and postoperative effect on urinary bladder (UB) capacity, we designed our study.
Objectives: This study compares laparoscopic TV versus EV repair of UVFs in terms of surgical success, intraoperative complications, postoperative UB capacity, and overactive bladder (OAB) symptoms.
Study design: A retrospective observational cohort study was conducted from January 1, 2020 to January 1, 2025, upon patients aged 18 years and older who underwent laparoscopic UVF repair at Ain Shams University Hospital, Cairo, Egypt. Data were collected through a chart review of routinely administered perioperative assessments, including the Overactive Bladder 8-Question Awareness Tool (OAB-V8) and a 3-day voiding diary.
Results: Patient demographic characteristics were similar in both groups. Success rates were similar between cohorts. One hysterectomy was performed in the EV group due to intraoperative bleeding. The EV approach had a higher complication rate than the TV group (P=0.014). The TV approach was associated with a significantly greater reduction in UB capacity compared with the EV approach (97.73±15.39 mL vs. 37.50±22.39 mL, respectively, P=0.001). Concurrently, the TV group demonstrated a significantly higher increase in OAB-V8 scores than the EV group (6.70±0.82 vs. 1.36±0.50, respectively, P=0.001).
Conclusion: Both techniques demonstrated efficacy in repairing fistulas. However, the EV approach offered superior functional outcomes, with significantly better preservation of UB capacity and a lower incidence of postoperative OAB symptoms. In contrast, the TV approach may remain preferable in younger patients or those seeking uterine preservation, as it enables precise dissection and repair while minimizing risk to uterine integrity.
{"title":"Laparoscopic Transvesical Versus Extravesical Uterovesical Fistula Repair.","authors":"Hisham Arafa, Waleed Mousa, Mahmoud Hossam, Mohammed Yassin, Ahmed Farouk","doi":"10.1097/SPV.0000000000001772","DOIUrl":"https://doi.org/10.1097/SPV.0000000000001772","url":null,"abstract":"<p><strong>Importance: </strong>Due to the lack of data comparing transvesical (TV) and extravesical (EV) techniques for uterovesical fistulas (UVFs), specifically comparing surgical success rates, intraoperative complications, and postoperative effect on urinary bladder (UB) capacity, we designed our study.</p><p><strong>Objectives: </strong>This study compares laparoscopic TV versus EV repair of UVFs in terms of surgical success, intraoperative complications, postoperative UB capacity, and overactive bladder (OAB) symptoms.</p><p><strong>Study design: </strong>A retrospective observational cohort study was conducted from January 1, 2020 to January 1, 2025, upon patients aged 18 years and older who underwent laparoscopic UVF repair at Ain Shams University Hospital, Cairo, Egypt. Data were collected through a chart review of routinely administered perioperative assessments, including the Overactive Bladder 8-Question Awareness Tool (OAB-V8) and a 3-day voiding diary.</p><p><strong>Results: </strong>Patient demographic characteristics were similar in both groups. Success rates were similar between cohorts. One hysterectomy was performed in the EV group due to intraoperative bleeding. The EV approach had a higher complication rate than the TV group (P=0.014). The TV approach was associated with a significantly greater reduction in UB capacity compared with the EV approach (97.73±15.39 mL vs. 37.50±22.39 mL, respectively, P=0.001). Concurrently, the TV group demonstrated a significantly higher increase in OAB-V8 scores than the EV group (6.70±0.82 vs. 1.36±0.50, respectively, P=0.001).</p><p><strong>Conclusion: </strong>Both techniques demonstrated efficacy in repairing fistulas. However, the EV approach offered superior functional outcomes, with significantly better preservation of UB capacity and a lower incidence of postoperative OAB symptoms. In contrast, the TV approach may remain preferable in younger patients or those seeking uterine preservation, as it enables precise dissection and repair while minimizing risk to uterine integrity.</p>","PeriodicalId":75288,"journal":{"name":"Urogynecology (Hagerstown, Md.)","volume":" ","pages":""},"PeriodicalIF":1.2,"publicationDate":"2025-11-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145566666","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-11-20DOI: 10.1097/SPV.0000000000001774
Erin E Mowers, Pamela Moalli, Lauren E Giugale
Importance: A lack of data on the time course of recovery following pelvic organ prolapse surgery limits evidence-based counseling.
Objectives: The objective of this study was to define the time course of recovery following vaginal native tissue prolapse repair and identify factors affecting recovery. We hypothesized that half of the patients would return to baseline activity by 6 weeks.
Study design: This was a secondary analysis of a previously published randomized controlled trial of perioperative pain control for women ≥18 years undergoing vaginal native tissue prolapse repair under general anesthesia and an enhanced recovery after surgery protocol. The Activities Assessment Scale was used to quantify perioperative functional status. Our primary outcome was the proportion of participants returning to baseline activity at 1,2, 6, and 12 weeks postoperatively. Secondary outcomes included factors associated with recovery.
Results: Sixty-five participants (aged: 69.1±10.2 years) undergoing vaginal apical prolapse procedures were included. More than half (52.3%) returned to their baseline activity by 1 week postoperatively, with 69.2%, 84.1%, and 93.6% returning to baseline activity by 2, 6, and 12 weeks, respectively. On final multivariable analysis, chronic obstructive pulmonary disease [OR: 0.02 (95% CI, 0.001-0.43), P<0.05], total intraoperative morphine equivalents [OR: 0.89 (95% CI, 0.80-0.98), P<0.05], and total postanesthesia care unit phase 2 morphine equivalents [OR: 0.72 (95% CI, 0.52-0.99), P<0.05] were negatively associated with 6-week recovery.
Conclusions: In women undergoing apical vaginal prolapse repair, >50% recovered baseline functional activity by 1 week, and >80% recovered by 6 weeks.
{"title":"Return to Baseline Activity Following Vaginal Pelvic Organ Prolapse Repair.","authors":"Erin E Mowers, Pamela Moalli, Lauren E Giugale","doi":"10.1097/SPV.0000000000001774","DOIUrl":"https://doi.org/10.1097/SPV.0000000000001774","url":null,"abstract":"<p><strong>Importance: </strong>A lack of data on the time course of recovery following pelvic organ prolapse surgery limits evidence-based counseling.</p><p><strong>Objectives: </strong>The objective of this study was to define the time course of recovery following vaginal native tissue prolapse repair and identify factors affecting recovery. We hypothesized that half of the patients would return to baseline activity by 6 weeks.</p><p><strong>Study design: </strong>This was a secondary analysis of a previously published randomized controlled trial of perioperative pain control for women ≥18 years undergoing vaginal native tissue prolapse repair under general anesthesia and an enhanced recovery after surgery protocol. The Activities Assessment Scale was used to quantify perioperative functional status. Our primary outcome was the proportion of participants returning to baseline activity at 1,2, 6, and 12 weeks postoperatively. Secondary outcomes included factors associated with recovery.</p><p><strong>Results: </strong>Sixty-five participants (aged: 69.1±10.2 years) undergoing vaginal apical prolapse procedures were included. More than half (52.3%) returned to their baseline activity by 1 week postoperatively, with 69.2%, 84.1%, and 93.6% returning to baseline activity by 2, 6, and 12 weeks, respectively. On final multivariable analysis, chronic obstructive pulmonary disease [OR: 0.02 (95% CI, 0.001-0.43), P<0.05], total intraoperative morphine equivalents [OR: 0.89 (95% CI, 0.80-0.98), P<0.05], and total postanesthesia care unit phase 2 morphine equivalents [OR: 0.72 (95% CI, 0.52-0.99), P<0.05] were negatively associated with 6-week recovery.</p><p><strong>Conclusions: </strong>In women undergoing apical vaginal prolapse repair, >50% recovered baseline functional activity by 1 week, and >80% recovered by 6 weeks.</p>","PeriodicalId":75288,"journal":{"name":"Urogynecology (Hagerstown, Md.)","volume":" ","pages":""},"PeriodicalIF":1.2,"publicationDate":"2025-11-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145566681","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-11-12DOI: 10.1097/SPV.0000000000001768
Martina Gabra, Katherine L Woodburn, Amr El Haraki, Anna Zdroik, Marisa Duong, Christina Mezes, Maya Fisher, Lyle Paukner, Catherine A Matthews
Importance: Unidirectional barbed suture may decrease suture time for vaginal mesh attachment in robotic sacrocolpopexy.
Objective: The objective of this study was to evaluate if absorbable unidirectional barbed suture decreases vaginal mesh attachment time compared with nonbarbed suture.
Study design: This single-blind, randomized trial of women undergoing robotic sacrocolpopexy for ≥stage 2 symptomatic pelvic organ prolapse assessed if absorbable unidirectional barbed suture resulted in a 50% faster vaginal mesh attachment compared with interrupted nonbarbed suture. Surgeon-reported ease of mesh attachment, appearance of mesh, and global satisfaction with each suture type was assessed with a 10-point Likert scale (1 worst, 10 best). Six-month patient-centered outcomes were assessed.
Results: In total, 52 participants were randomized, with 25 in the barbed suture group and 27 in the nonbarbed suture group. Vaginal mesh attachment was faster for barbed suture (13.2 vs. 19.7 min, P <0.01). However, this did not reach the primary outcome of a 50% decrease in suture time. When stratified by level of training, barbed suture remained significantly faster for resident and fellow surgeons but not for attending surgeons. Surgeons rated barbed suture higher than nonbarbed suture for ease of suture use and global satisfaction, with similar mesh appearance ratings. Total operative time was similar between groups (186.1 vs. 180.9 min, P =0.62). Six-month patient-centered outcomes were similar between groups.
Conclusions: Unidirectional barbed suture decreased mesh attachment time compared with nonbarbed suture, especially for novice surgeons. Surgeon satisfaction was higher for barbed suture, and there was a similar improvement in all patient-centered outcomes at 6 months.
{"title":"BEST: Barbed-suture Efficiency Study for Sacrocolpopexy: A Randomized Clinical Trial.","authors":"Martina Gabra, Katherine L Woodburn, Amr El Haraki, Anna Zdroik, Marisa Duong, Christina Mezes, Maya Fisher, Lyle Paukner, Catherine A Matthews","doi":"10.1097/SPV.0000000000001768","DOIUrl":"10.1097/SPV.0000000000001768","url":null,"abstract":"<p><strong>Importance: </strong>Unidirectional barbed suture may decrease suture time for vaginal mesh attachment in robotic sacrocolpopexy.</p><p><strong>Objective: </strong>The objective of this study was to evaluate if absorbable unidirectional barbed suture decreases vaginal mesh attachment time compared with nonbarbed suture.</p><p><strong>Study design: </strong>This single-blind, randomized trial of women undergoing robotic sacrocolpopexy for ≥stage 2 symptomatic pelvic organ prolapse assessed if absorbable unidirectional barbed suture resulted in a 50% faster vaginal mesh attachment compared with interrupted nonbarbed suture. Surgeon-reported ease of mesh attachment, appearance of mesh, and global satisfaction with each suture type was assessed with a 10-point Likert scale (1 worst, 10 best). Six-month patient-centered outcomes were assessed.</p><p><strong>Results: </strong>In total, 52 participants were randomized, with 25 in the barbed suture group and 27 in the nonbarbed suture group. Vaginal mesh attachment was faster for barbed suture (13.2 vs. 19.7 min, P <0.01). However, this did not reach the primary outcome of a 50% decrease in suture time. When stratified by level of training, barbed suture remained significantly faster for resident and fellow surgeons but not for attending surgeons. Surgeons rated barbed suture higher than nonbarbed suture for ease of suture use and global satisfaction, with similar mesh appearance ratings. Total operative time was similar between groups (186.1 vs. 180.9 min, P =0.62). Six-month patient-centered outcomes were similar between groups.</p><p><strong>Conclusions: </strong>Unidirectional barbed suture decreased mesh attachment time compared with nonbarbed suture, especially for novice surgeons. Surgeon satisfaction was higher for barbed suture, and there was a similar improvement in all patient-centered outcomes at 6 months.</p>","PeriodicalId":75288,"journal":{"name":"Urogynecology (Hagerstown, Md.)","volume":" ","pages":""},"PeriodicalIF":1.2,"publicationDate":"2025-11-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145544166","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}