Hypothesis / aims of study
Same day surgical discharge after vaginal reconstructive surgery is often appropriate but, in those with acute urinary retention, timing for repeat attempt at a voiding trial is not clear. Previously identified risk factors for failure of voiding trial after vaginal reconstruction come from a single retrospective study: age, degree of cystocele, intraoperative blood loss, Levator and Kelly Plication[1]. We present novel data analyzing a cohort of patients with routinely placed suprapubic catheters, providing insight into return of bladder function and risk factors for postoperative voiding dysfunction following vaginal prolapse repair. We aim to improve postoperative care by minimizing clinic visits for voiding trials.
Study design, materials and methods
We identified 127 women undergoing native tissue vaginal reconstruction from a single surgeon between 2012 and 2019 who routinely used suprapubic catheters. These patients all followed a specific catheter regimen postoperatively, giving reliable information about postvoid residual volumes (PVR) and thus bladder function. We used a PVR of <150 cc at 4 hours to be a surrogate marker for return of bladder function. Univariate and multivariate logistic regression analyses were used to identify risk factors for return of bladder function >4 days by surrogate marker. Variables included were age, baseline PVR, history of diabetes, stroke and/or smoking, leading edge of prolapse, stage of prolapse, type of apical suspension, estimated surgical blood loss (EBL), operative duration, anesthesia duration, concomitant hysterectomy and/or incontinence procedure. Primary outcome measure was PVR >150 cc measured by suprapubic catheter after 4 hours.
Interpretation of results
We present several clinically relevant findings which provide guidance on timing of voiding trials following prolapse repair. First, a concomitant hysterectomy demonstrated a 2.86-fold increased risk of delayed return of bladder function >4 days compared to patients with a vaginal vault suspension. We recommend repeating a void trial after 1 week in these patients given 80% of our cohort met criteria for return of bladder function by day 7. Second, surgical duration >120 minutes resulted in a 9.96-fold increased risk of delayed return of bladder function >4 days even when controlling for all other evaluated risk factors. We recommend considering surgical length along with other risk factors identified such as DM (5.65-fold), sacrospinous fixation (2.59-fold), and estimated blood loss (1.1-fold) when scheduling office visits. Third, in patients with an uncomplicated vaginal vault suspension and no other identified risk factors, we recommend voiding trial on postoperative day 5 as 80% of our cohort had return of bladder function by this time.
Limitations of the study are in the homogeneity of the cohort which could limit generalizability and in the retrospective design.