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For decades, transurethral resection of the prostate (TURP) has been regarded as the definitive surgical treatment for benign prostatic hyperplasia (BPH) (1,2). TURP, along with suprapubic enucleation techniques, remains the gold standard for relieving bladder outlet obstruction in clinical practice (3).
However, despite its widespread success, 5-10% of patients undergoing BPH surgery experience severe post-operative complications, most commonly urinary incontinence, followed by reoperation, recatheterization, urinary tract infections and perioperative bleeding (4,5).
Early post-operative incontinence has been reported in up to 30-40% of cases (6), underscoring a persistent challenge in optimizing functional outcomes following TURP. The pathophysiological mechanisms underlying post-TURP incontinence remain incompletely understood. It is generally accepted that conventional TURP involves the resection of the prostatic apex, a region intimately associated with the external urethral sphincter, which plays a critical role in passive urinary control (7).
The fundamental rationale for prostatic apex preservation is that maintaining a greater length of the urethral sphincter complex may protect more sphincteric muscle fibers, thereby preserving continence (8). Active continence is maintained by the levator ani muscle complex acting on the prostatic apex and membranous urethra (7), while the external urethral sphincter, located predominantly within the prostate between the apex and the verumontanum (9-11), provides essential closure function.
The preservation of the Denonvilliers' fascia, a tendinous structure extending from the prostate base to its apex, is also deemed to be vital, as it serves as a supportive fulcrum for both the prostate and the urethra (11,12). Moreover, Van der Poel et al (13) and Hoyland et al (14) demonstrated that the innervation of the prostatic apex and the urethral sphincter is intricately interconnected, suggesting that the maintenance of the prostatic urethra during surgery enhances post-operative continence outcomes.
Recently, several controlled clinical trials have investigated the efficacy of urethral mucosa preservation at the prostatic apex in the surgical management of BPH (15-18). However, individual studies have reported inconsistent results, and to date, to the best of our knowledge, no systematic review or meta-analysis has comprehensively compared the outcomes of apex-preserving versus apex-resecting techniques.
Therefore, the present study aimed to systematically review and quantitatively synthesize the available evidence on the clinical efficacy of prostatic apex preservation during BPH surgery, with particular attention to urinary continence and perioperative outcomes.
The present systematic review and meta-analysis adhered strictly to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines (19) and was prospectively registered in PROSPERO (CRD420250642661).
A comprehensive electronic search was conducted from database inception to January, 2025 across PubMed, Google Scholar and the Cochrane Library. Search terms included combinations of ‘prostatic apex preservation’, ‘benign prostatic hyperplasia’ and ‘outcomes’.
Additional manual searches of reference lists and clinical trial registries were performed to identify any relevant studies not indexed in the databases. The complete search algorithm is detailed in Table SI.
Study selection was guided by the Population, Intervention, Comparator, Outcome, and Study Design (PICOS) framework.
The inclusion criteria were the following: i) Population: Patients diagnosed with BPH, without restriction by age or comorbidities; ii) intervention: Surgical procedures that preserved the prostatic apex; iii) comparator: Conventional surgical approaches involving prostatic apex dissection; iv) primary outcome: Post-operative urinary incontinence rate; v) secondary outcomes: Intraoperative blood loss, volume of prostate tissue resected, International Prostate Symptom Score (IPSS), quality of life (QoL), peak urinary flow rate (Qmax) and duration of the surgery; vi) study design: Randomized controlled trials (RCTs) and non-randomized controlled clinical studies.
The exclusion criteria included the following: Studies not involving BPH or human participants, non-interventional or observational studies (e.g., reviews, editorials and case reports), non-English publications and studies for which full-text data were unavailable. The full PICOS schema used for eligibility assessment is summarized in Table SII.
Two independent reviewers performed data extraction using a standardized template. Discrepancies were resolved through discussion and consensus. The following data were extracted from each eligible study: First author, publication year and journal, study design and sample size, mean age of the participants, post-operative urinary incontinence rate, intraoperative blood loss, Qmax, IPSS, QoL score and prostate volume resected. When necessary, corresponding authors were contacted to clarify incomplete or ambiguous data.
The methodological quality of the included non-RCTs was evaluated using the Risk of Bias in Non-randomized Studies of Interventions (ROBINS-I) tool (20). In total, four studies met the inclusion criteria and were assessed in detail (15-18). The results of the ROBINS-I assessment are presented in Fig. 1.
Overall, studies demonstrated a low-to-moderate to moderate-to-severe risk of bias, primarily due to missing outcome data and selective reporting. Specifically, Liu and Yang (15) and Fujisaki et al (17) exhibited a low-to-moderate risk, Liang et al (16) had a moderate-to-severe risk due to incomplete data and selective outcome reporting, while Irani et al (18) was rated low-to-moderate.
All statistical analyses were conducted using Review Manager (RevMan) version 5.4(21). For continuous variables, outcomes are expressed as the mean difference (MD) with 95% confidence intervals (CIs). For dichotomous outcomes, the relative risk (RR) with 95% CI was calculated. Heterogeneity was evaluated using the Chi-squared (χ2) test and quantified by the I2 statistic. An I2 value >50% indicated substantial heterogeneity, and a P-value <0.05 was considered to indicate a statistically significant difference. The random effects model was used for the present study as a small number of studies and clinical heterogeneity are expected (21,22).
A total of 4,141 studies were identified via the databases. A total of 641 duplicate studies were detected. Following deduplication, 3,500 records were filtered. Subsequently, 3,442 were removed as they were not related to apex preservation. No automation tools were used in the screening part. The remaining 58 studies were refiltered for retrieval. A total of two studies were not retrieved for full text, and out of the 56 studies that were retrieved, 41 studies were excluded as they were not controlled trials, four studies were not related to the inclusion criteria, and seven studies did not cover the complication. Thus, four studies were included (15-18). Of these four studies, 638 participants were identified. The PRISMA flow chart (23) reflects the identification of studies via the databases and registers, rescreening and reassessment of the qualified studies (Fig. 2).
Of the total 638 participants, 452 were in the prostatic apex preservation group and 186 were in the apex dissection group. The characteristics of the studies included in the present systematic review are presented in Table I.
The characteristics of outcomes from each study, such as the duration of surgery, incontinence rate, intraoperative blood loss, prostate volume excised, IPSS, QoL and Qmax are presented in Table II.
The Grading of Assessment, Development, and Evaluation (GRADE) approach was used to assess the overall evidence concerning individual outcomes. The GRADEpro tool was applied to evaluate the certainty of the evidence (26,27). The summary assessment, development and evaluation of the findings according to the GRADE guidelines for the included studies (outcomes on urine incontinence and other outcomes that are moderate-quality evidence) are presented in Table III.
All studies analyzed the duration of surgery, involving 638 participants (452 in the prostatic apex preservation group and 186 in the apex dissection group). Random effects were used, and the results revealed that the surgery duration of the preserving technique was significantly shorter than that of the non-preserving technique (MD, -9.82; 95% CI, -13.91 to -5.73; P<0.00001) (Fig. 3).
All studies analyzed incontinence post-operatively, involving 638 participants (452 in the prostatic apex preservation group and 186 in the apex dissection group). Random effects were used, and the results revealed that the preserving group had a lower incontinence rate compared to the non-preserving group (RR, 0.18; 95% CI, 0.07 to 0.46; P=0.0004) (Fig. 4).
Liu and Yang (15), Liang et al (16), and Irani et al (17) analyzed the blood loss during surgery, involving 223 participants (112 in the prostatic apex preservation group and 111 in the apex dissection group). Random effects were used, and the results revealed that blood loss in the preserving group was also less than that in the non-preserving group (MD, -65.37; 95% CI, -121.97 to -8.77; P=0.02; Fig. 5).
Liang et al (16) and Fujisaki et al (17) analyzed the excised prostate volume, involving 505 participants (385 in the prostatic apex preservation group and 120 in the apex dissection group). Random effects models were used, and the results revealed similar volumes of excised tissue between the two groups (MD, 0.69; 95% CI, -5.96 to 7.34; P=0.84) (Fig. 6).
Liu and Yang (15) and Liang et al (16) analyzed the IPSS at 1 month post-operatively, while Irani et al (18) analyzed the IPSS at 6 months post-operatively, involving 223 participants (112 in the prostatic apex preservation group and 111 in the apex dissection group). Random effects were used, and the results revealed similar IPSS between the two groups (MD, -0.02; 95% CI, -0.65 to 0.62; P=0.96) (Fig. 7).
Liu and Yang (15) and Liang et al (16) analyzed the QoL post-operatively, involving 170 participants (85 in the prostatic apex preservation group and 85 in the apex dissection group). Random effects were used, and the results revealed similar QoL scores between the two groups (MD, -0.30; 95% CI, -0.50 to 0.11; P=0.003; Fig. 8).
Liu and Yang (15), Liang et al (16) and Fujisaki et al (17) analyzed the Qmax at 1 month post-operatively, while Irani et al (18) analyzed the Qmax at 6 months post-operatively, involving 638 participants (452 in the prostatic apex preservation group and 186 in the apex dissection group). Random effects were used, and the results revealed a similar Qmax score between the two groups (MD, 0.11; 95% CI, -0.38 to 0.59; P=0.66) (Fig. 9).
Leave-one-out analysis is a method used to evaluate the robustness of pooled estimation by individually excluding one study at a time and reanalyzing the data. In the present study, moderate to high heterogeneity was observed when pooling the effect sizes for urinary incontinence (I2=14% and P=0.32). The analysis revealed that the study by Fujisaki et al (17) had a significant influence on the pooled effect of the urinary incontinence results. When excluding the study by Fujisaki et al (17), the pooled urinary incontinence rate across all studies was 0.06 (I2=0%, P=0.99), as illustrated in the forest plot in Fig. 10. The forest plot, the study by Fujisaki et al (17), indicates that the urinary incontinence rate was 0.06 (95% CI, 0.01 to 0.33), which was lower than the first pooled rate of 0.18 (95% CI, 0.07 to 0.46), although not statistically significant. This result proposed that this meta-analysis is generally consistent.
The publication bias in urinary incontinence was assessed, as illustrated in the funnel plot in Fig. 11. The plot demonstrates the standard error and relative risk of urinary incontinence for each study. While it is hoped that a symmetrical distribution is achieved in the absence of publication bias, the funnel plot revealed some asymmetry, focusing on small studies in the left side, indicating a low prevalence due to the lack of data. Although the funnel plot visually revealed a potential risk of publication bias, Egger's regression test indicated potential small-study effects (bias estimate=-1.40; SE=0.11; P=0.0061). Due to the small number of studies (k=4), the results should be interpreted with caution, as Egger's regression test does not provide much value if the number of studies is <10.
Previous studies have highlighted the value of preserving the prostatic apex in reducing post-operative complications, particularly urinary incontinence following BPH surgery (15-18). Partin et al (7) suggested that the resection of the prostatic apex, which houses the external urethral sphincter responsible for passive urinary control, can compromise continence mechanisms and predispose patients to post-operative incontinence. Similarly, Zinner et al (24) emphasized the critical role of the urethral mucosa in maintaining urinary continence.
The surgical principle of preserving or reconstructing the urethral mucosa at the prostatic apex is to extend the mucosal length and create additional mucosal folds adjacent to the external urethral sphincter. This configuration provides a ‘sealing pad’ effect, improving urethral closure pressure and facilitating early post-operative continence (16).
In early research, transient urinary incontinence was reported in 4 of 15 patients (26.7%) undergoing conventional TURP, with all cases resolving within 6 months (25). Late incontinence has been linked to post-operative urinary tract infection, further reinforcing the importance of mucosal integrity in preserving urinary control (18).
Across studies, apex-preserving techniques have consistently achieved higher rates of immediate continence compared to conventional dissection (15-18). In the study by Irani et al (18), 6 patients (23%) in the control group developed immediate post-operative urge incontinence (4 cases recovered within 1 week and 2 cases within 3 months), whereas no cases occurred in the preservation group.
Liang et al (16) reported a similar pattern: In total, 7 patients (15%) in the control group experienced immediate incontinence (4 patients recovered in 1 week and 3 patients in 3 weeks); again there were no cases in the intervention group. Liu and Yang (15) observed 9 cases (22.5%) of transient incontinence in the control group, all resolving within 3 months, while the preservation group demonstrated 100% immediate continence. Fujisaki et al (17) documented an incontinence rate of 4.1% in the preservation group vs. 14.7% in controls immediately following catheter removal.
Across the included studies, the duration of the surgery was shorter in the apex-preservation group (15-18), and intraoperative blood loss was reduced in the majority of studies (15,16,18). In total, two studies reported comparable prostate resection volumes between the two approaches (16,17), and IPSS values at 3 months were similar across all cohorts (15,16,18).
QoL metrics, assessed in two studies, exhibited promising improvements in both groups with Qol scores comparable to each other (16,17), while Qmax, an indicator of functional recovery, was consistently satisfactory in all reports (15,16,18).
To the best of our knowledge, although several meta-analyses have examined ejaculatory function following prostatic apex preservation, the present study is the first to focus primarily on urinary functional outcomes. The findings presented herein indicate that preserving the prostatic apex during BPH surgery provides a clinically meaningful advantage in terms of early urinary continence, shorter operative duration and reduced intraoperative blood loss, without compromising long-term voiding efficacy.
Nevertheless, the present study has a few limitations which should be acknowledged. First, high heterogeneity was observed in outcomes, such as intraoperative blood loss (I2=97%) and IPSS (I2=60%), partly due to incomplete outcome reporting across studies. Second, surgical expertise and patient characteristics likely contributed to variability in results. Third, due to limited data availability, not all functional and perioperative parameters could be included in the pooled analysis. Fourth, the impact of ethnicity, lifestyle factors and patient comorbidities could not be evaluated. Lastly, reoperation outcomes could not be evaluated in the present meta-analysis as the included randomized controlled trials did not report reoperation data in a consistent, standardized, or extractable format. Finally, the majority of the included studies were small, single-center trials, emphasizing the need for larger, multicenter randomized studies with longer follow-up.
In conclusion, preserving the prostatic apex during BPH surgery appears to provide tangible benefits, including the earlier recovery of urinary continence, reduced intraoperative bleeding and a shorter surgery duration, while maintaining comparable postoperative urinary function. However, future large-scale, high-quality randomized trials with extended follow-up are warranted to validate these findings and establish the clinical superiority and safety of apex-preserving techniques in contemporary BPH management.
The authors would like to express their sincere gratitude to Professor Syah Mirsya Warli and Dr Bungaran Sihombing from Rumah Sakit Haji Adam Malik Medan City for the invaluable feedback and clinical support for this study. The present systematic review and meta-analysis has been registered in Prospero with the registration no. CRD420250642661.
Funding: No funding was received.
The data generated in the present study may be requested from the corresponding author.
All authors (DDK, BT and KAWY) contributed to the conception and design of the study. Material preparation, data collection and analysis were performed by DDK, BT and KAWY. The first draft of the manuscript was written by KAWY and BT, and all authors commented on previous versions of the manuscript. DDK, KAWY and BT confirm the authenticity of all the raw data. All authors (DDK, BT and KAWY) have read and approved the final manuscript.
Not applicable.
Not applicable.
The authors declare that they have no competing interests.
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