Efficacy of phosphodiesterase type 5 inhibitors in patients with erectile dysfunction after nerve-sparing radical prostatectomy: a systematic review and meta-analysis.

Background: Nerve-sparing radical prostatectomy (NSRP) had to be performed because approximately 94% of patients are diagnosed with localized prostate cancer (PCa). Although NSRP is generally done to improve functional outcomes, erectile dysfunction (ED) is one of the most prevailing complications after radical prostatectomy (RP). Phosphodiesterase type 5 inhibitors (PDE5-Is) are the most well-known treatment agent for postoperative ED. This study aimed to assess the efficacy of PDE5-Is in patients with ED after NSRP.
Methods: In this systematic literature review, randomized controlled trials on the efficacy and safety of PDE5-Is in patients who underwent NSRP were searched in MEDLINE, EMBASE, and the Cochrane Controlled Trials Register using the OVID platform. This study was conducted in accordance with the Preferred Reporting Items for Systematic Reviews and Meta-Analyses and Cochrane Review Methods. The quality of the evidence of the outcome data was evaluated using the Grading of Recommendations, Assessment, Development, and Evaluation (GRADE) approach.
Results: A total of 14 trials involving 2,822 patients were included. Significant improvements in the International Index of Erectile Function-Erectile Function (IIEF) domain score [mean difference (MD) =4.93; 95% confidence interval (CI): 4.14-5.71; P<0.00001] and erectile function recovery events [odds ratio (OR) =2.06; 95% CI: 1.45-2.94; P<0.0001] were observed after PDE5-I treatment. A higher positive response to Sexual Encounter Profile (SEP) question 2 (OR =2.27; 95% CI: 1.80-2.86; P<0.00001) and question 3 (OR =2.78; 95% CI: 1.97-3.91; P<0.00001) was also found after PDE5-I treatment. However, the incidence of treatment-emergent adverse events (TEAEs) was higher after PDE5-I treatment than after placebo treatment (OR =2.91; 95% CI: 1.84-4.61). Furthermore, the incidence of headache (OR =3.38; 95% CI: 2.40-4.75) and flushing (OR =9.44; 95% CI: 4.30-20.70) was also significantly higher after PDE5-I treatment (P<0.00001). In terms of the quality of the evidence of the outcome data, inconsistency problems were detected in all outcomes and imprecision problems in most outcomes. Discussion: PDE5-I treatment was more effective to placebo treatment in patients with ED after NSRP. No clinically serious complications were found in spite of the incidence of TEAEs being higher after PDE5-I treatment. 2022 Translational Andrology and Urology. All rights reserved.

Introduction

One in six men had been diagnosed with prostate cancer (PCa) in their lifetime, making PCa the most common type of cancer among men in Western countries (1,2). Approximately 94% of patients are diagnosed with localized PCa and thus need to undergo nerve-sparing radical prostatectomy (NSRP) (2,3). The number of radical prostatectomy (RP) operation has been rapidly increasing over years, and the age of patients seeking for this treatment has also increased correspondingly (4).

Despite the fact that NSRP is usually performed to promote the functional outcomes, such as erectile function, erectile dysfunction (ED) results frequently after the procedure. Postoperative ED has been reported in 15–18% of patients who undergo NSRP (5,6). It is a condition that can potentially take a toll on the patients’ everyday life (4). Therefore, if postoperative ED is less likely to occur, more patients will decide to receive NSRP (7). Various factors affect the development and severity of postoperative ED; these include patient age, preoperative potency, stage of the tumor, and surgeon’s experience (8-12). Postoperative ED can also cause vascular damage, neural injury, and smooth muscle damage (13,14).

The emergence of phosphodiesterase type 5 inhibitors (PDE5-Is) has innovated ED treatment with a success rate of approximately 60–70% (15,16). PDE5-Is are the most common treatment agent for postoperative ED. The efficacy and adverse effects of PDE5-Is have been reported; however, there is insufficient evidence to demonstrate the optimal use of PDE5-Is for penile rehabilitation. Several errors were found in meta-analyses and systematic reviews that have been performed to assess the efficacy and adverse effects of PDE5-Is (17-19). Therefore, we performed a systematic review and meta-analysis of randomized controlled trials to evaluate the efficacy and safety of PDE5-Is in patients with ED after NSRP.

We present the following article in accordance with the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) reporting checklist (available at https://tau.amegroups.com/article/view/10.21037/tau-21-881/rc).

Methods

We performed a systematic review to identify publications evaluating the efficacy and safety of PDE5-Is in patients with ED after NSRP. This systematic review and protocol was registered in PROSPERO database: CRD42020193371. There was no modifications to the protocol during the study process. This study was conducted in accordance with PRISMA and Meta-Analyses and Cochrane Review Methods (20).

Data and literature sources

We used the OVID platform to search for relevant literature in the following databases: EMBASE (from 1974), OVID MEDLINE (R) 1946 up to the present (OVID platform), OVID MEDLINE (R) Daily and MEDLINE In-Process and Other Non-Indexed Citations, the Cochrane Controlled Trials Register (OVID platform), and the Cochrane Database of Systematic Reviews (OVID platform) from inauguration to July 2020. In addition, a literature search of the Web of Science was conducted to find all relevant studies. We also manually searched the World Health Organization International Clinical Trials Registry Platform and ClinicalTrials.gov for additional unpublished and published studies. The main keywords used were ED, nerve-sparing prostatectomy, PDE5-I, and randomized controlled trial.

Study selection

All searched studies were independently selected by two reviewers according to predefined selection criteria. When disagreements occurred on primary study selection, a third reviewer arbitrated them. The predefined selection criteria in our meta-analysis were as follows: (I) randomized controlled trial published in any international journal in English language, (II) adult patients undergoing treatment with PDE5-Is for ED after nerve-sparing prostatectomy, (III) studies comparing the effects of PDE5-Is with those of placebo regardless of the treatment regimen, and (IV) the International Index of Erectile Function—Erectile Function (IIEF) domain score as the primary outcome, which was used for evaluating postoperative erectile function rehabilitation. In these studies, the number of patients who achieved erectile function recovery after PDE5-I treatment was also measured. The secondary outcomes were positive responses to Sexual Encounter Profile (SEP) questions 2 and 3, which were included for additional assessment of postoperative erectile function rehabilitation and the incidence of adverse events after PDE5-I treatment. The outcome variables were mean differences (MDs) or the incidence of events between the groups at designated times.

Data extraction

The two reviewers independently extracted data through a prespecified data extraction form, and the third reviewer reviewed the extracted data. The following variables were extracted: (I) patient characteristics and number of patients, (II) means and standard deviations or incidence of events; (III) administration and dosage of detailed interventions; (IV) treatment time; and (V) incidence of adverse events after each intervention. When the abovementioned variables were not mentioned in the study, the data were requested via email.

Assessment of methodological quality

The risks of bias in the studies were independently estimated by two reviewers using the Cochrane risk of bias tool. This tool evaluates the quality of randomized controlled studies by reviewing the generation of random sequences, blinding of participants, assessment of outcomes, allocation concealment, incompleteness in outcome data, selective outcome reporting, and other possible sources of risk of bias.

Quality of evidence

The quality of the evidence of the outcome data was evaluated using the Grading of Recommendations, Assessment, Development, and Evaluation (GRADE) approach (20). The two reviewers independently evaluated the quality of each outcome. The five categories of GRADE quality assessment were limitations of design, inconsistency, indirectness, imprecision, and publication bias. “Summary of findings” tables were presented using a GRADE profiler (GRADEpro) and included the following outcomes: (I) IIEF domain score, (II) erectile function recovery event, (III) improvement in the response to SEP question 2, (IV) improvement in the response to SEP question 3, (V) incidence of treatment-emergent adverse events (TEAEs), (VI) incidence of headache, and (VII) incidence of flushing.

Statistical analysis

Continuous data were presented as MDs and 95% confidence intervals (CIs) and were analyzed using weighted MDs and the generic inverse variance method. Binary outcomes, such as the incidence of adverse events, were analyzed by comparing odds ratios (ORs) with 95% CIs. Heterogeneity between studies was evaluated using the χ2 test and I2statistics (21). I2values of >50% and P values of <0.10 in the χ2 test were regarded as statistically significant. When significant clinical or statistical heterogeneity was found, random-effects models were applied.

A subgroup analysis was conducted according to the regimen of PDE5-I treatment, such as daily use and on-demand use. A sensitivity analysis was conducted to evaluate the influence of risk of bias on our estimates. When the study had 3 or more the unclear or high risk of bias, we excluded from analysis. All statistical analyses were performed using the Cochrane Collaboration Review Manager Software (RevMan version 5.4.). Publication bias was evaluated by the funnel plots in the meta-analysis.

Results

Identification of the studies

Initial searches of the databases identified 597 publications. After removal of 314 duplicated articles, 283 articles were further excluded after reviewing their titles and abstracts. The full text of the 28 remaining articles was obtained for scrutiny; of these, 14 were excluded because they were abstracts (n=4); they used a different study design (n=2); the study design was not randomized (n=4); or the same data were reported (n=4). Thus, 14 studies involving 2,822 participants were finally included in this meta-analysis () (22-35).

Figure 1

Flow chart of the literature search strategy.

Study characteristics and patient populations

Seven studies were performed in multiple centers and the other studies in three countries: Germany (n=3), Italy (n=2), and Turkey (n=2) between 2003 and 2015. Of these, four studies evaluated the efficacy of PDE5-Is after unilateral nerve-sparing radical prostatectomy (UNSRP) or bilateral nerve-sparing radical prostatectomy (BNSRP) (28,31,32,35) and nine studies after BNSRP (22-24,26,27,29,30,33,34). The characteristics of the studies are summarized in .

Table 1

Characteristics of the included randomized controlled trials

Study	Year	Country/region	Intervention	Control	Sample size		Treatment period	Surgical approach
					Intervention	Control
Aydogdu et al. (26)	2011	Turkey	Tadalafil 20 mg/day	Placebo	32	33	6 months	BNSRP
Bannowsky et al. (31)	2008	Germany	Sildenafil 25 mg/day	Placebo	23	18	52 weeks	UNSRP
								BNSRP
Bannowsky et al. (28)	2010	Germany	Sildenafil 25 mg/day	Placebo	23	18	78 weeks	UNSRP
								BNSRP
Bannowsky et al. A (25)	2012	Germany	Vardenafil 5 mg/day	Placebo	12	12	12 months	UNSRP
Bannowsky et al. B (25)			Vardenafil 10 mg/day		12
Brock et al. A (35)	2003	United States and Canada	Vardenafil 10 mg on demand	Placebo	140	140	3 months	UNSRP
Brock et al. B (35)			Vardenafil 20 mg on demand		147			BNSRP
Canat et al. A (22)	2015	Turkey	Tadalafil 20 mg three times/week	Placebo	38	34	12 months	BNSRP
Canat et al. B (22)			Tadalafil 20 mg on demand		40
Cavallini et al. (33)	2005	Italy	Sildenafil 100 mg on demand	Placebo	35	29	4 months	BNSRP
Montorsi et al. (34)	2004	Canada, Germany, Italy, The Netherlands, Spain, United States, and United Kingdom	Tadalafil 20 mg on demand	Placebo	201	102	3 months	BNSRP
Montorsi et al. A (30)	2008	Europe, United States, Canada, and South Africa	Vardenafil 10 mg/day	Placebo	137	145	9 months	BNSRP
Montorsi et al. B (30)			Vardenafil 10 mg (5 to 20 mg) on demand		141
Montorsi et al. A (23)	2014	Nine European countries and Canada	Tadalafil 5 mg/day	Placebo	138	141	9 months	BNSRP
Montorsi et al. B (23)			Tadalafil 20 mg on demand		143
Mulhall et al. A (24)	2013	53 sites in the United States	Avanafil 100 mg on demand	Placebo	99	100	3 months	BNSRP
Mulhall et al. B (24)			Avanafil 200 mg on demand		99
Nehra et al. A (32)	2005	United States and Canada	Vardenafil 10 mg on demand	Placebo	140	140	3 months	UNSRP
Nehra et al. B (32)			Vardenafil 20 mg on demand		147			BNSRP
Pace et al. (27)	2010	Italy	Sildenafil 50 or 100 mg/day	Placebo	20	20	6 months	BNSRP
Padma-Nathan et al. A (29)	2008	North America, France, Belgium, and Australia	Sildenafil 50 mg/day	Placebo	40	42	9 months	BNSRP
Padma-Nathan et al. B (29)			Sildenafil 100 mg/day		41

BNSRP, bilateral nerve-sparing radical prostatectomy; UNSRP, unilateral nerve-sparing radical prostatectomy.

Quality of the included studies

Although all 14 studies used a random method, most studies did not describe detailed allocation concealment methods. The risks of blinding of participants and outcome assessment were unclear in five studies. The risks of selective reporting, incomplete outcome data, and other bias were low. Risk of bias graphs and summaries are presented in ().

Figure 2

Risk of bias for all included randomized controlled trials. (A) Risk of bias graph. (B) Risk of bias summary.

Efficacy

IIEF domain score

Our meta-analysis found significant improvements in the IIEF domain score after PDE5-I treatment (MD =4.93; 95% CI: 4.14–5.71; P<0.00001; I2=53%) (). A subgroup analysis was conducted according to the regimen of PDE5-I treatment. The subgroup analysis revealed significantly improved IIEF domain scores for both daily use (MD =4.68; 95% CI: 3.89–5.46; P<0.00001; I2=0%) and on-demand use (MD =4.98; 95% CI: 3.57–6.39; P=0.0003; I2=74%).

Figure 3

Efficacy of phosphodiesterase type 5 inhibitor treatment. (A) Impact on the IIEF domain score. (B) Impact on the recovery events in relation to the IIEF domain score (patient number). PDE5-Is, phosphodiesterase type 5 inhibitors; CI, confidence interval; IIEF, International Index of Erectile Function—Erectile Function.

Erectile function recovery after PDE5-I treatment was determined at an IIEF domain score of >25 in four studies (26,27,30,34) and IIEF domain score of ≥22 in one study (23). The incidence of erectile function recovery events was also higher after PDE5-I treatment (OR =2.06; 95% CI: 1.45–2.94; P<0.0001; I2=42%) (). The subgroup analysis revealed that the incidence of these events was significantly higher for daily use (OR =1.68; 95% CI: 1.15–2.45; P=0.007; I2=0%) and on-demand use of PDE5-Is (OR =2.76; 95% CI: 1.34–5.69; P=0.006; I2=70%).

Response to the SEP questions

The rate of positive response to SEP question 2 was significantly higher after PDE5-I treatment (OR =2.27; 95% CI: 1.80–2.86; P<0.00001; I2=23%) (). The subgroup analysis revealed a significantly higher positive response rate for on-demand use of PDE5-Is (OR =2.39; 95% CI: 1.81–3.15; P<0.00001; I2=34%).

Figure 4

Efficacy of phosphodiesterase type 5 inhibitor treatment. (A) Impact on the response to SEP question 2. (B) Impact on the response to SEP question 3. PDE5-Is, phosphodiesterase type 5 inhibitors; CI, confidence interval; SEP, Sexual Encounter Profile.

Meanwhile, the rate of positive response to SEP question 3 was also significantly higher after PDE5-I treatment (OR =2.78; 95% CI: 1.97–3.91; P<0.00001; I2=64%) (). The subgroup analysis also revealed a higher positive response rate to SEP question 3 for daily use (OR =1.73; 95% CI: 1.19–2.50; P=0.004; I2=0%) and on-demand use of PDE5-Is (OR =3.32; 95% CI: 2.15–5.12; P<0.00001; I2=68%).

Safety

The incidence of TEAEs was reported in eight studies. In our analysis, we found a higher incidence of TEAEs after PDE5-I treatment than after placebo treatment (OR =2.91; 95% CI: 1.84–4.61; P<0.00001; I2=89%) (). In the subgroup analysis, the OR for the incidence of TEAEs for on-demand PDE5-I treatment (OR =3.44; 95% CI: 1.88–6.30; P<0.00001; I2=92%) was higher than that for daily PDE5-I treatment (OR =1.71; 95% CI: 1.17–2.49; P=0.005; I2=30%). However, clinically serious adverse events related to the study drug were not reported in the included studies.

Figure 5

Safety of phosphodiesterase type 5 inhibitor treatment. (A) Impact on the incidence of TEAEs. (B) Impact on the incidence of headache. PDE5-Is, phosphodiesterase type 5 inhibitors; CI, confidence interval; TEAEs, treatment-emergent adverse events.

In terms of headache, we found a significantly higher incidence in the patients who received PDE5-I treatment (OR =3.38; 95% CI: 2.40–4.75; P<0.00001; I2=23%) (). The subgroup analysis revealed that the incidence of headache was significantly higher for on-demand PDE5-I treatment (OR =4.33; 95% CI: 3.09–6.08; P<0.00001; I2=0%) than for daily PDE5-I treatment (OR =1.69; 95% CI: 0.98–2.91; P=0.06; I2=0%).

In terms of flushing (OR =9.44; 95% CI: 4.30–20.70; P<0.00001; I2=11%) (), dyspepsia (OR =4.49; 95% CI: 2.44–8.27; P<0.00001; I2=6%) (), and nasopharyngitis (OR =2.59; 95% CI: 1.97–4.18; P<0.00001; I2=0%), we found a significantly higher incidence in the patients who received PDE5-I treatment ().

Figure 6

Safety of phosphodiesterase type 5 inhibitor treatment. (A) Impact on the incidence of flushing. (B) Impact on the incidence of dyspepsia. (C) Impact on the incidence of nasopharyngitis. PDE5-Is, phosphodiesterase type 5 inhibitors; CI, confidence interval.

Sensitivity analysis

A sensitivity analysis was conducted to assess the influence of risk of bias on our estimates. Five studies (16,19,21,22,25) had unclear risk of bias in three components. These studies were included in the analysis of the improvements in IIEF score, the incidence of erectile function recovery events, and the incidence of TEAEs. The sensitivity analysis revealed that the risk of bias did not alter the outcome of this meta-analysis ().

Table 2

Sensitivity analysis of primary and secondary outcomes

Outcome	Studies, n	Phosphodiesterase type 5 inhibitors, n	Control patients, n	OR or MD	95% CI	P value for effect	P value for heterogeneity	I2 (%)
The improvements in IIEF score
Total studies	11 (22-25,27-29,31,33,34,35)	1,143	1,004	4.93	4.14 to 5.71	<0.00001	0.005	53
Including only studies with low risk of bias	6 (23,24,29,33-35)	973	856	4.99	3.78 to 6.20	<0.00001	0.002	65
The incidence of erectile function recovery events
Total studies	5 (23,26,27,30,34)	807	732	2.06	1.45 to 2.94	<0.0001	0.11	42
Including only studies with low risk of bias	4 (23,26,30,34)	787	712	2.07	1.40 to 3.05	0.0002	0.07	52
The incidence of TEAEs
Total studies	8 (23,24,27,29,30,32,34,35)	1,766	1,660	2.91	1.84 to 4.61	<0.00001	<0.00001	89
Including only studies with low risk of bias	7 (23,24,29,30,32,34,35)	1,746	1,640	2.91	1.84 to 4.61	<0.00001	<0.00001	89

n, the number of cases; OR, odds ratio; MD, mean difference; CI, confidence interval; IIEF, International Index of Erectile Function—Erectile Function; TEAEs, treatment-emergent adverse events.

The quality of the evidence of the outcome data, which was assessed using the GRADE approach, is presented in (). Herein, the quality ranged from low to moderate. Inconsistency problems were detected in all outcomes and imprecision problems in most outcomes. As the statistical power was low owing to the number of included studies (≤10), publication bias was not assessed (20).

Table 3

GRADE summary of findings table

Outcomes	Studies, n	Patients, n			Anticipated absolute effects (95% CI)		Relative effect (95% CI)	Quality of evidence (GRADE)
		PDE5-Is	Placebo		Risk with PDE5-Is	Risk with placebo
IIEF domain score	11 RCTs	1,143	1,004		The IIEF domain score was 4.93 higher (from 4.14 higher to 5.71 higher)			⨁⨁⨁◯
								MODERATE1
Recovery events in relation to the IIEF domain score	5 RCTs	252/807 (31.2%)	143/732 (19.5%)		138 more per 1,000 (from 65 more to 221 more)	195 per 1,000	OR =2.06 (1.45 to 2.94)	⨁⨁◯◯
								LOW1,2
Response to SEP question 2	7 RCTs	447/987 (45.3%)	233/886 (26.3%)		185 more per 1,000 (from 128 more to 242 more)	263 per 1,000	OR =2.27 (1.80 to 2.86)	⨁⨁◯◯
								LOW1,2
Response to SEP question 3	7 RCTs	469/1,301 (36.0%)	221/1,209 (18.3%)		201 more per 1,000 (from 123 more to 284 more)	183 per 1,000	OR =2.78 (1.97 to 3.91)	⨁⨁◯◯
								LOW1,2
Incidence of TEAEs	8 RCTs	1,014/1,766 (57.4%)	376/1,209 (31.1%)		157 more per 1,000 (from 110 more to 204 more)	311 per 1,000	OR =1.95 (1.61 to 2.35)	⨁⨁⨁◯
								MODERATE1
Incidence of headache	8 RCTs	207/1,781 (11.6%)	68/1,669 (4.1%)		85 more per 1,000 (from 52 more to 127 more)	41 per 1,000	OR =3.38 (2.40 to 4.75)	⨁⨁◯◯
								LOW1,2

The risk in the intervention group (and its 95% CI) was based on the assumed risk in the comparison group and the relative effect of the intervention (and its 95% CI). 1, downgraded by one level owing to inconsistency; 2, downgraded by one level owing to imprecision. GRADE Working Group quality of evidence. High quality, we are very confident that the true effect lies close to the estimate of the effect; Moderate quality, we are moderately confident in the effect estimate: the true effect is likely to be close to the estimate of the effect; however, there is a possibility that it is substantially different; Low quality, our confidence in the effect estimate is limited: the true effect may be substantially different from the estimate of the effect; Very low quality, we have very limited confidence in the effect estimate: the true effect is likely to be substantially different from the estimate of the effect. GRADE, Grading of Recommendations, Assessment, Development, and Evaluation; n, the number of cases; PDE5-I, phosphodiesterase type 5 inhibitor; CI, confidence interval; IIEF, International Index of Erectile Function—Erectile Function; RCT, randomized controlled trial; OR, odds ratio; SEP, Sexual Encounter Profile; TEAEs, treatment-emergent adverse events.

Discussion

Our meta-analysis and systematic review of the efficacy and safety of PDE5-Is demonstrated the feasibility of this treatment as penile rehabilitation after NSRP. The use of PDE5-Is improved the total IIEF domain score, erectile function recovery, and positive response rate to each SEP question. However, some adverse effects were noted, including headache, flushing, and dyspepsia.

Recovery of postoperative ED takes up to 4 years, and approximately 20–80% of patients recover their erectile function (16). Thermal damage to the cavernous nerve can result in permanent loss of potency after RP, and vascular damage in the accessory pudendal arteries can occur. Moreover, traction during RP can be damaged, resulting in conditions, such as neurapraxia. Neurapraxia can consequently result in structural changes in the endothelium and smooth muscle during RP (36).

New insights into the pathophysiology of postoperative ED led to the development of a rehabilitation strategy defined as the use of any drug or device in patients who have undergone RP to maximize the recovery of erectile function. The efficacy and adverse effects of PDE5-Is as penile rehabilitation were previously evaluated in meta-analyses and systematic reviews (17-19). However, concerns on the methodological quality have been raised in these reports. In these previous reports, errors in the data entered could be found, which has led to problems regarding the methodological query. In the age of evidence-based medicine, systematic review plays an important role in clinical decision making (37). In this situation, errors in the previous systematic reviews gave clinicians wrong information for decision making. These analyses were performed by entering the intention-to-treat population as the total number, and not the complete study population, or by entering the value of the score change as the value of the score. Additionally, there were cases in which the total population value and standard deviation value were incorrectly entered into the study data. Moreover, a retrospective study was included in a previous meta-analysis. Although the research subject of previous studies was the same as that of our study, our systematic review analyzed the results of 14 studies compared to only 6 to 8 studies included in the former. In addition, the quality of the evidence of the outcome data was evaluated using the GRADE approach in this systematic review. Taken together, our analysis provides a more accurate and reliable basis for penile rehabilitation, including the latest findings.

A part of the physiological process is the release of nitrous oxide (NO) in the blood vessels of the corpus cavernosum by sexual stimulation. NO activates the guanylate cyclase enzyme, which increases the number of annular cyclic guanosine monophosphate (cGMP). cGMP relaxes the catholic blood vessels, increasing blood flow and consequently evoking it. PDE5-I decomposition of cGMPs by phosphodiesterase type 5 increases the blood flow of the penis during sexual stimulation. Owing to this mechanism of action, PDE5-Is work only when there is sexual stimulation. Our analysis also demonstrated the superior efficacy of PDE5-Is with the improvements observed in the IIEF domain score, erectile function recovery, and positive response rate to SEP questions 2 and 3.

A subgroup analysis was conducted to assess the effects of the regimen of PDE5-I treatment, i.e., daily use and on-demand use. We found that on-demand use of PDE5-Is was more efficient than daily use of PDE5-Is. The pharmacokinetics of PDE5-Is showed a steady state after 5 days of daily use, with a total plasma concentration of 55 ng/mL achieving a reasonable drug dynamics goal, indicating maintenance of these concentrations over a 24-hour administration interval (18,38). In terms of side effects, daily use yielded a lower incidence than did on-demand use, and a fundamental change in the plasma concentration was expected. Considering these factors, the optimal administration methods can be considered depending on the degree of response.

In terms of safety, most studies have raised concerns on cardiovascular safety, although some studies have reported that PDE5-Is can have beneficial effects on the cardiovascular system (39-43). Because cardiovascular safety is directly linked to survival, it should be considered differently from other factors, even if it is less frequent. Although the total incidence of adverse events associated with PDE5-I administration was higher than that with placebo treatment, no serious cardiovascular adverse events were reported in our analysis. Our subgroup analysis showed that daily use of PDE5-Is had fewer side effects than on-demand use of PDE5-Is. A well-organized large-scale study is needed to confirm the difference in the effects of the regimen of PDE5-I treatment.

Nandipati et al. (44) reported the effectiveness of combination therapy in penile rehabilitation and reported that combination therapy of intra-cavenosal injection and PDE5-I were effective for ED. According to reporting by Deng et al. (45), the combination therapy of PDE5-I and vacuum erection device had a synergistic effect in penile rehabilitation. Although these studies were not included in this analysis because they did not meet the inclusion criteria, it should be considered that PDE5-I based combination therapy is effective in penile rehabilitation.

Limitations

First, clinical heterogeneity among the studies was observed. The type of treatment drug, drug dose, frequency of drug administration, and treatment period varied among the studies. Because of this heterogeneity, all outcomes were evaluated using a random-effects model. To eliminate heterogeneity in the frequency of drug administration, we conducted a subgroup analysis. Consequently, this heterogeneity did not affect the results. Second, the GRADE assessments demonstrated that the quality of the evidence of some outcome data was low. These outcome assessments revealed problems of imprecision and inconsistency. Lastly, only randomized controlled trials were included in this meta-analysis to increase the reliability of the assessments. It is possible that the incidence of TEAEs is low because the predetermined exclusion criteria used for the randomized controlled trials excluded uncommon clinical situations. Third, a patient’s age and comorbidities may be important factors that affect the PDE5-Is response rate. Although we made every effort to the effect of each factors using subgroup analysis, only the regimen of PDE5-I treatment was available for subgroup analysis. Further studies on the effect of the patient’s age and comorbidities on the PDE5-Is response rate are needed.

In terms of the level of evidence, although meta-analysis is at a high level, studies other than RCTs were not included. In addition, although there have been some studies on different subjects of penile rehabilitation, only studies satisfying the criteria for meta-analysis were included in this meta-analysis. In order to overcome these limitations, it is thought that analysis including all studies related to penile rehabilitation is necessary through systemic review in the further study.

Despite these limitations, this meta-analysis corrected some errors that could be found in previous meta-analyses and clearly showed the efficacy of PDE5-Is in patients with ED after NSRP.

Conclusions

This meta-analysis demonstrated the efficacy of PDE5-I treatment in patients with ED after NSRP based on the improvements observed in the IIEF domain score, erectile function recovery, and positive response rate to SEP questions 2 and 3. These efficacies were observed both for daily use and on-demand use of PDE5-Is. In terms of safety, clinically serious adverse effects were not found, although the incidence of TEAEs after PDE5-I treatment was higher than that after placebo treatment.

The article’s supplementary files as