| Literature DB >> 25785286 |
Fouad Aoun1, Alexandre Peltier1, Roland van Velthoven1.
Abstract
Erectile dysfunction is the most common complication after pelvic radical surgery. Rehabilitation programs are increasingly being used in clinical practice but there is no high level of evidence supporting its efficacy. The principle of early penile rehabilitation stems from animal studies showing early histological and molecular changes associated with penile corporal hypoxia after cavernous nerve injury. The concept of early penile rehabilitation was developed in late nineties with a subsequent number of clinical studies supporting early pharmacologic penile rehabilitation. These studies included all available phosphodiesterase type 5 inhibitors, intracavernosal injection and intraurethral use of prostaglandin E1 and to lesser extent vacuum erectile devices. However, these studies are of small number, difficult to interpret, and often with no control group. Furthermore, no studies have proven an in vivo derangement of endothelial or smooth muscle cell metabolism secondary to a prolonged flaccid state. The purpose of the present report is a synthetic overview of the literature in order to analyze the concept and the rationale of rehabilitation program of erectile dysfunction following radical pelvic surgery and the evidence of such programs in clinical practice. Emphasis will be placed on penile rehabilitation programs after radical cystoprostatectomy, radical prostatectomy, and rectal cancer treatment. Future perspectives are also analyzed.Entities:
Mesh:
Substances:
Year: 2015 PMID: 25785286 PMCID: PMC4345049 DOI: 10.1155/2015/876046
Source DB: PubMed Journal: ScientificWorldJournal ISSN: 1537-744X
Summary table of penile rehabilitation trials in patients undergoing pelvic cancer surgery.
| Author (year of publication) | Study design | Type of pelvic cancer surgery | Number of patients | Penile rehabilitation modality | Active drug (dosage) | Regimen | Duration | Outcomes |
|---|---|---|---|---|---|---|---|---|
| Montorsi et al. (1997) [ | PRCT | NSRP | 30 | ICI | Alprostadil (2.5–14 | 3 times weekly starting 1 month after surgery | 12 weeks | Recovery of spontaneous EF |
| Mulhall et al. (2005) [ | Prospective controlled nonrandomized trial | RP | 132 | PDE5I or ICI for nonresponders to PDE5I | Sildenafil (50–100 mg) and alprostadil | Daily oral PDE5I or 3 times weekly ICI for nonresponders | 18 months | 2.7 times higher spontaneous EF and statistically higher IIEF scores |
| Bannowsky et al. (2008) [ | PRCT | NSRP | 41 | PDE5I | Sildenafil (25 mg) | Nightly low dose starting the day of catheter removal | 52 weeks | Higher spontaneous EF and statistically higher IIEF scores |
| Padma-Nathan et al. (2008) [ | PRCT | BNSRP | 76 | PDE5I | Sildenafil (50–100 mg) | Nightly starting 4 weeks after surgery | 36 weeks | Improvement in spontaneous EF and satisfaction |
| Montorsi et al. (2004) [ | PRCT | BNSRP | 303 | PDE5I | Tadalafil (20 mg) | On demand 12 to 48 months after surgery | 12 weeks | Statistically higher IIEF scores and higher satisfaction |
| Brock et al. (2003) [ | PRCT | NSRP | 440 | PDE5I | Vardenafil (10–20 mg) | On demand | 12 weeks | Statistically higher IIEF scores |
| Raina et al. (2006) [ | PRCT | NSRP | 109 | VED | VED | Daily starting two weeks after surgery | 9 months | Improvement in spontaneous EF, IIEF scores, and satisfaction |
| Raina et al. (2007) [ | Prospective controlled nonrandomized trial | NSRP | 91 | Transurethral | MUSE (125 or 250 | 3 times weekly starting 3 weeks after the surgery | 9 months | Recovery of spontaneous EF |
|
Köhler et al. (2007) [ | PRCT | NSRP | 28 | VED | VED | Daily (10 mins) (immediate (1 month) versus delayed (6 months)) | 5 months | Improvement of EF and preservation of penile length |
| Montorsi et al. (2008) [ | PRCT | BNSRP | 628 | PDE5I | Vardenafil (10 mg nightly versus 5/20 mg on demand) | 10 mg nightly versus 5/20 mg on demand | 9 months | No difference in IIEF-EF between nightly dosing and on-demand dosing |
| McCullough (2008) [ | PRCT | NSRP | 54 | Transurethral versus PDE5I | MUSE (125 | Nightly starting 1 month after the surgery | 9 months | No differences in recovery |
|
Schwartz et al. (2004) [ | Prospective controlled nonrandomized trial | NSRP | 21 | PDE5I | Sildenafil (50 mg versus 100 mg) | Every other night beginning the day of catheter removal | 6 months | No loss of smooth muscle in 50 mg and gain of smooth muscle in 100 mg |
| Nandipati et al. (2006) [ | Prospective controlled nonrandomized trial | NSRP | 22 | PDE5I and ICI | Sildenafil (50 mg) and alprostadil (1–4 | Sildenafil daily and ICI 2-3 times weekly at hospital discharge | 6 months | Assisted early sexual activity and satisfaction; addition of PDE5I allows lower dose of ICI |
| Zippe et al. (2004) [ | Retrospective | RC | 49 | PDE5I | Sildenafil (?) | Not specified | Not specified | Successful |
| Hautmann et al. (2010) [ | Retrospective | RC | 9 | PDE5I | Sildenafil (?) | Not specified | Not specified | Partial tumescence in 5/9 patients |
| El-Bahnasawy et al. (2008) [ | Prospective nonrandomized trial | RC | 100 | PDE5I | Sildenafil (50–100 mg) | Daily | 4 weeks with 50 mg and then 4 weeks with 100 mg | Dose related effect |
| Nishizawa et al. (2011) [ | Prospective nonrandomized trial | Rectal cancer surgery | 49 | PDE5I | Sildenafil (25 mg) and vardenafil (5 mg) or | On demand | Not specified | Improvement in EF in 69% of patients |
| Lindsey et al. (2002) [ | PRCT | Rectal cancer and inflammatory bowel disease surgery | 32 | PDE5I | Sildenafil (25–50–100 mg) | Dose escalation | 4 weeks | 79% responded to |
PRCT: prospective randomized controlled trial; PDE5I: phosphodiesterase type 5 inhibitor; ICI: intracavernous injection; MUSE: medicated urethral system erection; RP: radical prostatectomy; RC: radical cystectomy; NSRP: nerve sparing radical prostatectomy; BNSRP: bilateral nerve sparing radical prostatectomy; EF: erectile function; IIEF: international index of erectile function; IIEF-EF: erectile function domain of the international index of erectile function.