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Review |
From the Sexual & Reproductive Medicine Program, Urology Service, Department of Surgery, Memorial Sloan-Kettering Cancer Center, New York, New York.
| Correspondence to: Dr John P. Mulhall, Department of Surgery, Urology Service, 525 E 68th St, New York, NY 10021 (e-mail: mulhalj1{at}mskcc.org). |
Since the introduction of the nerve-sparing radical prostatectomy (RP),
potency preservation rates of between 20% and 90% have been reported. It is
irrefutable that the nerve-sparing status of an RP is predictive of recovery
of erectile function. Bilateral nerve sparing is associated with superior
spontaneous and oral therapy–assisted recovery of erectile function
compared to unilateral nerve sparing, which in turn is more likely to lead to
functional erections than non–nerve-sparing surgery. Neural regeneration
is the mechanism by which erectile function improves over time following RP.
Although the degree of neural trauma that occurs intraoperatively is a
determinant of long-term recovery of neural function, biological factors
involved in neural regeneration are likely important determinants of the
completeness of neural recovery. Furthermore, these biological factors are
likely a major reason for the interindividual variation in recovery of
erectile function after this operation. Recently, the development of rat
models of cavernous nerve injury has facilitated the study of neuroprotective
and neuroregenerative agents. This paper reviews the current knowledge on
pharmacological neuromodulation as it pertains to the radical pelvic surgery
patient. The animal evidence is highly supportive of such agents' having a
positive impact on erectile function recovery after RP. Human trial data are
awaited.
Key words: Cavernous nerve, neuropraxia, immunophilin ligand, neuromodulation, erectile function
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