Dorsal Penile Nerve Block Prior to Inflatable Penile Prosthesis Placement: A Randomized, Placebo-Controlled Trial

Mathew C. Raynor, Angela Smith, Sachin N. Vyas, John P. Selph, Culley C. Carson

Research output: Contribution to journalArticle

  • 3 Citations

Abstract

Introduction. Dorsal penile nerve block (DPNB) has been previously shown to provide effective analgesia for penile surgeries. To date, few studies have examined the role of DPNB prior to inflatable penile prosthesis (IPP) implantation. Aim. The purpose of this study was to assess the efficacy of local penile nerve block prior to IPP implantation for postoperative pain control. Main Outcome Measures. The primary outcome was postoperative pain rated using the visual analog scale (VAS). Secondary outcome measures included total narcotic usage during hospitalization. Methods. Institutional Review Board approval was obtained. Patients with erectile dysfunction scheduled for IPP implantation were approached for study participation. Patients were excluded if they had a previous IPP scheduled for revision or replacement or were undergoing additional procedures during the same operative session. Patients were then randomized to either DPNB with 1% lidocaine and 0.5% bupivacaine without epinephrine or injectable saline placebo. Only the resident surgeon assisting in the case was aware of randomization. All procedures were performed by a single surgeon (C.C.C.). Postoperatively, patients were asked to rate their pain using a VAS hourly while in recovery, at 4 hours, and at 23 hours postoperatively. Total narcotic usage was also measured. Results. A total of 30 patients underwent randomization with 15 patients in each group. Baseline demographic data were similar in each group. There was a significant reduction in pain in the immediate postoperative period and at 4 hours after surgery in the treatment group when compared with placebo (VAS 2.5 vs. 5.3, P=0.009 at 0 hours; VAS 2.8 vs. 5.1, P=0.011 at 4 hours). Narcotic usage was similar among both groups. There were no perioperative or early postoperative complications in either group. Conclusions. DPNB is safe and effective for reducing pain in the early postoperative period following penile prosthesis implantation.

Original languageEnglish (US)
Pages (from-to)2975-2979
Number of pages5
JournalJournal of Sexual Medicine
Volume9
Issue number11
DOIs
StatePublished - 2012

Fingerprint

Penile Prosthesis
Pudendal Nerve
Nerve Block
Randomized Controlled Trials
Placebos
Penile Implantation
Visual Analog Scale
Narcotics
Pain
Postoperative Pain
Random Allocation
Postoperative Period
Outcome Assessment (Health Care)
Surgeons
Research Ethics Committees
Bupivacaine
Erectile Dysfunction
Lidocaine
Analgesia
Epinephrine

Keywords

  • Penile Implant Surgery
  • Penile Nerve Block
  • Penile Prosthesis
  • Randomized Trial

ASJC Scopus subject areas

  • Reproductive Medicine
  • Obstetrics and Gynecology
  • Urology

Cite this

Dorsal Penile Nerve Block Prior to Inflatable Penile Prosthesis Placement : A Randomized, Placebo-Controlled Trial. / Raynor, Mathew C.; Smith, Angela; Vyas, Sachin N.; Selph, John P.; Carson, Culley C.

In: Journal of Sexual Medicine, Vol. 9, No. 11, 2012, p. 2975-2979.

Research output: Contribution to journalArticle

Raynor, Mathew C.; Smith, Angela; Vyas, Sachin N.; Selph, John P.; Carson, Culley C. / Dorsal Penile Nerve Block Prior to Inflatable Penile Prosthesis Placement : A Randomized, Placebo-Controlled Trial.

In: Journal of Sexual Medicine, Vol. 9, No. 11, 2012, p. 2975-2979.

Research output: Contribution to journalArticle

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abstract = "Introduction. Dorsal penile nerve block (DPNB) has been previously shown to provide effective analgesia for penile surgeries. To date, few studies have examined the role of DPNB prior to inflatable penile prosthesis (IPP) implantation. Aim. The purpose of this study was to assess the efficacy of local penile nerve block prior to IPP implantation for postoperative pain control. Main Outcome Measures. The primary outcome was postoperative pain rated using the visual analog scale (VAS). Secondary outcome measures included total narcotic usage during hospitalization. Methods. Institutional Review Board approval was obtained. Patients with erectile dysfunction scheduled for IPP implantation were approached for study participation. Patients were excluded if they had a previous IPP scheduled for revision or replacement or were undergoing additional procedures during the same operative session. Patients were then randomized to either DPNB with 1% lidocaine and 0.5% bupivacaine without epinephrine or injectable saline placebo. Only the resident surgeon assisting in the case was aware of randomization. All procedures were performed by a single surgeon (C.C.C.). Postoperatively, patients were asked to rate their pain using a VAS hourly while in recovery, at 4 hours, and at 23 hours postoperatively. Total narcotic usage was also measured. Results. A total of 30 patients underwent randomization with 15 patients in each group. Baseline demographic data were similar in each group. There was a significant reduction in pain in the immediate postoperative period and at 4 hours after surgery in the treatment group when compared with placebo (VAS 2.5 vs. 5.3, P=0.009 at 0 hours; VAS 2.8 vs. 5.1, P=0.011 at 4 hours). Narcotic usage was similar among both groups. There were no perioperative or early postoperative complications in either group. Conclusions. DPNB is safe and effective for reducing pain in the early postoperative period following penile prosthesis implantation.",
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