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A Single Injection of Platelet-Rich Plasma Injection for the Treatment of Stress Urinary Incontinence in Females: A Randomized Placebo-Controlled Trial.
Ashton, Leah; Nakatsuka, Hannah; Johnson, Colin M; Kenne, Kimberly; Kreder, Karl J; Kruse, Ryan; Wendt, Linder; Takacs, Elizabeth B; Vollstedt, Annah J.
Affiliation
  • Ashton L; Medical University of South Carolina, Charleston, SC.
  • Nakatsuka H; University of Iowa Hospitals & Clinics, Iowa City, IA. Electronic address: hannah-nakatsuka@uiowa.edu.
  • Johnson CM; University of Iowa Hospitals & Clinics, Iowa City, IA. Electronic address: colin-johnson@uiowa.edu.
  • Kenne K; University of Iowa Hospitals & Clinics, Iowa City, IA. Electronic address: kimberly-kenne@uiowa.edu.
  • Kreder KJ; University of Iowa Hospitals & Clinics, Iowa City, IA. Electronic address: karl-kreder@uiowa.edu.
  • Kruse R; University of Iowa Hospitals & Clinics, Iowa City, IA. Electronic address: ryan-kruse@uiowa.edu.
  • Wendt L; Institute for Clinical and Translational Science, University of Iowa, Iowa City, IA. Electronic address: linder-windt@uiowa.edu.
  • Takacs EB; University of Iowa Hospitals & Clinics, Iowa City, IA.
  • Vollstedt AJ; University of Iowa Hospitals & Clinics, Iowa City, IA. Electronic address: annah-vollstedt@uiowa.edu.
Urology ; 2024 Jun 26.
Article in En | MEDLINE | ID: mdl-38942391
ABSTRACT

OBJECTIVE:

To determine the efficacy of a single injection of platelet-rich plasma (PRP) into the anterior vaginal wall at the mid-urethra compared to placebo, as there is emerging evidence that PRP may help treat female stress urinary incontinence (SUI).

METHODS:

This was a single-blind, randomized, placebo-controlled clinical trial at a single institution. Females with bothersome, demonstrable stress-predominant urinary incontinence were enrolled. Participants were randomized to either injection of 5 mL autologous PRP or saline at the anterior vaginal wall at the mid-urethra. The primary outcome was composite treatment success at 6 months, defined as a negative cough stress test and an answer of "much better" or "very much better" on the Patient's Global Impression of Improvement.

RESULTS:

Fifty patients were enrolled in the study and randomized to the PRP group (n = 25) or the saline placebo group (n = 25). There was no statistically significant difference in the primary outcome between the 2 groups. Adverse events were minor, and the rate of adverse events was similar between both groups.

CONCLUSION:

In this randomized placebo-controlled study, we were unable to demonstrate a difference in SUI treatment success between PRP and saline injections. At this time, there is insufficient evidence to offer a one-time PRP injection into the anterior vaginal wall for treatment of female SUI.

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Urology Year: 2024 Type: Article Affiliation country: Seychelles

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Urology Year: 2024 Type: Article Affiliation country: Seychelles