J 2023

Treatment of Vulvovaginal Laxity by Electroporation: The Jett Plasma Medical for Her II Study

FAIT, Tomas, Tivadar BALTAZAR, Leona BUBENÍČKOVÁ, Jan KESTRANEK, Martin STEPAN et. al.

Basic information

Original name

Treatment of Vulvovaginal Laxity by Electroporation: The Jett Plasma Medical for Her II Study

Authors

FAIT, Tomas (203 Czech Republic), Tivadar BALTAZAR (203 Czech Republic), Leona BUBENÍČKOVÁ (203 Czech Republic, belonging to the institution), Jan KESTRANEK (203 Czech Republic), Martin STEPAN (203 Czech Republic), Miroslav MULLER (203 Czech Republic) and Pavel TURCAN (203 Czech Republic, guarantor)

Edition

Journal of Clinical Medicine, Basel, MDPI, 2023, 2077-0383

Other information

Language

English

Type of outcome

Článek v odborném periodiku

Field of Study

30214 Obstetrics and gynaecology

Country of publisher

Switzerland

Confidentiality degree

není předmětem státního či obchodního tajemství

References:

Impact factor

Impact factor: 3.900 in 2022

RIV identification code

RIV/00216224:14110/23:00133376

Organization unit

Faculty of Medicine

UT WoS

001085248800001

Keywords in English

vaginal laxity; vulvovaginal laxity; nonsurgical vaginal tightening; incontinence; sexual function; urogenital distress; electroporation therapy

Tags

Tags

International impact, Reviewed
Změněno: 1/2/2024 10:59, Mgr. Tereza Miškechová

Abstract

V originále

Introduction: Vaginal laxity is a widespread and undertreated medical condition associated especially with vaginal parity. Aim: To evaluate the efficacy and safety of electroporation therapy treatment of vulvovaginal laxity by the Jett Plasma for Her II device. Methods: The Jett Plasma for Her II Study is a multicentric, prospective, randomized, single-blinded, and controlled study. Women presenting with vaginal laxity were randomized to receive electroporation therapy delivered to the vaginal tissue (active-82 patients) vs. therapy with zero intensity (placebo-9 patients). Results: A total of 91 subjects whose average age was 48.69 +/- 10.89 were included. Due to the results of a one-way analysis of variance, it may be concluded that in the case of the vaginal laxity questionnaire (VLQ), there is a statistically significant difference between actively treated patients and the placebo group (F-1,F-574 = 46.91; p < 0.001). In the case of the female sexual function index (FSFI), a one-way ANOVA test also showed a statistically significant difference between the actively treated patients and the placebo group (F-1,F-278 = 7.97; p = 0.005). In the case of the incontinence impact questionnaire-7 (IIQ-7), a one-way ANOVA test showed a statistically significant difference between the actively treated patients and the placebo group (F-1,F-384 = 15.51; p < 0.001). It confirms that improvement of vaginal laxity is conjoined with benefits in symptoms of urinary incontinence. Biopsy performed after the end of the treatment shows an increase in the vaginal mucosa thickness by an average of 100.04% in the active group. The treatment was well tolerated with no adverse events. No topical anesthetics were required. Conclusions: Treatments of vulvovaginal laxity by electroporation therapy achieved significant and sustainable 12-month effectiveness. Responses to the questionnaires also suggest subjective improvement in self-reported sexual function, incontinence, sexual satisfaction, and urogenital distress.