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A pilot randomized controlled trial of vaginal estrogen on postpartum atrophy, perineal pain, and sexual function.
Smith, Pamela E; McLaughlin, Eric M; Pandya, Lopa K; Hade, Erinn M; Lynch, Courtney D; Hudson, Catherine O.
Afiliação
  • Smith PE; Kaiser Permanente, Central Valley Area, 4601 Dale Road, Modesto, CA, 95356, USA. pamela.e1.smith@kp.org.
  • McLaughlin EM; Department of Biomedical Informatics, Center for Biostatistics, The Ohio State University, 200 Lincoln Tower, 1800 Cannon Drive, Columbus, OH, 43210, USA.
  • Pandya LK; Female Pelvic Medicine and Reconstructive Surgery, University of Illinois at Chicago, 820 S Wood St, CSN (MC808), Chicago, IL, 60612, USA.
  • Hade EM; Department of Population Health, Division of Biostatistics, NYU Grossman School of Medicine, 180 Madison Ave, Suite 5-53, New York, NY, 10016, USA.
  • Lynch CD; Department of Obstetrics & Gynecology, The Ohio State University, 395 W 12th Ave, Room 580, Columbus, OH, 43210, USA.
  • Hudson CO; Wellstar Urogynecology, 4900 Ivey Rd NW, Suite 1320, Acworth, GA, 37363, USA.
Int Urogynecol J ; 33(12): 3383-3390, 2022 12.
Article em En | MEDLINE | ID: mdl-35441854
ABSTRACT
INTRODUCTION AND

HYPOTHESIS:

Vulvovaginal symptoms following perineal laceration may be worsened by atrophy related to decreased estrogen. Our objective was to evaluate the effect of local estrogen therapy in this setting.

METHODS:

We conducted a single-center, pilot, randomized, placebo-controlled trial of local estradiol in primiparous women with a second-degree or greater perineal laceration following a term vaginal delivery. Participants were randomized to twice weekly estradiol or placebo cream from delivery through 3 months postpartum. The primary outcome was a validated measure of vulvovaginal symptoms at 12 weeks postpartum. Secondary outcomes included measures of perineal pain, quality of life, sexual function, ease of use, likelihood of continued use, and adverse events.

RESULTS:

We planned to enroll 70 women; however, due to human subjects research restrictions related to the COVID-19 pandemic, enrollment was stopped early. A total of 59 women were randomized, 31 to the estradiol group and 28 to the placebo group. Nearly all participants (95%) were followed through 12 weeks with suggestion of marginal improvement in Vulvar Assessment Scale scores [-0.10; 90% CI = (-0.20, 0.01)] in those randomized to estradiol compared to placebo. Local estradiol was not associated with improvement in other measures, and only one non-serious adverse event was observed.

CONCLUSIONS:

In primiparous women with a perineal laceration, use of local estradiol showed minimal clinical benefit in vulvovaginal atrophy and related symptoms but appears to be acceptable and safe for postpartum use. Larger adequately powered trials enrolling a diverse group of postpartum women are needed to affirm these findings.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Lacerações / COVID-19 Tipo de estudo: Clinical_trials Limite: Female / Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Lacerações / COVID-19 Tipo de estudo: Clinical_trials Limite: Female / Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article