Evidence map›Paper›PMID 29112594›Full record

Trial reportMenopause (New York, N.Y.)2018

Sexual activity and vaginal symptoms in the postintervention phase of the Women's Health Initiative Hormone Therapy Trials.

Margery Gass, Joseph Larson, Barbara Cochrane, JoAnn E Manson, Dorothy Lane, Vanessa Barnabei, Judith Ockene, Marcia L Stefanick, Charles Mouton

Open access · greenAbstract readMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in Menopause (New York, N.Y.), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.9field-weighted citation impact, top 23% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed, 12 citations in OpenAlex.

  1. Review
  2. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 6 institutions in 1 country.

Margery GassCleveland, OH.
Joseph LarsonFred Hutchinson Cancer Research Center, Seattle, WA.
Barbara CochraneFred Hutchinson Cancer Research Center, Seattle, WA.
JoAnn E MansonDivision of Preventive Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA.
Dorothy LaneDepartment of Preventive Medicine, Stony Brook University School of Medicine, Stony Brook, NY.
Vanessa BarnabeiDepartment of Obstetrics and Gynecology, School of Medicine and Biomedical Sciences, University at Buffalo, New York, NY.
Judith OckeneDivision of Preventive and Behavioral Medicine at the University of Massachusetts, Worcester, MA.
Marcia L StefanickStanford Prevention Research Center, Stanford University School of Medicine, Stanford, CA.
Charles MoutonOffice of Academic Affairs and Department of Family Medicine, University of Texas Medical Branch, Galveston, TX.
Fred Hutch Cancer Center · USHarvard University · USStanford University · USStony Brook University · USUniversity at Buffalo, State University of New York · USUniversity of Massachusetts Chan Medical School · US

Funding

CLIN CTR CLIN TRIAL/OBSERVATIONAL STUDY OF WHIN01WH042126 · WH · UNIVERSITY OF CINCINNATI · PI LIU, JAMES H. · 1994 to 2000
$1.0M
NHLBI NIH HHS HHSN268201600001CNHLBI NIH HHS HHSN268201600002CNHLBI NIH HHS HHSN268201600003CNHLBI NIH HHS HHSN268201600004CNHLBI NIH HHS HHSN268201600018CWHI NIH HHS N01 WH042126
6 · The paper itself

Abstract

objectiveTo assess the impact of discontinuing oral hormone therapy (HT) on sexual activity, vaginal symptoms, and sexual activity components among participants in the estrogen-progestin therapy (EPT) and estrogen therapy (ET) trial of the Women's Health Initiative.

methodsSurveys were sent postintervention to those who were still taking study pills and agreed to continue in the study when the trials were stopped. Comparisons between former HT and placebo users were accomplished with chi-square tests for categorical variables and t tests for continuous variables.

resultsIn all, 13,902 women with mean age at survey 69.9 years (EPT trial, women with intact uterus) and 71.7 years (ET trial, women with history of hysterectomy) responded. Prevalence of sexual activity postintervention was not significantly different between former EPT and placebo users (36.0% vs 34.2%; P = 0.37). Sexual activity of former ET users was 5.6% higher than placebo users (27.6% vs 22.0%; P = 0.001). The majority of sexually active women overall maintained orgasmic capacity and sexual satisfaction. Former EPT users were 10% to 12% more likely than former placebo users to report decreased desire, arousal, intercourse, climax, and satisfaction with sexual activity, and also increased dryness and dyspareunia upon discontinuing study drugs (P < 0.001). Former ET users were more likely than placebo users to report rare to no desire or arousal postintervention (P < 0.001).

conclusionsPostintervention ET trial participants formerly assigned to ET were significantly more likely to report sexual activity than those formerly assigned to placebo. Women who discontinued EPT were significantly more likely to report negative vaginal and sex-related effects.

Indexed as

MenopauseAgedAged, 80 and overEstrogen Replacement TherapyEstrogensFemaleFollow-Up StudiesHumansMiddle AgedProgestinsSexual BehaviorSexual PartnersSurveys and QuestionnairesSyndromeWomen's HealthEstrogensProgestins

Identifiers

PMID29112594
PMCPMC5821577
OpenAlexW2768811923

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.