Evidence map›Paper›PMID 30118684›Full record

ArticleContraception2018

Combined oral contraceptive interference with the ability of ulipristal acetate to delay ovulation: A prospective cohort study.

Alison B Edelman, Jeffrey T Jensen, Sara McCrimmon, Marci Messerle-Forbes, Andrea O'Donnell, Jon D Hennebold

Abstract read
In one paragraph

Article in Contraception, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
2.1field-weighted citation impact, top 13% 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

7 citing papers in PubMed, 1 synthesis or guideline pooled it, 24 citations in OpenAlex.

  1. U.S. Selected Practice Recommendations for Contraceptive Use, 2024.MMWR. Recommendations and reports : Morbidity and mortality weekly report. Recommendations and reports · 2024
    Guideline
  2. Trial
  3. Trial
  4. Trial
  5. Article
  6. Observational
  7. Observational
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 1 country.

Alison B EdelmanDepartment of Obstetrics & Gynecology, Oregon Health & Science University, Portland, Oregon; Division of Reproductive & Developmental Sciences, Oregon National Primate Research Center, Beaverton, Oregon. Electronic address: edelmana@ohsu.edu.
Jeffrey T JensenDepartment of Obstetrics & Gynecology, Oregon Health & Science University, Portland, Oregon; Division of Reproductive & Developmental Sciences, Oregon National Primate Research Center, Beaverton, Oregon.
Sara McCrimmonDepartment of Obstetrics & Gynecology, Oregon Health & Science University, Portland, Oregon.
Marci Messerle-ForbesDepartment of Obstetrics & Gynecology, Oregon Health & Science University, Portland, Oregon.
Andrea O'DonnellDepartment of Obstetrics & Gynecology, Oregon Health & Science University, Portland, Oregon.
Jon D HenneboldDepartment of Obstetrics & Gynecology, Oregon Health & Science University, Portland, Oregon; Division of Reproductive & Developmental Sciences, Oregon National Primate Research Center, Beaverton, Oregon.
Oregon Health & Science University · USOregon National Primate Research Center · US

Funding

Upgrade of confocal microscopy at the Oregon National Primate Research CenterP51OD011092 · OD · OREGON HEALTH & SCIENCE UNIVERSITY · PI Bonnie J. Nagel · 2012 to 2026
$203.9M
OREGON CLINICAL AND TRANSLATIONAL SCIENCE INSTITUTEUL1RR024140 · NCRR · OREGON HEALTH & SCIENCE UNIVERSITY · PI ORWOLL, ERIC S. · 2006 to 2011
$61.1M
NCRR NIH HHS UL1 RR024140NIH HHS P51 OD011092
6 · The paper itself

Abstract

objectiveTo determine if a combined oral contraceptive (COC) initiated shortly after ulipristal acetate (UPA) administration interferes with its mechanism of action. STUDY

designHealthy, reproductive-age women of normal BMI with proven ovulation (serum progesterone >3 ng/ml) were enrolled for three cycles (Cycle 1, UPA only; Cycle 2 washout; Cycle 3 UPA plus COC). During Cycles 1 and 3, subjects were monitored with transvaginal ultrasound and blood sampling for progesterone and LH every other day until a dominant follicle measuring >15 mm was visualized. In both treatment cycles, subjects received UPA (30mg) and were followed daily with similar monitoring for up to 7 days. In Cycle 3 only, subjects initiated a daily COC (0.15 mg levonorgestrel/30 μg ethinyl estradiol) 2 days after UPA. The study had 80% power to detect a 15% difference in the proportion of cycles with at least a 5-day delay in follicle rupture. We assessed follicle rupture as >50% decrease in mean size and adjudicated unclear outcomes with serum hormones.

resultsA total of 36 women enrolled and 33 completed all study procedures [age 28.4 years (SD 3.9); BMI 23.4 (SD 2.4)]. Compared to Cycle 1, more subjects demonstrated evidence of follicle rupture in <5 days in Cycle 3 [1/33 (3%) vs. 9/33 (27%), p = .008]. We also included data from 2 subjects who experienced rupture prior to COC dosing in the analysis.

conclusionUPA's effectiveness is significantly reduced by administering COCs 2 days later. IMPLICATIONS: This study demonstrates that UPA's efficacy as an emergency contraceptive is reduced with early exposure to COCs.

Indexed as

AdultContraceptive Agents, FemaleContraceptives, Oral, CombinedContraceptives, PostcoitalDrug CombinationsDrug InteractionsEthinyl EstradiolFemaleHealthy VolunteersHumansLevonorgestrelLuteinizing HormoneNorpregnadienesOvarian FollicleOvulationProgesteroneContraceptive Agents, FemaleContraceptives, Oral, CombinedContraceptives, PostcoitalDrug CombinationsEthinyl Estradiolethinyl estradiol, levonorgestrel drug combinationLevonorgestrelLuteinizing HormoneNorpregnadienesProgesteroneulipristal acetateContraceptive initiationEmergency contraceptionOral contraceptivesOvulation inhibitionPharmacodynamicsUlipristal acetate

Identifiers

PMID30118684
PMCPMC6204102
OpenAlexW2887714875

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.