Evidence map›Paper›PMID 39843375›Full record

ArticleBMJ open2025

Your period and your pregnancy, a cohort study of pregnant patients investigating the associations between menstruation and birth outcomes in Australia: study protocol.

Kirstin Tindal, Fiona Cousins, Kirsten Rebecca Palmer, Stacey Ellery, Beverley Vollenhoven, Caroline E Gargett, Adrienne Gordon, Billie Bradford, Miranda Davies-Tuck

Abstract read
In one paragraph

Article in BMJ open, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Kirstin TindalThe Ritchie Centre at Hudson Institute of Medical Research, Clayton, Victoria, Australia kirstin.street@monash.edu.ORCID http://orcid.org/0000-0002-5278-472X
Fiona CousinsThe Ritchie Centre at Hudson Institute of Medical Research, Clayton, Victoria, Australia.
Kirsten Rebecca PalmerObstetrics and Gynaecology, Monash University School of Clinical Sciences at Monash Health, Clayton, Victoria, Australia.ORCID http://orcid.org/0000-0001-7421-6291
Stacey ElleryThe Ritchie Centre at Hudson Institute of Medical Research, Clayton, Victoria, Australia.ORCID http://orcid.org/0000-0003-3769-1960
Beverley VollenhovenObstetrics and Gynaecology, Monash University School of Clinical Sciences at Monash Health, Clayton, Victoria, Australia.
Caroline E GargettThe Ritchie Centre at Hudson Institute of Medical Research, Clayton, Victoria, Australia.
Adrienne GordonDepartment of Paediatrics, University of Sydney - Camden Campus, Camden, New South Wales, Australia.
Billie BradfordObstetrics and Gynaecology, Monash University School of Clinical Sciences at Monash Health, Clayton, Victoria, Australia.
Miranda Davies-TuckThe Ritchie Centre at Hudson Institute of Medical Research, Clayton, Victoria, Australia.ORCID http://orcid.org/0000-0003-1918-5538

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionEarly pregnancy care involves the screening and identification of women with risk factors for adverse pregnancy outcomes, including stillbirth or preterm birth, to tailor pregnancy care and interventions accordingly. Most stillbirths and approximately two-thirds of preterm births, however, occur in the absence of evident risk factors. The majority of stillbirths occur in the preterm period, yet there are few interventions targeting this period, and progress to reduce stillbirth rates remains slow. Placental dysfunction is a major contributor to stillbirth, particularly, preterm stillbirth. Here, the endometrial environment may shed light on factors that influence placental development and the trajectory of a pregnancy. Menstrual symptoms or abnormal uterine bleeding (AUB) can indicate endometrial disorders, which are associated with infertility and adverse pregnancy outcomes. Whether AUB is associated with pregnancy outcomes in the absence of a diagnosed endometrial pathology, however, remains unknown. Limited information regarding a woman's menstrual cycle is captured in routine early pregnancy assessments, such as the last menstrual period and menstrual cycle length. Given the latent diagnosis of endometrial disorders and that up to a third of all women experience AUB during their lifetime, determining the association between menstrual characteristics and pregnancy outcomes has the potential to uncover new clinical strategies to reduce adverse pregnancy outcomes. Therefore, this study aims to understand the association between menstruation and pregnancy outcomes to identify which menstrual characteristics could provide value as a pregnancy risk assessment tool. METHODS AND ANALYSIS: This is a prospective study of women aged 18-45 with a singleton pregnancy. Participants will be recruited in early pregnancy at their antenatal appointment and not have a known diagnosed endometrial pathology (endometriosis, adenomyosis, endometrial cancer or an endometrial submucosal fibroid) or have had an endometrial ablation. Participants will also be excluded if there is a planned termination of pregnancy or a termination of pregnancy for psychosocial reasons. Women will complete a menstrual history survey to capture menstrual cycle length, regularity, level of pain, heaviness of flow and other menstrual symptoms. Participants will consent to having the survey data linked with their pregnancy and birth outcome information. The primary outcome is a composite of stillbirth, spontaneous preterm birth, pre-eclampsia or fetal growth restriction. Participants will also be invited to complete an optional fetal movements survey at 28-32 and 36+ weeks' gestation, and consent for placental collection at the time of birth will be sought. ETHICS AND DISSEMINATION: Ethics approval was obtained from Monash Health Human Research Ethics Committee (83559) on 24 April 2024. The study will be conducted in accordance with these conditions. Findings will be disseminated through peer-reviewed publications and conference presentations.

Indexed as

MenstruationMenstruation DisturbancesPregnancy OutcomePremature BirthAdultAustraliaCohort StudiesFemaleHumansPregnancyProspective StudiesResearch DesignRisk FactorsStillbirthDysmenorrheaFetal medicineGYNAECOLOGYOBSTETRICSPregnancyPUBLIC HEALTH

Identifiers

PMID39843375
PMCPMC11784170

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Registered trials

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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.