Evidence map›Paper›PMID 40885901›Full record

ArticleBMC pregnancy and childbirth2025

The implication of chlamydia and bacterial vaginosis among low-risk pregnant women with preterm birth: a prospective multicentric cohort study.

Wassan Nori, Wisam Akram, Rafal Mustafa Murshid, Reia Jaber

Abstract readMulticenter Study
In one paragraph

Article in BMC pregnancy and childbirth, 2025. 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
–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

2 citing papers in PubMed.

  1. Article
  2. Article
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

4 authors.

Wassan Nori *College of Medicine, Department of Obstetrics and Gynecology, Mustansiriyah University, Baghdad, Iraq. Dr.wassan76@uomustansiriyah.edu.iq.ORCID http://orcid.org/0000-0002-8749-2444
Wisam Akram *College of Medicine, Department of Obstetrics and Gynecology, Mustansiriyah University, Baghdad, Iraq.ORCID http://orcid.org/0000-0002-1968-7004
Rafal Mustafa MurshidCollege of Medicine, Department of Obstetrics and Gynecology, University of Anbar, Ramadi, 31001, Iraq.ORCID http://orcid.org/0000-0002-4910-2185
Reia JaberDepartment of Infection Prevention & Control. Florida, Orlando Health, Orlando, 32806, USA.ORCID http://orcid.org/0009-0003-0250-8262

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPreterm birth (PTB) is a multifactorial pathology that raises feto-maternal morbidity. Infection was associated with higher PTB risk. Earlier studies discussed the inconsistent role of Chlamydia trachomatis (CT) with PTB. To examine the contribution of CT to the overall incidence of PL in our population and to verify the concurrent impact of bacterial vaginosis (BV) on PTB risk.

methodsA prospective cohort study enrolled low-risk pregnant women attending an antenatal clinic at a gestational age of 24-28 weeks. They were screened for CT and BV using cervical smears and subdivided into two groups: positive CT cases (study group; N = 79) and negative CT cases (control group; N = 235). They were followed until delivery. For each, maternal parameters [Maternal age, parity, socioeconomic class, BV, preterm labor, tocolytic, progestogen drugs, and dexamethasone] and Fetal parameters [Gestational age at delivery, fetal birth weight, admission to intensive care unit for respiratory distress syndrome] were recorded.

resultsPositive CT cases had significantly higher PBT; 20/79 (25.3%) vs. 21/235 (9%) among negative CT cases. Stratifying PTB results according to infection status revealed that 6.3% (12/189) of PTB cases were negative for both CT and BV, 12.2% (5/41) had CT alone, and 19.6% (9/46) were positive for BV alone. 39.5% (15/38) of PTB cases screened positive for CT and BV, thus highlighting a potential synergistic effect between the infection and PTB risk. Positive CT cases had higher BV incidence; 38/79 (48.1%), and higher use of tocolytic; 21/79 (26.6%), progestogen; 20/79 (25.3%), and dexamethasone drugs; 24/79 (30.4%); (P = 0.03, 0.006, 0.02, 0.009, and 0.01, respectively). Multiple logistic regression showed that positive BV cases had an increased risk of adverse outcomes, OR = 3.78. Overall model fit confirmed CT contribution to overall PTB 3-7%. Cochran-Mantel-Haenszel test discussed a BV synergistic role in PTB; OR = 2.55; 95%CI:1.44 to 4.51; P = 0.002.

conclusionThe current findings suggest that CT infection, especially when combined with BV, may significantly increase the risk of PTB even when both infections are appropriately treated during pregnancy. The observed synergistic interaction highlights the potential role of screening for co-infection during pregnancy and reinforces an integrated management approach beyond treatment.

Indexed as

Chlamydia InfectionsChlamydia trachomatisPregnancy Complications, InfectiousPremature BirthVaginosis, BacterialAdultFemaleGestational AgeHumansIncidenceInfant, NewbornPregnancyProspective StudiesRisk FactorsVaginal SmearsYoung AdultBacterial vaginosisChlamydia trachomatisInfectionPCRPreterm labor

Identifiers

PMID40885901
PMCPMC12399010

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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 Socratic graph.