Intra-amniotic infection
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patients with singleton pregnancies (between August 2014 and April 2020) who underwent inpatient management at our department for PPROM, preterm labor, cervical insufficiency, and asymptomatic cervical shortening between 22 weeks 0 days and 33 weeks 6 days of gestation were included.
Exclusion criteria
Exclusion criteria: Exclusion criteria were as follows: delivery after 34 gestational weeks, fetal chromosomal abnormalities or multiple malformations, intrauterine fetal death, delivery at another hospital, MIAC in which Ureaplasma spp. and Mycoplasma hominis were not identified, and an unclear placental pathology or umbilical vein blood interleukin (IL)-6 concentration in patients in whom intra-amniotic inflammation or MIAC was not detected by amniocentesis or for whom amniocentesis was not indicated.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary study outcomes were the relationships between the prevalence of BPD and intra-amniotic infection with or without Ureaplasma spp. and intra-amniotic inflammation without MIAC after adjusting for gestational age at birth. | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary study outcomes were the relationships between the prevalence of adverse neonatal outcomes, and intra-amniotic infection with or without Ureaplasma spp. and intra-amniotic inflammation without MIAC after adjusting for potential confounders. | — |
Countries
Japan
Contacts
National Hospital Organization, Saga National Hospital Department of Obstetrics and Gynecology