Preterm Prelabor Rupture of Membranes between 34 and 37 Weeks: A Point-of-Care Test of Vaginal Fluid Interleukin-6 Concentrations for a Noninvasive Detection of Intra-Amniotic Inflammation
Language English Country Switzerland Media print-electronic
Document type Journal Article
PubMed
28796999
DOI
10.1159/000477617
PII: 000477617
Knihovny.cz E-resources
- Keywords
- Amniotic fluid, Cytokine, Intra-amniotic inflammation, Late PPROM, Lateral flow-based immunoassay, Microbial invasion of the amniotic cavity, Noninvasive procedure, Preterm delivery, Rapid test,
- MeSH
- Adult MeSH
- Infections diagnosis MeSH
- Interleukin-6 analysis MeSH
- Humans MeSH
- Young Adult MeSH
- Infant, Newborn, Diseases MeSH
- Infant, Newborn MeSH
- Point-of-Care Testing MeSH
- Fetal Membranes, Premature Rupture * MeSH
- Prospective Studies MeSH
- Pregnancy MeSH
- Vagina chemistry MeSH
- Check Tag
- Adult MeSH
- Humans MeSH
- Young Adult MeSH
- Infant, Newborn MeSH
- Pregnancy MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- IL6 protein, human MeSH Browser
- Interleukin-6 MeSH
OBJECTIVE: The aim of this study was to investigate whether a previously reported vaginal fluid point-of-care interleukin (IL)-6 cut-off value of 2,500 pg/mL can be used for the identification intra-amniotic inflammation in women with preterm prelabor rupture of membranes (PPROM) between 34 and 37 weeks. MATERIAL AND METHODS: A prospective cohort study was conducted in women with singleton gestation complicated by PPROM between 34 + 0 and 36 + 6 weeks. Vaginal fluid was successfully obtained in 118 women from the posterior vaginal fornix via aspiration using a sterile urine sample tube with a suction tip. Amniotic fluid was obtained via transabdominal amniocentesis. IL-6 concentrations were assessed in both fluids immediately after sampling. Intra-amniotic inflammation was defined as an amniotic fluid point-of-care IL-6 concentration of ≥745 pg/mL. RESULTS: The tested vaginal fluid IL-6 cut-off value had a sensitivity of 91%, specificity of 91%, positive predictive value of 50%, negative predictive value of 99%, positive likelihood ratio of 9.7, and negative likelihood ratio of 0.1 for the identification of intra-amniotic inflammation. CONCLUSION: The point-of-care vaginal fluid IL-6 test with a cut-off value of 2,500 pg/mL shows good sensitivity, specificity, and negative predictive value for the identification of intra-amniotic inflammation in PPROM between 34 and 37 weeks.
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