External validation of a non-invasive vaginal tool to assess the risk of intra-amniotic inflammation in pregnant women with preterm labor and intact membranes

dc.contributor.authorCobo Cobo, María Teresa
dc.contributor.authorBurgos Artizzu, Xavier P.
dc.contributor.authorFerrero Martínez, Silvia
dc.contributor.authorBalcells, Judith
dc.contributor.authorBosch, Jaime
dc.contributor.authorGené, Amadeu
dc.contributor.authorMurillo Bravo, Clara
dc.contributor.authorRueda, Claudia
dc.contributor.authorBoada, David
dc.contributor.authorSánchez Antón, Maria Teresa
dc.contributor.authorKacerovsky, Marian
dc.contributor.authorJacobsson, Bo
dc.contributor.authorPalacio, Montse
dc.date.accessioned2025-03-25T11:15:24Z
dc.date.available2025-03-25T11:15:24Z
dc.date.issued2024
dc.date.updated2025-03-25T11:15:24Z
dc.description.abstractObjectives: To prospectively validate the diagnostic performance of a non-invasive point-of-care tool (Rapid IAI System), including vaginal alpha-fetoprotein and interleukin-6, to predict the occurrence of intra-amniotic inflammation in a Spanish cohort of patients admitted with a diagnosis of preterm labor and intact membranes. Methods: From 2017 to 2022, we prospectively evaluated a cohort of pregnant women diagnosed with preterm labor and intact membranes admitted below 34+0 weeks who underwent amniocentesis to rule-in/out intra-amniotic infection and/or inflammation. Vaginal sampling was performed at the time of amniocentesis or within 24-48 h. Amniotic fluid IL-6, vaginal alpha-fetoprotein and vaginal IL-6 concentrations were measured using a point-of-care tool provided by Hologic Inc., "Rapid IAI System". We defined intra-amniotic inflammation when amniotic fluid IL-6 values were greater than 11.3 ng/mL. During recruitment, clinicians were blinded to the results of the point-of-care tool. The original prediction model proposed by Hologic Inc. to predict intra-amniotic inflammation was validated in this cohort of patients. Results: We included 151 patients diagnosed with preterm labor and intact membranes. Among these, 29 (19.2 %) had intra-amniotic inflammation. The algorithm including vaginal IL-6 and alpha-fetoprotein showed an area under curve to predict intra-amniotic inflammation of 80.3 % (±5.3 %) with a sensitivity of 72.4 %, specificity of 84.6 %, positive predictive valuve (PPV) of 52.5 %, negative predictive value (NPV) of 92.9 %, and a positive likelihood ratio (LR+) of 4.6 and negative likelihood ratio (LR-) of 0.33. Conclusions: External validation of a non-invasive rapid point-of-care tool, including vaginal alpha-fetoprotein and IL-6, showed very good diagnostic performance for predicting the absence of intra-amniotic inflammation in women with preterm labor and intact membranes.
dc.format.extent9 p.
dc.format.mimetypeapplication/pdf
dc.identifier.idgrec757472
dc.identifier.issn0300-5577
dc.identifier.pmid39575693
dc.identifier.urihttps://hdl.handle.net/2445/219980
dc.language.isoeng
dc.publisherWalter de Gruyter
dc.relation.isformatofReproducció del document publicat a: https://doi.org/10.1515/jpm-2024-0178
dc.relation.ispartofJournal of Perinatal Medicine, 2024, vol. 53, num.2, p. 170-178
dc.relation.urihttps://doi.org/10.1515/jpm-2024-0178
dc.rights(c) Walter de Gruyter, 2024
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess
dc.sourceArticles publicats en revistes (Cirurgia i Especialitats Medicoquirúrgiques)
dc.subject.classificationPart prematur
dc.subject.classificationLíquid amniòtic
dc.subject.classificationEmbarassades
dc.subject.otherPremature labor
dc.subject.otherAmniotic liquid
dc.subject.otherPregnant women
dc.titleExternal validation of a non-invasive vaginal tool to assess the risk of intra-amniotic inflammation in pregnant women with preterm labor and intact membranes
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion

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