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.author
Cobo Cobo, María Teresa
dc.contributor.author
Burgos Artizzu, Xavier P.
dc.contributor.author
Ferrero Martínez, Silvia
dc.contributor.author
Balcells, Judith
dc.contributor.author
Bosch, Jaime
dc.contributor.author
Gené, Amadeu
dc.contributor.author
Murillo Bravo, Clara
dc.contributor.author
Rueda, Claudia
dc.contributor.author
Boada, David
dc.contributor.author
Sánchez Antón, Maria Teresa
dc.contributor.author
Kacerovsky, Marian
dc.contributor.author
Jacobsson, Bo
dc.contributor.author
Palacio, Montse
dc.date.issued
2025-03-25T11:15:24Z
dc.date.issued
2025-03-25T11:15:24Z
dc.date.issued
2024
dc.date.issued
2025-03-25T11:15:24Z
dc.identifier
0300-5577
dc.identifier
https://hdl.handle.net/2445/219980
dc.identifier
757472
dc.identifier
39575693
dc.description.abstract
Objectives: 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
9 p.
dc.format
application/pdf
dc.language
eng
dc.publisher
Walter de Gruyter
dc.relation
Reproducció del document publicat a: https://doi.org/10.1515/jpm-2024-0178
dc.relation
Journal of Perinatal Medicine, 2024, vol. 53, num.2, p. 170-178
dc.relation
https://doi.org/10.1515/jpm-2024-0178
dc.rights
(c) Walter de Gruyter, 2024
dc.rights
info:eu-repo/semantics/openAccess
dc.source
Articles publicats en revistes (Cirurgia i Especialitats Medicoquirúrgiques)
dc.subject
Part prematur
dc.subject
Líquid amniòtic
dc.subject
Embarassades
dc.subject
Premature labor
dc.subject
Amniotic liquid
dc.subject
Pregnant women
dc.title
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.type
info:eu-repo/semantics/article
dc.type
info:eu-repo/semantics/publishedVersion


Ficheros en el ítem

FicherosTamañoFormatoVer

No hay ficheros asociados a este ítem.