Cobo, TeresaAldecoa, VictoriaBartha, José LuisBugatto, FernandoCarrillo Badillo, María PazComas, CarminaDiago Almeda, VicenteFerrero, SilviaGoya, MariaHerraiz, IgnacioMartí Malgosa, LaiaOlivella, AnnaPaules, CristinaFerrero, SilviaFigueras Retuerta, FrancescPalacio, MontseGratacós Solsona, EduardOPTIM-PTL group2023-03-292023-03-292021-09-282044-6055https://hdl.handle.net/2445/196209Introduction: The majority of women admitted with threatened preterm labour (PTL) do not delivery prematurely. While those with microbial invasion of the amniotic cavity (MIAC) represent the highest risk group, this is a condition that is not routinely ruled out since it requires amniocentesis. Identification of low-risk or high-risk cases might allow individualisation of care, that is, reducing overtreatment with corticosteroids and shorten hospital stay in low-risk women, while allowing early antibiotic therapy in those with MIAC. Benefits versus risks of amniocentesis-based predictor models of spontaneous delivery within 7 days and/or MIAC have not been evaluated. Methods and analysis: This will be a Spanish randomised, multicentre clinical trial in singleton pregnancies (23.0-34.6 weeks) with PTL, conducted in 13 tertiary centres. The intervention arm will consist in the use of amniocentesis-based predictor models: if low risk, hospital discharge within 24 hours of results with no further medication will be recommended. If high risk, antibiotics will be added to standard management. The control group will be managed according to standard institutional protocols, without performing amniocentesis for this indication. The primary outcome will be total antenatal doses of corticosteroids, and secondary outcomes will be days of maternal stay and the occurrence of clinical chorioamnionitis. A cost analysis will be undertaken. To observe a reduction from 90% to 70% in corticosteroid doses, a reduction in 1 day of hospital stay (SD of 2) and a reduction from 24% to 12% of clinical chorioamnionitis, a total of 340 eligible patients randomised 1 to 1 to each study arm is required (power of 80%, with type I error α=0.05 and two-sided test, considering a dropout rate of 20%). Randomisation will be stratified by gestational age and centre.6 p.application/pdfengcc-by-nc (c) Cobo, Teresa et al., 2021https://creativecommons.org/licenses/by-nc/4.0/Part prematurAvaluació del risc per la salutLíquid amniòticInfeccionsServeis de salut maternalCorticosteroidesEcografiaPremature laborHealth risk assessmentAmniotic liquidInfectionsMaternal health servicesAdrenocortical hormonesUltrasonic imaginginfo:eu-repo/semantics/article7216542023-03-29info:eu-repo/semantics/openAccess34588268