Mode of birth in women with low-lying placenta: protocol for a prospective multicentre 1:3 matched case-control study in Italy (the MODEL-PLACENTA study).

INTRODUCTION: The term placenta praevia defines a placenta that lies over the internal os, whereas the term low-lying placenta identifies a placenta that is partially implanted in the lower uterine segment with the inferior placental edge located at 1-20 mm from the internal cervical os (internal-os-distance). The most appropriate mode of birth in women with low-lying placenta is still controversial, with the majority of them undergoing caesarean section. The current project aims to evaluate the rate of vaginal birth and caesarean section in labour due to bleeding by offering a trial of labour to all women with an internal-os-distance >5 mm as assessed by transvaginal sonography in the late third trimester. METHODS AND ANALYSIS: The MODEL-PLACENTA is a prospective, multicentre, 1:3 matched case-control study involving 17 Maternity Units across Lombardy and Emilia-Romagna regions, Italy. The study includes women with a placenta located in the lower uterine segment at the second trimester scan. Women with a normally located placenta will be enrolled as controls. A sample size of 30 women with an internal-os-distance >5 mm at the late third trimester scan is needed at each participating Unit. Since the incidence of low-lying placenta decreases from 2% in the second trimester to 0.4% at the end of pregnancy, 150 women should be recruited at each centre at the second trimester scan. A vaginal birth rate ≥60% in women with an internal-os-distance >5 mm will be considered appropriate to start routinely admitting to labour these women. ETHICS AND DISSEMINATION: Ethical approval for the study was given by the Brianza Ethics Committee (No 3157, 2019). Written informed consent will be obtained from study participants. Results will be disseminated by publication in peer-reviewed journals and presentation in international conferences. TRIAL REGISTRATION NUMBER: NCT04827433 (pre-results stage).

The effect of a maternal infusion of amino acids on umbilical uptake in pregnancies complicated by intrauterine growth restriction.

OBJECTIVE: To establish whether, in human pregnancies complicated by intrauterine growth restriction (IUGR), the maternal intravenous infusion of amino acids can increase fetal amino acid concentrations and umbilical uptake. STUDY DESIGN: Before elective cesarean delivery, a solution of amino acids was infused into a maternal vein in 8 patients with pregnancies complicated by IUGR (experimental group). At cesarean delivery, maternal, umbilical venous, and arterial blood samples were obtained. Ten comparable IUGR pregnancies were compared with those in the experimental group. RESULTS: In the experimental group, all maternal amino acid concentrations were increased significantly. In the umbilical vein, valine, methionine, isoleucine, leucine, phenylalanine, arginine, serine, glycine, and proline concentrations were elevated. Umbilical venoarterial differences of amino acid per mole of oxygen for leucine, isoleucine, methionine, arginine, glycine, serine, and proline were elevated but not for lysine, histidine, threonine, valine, and phenylalanine. CONCLUSION: In pregnancies complicated by IUGR, increasing the maternal concentration of amino acids leads to an increased umbilical uptake of some of the amino acids to the fetus. There was no evidence of a change in the uptake of 3 essential amino acids: lysine, histidine, and threonine.