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Third-degree AVB was defined as the complete dissociation of atrial and ventricular contractions, with constant intervals between atrial contractions. We recorded information on the diagnosis and therapeutic approach for each case: watchful waiting, intrauterine treatment, or delivery. The primary outcomes were the survival of the foetus and the efficacy of the treatment given (assessing reduction of the degree of AVB or haemodynamic improvement). We collected data on the antibody status of the mother, the association with structural cardiopathies, and the detection of signs of hydrops or ventricular dysfunction (VD). We documented the outcomes of the foetuses and the need for pacemakers in postnatal life. In the statistical analysis, we used Student's t test to compare means, and Fisher's Ribociclib supplier exact test to analyse categorical variables. The level of statistical significance was set at P?Cobimetinib molecular weight pregnancy in 1 case in which the foetus had XO monosomy, omphalocoele, and hydrops. Another foetus received a diagnosis of mitochondrial disease after birth and developed severe neurologic abnormalities. The third foetus, whose mother was positive for anti-Ro/anti-La antibodies, alternated episodes of bradycardia and tachycardia, Rolziracetam received a diagnosis of sick sinus syndrome at birth, and required a pacemaker. The mean age at diagnosis was 23.5 WGA (range, 14�C31; SD, 4.3), and in cases associated with CHD was 18 WGA, and 23.9 WGA in cases with no CHD. Table 1 summarises data on the diagnosis, management, and outcome of each foetus. Table 2 shows the analysed data, both overall and for each subset. Of the 19 foetuses, 2 (10%) had second-degree AVB, and 17 (90%) had third-degree AVB. Congenital heart disease was detected in 3 foetuses (16%), and was severe and associated to isomerism in all. Maternal antibodies were found in 12 (63%). The aetiology was unknown in the remaining 4 (21%). The overall mortality was 20% (or 37% if we include voluntary terminations of pregnancy [VTP]). We also analysed mortality in each subset. All 3 patients with AVB associated to CHD died (1 spontaneously and 2 by VTP). There was 1 death in the group of AVB of unknown aetiology, a foetus with hydrops and severe VD born at week 27 of gestation.