{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,5,13]],"date-time":"2025-05-13T15:50:18Z","timestamp":1747151418856,"version":"3.40.5"},"reference-count":21,"publisher":"Wiley","issue":"5","license":[{"start":{"date-parts":[[2020,2,16]],"date-time":"2020-02-16T00:00:00Z","timestamp":1581811200000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":["obgyn.onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["Prenatal Diagnosis"],"published-print":{"date-parts":[[2020,4]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:sec><jats:label\/><jats:p>Assessing cardiac function and risk stratification in a fetal anti\u2010Sj\u00f6gren syndrome type A (SSA) or anti\u2010Sj\u00f6gren syndrome type B (SSB) complete atrioventricular block (CAVB) is challenging. We aimed to evaluate the cardiovascular profile score (CVP) and its components in surveillance of fetuses with autoimmune CAVB.<\/jats:p><\/jats:sec><jats:sec><jats:title>Methods<\/jats:title><jats:p>Retrospective cohort review of CAVB pregnancies, excluding fetuses with significant cardiac anomalies.<\/jats:p><\/jats:sec><jats:sec><jats:title>Results<\/jats:title><jats:p>CAVBs are in 17 fetuses, diagnosed at mean gestational age of 23\u2009\u00b1\u20095\u2009weeks. Overall mortality is 18%: 1 termination, 1 fetal demise (intrauterine fetal demise [IUFD]), and 1 postnatal death. Both mortalities had intrauterine growth restriction; IUFD had placental infarction.<\/jats:p><jats:p>Presenting CVP 8.7\u2009\u00b1\u20091. No fetus had CVP &lt;7; the score correlated with increased risk of perinatal death. The 2 mortalities had initial CVP scores of 8 and 9; both increased to 10 on subsequent exams.<\/jats:p><jats:p>30% of fetuses had low middle cerebral artery pulsatility (MCA\u2010PI) on the last study. All had high umbilical artery pulsatility (UA\u2010PI) throughout gestation. The 2 deaths had the lowest MCA\u2010PI.<\/jats:p><\/jats:sec><jats:sec><jats:title>Conclusion<\/jats:title><jats:p>Despite low heart rates, high CVP scores in our cohort remained high and were not predictive of mortality. Abnormalities in MCA flow reflects fetal cerebral vasodilation that may indicate altered hemodynamics and be predictive of outcomes, but data is limited. Abnormal umbilical artery (UA) flow suggests that perinatal mortality may also be related to placental disease.<\/jats:p><\/jats:sec>","DOI":"10.1002\/pd.5637","type":"journal-article","created":{"date-parts":[[2020,1,8]],"date-time":"2020-01-08T15:12:54Z","timestamp":1578496374000},"page":"557-564","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":2,"title":["Prediction of outcome in fetal autoimmune complete heart block"],"prefix":"10.1002","volume":"40","author":[{"ORCID":"https:\/\/orcid.org\/0000-0003-4495-3578","authenticated-orcid":false,"given":"Neeta","family":"Sethi","sequence":"first","affiliation":[{"name":"Division of Cardiology Children's National Hospital  Washington, DC"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Anita","family":"Krishnan","sequence":"additional","affiliation":[{"name":"Division of Cardiology Children's National Hospital  Washington, DC"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Mary","family":"Donofrio","sequence":"additional","affiliation":[{"name":"Division of Cardiology Children's National Hospital  Washington, 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