Key result
Dexamethasone 8 mg/day initiated ≤24 weeks restored AV conduction in 17% of CAVB fetuses vs 0% with later/lower dose treatment (OR 13.69; 95% CI 0.72-260.13; p=0.024).
Why the study?
Antibody-mediated complete atrioventricular block is considered irreversible, prompting investigation into the effects of transplacental steroids on fetal AV conduction.
Does early, high-dose transplacental dexamethasone therapy improve fetal AV conduction in fetuses with immune-mediated complete heart block?
Cohort (n=59)
No
Does early, high-dose transplacental dexamethasone therapy improve fetal AV conduction in fetuses with immune-mediated complete heart block?
Early, high-dose transplacental dexamethasone therapy may transiently restore AV conduction in a subgroup of fetuses with complete heart block, which is associated with a reduced need for postnatal pacing.
Should not yet alter fetal CAVB management; hypothesis-generating and requires RCT confirmation.
INTRODUCTION: Antibody-mediated complete atrioventricular block (CAVB) is considered irreversible. We sought to examine the effects of transplacental steroids on fetal AV conduction. METHODS: Fifty-nine fetuses diagnosed with CAVB at our center from 1996 to 2018 were reviewed. Routine dexamethasone administration to birth was used to limit cardiac inflammatory damage. Restoration of fetal AV conduction was classified as "unexpected" treatment response. RESULTS: CAVB resolved in 5/29 (17%) fetuses first treated ≤24-week gestation with 8 mg/day of dexamethasone, when compared with 0/30 (0%) when treatment was initiated later and/or at a starting dose of 4 mg/day (odds ratio 13.69; 95% confidence interval 0.72-260.13; p = 0.024). Treatment response was also associated with a faster ventricular rate at diagnosis (median [range]: 80 [60-97] beats per minute [bpm] vs. 58 [38-92] bpm; p = 0.0036). CAVB reappeared in all 5 responders either prenatally (n = 1) or postnatally before (n = 3) or after (n = 1) the first year of life. When compared with infants with treatment-resistant CAVB (median follow-up 10.3 years), responders (median follow-up 12.3 years) required postnatal pacing less frequent (2/5 [40%] vs. 45/49 [92%]; p = 0.013). CONCLUSIONS: In a subgroup of CAVB fetuses, dexamethasone transiently restored AV conduction. This was associated with a lower rate of postnatal pacing when compared with nonresponders.
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Saito et al. (2021) conducted a cohort in Antibody-mediated complete atrioventricular block (CAVB) (n=59). Dexamethasone initiated ≤24-week gestation vs. Treatment initiated later and/or at a starting dose of 4 mg/day was evaluated on Restoration of fetal AV conduction (OR 13.69, 95% CI 0.72-260.13, p=0.024). Dexamethasone 8 mg/day initiated ≤24 weeks restored AV conduction in 17% of CAVB fetuses vs 0% with later/lower dose treatment (OR 13.69; 95% CI 0.72-260.13; p=0.024).
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