Transplacental fetal treatment improves the outcome of prenatally diagnosed complete atrioventricular block without structural heart disease

Circulation. 2004 Sep 21;110(12):1542-8. doi: 10.1161/01.CIR.0000142046.58632.3A. Epub 2004 Sep 7.

Abstract

Background: Untreated isolated fetal complete atrioventricular block (CAVB) has a significant mortality rate. A standardized treatment approach, including maternal dexamethasone at CAVB diagnosis and beta-stimulation for fetal heart rates <55 bpm, has been used at our institutions since 1997. The study presents the impact of this approach.

Methods and results: Thirty-seven consecutive cases of fetal CAVB since 1990 were studied. Mean age at diagnosis was 25.6+/-5.2 gestational weeks. In 33 patients (92%), CAVB was associated with maternal anti-Ro/La autoantibodies. Patients were separated into those diagnosed between 1990 and 1996 (group 1; n=16) and those diagnosed between 1997 and 2003 (group 2; n=21). The 2 study groups were comparable in the clinical presentation at CAVB diagnosis but did differ in prenatal management (treated patients: group 1, 4/16; group 2, 18/21; P<0.0001). Overall, 22 fetuses were treated, 21 with dexamethasone and 9 with beta-stimulation for a mean of 7.5+/-4.5 weeks. Live-birth and 1-year survival rates of group 1 were 80% and 47%, and these improved to 95% for group 2 patients (P<0.01). The 21 patients treated with dexamethasone had a 1-year survival rate of 90%, compared with 46% without glucocorticoid therapy (P<0.02). Immune-mediated conditions (myocarditis, hepatitis, cardiomyopathy) resulting in postnatal death or heart transplantation were significantly more common in untreated anti-Ro/La antibody-associated pregnancies compared with patients treated with steroids (0/18 versus 4/9 live births; P=0.007).

Conclusions: A standardized treatment approach, including transplacental fetal administration of dexamethasone and beta-stimulation at heart rates <55 bpm, reduced the morbidity and improved the outcome of isolated fetal CAVB.

Publication types

  • Comparative Study
  • Evaluation Study
  • Review

MeSH terms

  • Adrenergic beta-Agonists / administration & dosage
  • Adrenergic beta-Agonists / pharmacokinetics
  • Adrenergic beta-Agonists / therapeutic use*
  • Adult
  • Antibodies, Antinuclear / immunology
  • Autoimmune Diseases / drug therapy
  • Autoimmune Diseases / immunology
  • Dexamethasone / administration & dosage
  • Dexamethasone / pharmacokinetics
  • Dexamethasone / therapeutic use*
  • Drug Therapy, Combination
  • Female
  • Fetal Death / epidemiology
  • Fetal Death / etiology
  • Fetal Diseases / drug therapy
  • Fetal Diseases / mortality
  • Fetal Heart / drug effects
  • Fetal Heart / pathology
  • Fetal Therapies*
  • Gestational Age
  • Heart Block / drug therapy*
  • Heart Block / embryology*
  • Humans
  • Immunosuppressive Agents / administration & dosage
  • Immunosuppressive Agents / pharmacokinetics
  • Immunosuppressive Agents / therapeutic use*
  • Infant, Newborn
  • Life Tables
  • Male
  • Maternal-Fetal Exchange
  • Myocarditis / drug therapy
  • Myocarditis / embryology
  • Myocarditis / etiology
  • Pregnancy
  • Pregnancy Complications / drug therapy
  • Pregnancy Complications / immunology
  • Pregnancy Outcome
  • Prenatal Diagnosis
  • Retrospective Studies
  • Survival Analysis
  • Treatment Outcome

Substances

  • Adrenergic beta-Agonists
  • Antibodies, Antinuclear
  • Immunosuppressive Agents
  • SS-A antibodies
  • SS-B antibodies
  • Dexamethasone