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Factors associated with long-term cardiac dysfunction in neonatal lupus.
Saxena, Amit; Izmirly, Peter M; Bomar, Rebecca P; Golpanian, Rachel Shireen; Friedman, Deborah M; Eisenberg, Ruth; Kim, Mimi Y; Buyon, Jill P.
Affiliation
  • Saxena A; Medicine, NYU School of Medicine, New York, New York, United States amit.saxena@nyulangone.org.
  • Izmirly PM; Medicine, NYU School of Medicine, New York, New York, United States.
  • Bomar RP; Medicine, NYU School of Medicine, New York, New York, United States.
  • Golpanian RS; Medicine, NYU School of Medicine, New York, New York, United States.
  • Friedman DM; Pediatrics, New York Medical College, Valhalla, New York, USA.
  • Eisenberg R; Epidemiology and Population Health, Albert Einstein College of Medicine, Bronx, New York, USA.
  • Kim MY; Epidemiology and Population Health, Albert Einstein College of Medicine, Bronx, New York, USA.
  • Buyon JP; Medicine, NYU School of Medicine, New York, New York, United States.
Ann Rheum Dis ; 79(2): 217-224, 2020 02.
Article in En | MEDLINE | ID: mdl-31672776
ABSTRACT

OBJECTIVES:

Cardiac manifestations of neonatal lupus (NL) have been associated with significant morbidity and mortality; however, there is minimal information on long-term outcomes of affected individuals. This study was initiated to evaluate the presence of and the risk factors associated with cardiac dysfunction in NL after birth in multiple age groups to improve counselling, to further understand pathogenesis and to provide potential preventative strategies.

METHODS:

Echocardiogram reports were evaluated in 239 individuals with cardiac NL 143 from age 0-1 year, 176 from age >1-17 years and 64 from age >17 years. Logistic regression analyses evaluated associations of cardiac dysfunction at each age group with demographic, fetal and postnatal factors, using imputation to address missing data.

RESULTS:

Cardiac dysfunction was identified in 22.4% at age 0-1 year, 14.8% at age >1-17 years and 28.1% at age >17 years. Dysfunction in various age groups was significantly associated with male sex, black race, lower fetal heart rates, fetal extranodal cardiac disease and length of time paced. In 106 children with echocardiograms at ages 0-1 year and >1-17 years, 43.8% with dysfunction at age 0-1 year were also affected at age >1-17 years, while the others reverted to normal. Of children without dysfunction at age 0-1 year, 8.9% developed new dysfunction between ages >1 and 17 years. Among 34 with echocardiograms at ages >1-17 years and >17 years, 6.5% with normal function at age >1-17 years developed dysfunction in adulthood.

CONCLUSIONS:

Risk factors in fetal life can influence cardiac morbidity into adulthood.Although limited by a small number of cases, cardiac dysfunction in the first year often normalises by later childhood. New-onset dysfunction, although rare, can occur de novo after the first year.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Time Factors / Echocardiography / Heart Diseases / Lupus Erythematosus, Systemic Type of study: Etiology_studies / Evaluation_studies / Prognostic_studies / Risk_factors_studies Limits: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male / Newborn Language: En Journal: Ann Rheum Dis Year: 2020 Type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Time Factors / Echocardiography / Heart Diseases / Lupus Erythematosus, Systemic Type of study: Etiology_studies / Evaluation_studies / Prognostic_studies / Risk_factors_studies Limits: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male / Newborn Language: En Journal: Ann Rheum Dis Year: 2020 Type: Article Affiliation country: United States