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J Am Coll Cardiol, 1998; 32:1749-1755
© 1998 by the American College of Cardiology Foundation
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CLINICAL STUDIES

Prevalence of congenital cardiovascular malformations in children of human immunodeficiency virus-infected women

The prospective P2C2 HIV multicenter study

Wyman W. Lai, MD, MPH, FACC*, Steven E. Lipshultz, MD{dagger} {dagger},1, Kirk A. Easley, MS{ddagger}, Thomas J. Starc, MD||, Stacey E. Drant, MD, J. Timothy Bricker, MD, FACC#, Steven D. Colan, MD, FACC{dagger} {dagger}, Douglas S. Moodie, MD, FACC§, George Sopko, MD, MPH**, Samuel Kaplan, MD, FACC for the P2C2 HIV Study Group National Heart Lung and Blood Institute Bethesda Maryland

* Department of Pediatrics, Division of Pediatric Cardiology, Mount Sinai School of Medicine, New York, New York, USA
{dagger} Department of Cardiology, Children’s Hospital, Boston, Massachusetts, USA
{dagger} Department of Pediatrics, Harvard Medical School, Boston, Massachusetts, USA
{ddagger} Department of Biostatistics and Epidemiology, Division of Pediatric Cardiology, Cleveland Clinic Foundation, Cleveland, Ohio, USA
§ Department of Pediatrics, Division of Pediatric Cardiology, Cleveland Clinic Foundation, Cleveland, Ohio, USA
|| Department of Pediatrics, Division of Pediatric Cardiology, Presbyterian Hospital/Columbia University School of Medicine, New York, New York, USA
Department of Pediatrics, Division of Pediatric Cardiology, University of California, Los Angeles School of Medicine, Los Angeles, California, USA
# Department of Pediatrics, Division of Pediatric Cardiology, Baylor College of Medicine, Houston, Texas, USA
** Division of Heart and Vascular Diseases, National Heart, Lung, and Blood Institute, Bethesda, Maryland, USA

Manuscript received December 18, 1997; revised manuscript received July 8, 1998, accepted July 29, 1998.

Address for correspondence: Dr. Wyman W. Lai, Division of Pediatric Cardiology, Box 1201, The Mount Sinai Medical Center, One Gustave L. Levy Place, New York, New York 10029-6574
Wyman_Lai{at}smtplink.mssm.edu

Objectives. The purpose of the study was to assess the effects of maternal HIV-1 (human immunodeficiency virus) infection and vertically transmitted HIV-1 infection on the prevalence of congenital cardiovascular malformations in children.

Background. In the United States, an estimated 7000 children are born to HIV-infected women annually. Previous limited reports have suggested an increase in the prevalence of congenital cardiovascular malformations in vertically transmitted HIV-infected children.

Methods. In a prospective longitudinal multicenter study, diagnostic echocardiograms were performed at 4–6-month intervals on two cohorts of children exposed to maternal HIV-1 infection: 1) a Neonatal Cohort of 90 HIV-infected, 449 HIV-uninfected and 19 HIV-indeterminate children; and 2) an Older HIV-Infected Cohort of 201 children with vertically transmitted HIV-1 infection recruited after 28 days of age.

Results. In the Neonatal Cohort, 36 lesions were seen in 36 patients, yielding an overall congenital cardiovascular malformation prevalence of 6.5% (36/558), with a 8.9% (8/90) prevalence in HIV-infected children and a 5.6% (25/449) prevalence in HIV-uninfected children. Two children (2/558, 0.4%) had cyanotic lesions. In the Older HIV-Infected Cohort, there was a congenital cardiovascular malformation prevalence of 7.5% (15/201). The distribution of lesions did not differ significantly between the groups.

Conclusions. There was no statistically significant difference in congenital cardiovascular malformation prevalence in HIV-infected versus HIV-uninfected children born to HIV-infected women. With the use of early screening echocardiography, rates of congenital cardiovascular malformations in both the HIV-infected and HIV-uninfected children were five- to ten-fold higher than rates reported in population-based epidemiologic studies but not higher than in normal populations similarly screened. Potentially important subclinical congenital cardiovascular malformations were detected.

Abbreviations and Acronyms
  HIV = human immunodeficiency virus
  P2C2 = pediatric pulmonary and cardiac complications




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