Infective endocarditis in New Zealand children 1994-2012

Rachel Webb1, Lesley Voss, Sally Roberts

  • 1From the *Department of Pediatric Infectious Diseases, Starship Children's Hospital, Auckland; †Department of Microbiology, Auckland District Health Board; ‡Department of Pediatric and Congenital Cardiac Services, Starship Children's Hospital, Auckland; and §School of Population Child and Youth Health, University of Auckland, Auckland, New Zealand.

Abstract

Insights

Infective endocarditis (IE) in New Zealand children is often linked to congenital heart disease, but rheumatic heart disease is also a significant risk factor. Staphylococcus aureus is a common cause, alongside unusual pathogens like Corynebacterium diphtheriae.

Area of Science:

  • Pediatric Infectious Diseases
  • Cardiology
  • Microbiology

Background:

  • New Zealand faces a high incidence of bacterial infections and postinfectious conditions like rheumatic heart disease.
  • Infective endocarditis (IE) is a serious concern in children, necessitating a clear understanding of its clinical and microbiological landscape.

Purpose of the Study:

  • To delineate the clinical and microbiological characteristics of infective endocarditis (IE) in children in New Zealand.
  • To identify primary risk factors and common pathogens associated with pediatric IE in the region.

Main Methods:

  • A retrospective review was conducted on hospital records of patients under 16 years old diagnosed with IE.
  • Cases were classified as Definite or Possible IE using modified Duke criteria.

Main Results:

  • 85 IE episodes occurred in 82 children; 60% had congenital heart disease, and rheumatic heart disease was also noted.
  • Healthcare-associated IE accounted for 41% of cases. Staphylococcus aureus was the most frequent pathogen (30.6%), with Corynebacterium diphtheriae (11.8%) and Streptococcus pyogenes (8.2%) also identified.
  • Mortality was 4.7%, with 9% of survivors experiencing neurologic sequelae. 16S ribosomal RNA testing aided diagnosis in culture-negative cases.

Conclusions:

  • Congenital heart disease is the primary risk factor for pediatric IE in New Zealand, with rheumatic heart disease also being significant.
  • The study highlights a substantial burden of healthcare-associated IE and identifies key bacterial pathogens, including S. aureus, C. diphtheriae, and S. pyogenes.
  • 16S ribosomal RNA testing is valuable for diagnosing culture-negative IE, informing prophylaxis recommendations.

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