Two-year evolution of latent rheumatic heart disease in Malawi

Amy Sanyahumbi1, Andrea Beaton2, Danielle Guffey3

  • 1Division of Pediatric Cardiology, Department of Pediatrics, Baylor College of Medicine, Texas Children's Hospital, Houston, Texas.

Congenital Heart Disease
|February 2, 2019
PubMed

Insights

Rheumatic heart disease (RHD) screening in children showed low progression rates. Borderline RHD cases rarely advanced to definite RHD, indicating a favorable prognosis in this group.

Area of Science:

  • Cardiology
  • Pediatrics
  • Public Health

Background:

  • Screening echocardiography is used to detect latent rheumatic heart disease (RHD) in asymptomatic children.
  • World Heart Federation guidelines categorize RHD as definite, borderline, or absent based on echocardiogram findings.
  • The natural progression of RHD diagnosed via screening is largely unknown.

Purpose of the Study:

  • To evaluate the 2-year evolution of rheumatic heart disease (RHD) in children initially diagnosed through screening echocardiography.
  • To assess progression and regression rates in both definite and borderline RHD cases.

Main Methods:

  • Follow-up echocardiograms were performed after two years on children diagnosed with latent RHD.
  • Echocardiogram readings involved a multi-reader approach to ensure accuracy.
  • Factors such as penicillin adherence, age, gender, and socioeconomic status were compared between RHD progression groups.

Main Results:

  • Among 39 borderline RHD cases, only 2.6% progressed to definite RHD; 43.6% regressed to normal.
  • Of 11 definite RHD cases, 36.4% regressed to borderline, and 9.1% regressed to normal.
  • No significant differences in adherence or demographic factors were found between those who regressed and those who did not.

Conclusions:

  • Children diagnosed with borderline rheumatic heart disease (RHD) exhibit a low rate of progression to definite RHD.
  • The study achieved a high participant retention rate of 98%.
  • Further long-term follow-up is necessary to fully understand the expected disease trajectory of RHD detected through screening.
Abstract

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