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Outcomes of borderline rheumatic heart disease: A prospective cohort study
Geneviève Bertaina1, Bernard Rouchon2, Bertrand Huon2
1INSERMU970, Paris Cardiovascular Research Centre-PARCC, Paris, France.
Insights
Borderline rheumatic heart disease (RHD) in children often remains stable over two years. Consistent diagnosis of borderline RHD may require review by two specialists.
Area of Science:
- Cardiology
- Pediatrics
- Public Health
Background:
- Systematic echocardiography screening for rheumatic heart disease (RHD) in endemic areas identifies a new category: borderline RHD.
- The clinical significance and natural progression of borderline RHD require further investigation.
Purpose of the Study:
- To evaluate the outcomes of children diagnosed with borderline RHD through echocardiographic screening.
- To understand the natural history and clinical course of borderline RHD in a pediatric population.
Main Methods:
- Prospective echocardiographic screening for RHD was conducted in 4th-grade schoolchildren (aged 9-10 years) in New Caledonia.
- Children with borderline RHD, confirmed by two independent cardiologists, were included and followed up for a median of 23 months.
Main Results:
- Of 8684 screened children, 25 were diagnosed with borderline RHD and followed up.
- After a median of 23 months, 60% showed stable valvular lesions, and 32% had normal findings.
- Two children (8%) progressed to definite RHD, with no clinical events reported during the follow-up period.
Conclusions:
- Borderline RHD identified through systematic screening in high-risk populations generally shows stability over two years.
- Consistent diagnosis of borderline RHD may necessitate a consensus review by two independent cardiologists.
Context And Aims:
The advent of systematic screening for rheumatic heart disease (RHD) by echocardiography in endemic regions has led to a new entity: borderline RHD. The pathogenicity and natural history of borderline RHD needs to be addressed. The aim of this study was to assess the outcomes of children detected by echocardiography as having borderline RHD.
Methods:
Schoolchildren in 4th grade (i.e., aged 9-10years) who were prospectively echo-screened for RHD (2012-2014) in Nouméa, New Caledonia, were asked to participate. Children with borderline RHD according to consistent independent review by two cardiologists were included and followed-up in 2015.
Results:
Among the 8684 schoolchildren screened, 49 were diagnosed with borderline RHD according to the Cardiologist clinically involved in the child's management plan. After independent review by two cardiologists, 25 children were consistently diagnosed with borderline RHD and included in the follow-up study. Overall, inter-observer agreement was moderate with diagnostic kappa values of 0.63 (95% CI 0.45-0.78). After a median follow-up of 23months (IQR (20.5-33.0), 15 children (60.0%) had stability of valvular lesions, 8 (32.0%) had normal findings according to the WHF criteria. Two children (8.0%) had definite RHD on the follow-up echocardiogram, but no clinical events or audible pathological murmur during the study period. No factor could be identified as prognostic of either stability or progression.
Conclusions:
Borderline RHD diagnosed by systematic screening in high-risk populations remains mostly unchanged at 2years follow-up. Diagnosis of borderline RHD may require two reviewers for consistency.
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