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Paediatric follow-up of haemodynamically insignificant congenital cardiac lesions
Benjamin G Smith1, Shakeel A Qureshi
1Department of Paediatric Cardiology, Royal Hospital for Sick Children, Glasgow, United Kingdom.
Insights
Follow-up for hemodynamically insignificant congenital cardiac lesions (HICCL) in the UK varies widely. A rationalized approach suggests limited follow-up after age two, with only two assessments recommended for most HICCL cases.
Area of Science:
- Pediatric Cardiology
- Congenital Heart Disease
- Echocardiography
Background:
- Hemodynamically insignificant congenital cardiac lesions (HICCL) represent a spectrum of heart conditions in children.
- Current follow-up practices for HICCL in the UK are not standardized.
- Advanced echocardiography may lead to over-investigation and prolonged follow-up.
Purpose of the Study:
- To describe current follow-up practices for HICCL in the UK.
- To propose a rationalized follow-up strategy based on the natural history of these lesions.
Main Methods:
- An internet-based survey was conducted among 170 UK pediatric cardiologists and general pediatricians.
- Respondents were presented with five common HICCL scenarios: VSD, ASD, PFO, mild PS, and PDA.
- 52 responses were analyzed to identify trends in follow-up beliefs and practices.
Main Results:
- Significant variation in follow-up practices for HICCL was observed among respondents.
- A tendency to discharge patients with patent foramen ovale (PFO) was noted.
- Most other HICCL lesions were followed, often with frequent reviews.
Conclusions:
- Over-reliance on advanced echocardiography may result in unnecessary frequent reviews of HICCL.
- A rationalized follow-up protocol is proposed, recommending no more than two assessments after age two for most HICCL.
- These recommended assessments should occur in late childhood and near full growth.
Aim:
To describe the prevailing follow-up of haemodynamically insignificant congenital cardiac lesions (HICCL) in the UK. To suggest a rationalisation of follow-up based on the known natural history of these lesions.
Methods:
An internet-based survey of 170 paediatric cardiologists and general paediatricians with an interest in cardiology in the UK. Five scenarios concerning common HICCL were presented: ventricular and atrial septal defects, patent foramen ovale, mild pulmonary stenosis and persistent ductus arteriosus.
Results:
There were 52 respondents. There was a broad range of beliefs and practices. However, there were tendencies to discharge children with a patent foramen ovale and follow patients with all other lesions, often on a relatively frequent basis.
Conclusions:
The increasingly sensitive and advanced nature of echocardiography and the subsequent reliance upon it may be contributing to unnecessarily frequent review of HICCL and a reluctance to discharge patients. In the majority of patients with HICCL, no more than two assessments of HICCL are required after 2 years of age - once in late childhood and once near full growth.
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