Non-invasive pressure-volume loops show high arterial elastance in children with repaired tetralogy of Fallot.


Journal

Scandinavian cardiovascular journal : SCJ
ISSN: 1651-2006
Titre abrégé: Scand Cardiovasc J
Pays: England
ID NLM: 9708377

Informations de publication

Date de publication:
Dec 2024
Historique:
medline: 24 10 2024
pubmed: 24 10 2024
entrez: 24 10 2024
Statut: ppublish

Résumé

Children with repaired tetralogy of Fallot (rToF) often have pulmonary regurgitation with right ventricular (RV) dilatation and dysfunction, whereas less is known about the effect on the left ventricle (LV). The aim was to investigate LV haemodynamic variables derived from non-invasive pressure-volume loops in children with rToF and how they compare to controls and previous research on adults. Ten children with rToF and pulmonary regurgitation (12 years [10-13], 6 males) and 10 age- and sex-matched healthy controls (12 years [10-14], 6 males) underwent brachial blood pressure in conjunction with cardiac magnetic resonance imaging. Pressure-volume loops were derived by brachial blood pressure together with LV volumes throughout the cardiac cycle in short-axis cine images yielding several haemodynamic variables, including arterial elastance. The RV endocardial border was delineated in end-diastole and end-systole. Children with rToF and pulmonary regurgitation had larger RV end-diastolic volume (136 [114-156]) than controls (100 [94-112] ml/m Children with rToF had higher arterial elastance and heart rate than controls, likely due to increased sympathetic tone to compensate for impaired LV filling following pulmonary regurgitation. If this contributes to increased risk of adverse cardiovascular and cerebrovascular events remains to be studied.

Sections du résumé

BACKGROUND UNASSIGNED
Children with repaired tetralogy of Fallot (rToF) often have pulmonary regurgitation with right ventricular (RV) dilatation and dysfunction, whereas less is known about the effect on the left ventricle (LV). The aim was to investigate LV haemodynamic variables derived from non-invasive pressure-volume loops in children with rToF and how they compare to controls and previous research on adults.
MATERIALS AND METHODS UNASSIGNED
Ten children with rToF and pulmonary regurgitation (12 years [10-13], 6 males) and 10 age- and sex-matched healthy controls (12 years [10-14], 6 males) underwent brachial blood pressure in conjunction with cardiac magnetic resonance imaging. Pressure-volume loops were derived by brachial blood pressure together with LV volumes throughout the cardiac cycle in short-axis cine images yielding several haemodynamic variables, including arterial elastance. The RV endocardial border was delineated in end-diastole and end-systole.
RESULTS UNASSIGNED
Children with rToF and pulmonary regurgitation had larger RV end-diastolic volume (136 [114-156]) than controls (100 [94-112] ml/m
CONCLUSION UNASSIGNED
Children with rToF had higher arterial elastance and heart rate than controls, likely due to increased sympathetic tone to compensate for impaired LV filling following pulmonary regurgitation. If this contributes to increased risk of adverse cardiovascular and cerebrovascular events remains to be studied.

Identifiants

pubmed: 39445438
doi: 10.1080/14017431.2024.2418085
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

2418085

Auteurs

Viggo Klementsson (V)

Clinical Physiology, Department of Clinical Sciences Lund, Skåne University Hospital, Lund University, Lund, Sweden.
Department of Clinical Physiology, Skåne University Hospital, Lund, Sweden.

Misha Bhat (M)

Paediatric Cardiology, Children's Heart Centre, Skåne University Hospital, Lund, Sweden.
Paediatrics, Department of Clinical Sciences Lund, Lund University, Lund, Sweden.

Katarina Steding-Ehrenborg (K)

Clinical Physiology, Department of Clinical Sciences Lund, Skåne University Hospital, Lund University, Lund, Sweden.
Department of Clinical Physiology, Skåne University Hospital, Lund, Sweden.

Erik Hedström (E)

Clinical Physiology, Department of Clinical Sciences Lund, Skåne University Hospital, Lund University, Lund, Sweden.
Department of Clinical Physiology, Skåne University Hospital, Lund, Sweden.
Diagnostic Radiology, Department of Clinical Sciences Lund, Lund University, Lund, Sweden.
Department of Radiology, Skåne University Hospital, Lund, Sweden.

Petru Liuba (P)

Paediatric Cardiology, Children's Heart Centre, Skåne University Hospital, Lund, Sweden.
Paediatrics, Department of Clinical Sciences Lund, Lund University, Lund, Sweden.

Pia Sjöberg (P)

Clinical Physiology, Department of Clinical Sciences Lund, Skåne University Hospital, Lund University, Lund, Sweden.
Department of Clinical Physiology, Skåne University Hospital, Lund, Sweden.

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Classifications MeSH