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Angiographic tool to detect pulmonary arteriovenous malformations in single ventricle physiology.
Spurgin, Stephen B; Arar, Yousef M; Zellers, Thomas M; Wang, Jijia; Madsen, Nicolas L; Veeram Reddy, Surendranath R; Cleaver, Ondine; Divekar, Abhay A.
Affiliation
  • Spurgin SB; Department of Pediatrics, Southwestern Medical Center, Dallas, TX, USA.
  • Arar YM; Pediatric Cardiology, Children's Medical Center, Dallas, TX, USA.
  • Zellers TM; Department of Pediatrics, Southwestern Medical Center, Dallas, TX, USA.
  • Wang J; Pediatric Cardiology, Children's Medical Center, Dallas, TX, USA.
  • Madsen NL; Department of Pediatrics, Southwestern Medical Center, Dallas, TX, USA.
  • Veeram Reddy SR; Pediatric Cardiology, Children's Medical Center, Dallas, TX, USA.
  • Cleaver O; Department of Applied Clinical Research, University of Texas Southwestern Medical Center, Dallas, TX, USA.
  • Divekar AA; Department of Pediatrics, Southwestern Medical Center, Dallas, TX, USA.
Cardiol Young ; : 1-6, 2024 May 10.
Article de En | MEDLINE | ID: mdl-38724470
ABSTRACT

OBJECTIVE:

Individuals with single ventricle physiology who are palliated with superior cavopulmonary anastomosis (Glenn surgery) may develop pulmonary arteriovenous malformations. The traditional tools for pulmonary arteriovenous malformation diagnosis are often of limited diagnostic utility in this patient population. We sought to measure the pulmonary capillary transit time to determine its value as a tool to identify pulmonary arteriovenous malformations in patients with single ventricle physiology.

METHODS:

We defined the angiographic pulmonary capillary transit time as the number of cardiac cycles required for transit of contrast from the distal pulmonary arteries to the pulmonary veins. Patients were retrospectively recruited from a single quaternary North American paediatric centre, and angiographic and clinical data were reviewed. Pulmonary capillary transit time was calculated in 20 control patients and compared to 20 single ventricle patients at the pre-Glenn, Glenn, and Fontan surgical stages (which were compared with a linear-mixed model). Correlation (Pearson) between pulmonary capillary transit time and haemodynamic and injection parameters was assessed using angiograms from 84 Glenn patients. Five independent observers calculated pulmonary capillary transit time to measure reproducibility (intraclass correlation coefficient).

RESULTS:

Mean pulmonary capillary transit time was 3.3 cardiac cycles in the control population, and 3.5, 2.4, and 3.5 in the pre-Glenn, Glenn, and Fontan stages, respectively. Pulmonary capillary transit time in the Glenn population did not correlate with injection conditions. Intraclass correlation coefficient was 0.87.

CONCLUSIONS:

Pulmonary angiography can be used to calculate the pulmonary capillary transit time, which is reproducible between observers. Pulmonary capillary transit time accelerates in the Glenn stage, correlating with absence of direct hepatopulmonary venous flow.
Mots clés

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Langue: En Journal: Cardiol Young Sujet du journal: ANGIOLOGIA / CARDIOLOGIA / PEDIATRIA Année: 2024 Type de document: Article Pays d'affiliation: États-Unis d'Amérique

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Langue: En Journal: Cardiol Young Sujet du journal: ANGIOLOGIA / CARDIOLOGIA / PEDIATRIA Année: 2024 Type de document: Article Pays d'affiliation: États-Unis d'Amérique