The French experience with a population-based esophageal atresia registry (RENATO). - Université de Lille
Article Dans Une Revue European Journal of Pediatric Surgery Année : 2023

The French experience with a population-based esophageal atresia registry (RENATO).

Résumé

In this paper, is presented a national register for esophageal atresia (EA) started in January 2008. We report our experience about the conception of this database and its coordiantion. Data management and data quality are also detailed. In 2023, more then 2500 patients with esophageal atresia are included. Prevalence of EA in France was calculated at 1.8/10000 living birth. Main clinical results are listed with scientifc publications issued directly from the register.
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Dates et versions

hal-04384094 , version 1 (10-01-2024)

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Citer

Rony Sfeir, Dyuti Sharma, Julien Labreuche, Luc Dauchet, Frederic Gottrand. The French experience with a population-based esophageal atresia registry (RENATO).. European Journal of Pediatric Surgery, 2023, European Journal of Pediatric Surgery, ⟨10.1055/a-2206-6837⟩. ⟨hal-04384094⟩

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