Publications by authors named "Aurelie Berot"

The transition of young type 1 diabetic (T1D) patients from pediatric to adult healthcare is a high-risk period of loss to follow-up. Since 2015, we have implemented a transition program, involving both pediatric and adult clinicians. The main objective was to evaluate the number of patients who had succeeded this transition program at 1 year.

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The follow-up of diabetic patients is marked by a period of transition from pediatric care to adult services. The major challenge of this transition is to ensure continuity of care under the best possible conditions. Socio-economic factors must be taken into account to ensure that care is adapted to patients' needs.

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Article Synopsis
  • The study investigates how the transition process for adolescents with type 1 diabetes is organized to maintain their health and minimize follow-up losses.
  • A systematic review of literature from 2010 to 2023 was conducted, focusing on transition programs for this demographic, resulting in 18 studies being included.
  • Findings show that socioeconomic factors, particularly educational levels, are poorly represented in transition programs, with limited impact on patient management and outcomes.
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The adoption of electronic health records in hospitals has ensured the availability of large datasets that can be used to predict medical complications. The trajectories of patients in real-world settings are highly variable, making longitudinal data modeling challenging. In recent years, significant progress has been made in the study of deep learning models applied to time series; however, the application of these models to irregular medical time series (IMTS) remains limited.

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French health insurance data showed that the incidence of type 1 diabetes mellitus (T1DM) in children increased over the years to 2015. The objective of our study was to assess the evolution of the number of incident cases of paediatric and adult type 1 diabetes in our institution, and to describe their clinical presentation and its evolution. All patients with T1DM managed at diagnosis at Reims University Hospital between 1997 and 2019 were included.

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Article Synopsis
  • The study focuses on the features and genetic factors of primary hyperparathyroidism (PHPT) in children, analyzing data from 63 cases over 20 years.
  • Infants often show milder and asymptomatic forms of PHPT, while older children exhibit more nonspecific symptoms, and about 52% of cases have a genetic basis.
  • Genetic mutations related to calcium-sensing are prevalent in infants, whereas mutations affecting parathyroid cell growth are more common in older children, highlighting different underlying mechanisms in various age groups.
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