Publications by authors named "H P Hebestreit"

Objective: Unlocking the potential of routine medical data for clinical research requires the analysis of data from multiple healthcare institutions. However, according to German data protection regulations, data can often not leave the individual institutions and decentralized approaches are needed. Decentralized studies face challenges regarding coordination, technical infrastructure, interoperability and regulatory compliance.

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Article Synopsis
  • The review discusses current research and discussions in pediatric rhinology, focusing on the collaboration between otorhinolaryngologists and pediatricians.
  • It covers congenital malformations like choanal atresia and nasal dermoid cysts, along with treatments for sinogenic orbital complications and chronic rhinosinusitis in children.
  • Additionally, it updates on the ENT specialist's role in managing children with cystic fibrosis and primary ciliary dyskinesia.
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Cystic Fibrosis (CF) is the most common autosomal recessive genetic multisystemic disease. In Germany, it affects at least 8000 people. The disease is caused by mutations in the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) gene leading to dysfunction of CFTR, a transmembrane chloride channel.

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Introduction: Childhood cancer survivors (CCS) are at risk of experiencing lower quality-of-life, fatigue, and depression. Few randomized controlled trials have studied the effect of physical activity (PA) on these in adult long-term CCS. This study investigated the effect of a 1-year individualized PA intervention on health-related quality-of-life (HRQOL), fatigue, and distress symptoms in adult CCS.

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