Publications by authors named "F B Langer"

Introduction: Evidence-based clinical practice guidelines drive optimal patient care and facilitate access to high-quality treatment. Creating guidelines for rare diseases such as haemophilia, where evidence does not often come from randomized controlled trials but from non-randomized and well-designed observational studies and real-world data, is challenging. The methodology used for assessing available evidence should consider this critical fact.

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Since the 1970s, specialized hemophilia centers have been established to optimize the complex and costly treatment of patients with severe bleeding disorders. In 2019, the first GTH guidelines on the structural and process quality of hemophilia centers were published. On this basis, a procedure for the certification of hemophilia centers has been established under the technical leadership of the GTH.

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Background: Although hemophilia A mainly affects males, carriers (defined as females with hemophilia A, as well as symptomatic or asymptomatic hemophilia A carriers) are at risk of excessive bleeding, particularly during trauma or during surgical procedures. Clinical trials have focused on male patients with severe disease, and data for females are limited. Improved, evidence-based treatment guidelines for management of hemophilia A carriers are required.

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Article Synopsis
  • Impaired interaction between fibroblasts and AT2 pneumocytes contributes to chronic lung diseases like idiopathic pulmonary fibrosis (IPF), with Mucin 5B (MUC5B) being associated with the condition.
  • Research using an organoid model showed that fibroblasts with high fibrosis markers can alter STAT3 signaling in AT2 cells, leading to cystic growth and increased MUC5B expression, influenced by the cytokine IL-6.
  • The study also demonstrated that the drug dasatinib can block the formation of these cystic organoids, suggesting a potential avenue for drug development to address these interactions in IPF.
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