Publications by authors named "R Kaczmarek"

Introduction: The 2024 ISTH clinical practice guideline (CPG) for treatment of congenital haemophilia, the NBDF-McMaster Guideline on Care Models for Haemophilia Management, and ASH ISTH NBDF WFH guidelines on the diagnosis and management of VWD all utilised GRADE methodology.

Aim: Discuss missed opportunities and the methodological approach of the ISTH Guideline in contrast to how GRADE was previously applied in rare diseases.

Methods: Critically analyse the methodology of each guideline along with best practices in the use of GRADE.

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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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Article Synopsis
  • Human Gb3/CD77 synthase, an enzyme, creates Galα1→4Gal structures on glycosphingolipids and glycoproteins, which are important for bacterial recognition in infections.
  • The major product, Globotriaosylceramide (Gb3), acts as a receptor for harmful toxins from certain bacteria and is also linked to symptoms of Anderson-Fabry disease due to enzyme deficiency.
  • Additionally, the synthase is implicated in cancer biology, playing a role in cancer cell survival and resistance to treatments, and influencing the P1PK blood group system.
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