Publications by authors named "E Gouider"

In recent years, there has been a growing interest in the activated partial thromboplastin time clot waveform analysis (APTT-CWA), which reflects clot formation. It was mainly studied in hemophilia and disseminated intravascular coagulation. The aim of this study was to evaluate the usefulness of APTT-CWA in hemophilia carriers.

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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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Introduction: Prophylaxis is the recommended management strategy for all persons with hemophilia (PwH), yet its adoption is uneven worldwide.

Areas Covered: This analysis examines global disparities in hemophilia care, focusing on global prophylactic coverage and its correlation with the World Bank's world development indicators. It outlines the disproportionate consumption of clotting factors and non-factor concentrates in high-income countries compared to lower-income counterparts and the challenges of expanding prophylaxis coverage in under-resourced settings.

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Article Synopsis
  • Blastic plasmacytoid dendritic-cell neoplasm (BPDCN) is a rare and aggressive cancer that arises from dendritic cells and is known for its poor prognosis and unique surface markers (CD4 and CD56).
  • The disease has had various names over time, highlighting the complications in understanding its origin and diagnosing it, particularly due to similarities with other conditions like acute myeloid leukemia (AML) and histiocytic sarcoma (HS).
  • A case study of a 42-year-old male revealed diagnostic challenges, as initial suspicions of BPDCN were complicated by conflict from pathologists, leading to ineffective treatment and a rapid decline in the patient’s condition.
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