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Inherited Hemophilia-A Multidimensional Chronic Disease That Requires a Multidisciplinary Approach
Cristina Claudia Tarniceriu1,2, Loredana Liliana Hurjui3, Daniela Maria Tanase4
1Department of Morpho-Functional Science I, Discipline of Anatomy, "Grigore T. Popa" University of Medicine and Pharmacy, 700115 Iasi, Romania.
Hereditary hemophilia causes severe joint damage, particularly in knees and ankles. Comprehensive, multidisciplinary care is essential for managing hemophilia complications and comorbidities.
Area of Science:
- Orthopedics and Sports Medicine
- Hematology
- Rheumatology
Background:
- Articular damage is a significant complication of hereditary hemophilia, affecting large joints.
- Hereditary coagulopathies like hemophilia A and B necessitate a multidisciplinary approach due to their complexity.
- Hemophilic arthropathy prevalence and joint involvement patterns require further investigation.
Purpose of the Study:
- To determine the prevalence of hemophilic arthropathy in northeastern Romania.
- To identify commonly affected joints in hemophilia patients.
- To assess correlations between arthropathy, hemophilia type, treatment, and comorbidities.
Main Methods:
- Retrospective study of 36 adults with hemophilia A and B.
- Osteoarticular system evaluation using the modified Hemophilia Joint Health Score (mHJHS).
- Assessment of 12 joints based on swelling, pain, atrophy, crepitus, and range of motion loss.
Main Results:
- Severe joint damage was most frequent in knees, ankles, elbows, and wrists.
- Severe hemophilia correlated with severe joint damage (p < 0.05).
- Hepatitis C virus (HCV) infection was linked to severe joint damage and intermittent prophylaxis.
Conclusions:
- Multidisciplinary medical services are crucial for comprehensive hemophilia care.
- Effective management requires addressing the condition's complications and comorbidities.
- Tailored treatment strategies, considering disease severity and comorbidities, are vital.
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