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PubMed Narrative Review Evidence Moderate

Unmet needs in hemophilic arthropathy.

Blood reviews | 2025 | Dargaud Y, Lobet S, Roussel N, Valentino LA

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Source
PubMed
Type
Narrative Review
Evidence
Moderate

Abstract

[Indexed for MEDLINE] Conflict of interest statement: Declaration of competing interest The authors declare no conflicts of interest related to this article. 3. Orthopedics. 2017 Nov 1;40(6):e940-e946. doi: 10.3928/01477447-20170619-05. Epub 2017 Jun 30. Hemophilic Arthropathy. Nacca CR, Harris AP, Tuttle JR. The musculoskeletal manifestations of hemophilia A and B are some of the most common presenting symptoms and continue to be challenging to practitioners. Hemophilic arthropathy, if not initially adequately treated and managed, may lead to debilitating disease and eventually require the consideration of major surgery, including total joint arthroplasty. Thorough comprehension of the pathophysiology, diagnosis, and both medical and surgical interventions is critical in establishing an appropriate treatment regimen for these patients. Furthermore, a true multidisciplinary approach involving hematology, orthopedics, and physical therapy is essential for a patient with hemophilic arthropathy. The authors present a comprehensive review of hemophilic arthropathy from an orthopedist's perspective. [Orthopedics. 2017; 40(6):e940-e946.]. Copyright 2017, SLACK Incorporated. DOI: 10.3928/01477447-20170619-05

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