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ABSTRACT: Objective
To determine the incidence and causes of skin reactions to the synthetic pentasaccharide fondaparinux.Patients and methods
Patients who received prophylactic/therapeutic subcutaneous fondaparinux treatment for more than 7 days were prospectively examined for cutaneous adverse effects between September 1, 2008, and April 30, 2009. When indicated, other procedures, such as skin biopsy, allergy testing, and clinical/laboratory assessment for thrombosis and heparin-induced thrombocytopenia, were performed.Results
Overall, 231 patients were enrolled. No patient developed typical delayed type IV hypersensitivity (DTH) erythematous skin lesions. However, one female patient experienced abdominal pruritus at sites of injection. Histology revealed a mild lymphohisti
SUBMITTER: Schindewolf M
PROVIDER: S-EPMC2947963 | biostudies-literature | 2010 Oct
REPOSITORIES: biostudies-literature