<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>85(10)</volume><submitter>Schindewolf M</submitter><pubmed_abstract>&lt;h4>Objective&lt;/h4>To determine the incidence and causes of skin reactions to the synthetic pentasaccharide fondaparinux.&lt;h4>Patients and methods&lt;/h4>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.&lt;h4>Results&lt;/h4>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</pubmed_abstract><journal>Mayo Clinic proceedings</journal><pagination>913-9</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC2947963</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Low allergenic potential with fondaparinux: results of a prospective investigation.</pubmed_title><pmcid>PMC2947963</pmcid><pubmed_authors>Hecking C</pubmed_authors><pubmed_authors>Lindhoff-Last E</pubmed_authors><pubmed_authors>Marzi I</pubmed_authors><pubmed_authors>Schindewolf M</pubmed_authors><pubmed_authors>Boehncke WH</pubmed_authors><pubmed_authors>Garbaraviciene J</pubmed_authors><pubmed_authors>Kroll H</pubmed_authors><pubmed_authors>Scheuermann J</pubmed_authors><pubmed_authors>Wolter M</pubmed_authors><pubmed_authors>Kaufmann R</pubmed_authors><pubmed_authors>Ludwig RJ</pubmed_authors></additional><is_claimable>false</is_claimable><name>Low allergenic potential with fondaparinux: results of a prospective investigation.</name><description>&lt;h4>Objective&lt;/h4>To determine the incidence and causes of skin reactions to the synthetic pentasaccharide fondaparinux.&lt;h4>Patients and methods&lt;/h4>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.&lt;h4>Results&lt;/h4>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</description><dates><release>2010-01-01T00:00:00Z</release><publication>2010 Oct</publication><modification>2025-04-05T13:40:54.68Z</modification><creation>2019-03-27T00:34:30Z</creation></dates><accession>S-EPMC2947963</accession><cross_references><pubmed>20843983</pubmed><doi>10.4065/mcp.2010.0346</doi></cross_references></HashMap>