Diagnosis and management of the antiphospholipid syndrome
The antiphospholipid syndrome is a systemic autoimmune disease defined by thrombotic or obstetrical events that occur in patients with persistent antiphospholipid antibodies. Thrombotic antiphospholipid syndrome is characterized by venous, arterial, or microvascular thrombosis. Patients with catastr...
| Authors: | , |
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| Format: | article |
| Status: | Published version |
| Publication Date: | 2018 |
| Country: | España |
| Institution: | Universidad de Barcelona |
| Repository: | Dipòsit Digital de la UB |
| OAI Identifier: | oai:diposit.ub.edu:2445/178505 |
| Online Access: | https://hdl.handle.net/2445/178505 |
| Access Level: | Open access |
| Keyword: | Síndrome antifosfolipídica Diagnòstic Trombosi Antiphospholipid syndrome Diagnosis Thrombosis |
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Diagnosis and management of the antiphospholipid syndromeRiera Mestre, AntoniVidaller Palacín, AntonioSíndrome antifosfolipídicaDiagnòsticTrombosiAntiphospholipid syndromeDiagnosisThrombosisThe antiphospholipid syndrome is a systemic autoimmune disease defined by thrombotic or obstetrical events that occur in patients with persistent antiphospholipid antibodies. Thrombotic antiphospholipid syndrome is characterized by venous, arterial, or microvascular thrombosis. Patients with catastrophic antiphospholipid syndrome present with thrombosis involving multiple organs. Obstetrical antiphospholipid syndrome is characterized by fetal loss after the 10th week of gestation, recurrent early miscarriages, intrauterine growth restriction, or severe preeclampsia.1 The major nonthrombotic manifestations of antiphospholipid-antibody positivity include valvular heart disease, livedo, antiphospholipidantibody-related nephropathy, thrombocytopenia, hemolytic anemia, and cognitive dysfunction. The antiphospholipid syndrome is often associated with other systemic autoimmune diseases such as systemic lupus erythematosus (SLE); however, it commonly occurs without other autoimmune manifestations (primary antiphospholipid syndrome).Massachusetts Medical Society2018info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://hdl.handle.net/2445/178505Articles publicats en revistes (Ciències Clíniques)reponame:Dipòsit Digital de la UBinstname:Universidad de BarcelonaInglésReproducció del document publicat a: https://doi.org/10.1056/NEJMc1808253New England Journal of Medicine, 2018, vol. 379, num. 13, p. 1289-1290https://doi.org/10.1056/NEJMc1808253(c) Massachusetts Medical Society, 2018info:eu-repo/semantics/openAccessoai:diposit.ub.edu:2445/1785052026-05-27T06:46:51Z |
| dc.title.none.fl_str_mv |
Diagnosis and management of the antiphospholipid syndrome |
| title |
Diagnosis and management of the antiphospholipid syndrome |
| spellingShingle |
Diagnosis and management of the antiphospholipid syndrome Riera Mestre, Antoni Síndrome antifosfolipídica Diagnòstic Trombosi Antiphospholipid syndrome Diagnosis Thrombosis |
| title_short |
Diagnosis and management of the antiphospholipid syndrome |
| title_full |
Diagnosis and management of the antiphospholipid syndrome |
| title_fullStr |
Diagnosis and management of the antiphospholipid syndrome |
| title_full_unstemmed |
Diagnosis and management of the antiphospholipid syndrome |
| title_sort |
Diagnosis and management of the antiphospholipid syndrome |
| dc.creator.none.fl_str_mv |
Riera Mestre, Antoni Vidaller Palacín, Antonio |
| author |
Riera Mestre, Antoni |
| author_facet |
Riera Mestre, Antoni Vidaller Palacín, Antonio |
| author_role |
author |
| author2 |
Vidaller Palacín, Antonio |
| author2_role |
author |
| dc.subject.none.fl_str_mv |
Síndrome antifosfolipídica Diagnòstic Trombosi Antiphospholipid syndrome Diagnosis Thrombosis |
| topic |
Síndrome antifosfolipídica Diagnòstic Trombosi Antiphospholipid syndrome Diagnosis Thrombosis |
| description |
The antiphospholipid syndrome is a systemic autoimmune disease defined by thrombotic or obstetrical events that occur in patients with persistent antiphospholipid antibodies. Thrombotic antiphospholipid syndrome is characterized by venous, arterial, or microvascular thrombosis. Patients with catastrophic antiphospholipid syndrome present with thrombosis involving multiple organs. Obstetrical antiphospholipid syndrome is characterized by fetal loss after the 10th week of gestation, recurrent early miscarriages, intrauterine growth restriction, or severe preeclampsia.1 The major nonthrombotic manifestations of antiphospholipid-antibody positivity include valvular heart disease, livedo, antiphospholipidantibody-related nephropathy, thrombocytopenia, hemolytic anemia, and cognitive dysfunction. The antiphospholipid syndrome is often associated with other systemic autoimmune diseases such as systemic lupus erythematosus (SLE); however, it commonly occurs without other autoimmune manifestations (primary antiphospholipid syndrome). |
| publishDate |
2018 |
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2018 |
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info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion |
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article |
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publishedVersion |
| dc.identifier.none.fl_str_mv |
https://hdl.handle.net/2445/178505 |
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https://hdl.handle.net/2445/178505 |
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Inglés |
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Inglés |
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Reproducció del document publicat a: https://doi.org/10.1056/NEJMc1808253 New England Journal of Medicine, 2018, vol. 379, num. 13, p. 1289-1290 https://doi.org/10.1056/NEJMc1808253 |
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(c) Massachusetts Medical Society, 2018 info:eu-repo/semantics/openAccess |
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(c) Massachusetts Medical Society, 2018 |
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openAccess |
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application/pdf |
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Massachusetts Medical Society |
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Massachusetts Medical Society |
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Articles publicats en revistes (Ciències Clíniques) reponame:Dipòsit Digital de la UB instname:Universidad de Barcelona |
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Universidad de Barcelona |
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Dipòsit Digital de la UB |
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Dipòsit Digital de la UB |
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