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        "resumen" => "<p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">The classical clinical picture of the antiphospholipid syndrome &#40;APS&#41; is characterized by venous or arterial thromboses&#44; fetal losses and thrombocytopenia&#44; in the presence of antiphospholipid antibodies &#40;aPL&#41;&#44; namely lupus anticoagulant&#44; anticardiolipin antibodies or antibodies directed to various proteins&#44; mainly &#946;2 glycoprotein I&#44; or all three&#46; Apart from being &#8220;primary&#8221; &#40;without any discernable underlying systemic autoimmune disease&#41;&#44; or associated to another disease &#40;usually to systemic lupus erythematosus&#41;&#44; it may also occur rapidly over days or weeks when it has been termed &#8220;catastrophic&#8221; APS&#46; Therapy should not primarily be directed at effectively reducing the aPL levels and the use of immunotherapy &#40;including high dose steroid administration&#44; immunosuppression or plasma exchange&#41; is generally not indicated&#44; unless in the catastrophic APS&#46; Treatment of APS patients should be based on the use of antiaggregant and anticoagulant therapy&#46;</p>"
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        "resumen" => "<p id="spar0010" class="elsevierStyleSimplePara elsevierViewall">El s&#237;ndrome antifosfolip&#237;dico &#40;SAF&#41; se caracteriza por la asociaci&#243;n de los anticuerpos antifosfolip&#237;dicos &#40;AAF&#41; con trombosis de repetici&#243;n&#44; abortos o p&#233;rdidas fetales recurrentes y trombocitopenia&#46; Los AAF m&#225;s estudiados son los anticuerpos anticardiolipina&#44; el anticoagulante l&#250;pico y los anticuerpos anti-&#946;2-glucoprote&#237;na I&#46; El SAF puede presentarse de forma aislada&#44; denomin&#225;ndose SAF primario&#44; o bien asociado a otras enfermedades autoinmunes sist&#233;micas&#44; fundamentalmente a lupus eritematoso sist&#233;mico&#46; M&#225;s recientemente&#44; se ha descrito un subgrupo de SAF en el que los pacientes desarrollan m&#250;ltiples trombosis durante un corto espacio de tiempo&#44; que se ha denominado SAF catastr&#243;fico&#46; Aunque parece clara la asociaci&#243;n entre la presencia de AAF y trombosis&#44; la actitud terap&#233;utica no debe ir dirigida primariamente a la eliminaci&#243;n o a la reducci&#243;n de los niveles de estos anticuerpos mediante recambios plasm&#225;ticos&#44; gammaglobulinas intravenosas o inmunodepresores &#40;excepto en el SAF catastr&#243;fico&#41;&#44; y a que no existe una clara correlaci&#243;n entre los niveles de los AAF y los episodios tromb&#243;ticos&#46; El tratamiento de estos pacientes debe basarse en el uso de antiagregantes plaquetarios o anticoagulantes&#46;</p>"
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Therapeutic strategies in antiphospholipid syndrome
Estrategias terapéuticas en el síndrome antifosfolipídico
Ricard Cervera
Servicio de Enfermedades Autoinmunes, Hospital Clínic, Barcelona, Spain
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        "resumen" => "<p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">The classical clinical picture of the antiphospholipid syndrome &#40;APS&#41; is characterized by venous or arterial thromboses&#44; fetal losses and thrombocytopenia&#44; in the presence of antiphospholipid antibodies &#40;aPL&#41;&#44; namely lupus anticoagulant&#44; anticardiolipin antibodies or antibodies directed to various proteins&#44; mainly &#946;2 glycoprotein I&#44; or all three&#46; Apart from being &#8220;primary&#8221; &#40;without any discernable underlying systemic autoimmune disease&#41;&#44; or associated to another disease &#40;usually to systemic lupus erythematosus&#41;&#44; it may also occur rapidly over days or weeks when it has been termed &#8220;catastrophic&#8221; APS&#46; Therapy should not primarily be directed at effectively reducing the aPL levels and the use of immunotherapy &#40;including high dose steroid administration&#44; immunosuppression or plasma exchange&#41; is generally not indicated&#44; unless in the catastrophic APS&#46; Treatment of APS patients should be based on the use of antiaggregant and anticoagulant therapy&#46;</p>"
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Article information
ISSN: 21735743
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