作者
Marta Tonello,Ariela Hoxha,Savino Sciascia,María José Cuadrado,José Omar Latino,Sebastián Udry,Т. М. Reshetnyak,N. Costedoat‐Chalumeau,N. Costedoat‐Chalumeau,Luca Marozio,Anǵela Tincani,Laura Andréoli,Ewa Haładyj,Pier Luigi Meroni,Maria Gerosa,Jaume Alijotas‐Reig,Sara Tenti,K Mayer-Pickel,Michal J. Simchen,Maria Tiziana Bertero,Sara De Carolis,Véronique Ramoni,A. Mékinian,Elvira Grandone,Aldo Maina,Fátima Serrano,Vittorio Pengo,Munther A. Khamashta,Amelia Ruffatti
摘要
Abstract The effect of additional treatments combined with conventional therapy on pregnancy outcomes was examined in high-risk primary antiphospholipid syndrome (PAPS) patients to identify the most effective treatment strategy. The study's inclusion criteria were (1) positivity to lupus anticoagulant alone or associated with anticardiolipin and/or anti-β2 glycoprotein I antibodies; (2) a history of severe maternal–foetal complications (Group I) or a history of one or more pregnancies refractory to conventional therapy leading to unexplained foetal deaths not associated with severe maternal–foetal complications (Group II). Two different additional treatments were considered: oral—low-dose steroids (10–20 mg prednisone daily) and/or 200 to 400 mg daily doses of hydroxychloroquine and parenteral—intravenous immunoglobulins at 2 g/kg per month and/or plasma exchange. The study's primary outcomes were live birth rates and pregnancy complications. A total of 194 pregnant PAPS patients attending 20 tertiary centres were retrospectively enrolled. Hydroxychloroquine was found to be linked to a significantly higher live birth rate with respect to the other oral treatments in the Group II patients. The high (400 mg) versus low (200 mg) doses of hydroxychloroquine (p = 0.036) and its administration before versus during pregnancy (p = 0.021) were associated with a significantly higher live birth rate. Hydroxychloroquine therapy appeared particularly efficacious in the PAPS patients without previous thrombosis. Parenteral treatments were associated with a significantly higher live birth rate with respect to the oral ones (p = 0.037), particularly in the Group I patients. In conclusion, some additional treatments were found to be safe and efficacious in high-risk PAPS pregnant women.