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原发性抗磷脂综合征经食管超声心动图检查的五年随访

Five-year follow-up by transesophageal echocardiographic studies in primary antiphospholipid syndrome.

作者信息

Turiel Maurizio, Sarzi-Puttini Piercarlo, Peretti Rossana, Bonizzato Sara, Muzzupappa Sabrina, Atzeni Fabiola, Rossi Edoardo, Doria Andrea

机构信息

Department of Cardiology, Istituto Ortopedico Galeazzi, Italy.

出版信息

Am J Cardiol. 2005 Aug 15;96(4):574-9. doi: 10.1016/j.amjcard.2005.04.022.

DOI:10.1016/j.amjcard.2005.04.022
PMID:16098314
Abstract

This prospective study describes valvular abnormalities assessed by transesophageal echocardiography (TEE) in patients with primary antiphospholipid syndrome (APLS) over a 5-year follow-up. Of the 56 patients with APLS evaluated at baseline, 47 (84%) had repeat TEE examinations, including 3 patients who died before the end of the follow-up. The first TEE study showed cardiac involvement (thickening or vegetations and embolic sources) in 34 subjects (61%), with mitral valve thickening, the most common abnormality, present in 30 patients (54%). Embolic sources were found in 14 patients (25%; 9 severe spontaneous echocardiographic contrast, 5 Libman-Sacks endocarditis), associated with mitral valve thickening or stenosis in 10 patients. Over the 5-year follow-up, cardiac involvement was unchanged in 30 subjects (64%). New cardiac abnormalities were observed in 17 patients (36%), 15 (88%) with high immunoglobulin-G (IgG) anticardiolipin antibody (aCL) titers and 2 (12%) with low IgG aCL titers. In conclusion, this study showed that mitral valve thickening and embolic sources are frequently observed in patients with APLS. Anticoagulant and/or antiplatelet treatment was ineffective in terms of valvular lesion regression. New appearances of cardiac involvement are significantly related to high IgG aCL titers.

摘要

这项前瞻性研究描述了在5年随访期间,经食管超声心动图(TEE)评估的原发性抗磷脂综合征(APLS)患者的瓣膜异常情况。在基线时评估的56例APLS患者中,47例(84%)接受了重复TEE检查,其中3例在随访结束前死亡。首次TEE研究显示34例患者(61%)存在心脏受累(增厚或赘生物及栓子来源),最常见的异常为二尖瓣增厚,30例患者(54%)存在该情况。14例患者(25%)发现栓子来源(9例严重自发超声心动图造影,5例Libman-Sacks心内膜炎),其中10例与二尖瓣增厚或狭窄相关。在5年随访期间,30例患者(64%)的心脏受累情况无变化。17例患者(36%)出现新的心脏异常,其中15例(88%)免疫球蛋白G(IgG)抗心磷脂抗体(aCL)滴度高,2例(12%)IgG aCL滴度低。总之,本研究表明APLS患者常出现二尖瓣增厚和栓子来源。抗凝和/或抗血小板治疗在瓣膜病变消退方面无效。心脏受累的新出现与高IgG aCL滴度显著相关。

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