Descriptive analysis of patients positive for anti-phospholipid antibodies included in two Italian registries

Vittorio Pengo, Luca Sarti, Emilia Antonucci, Stefania Di Agostino, Elisa Bison, Gentian Denas, Daniela Poli, Pier Luigi Meroni, Roberto Gerli, Antonella Radice, Gualtiero Palareti, On behalf of FIRMA group and START collaborators
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Abstract

The definite diagnosis of antiphospholipid syndrome (APS) depends on the laboratory performance and clinicians’ interpre- tation. Results from two Italian inception cohort studies of anti- phospholipid antibodies (aPL)-positive subjects, the Italian Survey on ANtiphoSpholipid antibody Positive Individuals Reg- istry (INSPIRE) and the Survey on AnTicoagulated Patients- Reg- isTry (START) have been compared. Data from INSPIRE were collected by rheumatologists of the FIRMA group while those of START by physicians working in Italian thrombosis centers. Ev- idence on several, still unraveled, clinical and methodological as- pects of ‘real life’ aPL testing and APS diagnosis was collected. In this paper, we report the characteristics of 123 cases enrolled in INSPIRE and 229 in START registries, with particular refer- ence to the reasons why these tests were requested, the obtained aPL profile, and consequent treatment. Laboratory testing for aPL in the absence of clinical criteria defining APS was more frequent in INSPIRE (p<0.0001). The rate of patients in classification cat- egory I (more than one aPL test positive) was significantly higher in START (p<0.0001) as well as the use of warfarin. A wide va- riety of treatments has been observed in patients in classification category II (single aPL positivity). These data indicate that there is a need to harmonize many aspects among the various specialists dealing with APS.
对意大利两个登记处中抗磷脂抗体阳性患者的描述性分析
抗磷脂综合征(APS)的明确诊断取决于实验室表现和临床医生的解释。意大利两项抗磷脂抗体(aPL)阳性受试者的初始队列研究结果,意大利抗磷脂抗体阳性个体登记调查(INSPIRE)和抗凝患者登记调查(START)进行了比较。INSPIRE的数据由FIRMA组的风湿病学家收集,而START的数据由意大利血栓中心的医生收集。收集了关于“现实生活”aPL检测和APS诊断的几个临床和方法学方面的证据。在本文中,我们报告了123例在INSPIRE注册的病例和229例在START注册的病例的特征,特别提到了要求进行这些测试的原因、获得的aPL概况以及随后的治疗。在没有APS临床标准的情况下,实验室检测aPL在INSPIRE中更为常见(p<0.0001)。在START (p<0.0001)和华法林的使用中,I类(超过1例aPL检测阳性)患者的比例显著高于对照组(p < 0.01)。在II类(单aPL阳性)患者中观察到多种治疗方法。这些数据表明,有必要协调处理APS的各种专家之间的许多方面。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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