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Triple positive profile in antiphospholipid syndrome: prognosis, relapse and management from a retrospective multicentre study

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Objective Antiphospholipid syndrome (APS) is defined by the association of thromboembolic and/or obstetrical clinical manifestations and the presence of antiphospholipid antibodies. The objective of our study was to evaluate the impact of the triple-positive profile in a cohort of 204 APS patients. Methods We conducted a retrospective study, including patients with primary or secondary APS, meeting the Sydney criteria with at least one thrombotic and/or obstetrical complication. Clinical characteristics and the risk of relapse (defined by the occurrence of a new thrombotic event and/or a new adverse obstetrical event) between triple-positive and non-triple-positive APS patients were compared. Results 204 patients were included in our study, 68 were triple-positive and 136 were single or double positive. 122 patients (59.8%) had primary APS. 67 patients (32.8%) had obstetrical APS, with a higher rate among triple-positive patients (45.6% vs 26.5%, p=0.010), and 170 patients (83.3%) had thrombotic APS, without difference between triple-positive and others. Thrombotic events were more often venous (56.4%) than arterial (37.7%). Triple-positive patients had more placental complications than others (17.6% vs 2.9%, p=0.001) and more non-criteria events (48.5% vs 25.7%, p=0.002). Among non-criteria events, there was a higher frequency of Sneddon syndrome in triple-positive patients (7.4% vs 0.7%, p=0.028). The relapse rate was higher in triple-positive patients than in others (63.2% vs 39,7%, p=0002). In multivariate analysis, the triple-positive profile was associated with a higher risk of relapse (HR 1.63; 95% CI 1.04 to 2.55; p=0.031). Conclusion The triple-positivity is associated with a higher risk of relapse and obstetrical complications.
Title: Triple positive profile in antiphospholipid syndrome: prognosis, relapse and management from a retrospective multicentre study
Description:
Objective Antiphospholipid syndrome (APS) is defined by the association of thromboembolic and/or obstetrical clinical manifestations and the presence of antiphospholipid antibodies.
The objective of our study was to evaluate the impact of the triple-positive profile in a cohort of 204 APS patients.
Methods We conducted a retrospective study, including patients with primary or secondary APS, meeting the Sydney criteria with at least one thrombotic and/or obstetrical complication.
Clinical characteristics and the risk of relapse (defined by the occurrence of a new thrombotic event and/or a new adverse obstetrical event) between triple-positive and non-triple-positive APS patients were compared.
Results 204 patients were included in our study, 68 were triple-positive and 136 were single or double positive.
122 patients (59.
8%) had primary APS.
67 patients (32.
8%) had obstetrical APS, with a higher rate among triple-positive patients (45.
6% vs 26.
5%, p=0.
010), and 170 patients (83.
3%) had thrombotic APS, without difference between triple-positive and others.
Thrombotic events were more often venous (56.
4%) than arterial (37.
7%).
Triple-positive patients had more placental complications than others (17.
6% vs 2.
9%, p=0.
001) and more non-criteria events (48.
5% vs 25.
7%, p=0.
002).
Among non-criteria events, there was a higher frequency of Sneddon syndrome in triple-positive patients (7.
4% vs 0.
7%, p=0.
028).
The relapse rate was higher in triple-positive patients than in others (63.
2% vs 39,7%, p=0002).
In multivariate analysis, the triple-positive profile was associated with a higher risk of relapse (HR 1.
63; 95% CI 1.
04 to 2.
55; p=0.
031).
Conclusion The triple-positivity is associated with a higher risk of relapse and obstetrical complications.

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