摘要 18 - 香港华裔抗磷脂综合征患者的标准化死亡率以及死亡和复发的风险因素

Carolyn Lee
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On presentation, 369 patients had thrombotic events. Arterial thrombosis occurred in 177 patients and venous thrombosis occurred in 189 patients. Obstetric morbidities occurred in 77 patients. Twenty three patients had both obstetric and thrombotic events. Over a mean follow-up of 9.7±7.2 years, 75 (17.7%) patients succumbed. The age and sex adjusted SMR relative to general population was 4.34[95% CI 3.44-5.41]. In thrombotic APS patients, mortality was associated with age [Formula: see text]60 years at diagnosis (HR 5.30 [95% CI 3.11-9.03]; p<0.001), presence of arterial hypertension (HR 1.89 [95% CI 1.11-3.19]; p =0.018), and presence of arterial thrombosis (HR 1.81 [95% CI 1.06-3.10]; p=0.031). Recurrence of thrombosis occurred in 89 (21%) patients (15% arterial, 5.2% venous). Recurrence of thrombosis was found to be associated with triple positive antibodies (HR 2.71 [95% CI 1.15-6.42]; p=0.023) independent of other risk factors in a multivariate model. 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引用次数: 0

摘要

背景 报告标准死亡率(SMR),并评估香港华裔抗磷脂综合征(APS)患者死亡和复发的风险因素。方法 通过医院管理局临床数据检索系统(CDARS),使用抗磷脂综合征的 ICD-10 诊断代码识别在香港 16 家公立医院接受随访的患者。他们的诊断是根据2006年修订的APS共识标准(1)核实的。采用 Kaplan-Meier 法和 Cox 回归法研究了死亡率、血栓复发率及其相关风险因素。结果 共发现 423 名中国 APS 患者。其中,288 名患者符合 2006 年 APS 标准,被归类为确诊 APS,135 名患者为疑似 APS。204 名患者为原发性 APS,219 名患者为继发性 APS。369 名患者在就诊时发生了血栓事件。177名患者发生动脉血栓,189名患者发生静脉血栓。77名患者发生了产科疾病。23 名患者同时发生了产科和血栓事件。在平均为 9.7±7.2 年的随访中,75 名患者(17.7%)死亡。经年龄和性别调整后,相对于普通人群的SMR为4.34[95% CI 3.44-5.41]。在血栓性 APS 患者中,死亡率与诊断时的年龄[计算公式:见正文]60 岁(HR 5.30 [95% CI 3.11-9.03];P<0.001)、动脉高血压(HR 1.89 [95% CI 1.11-3.19];P=0.018)和动脉血栓形成(HR 1.81 [95% CI 1.06-3.10];P=0.031)有关。89例(21%)患者出现血栓复发(15%动脉血栓,5.2%静脉血栓)。在多变量模型中发现,血栓复发与三抗体阳性有关(HR 2.71 [95% CI 1.15-6.42];P=0.023),与其他风险因素无关。结论 中国 APS 患者死亡率升高,诊断时年龄较大、动脉高血压和动脉血栓形成是导致死亡的独立风险因素。血栓事件的复发并不少见,且与 aPL 抗体三项阳性有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Abstract 18 — Standardized Mortality Ratio and Risk Factors for Mortality and Recurrence in Hong Kong Chinese Patients with Antiphospholipid Syndrome
Background To report standardized mortality ratio (SMR) and assess risk factors for mortality and recurrence in Hong Kong Chinese patients with antiphospholipid syndrome (APS). Methods Patients followed up in 16 public hospitals in Hong Kong were identified by the Hospital Authority Clinical Data Retrieval System (CDARS) using the ICD-10 diagnostic code of APS. Their diagnoses were verified using the 2006 modified consensus criteria (1) for APS. The mortality, thrombosis recurrence rate and their associated risk factors were studied by Kaplan-Meier method and Cox Regression. Results Four hundred twenty-three Chinses APS patients were identified. Among them, 288 patients fulfilled the 2006 criteria for APS and were classified as definite APS, while 135 patients had probable APS. APS was primary in 204 patients and secondary in 219 patients. On presentation, 369 patients had thrombotic events. Arterial thrombosis occurred in 177 patients and venous thrombosis occurred in 189 patients. Obstetric morbidities occurred in 77 patients. Twenty three patients had both obstetric and thrombotic events. Over a mean follow-up of 9.7±7.2 years, 75 (17.7%) patients succumbed. The age and sex adjusted SMR relative to general population was 4.34[95% CI 3.44-5.41]. In thrombotic APS patients, mortality was associated with age [Formula: see text]60 years at diagnosis (HR 5.30 [95% CI 3.11-9.03]; p<0.001), presence of arterial hypertension (HR 1.89 [95% CI 1.11-3.19]; p =0.018), and presence of arterial thrombosis (HR 1.81 [95% CI 1.06-3.10]; p=0.031). Recurrence of thrombosis occurred in 89 (21%) patients (15% arterial, 5.2% venous). Recurrence of thrombosis was found to be associated with triple positive antibodies (HR 2.71 [95% CI 1.15-6.42]; p=0.023) independent of other risk factors in a multivariate model. Conclusion Increased mortality rate was observed in Chinese APS patient, with older age at diagnosis, presence of arterial hypertension and arterial thrombosis being independent risk factors for mortality. Recurrence of thrombotic events was not uncommon and associated with the presence of triple positive aPL antibodies.
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