Miller David P, Kaye James A, Shea Kathleen, Ziyadeh Najat, Cali Clorinda, Black Corri, Walker Alexander M
Ingenix, Newton, Massachusetts 02466, USA.
Epidemiology. 2004 Mar;15(2):208-15. doi: 10.1097/01.ede.0000113273.14807.53.
Thrombotic thrombocytopenic purpura and hemolytic uremic syndrome are rare disorders characterized by platelet aggregation, microthrombi, and resulting tissue damage. We studied the incidence and possible risk factors for these diseases in 3 large populations in the United States, United Kingdom, and Canada.
Data were derived from a large health insurer in the United States, general practices in the United Kingdom, and the Province of Saskatchewan. We identified potential cases of thrombotic thrombocytopenia purpura and hemolytic uremic syndrome in computerized data and verified them by medical record review. We estimated incidence rates for thrombotic thrombocytopenia purpura and hemolytic uremic syndrome together and separately, and we conducted a case-control study to evaluate potential risk factors.
The age-sex standardized incidence of thrombotic thrombocytopenia purpura and hemolytic uremic syndrome was higher than previously reported (6.5, 2.2, and 3.2 per million per year in the United States, United Kingdom, and Saskatchewan, respectively), but there was no secular trend. The incidence of thrombotic thrombocytopenia purpura and hemolytic uremic syndrome was higher in women than men. Most cases of hemolytic uremic syndrome occurred before 20 years of age. We confirmed several known risk factors for thrombotic thrombocytopenia purpura and hemolytic uremic syndrome (cancer, bone marrow transplantation, pregnancy).
The incidence of thrombotic thrombocytopenia purpura and hemolytic uremic syndrome is higher than previously reported but does not appear to be rising. Apparent international differences in incidence could be the result of imprecision in identifying thrombotic thrombocytopenia purpura and hemolytic uremic syndrome in large research databases.
血栓性血小板减少性紫癜和溶血性尿毒症综合征是罕见疾病,其特征为血小板聚集、微血栓形成及由此导致的组织损伤。我们在美国、英国和加拿大的3个大型人群中研究了这些疾病的发病率及可能的危险因素。
数据来源于美国一家大型健康保险公司、英国的全科医疗以及萨斯喀彻温省。我们在计算机化数据中识别出血栓性血小板减少性紫癜和溶血性尿毒症综合征的潜在病例,并通过病历审查进行核实。我们分别估算了血栓性血小板减少性紫癜和溶血性尿毒症综合征的发病率,还开展了一项病例对照研究以评估潜在危险因素。
血栓性血小板减少性紫癜和溶血性尿毒症综合征的年龄性别标准化发病率高于此前报告的数据(美国、英国和萨斯喀彻温省每年每百万人口中分别为6.5、2.2和3.2例),但无长期趋势。血栓性血小板减少性紫癜和溶血性尿毒症综合征的发病率女性高于男性。大多数溶血性尿毒症综合征病例发生在20岁之前。我们证实了血栓性血小板减少性紫癜和溶血性尿毒症综合征的几个已知危险因素(癌症、骨髓移植、妊娠)。
血栓性血小板减少性紫癜和溶血性尿毒症综合征的发病率高于此前报告,但似乎并未上升。发病率明显的国际差异可能是由于在大型研究数据库中识别血栓性血小板减少性紫癜和溶血性尿毒症综合征存在不精确性所致。