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A Population-Based, Multisite Cohort Study of the Predictors of Chronic Idiopathic Thrombocytopenic Purpura in Children

机译:基于人群的儿童慢性特发性血小板减少性紫癜预测因素的多地点队列研究

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OBJECTIVE. The objective of this study was to identify risk factors for developing chronic idiopathic thrombocytopenic purpura in a cohort of pediatric patients with idiopathic thrombocytopenic purpura.METHODS. We conducted a retrospective cohort analysis of 259 children who were diagnosed with idiopathic thrombocytopenic purpura between 1991 and 2000 at 1 of 8 managed care organizations that comprise the Vaccine Safety Datalink. We reviewed the charts of 595 potential patients with idiopathic thrombocytopenic purpura from the 8 Vaccine Safety Datalink sites and excluded patients with known causes of thrombocytopenia. Chronic idiopathic thrombocytopenic purpura was defined as having thrombocytopenia for 6 months beyond the initial diagnosis. The risk for developing chronic idiopathic thrombocytopenic purpura was assessed using simple and multivariable analyses.RESULTS. Of the 259 cases of idiopathic thrombocytopenic purpura, 197 (76%) were acute, 60 (23%) were chronic, and 2 (1%) could not be determined. Among the acute cases, the mean duration of illness was 22 days. There was 1 serious bleeding outcome in the cohort. In multivariable regression analysis, the patients with chronic illness were older, less likely to present with mucosal bleeding, less likely to have had an acute illness before diagnosis, and more likely to present with a platelet count 20000/μL than children with acute idiopathic thrombocytopenic purpura. In particular, children whose illness was diagnosed at ≥10 years of age and who had platelet counts ≥20000/μL had an approximate fivefold risk for progressing to chronic disease when compared with children who presented at ≤2 years of age with platelet counts 20000/μL.CONCLUSIONS. Although idiopathic thrombocytopenic purpura tends to be a benign and self-limited condition, acute and chronic idiopathic thrombocytopenic purpura seem to be distinct illnesses defined by age, platelet count, bleeding symptoms, and the presence of acute illness before diagnosis. Physicians should be aware of these differences when advising their patients and families.
机译:目的。这项研究的目的是确定一组患儿特发性血小板减少性紫癜的慢性特发性血小板减少性紫癜的危险因素。我们对构成疫苗安全性数据链接的8个管理医疗机构中的1个,对1991年至2000年之间被诊断为特发性血小板减少性紫癜的259名儿童进行了回顾性队列分析。我们从8个Vaccine Safety Datalink网站上回顾了595位潜在的特发性血小板减少性紫癜患者的图表,并排除了已知的血小板减少原因的患者。慢性特发性血小板减少性紫癜的定义是在最初诊断后6个月内出现血小板减少症。使用简单和多变量分析评估了发生慢性特发性血小板减少性紫癜的风险。在259例特发性血小板减少性紫癜中,有197例(76%)是急性的,有60例(23%)是慢性的,有2例(1%)无法确定。在急性病例中,平均病程为22天。该队列中有1人严重出血。在多变量回归分析中,与急性特发性儿童相比,慢性病患者年龄更大,出现粘膜出血的可能性较小,在诊断前患有急性疾病的可能性较小,血小板计数> 20000 /μL的可能性较高。血小板减少性紫癜。尤其是,被诊断出疾病≥10岁且血小板计数≥20000/μL的儿童,与≤2岁的血小板计数<20000的儿童相比,患慢性病的风险约为五倍/μL结论尽管特发性血小板减少性紫癜往往是良性和自限性疾病,但急性和慢性特发性血小板减少性紫癜似乎是由年龄,血小板计数,出血症状以及诊断前是否存在急性疾病定义的不同疾病。在为患者和家人提供建议时,医师应意识到这些差异。

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