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原发性血小板增多症和特发性骨髓化生基于人群的发病率及生存率数据:一项奥尔姆斯特德县研究,1976 - 1995年

Population-based incidence and survival figures in essential thrombocythemia and agnogenic myeloid metaplasia: an Olmsted County Study, 1976-1995.

作者信息

Mesa R A, Silverstein M N, Jacobsen S J, Wollan P C, Tefferi A

机构信息

Division of Hematology and Internal Medicine, Mayo Clinic and Mayo Foundation, Rochester, Minnesota 55905, USA.

出版信息

Am J Hematol. 1999 May;61(1):10-5. doi: 10.1002/(sici)1096-8652(199905)61:1<10::aid-ajh3>3.0.co;2-i.

Abstract

To provide basic information about occurrence and outcome of essential thrombocythemia (ET) and agnogenic myeloid metaplasia (AMM), we used the Rochester Epidemiology Project medical record linkage system for residents of Olmsted County, Minnesota. We identified all residents who were diagnosed with ET or AMM from 1976 to 1995. Community inpatient and outpatient medical records were reviewed to verify the diagnosis of ET or AMM, and patients were followed passively through their medical records to determine the outcome after diagnosis. We identified 39 cases of ET and 21 of AMM, with age- and sex-adjusted incidence rates of 2.53 and 1.46 cases/100,000 population annually, respectively. The respective median ages at diagnosis were 72 and 67 years. The female-to-male ratios were 1.8 and 1.6 for ET and AMM, respectively, and when adjusted for age, there was no difference in risk. The median follow-up period was 62.9 months for ET and 33.2 months for AMM. Five- and 10-year survivals were 74.4% and 61.3%, respectively, for ET and were significantly lower than expected for age-matched controls (P = 0.012). Prognosis was worse for AMM, with a median progression time of 7 months and a 3-year survival of 52.4%. This was significantly worse than for age-matched controls (P < 0.001). This study provides population-based incidence and comparative survival figures in ET and AMM.

摘要

为了提供原发性血小板增多症(ET)和原因不明的髓样化生(AMM)的发病情况及预后的基本信息,我们使用了明尼苏达州奥尔姆斯特德县居民的罗切斯特流行病学项目医疗记录链接系统。我们确定了1976年至1995年期间所有被诊断为ET或AMM的居民。查阅社区住院和门诊医疗记录以核实ET或AMM的诊断,并通过患者的医疗记录对患者进行被动随访,以确定诊断后的预后情况。我们确定了39例ET和21例AMM,年龄和性别调整后的发病率分别为每年2.53例/10万人口和1.46例/10万人口。诊断时的中位年龄分别为72岁和67岁。ET和AMM的女性与男性比例分别为1.8和1.6,调整年龄后,风险无差异。ET的中位随访期为62.9个月,AMM为33.2个月。ET的5年和10年生存率分别为74.4%和61.3%,显著低于年龄匹配对照组的预期生存率(P = 0.012)。AMM的预后更差,中位进展时间为7个月,3年生存率为52.4%。这明显比年龄匹配对照组差(P < 0.001)。本研究提供了基于人群的ET和AMM的发病率及比较生存数据。

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