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美国管理式医疗计划中成人特发性炎性肌病的流行病学。

Epidemiology of adult idiopathic inflammatory myopathies in a U.S. managed care plan.

机构信息

Department of Rheumatology, Geffen School of Medicine, University of California, Los Angeles, California, USA.

出版信息

Muscle Nerve. 2012 May;45(5):676-83. doi: 10.1002/mus.23302.

Abstract

INTRODUCTION

Idiopathic inflammatory myopathies have a reported incidence of 0.1 to 1 per 100,000 person-years and prevalence of 0.55 to 6 per 100,000 in the United States.

METHODS

We retrospectively examined medical claims for adults aged ≥18 years with myositis (International Classification of Diseases, Ninth Revision, Clinical Modification codes 710.3 [dermatomyositis], 710.4 [polymyositis], and 728.81 [interstitial myositis]) from 2003 to 2008 in a large US managed care database.

RESULTS

The incidence and prevalence cohorts comprised 1,941 and 3,112 subjects, respectively. From 2003 to 2008, the adjusted annual incidence of myositis ranged from 5.8 to 7.9 per 100,000 person-years, and the annual prevalence of myositis ranged from 14.0 to 17.4 per 100,000.

CONCLUSIONS

The incidence and prevalence of idiopathic inflammatory myopathies in the managed care plan studied was higher than previously reported in the United States. Because of the limitations inherent in claims analysis, additional research is needed to substantiate these results.

摘要

简介

特发性炎性肌病在美国的发病率为每 10 万人 0.1 至 1 人年,患病率为每 10 万人 0.55 至 6 人。

方法

我们回顾性地检查了 2003 年至 2008 年期间,一家大型美国管理式医疗保健数据库中年龄≥18 岁的肌炎(国际疾病分类,第九版,临床修正码 710.3[皮肌炎]、710.4[多发性肌炎]和 728.81[间质性肌炎])患者的医疗索赔。

结果

发病率和患病率队列分别包含 1941 名和 3112 名患者。2003 年至 2008 年,肌炎的调整后年发病率范围为每 10 万人 5.8 至 7.9 人年,肌炎的年患病率范围为每 10 万人 14.0 至 17.4 人。

结论

在所研究的管理式医疗保健计划中,特发性炎性肌病的发病率和患病率高于美国以前的报告。由于索赔分析固有的局限性,需要进一步的研究来证实这些结果。

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