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美国确诊的原发性免疫缺陷疾病的人群患病率。

Population prevalence of diagnosed primary immunodeficiency diseases in the United States.

作者信息

Boyle J M, Buckley R H

机构信息

SRBI, Silver Spring, MD, USA.

出版信息

J Clin Immunol. 2007 Sep;27(5):497-502. doi: 10.1007/s10875-007-9103-1. Epub 2007 Jun 19.

Abstract

RATIONALE

Although health surveys are routinely used to estimate the population incidence and prevalence of many chronic and acute conditions in the U.S. population, they have infrequently been used for "rare" conditions such as primary immunodeficiency diseases (PID). Accurate prevalence measures are needed to separate the truly rare condition from those that primary care doctors are likely to see in their practices today, if early diagnosis and treatment are to be achieved.

METHODS

A national probability sample of 10,000 households was sampled by random digit dialing and screened by telephone to identify how many of the nearly 27,000 household members had been diagnosed with a PID.

RESULTS

A total of 23 household members in 18 households were reported with a specific diagnosis for PID (CVID, IgA, IgG, XLA, SCID, CGD), whereas additional cases were reported as a PID without a confirmatory diagnosis. These findings suggest a population prevalence of diagnosed PID in the United States at approximately 1 in 1,200 persons.

CONCLUSIONS

Diagnoses of PID in the United States are far more common than suggested in the literature.

摘要

理论依据

尽管健康调查通常用于估计美国人群中许多慢性和急性疾病的发病率和患病率,但它们很少用于诸如原发性免疫缺陷病(PID)等“罕见”疾病。如果要实现早期诊断和治疗,就需要准确的患病率测量方法,以将真正的罕见疾病与初级保健医生在其临床实践中可能遇到的疾病区分开来。

方法

通过随机数字拨号对10000户家庭进行全国概率抽样,并通过电话进行筛查,以确定近27000名家庭成员中有多少人被诊断患有PID。

结果

18户家庭中的23名家庭成员被报告患有特定诊断的PID(常见变异型免疫缺陷、IgA、IgG、X连锁无丙种球蛋白血症、重症联合免疫缺陷、慢性肉芽肿病),而其他病例被报告为患有PID但未经确诊。这些发现表明,美国确诊PID的人群患病率约为1/1200。

结论

美国PID的诊断比文献中所显示的要普遍得多。

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