Division of Vector-Borne Diseases, National Center for Emerging and Zoonotic Infectious Diseases, CDC.
MMWR Morb Mortal Wkly Rep. 2019 Mar 15;68(10):243-246. doi: 10.15585/mmwr.mm6810a3.
Spotted fever rickettsioses (SFR), including Rocky Mountain spotted fever (RMSF), are nationally notifiable diseases in the United States caused by spotted fever group Rickettsia. The annual incidence of SFR increased from 1.7 cases per 1 million persons in 2000 to 13.2 in 2016 (1,2). Although this demonstrates a substantial increase in SFR cases, the actual magnitude of the increase is questionable because the current case definition allows for nonspecific laboratory criteria to support diagnosis (3). To analyze the quality of laboratory data used to support the diagnosis of SFR cases with illness onset during 2010-2015, CDC examined supplementary case report forms. Among 16,807 reported cases, only 167 (1.0%) met the confirmed case definition, and the remaining 16,640 (99.0%) met the probable case definition. The most common supportive laboratory evidence for probable cases was elevated immunoglobulin G (IgG) antibody titer by indirect immunofluorescence assay (IFA), which was reported for 14,784 (88.8%) probable cases. Antibodies to spotted fever group Rickettsia can persist for months or years following infection, making a single antibody titer unreliable for diagnosing incident disease without a convalescent specimen. Increased use of molecular assays and use of paired and appropriately timed IFA IgG testing practices could improve understanding of SFR epidemiology and increase the accuracy of disease incidence estimates.
斑点热立克次体病(SFR),包括落矶山斑点热(RMSF),是美国全国性报告疾病,由斑点热群立克次体引起。SFR 的年发病率从 2000 年的每百万人 1.7 例增加到 2016 年的 13.2 例(1,2)。尽管这表明 SFR 病例大幅增加,但实际增加幅度值得怀疑,因为当前的病例定义允许非特异性实验室标准来支持诊断(3)。为了分析用于支持 2010-2015 年发病的 SFR 病例诊断的实验室数据质量,CDC 检查了补充病例报告表。在报告的 16807 例病例中,只有 167 例(1.0%)符合确诊病例定义,其余 16640 例(99.0%)符合可能病例定义。可能病例最常见的支持性实验室证据是间接免疫荧光法(IFA)检测到的升高的免疫球蛋白 G(IgG)抗体滴度,在 14784 例(88.8%)可能病例中报告了这种证据。感染后,针对斑点热群立克次体的抗体可能会持续数月或数年,因此在没有恢复期标本的情况下,单次抗体滴度不可靠用于诊断新发病例。增加使用分子检测,并采用配对和适当时间的 IFA IgG 检测实践,可以更好地了解 SFR 流行病学,并提高疾病发病率估计的准确性。