Division of Vector-Borne Diseases, Centers for Disease Control and Prevention, Fort Collins, Colorado, USA.
New Jersey Department of Health, Trenton, New Jersey, USA.
Zoonoses Public Health. 2022 Aug;69(5):451-457. doi: 10.1111/zph.12933. Epub 2022 Mar 6.
Historically, public health surveillance for Lyme disease has required clinical follow-up on positive laboratory reports for the purpose of case classification. In areas with sustained high incidence of the disease, this resource-intensive activity yields a limited benefit to public health practice. A range of burden-reducing strategies have been implemented in many states, creating inconsistencies that limit the ability to decipher trends. Laboratory-based surveillance, or surveillance based solely on positive laboratory reports without follow-up for clinical information on positive laboratory reports, emerged as a feasible alternative to improve standardization in already high-incidence areas. To inform expectations of a laboratory-based surveillance model, we conducted a retrospective analysis of Lyme disease data collected during 2012-2018 from 10 high-incidence states. The number of individuals with laboratory evidence of infection ranged from 1302 to 20,994 per state and year. On average, 55% of those were ultimately classified as confirmed or probable cases (range: 29%-86%). Among all individuals with positive laboratory evidence, 18% (range: 2%-37%) were determined to be 'not a case' upon investigation and 23% (range: 2%-52%) were classified as suspect cases due to lack of associated clinical information and thus were not reported to the Centers for Disease Control and Prevention (CDC). The number of reported cases under a laboratory-based approach to surveillance in high-incidence states using recommended two-tier testing algorithms is likely to be, on average, 1.2 times higher (range: 0.6-1.8 times) than what was reported to CDC during 2012-2018. A laboratory-based surveillance approach for high-incidence states will improve standardization and reduce burden on public health systems, allowing public health resources to focus on prevention messaging, exploration of novel prevention strategies and alternative data sources to yield information on the epidemiology of Lyme disease.
从历史上看,莱姆病的公共卫生监测需要对实验室阳性报告进行临床随访,以便对病例进行分类。在疾病持续高发的地区,这种资源密集型活动对公共卫生实践的益处有限。许多州已经实施了一系列减轻负担的策略,这些策略存在差异,限制了对趋势的解读能力。基于实验室的监测,或仅基于实验室阳性报告而不随访临床阳性实验室报告信息的监测,已成为改善已经高发病率地区标准化的可行替代方法。为了了解基于实验室的监测模型的预期,我们对 2012-2018 年来自 10 个高发病率州的莱姆病数据进行了回顾性分析。每个州和年份的实验室感染证据人数从 1302 人到 20994 人不等。平均而言,其中 55%的人最终被归类为确诊或可能病例(范围:29%-86%)。在所有具有阳性实验室证据的个体中,18%(范围:2%-37%)经调查被确定为“非病例”,23%(范围:2%-52%)因缺乏相关临床信息而被归类为疑似病例,因此未向疾病预防控制中心(CDC)报告。在高发病率州,采用推荐的两级检测算法的基于实验室的监测方法,报告的病例数可能平均增加 1.2 倍(范围:0.6-1.8 倍),比 2012-2018 年向 CDC 报告的病例数增加。对于高发病率州,基于实验室的监测方法将提高标准化程度并减轻公共卫生系统的负担,使公共卫生资源能够专注于预防信息、探索新的预防策略和替代数据来源,以获取莱姆病流行病学信息。