Department of Biological Sciences and Eck Institute for Global Health, University of Notre Dame, Notre Dame, Indiana, United States of America.
PLoS Negl Trop Dis. 2021 Mar 1;15(3):e0009208. doi: 10.1371/journal.pntd.0009208. eCollection 2021 Mar.
During the 2015-2017 Zika epidemic, dengue and chikungunya-two other viral diseases with the same vector as Zika-were also in circulation. Clinical presentation of these diseases can vary from person to person in terms of symptoms and severity, making it difficult to differentially diagnose them. Under these circumstances, it is possible that numerous cases of Zika could have been misdiagnosed as dengue or chikungunya, or vice versa. Given the importance of surveillance data for informing epidemiological analyses, our aim was to quantify the potential extent of misdiagnosis during this epidemic. Using basic principles of probability and empirical estimates of diagnostic sensitivity and specificity, we generated revised estimates of reported cases of Zika that accounted for the accuracy of diagnoses made on the basis of clinical presentation with or without laboratory confirmation. Applying this method to weekly reported case data from 43 countries throughout Latin America and the Caribbean, we estimated that 944,700 (95% CrI: 884,900-996,400) Zika cases occurred when assuming all confirmed cases were diagnosed using molecular methods versus 608,400 (95% CrI: 442,000-821,800) Zika cases that occurred when assuming all confirmed cases were diagnosed using serological methods. Our results imply that misdiagnosis was more common in countries with proportionally higher reported cases of dengue and chikungunya, such as Brazil. Given that Zika, dengue, and chikungunya appear likely to co-circulate in the Americas and elsewhere for years to come, our methodology has the potential to enhance the interpretation of passive surveillance data for these diseases going forward. Likewise, our methodology could also be used to help resolve transmission dynamics of other co-circulating diseases with similarities in symptomatology and potential for misdiagnosis.
在 2015 年至 2017 年寨卡病毒疫情期间,登革热和基孔肯雅热——这两种与寨卡病毒具有相同传播媒介的其他病毒疾病——也在流行。这些疾病的临床表现因人而异,症状和严重程度各不相同,因此难以进行鉴别诊断。在这种情况下,可能有许多寨卡病毒病例被误诊为登革热或基孔肯雅热,反之亦然。鉴于监测数据对于进行流行病学分析的重要性,我们的目的是量化在此次疫情中可能出现的误诊程度。利用概率论的基本原理和诊断敏感性与特异性的经验估计,我们生成了经过修正的寨卡病毒报告病例估计数,这些估计数考虑了根据临床表现(无论有无实验室确认)做出诊断的准确性。我们将这种方法应用于拉丁美洲和加勒比地区 43 个国家每周报告的病例数据,结果估计,如果假设所有确诊病例均使用分子方法进行诊断,则有 944700 例(95%置信区间:884900-996400)寨卡病毒病例;如果假设所有确诊病例均使用血清学方法进行诊断,则有 608400 例(95%置信区间:442000-821800)寨卡病毒病例。我们的研究结果表明,在报告的登革热和基孔肯雅热病例比例较高的国家,误诊更为常见,例如巴西。鉴于寨卡病毒、登革热和基孔肯雅热在未来几年可能会在美洲及其他地区共同流行,我们的方法有潜力增强对这些疾病进行被动监测数据的解释。同样,我们的方法也可以用于帮助解决其他具有相似症状和误诊可能性的共同流行疾病的传播动态。