Division of Vector-Borne Diseases, National Center for Emerging and Zoonotic Infectious Diseases, CDC.
MMWR Recomm Rep. 2019 Jun 14;68(1):1-10. doi: 10.15585/mmwr.rr6801a1.
Dengue and Zika viruses are closely related mosquitoborne flaviviruses with similar transmission cycles, distribution throughout the tropics and subtropics, and disease manifestations including fever, rash, myalgia, and arthralgia. For patients with suspected dengue or Zika virus disease, nucleic acid amplification tests (NAATs) are the preferred method of diagnosis. Immunoglobulin M (IgM) antibody testing can identify additional infections and remains an important tool for the diagnosis of these diseases, but interpreting the results is complicated by cross-reactivity, and determining the specific timing of infection can be difficult. These limitations are a particular challenge for pregnant women in determining whether Zika virus infection occurred during or before the pregnancy.This report summarizes existing and new guidance on dengue and Zika virus diagnostic testing for patients with a clinically compatible illness who live in or recently traveled to an area where there is risk for infection with both viruses. CDC recommendations for screening of asymptomatic pregnant women with possible Zika virus exposure are unchanged. For symptomatic nonpregnant persons, dengue and Zika virus NAATs should be performed on serum collected ≤7 days after symptom onset. Dengue and Zika virus IgM antibody testing should be performed on NAAT-negative serum specimens or serum collected >7 days after onset of symptoms. For symptomatic pregnant women, serum and urine specimens should be collected as soon as possible within 12 weeks of symptom onset for concurrent dengue and Zika virus NAATs and IgM antibody testing. Positive IgM antibody test results with negative NAAT results should be confirmed by neutralizing antibody tests when clinically or epidemiologically indicated, including for all pregnant women. Data on the epidemiology of viruses known to be circulating at the location of exposure and clinical findings should be considered when deciding which tests to perform and for interpreting results.Patients with clinically suspected dengue should receive appropriate management to monitor and treat shock and hemorrhage. Women with laboratory evidence of possible Zika virus infection during pregnancy and their infants should be evaluated and managed for possible adverse outcomes. Dengue and Zika virus disease are nationally notifiable conditions, and cases should be reported to public health authorities.
登革热和寨卡病毒是密切相关的蚊媒黄病毒,具有相似的传播周期、在热带和亚热带的分布以及包括发热、皮疹、肌痛和关节痛在内的疾病表现。对于疑似登革热或寨卡病毒病的患者,核酸扩增检测(NAAT)是首选的诊断方法。免疫球蛋白 M(IgM)抗体检测可识别其他感染,并仍然是这些疾病诊断的重要工具,但由于交叉反应,解释结果较为复杂,并且确定感染的具体时间可能较为困难。这些限制对于确定寨卡病毒感染是否发生在妊娠期间或之前的孕妇来说是一个特别的挑战。
本报告总结了现有和新的登革热和寨卡病毒诊断检测指南,适用于居住在或最近前往存在感染这两种病毒风险的地区且临床表现符合疾病的患者。CDC 对可能暴露于寨卡病毒的无症状孕妇的筛查建议保持不变。对于有症状的非孕妇,应在症状出现后≤7 天采集血清进行登革热和寨卡病毒 NAAT。对于无 NAAT 阴性血清标本或症状出现后>7 天采集的血清,应进行登革热和寨卡病毒 IgM 抗体检测。对于有症状的孕妇,应尽快在症状出现后 12 周内采集血清和尿液标本,同时进行登革热和寨卡病毒 NAAT 和 IgM 抗体检测。当临床或流行病学指征需要时,对于出现 IgM 抗体阳性而 NAAT 结果阴性的情况,应通过中和抗体检测进行确认,包括所有孕妇。在决定进行哪些检测和解释检测结果时,应考虑暴露地点已知病毒的流行病学数据和临床发现。
对于有临床疑似登革热的患者,应进行适当的管理以监测和治疗休克和出血。对于妊娠期间实验室证据提示可能感染寨卡病毒的妇女及其婴儿,应进行评估和管理以确定是否存在不良结局。登革热和寨卡病毒病是全国法定报告的疾病,应向公共卫生部门报告病例。