登革热和寨卡病毒诊断检测患者的临床相容疾病和感染两种病毒的风险。

IF 33.7 1区 医学 Q1 Medicine
Tyler M Sharp, Marc Fischer, Jorge L Muñoz-Jordán, Gabriela Paz-Bailey, J Erin Staples, Christopher J Gregory, Stephen H Waterman
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引用次数: 74

摘要

登革热病毒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,分布于整个热带和亚热带,疾病表现包括发烧、皮疹、肌痛和关节痛。对于疑似登革热或寨卡病毒病的患者,核酸扩增试验(NAATs)是首选的诊断方法。免疫球蛋白M (IgM)抗体检测可以识别其他感染,并且仍然是诊断这些疾病的重要工具,但由于交叉反应性,解释结果很复杂,并且确定感染的具体时间可能很困难。这些限制对孕妇在确定寨卡病毒感染是否发生在怀孕期间或之前是一个特别的挑战。本报告总结了对居住或最近曾到有感染两种病毒风险地区的临床相容疾病患者进行登革热和寨卡病毒诊断检测的现有和新指南。疾病预防控制中心对筛查可能接触寨卡病毒的无症状孕妇的建议保持不变。对于有症状的非孕妇,应在症状出现后≤7天对采集的血清进行登革热和寨卡病毒NAATs检测。应对naat阴性血清标本或在出现症状后>7天采集的血清进行登革热和寨卡病毒IgM抗体检测。对于有症状的孕妇,应在症状出现后12周内尽快采集血清和尿液标本,同时进行登革热和寨卡病毒NAATs和IgM抗体检测。当临床或流行病学指示时,应通过中和抗体试验确认IgM抗体阳性和NAAT阴性,包括所有孕妇。在决定进行何种检测和解释检测结果时,应考虑在接触地点已知正在传播的病毒的流行病学数据和临床结果。临床疑似登革热患者应接受适当的管理,以监测和治疗休克和出血。在怀孕期间有实验室证据表明可能感染寨卡病毒的妇女及其婴儿,应对可能的不良后果进行评估和管理。登革热和寨卡病毒病是国家必须通报的疾病,病例应向公共卫生当局报告。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Dengue and Zika Virus Diagnostic Testing for Patients with a Clinically Compatible Illness and Risk for Infection with Both Viruses.

Dengue and Zika Virus Diagnostic Testing for Patients with a Clinically Compatible Illness and Risk for Infection with Both Viruses.

Dengue and Zika Virus Diagnostic Testing for Patients with a Clinically Compatible Illness and Risk for Infection with Both Viruses.

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.

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来源期刊
Mmwr Recommendations and Reports
Mmwr Recommendations and Reports PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH-
CiteScore
36.00
自引率
0.00%
发文量
3
期刊介绍: The MMWR series of publications is published by the Office of Science, Centers for Disease Control and Prevention (CDC), U.S. The MMWR Recommendations and Reports contain in-depth articles that relay policy statements for prevention and treatment in all areas in the CDC’s scope of responsibility (e.g., recommendations from the Advisory Committee on Immunization Practices).
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