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2016年1月1日至2017年6月30日纽约市寨卡病毒病例的流行病学特征及实验室检查结果

Epidemiological Characteristics and Laboratory Findings of Zika Virus Cases in New York City, January 1, 2016-June 30, 2017.

作者信息

McGibbon Emily, Moy Morgan, Vora Neil M, Dupuis Alan, Fine Annie, Kulas Karen, Limberger Ronald, Liu Dakai, Rakeman Jennifer, St George Kirsten, Slavinski Sally

机构信息

1 Bureau of Communicable Diseases , New York City Department of Health and Mental Hygiene, Long Island City, New York.

2 Public Health Laboratory , New York City Department of Health and Mental Hygiene, New York City, New York.

出版信息

Vector Borne Zoonotic Dis. 2018 Jul;18(7):382-389. doi: 10.1089/vbz.2017.2223. Epub 2018 May 9.

Abstract

BACKGROUND

An outbreak of Zika virus (ZIKV) began in May 2015 in Brazil and rapidly spread throughout the Americas; New York City (NYC) has a diverse population with ∼1.8 million residents who were born in ZIKV-affected areas. Before July 24, 2017, the Centers for Disease Control and Prevention (CDC) ZIKV testing recommendations included nucleic acid amplification-based tests for serum and urine specimens collected ≤14 days of illness onset or last potential exposure, and ZIKV immunoglobulin M (IgM) assay when ZIKV RNA is not detected or for specimens collected within 2-12 weeks of illness onset or last potential exposure, followed by a plaque reduction neutralization test (PRNT). However, the New York public health laboratories and commercial laboratories tested specimens collected beyond these time frames.

METHODS

We analyzed 1080 noncongenital ZIKV cases in NYC residents who met the Council for State and Territorial Epidemiologist's ZIKV case definitions.

RESULTS

Among cases, 98% were travel associated, 1% were sexually transmitted, and 1% had unknown exposures; 412 (38%) cases were pregnant women. Of 672 patients with ZIKV RNA detected in serum or urine specimens, 48 (7%) tested positive >14 days after either symptom onset or last potential exposure date (range 15-99 days). Of 390 patients diagnosed based on serology alone (i.e., not tested or not detectable for ZIKV RNA), 60 (15%) had a positive ZIKV IgM and PRNT >12 weeks after symptom onset or last potential exposure date (range 85-273 days).

CONCLUSION

Our findings correspond with CDC's updated guidance to test symptomatic pregnant women up to 12 weeks past onset of symptoms. ZIKV IgM antibody testing may also be warranted for pregnant women regardless of symptoms if their exposure occurred during their pregnancy or periconception period. Providers should understand the scope of diagnostic testing and its limitations to appropriately counsel patients, especially pregnant women.

摘要

背景

寨卡病毒(ZIKV)疫情于2015年5月在巴西爆发,并迅速蔓延至整个美洲;纽约市人口多样化,约有180万居民出生在寨卡病毒感染地区。在2017年7月24日之前,美国疾病控制与预防中心(CDC)的寨卡病毒检测建议包括,对发病或最后一次可能接触病毒≤14天内采集的血清和尿液标本进行基于核酸扩增的检测,以及在未检测到寨卡病毒RNA时或发病或最后一次可能接触病毒2 - 12周内采集的标本进行寨卡病毒免疫球蛋白M(IgM)检测,随后进行蚀斑减少中和试验(PRNT)。然而,纽约公共卫生实验室和商业实验室对超出这些时间范围采集的标本进行了检测。

方法

我们分析了1080例符合州和地区流行病学家委员会寨卡病毒病例定义的纽约市居民非先天性寨卡病毒病例。

结果

在这些病例中,98%与旅行相关,1%通过性传播,1%的暴露情况不明;412例(38%)病例为孕妇。在血清或尿液标本中检测到寨卡病毒RNA的672例患者中,48例(7%)在症状出现或最后一次可能接触日期>14天后检测呈阳性(范围为15 - 99天)。在仅基于血清学诊断的390例患者(即未检测或未检测到寨卡病毒RNA)中,60例(15%)在症状出现或最后一次可能接触日期>12周后寨卡病毒IgM和PRNT呈阳性(范围为85 - 273天)。

结论

我们的研究结果与CDC的最新指南一致,即对症状出现后长达12周的有症状孕妇进行检测。如果孕妇在孕期或围孕期有暴露史,无论有无症状,也可能需要进行寨卡病毒IgM抗体检测。医疗服务提供者应了解诊断检测的范围及其局限性,以便为患者,尤其是孕妇提供适当的咨询。

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