Evidence map›Paper›PMID 31194720›Full record

GuidelineMMWR. Recommendations and reports : Morbidity and mortality weekly report. Recommendations and reports2019

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

Tyler M Sharp, Marc Fischer, Jorge L Muñoz-Jordán, Gabriela Paz-Bailey, J Erin Staples, Christopher J Gregory, Stephen H Waterman

Abstract readPractice Guideline
In one paragraph

Guideline in MMWR. Recommendations and reports : Morbidity and mortality weekly report. Recommendations and reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 69 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
69citing papers in PubMed, 2 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

69 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Zika virus infection in the genital tract of non-pregnant females: a systematic review.Revista do Instituto de Medicina Tropical de Sao Paulo · 2020
    Pooled it
  3. Review
  4. Review
  5. Review
  6. Article
  7. Article
  8. Article
  9. Diagnostic Techniques for Dengue Virus.Current topics in microbiology and immunology · 2026
    Review
  10. Article
  11. Article
  12. Review
  13. Review
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Review
  20. Article

9 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Tyler M SharpDivision of Vector-Borne Diseases, National Center for Emerging and Zoonotic Infectious Diseases, CDC.
Marc FischerDivision of Vector-Borne Diseases, National Center for Emerging and Zoonotic Infectious Diseases, CDC.
Jorge L Muñoz-JordánDivision of Vector-Borne Diseases, National Center for Emerging and Zoonotic Infectious Diseases, CDC.
Gabriela Paz-BaileyDivision of Vector-Borne Diseases, National Center for Emerging and Zoonotic Infectious Diseases, CDC.
J Erin StaplesDivision of Vector-Borne Diseases, National Center for Emerging and Zoonotic Infectious Diseases, CDC.
Christopher J GregoryDivision of Vector-Borne Diseases, National Center for Emerging and Zoonotic Infectious Diseases, CDC.
Stephen H WatermanDivision of Vector-Borne Diseases, National Center for Emerging and Zoonotic Infectious Diseases, CDC.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

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.

Indexed as

Diagnostic Tests, RoutineCenters for Disease Control and Prevention, U.S.CoinfectionDengueDengue VirusDiagnosis, DifferentialFemaleHumansPregnancyPregnancy Complications, InfectiousRisk AssessmentTravel-Related IllnessUnited StatesZika VirusZika Virus Infection

Identifiers

PMID31194720
PMCPMC6581290

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.