Evidence map›Paper›PMID 31625835›Full record

Trial reportEmerging infectious diseases2019

Lack of Efficacy of High-Titered Immunoglobulin in Patients with West Nile Virus Central Nervous System Disease.

John W Gnann, Amy Agrawal, John Hart, Martha Buitrago, Paul Carson, Diane Hanfelt-Goade, Ken Tyler, Jared Spotkov, Alison Freifeld, Thomas Moore and 9 more

Registry-linked trialOpen access · diamondAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Emerging infectious diseases, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06590207 (Administering Convalescent Plasma Rich With Neutralizing Abs. to Hospitalized Adults With WNV - a Double-blind Randomized Controlled Study), which is not on this map. Cited by 27 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed, 1 pooled it
5.1field-weighted citation impact, top 5% of its field
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.

NCT06590207 phase3completednot on this mapstarted 2024, after this paper: background citation

Administering Convalescent Plasma Rich With Neutralizing Abs. to Hospitalized Adults With WNV - a Double-blind Randomized Controlled Study

TypeinterventionalSponsorSheba Medical CenterRan2024 to 2025Enrolled200ConditionsWest Nile Fever With Neurologic Manifestation (Diagnosis), West Nile Fever Without ComplicationsArmsplasma rich with WNV neutralizing antibodies, Saline
3 · Its place in the literature

Who cites it

27 citing papers in PubMed, 1 synthesis or guideline pooled it, 53 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Article
  5. Review
  6. Human antibodies against West Nile and related orthoflaviviruses.bioRxiv : the preprint server for biology · 2026
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Variations in West Nile viral infections across North and Central Texas.Proceedings (Baylor University. Medical Center) · 2025
    Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Review
  19. Neurology of Acute Viral Infections.The Neurohospitalist · 2022
    Review
  20. Review
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

19 authors.

John W Gnann
Amy Agrawal
John Hart
Martha Buitrago
Paul Carson
Diane Hanfelt-Goade
Ken Tyler
Jared Spotkov
Alison Freifeld
Thomas Moore
Jorge Reyno
Henry Masur
Penelope Jester
Ilet Dale
Yufeng Li
Inmaculada Aban
Fred D Lakeman
Richard J Whitley
National Institute of Allergy and Infectious Diseases Collaborative Antiviral Study Group

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

West Nile Virus (WNV) can result in clinically severe neurologic disease. There is no treatment for WNV infection, but administration of anti-WNV polyclonal human antibody has demonstrated efficacy in animal models. We compared Omr-IgG-am, an immunoglobulin product with high titers of anti-WNV antibody, with intravenous immunoglobulin (IVIG) and normal saline to assess safety and efficacy in patients with WNV neuroinvasive disease as part of a phase I/II, randomized, double-blind, multicenter study in North America. During 2003-2006, a total of 62 hospitalized patients were randomized to receive Omr-IgG-am, standard IVIG, or normal saline (3:1:1). The primary endpoint was medication safety. Secondary endpoints were morbidity and mortality, measured using 4 standardized assessments of cognitive and functional status. The death rate in the study population was 12.9%. No significant differences were found between groups receiving Omr-IgG-am compared with IVIG or saline for either the safety or efficacy endpoints.

Indexed as

West Nile virusAdultAgedAntibodies, NeutralizingAntibodies, ViralCentral Nervous System Viral DiseasesFemaleHumansImmunoglobulin GImmunoglobulins, IntravenousMaleMiddle AgedTreatment OutcomeWest Nile FeverAntibodies, NeutralizingAntibodies, ViralImmunoglobulin GImmunoglobulins, Intravenouscentral nervous system diseaseencephalitisflavivirusimmunoglobulinneuroinvasive diseaseNorth AmericaOmr-IgG-amPolygamUnited StatesvirusesWest Nile virusWNV

Identifiers

PMID31625835
PMCPMC6810207
OpenAlexW2980092607

What OpenQuestion holds

Textmetadata
LicenceCC BY
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Registered trials

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.