Evidence map›Paper›PMID 25946164›Full record

ArticlePloS one2015

Constructing rigorous and broad biosurveillance networks for detecting emerging zoonotic outbreaks.

Mac Brown, Leslie Moore, Benjamin McMahon, Dennis Powell, Montiago LaBute, James M Hyman, Ariel Rivas, Mark Jankowski, Joel Berendzen, Jason Loeppky and 2 more

Abstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
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

12 authors.

Mac BrownUniversity of California-Santa Barbara, Department of Economics, Santa Barbara, California, 93111, United States of America.
Leslie MooreStatistical Sciences, Los Alamos National Laboratory, Los Alamos, New Mexico, 87545, United States of America.
Benjamin McMahonLos Alamos National Laboratory, Theoretical Biology and Biophysics, Los Alamos, New Mexico, 87545, United States of America.
Dennis PowellEnergy and Infrastructure Analysis, Los Alamos National Laboratory, Los Alamos, New Mexico, 87545, United States of America.
Montiago LaButeLawrence Livermore National Laboratory, Applied Statistics Group-Computational Engineering Division, Mailstop L-174, 7000 East Ave. Livermore, California, 94550, United States of America.
James M HymanDepartment of Mathematics, Tulane University, New Orleans, Louisiana, 70118, United States of America.
Ariel RivasCenter for Global Health, Health Sciences Center, University of New Mexico, Albuquerque, New Mexico, 87131, United States of America.
Mark JankowskiMinnesota Pollution Control Agency, Environmental Analysis & Outcomes Division, St. Paul, Minnesota, 55155, United States of America.
Joel BerendzenLos Alamos National Laboratory, Applied Modern Physics, Mailstop D454, Los Alamos, New Mexico, 87545, United States of America.
Jason LoeppkyUniversity of British Columbia, Okanagan, 3333 University Way, Kelowna, B.C. V1V 1V7, Canada.
Carrie ManoreCenter for Computational Science, Tulane University, New Orleans, Louisiana, 70118, United States of America.
Jeanne FairLos Alamos National Laboratory, Environmental Stewardship, K404, Los Alamos, New Mexico, 87545, United States of America.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Determining optimal surveillance networks for an emerging pathogen is difficult since it is not known beforehand what the characteristics of a pathogen will be or where it will emerge. The resources for surveillance of infectious diseases in animals and wildlife are often limited and mathematical modeling can play a supporting role in examining a wide range of scenarios of pathogen spread. We demonstrate how a hierarchy of mathematical and statistical tools can be used in surveillance planning help guide successful surveillance and mitigation policies for a wide range of zoonotic pathogens. The model forecasts can help clarify the complexities of potential scenarios, and optimize biosurveillance programs for rapidly detecting infectious diseases. Using the highly pathogenic zoonotic H5N1 avian influenza 2006-2007 epidemic in Nigeria as an example, we determined the risk for infection for localized areas in an outbreak and designed biosurveillance stations that are effective for different pathogen strains and a range of possible outbreak locations. We created a general multi-scale, multi-host stochastic SEIR epidemiological network model, with both short and long-range movement, to simulate the spread of an infectious disease through Nigerian human, poultry, backyard duck, and wild bird populations. We chose parameter ranges specific to avian influenza (but not to a particular strain) and used a Latin hypercube sample experimental design to investigate epidemic predictions in a thousand simulations. We ranked the risk of local regions by the number of times they became infected in the ensemble of simulations. These spatial statistics were then complied into a potential risk map of infection. Finally, we validated the results with a known outbreak, using spatial analysis of all the simulation runs to show the progression matched closely with the observed location of the farms infected in the 2006-2007 epidemic.

Indexed as

Models, StatisticalAnimalsEpidemiological MonitoringHumansInfluenza A Virus, H5N1 SubtypeInfluenza, HumanInfluenza in BirdsPoultryZoonoses

Identifiers

PMID25946164
PMCPMC4422680

What OpenQuestion holds

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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.