Evidence map›Paper›PMID 30359419›Full record

ArticlePloS one2018

Initial validation of a simulation model for estimating the impact of serogroup A Neisseria meningitidis vaccination in the African meningitis belt.

Michael L Jackson, Alpha Oumar Diallo, Isaie Médah, Brice Wilfried Bicaba, Issaka Yaméogo, Daouda Koussoubé, Rasmata Ouédraogo, Lassané Sangaré, Sarah A Mbaeyi

Abstract readValidation Study
In one paragraph

Article in PloS one, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. 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

9 authors.

Michael L JacksonKaiser Permanente Washington Health Research Institute, Kaiser Permanente Washington, Seattle, Washington, United States of America.ORCID 0000-0002-2340-0256
Alpha Oumar DialloNational Center for Immunization and Respiratory Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia, United States of America.
Isaie MédahDirection de la Lutte Contre la Maladie, Ministère de la Santé, Ouagadougou, Burkina Faso.
Brice Wilfried BicabaDirection de la Lutte Contre la Maladie, Ministère de la Santé, Ouagadougou, Burkina Faso.
Issaka YaméogoDirection de la Lutte Contre la Maladie, Ministère de la Santé, Ouagadougou, Burkina Faso.
Daouda KoussoubéDirection de la Lutte Contre la Maladie, Ministère de la Santé, Ouagadougou, Burkina Faso.
Rasmata OuédraogoDirection de la Lutte Contre la Maladie, Ministère de la Santé, Ouagadougou, Burkina Faso.
Lassané SangaréDirection de la Lutte Contre la Maladie, Ministère de la Santé, Ouagadougou, Burkina Faso.
Sarah A MbaeyiNational Center for Immunization and Respiratory Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia, United States of America.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We previously developed a mathematical simulation of serogroup A Neisseria meningitidis (NmA) transmission in Burkina Faso, with the goal of forecasting the relative benefit of different vaccination programs. Here, we revisit key structural assumptions of the model by comparing how accurately the different assumptions reproduce observed NmA trends following vaccine introduction. A priori, we updated several of the model's parameters based on recently published studies. We simulated NmA disease under different assumptions about duration of vaccine-induced protection (including the possibility that vaccine-induced protection may last longer than natural immunity). We compared simulated and observed case counts from 2011-2017. We then used the best-fit model to forecast the impact of different vaccination strategies. Our updated model, with the assumption that vaccine-induced immunity lasts longer than immunity following NmA colonization, was able to reproduce observed trends in NmA disease. The updated model predicts that, following a mass campaign among persons 1-29 years of age, either routine immunization of 9 month-old children or periodic mini-campaigns among children 1-4 years of age will lead to sustained control of epidemic NmA in Burkina Faso. This validated model can help public health officials set policies for meningococcal vaccination in Africa.

Indexed as

Computer SimulationVaccinationAdolescentAdultBurkina FasoChildChild, PreschoolFemaleHumansImmunization ProgramsInfantMaleMeningitis, MeningococcalMeningococcal VaccinesNeisseria meningitidis, Serogroup ASerogroupMeningococcal Vaccines

Identifiers

PMID30359419
PMCPMC6201925

What OpenQuestion holds

Textmetadata
LicenceCC0
Read underepoch 390

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.