Evidence map›Paper›PMID 30300411›Full record

ArticlePloS one2018

Antimicrobial treatment practices among Ugandan children with suspicion of central nervous system infection.

Elizabeth Kemigisha, Deborah Nanjebe, Yap Boum, Céline Langendorf, Said Aberrane, Dan Nyehangane, Fabienne Nackers, Yolanda Mueller, Rémi Charrel, Richard A Murphy and 2 more

Open access · goldAbstract read
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 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 pooled it
1.0field-weighted citation impact, top 23% 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.

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

6 citing papers in PubMed, 1 synthesis or guideline pooled it, 8 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. 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 at 3 institutions in 2 countries.

Elizabeth KemigishaEpicentre Mbarara Research Centre, Mbarara, Uganda.
Deborah NanjebeEpicentre Mbarara Research Centre, Mbarara, Uganda.
Yap BoumEpicentre Mbarara Research Centre, Mbarara, Uganda.
Céline LangendorfEpicentre, Paris, France.
Said AberraneMicrobiology Laboratory, Créteil Hospital, France.
Dan NyehanganeEpicentre Mbarara Research Centre, Mbarara, Uganda.
Fabienne NackersEpicentre, Paris, France.
Yolanda MuellerCentre de recherche et de développement Policlinique Médicale Universitaire, Lausanne, Switzerland.
Rémi CharrelEPV Emergence des Pathologies, UMR D 190, Marseille, France.
Richard A MurphyDivision of Infectious Diseases, Los Angeles Biomedical Research Institute at Harbor-UCLA Medical Center, Torrance, CA, United States of America.
Anne-Laure PageEpicentre, Paris, France.
Juliet Mwanga-AmumpaireEpicentre Mbarara Research Centre, Mbarara, Uganda.ORCID 0000-0002-6738-477X
Mbarara University of Science and Technology · UGEpicentre Uganda · UGThe Lundquist Institute · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Acute central nervous system (CNS) infections in children in sub-Saharan Africa are often fatal. Potential contributors include late presentation, limited diagnostic capacity and inadequate treatment. A more nuanced understanding of treatment practices with a goal of optimizing such practices is critical to prevent avoidable case fatality. We describe empiric antimicrobial treatment, antibiotic resistance and treatment adequacy in a prospective cohort of 459 children aged two months to 12 years hospitalised for suspected acute CNS infections in Mbarara, Uganda, from 2009 to 2012. Among these 459 children, 155 had a laboratory-confirmed diagnosis of malaria (case-fatality rate [CFR] 14%), 58 had bacterial infections (CFR 24%) and 6 children had mixed malaria and bacterial infections (CFR 17%). Overall case fatality was 18.1% (n = 83). Of 219 children with laboratory-confirmed malaria and/or bacterial infections, 182 (83.1%) received an adequate antimalarial and/or antibiotic on the day of admission and 211 (96.3%) within 48 hours of admission. The proportion of those receiving adequate treatment was similar among survivors and non-survivors. All bacterial isolates were sensitive to ceftriaxone except one Escherichia coli isolate with extended-spectrum beta-lactamase (ESBL). The observed high mortality was not a result of inadequate initial antimicrobial treatment at the hospital. The epidemiology of CNS infection in this setting justifies empirical use of a third-generation cephalosporin, however antibiotic resistance should be monitored closely.

Indexed as

Anti-Bacterial AgentsAnti-Infective Agentsbeta-LactamasesCeftriaxoneCentral Nervous System InfectionsChildChild, PreschoolCoinfectionDrug Resistance, BacterialEscherichia coliEscherichia coli InfectionsFemaleHumansInfantMalariaMaleAnti-Bacterial AgentsAnti-Infective Agentsbeta-LactamasesCeftriaxone

Identifiers

PMID30300411
PMCPMC6177169
OpenAlexW2897348552

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.