Evidence map›Paper›PMID 26021376›Full record

ArticleBMC medicine2015

Severe malaria in children leads to a significant impairment of transitory otoacoustic emissions--a prospective multicenter cohort study.

Joachim Schmutzhard, Peter Lackner, Raimund Helbok, Helene Verena Hurth, Fabian Cedric Aregger, Veronika Muigg, Josua Kegele, Sebastian Bunk, Lukas Oberhammer, Natalie Fischer and 12 more

Erratum issuedAbstract readMulticenter Study
In one paragraph

Article in BMC medicine, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Review
  2. Article
  3. A retinal model of cerebral malaria.Scientific reports · 2019
    Article
  4. A Clinical Study of Effect of Hyperpyrexia on Otoacoustic Emissions in Children.Indian journal of otolaryngology and head and neck surgery : official publication of the Association of Otolaryngologists of India · 2018
    Article
  5. Review
  6. Article
  7. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

22 authors.

Joachim SchmutzhardDepartment of Otorhinolaryngology, Medical University Innsbruck, Anichstrasse 35, A-6020, Innsbruck, Austria. Joachim.Schmutzhard@i-med.ac.at.
Peter LacknerDepartment of Neurology, NICU, Medical University Innsbruck, Innsbruck, Austria. Peter.Lackner@i-med.ac.at.
Raimund HelbokDepartment of Neurology, NICU, Medical University Innsbruck, Innsbruck, Austria. Raimund.Helbok@uki.at.
Helene Verena HurthDepartment of Neurology, NICU, Medical University Innsbruck, Innsbruck, Austria. helene.hurth@gmx.at.
Fabian Cedric AreggerDepartment of Neurology, NICU, Medical University Innsbruck, Innsbruck, Austria. faregger@gmail.com.
Veronika MuiggCentre de Recherches Médicales de Lambaréné, Albert Schweitzer Hospital (MRUG), Lambaréné, Gabon. Veronika.Muigg@student.i-med.ac.at.
Josua KegeleDepartment of Neurology, NICU, Medical University Innsbruck, Innsbruck, Austria. josua.kegele@gmail.com.
Sebastian BunkDepartment of Neurology, NICU, Medical University Innsbruck, Innsbruck, Austria. Sebastian.Bunk@student.i-med.ac.at.
Lukas OberhammerCentre de Recherches Médicales de Lambaréné, Albert Schweitzer Hospital (MRUG), Lambaréné, Gabon. Lukas.Oberhammer@student.i-med.ac.at.
Natalie FischerDepartment of Otorhinolaryngology, Medical University Innsbruck, Anichstrasse 35, A-6020, Innsbruck, Austria. Natalie.Fischer@i-med.ac.at.
Leyla PinggeraDepartment of Otorhinolaryngology, Medical University Innsbruck, Anichstrasse 35, A-6020, Innsbruck, Austria. Leyla.Pinggera@i-med.ac.at.
Allan OtienoCenter for Clinical Research, Kenya Medical Research Institute, Kisumu, Kenya. gaotieno@gmail.com.
Bernards OgutuCenter for Clinical Research, Kenya Medical Research Institute, Kisumu, Kenya. Bernhards.Ogutu@usamru-k.org.
Tsiri AgbenyegaKomfo Anokye Teaching Hospita & Kwame Nkrumah University of Science and Technology, Kumasi, Ghana. tsiri@ghana.com.
Daniel AnsongKomfo Anokye Teaching Hospita & Kwame Nkrumah University of Science and Technology, Kumasi, Ghana. ansongd@yahoo.com.
Ayola A AdegnikaCentre de Recherches Médicales de Lambaréné, Albert Schweitzer Hospital (MRUG), Lambaréné, Gabon. a.a.adegnika@medizin.uni-tuebingen.de.
Saadou IssifouCentre de Recherches Médicales de Lambaréné, Albert Schweitzer Hospital (MRUG), Lambaréné, Gabon. isaadou2002@yahoo.fr.
Patrick ZorowkaDepartment of Hearing, Speech and Voice Disorders, Medical University, Innsbruck, Austria. Patrick.Zorowka@i-med.ac.at.
Sanjeev KrishnaSt. George's University of London, London, UK. sgjf100@sgul.ac.uk.
Benjamin MordmüllerCentre de Recherches Médicales de Lambaréné, Albert Schweitzer Hospital (MRUG), Lambaréné, Gabon. benjamin.mordmueller@uni-tuebingen.de.
Erich SchmutzhardDepartment of Neurology, NICU, Medical University Innsbruck, Innsbruck, Austria. Erich.Schmutzhard@i-med.ac.at.
Peter KremsnerCentre de Recherches Médicales de Lambaréné, Albert Schweitzer Hospital (MRUG), Lambaréné, Gabon. peter.kremsner@uni-tuebingen.de.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSevere malaria may influence inner ear function, although this possibility has not been examined prospectively. In a retrospective analysis, hearing impairment was found in 9 of 23 patients with cerebral malaria. An objective method to quickly evaluate the function of the inner ear are the otoacoustic emissions. Negative transient otoacoustic emissions are associated with a threshold shift of 20 dB and above.

methodsThis prospective multicenter study analyses otoacoustic emissions in patients with severe malaria up to the age of 10 years. In three study sites (Ghana, Gabon, Kenya) 144 patients with severe malaria and 108 control children were included. All malaria patients were treated with parental artesunate.

resultsIn the control group, 92.6 % (n = 108, 95 % confidence interval 86.19-6.2 %) passed otoacoustic emission screening. In malaria patients, 58.5 % (n = 94, malaria vs controls p < 0.001, 95 % confidence interval 48.4-67.9 %) passed otoacoustic emission screening at the baseline measurement. The value increased to 65.2 % (n = 66, p < 0.001, 95 % confidence interval 53.1-75.5 %) at follow up 14-28 days after diagnosis of malaria. The study population was divided into severe non-cerebral malaria and severe malaria with neurological symptoms (cerebral malaria). Whereas otoacoustic emissions in severe malaria improved to a passing percentage of 72.9 % (n = 48, 95 % confidence interval 59-83.4 %) at follow-up, the patients with cerebral malaria showed a drop in the passing percentage to 33 % (n = 18) 3-7 days after diagnosis. This shows a significant impairment in the cerebral malaria group (p = 0.012 at days 3-7, 95 % confidence interval 16.3-56.3 %; p = 0.031 at day 14-28, 95 % confidence interval 24.5-66.3 %).

conclusionThe presented data show that 40 % of children have involvement of the inner ear early in severe malaria. In children, audiological screening after severe malaria infection is not currently recommended, but is worth investigating in larger studies.

Indexed as

Otoacoustic Emissions, SpontaneousChildChild, PreschoolCohort StudiesFemaleGabonGhanaHearing LossHumansKenyaMalaria, CerebralMalaria, FalciparumMaleProspective Studies

Identifiers

PMID26021376
PMCPMC4457990

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Registered trials

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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.