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

Schmutzhard, J; Lackner, P; Helbok, R; Hurth, HV; Aregger, FC; Muigg, V; Kegele, J; Bunk, S; Oberhammer, L; Fischer, N; et al. Schmutzhard, J; Lackner, P; Helbok, R; Hurth, HV; Aregger, FC; Muigg, V; Kegele, J; Bunk, S; Oberhammer, L; Fischer, N; Pinggera, L; Otieno, A; Ogutu, B; Agbenyega, T; Ansong, D; Adegnika, AA; Issifou, S; Zorowka, P; Krishna, S; Mordmüller, B; Schmutzhard, E; Kremsner, P (2015) Severe malaria in children leads to a significant impairment of transitory otoacoustic emissions--a prospective multicenter cohort study. BMC Medicine, 13. p. 125. ISSN 1741-7015 https://doi.org/10.1186/s12916-015-0366-8
SGUL Authors: Krishna, Sanjeev

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Abstract

BACKGROUND: Severe 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. METHODS: This 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. RESULTS: In 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 %). CONCLUSION: The 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.

Item Type: Article
Additional Information: There is an erratum for this record: http://openaccess.sgul.ac.uk/108359/ © 2015 Schmutzhard et al. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http:// creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
Keywords: Child, Child, Preschool, Cohort Studies, Female, Gabon, Ghana, Hearing Loss, Humans, Kenya, Malaria, Cerebral, Malaria, Falciparum, Male, Otoacoustic Emissions, Spontaneous, Prospective Studies, Humans, Malaria, Cerebral, Malaria, Falciparum, Hearing Loss, Cohort Studies, Prospective Studies, Otoacoustic Emissions, Spontaneous, Child, Child, Preschool, Gabon, Kenya, Ghana, Female, Male, Hearing impairment, Otoacoustic emissions, Severe malaria, General & Internal Medicine, 11 Medical And Health Sciences
SGUL Research Institute / Research Centre: Academic Structure > Infection and Immunity Research Institute (INII)
Journal or Publication Title: BMC Medicine
ISSN: 1741-7015
Language: ENG
Dates:
DateEvent
28 May 2015Published
13 May 2015Accepted
Publisher License: Creative Commons: Attribution 4.0
PubMed ID: 26021376
Web of Science ID: WOS:000355970000001
Go to PubMed abstract
URI: https://openaccess.sgul.ac.uk/id/eprint/108358
Publisher's version: https://doi.org/10.1186/s12916-015-0366-8

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