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A long-term follow-up study on otoacoustic emissions testing in paediatric patients with severe malaria in Gabon

BACKGROUND: In a previous study, severe and cerebral malaria have been connected with acute cochlear malfunction in children, demonstrated by a decrease of transitory evoked otoacoustic emissions (TEOAEs) reproducibility. This study aims to determine whether cochlear malfunction persists for 4 years...

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Autores principales: Reiterer, Elisa, Reider, Simon, Lackner, Peter, Fischer, Natalie, Dejaco, Daniel, Riechelmann, Herbert, Zorowka, Patrick, Kremsner, Peter G., Adegnika, Ayola Akim, Schmutzhard, Erich, Schmutzhard, Joachim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6591898/
https://www.ncbi.nlm.nih.gov/pubmed/31234890
http://dx.doi.org/10.1186/s12936-019-2840-9
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author Reiterer, Elisa
Reider, Simon
Lackner, Peter
Fischer, Natalie
Dejaco, Daniel
Riechelmann, Herbert
Zorowka, Patrick
Kremsner, Peter G.
Adegnika, Ayola Akim
Schmutzhard, Erich
Schmutzhard, Joachim
author_facet Reiterer, Elisa
Reider, Simon
Lackner, Peter
Fischer, Natalie
Dejaco, Daniel
Riechelmann, Herbert
Zorowka, Patrick
Kremsner, Peter G.
Adegnika, Ayola Akim
Schmutzhard, Erich
Schmutzhard, Joachim
author_sort Reiterer, Elisa
collection PubMed
description BACKGROUND: In a previous study, severe and cerebral malaria have been connected with acute cochlear malfunction in children, demonstrated by a decrease of transitory evoked otoacoustic emissions (TEOAEs) reproducibility. This study aims to determine whether cochlear malfunction persists for 4 years after recovery from severe malaria in a subset of the previous study’s collective. Follow-up TEOAEs were performed on site (CERMEL, Hôpital Albert Schweitzer, Lambaréné, Gabon) or at the participants’ homes; 33 out of 90 participants included in the initial investigation by Schmutzhard et al. could be retrieved and were re-examined, 31/33 could be included. Of the 57 missing participants, 51 could not be contacted, 1 had moved away, 4 refused to cooperate, and 1 had died. METHODS: As in the initial investigation, participants of this prospective follow-up study were subjected to TEOAE examination on both ears separately. A wave correlation rate of > 60% on both ears was considered a “pass”; if one ear failed to pass, the examination was considered a “fail”. The results were compared to the primary control group. Additionally, a questionnaire has been applied focusing on subsequent malaria infections between the primary inclusion and follow-up and subjective impairment of hearing and/or understanding. RESULTS: The cohort’s mean age was 9 years, 14 children were female, 18 male. 31 had been originally admitted with severe, one with cerebral malaria. 83.8% of participants (n = 26) presented with a TEOAE correlation rate of > 60% on both ears (the cut-off for good cochlear function); in the control group, 92.2% (n = 83) had passed TEOAE examination on both ears. Recurrent severe malaria was associated with a worse TEOAE correlation rate. Age at infection and gender had no influence on the outcome. CONCLUSIONS: Cochlear malfunction seems to be persistent after 4 years in more than 16% of children hospitalized for malaria. In a healthy control group, this proportion was 7.8%. Yet, the severity of the initial TEOAE-decrease did not predict a worse outcome. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12936-019-2840-9) contains supplementary material, which is available to authorized users.
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spelling pubmed-65918982019-07-08 A long-term follow-up study on otoacoustic emissions testing in paediatric patients with severe malaria in Gabon Reiterer, Elisa Reider, Simon Lackner, Peter Fischer, Natalie Dejaco, Daniel Riechelmann, Herbert Zorowka, Patrick Kremsner, Peter G. Adegnika, Ayola Akim Schmutzhard, Erich Schmutzhard, Joachim Malar J Research BACKGROUND: In a previous study, severe and cerebral malaria have been connected with acute cochlear malfunction in children, demonstrated by a decrease of transitory evoked otoacoustic emissions (TEOAEs) reproducibility. This study aims to determine whether cochlear malfunction persists for 4 years after recovery from severe malaria in a subset of the previous study’s collective. Follow-up TEOAEs were performed on site (CERMEL, Hôpital Albert Schweitzer, Lambaréné, Gabon) or at the participants’ homes; 33 out of 90 participants included in the initial investigation by Schmutzhard et al. could be retrieved and were re-examined, 31/33 could be included. Of the 57 missing participants, 51 could not be contacted, 1 had moved away, 4 refused to cooperate, and 1 had died. METHODS: As in the initial investigation, participants of this prospective follow-up study were subjected to TEOAE examination on both ears separately. A wave correlation rate of > 60% on both ears was considered a “pass”; if one ear failed to pass, the examination was considered a “fail”. The results were compared to the primary control group. Additionally, a questionnaire has been applied focusing on subsequent malaria infections between the primary inclusion and follow-up and subjective impairment of hearing and/or understanding. RESULTS: The cohort’s mean age was 9 years, 14 children were female, 18 male. 31 had been originally admitted with severe, one with cerebral malaria. 83.8% of participants (n = 26) presented with a TEOAE correlation rate of > 60% on both ears (the cut-off for good cochlear function); in the control group, 92.2% (n = 83) had passed TEOAE examination on both ears. Recurrent severe malaria was associated with a worse TEOAE correlation rate. Age at infection and gender had no influence on the outcome. CONCLUSIONS: Cochlear malfunction seems to be persistent after 4 years in more than 16% of children hospitalized for malaria. In a healthy control group, this proportion was 7.8%. Yet, the severity of the initial TEOAE-decrease did not predict a worse outcome. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12936-019-2840-9) contains supplementary material, which is available to authorized users. BioMed Central 2019-06-24 /pmc/articles/PMC6591898/ /pubmed/31234890 http://dx.doi.org/10.1186/s12936-019-2840-9 Text en © The Author(s) 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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.
spellingShingle Research
Reiterer, Elisa
Reider, Simon
Lackner, Peter
Fischer, Natalie
Dejaco, Daniel
Riechelmann, Herbert
Zorowka, Patrick
Kremsner, Peter G.
Adegnika, Ayola Akim
Schmutzhard, Erich
Schmutzhard, Joachim
A long-term follow-up study on otoacoustic emissions testing in paediatric patients with severe malaria in Gabon
title A long-term follow-up study on otoacoustic emissions testing in paediatric patients with severe malaria in Gabon
title_full A long-term follow-up study on otoacoustic emissions testing in paediatric patients with severe malaria in Gabon
title_fullStr A long-term follow-up study on otoacoustic emissions testing in paediatric patients with severe malaria in Gabon
title_full_unstemmed A long-term follow-up study on otoacoustic emissions testing in paediatric patients with severe malaria in Gabon
title_short A long-term follow-up study on otoacoustic emissions testing in paediatric patients with severe malaria in Gabon
title_sort long-term follow-up study on otoacoustic emissions testing in paediatric patients with severe malaria in gabon
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6591898/
https://www.ncbi.nlm.nih.gov/pubmed/31234890
http://dx.doi.org/10.1186/s12936-019-2840-9
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