Cargando…
Gentamicin-mediated ototoxicity and nephrotoxicity: A clinical trial study
BACKGROUND: Aminoglycosides and mainly gentamicin are the most important antimicrobial agents. Two different methods of administration exist: Single and multiple doses. There has always been a controversy about the less harmful administration method, to minimize adverse effects of gentamicin – deafn...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5126748/ https://www.ncbi.nlm.nih.gov/pubmed/27942103 http://dx.doi.org/10.4103/0300-1652.193861 |
_version_ | 1782470158841806848 |
---|---|
author | Saleh, Parviz Abbasalizadeh, Shamsi Rezaeian, Saman Naghavi-Behzad, Mohammad Piri, Reza Pourfeizi, Hojjat Hossein |
author_facet | Saleh, Parviz Abbasalizadeh, Shamsi Rezaeian, Saman Naghavi-Behzad, Mohammad Piri, Reza Pourfeizi, Hojjat Hossein |
author_sort | Saleh, Parviz |
collection | PubMed |
description | BACKGROUND: Aminoglycosides and mainly gentamicin are the most important antimicrobial agents. Two different methods of administration exist: Single and multiple doses. There has always been a controversy about the less harmful administration method, to minimize adverse effects of gentamicin – deafness and renal insufficiency. In this study, it was aimed to compare two different methods of administration to figure out the least harmful treatment method. MATERIALS AND METHODS: In a clinical study, eighty patients aged 12–55 years who were admitted with sepsis syndrome were included in the study; they were divided into two groups: The first group received single-dose treatment (5 mg/kg) whereas the second group was treated with multiple doses (1.7 mg/kg three times a day) of gentamicin. RESULTS: The results show that blood urea nitrogen (BUN) and creatinine (CR) levels were decreased in the first group. Both blood urea nitrogen and creatinine and also mean glomerular filtration rate was increased in the same group. In the second group, mean BUN and CR levels were increased while the GFR was decreased in the same group. There was also a gradual increase in GFR in the first group. GFR <80 was decreased from 20% to 5.1% in the first group while increased from 5% to 27.5% in the second group. Results of audiometric studies show 6.1% hearing problem in the first group and 12.8% in the second one. CONCLUSIONS: Results of the present study showed that nephrotoxicity and ototoxicity are minimized in single-dose administration compared to multiples doses. |
format | Online Article Text |
id | pubmed-5126748 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-51267482016-12-09 Gentamicin-mediated ototoxicity and nephrotoxicity: A clinical trial study Saleh, Parviz Abbasalizadeh, Shamsi Rezaeian, Saman Naghavi-Behzad, Mohammad Piri, Reza Pourfeizi, Hojjat Hossein Niger Med J Original Article BACKGROUND: Aminoglycosides and mainly gentamicin are the most important antimicrobial agents. Two different methods of administration exist: Single and multiple doses. There has always been a controversy about the less harmful administration method, to minimize adverse effects of gentamicin – deafness and renal insufficiency. In this study, it was aimed to compare two different methods of administration to figure out the least harmful treatment method. MATERIALS AND METHODS: In a clinical study, eighty patients aged 12–55 years who were admitted with sepsis syndrome were included in the study; they were divided into two groups: The first group received single-dose treatment (5 mg/kg) whereas the second group was treated with multiple doses (1.7 mg/kg three times a day) of gentamicin. RESULTS: The results show that blood urea nitrogen (BUN) and creatinine (CR) levels were decreased in the first group. Both blood urea nitrogen and creatinine and also mean glomerular filtration rate was increased in the same group. In the second group, mean BUN and CR levels were increased while the GFR was decreased in the same group. There was also a gradual increase in GFR in the first group. GFR <80 was decreased from 20% to 5.1% in the first group while increased from 5% to 27.5% in the second group. Results of audiometric studies show 6.1% hearing problem in the first group and 12.8% in the second one. CONCLUSIONS: Results of the present study showed that nephrotoxicity and ototoxicity are minimized in single-dose administration compared to multiples doses. Medknow Publications & Media Pvt Ltd 2016 /pmc/articles/PMC5126748/ /pubmed/27942103 http://dx.doi.org/10.4103/0300-1652.193861 Text en Copyright: © 2016 Nigerian Medical Journal http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms. |
spellingShingle | Original Article Saleh, Parviz Abbasalizadeh, Shamsi Rezaeian, Saman Naghavi-Behzad, Mohammad Piri, Reza Pourfeizi, Hojjat Hossein Gentamicin-mediated ototoxicity and nephrotoxicity: A clinical trial study |
title | Gentamicin-mediated ototoxicity and nephrotoxicity: A clinical trial study |
title_full | Gentamicin-mediated ototoxicity and nephrotoxicity: A clinical trial study |
title_fullStr | Gentamicin-mediated ototoxicity and nephrotoxicity: A clinical trial study |
title_full_unstemmed | Gentamicin-mediated ototoxicity and nephrotoxicity: A clinical trial study |
title_short | Gentamicin-mediated ototoxicity and nephrotoxicity: A clinical trial study |
title_sort | gentamicin-mediated ototoxicity and nephrotoxicity: a clinical trial study |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5126748/ https://www.ncbi.nlm.nih.gov/pubmed/27942103 http://dx.doi.org/10.4103/0300-1652.193861 |
work_keys_str_mv | AT salehparviz gentamicinmediatedototoxicityandnephrotoxicityaclinicaltrialstudy AT abbasalizadehshamsi gentamicinmediatedototoxicityandnephrotoxicityaclinicaltrialstudy AT rezaeiansaman gentamicinmediatedototoxicityandnephrotoxicityaclinicaltrialstudy AT naghavibehzadmohammad gentamicinmediatedototoxicityandnephrotoxicityaclinicaltrialstudy AT pirireza gentamicinmediatedototoxicityandnephrotoxicityaclinicaltrialstudy AT pourfeizihojjathossein gentamicinmediatedototoxicityandnephrotoxicityaclinicaltrialstudy |