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Indoor air bacterial load and antibiotic susceptibility pattern of isolates at Adare General Hospital in Hawassa, Ethiopia

BACKGROUND: Air is the agent of pathogenic microbes that cause significant problems in the hospital environment. Multidrug resistance poses a major therapeutic challenge to these airborne microorganisms in hospital indoor environments. METHOD AND MATERIALS: This study was conducted at Adare General...

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Autores principales: Atalay, Yibeltal Assefa, Mengistie, Embialle, Tolcha, Alemu, Birhan, Belete, Asmare, Getachew, Gebeyehu, Natnael Atnafu, Gelaw, Kelemu Abebe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10653387/
https://www.ncbi.nlm.nih.gov/pubmed/38026319
http://dx.doi.org/10.3389/fpubh.2023.1194850
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author Atalay, Yibeltal Assefa
Mengistie, Embialle
Tolcha, Alemu
Birhan, Belete
Asmare, Getachew
Gebeyehu, Natnael Atnafu
Gelaw, Kelemu Abebe
author_facet Atalay, Yibeltal Assefa
Mengistie, Embialle
Tolcha, Alemu
Birhan, Belete
Asmare, Getachew
Gebeyehu, Natnael Atnafu
Gelaw, Kelemu Abebe
author_sort Atalay, Yibeltal Assefa
collection PubMed
description BACKGROUND: Air is the agent of pathogenic microbes that cause significant problems in the hospital environment. Multidrug resistance poses a major therapeutic challenge to these airborne microorganisms in hospital indoor environments. METHOD AND MATERIALS: This study was conducted at Adare General Hospital in Hawassa City, Sidama, Ethiopia. A cross-sectional study was conducted. The proportional allocation method was used to select the sampled 50 rooms from the total available rooms in each category of wards and staff offices. A total of 100 indoor air samples were collected using settle plates in all units twice a day, morning (9:00–4:00 a.m.) and afternoon (3:00–4:00 p.m.). The types and number of colonies were determined in the laboratory, and the pathogenic bacteria were isolated by appropriate bacteriological techniques. Antimicrobial susceptibility testing was performed on Mueller-Hinton agar for each potentially pathogenic bacterium isolated. For each bacterium, a total of 12 antibiotics were tested using the Kirby-Bauer disk diffusion method. The test organism was adjusted to McFarland turbidity standards of 0.5. Data were entered and analyzed using the SPSS version 25 window. Descriptive analysis and one-way analysis of variance were performed. RESULTS: The indoor air bacterial load of Adare General Hospital was found in the range between 210 and 3,224 CFU/m(3). The highest indoor air bacterial load was identified from the gynecology ward with a mean of 2,542.5CFU/m(3) at p < 0.05. From 100 indoor air samples, a total of 116 bacterial pathogen isolates were obtained. Gram-positive isolates predominated at 72.4%, of which 37.1% were Staphylococcus aureus, 26.7% were coagulase-negative Staphylococci, and the rest 8.6% were Streptococcus pyogenes. The isolation of pathogenic bacteria Staphylococcus aureus and coagulase-negative Staphylococci showed a high level of resistance to ampicillin. CONCLUSION: A high bacterial load was found in the study area as compared to different indoor air biological standards. Staphylococcus aureus and coagulase-negative Staphylococci were the isolated predominant bacteria. Attention should be given to preventing and minimizing those environmental factors that favor the multiplication of bacteria in the indoor environment of a hospital for the safe health of patients, visitors, and staff.
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spelling pubmed-106533872023-11-02 Indoor air bacterial load and antibiotic susceptibility pattern of isolates at Adare General Hospital in Hawassa, Ethiopia Atalay, Yibeltal Assefa Mengistie, Embialle Tolcha, Alemu Birhan, Belete Asmare, Getachew Gebeyehu, Natnael Atnafu Gelaw, Kelemu Abebe Front Public Health Public Health BACKGROUND: Air is the agent of pathogenic microbes that cause significant problems in the hospital environment. Multidrug resistance poses a major therapeutic challenge to these airborne microorganisms in hospital indoor environments. METHOD AND MATERIALS: This study was conducted at Adare General Hospital in Hawassa City, Sidama, Ethiopia. A cross-sectional study was conducted. The proportional allocation method was used to select the sampled 50 rooms from the total available rooms in each category of wards and staff offices. A total of 100 indoor air samples were collected using settle plates in all units twice a day, morning (9:00–4:00 a.m.) and afternoon (3:00–4:00 p.m.). The types and number of colonies were determined in the laboratory, and the pathogenic bacteria were isolated by appropriate bacteriological techniques. Antimicrobial susceptibility testing was performed on Mueller-Hinton agar for each potentially pathogenic bacterium isolated. For each bacterium, a total of 12 antibiotics were tested using the Kirby-Bauer disk diffusion method. The test organism was adjusted to McFarland turbidity standards of 0.5. Data were entered and analyzed using the SPSS version 25 window. Descriptive analysis and one-way analysis of variance were performed. RESULTS: The indoor air bacterial load of Adare General Hospital was found in the range between 210 and 3,224 CFU/m(3). The highest indoor air bacterial load was identified from the gynecology ward with a mean of 2,542.5CFU/m(3) at p < 0.05. From 100 indoor air samples, a total of 116 bacterial pathogen isolates were obtained. Gram-positive isolates predominated at 72.4%, of which 37.1% were Staphylococcus aureus, 26.7% were coagulase-negative Staphylococci, and the rest 8.6% were Streptococcus pyogenes. The isolation of pathogenic bacteria Staphylococcus aureus and coagulase-negative Staphylococci showed a high level of resistance to ampicillin. CONCLUSION: A high bacterial load was found in the study area as compared to different indoor air biological standards. Staphylococcus aureus and coagulase-negative Staphylococci were the isolated predominant bacteria. Attention should be given to preventing and minimizing those environmental factors that favor the multiplication of bacteria in the indoor environment of a hospital for the safe health of patients, visitors, and staff. Frontiers Media S.A. 2023-11-02 /pmc/articles/PMC10653387/ /pubmed/38026319 http://dx.doi.org/10.3389/fpubh.2023.1194850 Text en Copyright © 2023 Atalay, Mengistie, Tolcha, Birhan, Asmare, Gebeyehu and Gelaw. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Public Health
Atalay, Yibeltal Assefa
Mengistie, Embialle
Tolcha, Alemu
Birhan, Belete
Asmare, Getachew
Gebeyehu, Natnael Atnafu
Gelaw, Kelemu Abebe
Indoor air bacterial load and antibiotic susceptibility pattern of isolates at Adare General Hospital in Hawassa, Ethiopia
title Indoor air bacterial load and antibiotic susceptibility pattern of isolates at Adare General Hospital in Hawassa, Ethiopia
title_full Indoor air bacterial load and antibiotic susceptibility pattern of isolates at Adare General Hospital in Hawassa, Ethiopia
title_fullStr Indoor air bacterial load and antibiotic susceptibility pattern of isolates at Adare General Hospital in Hawassa, Ethiopia
title_full_unstemmed Indoor air bacterial load and antibiotic susceptibility pattern of isolates at Adare General Hospital in Hawassa, Ethiopia
title_short Indoor air bacterial load and antibiotic susceptibility pattern of isolates at Adare General Hospital in Hawassa, Ethiopia
title_sort indoor air bacterial load and antibiotic susceptibility pattern of isolates at adare general hospital in hawassa, ethiopia
topic Public Health
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10653387/
https://www.ncbi.nlm.nih.gov/pubmed/38026319
http://dx.doi.org/10.3389/fpubh.2023.1194850
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