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Emerging Trends of Nosocomial Pneumonia in Intensive Care Unit of a Tertiary Care Public Teaching Hospital in Western India

BACKGROUND: Nosocomial pneumonia poses great challenge to an intensivist. Detailed information about hospital-acquired pneumonia (HAP) and ventilator-acquired pneumonia (VAP) is crucial for prevention and optimal management, thus improving quality Intensive Care Unit (ICU) care. Hence, we aimed to s...

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Autores principales: Bhadade, Rakesh, Harde, Minal, deSouza, Rosemarie, More, Ashwini, Bharmal, Ramesh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5579893/
https://www.ncbi.nlm.nih.gov/pubmed/28671150
http://dx.doi.org/10.4103/aam.aam_7_17
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author Bhadade, Rakesh
Harde, Minal
deSouza, Rosemarie
More, Ashwini
Bharmal, Ramesh
author_facet Bhadade, Rakesh
Harde, Minal
deSouza, Rosemarie
More, Ashwini
Bharmal, Ramesh
author_sort Bhadade, Rakesh
collection PubMed
description BACKGROUND: Nosocomial pneumonia poses great challenge to an intensivist. Detailed information about hospital-acquired pneumonia (HAP) and ventilator-acquired pneumonia (VAP) is crucial for prevention and optimal management, thus improving quality Intensive Care Unit (ICU) care. Hence, we aimed to study the current trend of nosocomial pneumonia in ICU. MATERIALS AND METHODS: It was a prospective observational cohort study, conducted in the ICU of a tertiary care teaching public hospital over a period of 18 months. We studied clinical profile and outcome of 120 adult patients who developed VAP/HAP during the study period. We also analyzed the causative organisms, antibiotic sensitivity, and resistance pattern in these patients. RESULTS: Out of 120 patients, 29 patients were HAP and 91 patients were VAP. Mortality was 60% (72), and development of VAP and requirement of mechanical ventilation showed significant association with mortality (P < 0.00001). Most common organism causing HAP was Staphylococcus aureus (43.4%) and VAP was Klebsiella pneumoniae (49%). Maximum antibiotic sensitivity was found to piperacillin + tazobactam (58.8%), followed by imipenem (49.5%) and meropenem (41.8%), whereas maximum antibiotic resistance was found to cefepime (95.1%), followed by ceftazidime and amoxicillin (91.2%). CONCLUSION: Nosocomial pneumonia showed high incidence (17.44%) and mortality (60%). Common organisms identified were S. aureus and K. pneumoniae. Resistance was high for commonly used antibiotics and high antibiotic sensitivity for piperacillin + tazobactam and carbapenem.
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spelling pubmed-55798932017-09-08 Emerging Trends of Nosocomial Pneumonia in Intensive Care Unit of a Tertiary Care Public Teaching Hospital in Western India Bhadade, Rakesh Harde, Minal deSouza, Rosemarie More, Ashwini Bharmal, Ramesh Ann Afr Med Original Article BACKGROUND: Nosocomial pneumonia poses great challenge to an intensivist. Detailed information about hospital-acquired pneumonia (HAP) and ventilator-acquired pneumonia (VAP) is crucial for prevention and optimal management, thus improving quality Intensive Care Unit (ICU) care. Hence, we aimed to study the current trend of nosocomial pneumonia in ICU. MATERIALS AND METHODS: It was a prospective observational cohort study, conducted in the ICU of a tertiary care teaching public hospital over a period of 18 months. We studied clinical profile and outcome of 120 adult patients who developed VAP/HAP during the study period. We also analyzed the causative organisms, antibiotic sensitivity, and resistance pattern in these patients. RESULTS: Out of 120 patients, 29 patients were HAP and 91 patients were VAP. Mortality was 60% (72), and development of VAP and requirement of mechanical ventilation showed significant association with mortality (P < 0.00001). Most common organism causing HAP was Staphylococcus aureus (43.4%) and VAP was Klebsiella pneumoniae (49%). Maximum antibiotic sensitivity was found to piperacillin + tazobactam (58.8%), followed by imipenem (49.5%) and meropenem (41.8%), whereas maximum antibiotic resistance was found to cefepime (95.1%), followed by ceftazidime and amoxicillin (91.2%). CONCLUSION: Nosocomial pneumonia showed high incidence (17.44%) and mortality (60%). Common organisms identified were S. aureus and K. pneumoniae. Resistance was high for commonly used antibiotics and high antibiotic sensitivity for piperacillin + tazobactam and carbapenem. Medknow Publications & Media Pvt Ltd 2017 /pmc/articles/PMC5579893/ /pubmed/28671150 http://dx.doi.org/10.4103/aam.aam_7_17 Text en Copyright: © 2017 Annals of African Medicine 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
Bhadade, Rakesh
Harde, Minal
deSouza, Rosemarie
More, Ashwini
Bharmal, Ramesh
Emerging Trends of Nosocomial Pneumonia in Intensive Care Unit of a Tertiary Care Public Teaching Hospital in Western India
title Emerging Trends of Nosocomial Pneumonia in Intensive Care Unit of a Tertiary Care Public Teaching Hospital in Western India
title_full Emerging Trends of Nosocomial Pneumonia in Intensive Care Unit of a Tertiary Care Public Teaching Hospital in Western India
title_fullStr Emerging Trends of Nosocomial Pneumonia in Intensive Care Unit of a Tertiary Care Public Teaching Hospital in Western India
title_full_unstemmed Emerging Trends of Nosocomial Pneumonia in Intensive Care Unit of a Tertiary Care Public Teaching Hospital in Western India
title_short Emerging Trends of Nosocomial Pneumonia in Intensive Care Unit of a Tertiary Care Public Teaching Hospital in Western India
title_sort emerging trends of nosocomial pneumonia in intensive care unit of a tertiary care public teaching hospital in western india
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5579893/
https://www.ncbi.nlm.nih.gov/pubmed/28671150
http://dx.doi.org/10.4103/aam.aam_7_17
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