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International Journal of Trend in Scientific Research and Development (IJTSRD)
Volume 6 Issue 3, March-April 2022 Available Online: www.ijtsrd.com e-ISSN: 2456 – 6470
@ IJTSRD | Unique Paper ID – IJTSRD49780 | Volume – 6 | Issue – 3 | Mar-Apr 2022 Page 1539
Emerging Trends in Antimicrobial Resistance
Arnab Majhi
Department of Physiology, Sonarpur Mahavidyalaya, Sahid Biswanath Sarani, Kolkata, West Bengal, India
ABSTRACT
Burn injury is associated with high morbidity, long term disability
and mortality. This phenomenon is seen all over the world, but is
more pronounced in economically developing countries. Treatment
of burn patients has evolved to a great extent today, but infection still
continues to be the main cause of morbidity and mortality in the burn
patients. Invasion of the burn wound by microbial pathogens leads to
burn wound infections in burn patients. The risk of contracting a life
threatening infection is high in burn patient due to the nature of the
injury, an immunocompromised state, prolonged hospital stay and
multiple interventions. Septic processes account for approximately
73% of all deaths within the initial five days of post-burn.
Burn patients usually have a prolonged stay in the burn unit. The
microbiological profile of the organisms invading the burn wounds
changes over time. A burn wound typically has large amounts of
protein rich fluid exudate, which forms a healthy medium for
bacterial growth. New burn admissions usually show the
predominance of gram positive organisms in their wounds. Gram
negative organisms become more prevalent as the duration of
treatment increases. These organisms are potentially more invasive.
Endogenous gram-negative flora from the patient’s gut colonize the
wounds within a few days of the burn. The gram-positive flora, are
the natural inhabitants of the skin. Infection in burn patient is not
only one of the major reasons for mortality, but also for prolonging
the hospital stay and delay skin cover procedures such as skin
grafting. It is hence considered prudent for every burn institute to
determine the changing anti-microbial profile of the burn patients and
their sensitivity pattern over time.
The microbial flora affecting the burn wound is a dynamic entity and
continues to evolve as the burn wound progresses. This change in the
microbiological profile of the wound varies with each patient over
the duration of his admission for the treatment of his burn injury and
also in each burn unit over the time. Nosocomial organisms are
commonly seen infecting the burn wounds and have multi-drug
resistance antimicrobial profiles.
In addition, there was no comprehensive study done on the changing
trends in the burn wound microbiology with emphasis on changing
trends in the microbiological profile of burn wounds
KEYWORDS: wounds, microbiology, noscomial, patients,
immunocompromised, burn
How to cite this paper: Arnab Majhi
"Emerging Trends in Antimicrobial
Resistance"
Published in
International Journal
of Trend in Scientific
Research and
Development (ijtsrd),
ISSN: 2456-6470,
Volume-6 | Issue-3,
April 2022, pp.1539-1543, URL:
www.ijtsrd.com/papers/ijtsrd49780.pdf
Copyright © 2022 by author (s) and
International Journal of Trend in
Scientific Research and Development
Journal. This is an
Open Access article
distributed under the
terms of the Creative Commons
Attribution License (CC BY 4.0)
(http://creativecommons.org/licenses/by/4.0)
INTRODUCTION
Antimicrobial resistance (AMR) is one of the most
serious public health threats of the twenty-first
century [1]. Globally, about 700,000 people die due
to AMR related illnesses every year. It is estimated
that by 2050 these deaths will reach10 million,
costing the world US$100 trillion [2]. In 2014, the
World Health Organisation (WHO) reported > 25%
resistance to penicillin by Streptococcus pneumoniae
IJTSRD49780
International Journal of Trend in Scientific Research and Development @ www.ijtsrd.com eISSN: 2456-6470
@ IJTSRD | Unique Paper ID – IJTSRD49780 | Volume – 6 | Issue – 3 | Mar-Apr 2022 Page 1540
in all its six regions. Five out of the six regions
reported > 50% resistance to 3rd generation
cephalosporins by Eschericia coli. WHO reported
resistance to last resort antibiotics like vancomycin,
3rd generation cephalosporins, clindamycin and
carbapenems by some organisms. Resistance to these
last line antibiotics led the WHO to advocate for
research and development of more antimicrobials for
treatment of these priority organisms in 2017 [4]. We
estimated deaths and disability-adjusted life-years
(DALYs) attributable to and associated with bacterial
AMR for 23 pathogens and 88 pathogen–drug
combinations in 204 countries and territories in 2019.
We obtained data from systematic literature reviews,
hospital systems, surveillance systems, and other
sources, covering 471 million individual records or
isolates and 7585 study-location-years. We used
predictive statistical modelling to produce estimates
of AMR burden for all locations, including for
locations with no data. Our approach can be divided
into five broad components: number of deaths where
infection played a role, proportion of infectious
deaths attributable to a given infectious syndrome,
proportion of infectious syndrome deaths attributable
to a given pathogen, the percentage of a given
pathogen resistant to an antibiotic of interest, and the
excess risk of death or duration of an infection
associated with this resistance. [1,2]
Using these components, we estimated disease burden
based on two counterfactuals: deaths attributable to
AMR (based on an alternative scenario in which all
drug-resistant infections were replaced by drug-
susceptible infections), and deaths associated with
AMR (based on an alternative scenario in which all
drug-resistant infections were replaced by no
infection). We generated 95% uncertainty intervals
(UIs) for final estimates as the 25th and 975th ordered
values across 1000 posterior draws, and models were
cross-validated for out-of-sample predictive validity.
We present final estimates aggregated to the global
and regional level. The six leading pathogens for
deaths associated with resistance (Escherichia coli,
followed by Staphylococcus aureus, Klebsiella
pneumoniae, Streptococcus pneumoniae,
Acinetobacter baumannii, and Pseudomonas
aeruginosa) were responsible for 929 000 (660 000–
1 270 000) deaths attributable to AMR and 3·57
million (2·62–4·78) deaths associated with AMR in
2019. One pathogen–drug combination, meticillin-
resistant S aureus, caused more than 100 000 deaths
attributable to AMR in 2019, while six more each
caused 50 000–100 000 deaths: multidrug-resistant
excluding extensively drug-resistant tuberculosis,
third-generation cephalosporin-resistant E coli,
carbapenem-resistant A baumannii, fluoroquinolone-
resistant E coli, carbapenem-resistant K pneumoniae,
and third-generation cephalosporin-resistant K
pneumoniae.[3,4]
Antimicrobial resistance experiment
Many bacteria are demonstrating increasing levels of resistance to commonly used antibiotics. While this has
implications for the healthcare system as a whole, many patients infected with these resistant organisms will
initially present to the emergency department (ED).[5]
Discussion and Results
Burn wound infection is a dynamic entity that is one of the major determining factors of the patient’s hospital
stay, mortality and morbidity. The analysis of the changing trends in the burn wounds microbiological profile
will help deciding a more effective empirical therapy for burn wound infection. The gram-positive organisms
have become more common in 2017 in the first week of burn admission as compared to previous years. From the
second week onwards the gram-negative organisms are the more prevalent organisms. Non-fermenting gram-
International Journal of Trend in Scientific Research and Development @ www.ijtsrd.com eISSN: 2456-6470
@ IJTSRD | Unique Paper ID – IJTSRD49780 | Volume – 6 | Issue – 3 | Mar-Apr 2022 Page 1541
negative bacilli, Pseudomonas aeruginosa and Staphylococci are the most commonly seen organisms. The
patients with a rapid progression of sepsis with burn wound infected with Pseudomonas and non-fermenting
gram-negative bacilli will benefit from starting of Colistin at an early stage. Similarly, those with Staphylococci
growing in the burn wounds can benefit from Linezolid, Chloramphenicol.[6,7]
Percentage of different organisms isolated from burn wounds over 1st to 4th week
Susceptibility of Non-fermenting gram negative bacilli to different antibiotics over 1st to 4th week
Non-fermenting gram-negative bacilli (NFGNB) were the most commonly isolated organisms over all in the
5 years of the study. In the first week Enterococcus, NFGNB and coagulase negative staphylococci were isolated
from the burn wounds. In the second week, the most common organism isolated was NFGNB in all 5 years. In
the 3rd week and 4th week, Pseudomonas Aeruginosa was the most common organism isolated in all 5 years.
The most common bacterial isolate (in numbers) from cultures was Non-fermenting gram negative bacilli with
212 isolates, which was in contrast with the other studies. Gram negative bacteria were resistant to majority of
antibiotics with the sensitivity progressively diminishing as the duration of the burn injury progresses.[8,9]
However, they remained sensitive to Colistin. This was in contrast to other studies which found Polymixin to be
effective drug for the treatment of gram negative bacilli.
International Journal of Trend in Scientific Research and Development @ www.ijtsrd.com eISSN: 2456-6470
@ IJTSRD | Unique Paper ID – IJTSRD49780 | Volume – 6 | Issue – 3 | Mar-Apr 2022 Page 1542
Complete sensitivity is shown by Pseudomonas aeruginosa only to Colistin in the first week. 1st line drugs i.e.
Amikacin, Magnex, Ceftazidime, Levoflox and Piperacillin tazobactam show sensitivityin the range of 50–70%
and resistance of 20–30%. This trend continues almost the same over the 2nd and the 3rd week. In the 4th week,
minimal Colistin resistance is noted (5.6%) with sensitivity of 94.4%. All the first line drugs mentioned above
show a higher level of resistance ranging between 65 and 80%.[10]
In the first week, Methicillin Resistant
Staphylococcus aureus (MRSA) was present in high
percentage of nearly 81%. Chloramphenicol,
Netilmicin, Linezolid and Rifampicin have 100%
sensitivity. Similar trend continues over 2nd and 3rd
week with minimal resistance developing towards
Chloramphenicol (7.69%) and Netilmicin (10%). In
the 4th week MRSA has gone up to 86.67% with
developing resistance against Netilmicin (12.5%) and
Rifampicin (33.33%) but it was still 100% sensitive
to Chloremphenicol and Linezolid.
Pseudomonas and NFGNB species were sensitive to
Colistin, throughout the course of the admission.
Their resistance to 1st line drugs like Amikacin,
Ceftazidime, Magnex, Piptaz was noted, on an
increasing scale from the 1st culture to the 4th
culture.
There is an increase in the presence of MRSA from
80% in the first culture to 86% in the 4th culture.
Though it still carries 100% of sensitivity for
Linezolid, Chloramphenicol.[11]
Conclusions
We conclude from our study that gram positive
organisms have emerged as the common organisms
isolated from the burn wounds in the first week of
burn admission in 2016 and 2017 as compared to
previous years. From the second week, the gram-
negative organisms are the more prevalent organisms.
Their presence in the burn wound and their antibiotic
International Journal of Trend in Scientific Research and Development @ www.ijtsrd.com eISSN: 2456-6470
@ IJTSRD | Unique Paper ID – IJTSRD49780 | Volume – 6 | Issue – 3 | Mar-Apr 2022 Page 1543
resistance keeps progressively increasing as time
passes.
Overall, Non-fermenting gram-negative bacilli,
Pseudomonas aeruginosa and Staphylococci are the
most commonly isolated organisms over the last
5 years. The patients with a rapid progression of
sepsis with burn wound infected with Pseudomonas
and non-fermenting gram-negative bacilli will benefit
from starting of Colistinat an early stage. Similarly,
those with Staphylococci (MRSA) growing in the
burn wounds will benefit from Linezolid,
Chloramphenicol. [12]
Microbial flora of the burn wound and its antibiotic
profile is an ever-changing entity. Constant
evaluation and analysis of the wound cultures will
help the treating physicians to keep abreast with the
pathogens and give the patient a fighting chance in
this battle for survival. Each burn centre should have
its own system of audit and should review its burn
wounds cultures periodically, as the results will
change for different centres depending on location,
population served and the type of injury sustained.
Antimicrobial susceptibility difference are also to be
followed as different for different centres.[13]
References
[1] Kirby-Bauer Disk Diffusion SusceptibilityTest
Protocol Archived 26 June 2011 at the
Wayback Machine, Jan Hudzicki, ASM
[2] "Antimicrobial resistance Fact sheet N°194".
who.int. April 2014. Archived from the original
on 10 March 2015. Retrieved 7 March 2015.
[3] A.-P. Magiorakos, A. Srinivasan, R. B. Carey,
Y. Carmeli, M. E. Falagas, C. G. Giske, S.
Harbarth, J. F. Hinndler et al. Multidrug-
resistant, extensively drug-resistant and
pandrug-resistant bacteria.... Clinical
Microbiology and Infection, Vol 8, Iss. 3 first
published 27 July 2011 [via Wiley Online
Library]. Retrieved 28 August 2020
[4] "General Background: About Antibiotic
Resistance". www.tufts.edu. Archived from the
original on 23 October 2015. Retrieved 30
October 2015.
[5] "About Antimicrobial Resistance".
www.cdc.gov. 10 September 2018. Archived
from the original on 1 October 2017. Retrieved
30 October 2015.
[6] Jump up to:a b Swedish work on containment
of antibiotic resistance – Tools, methods and
experiences (PDF). Stockholm: Public Health
Agency of Sweden. 2014. pp. 16–17, 121–128.
ISBN 978-91-7603-011-0. Archived (PDF)
from the original on 23 July 2015. Retrieved 23
July 2015.
[7] "Duration of antibiotic therapy and resistance".
NPS Medicinewise. National Prescribing
Service Limited trading, Australia. 13 June
2013. Archived from the original on 23 July
2015. Retrieved 22 July 2015.
[8] Gerber JS, Ross RK, Bryan M, Localio AR,
Szymczak JE, Wasserman R, et al. (December
2017). "Association of Broad- vs Narrow-
Spectrum Antibiotics With Treatment Failure,
Adverse Events, and Quality of Life in
Children With Acute Respiratory Tract
Infections". JAMA. 318 (23): 2325–2336.
doi:10.1001/jama.2017.18715. PMC 5820700.
PMID 29260224.
[9] "CDC Features – Mission Critical: Preventing
Antibiotic Resistance". www.cdc.gov. 4 April
2018. Archived from the original on 8
November 2017. Retrieved 22 July 2015.
[10] Changing Markets (February 2016). "Impacts
of Pharmaceutical Pollution on Communities
and Environment in India" (PDF). Nordea.
Nordea. Archived (PDF) from the original on
20 May 2017. Retrieved 1 May 2018.
[11] Gullberg E, Cao S, Berg OG, Ilbäck C,
Sandegren L, Hughes D, Andersson DI (July
2011). "Selection of resistant bacteria at very
low antibiotic concentrations". PLOS
Pathogens. 7 (7): e1002158.
doi:10.1371/journal.ppat.1002158. PMC
3141051. PMID 21811410.
[12] Cassir N, Rolain JM, Brouqui P (2014). "A new
strategy to fight antimicrobial resistance: the
revival of old antibiotics". Frontiers in
Microbiology. 5: 551.
doi:10.3389/fmicb.2014.00551. PMC 4202707.
PMID 25368610.
[13] Sample I (26 March 2018). "Calls to rein in
antibiotic use after study shows 65% increase
worldwide". The Guardian. Archived from the
original on 8 April 2018. Retrieved 28 March
2018.

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Emerging Trends in Antimicrobial Resistance

  • 1. International Journal of Trend in Scientific Research and Development (IJTSRD) Volume 6 Issue 3, March-April 2022 Available Online: www.ijtsrd.com e-ISSN: 2456 – 6470 @ IJTSRD | Unique Paper ID – IJTSRD49780 | Volume – 6 | Issue – 3 | Mar-Apr 2022 Page 1539 Emerging Trends in Antimicrobial Resistance Arnab Majhi Department of Physiology, Sonarpur Mahavidyalaya, Sahid Biswanath Sarani, Kolkata, West Bengal, India ABSTRACT Burn injury is associated with high morbidity, long term disability and mortality. This phenomenon is seen all over the world, but is more pronounced in economically developing countries. Treatment of burn patients has evolved to a great extent today, but infection still continues to be the main cause of morbidity and mortality in the burn patients. Invasion of the burn wound by microbial pathogens leads to burn wound infections in burn patients. The risk of contracting a life threatening infection is high in burn patient due to the nature of the injury, an immunocompromised state, prolonged hospital stay and multiple interventions. Septic processes account for approximately 73% of all deaths within the initial five days of post-burn. Burn patients usually have a prolonged stay in the burn unit. The microbiological profile of the organisms invading the burn wounds changes over time. A burn wound typically has large amounts of protein rich fluid exudate, which forms a healthy medium for bacterial growth. New burn admissions usually show the predominance of gram positive organisms in their wounds. Gram negative organisms become more prevalent as the duration of treatment increases. These organisms are potentially more invasive. Endogenous gram-negative flora from the patient’s gut colonize the wounds within a few days of the burn. The gram-positive flora, are the natural inhabitants of the skin. Infection in burn patient is not only one of the major reasons for mortality, but also for prolonging the hospital stay and delay skin cover procedures such as skin grafting. It is hence considered prudent for every burn institute to determine the changing anti-microbial profile of the burn patients and their sensitivity pattern over time. The microbial flora affecting the burn wound is a dynamic entity and continues to evolve as the burn wound progresses. This change in the microbiological profile of the wound varies with each patient over the duration of his admission for the treatment of his burn injury and also in each burn unit over the time. Nosocomial organisms are commonly seen infecting the burn wounds and have multi-drug resistance antimicrobial profiles. In addition, there was no comprehensive study done on the changing trends in the burn wound microbiology with emphasis on changing trends in the microbiological profile of burn wounds KEYWORDS: wounds, microbiology, noscomial, patients, immunocompromised, burn How to cite this paper: Arnab Majhi "Emerging Trends in Antimicrobial Resistance" Published in International Journal of Trend in Scientific Research and Development (ijtsrd), ISSN: 2456-6470, Volume-6 | Issue-3, April 2022, pp.1539-1543, URL: www.ijtsrd.com/papers/ijtsrd49780.pdf Copyright © 2022 by author (s) and International Journal of Trend in Scientific Research and Development Journal. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (CC BY 4.0) (http://creativecommons.org/licenses/by/4.0) INTRODUCTION Antimicrobial resistance (AMR) is one of the most serious public health threats of the twenty-first century [1]. Globally, about 700,000 people die due to AMR related illnesses every year. It is estimated that by 2050 these deaths will reach10 million, costing the world US$100 trillion [2]. In 2014, the World Health Organisation (WHO) reported > 25% resistance to penicillin by Streptococcus pneumoniae IJTSRD49780
  • 2. International Journal of Trend in Scientific Research and Development @ www.ijtsrd.com eISSN: 2456-6470 @ IJTSRD | Unique Paper ID – IJTSRD49780 | Volume – 6 | Issue – 3 | Mar-Apr 2022 Page 1540 in all its six regions. Five out of the six regions reported > 50% resistance to 3rd generation cephalosporins by Eschericia coli. WHO reported resistance to last resort antibiotics like vancomycin, 3rd generation cephalosporins, clindamycin and carbapenems by some organisms. Resistance to these last line antibiotics led the WHO to advocate for research and development of more antimicrobials for treatment of these priority organisms in 2017 [4]. We estimated deaths and disability-adjusted life-years (DALYs) attributable to and associated with bacterial AMR for 23 pathogens and 88 pathogen–drug combinations in 204 countries and territories in 2019. We obtained data from systematic literature reviews, hospital systems, surveillance systems, and other sources, covering 471 million individual records or isolates and 7585 study-location-years. We used predictive statistical modelling to produce estimates of AMR burden for all locations, including for locations with no data. Our approach can be divided into five broad components: number of deaths where infection played a role, proportion of infectious deaths attributable to a given infectious syndrome, proportion of infectious syndrome deaths attributable to a given pathogen, the percentage of a given pathogen resistant to an antibiotic of interest, and the excess risk of death or duration of an infection associated with this resistance. [1,2] Using these components, we estimated disease burden based on two counterfactuals: deaths attributable to AMR (based on an alternative scenario in which all drug-resistant infections were replaced by drug- susceptible infections), and deaths associated with AMR (based on an alternative scenario in which all drug-resistant infections were replaced by no infection). We generated 95% uncertainty intervals (UIs) for final estimates as the 25th and 975th ordered values across 1000 posterior draws, and models were cross-validated for out-of-sample predictive validity. We present final estimates aggregated to the global and regional level. The six leading pathogens for deaths associated with resistance (Escherichia coli, followed by Staphylococcus aureus, Klebsiella pneumoniae, Streptococcus pneumoniae, Acinetobacter baumannii, and Pseudomonas aeruginosa) were responsible for 929 000 (660 000– 1 270 000) deaths attributable to AMR and 3·57 million (2·62–4·78) deaths associated with AMR in 2019. One pathogen–drug combination, meticillin- resistant S aureus, caused more than 100 000 deaths attributable to AMR in 2019, while six more each caused 50 000–100 000 deaths: multidrug-resistant excluding extensively drug-resistant tuberculosis, third-generation cephalosporin-resistant E coli, carbapenem-resistant A baumannii, fluoroquinolone- resistant E coli, carbapenem-resistant K pneumoniae, and third-generation cephalosporin-resistant K pneumoniae.[3,4] Antimicrobial resistance experiment Many bacteria are demonstrating increasing levels of resistance to commonly used antibiotics. While this has implications for the healthcare system as a whole, many patients infected with these resistant organisms will initially present to the emergency department (ED).[5] Discussion and Results Burn wound infection is a dynamic entity that is one of the major determining factors of the patient’s hospital stay, mortality and morbidity. The analysis of the changing trends in the burn wounds microbiological profile will help deciding a more effective empirical therapy for burn wound infection. The gram-positive organisms have become more common in 2017 in the first week of burn admission as compared to previous years. From the second week onwards the gram-negative organisms are the more prevalent organisms. Non-fermenting gram-
  • 3. International Journal of Trend in Scientific Research and Development @ www.ijtsrd.com eISSN: 2456-6470 @ IJTSRD | Unique Paper ID – IJTSRD49780 | Volume – 6 | Issue – 3 | Mar-Apr 2022 Page 1541 negative bacilli, Pseudomonas aeruginosa and Staphylococci are the most commonly seen organisms. The patients with a rapid progression of sepsis with burn wound infected with Pseudomonas and non-fermenting gram-negative bacilli will benefit from starting of Colistin at an early stage. Similarly, those with Staphylococci growing in the burn wounds can benefit from Linezolid, Chloramphenicol.[6,7] Percentage of different organisms isolated from burn wounds over 1st to 4th week Susceptibility of Non-fermenting gram negative bacilli to different antibiotics over 1st to 4th week Non-fermenting gram-negative bacilli (NFGNB) were the most commonly isolated organisms over all in the 5 years of the study. In the first week Enterococcus, NFGNB and coagulase negative staphylococci were isolated from the burn wounds. In the second week, the most common organism isolated was NFGNB in all 5 years. In the 3rd week and 4th week, Pseudomonas Aeruginosa was the most common organism isolated in all 5 years. The most common bacterial isolate (in numbers) from cultures was Non-fermenting gram negative bacilli with 212 isolates, which was in contrast with the other studies. Gram negative bacteria were resistant to majority of antibiotics with the sensitivity progressively diminishing as the duration of the burn injury progresses.[8,9] However, they remained sensitive to Colistin. This was in contrast to other studies which found Polymixin to be effective drug for the treatment of gram negative bacilli.
  • 4. International Journal of Trend in Scientific Research and Development @ www.ijtsrd.com eISSN: 2456-6470 @ IJTSRD | Unique Paper ID – IJTSRD49780 | Volume – 6 | Issue – 3 | Mar-Apr 2022 Page 1542 Complete sensitivity is shown by Pseudomonas aeruginosa only to Colistin in the first week. 1st line drugs i.e. Amikacin, Magnex, Ceftazidime, Levoflox and Piperacillin tazobactam show sensitivityin the range of 50–70% and resistance of 20–30%. This trend continues almost the same over the 2nd and the 3rd week. In the 4th week, minimal Colistin resistance is noted (5.6%) with sensitivity of 94.4%. All the first line drugs mentioned above show a higher level of resistance ranging between 65 and 80%.[10] In the first week, Methicillin Resistant Staphylococcus aureus (MRSA) was present in high percentage of nearly 81%. Chloramphenicol, Netilmicin, Linezolid and Rifampicin have 100% sensitivity. Similar trend continues over 2nd and 3rd week with minimal resistance developing towards Chloramphenicol (7.69%) and Netilmicin (10%). In the 4th week MRSA has gone up to 86.67% with developing resistance against Netilmicin (12.5%) and Rifampicin (33.33%) but it was still 100% sensitive to Chloremphenicol and Linezolid. Pseudomonas and NFGNB species were sensitive to Colistin, throughout the course of the admission. Their resistance to 1st line drugs like Amikacin, Ceftazidime, Magnex, Piptaz was noted, on an increasing scale from the 1st culture to the 4th culture. There is an increase in the presence of MRSA from 80% in the first culture to 86% in the 4th culture. Though it still carries 100% of sensitivity for Linezolid, Chloramphenicol.[11] Conclusions We conclude from our study that gram positive organisms have emerged as the common organisms isolated from the burn wounds in the first week of burn admission in 2016 and 2017 as compared to previous years. From the second week, the gram- negative organisms are the more prevalent organisms. Their presence in the burn wound and their antibiotic
  • 5. International Journal of Trend in Scientific Research and Development @ www.ijtsrd.com eISSN: 2456-6470 @ IJTSRD | Unique Paper ID – IJTSRD49780 | Volume – 6 | Issue – 3 | Mar-Apr 2022 Page 1543 resistance keeps progressively increasing as time passes. Overall, Non-fermenting gram-negative bacilli, Pseudomonas aeruginosa and Staphylococci are the most commonly isolated organisms over the last 5 years. The patients with a rapid progression of sepsis with burn wound infected with Pseudomonas and non-fermenting gram-negative bacilli will benefit from starting of Colistinat an early stage. Similarly, those with Staphylococci (MRSA) growing in the burn wounds will benefit from Linezolid, Chloramphenicol. [12] Microbial flora of the burn wound and its antibiotic profile is an ever-changing entity. Constant evaluation and analysis of the wound cultures will help the treating physicians to keep abreast with the pathogens and give the patient a fighting chance in this battle for survival. Each burn centre should have its own system of audit and should review its burn wounds cultures periodically, as the results will change for different centres depending on location, population served and the type of injury sustained. Antimicrobial susceptibility difference are also to be followed as different for different centres.[13] References [1] Kirby-Bauer Disk Diffusion SusceptibilityTest Protocol Archived 26 June 2011 at the Wayback Machine, Jan Hudzicki, ASM [2] "Antimicrobial resistance Fact sheet N°194". who.int. April 2014. Archived from the original on 10 March 2015. Retrieved 7 March 2015. [3] A.-P. Magiorakos, A. Srinivasan, R. B. Carey, Y. Carmeli, M. E. Falagas, C. G. Giske, S. Harbarth, J. F. Hinndler et al. Multidrug- resistant, extensively drug-resistant and pandrug-resistant bacteria.... Clinical Microbiology and Infection, Vol 8, Iss. 3 first published 27 July 2011 [via Wiley Online Library]. Retrieved 28 August 2020 [4] "General Background: About Antibiotic Resistance". www.tufts.edu. Archived from the original on 23 October 2015. Retrieved 30 October 2015. [5] "About Antimicrobial Resistance". www.cdc.gov. 10 September 2018. Archived from the original on 1 October 2017. Retrieved 30 October 2015. [6] Jump up to:a b Swedish work on containment of antibiotic resistance – Tools, methods and experiences (PDF). Stockholm: Public Health Agency of Sweden. 2014. pp. 16–17, 121–128. ISBN 978-91-7603-011-0. Archived (PDF) from the original on 23 July 2015. Retrieved 23 July 2015. [7] "Duration of antibiotic therapy and resistance". NPS Medicinewise. National Prescribing Service Limited trading, Australia. 13 June 2013. Archived from the original on 23 July 2015. Retrieved 22 July 2015. [8] Gerber JS, Ross RK, Bryan M, Localio AR, Szymczak JE, Wasserman R, et al. (December 2017). "Association of Broad- vs Narrow- Spectrum Antibiotics With Treatment Failure, Adverse Events, and Quality of Life in Children With Acute Respiratory Tract Infections". JAMA. 318 (23): 2325–2336. doi:10.1001/jama.2017.18715. PMC 5820700. PMID 29260224. [9] "CDC Features – Mission Critical: Preventing Antibiotic Resistance". www.cdc.gov. 4 April 2018. Archived from the original on 8 November 2017. Retrieved 22 July 2015. [10] Changing Markets (February 2016). "Impacts of Pharmaceutical Pollution on Communities and Environment in India" (PDF). Nordea. Nordea. Archived (PDF) from the original on 20 May 2017. Retrieved 1 May 2018. [11] Gullberg E, Cao S, Berg OG, Ilbäck C, Sandegren L, Hughes D, Andersson DI (July 2011). "Selection of resistant bacteria at very low antibiotic concentrations". PLOS Pathogens. 7 (7): e1002158. doi:10.1371/journal.ppat.1002158. PMC 3141051. PMID 21811410. [12] Cassir N, Rolain JM, Brouqui P (2014). "A new strategy to fight antimicrobial resistance: the revival of old antibiotics". Frontiers in Microbiology. 5: 551. doi:10.3389/fmicb.2014.00551. PMC 4202707. PMID 25368610. [13] Sample I (26 March 2018). "Calls to rein in antibiotic use after study shows 65% increase worldwide". The Guardian. Archived from the original on 8 April 2018. Retrieved 28 March 2018.