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DOI: http://doi.org/10.54079/jpmi.36.4.

3027 ORIGINAL ARTICLE

ANTIBIOTIC SUSCEPTIBILITY PATTERN OF CARBAPENEM


RESISTANT ENTEROBACTERIACEAE AMONG UROPATHOGENS
ISOLATED IN A REFERRAL LABORATORY OF KARACHI
Department of Pathology Saima Naseem , Ambreen Fatima, Fatima Fasih, Sahar Iqbal, Hareem Gohar, Fouzia Zeeshan
Dow University of Health
Sciences, Karachi - Pakistan ABSTRACT
Address for correspondence: Objective: To determine the antibiotic susceptibility pattern of Carbapenem resistant Enterobacteriaceae among
Saima Naseem uropathogens isolated in a referral laboratory in Karachi.
Department of Pathology
Dow University of Health Methodology: It is a retrospective cross-sectional study, carried out at the Department of Microbiology of Dow
Sciences, Karachi - Pakistan Diagnostic Research and Reference Laboratory. All urine samples collected during the study period of 6 months
from October 2020 to March 2021 were tested for culture and sensitivity patterns by the disc diffusion method.
E-mail:
[email protected].
Data of urine culture and sensitivity test reports were taken from the medical record. and analyzed by using SPSS
pk version 16.

Date Received:
Results: Out of the total 10925 uropathogens isolated, 67% belonged to Enterobacteriaceae family. The most fre-
December, 10th 2021 quent isolate among them was Escherichia coli 84% followed by Klebsiella species at 10%. The overall prevalence
Date Revised: of Carbapenem resistance was 6%. The frequency of Carbapenem resistance was higher in Klebsiella species
August, 3rd 2022 27% than Escherichia coli 8%. Multi-drug resistance was observed in both Escherichia coli and Klebsiella species
Date Accepted: especially against Ampicillin, followed by Cefixime, Cefuroxime, Ceftriaxone, Cotrimoxazole and Ciprofloxacin.
September, 27th 2022
Conclusion: The study showed a significant rate of Carbapenem resistance among Enterobacteriaceae which
emphasizes the need for formulating an antimicrobial policy with its strict implementation and regular surveillance
to control the spread of Carbapenem resistant Enterobacteriaceae at the hospital and community level.
Keywords: Carbapenem; Enterobacteriaceae; Escherichia coli; Resistance

INTRODUCTION meropenem, imipenem, ertapenem, & doripenem.3,4


However, production of carbapenemase hydrolyting
A Urinary Tract Infection (UTI) is considered one of enzymes, coded by blaKPC, blaVIM and blaIMP, has
the most prevailing bacterial infections after the upper further increased resistance among Enterobacteriace-
respiratory tract infection. It is often associated with ae.5 In United Kingdom, a new metallo-ß–lactamase
prolonged hospital stay and increased mortality rate was identified as New Delhi metallo-ß-lactamase
due to septicemia. Every year, 150 million people de- (blaNDM) in clinical isolates of Escherichia coli (E. coli)
velop UTI globally costing health care an approximate and Klebsiella pneumonia in a Swedish patient who
of 6 billion dollars.1 Gram negative bacteria, especially visited India.6 Other studies have also reported similar
the family of Enterobacteriaceae, are the most pre- resistance gene which have posed high level of resis-
dominant cause of both Nosocomial and community tance to the available antimicrobials, making them in-
acquired UTIs. They have developed a multidrug resis- effective in treating infections. It can eventually result
This article may be cited as tance to both the first and second line of antimicrobi- in an increased risk to the public health by spreading
Nassem S, Fatima A, Fasih F, als.2 resistance widely and causing high mortality rates. Lit-
Iqbal S, Gohar H, Zeeshan
erature shows that amongst Enterobacteriaceae, the
F. Antibiotic susceptibility
pattern of Carbapenem re- Earlier, one of the main causes of development of most common isolates with Carbapenem resistance
sistant Enterobacteriaceae resistance in Enterobacteriaceae was the production were E. coli and Klebsiella species (sp.).7 Patients who
among uropathogens iso- of antibiotic degrading enzymes, like pencillinases, are on invasive devices like intravenous catheter, uri-
lated in a referral laboratory cephalosorinases, and extended spectrum ß-lact- nary catheters, nasogastric tubes or ventilators as well
of Karachi. J Postgrad Med
Inst 2022;36(4):230-34.
amase (ESBL). Currently the last antibiotic option avail- as those suffering from recurrent infections and taking
https://doi.org/10.54079/ able to treat ESBL producing Enterobacteriaceae is a antibiotics for a long period of time are key victims of
jpmi.36.4.3027. Carbapenem group of ß-lactam antibiotics including Carbapenem resistant Enterobacteriaceae (CRE).8

230 VOL. 36 NO. 4 | Journal of Postgraduate Medical Institute


Antibiotic susceptibility pattern of Carbapenem resistant Enterobacteriaceae among uropathogens isolated in a referral laboratory of Karachi

While understanding the magnitude of power of the study was taken for Klebsiella cross tab to compare frequency of uropatho-
the problem, there is a need to have up- sp. with a 10% prevalence. Each report has gens with age groups and also to compare
dated information regarding prevalence and data of patient’s age, gender, isolated organ- sensitivity pattern of uropathogens against
antimicrobial susceptibility pattern of the ism and its antibiotic susceptibility pattern. antibiotics.
Enterobacteriaceae in urinary isolates for Culture reports having complete information
appropriate empirical therapy of urinary tract regarding patient’s age, gender, and iso- RESULTS
infection. Therefore, this study was designed lated organism were included in the study.
to determine prevalence and antibiotic sus- Moreover antibiotic susceptibility pattern of In this study, a total 28,505 urine cul-
ceptibility pattern of Enterobacteriaceae iso- only gram negative bacteria belonging to the tures and sensitivity test report data was
lated from urinary tract infected patients. family of Enterobactericeae were included in taken from medical record of a period of 6
the study. . Culture reports having a lack of months from October 2020 to March 2021.
METHODOLOGY above mentioned in a patient’s information Out of these, 10,925 (38%) showed positive
were excluded from the study. The antibiotic bacterial growth having a female to male ra-
This retrospective, cross-sectional study susceptibility pattern of organisms other than tio of 2.6:1. Amongst these, 7,849 (72%) of
was conducted at the Department of Micro- family of Enterobacteriaceae were excluded specimens belonged to female patients and
biology Dow Diagnostic Research and Refer- as well. In Microbiology lab, urine samples 3,076 (28%) of specimens were of male pa-
ence Laboratory (DDRRL). The data of urine were processed according to standard mi- tients with overall mean age of the patient
and culture sensitivity test report was col- crobiological procedures and antibiotic sus- found to be 42.5 years. Significant bacterial
lected from the medical record of Microbi- ceptibility test was performed as stated in growth was found much higher in the pa-
ology section after getting approval from In- CLSI guidelines 2021.(9) The antibiotic discs tients having age ranging between 21-30
stitutional Review Board (IRB) with Reference used for susceptibility testing of gram neg- years followed by 51-60 years in compari-
No. IRB-1794/DUHS/Approval/2021. The ative bacteria of family Enterobacteriaceae son to other age groups. (Figure-I).
culture reports included samples from both included Ampicillin 10µg, Amoxicillin / Clavu-
inpatient and outpatient department during lanic acid 30µg, Piperacillin / Tazobactam Out of the total 10,925 uropathogens
a period of six months from October 2020 110µg, Amikacin 30µg, Meropenem 10µg, isolated, 67% (7,285) belonged to Entero-
to March 2021. A sample size of 28,505 Gentamicin 10µg, Cefixime 5µg Ceftriaxone bacteriaceae family. The most frequent iso-
subjects was taken, that have achieved 30µg, Cefuroxime 30µg, Ciprofloxacin 5µg, late among them was E. coli 6,135 (84%)
more than 99% power to detect a marginal Cotrimaxazole 25µg, Nitrofurantoin 300µg followed by Klebsiella sp. 704 (10%). (Fig-
error of 5%, a 95% confidence interval, and and Fosfomycin 200µg. The entire data was ure- II)
an 84% prevalence of E. coli using PASS entered in SPSS version 16 and descriptive
version 15 software. A one-sample test statistics was measured in percentages. Fur- Antibiotic sensitivity pattern of only E. coli
was used to calculate proportion. The same ther statistical analysis was done by using and Klebsiella sp. were analyzed as other

Figure 1: Age group wise distribution of isolated uropathogens in %

VOL. 36 NO. 4 | Journal of Postgraduate Medical Institute 231


Antibiotic susceptibility pattern of Carbapenem resistant Enterobacteriaceae among uropathogens isolated in a referral laboratory of Karachi

Figure 2: Frequency of isolated Enterobacteriaceae in %

Table 1: Antibiotic resistance pattern of isolated Enterobacteriaceae


Escherichia coli N= 84%
Antibiotics Klebsiella sp. N= 10% (704)
(6,135)
Ampicillin 5276 (86%)* -
Amoxicillin / Clavulanic acid 2024 (33%) 190 (27%)
Piperacillin / Tazobactam 613 (10%) 105 (15%)
Ceftriaxone 4171 (68%)* 282 (40%)
Cefixime 4539 (74%)* 330 (47%)*
Cefuroxime 4539 (74%)* 330 (47%)*
Meropenem 491(8%) 190(27%)
Gentamicin 1533 (25%) 133 (19%)
Amikacin 122 (2%) 77 (11%)
Ciprofloxacin 3865 (63%)* 211(30%)
Cotrimoxazole 4171 (68%)* 295 (42%)*
Fosfomycin 491 (8%) 77 (11%)
Nitrofurantoin 306 (5%) 147 (21%)
*Microorganisms showing increased resistance to antibiotics, - Antibiotics not tested

members of Enterobacteriaceae isolated most sensitive antibiotics to Klebsiella sp. M. et al.10 and in North India by P Datta et
were in very less number. Therefore, a total were Amikacin 89%, Fosfomycin 89% and al.11 However, a high prevalence of CRE was
of 6,839 Enterobacteriaceae isolates (E. coli Tazobactam 85% respectively. (Table-I). reported by Gurung S. et al12 and Wattal C et
6,135 & Klebsiella sp. 704) were analyzed al13 in Nepal and Delhi respectively.
for antibiotic sensitivity pattern. Overall prev- DISCUSSION
alence of Carbapenem resistance among Further in this study, a higher rate of
them was 6% (390/ 6,839). The frequency This study emphasized on the frequency Carbapenem resistance (CR) was noticed
of Carbapenem resistance was higher in of Carbapenem resistant Enterobacteriace- in Klebsiella sp. 27% than in E. coli 8%.
Klebsiella sp. 190 (27%) than E. coli 491 ae (CRE) among urinary isolates which has Similar findings were found in studies con-
(8%). Most sensitive antibiotics to E. coli become an emerging threat to public health. ducted by Shields R.K. et al14 and Matar et
were Amikacin 98 %, Nitrofurantoin 95%, Statistical analysis of the data showed a al.15 In contrast, in Mumbai, Nirangan et al
Meropenem 92%, Fosfomycin 92% and frequency of 6% CRE in this study. Similar reported a higher prevalence of CR in E. coli
Tazobactam 90% respectively. However, the results were observed in Nigeria by Suwaiba 49.8% than in K. pneumonia 37.4%.16 Re-

232 VOL. 36 NO. 4 | Journal of Postgraduate Medical Institute


Antibiotic susceptibility pattern of Carbapenem resistant Enterobacteriaceae among uropathogens isolated in a referral laboratory of Karachi

search studies showed that factors causing veillance programs should be established on 2009;99(8):584-7.
an increased CR in gram negative bacteria regular basis to identify and monitor emer- 6. Yong D, Toleman MA, Giske CG, Cho
include production of carbapenemase en- gence of antibiotics resistance. In-depth HS, Sundman K, Lee K, et al. Char-
zymes, loss of porin proteins, increased ex- knowledge of the prevalence and resistance acterization of a new metallo-β-lact-
pression of efflux pumps and modification in pattern of CPE may help infection control amase gene, bla NDM-1, and a novel
penicillin binding proteins.17 team to take necessary actions to combat erythromycin esterase gene carried on
widespread dissemination of CRE. a unique genetic structure in Klebsiel-
Moreover, it has been observed that the la pneumoniae sequence type 14 from
prevalence of CRE in different studies is dis- REFERENCES India. Antimicrobial agents and chemo-
tinct from each other which can be due to therapy. 2009;53(12):5046-54. DOI:
the difference in consumption of Carbapen- 1. Eshetie S, Unakal C, Gelaw A, Ayelign 10.1128/AAC.00774-09.
em and other antibiotics in those geographi- B, Endris M, Moges F. Multidrug resis- 7. Gupta N, Limbago BM, Patel JB, Kallen
cal areas and study population. tant and carbapenemase producing AJ. Carbapenem-resistant Entero-
Enterobacteriaceae among patients bacteriaceae: epidemiology and pre-
It is necessary to implement antimicro- with urinary tract infection at referral vention. Clinical infectious diseases.
bial stewardship in all health care centers Hospital, Northwest Ethiopia. Antimi- 2011;53(1):60-7. DOI: 10.1093/cid/
by reserving broad spectrum antimicrobial crobial resistance and infection control. cir202.
agents and using them only when it is highly 2015;4(1):1-8. DOI: 10.1186/s13756- 8. Hayden MK, Lin MY, Lolans K, Weiner S,
recommended.18 As shown in multiple re- 015-0054-7 Blom D, Moore NM, et al. Prevention of
search reports, CRE have rapidly increased 2. Woodford N, Xu-McCrae L, Mushtaq colonization and infection by Klebsiella
in number within the last few years, which is S, Wu HHT, Ellington MJ, Lancaster O, pneumoniae carbapenemase–produc-
an alarming threat for the health care sector. et al. Prevalence of carbapenem resis- ing Enterobacteriaceae in long-term
It can become the source of a nation-wide tance and carbapenemase production acute-care hospitals. Clinical Infectious
surge of healthcare associated infections in among Enterobacteriaceae isolated Diseases. 2015;60(8):1153-61. DOI:
near future. The lack of any infection control from urine in the UK: results of the UK 10.1093/cid/ciu1173.
plan in the health care system to limit the infection-Carbapenem Resistance Eval- 9. Humphries R, Bobenchik AM, Hindler
spread of CR can result in a very devastating uation Surveillance Trial (iCREST-UK). JA, Schuetz AN. Overview of Changes
situation for public health. Journal of Antimicrobial Chemotherapy. to the Clinical and Laboratory Stan-
2018;73(3):698-702. DOI: 10.1093/ dards Institute Performance Standards
According to the World Health Organi- jac/dkx471 for Antimicrobial Susceptibility Testing,
zation report of 2014,19 ample data on the 3. Huttner A, Harbarth S, Carlet J, Cos- M100. Journal of Clinical Microbiology.
prevalence of CPE is not available in de- grove S, Goossens H, Holmes A, et al. 2021;59(12):00213-21. DOI: 10.1128/
veloping countries. Therefore, it has been Antimicrobial resistance: a global view JCM.00213-21
emphasized in the report to conduct sur- from the 2013 World Healthcare-As- 10. Suwaiba M, Dadah AJ, Sanusi SB. Prev-
veillance programs in these countries on a sociated Infections Forum. Antimicro- alence of carbapenem resistant esch-
regular basis to identify the magnitude of bial resistance and infection control. erichia coli and klebsiella pneumoniae
resistance strains in these areas. 2013;2(1):1-13. DOI: 10.1186/2047- in urine samples of patients attending
2994-2-31 selected general hospitals within Kadu-
CONCLUSION 4. Nordmann P, Cuzon G, Naas T. The na Metropolis. Science World Journal.
real threat of Klebsiella pneumoniae 2020;15(4):99-107.
Multi-drug resistance has been observed carbapenemase-producing bacte- 11. Datta P, Gupta V, Garg S, Chander J.
in both Klebsiella sp. and E. coli especially ria. The Lancet infectious diseases. Phenotypic method for differentiation
against Ampicillin, followed by Cefixime, 2009;9(4):228-36. DOI: 10.1016/ of carbapenemases in Enterobacteri-
Cefuroxime, Ceftriaxone, Cotrimoxazole and S1473-3099(09)70054-4. aceae: Study from north India. Indian
Ciprofloxacin. Moreover, the overall preva- 5. Habte TM, Dube S, Ismail N, Hoosen AA. Journal of Pathology and Microbiology.
lence of CRE was found to be 6%, with a Hospital and community isolates of uro- 2012;55(3):357.
higher percentage of resistance in Klebsiella pathogens at a tertiary hospital in South 12. Gurung S, Kafle S, Dhungel B, Adhikari
sp. was 27% than 8% in E. coli. Local sur- Africa. South African Medical Journal. N, Shrestha UT, Adhikari B, et al. De-

VOL. 36 NO. 4 | Journal of Postgraduate Medical Institute 233


Antibiotic susceptibility pattern of Carbapenem resistant Enterobacteriaceae among uropathogens isolated in a referral laboratory of Karachi

tection of OXA-48 gene in carbape- 15. Matar GM, Dandache I, Carrër A, Khai- 17. Papp-Wallace KM, Endimiani A. taracila
nem-resistant Escherichia coli and rallah MT, Nordmann P, Sabra A, et al. MA, Bonomo rA. Carbapenems: past,
Klebsiella pneumoniae from urine sam- Spread of OXA-48-mediated resistance present, and future Antimicrob Agents
ples. Infection and Drug Resistance. to carbapenems in Lebanese Klebsiella Chemother. 2011;55(11):4943-60.
2020;13:2311-2321. DOI: 10.2147/ pneumoniae and Escherichia coli that DOI: 10.1128/AAC.00296-11
IDR.S259967 produce extended spectrum β-lact- 18. Siegel JD, Rhinehart E, Jackson M,
13. Wattal C, Goel N, Oberoi JK, Raveendran amase. Annals of Tropical Medicine & Chiarello L. Management of multi-
R, Datta S, Prasad KJ. Surveillance of Parasitology. 2010;104(3):271-4. DOI: drug-resistant organisms in health care
multidrug resistant organisms in tertia- 10.1179/136485910X12647085215 settings, 2006. American journal of in-
ry care hospital in Delhi, India. J Assoc 651 fection control. 2007;35(10):S165-S93.
Physicians India. 2010;58(Suppl):32-6. 16. Patil NB, Sharma S, Aggarwal M, Vora DOI: 10.1016/j.ajic.2007.10.006
14. Shields RK, Zhou Y, Kanakamedala H, Cai M, Virani Z, Gupte P, et al. Prevalence 19. World Health Organization (WHO). An-
B. Burden of illness in US hospitals due and susceptibility analysis of gram neg- timicrobial resistance global report on
to carbapenem-resistant Gram-nega- ative pathogens in tertiary care trans- surveillance: 2014 summary. World
tive urinary tract infections in patients plant hospital, Mumbai. Asian Journal Health Organization, 2014. Avaliable
with or without bacteraemia. BMC in- of Research in Medical and Pharma- from URL: https://apps.who.int/iris/
fectious diseases. 2021;21(1):1-12. ceutical Sciences. 2018;4(2):1-8. handle/10665/112642.
DOI: 10.1186/s12879-021-06229-x DOI:10.9734/AJRIMPS/2018/41893

Author’s Contribution
SN Performed the data analysis and interpretation of data. AF contributed in the literature search and helped in the analysis of data. FF, SI, and HG
contributed in data collection and drafted the manuscript for final approval. FZ conceived the idea and helped in the write-up of the manuscript.
Authors agree to be accountable for all aspects of the work in ensuring that questions related to the accuracy or integrity of any part of the work
are appropriately investigated and resolved.

Conflict of Interest Grant Support and Financial Disclosure


Authors declared no conflict of interest None

Data Sharing Statement


The data that support the findings of this study are available from the corresponding author upon reasonable request.

234 VOL. 36 NO. 4 | Journal of Postgraduate Medical Institute

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