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Article

Prevalence of Escherichia coli Producing Extended Spectrum Beta-Lactamase (ESBL) Driven Septicaemia in Children Aged 0–2 Years in Two Districts Hospitals in Yaounde, Cameroon

1
Department of Microbiology, Faculty of Health Sciences, Université des Montagnes, Bangangté BP 208, Cameroon
2
Faculty of Medicine, Sorbonne Université Paris, 75006 Paris, France
3
Division of Hepatology, Department of Medecine II, Leipzig University Medical Center, University of Leipzig, 04109 Leipzig, Germany
4
Bacteriology Unit, University Teaching Hospital of Yaounde, Yaoundé 00237, Cameroon
5
Department of Medical Laboratory Science, Faculty of Health Sciences, University of Buéa, Buéa P.O. Box 63, Cameroon
6
Faculty of Health Sciences & National Health Laboratory Services, Walter Sisulu University, Mthatha 5117, South Africa
*
Author to whom correspondence should be addressed.
Bacteria 2022, 1(4), 294-301; https://doi.org/10.3390/bacteria1040022
Submission received: 31 October 2022 / Revised: 23 November 2022 / Accepted: 2 December 2022 / Published: 7 December 2022

Abstract

:
Septicaemia is public health problem worldwide with a high rate of mortality among children. Epidemiological data on this phenomenon in Cameroon are still scarce. This study aimed to determine the prevalence and associated factors to septicaemia due to E. coli strains producing extended spectrum beta-lactamase (ESBL) in two hospitals in Yaoundé, Cameroon. A prospective, cross-sectional study was conducted on infants aged 0 to 2 years old at the consultation and neonatology care unit of two district hospitals of Yaoundé (UTHY and YGOPH) during a period of seven months (from August 2019 to March 2020). Each blood sample collected per infant was cultured in hemoline performance vials, and bacterial strains were identified using the Api-20 E system. In addition, an antibiotic resistant profile of isolates as well as the ESBL production were performed in accordance with the recommendations of the Antibiogram committee of the French Society of Microbiology 2019. Data were analysed in Epi-Info7.0 and for p less than 0.05, the difference was statistically significant. Of the 300 children enrolled, 130 (43.33%) were blood culture positive, and E. coli. was the most prevalent (69.23% (90/130)). Then antibiotic susceptibility test revealed that 77 over 90 E. coli strains were resistant to penicillin (with 85.55% to amoxicillin), and 34.44% were producing ESBL. Factors such as immunodeficiency, being on antibiotics, and particularly taking β-lactam were significantly associated with E. coli ESBL production ([aOR = 19.93; p = 0.0001], [aOR = 1.97; p = 0.04], and [aOR = 3.54; p = 0.01], respectively). Moreover, co-resistance to aminoglycosides, quinolones, fluoroquinolones, and cotrimoxazole were also found. This study highlighted a high prevalence of E. coli ESBL in blood samples of children aged 0–2 years in Yaoundé and prompts the development of more efficient strategies against E. coli ESBL associated mortality in infants in Cameroon.

1. Introduction

Septicaemia is a generalised infection due to repeated discharge of pathogenic bacteria into the blood stream and is responsible for in- and outpatients hospital admission [1]. Clinical manifestations documented include hyperthermia, hypothermia, rise in respiratory frequency, tachycardia, hyperleukocytosis, and leukopenia [2]. Septicaemia is frequent in newborns and children due to their immature immune system [3] and includes mostly bacteria such as Escherichia coli, group B Streptococcus and Klebsiella [3]. According to the WHO, 49 million cases of sepsis and 11 million sepsis-related deaths occurred worldwide in 2017, accounting for approximately 20% of all-cause deaths, and 41% (20 million) of all global sepsis cases in 2017 were amongst children under five years of age [4]. In emerging countries of sub-Saharan Africa, neonatal septicaemia is responsible for about 6 million deaths annually [3]. In Cameroon, previous studies reported in 2016 an incidence of 20.34% and 2.8% of neonatal infections due to septicaemia in Yaoundé [5] and Douala, respectively [6]. Other research works showed an incidence of 26% in University Teaching Hospital Center in Yaoundé in 2000 [7] and 48.2% at the Yaoundé Gynae-Obstetric and Pediatrics hospital in 2006 [8]. Treatment options are chosen on the basis of the severity of clinical signs, suspected pathogen, bactericidal antibiotic diffusion, and immune status [9]. In the presence of symptoms, a probabilistic treatment using broad spectrum antibiotics are generally initiated 4–8 h prior to antibiogram results [9]. Compared to monotherapy, cefoxitin (C3G) combined with aminoglycosides (gentamycin) has been shown to be more efficient in immuno-deficient children [3,10].
Previous studies in bloodstream infections have reported an increased incidence and antimicrobial resistance (AMR) in Escherichia coli, one of the most frequent pathogens causing bacteremia [11,12,13]. An antimicrobial resistant organism may be acquired by emergence of resistance in endogenous flora or by acquisition from other patients and the environment [14]. The most problematic mechanisms in E. coli correspond to the acquisition of genes coding for carbapenemases (conferring resistance to carbapenems), 16S rRNA methylases (conferring pan-resistance to aminoglycosides), plasmid-mediated quinolone resistance (PMQR) genes (conferring resistance to (fluoro)quinolones), mcr genes (conferring resistance to polymyxins), and extended-spectrum β-lactamases (conferring resistance to broad-spectrum cephalosporins) [15]
In vitro, carbapenems (ertapenem, imipenem) have been demonstrated to have better efficacy on Escherichia coli producing broad spectrum β-lactamases (ESBL), with an inhibition of about 98% of strains [16]. However, modern medicine has only driven further evolution of antimicrobial resistance by misuse, overuse, and abuse of antibiotics [17]. This can shortly lead to therapeutic crisis. One leading factor of antimicrobial resistance (AMR) in developed countries is the over-prescription by physicians of antimicrobials, particularly antibiotics, even in the absence of appropriate indications [14]; in low- and middle-income countries, on the contrary, it is self-medication due to poverty and poor education [18].
This study aimed to determine the prevalence and associated factors to septicaemia due to E. coli strains producing extended spectrum beta-lactamase (ESBL) in two hospitals in Yaoundé, Cameroon.

2. Results

Out of 300 neonates enrolled in this study, a female predominance with 55% (165/300) was observed. Equally, 77.66% (233/300) were immunocompromised, and 10.66% (32/300) have been admitted in the hospital for 3 months and above.

2.1. E. coli Isolation from Blood Culture and ESBL Production

Blood culture positivity accounted for 43.33% (130/300), with Escherichia coli being the predominant microorganism with 69.23% (90/130). About 34.44% (31/90) of the isolated E. coli strains produced ESBL (Figure 1).

2.2. Resistance Profile of E. coli Strains to β-Lactams

Antibiotic susceptibility testing of E. coli strains showed varying resistance levels to the antibiotics of the beta-lactams family. The greatest being amoxicillin with 85.55%, followed by cefoxitin with 62.5% and cefotaxim with 60.3% (Figure 2).

2.3. E. coli Antibiotic Susceptibility Testing to Other Antibiotic Families

The E. coli strains exhibited different levels of resistance to aminosides (54.6% to Amikacin, 57.8% to gentamicin, 27.3%), to quinolones (27.3% to ofloxacin and 34.5% to nalidixic acid), and to cotrimoxazole (92.2%) (Figure 3).

2.4. Univariate and Multivariate Analyses of Factors Associated with E. coli Producing ESBL

The univariate analysis of factors associated with E. coli producing ESBL revealed a significant association with admission to hospital for at least 3 months (p = 0.03), antibiotherapy (p = 0.02), B-lactams resistance (p = 0.003), and immunodeficiency (p = 0.0001) (Table 1).
Concerning multivariate analysis, no significant association was found between admission into hospital for at least 3 months and the presence of E. coli producing ESBL among children aged 0–2 years (aOR = 2.94; 95% CI = 0.97; 8.91; p = 0.06). However, immunodeficiency and antibiotics such as β-lactams were significantly linked to the presence of E. coli producing ESBL (aOR = 1.97; 95%CI = 8.82; 45.32; p = 0.0001; and aOR = 3.54; 95% CI = 1.28; 9.80; p = 0.014), respectively (Table 2).

3. Discussion

In total, 300 blood samples were cultured from symptomatic neonates; 43.33% had a positive blood culture of which 69% were E. coli. A recent study in Niger and Nigeria found similar high prevalence of septicaemia among neonates (55.1% and 42%, respectively), and the same study equally reported septicaemia as the main cause of morbidity and mortality among neonates [19,20]. Moreover, the high rate of E. coli in this study is quite similar to other studies in Abidjan [21] and England [22] with 68% and 36.4%, respectively. This can be explained by the fact that E. coli is present in the genital tract of about 13% of women at the time of delivery [23]. In addition, newborns have been shown to be highly colonized with E. coli at birth [24]. This clearly shows that hygienic measures among pregnant women are not always observed.
Drug susceptibility showed a synergic effect between clavulanic acid and third-generation cephalosporin on E. coli strains in 34.44% cases. A similar study in England found a slightly higher result in 2015 (43%) [22]. This difference could be related to the method used for strain identification. In their study, the diagnostic tool includes the molecular technique which is a much more specific than the Mueller–Hinton agar double synergy test used in ours [25].
Higher levels of co-resistances to aminoglycosides, quinolones, fluoroquinolones and cotrimoxazole were observed in this study. These results are similar to those reported in 2016 in Mali [26]. Indeed, most ESBL-producing strains are not only resistant to the majority of β-lactam antibiotics but also to many antibiotics of other families such as fluoroquinolones, aminosides, co-trimoxazole, and quinolones [27]. Moreover, immunodeficiency and antibiotics such as β-lactams were significantly linked to the presence of E. coli producing ESBL. It has been shown that newborns with immature immune systems promote the development of E. coli ESBL related septicaemia [28]. A significant association between antibiotics and ESBL production has also been reported [29,30]. These findings strongly suggests that the overuse of broad-spectrum antibiotics may lead to the development of resistance mechanisms such as the production of ESBLs by such species [31].

4. Materials and Methods

4.1. Study Type and Location

A cross-sectional, descriptive study was conducted to determine the prevalence of (ESBL) linked to septicaemia in children aged 0–2 years old admitted at the neonatal unit of the University Teaching Hospital, Yaoundé (UTCH) and the Yaoundé Gynaeco-Obstetrics and Pediatrics Hospital (YGOPH).

4.2. Study Duration

Samples were collected and analysed over a seven-month period from 17 August 2019 to 17 March 2020. A written informed consent of the parents or guardian of children and infants included in the study was obtained.

4.3. Sample Collection

Venous blood (1–3 mL) was collected per patient into cryovial tube following strict aseptic measures, and all samples were processed in the bacteriology laboratories of the UTCH and YGOPH. All infants living with HIV, those with recurrent infections, and admitted infants undergoing blood transfusion were considered as immunocompromised.

4.4. Bacteria Culture and Identification

The selective Medium Eosine Methylene Blue was used for Enterobacteriae culture, growth, and selection. Strain identification of the isolates was performed using Api 20E system. Each mini-gallery API 20E was inoculated with a bacteria suspension prepared with an opacity of 0.5 on the McFarland scale.

4.5. Antibiotic Susceptibility Testing for ESBL Phenotype

Antibiotic susceptibility test was performed using the Kirby–Bauer disk diffusion method on Mueller–Hinton agar as recommended by the (AC-FSM) 2017. The following antibiotics were tested: amoxicillin (30 µg); amoxicillin + Clavulanic acid (30 µg); cefotaxime (5 µg); ceftazidime (10 µg); cefepime (30 µg); cefoxitin (30 µg); amikacin (10 µg); Nalidixic acid (10 µg); ertapenem (10 µg); ciprofloxacin (10 µg); ofloxacin (5 µg); Fosfomycin (200 µg); Amikacin (10 µg); cotrimoxazole (25 µg); gentamycin (10 µg); and ticarcillin (75 µg). Inhibition zone diameters were indicative of sensitivity or resistance to each antibiotic. The production of broad-spectrum beta-lactamase (ESBL) by E. coli was indicated by the presence of a characteristic champagne cork obtained from the synergy between a third-generation cephalosporin (C3G) and beta-lactamases inhibitor (Augmentin disk).

4.6. Data Analysis and Interpretation

The different variables and results obtained after verification of their conformity were recorded in Excel 2010 software then analysed with the statistical software Statview 5.0 (SAS Institute Inc, Cary, NC, USA). The analyses included the calculation of the frequency (for qualitative variables) and mean or median (for quantitative variables).

4.7. Ethical Considerations

Prior to the study, authorisations from the head of each health facility involved as well as institutional ethical clearance was obtained from the institutional ethic committee of Université des Montagnes (N°2020/205/UdM/PR/CM, 3 June 2020).

5. Conclusions

In this study, a high prevalence and resistance rate to antibiotics of Escherichia coli ESBL in the blood of children aged 0–2 years in Yaoundé were highlighted. The significant associated factors to E. coli ESBL production were: admission to hospital for at least 3 months; antibiotherapy; resistance to B-lactams; and immunodeficiency. This study prompts the development of more efficient strategies against E. coli ESBL associated mortality in infants in Cameroon.

Author Contributions

C.I.D. conceived the project and designed the study. C.I.D. and P.D.D.D. searched relevant literature, scrutinized all relevant information, and drafted the manuscript. C.I.D. and B.D.T.P. conducted and coordinated the field study. S.T.L. and A.D. collected and processed the samples and data. P.D.D.D., R.K.W., H.G.K. and C.I.D. analysed the data and wrote the article. C.I.D., B.D.T.P. and T.A. revised the manuscript. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Institutional Review Board Statement

The study was conducted in accordance with the Declaration of Helsinki and approved by the institutional ethic committee of Université des Montagnes (N°2020/205/UdM/PR/CM, 3 June 2020).

Informed Consent Statement

Informed consent was obtained from all subjects involved in the study.

Data Availability Statement

All data generated or analysed in the course of this study are included in this manuscript.

Acknowledgments

The authors hereby thank the directors and the staff of the University Teaching Hospital and the Yaoundé Gynaeco-Obstetric and Pediatric Hospital for their financial and material support. The authors are also grateful to the data collectors and participants of the study.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Lever, A.; Mackenzie, I. Sepsis: Definition, epidemiology, and diagnosis. BMJ 2007, 335, 879–883. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  2. Randolph, A.G.; McCulloh, R.J. Pediatric sepsis: Important considerations for diagnosing and managing severe infections in infants, children, and adolescents. Virulence 2014, 5, 179–189. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  3. Francois, X.W. Escherichia coli. Jeurotext; Pastor Institute: Paris, France, 2012; Volume 15. [Google Scholar]
  4. Global Report on the Epidemiology and Burden of Sepsis: Current Evidence, Identifying Gaps and Future Directions; World Health Organization: Geneva, Switzerland, 2020.
  5. Moudjongue, S. Implementation of an Antibiotic Monitoring System: Case of Blood Cultures at the Rodolphe Merieux Laboratory in Bamako. Ph.D. Thesis, University of Bamako, Bamako, Mali, 2014. [Google Scholar]
  6. Nouetchognou, J.; Ateudjieu, J.; Jemea, B.; Mbanya, D. Accidental exposures to blood and body fluids among health care workers in a referral Hospital of Cameroon. BMC Res. Notes 2016, 9, 94. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  7. Moffo, J. Contribution to the Study of Perinatal and Neonatal Hospital Morbidity and Mortality at the Center Hospitalier et Universitaire de Yaoundé. Medical Thesis, University of Yaoundé I FMSB, Yaoundé, Cameroon, 2000; 245p. [Google Scholar]
  8. Eloundou, O. Neonatal Morbidity and Mortality at the Gyneco and Pediatric Hospital of Yaoundé. Medical Thesis, FMSB, University of Yaoundé I, Yaoundé, Cameroon, 2007; 576p. [Google Scholar]
  9. Makki, A. Sepsis and Septic Shock. Master’s Thesis, Lebanese University, Beirut, Lebanon, 2007; 17p. [Google Scholar]
  10. Hoban, D.J.; Nicolle, L.E.; Hawser, S.; Bouchillon, S.; Badal, R. Antimicrobial susceptibility of global in patient urinary tract isolates of E. coli: Results from the Study for Monitoring Antimicrobial Resistance Trends (SMART) program: 2009–2010. Diagn. Microbiol. Infect. Dis. 2011, 70, 507–511. [Google Scholar] [CrossRef] [PubMed]
  11. MacKinnon, M.C.; McEwen, S.A.; Pearl, D.L.; Lyytikäinen, O.; Jacobsson, G.; Collignon, P.; Gregson, D.B.; Valiquette, L.; Laupland, K.B. Increasing incidence and antimicrobial resistance in Escherichia coli bloodstream infections: A multinational population-based cohort study. Antimicrob. Resist. Infect. Control 2021, 10, 131. [Google Scholar] [CrossRef]
  12. Bonten, M.; Johnson, J.R.; Biggelaar, A.H.J.V.D.; Georgalis, L.; Geurtsen, J.; de Palacios, P.I.; Gravenstein, S.; Verstraeten, T.; Hermans, P.; Poolman, J.T. Epidemiology of Escherichia coli Bacteremia: A Systematic Literature Review. Clin. Infect. Dis. 2021, 72, 1211–1219. [Google Scholar] [CrossRef]
  13. Akova, M. Epidemiology of antimicrobial resistance in bloodstream infections. Virulence 2016, 7, 252–266. [Google Scholar] [CrossRef]
  14. Institute of Medicine (US) Forum on Emerging Infections. The Resistance Phenomenon in Microbes and Infectious Disease Vectors: Implications for Human Health and Strategies for Containment: Workshop Summary; Knobler, S.L., Lemon, S.M., Najafi, M., Burroughs, T., Eds.; National Academies Press (US): Washington, DC, USA, 2003. [Google Scholar]
  15. Poirel, L.; Madec, J.-Y.; Lupo, A.; Schink, A.-K.; Kieffer, N.; Nordmann, P.; Schwarz, S. Antimicrobial Resistance in Escherichia coli. Microbiol. Spectr. 2018, 6. [Google Scholar] [CrossRef] [Green Version]
  16. Pitout, J.D.D.; Laupland, K.B. Extended spectrum béta-lactamases producing enterobacteriaceae: An emerging public-health concern. Lancet Infect. Dis. 2008, 8, 159–166. [Google Scholar] [CrossRef]
  17. Subramaniam, G.; Girish, M. Antibiotic Resistance—A Cause for Reemergence of Infections. Indian J. Pediatr. 2020, 87, 937–944. [Google Scholar] [CrossRef]
  18. Pokharel, S.; Raut, S.; Adhikari, B. Tackling antimicrobial resistance in low-income and middle-income countries. BMJ Glob. Health 2019, 4, e002104. [Google Scholar] [CrossRef]
  19. Ada, A.; Moustapha, M.O.; Habou, H.; Amadou, O.; Magagi, I.O.; IdéBana, M.B.; Adamou, R.; Magagi, H.; Abarchi, A.I.H. Morbidity and mortality of neonatal visceral surgical emergencies in Niger. Afr. J. Surg. Spec. 2020, 14, 5–9. [Google Scholar]
  20. Pius, S.; Bello, M.; Galadima, G.B.; Ibrahim, H.A.; Yerima, S.T.; Ambe, J.P. Neonatal septicaemia, bacterial isolates and antibiogram sensitivity in Maiduguri North-Eastern Nigeria. Niger. Postgrad. Med. J. 2016, 23, 146. [Google Scholar] [CrossRef]
  21. Akaffou, E.; Amon-tanoh, D.F.; Amangoua, E.; Kangah, D. Neonatal bacterial infections in hospitals in Abidjan. Med. Afr. Noire 2000, 48, 698–709. [Google Scholar]
  22. Abernethy, J.K.; Johnson, A.P.; Guy, R.; Hinton, N.; Sheridan, E.A.; Hope, R.J. Thirty dall-cause mortality in patients with Escherichia coli bacteraemia in England. Clin. Microbiol. Ang Infect. 2015, 21, 251.e1–251.e8. [Google Scholar]
  23. Sáez-López, E.; Guiral, E.; Orth, D.F.; Villanueva, S.; Goncé, A.; López, M.; Teixidó, I.; Pericot, A.; Figueras, F.; Palacio, M.; et al. Vaginal versus Obstetric Infection Escherichia coli Isolates among Pregnant Women: Antimicrobial Resistance and Genetic Virulence Profile. PLoS ONE 2016, 11, e0146531. [Google Scholar] [CrossRef] [Green Version]
  24. Al-Balawi, M.; Morsy, F.M. Prenatal versus Postnatal Initial Colonization of Healthy Neonates’ Colon Ecosystem by the Enterobacterium Escherichia coli. Microbiol. Spectr. 2021, 9. [Google Scholar] [CrossRef]
  25. Lagha, N. Study of the Resistance to Antibiotics of Enterobacteria Producing Extended-Spectrum Beta-Lactamases (ESBL) Isolated from the Hospital of Laghouat. Ph.D. Thesis, Abu Bekr Belkaid, University of Tlemcen, Tlemcen, Algeria, 2015. [Google Scholar]
  26. Sangare, S.A.; Maiga, A.I.; Guindo, I.; Maiga, A.; Camara, N.; Dicko, O.A.; Diallo, S.; Bougoudogo, F.; Armand-Lefevre, L.; Andremont, A.; et al. Prevalence of ESBL-producing Enterobacteriaceae isolated from blood culture in Mali. J. Infect. Dev. Ctries 2016, 10, 1059–1064. [Google Scholar] [CrossRef] [Green Version]
  27. Moghadam, M.; Shariati, A.; Mirkalantari, S.; Karmostaji, A. The complex genetic region conferring transferable antibiotic resistance in multidrug-resistant and extremely drug-resistant Klebsiella pneumoniae clinical isolates. New Microbes New Infect. 2020, 36, 100693. [Google Scholar] [CrossRef]
  28. Dolma, K.; Summerlin, T.L.; Wongprasert, H.; Lal, C.V.; Iii, J.B.P.; Winter, L. Early-Onset Neonatal Sepsis with Extended Spectrum Beta-Lactamase Producing Escherichia Coli in Infants Born to South and South East Asian Immigrants: A Case Series. Am. J. Perinatol. Rep. 2018, 08, e277–e279. [Google Scholar] [CrossRef] [Green Version]
  29. Kim, J.Y.; Yum, Y.; Joo, H.J.; An, H.; Yoon, Y.K.; Kim, J.H.; Sohn, J.W. Impact of antibiotic usage on extended-spectrum β-lactamase producing Escherichia coli prevalence. Sci. Rep. 2021, 11, 13024. [Google Scholar] [CrossRef] [PubMed]
  30. Tornberg-Belanger, S.N.; Rwigi, D.; Mugo, M.; Kitheka, L.; Onamu, N.; Ounga, D.; Diakhate, M.M.; Atlas, H.E.; Wald, A.; McClelland, R.S.; et al. Antimicrobial resistance including Extended Spectrum Beta Lactamases (ESBL) among E. coli isolated from kenyan children at hospital discharge. PLoS Negl. Trop. Dis. 2022, 16, e0010283. [Google Scholar] [CrossRef] [PubMed]
  31. Zheng, Z.J.; Tang, Y.M. Drug resistance of extended-spectrum-β-lactamases-producing bacteria in children with hematological malignancy after chemotherapy. Zhongguo Dang Dai Er Ke Za Zhi 2012, 14, 518–520. (In Chinese) [Google Scholar] [PubMed]
Figure 1. Prevalence of E. coli isolated from blood culture and ESBL producing E. coli.
Figure 1. Prevalence of E. coli isolated from blood culture and ESBL producing E. coli.
Bacteria 01 00022 g001
Figure 2. β-lactam susceptibility profile.
Figure 2. β-lactam susceptibility profile.
Bacteria 01 00022 g002
Figure 3. Susceptibility profile to other families of antibiotics.
Figure 3. Susceptibility profile to other families of antibiotics.
Bacteria 01 00022 g003
Table 1. Factors associated with E. coli producing ESBL.
Table 1. Factors associated with E. coli producing ESBL.
FactorsTotal
(N)
E. coli ESBL
n (%)
E. coli Non-ESBL
n (%)
p-Value
Admission (≥3 months)
No26822 (8.21%)246 (91.79%)
Yes3209 (28.13%)23 (71.88%)0.03
Use of Antibiotic
No23017 (7.39%)213 (92.61%)
Yes7014 (20%)56 (80%)0.02
Β-lactams (N = 70)
No041 (25%)3 (75%)
Yes6612 (18.19%)48 (72.72%)0.003
Quinolone (N = 70)
No3713 (35.14%)24 (64.87%)
Yes335 (15.15%)28 (84.85%)0.45
Aminosides (N = 70)
No102 (20%)8 (80%)
Yes6012 (20%)48 (80%)0.24
Others
Bacterial infection10 (0.0%)1 (100%)0.99
Immunodeficiency23314 (6.10%)219 (94%)0.0001
Blood Transfusion200 (0.0%)20 (100%)0.06
Table 2. Multivariate analysis of factors associated with E. coli producing ESBL.
Table 2. Multivariate analysis of factors associated with E. coli producing ESBL.
FactorsaOR95% CIp-Value
Admission (≥3 months)
No1
Yes2.94[0.97–8.91]0.06
On Antibiotic
No1
Yes1.97[1.02–3.83]0.04
Β-lactams
No1
Yes3.54[1.28–9.80]0.01
Aminosides
No1
Yes1[1–1.33]0.41
Associated factors
Immunodeficiency19.93[8.82–45.32]0.0001
Blood transfusion2.48[0.95–6.45]0.06
Bacterial infection3.45[1.19–2.95]0.99
aOR = Adjusted OR; 95%CI = 95% Confidence interval.
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Djuikoue, C.I.; Djouela Djoulako, P.D.; Wouambo, R.K.; Lacmago, S.T.; Dayomo, A.; Kamga, H.G.; Thumamo Pokam, B.D.; Apalata, T. Prevalence of Escherichia coli Producing Extended Spectrum Beta-Lactamase (ESBL) Driven Septicaemia in Children Aged 0–2 Years in Two Districts Hospitals in Yaounde, Cameroon. Bacteria 2022, 1, 294-301. https://doi.org/10.3390/bacteria1040022

AMA Style

Djuikoue CI, Djouela Djoulako PD, Wouambo RK, Lacmago ST, Dayomo A, Kamga HG, Thumamo Pokam BD, Apalata T. Prevalence of Escherichia coli Producing Extended Spectrum Beta-Lactamase (ESBL) Driven Septicaemia in Children Aged 0–2 Years in Two Districts Hospitals in Yaounde, Cameroon. Bacteria. 2022; 1(4):294-301. https://doi.org/10.3390/bacteria1040022

Chicago/Turabian Style

Djuikoue, Cécile Ingrid, Paule Dana Djouela Djoulako, Rodrigue Kamga Wouambo, Suzie Titsamp Lacmago, Audrey Dayomo, Hortense Gonsu Kamga, Benjamin D. Thumamo Pokam, and Teke Apalata. 2022. "Prevalence of Escherichia coli Producing Extended Spectrum Beta-Lactamase (ESBL) Driven Septicaemia in Children Aged 0–2 Years in Two Districts Hospitals in Yaounde, Cameroon" Bacteria 1, no. 4: 294-301. https://doi.org/10.3390/bacteria1040022

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