Please use this identifier to cite or link to this item: https://doi.org/10.1186/1471-2334-5-86
DC FieldValue
dc.titleExtended spectrum β-lactamases among Gram-negative bacteria of nosocomial origin from an Intensive Care Unit of a tertiary health facility in Tanzania
dc.contributor.authorNdugulile, F
dc.contributor.authorJureen, R
dc.contributor.authorHarthug, S
dc.contributor.authorUrassa, W
dc.contributor.authorLangeland, N
dc.date.accessioned2020-10-20T04:52:09Z
dc.date.available2020-10-20T04:52:09Z
dc.date.issued2005
dc.identifier.citationNdugulile, F, Jureen, R, Harthug, S, Urassa, W, Langeland, N (2005). Extended spectrum β-lactamases among Gram-negative bacteria of nosocomial origin from an Intensive Care Unit of a tertiary health facility in Tanzania. BMC Infectious Diseases 5 : 86. ScholarBank@NUS Repository. https://doi.org/10.1186/1471-2334-5-86
dc.identifier.issn14712334
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/178026
dc.description.abstractBackground: Resistance to third generation cephalosporins due to acquisition and expression of extended spectrum β- lactamase (ESBL) enzymes among Gram-negative bacteria is on the increase. Presence of ESBL producing organisms has been reported to significantly affect the course and outcome of an infection. Therefore infections due to ESBL isolates continue to pose a challenge to infection management worldwide. The aim of this study was to determine the existence and to describe phenotypic and genotypic characteristics of ESBLs in an Intensive Care Unit (ICU) setting in Tanzania. Methods: Between October 2002 and April 2003, clinical information and samples were collected from patients suspected to have nosocomial infections in an Intensive Care Unit of a tertiary hospital in Tanzania. The isolates were identified, tested for antimicrobial susceptibility and analysed for presence of ESBL genes. Results: Thirty-nine Gram-nega tive bacteria were isolated from clinical samples of 39 patients. These isolates included 13 Escherichia coli, 12 Enterobacter spp, 5 Pseudomonas spp, 4 Proteus spp, 2 Klebsiella. pneumoniae, 2 Citrobacter freundii and 1 Chryseomonas luteola. Eleven (28.2%) of these isolates were ESBL producing. The ESBL genes characterised were SHV-12, SHV-28 and CTX-M-15. The ESBL producing isolates were more resistant to gentamicin and ciprofloxacin than non-ESBL producing isolates. Conclusion: This study shows the presence of ESBL genes among Gram-negative bacteria in the ICU setting in Tanzania. There is a need to institute strict hospital infection control policy and a regular surveillance of resistance to antimicrobial agents. © 2005 Ndugulile et al., licensee BioMed Central Ltd.
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceUnpaywall 20201031
dc.subjectamoxicillin plus clavulanic acid
dc.subjectampicillin
dc.subjectantibiotic agent
dc.subjectantiinfective agent
dc.subjectbacterial enzyme
dc.subjectbeta lactamase
dc.subjectcefepime
dc.subjectceftazidime
dc.subjectceftriaxone
dc.subjectcefuroxime
dc.subjectcephalosporin derivative
dc.subjectchloramphenicol
dc.subjectciprofloxacin
dc.subjectclavulanic acid
dc.subjectcotrimoxazole
dc.subjectdoxycycline
dc.subjectgentamicin
dc.subjectimipenem
dc.subjecttobramycin
dc.subjectantiinfective agent
dc.subjectbeta lactamase
dc.subjectantibiotic resistance
dc.subjectantibiotic sensitivity
dc.subjectarticle
dc.subjectbacterial gene
dc.subjectbacterium identification
dc.subjectbacterium isolate
dc.subjectbacterium isolation
dc.subjectChryseobacterium
dc.subjectCitrobacter freundii
dc.subjectclinical article
dc.subjectcontrolled study
dc.subjectEnterobacter
dc.subjectenzyme synthesis
dc.subjectEscherichia coli
dc.subjectgenetic analysis
dc.subjectgenotype
dc.subjectGram negative bacterium
dc.subjecthealth care facility
dc.subjecthealth care policy
dc.subjecthealth survey
dc.subjecthospital infection
dc.subjecthuman
dc.subjectinfection control
dc.subjectintensive care unit
dc.subjectKlebsiella pneumoniae
dc.subjectminimum inhibitory concentration
dc.subjectnonhuman
dc.subjectphenotype
dc.subjectProteus
dc.subjectPseudomonas
dc.subjectsampling
dc.subjectspecies
dc.subjectTanzania
dc.subjectcross infection
dc.subjectdrug effect
dc.subjectenzymology
dc.subjectGram negative infection
dc.subjectmetabolism
dc.subjectmicrobiology
dc.subjectmultidrug resistance
dc.subjectAnti-Bacterial Agents
dc.subjectbeta-Lactamases
dc.subjectCross Infection
dc.subjectDrug Resistance, Multiple, Bacterial
dc.subjectGram-Negative Bacteria
dc.subjectGram-Negative Bacterial Infections
dc.subjectHumans
dc.subjectIntensive Care Units
dc.subjectTanzania
dc.typeArticle
dc.contributor.departmentPATHOLOGY
dc.description.doi10.1186/1471-2334-5-86
dc.description.sourcetitleBMC Infectious Diseases
dc.description.volume5
dc.description.page86
dc.published.statePublished
Appears in Collections:Staff Publications
Elements

Show simple item record
Files in This Item:
File Description SizeFormatAccess SettingsVersion 
10_1186_1471-2334-5-86.pdf240.46 kBAdobe PDF

OPEN

NoneView/Download

Google ScholarTM

Check

Altmetric


This item is licensed under a Creative Commons License Creative Commons