Feglo P.K.1, Acheampong D.O.2, Gbedema S.Y.3*
1Department of Clinical Microbiology, School of Medical Sciences, College of Health Sciences, KNUST, Kumasi, Ghana
2Department of Clinical Microbiology, School of Medical Sciences, College of Health Sciences, KNUST, Kumasi, Ghana
3Department of Pharmaceutics, Faculty of Pharmacy and Pharmaceutical Sciences, College of Health Sciences, KNUST, Kumasi, Ghana
* Corresponding Author : sgbedema.pharm@knust.edu.gh
Received : - Accepted : - Published : 21-12-2010
Volume : 1 Issue : 2 Pages : 4 - 8
J Clin Res Lett 1.2 (2010):4-8
DOI : http://dx.doi.org/10.9735/0976-7061.1.2.4-8
Keywords : Klebsiella species, antibiotic resistance, aminoglycosides, cephalosporins
Conflict of Interest : None declared
Acknowledgements/Funding : We are grateful to Mr R. Lartey and the staff of
the Clinical Microbiology Laboratory, KATH, for
providing technical guidance and most of the
logistics for this work.
Background and Objective: The antibiogram of the various species of Klebsiella implicated in many infections in Ghana are not known. This study was designed to determine the antibiogram of the various species of Klebsiella isolated from clinical samples in Komfo Anokye Teaching Hospital (KATH) in Kumasi, Ghana. Materials and Methods: 2197 clinical specimens from the hospital were cultured on blood agar and MacConkey agar and the isolates investigated. The antibiogram of the various Klebsiella species isolated were determined and compared with antibiotics chosen for empirical treatment of 51 paediatric patients in the hospital. Results: Klebsiella species were recovered from 205 clinical samples (9.3% prevalence rate) with K. pneumoniae being the highest recovered species (74.1%), followed by K. oxytoca (24.4%), K. rhinoscleromatis (1%) and K. ozaenae (0.5%). Amikacin was the most potent (80%) against the recovered species whilst cefotaxime, ceftriaxone and gentamicin exhibited approximately 60% potencies. Cefuroxime and ampicillin on the other hand were respectively 75% and 100% resistant. Conclusion: The dominant species of Klebsiella infections were K. pnuemoniae and K. oxytoca. The third generation cephalosporins and aminoglycosides were the potent antibiotics for treatment of Klebsiella infections reported in KATH.
[1] Podschun R., Ullmann U. (1998)
Clinical Microbiology Reviews, 11 (4):
589-603.
» CrossRef » Google Scholar » PubMed » DOAJ » CAS » Scopus
[2] Liam C.K., Lim K.H., Wong C.M.
(2001) Respirology, 6 (3): 259-264.
» CrossRef » Google Scholar » PubMed » DOAJ » CAS » Scopus
[3] Meremikwu M.M., Nwachukwu C.E.,
Asuquo A.E., Okebe J.U., Utsalo S.J.
(2005) BMC Infectious Diseases.,
5:110.
» CrossRef » Google Scholar » PubMed » DOAJ » CAS » Scopus
[4] Anderson D.J., Engemann J.J., Harrell
L.J., Carmeli Y., Reller L.B., Kaye K.S.
(2006) Antimicrobial Agents and
Chemotherapy, 50: 1715-1720.
» CrossRef » Google Scholar » PubMed » DOAJ » CAS » Scopus
[5] Ozumba U.C. (2005) Nigerian Journal
of Clinical Practice, 2:107-109.
» CrossRef » Google Scholar » PubMed » DOAJ » CAS » Scopus
[6] Wu C.J., Lee H.C., Lee N.Y., Shih H.I.
(2006) Journal of Microbiology,
Immunology and Infection, 39 (2):
135-43.
» CrossRef » Google Scholar » PubMed » DOAJ » CAS » Scopus
[7] Barrow G.I., Felthan R.K.A. (2003)
Cowan and Steel’s Manual for the
Identification of Medical Bacteria. 3rd
Ed. Cambridge University Press.
Cambridge UK; pp: 351-353.
» CrossRef » Google Scholar » PubMed » DOAJ » CAS » Scopus
[8] Newman M.J., Frimpong E.,
Asamoah-Adu A., Sampane-Donkor
E. (2006) Resistance to Antimicrbial
Drugs in Ghana. The Ghanaian–Dutch
collaboration for Health Research and
Development, pp: 1-6.
» CrossRef » Google Scholar » PubMed » DOAJ » CAS » Scopus
[9] Cheesebrough M. (2000) District
Laboratory Practice in Tropical
Countries. !st Edn., Press Syndicate
of the University of Cambridge,
Cambridge UK; pp:132 – 143.
» CrossRef » Google Scholar » PubMed » DOAJ » CAS » Scopus
[10] Farmer J.J. (1999)
Enterobacteriaceae: Introduction and
identification. In: Murray P.R, E.J.
Baron, M.A. Pfaller, (eds). Manual of
Clinical Microbiology. 7th ed.
Washington, DC; American Society for
Microbiology, pp: 438-447.
» CrossRef » Google Scholar » PubMed » DOAJ » CAS » Scopus
[11] Kaye K.S., Fraimow H.S., Abrutyn E.
(2000) Infectious Disease Clinics of
North America, 14 (2): 293-319
» CrossRef » Google Scholar » PubMed » DOAJ » CAS » Scopus
[12] Ohene A. (1997) East African Medical
Journal, 74 (7): 450-455.
» CrossRef » Google Scholar » PubMed » DOAJ » CAS » Scopus
[13] Livermore D.M., Brown D.F. (2001)
Journal of Antimicrobial
Chemotherapy, 48 Suppl 1: S59-S64.
» CrossRef » Google Scholar » PubMed » DOAJ » CAS » Scopus
[14] Goldman D.A. (1996) Journal of
American Medical Association, 275:
234–240.
» CrossRef » Google Scholar » PubMed » DOAJ » CAS » Scopus
[15] Nicolle L.E. (2001) Infection Control
and Hospital Epidemiology, 20: 202–
205.
» CrossRef » Google Scholar » PubMed » DOAJ » CAS » Scopus
[16] Leibovici L., Shraga I., Ducker M.,
Konigsberger H., Samra Z., Pitlik S.D.
(1998) Journal of Internal Medicine,
244: 379-386.
» CrossRef » Google Scholar » PubMed » DOAJ » CAS » Scopus
[17] Kristensen B., Larsen S.,
Schoenheyder H.C., Leibovici L., Paul
M., Frank U., Andreassen S. (2001)
Interscience Conference on
Antimicrobial Agents and
Chemotherapy, Abstract no. L-2063.
» CrossRef » Google Scholar » PubMed » DOAJ » CAS » Scopus
[18] Abe-Aibinu I.E. (2000) Journal of the
Nigerian Infection Control Association,
3 (2): 14-17.
» CrossRef » Google Scholar » PubMed » DOAJ » CAS » Scopus
[19] Rice L. (2001) Evolution and clinical
importance of extended-spectrum
beta-lactamases. Chest, 119;
Supplement 2, 391S-396S.
» CrossRef » Google Scholar » PubMed » DOAJ » CAS » Scopus