EVALUATION OF MINIMAL INHIBITORY CONCENTRATIONS OF CEFTAROLINE, TEICOPLANIN AND DAPTOMYCIN FOR TREATMENT OF METHICILLIN RESISTANT STAPHYLOCOCCUS AUREUS IN A TERTIARY CARE SETTING

Objective: To evaluate Minimal Inhibitory Concentrations of ceftaroline, teicoplanin & daptomycin for treatment of methicillinresistant Staphylococcus aureus in a tertiary care setting.Study Design: Experimental study.Place and Duration of Study: Department of Pathology, Microbiology Laboratory...

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Veröffentlicht in:Pakistan Armed Forces medical journal 2024-09, Vol.73 (6), p.1862-1865
Hauptverfasser: Aneela Khawaja, Muhammad Abid Farooque, Faiqa Arshad, Namra Yunus, Nusrat Alavi, Qurat-ul Ain, Aiman Naveed
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Sprache:eng
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Zusammenfassung:Objective: To evaluate Minimal Inhibitory Concentrations of ceftaroline, teicoplanin & daptomycin for treatment of methicillinresistant Staphylococcus aureus in a tertiary care setting.Study Design: Experimental study.Place and Duration of Study: Department of Pathology, Microbiology Laboratory from Nov 2021 to Oct 2022.Methodology: All the isolated Staph. aureus was processed and identified by colony morphology on blood agar, gram stain,and biochemical tests i.e., catalase, coagulase and DNAase test. Minimal Inhibitory Concentration was evaluated using Estrips for ceftaroline, teicoplanin & daptomycin for all the MRSA strains during the study period.Results: A total of 924 S.aureus strains were processed, and 270 (29.22%) MRSA were recovered during the study period. Thehighest percentage 50 was observed in sputum (n=2), followed by 41.66% in endobronchial washing (n=10), pus 160 (31.25%),tissue 30 (31.25%), pus swab 50 (29.76%), high vaginal swab 2 (25%), and least in blood 16 (14.54%). MICs for all the MRSAisolates to teicoplanin were in susceptible range (≤8µg/ml). MIC of 22 (8.14%) and 14 (5.18%) MRSA isolates for Ceftarolineand daptomycin were in susceptible dose-dependent (SDD=2-4µg/ml) range.Conclusion: The diagnostic modality, antimicrobial susceptibility testing, and MIC determination were found to be the bestapproach for adequate management of MRSA.
ISSN:0030-9648
2411-8842
DOI:10.51253/pafmj.v73i6.12718