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DOI 10.2147/idr.s151783

Медицинская библиотека · Infection and drug resistance · 2018

Ambulance vehicles as a source of multidrug-resistant infections: a multicenter study in Assiut City, Egypt.

El-Mokhtar Mohamed A, Hetta Helal F

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Аннотация

BACKGROUND

Ambulances may represent a potential source of infection to patients, patients' relatives, and paramedical staffs. In this study, we analyzed the extent of bacterial contamination in ambulance vehicles and measured the degree of antimicrobial resistance among isolated pathogens.

MATERIALS AND

METHODS

Twenty-five vehicles were included and 16 sampling points were swabbed in each vehicle. Then the swabs were immediately transferred to the laboratory to identify bacterial contaminants utilizing standard microbiological procedures and API® systems. Antibiotic susceptibility testing and screening for methicillin-resistant staphylococci and extended spectrum β-lactamases (ESBLs)-producing Gram-negative rods were carried out.

RESULTS

A total of 400 samples were collected, 589 bacteria were isolated and 286 (48.6%) of the isolates were potentially pathogenic. The highest contamination rate with pathogenic bacteria was detected in suction devices (75.8%) and stethoscopes (67.7%). Staphylococci were the most frequently detected microorganisms (n=184) followed by Klebsiella spp. (49), Escherichia coli (40), Citrobacter spp. (7), and Proteus spp. (6). Staphylococci were mostly sensitive to vancomycin, whereas Gram-negative bacteria were sensitive to imipenem. Overall, 46.1% of Staphylococcus aureus were methicillin resistant, whereas 20.4% of the coagulase-negative staphylococci were methicillin resistant. Moreover, 36.7% of Klebsiella spp. and 27.5% of E. coli were ESBL producers.

CONCLUSION

Our study provides evidence that ambulances represent a source of prehospital multidrug-resistant infections.

Для цитирования: El-Mokhtar Mohamed A, Hetta Helal F. Ambulance vehicles as a source of multidrug-resistant infections: a multicenter study in Assiut City, Egypt.. Infection and drug resistance. 2018. DOI: 10.2147/idr.s151783.
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