Abstract:
OBJECTIVE To analyze the drug resistance and clinical distribution of
Pseudomonas aeruginosa in hospital caused lower respiratory tract infection, so as to provide reference for rational use of drugs in hospital.
METHODS Samples in lower respiratory of patients in the department of outpatients and inpatients of hospital from Jan. 2013 to Dec. 2015 were collected, which were inoculated on blood plate and Macconkey tablet followed by National Clinical Laboratory Procedures and cultured in CO
2 incubator under 35 ℃. API20NF was used to identify bacteria, and K-B was used for drug sensitivity test.WHONET 5.3 was used for data analysis.
RESULTS A total of 9847 strains of
P.aeruginosa were isolated in from the hospitalized patients 2013~2015,and 1 257 strains of
P.aeruginosa were isolated, the isolation rate in each year was 9.50%,13.70%,15.20%, with an increasing trend year by year. A total of 1 147 strains were isolated from the patients in department of inpatients, accounting for 91.25%, mainly in Department of Respiration ICU, Surgery ICU and Neurology, accounting for 25.46%, 20.29%, and 14.40%,while 110 strains detected from the department of outpatients, accounting for 8.75%. In 2013,the top 3 drugs resistance rate of
Pseudomonas aeruginosa were aztreonam, imipenem and piperacillin, accounting for 32.52%,30.67% and 30.37% respectively. In 2014, the top three were cefoperazone, aztreonam and piperacillin, accounting for 31.68%, 29.95% and 29.31% respectively, and in 2015 cefoperazone, aztreonam and imipenem, accounting for 34.54%, 29.41% and 29.03% respectively, while the resistance rate to amikacin kept the lowest in these three years which were 15.30%, 14.30% and 13.50% respectively.
CONCLUSION The hospital lower respiratory tract infection induced by
P. aeruginosa has an increasing trend yearly from 2013 to 2015. The changes and characteristics of drug resistance of
P. aeruginosa should be paid more attention in the treatment to reduce the use of antibiotics like carbapenem,and promote the rational use of amikacin and cefoperazone/sulbactam.