The analysis in this article is based on existing data, and does

The analysis in this article is based on existing data, and does not involve any new

studies of human or animal subjects performed by any of the authors. Susceptibility data for inpatient-derived P. aeruginosa isolates collected between January 1, 2006 and December 31, 2012 were retrieved from hospital microbiology records and antibiotic use data were retrieved from the pharmacy database. The antibiotics of MK-1775 solubility dmso interest were amikacin, cefepime, ciprofloxacin, gentamicin, meropenem, piperacillin/tazobactam, and tobramycin and all drug use was expressed as grams/1,000 patient SN-38 mouse days. To have a statistically valid sample of tested isolates (≥30), periods of analysis were divided into six quarter increments (e.g., January 2006 through June 2007) and we thereby analyzed a total of six periods within the 7-year time

span. Analysis of potentially significant changes in either antibiotic use or susceptibility, over time (period 1 vs. period 4), was performed via paired t test and Chi-square test, respectively. A trend analysis ALK inhibitor (linear regression) of susceptibility over time was also completed. All statistical analyses were performed using SPSS v.21 (IBM, Armonk, NY, USA). Results Little change was observed in susceptibility of P. aeruginosa over the time period of interest with the biggest change being a 12% difference from period 1 to period 4 for aztreonam (Table 1). Conversely, the utilization of most of the antibiotics increased over time with the greatest change observed for piperacillin/tazobactam (92% increase), although overall antibiotic utilization change was not statistically significant (Table 1). As a group, utilization of aminoglycosides decreased (14.5% decrease for the class). Use of both amikacin and gentamicin decreased while that of tobramycin increased. No changes in either susceptibility proportions or antibiotic utilization were statistically significant (P > 0.05). Trend analysis of susceptibility over time revealed poor data fits (as reflected by R 2) suggesting no or weak linearity. As susceptibility of P. aeruginosa was relatively stable over this time period, Pregnenolone tests of correlation or cause-and-effect between antibiotic use over time and susceptibility

over time were not pursued. Table 1 Changes in susceptibility (%) and antibiotic use (grams/1,000 PD) over time   Isolates tested, n Antibiotic Amikacin Aztreonam Cefepime Ciprofloxacin Gentamicin Meropenem Piperacillin/Tazobactam Tobramycin Susceptibility, %  Period   1 34 100 85.3 91.2 97.1 94.1 91.2 91.2 100   2 44 97.7 81.8 100 100 97.7 100 100 97.7   3 44 100 87.8 100 97.6 100 100 100 100   4 61 91.1 73.8 88.5 90.2 93.4 91.8 88.5 91.3   P a   0.09 0.19 0.69 0.22 0.90 0.92 0.69 0.90   Absolute changeb   −8.9 −11.5 −2.7 −6.9 −0.7 0.6 −2.7 −8.7   R 2 c   0.560 0.364 0.031 0.501 <0.001 0.002 0.031 0.558   P d   0.252 0.397 0.825 0.292 0.992 0.953 0.825 0.253 Antibiotic use, grams/1,000 PD  Period   1   0.65 ND 75.47 6.11 5.12 34.67 172.36 6.83   2   1.26 ND 72.26 7.

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