Table 3.
Variable | Univariable analysis | Multivariable analysis | |||
---|---|---|---|---|---|
OR | p | OR | p a | 95% CI | |
Type of ward (reference: Medical) | |||||
ICU | 0.94 | 0.83 | 0.07 | 0.005 | 0.01–0.46 |
Surgical | 0.95 | 0.81 | 0.66 | 0.19 | 0.35–1.23 |
Ward size in 2013, per increase of 50 beds | 0.90 | 0.14 | 0.79 | 0.02 | 0.64–0.97 |
Type of HCF (reference: General hospital) | |||||
University hospital | 0.42 | 0.35 | 0.28 | 0.25 | 0.03–2.39 |
Private hospital | 1.06 | 0.85 | 0.66 | 0.28 | 0.31–1.40 |
Cancer centre | 0.37 | 0.29 | 0.09 | 0.04 | 0.01–0.88 |
Local hospital | 2.33 | 0.18 | 1.19 | 0.83 | 0.25–5.54 |
Rehabilitation and long-term care facility | 0.38 | 0.50 | 0.24 | 0.40 | 0.01–6.59 |
Military hospital | 0.43 | 0.34 | 0.18 | 0.09 | 0.02–1.28 |
Geographical area (reference: South-east) | |||||
North | 1.42 | 0.42 | 2.33 | 0.09 | 0.88–6.16 |
West | 1.15 | 0.80 | 1.09 | 0.90 | 0.30–3.94 |
East | 1.93 | 0.15 | 3.11 | 0.03 | 1.10–8.77 |
South-west | 1.78 | 0.17 | 1.57 | 0.36 | 0.60–4.12 |
Antibiotic use, DDDs per 1000 patients-days | |||||
Initial CBP useb | 1.01 | 0.01 | 0.97 | 0.08 | 0.95–1.00 |
Initial prescribing profile of CBPsc | 1.22 | 0.002 | 3.16 | < 0.001 | 1.88–5.34 |
Initial 3GC useb | 1.00 | 0.79 | |||
Initial prescribing profile of 3GCsc | 0.97 | 0.16 | 0.89 | 0.002 | 0.83–0.96 |
Reduction in 3GC used | 1.34 | 0.23 | |||
Initial FQ useb | 1.00 | 0.25 | |||
Initial prescribing profile of FQsc | 1.02 | 0.29 | |||
Reduction in FQ used | 2.21 | 0.004 | 2.3 | 0.02 | 1.17–4.53 |
Initial AG useb | 1.00 | 0.50 | |||
Initial prescribing profile of AGsc | 0.97 | 0.44 | |||
Reduction in AG used | 1.56 | 0.06 | 1.13 | 0.67 | 0.65–1.96 |
Initial AP ± BLI useb | 1.00 | 0.83 | |||
Initial prescribing profile of AP±BLIsc | 1.00 | 0.99 | |||
Reduction in AP ± BLI used | 1.10 | 0.68 | |||
Initial Imidazole useb | 1.00 | 0.98 | |||
Initial prescribing profile of imidazolesc | 0.97 | 0.45 | |||
Reduction in imidazole used | 1.65 | 0.03 | 1.50 | 0.15 | 0.87–2.59 |
Initial GP useb | 1.00 | 0.95 | |||
Initial prescribing profile of GPsc | 0.97 | 0.61 | |||
Reduction in GP used | 1.83 | 0.01 | 1.98 | 0.02 | 1.13–3.45 |
Initial TZP useb | 1.00 | 0.99 | |||
Initial prescribing profile of TZPc | 0.95 | 0.33 | |||
Reduction in TZP used | 4.24 | < 0.001 | 4.02 | < 0.001 | 1.99–8.14 |
Initial use of other alternatives to CBPsb | 1.00 | 0.88 | |||
Initial prescribing profile of other alternatives to CBPsc | 1.31 | 0.25 | |||
Reduction in the use of other alternatives to CBPsd | 1.07 | 0.79 | |||
Initial overall antibiotic useb | 1.00 | 0.72 | 1.00 | 0.97 | 0.99–1.01 |
Reduction in the overall antibiotic used | 2.02 | 0.003 | 1.38 | 0.29 | 0.76–2.51 |
Region with high ESBL-PE incidence rate in acute care settingse | 0.65 | 0.12 | 0.40 | 0.01 | 0.19–0.82 |
OR odds ratio, CI confidence interval, ICU intensive care unit, HCF healthcare facility, DDD defined daily dose, CBP carbapenem, 3GC third-generation cephalosporin, FQ fluoroquinolone, AG aminoglycoside, AP ± BLI aminopenicillin ± β-lactamase inhibitor, GP glycopeptide, TZP piperacillin/tazobactam. ESBL-PE extended-spectrum β-lactamase-producing Enterobacteriaceae
aSignificant associations (p < 0.05) from multivariable analysis are highlighted in bold italic
bConsumption of a given antibiotic in 2009
cProportion (%) of a given antibiotic in the total antibiotic consumption in 2009
dReduction in the consumption of a given antibiotic between 2009 and 2013
eData from the French multidrug-resistant bacteria surveillance network; BMR-RAISIN, 2011