Table 1.
Organism/antimicrobial agent | MIC50 (mg/L) | MIC90 (mg/L) | Percentage susceptible (%S)/percentage resistant (%R) using EUCAST criteriaa |
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---|---|---|---|---|---|---|---|---|
Europe |
Eastern Europe |
Western Europe |
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%S | %R | %S | %R | %S | %R | |||
Enterobacterales (n) | (6846) | (1724) | (5122) | |||||
meropenem/vaborbactam | 0.03 | 0.06 | 98.0 | 2 | 92.7 | 7.3 | 99.8 | 0.2 |
meropenem | 0.03 | 0.12 | 95.1 | 3.4 | 86.1 | 9.5 | 98.1 | 1.3 |
imipenem | 0.25 | 2 | b | 3.9 | b | 10.3 | b | 1.7 |
amikacin | 2 | 4 | 94.2c | 5.8 | 83.1c | 16.9 | 97.9c | 2.1 |
aztreonam | ≤0.12 | >16 | 72.9 | 24.4 | 52.5 | 45 | 79.8 | 17.4 |
cefepime | ≤0.5 | >16 | 77.4 | 18.9 | 53.8 | 42.3 | 85.3 | 11 |
ceftazidime | 0.25 | >32 | 72.0 | 23.1 | 51.9 | 44.1 | 78.8 | 16 |
colistin | ≤0.5 | >8 | 76.8 | 23.2 | 80.1 | 19.9 | 75.7 | 24.3 |
gentamicin | ≤1 | >8 | 85.3c | 14.7 | 69.2c | 30.8 | 90.7c | 9.3 |
levofloxacin | ≤0.12 | >4 | 75.0 | 21.9 | 55.4 | 40.6 | 81.5 | 15.6 |
piperacillin/tazobactam | 2 | >64 | 75.6 | 19.4 | 59.8 | 34.2 | 80.9 | 14.4 |
CRE (n) | (362) | (260) | (102) | |||||
meropenem/vaborbactam | 4 | >32 | 63.0 | 37.0 | 51.5 | 48.5 | 92.2 | 7.8 |
meropenem | 16 | >32 | 7.7 | 63.5 | 8.1 | 63.1 | 6.9 | 64.7 |
imipenem | 8 | >8 | b | 71.8 | b | 68.1 | b | 81.4 |
amikacin | 16 | >32 | 41.4c | 58.6 | 34.2c | 65.8 | 59.8c | 40.2 |
aztreonam | >16 | >16 | 8.8 | 90.6 | 10.8 | 88.5 | 3.9 | 96.1 |
cefepime | >16 | >16 | 4.7 | 90.6 | 5.8 | 90 | 2.0 | 92.2 |
ceftazidime | >32 | >32 | 6.6 | 92.3 | 8.1 | 90.4 | 2.9 | 97.1 |
colistin | ≤0.5 | >8 | 74.2 | 25.8 | 72.6 | 27.4 | 78.4 | 21.6 |
gentamicin | >8 | >8 | 39.8c | 60.2 | 34.2c | 65.8 | 53.9c | 46.1 |
levofloxacin | >4 | >4 | 8.9 | 88.1 | 6.6 | 90 | 14.7 | 83.3 |
piperacillin/tazobactam | >64 | >64 | 0.3 | 99.4 | 0.4 | 99.6 | 0 | 99 |
KPC-producing CRE (n) | (114) | (40) | (74) | |||||
meropenem/vaborbactam | 0.12 | 1 | 99.1 | 0.9 | 97.5 | 2.5 | 100 | 0 |
meropenem | 32 | >32 | 1.8 | 75.4 | 5.0 | 75 | 0 | 75.7 |
imipenem | >8 | >8 | 3.5 | 92.1 | 10.0 | 87.5 | 0 | 94.6 |
amikacin | 16 | >32 | 43.0c | 57 | 22.5c | 77.5 | 54.1c | 45.9 |
aztreonam | >16 | >16 | 0 | 100.0 | 0 | 100.0 | 0 | 100.0 |
cefepime | >16 | >16 | 0 | 99.1 | 0 | 100.0 | 0 | 98.6 |
ceftazidime | >32 | >32 | 0 | 100.0 | 0 | 100.0 | 0 | 100.0 |
colistin | ≤0.5 | >8 | 72.8 | 27.2 | 62.5 | 37.5 | 78.4 | 21.6 |
gentamicin | 2 | >8 | 59.6c | 40.4 | 65.0c | 35 | 56.8c | 43.2 |
levofloxacin | >4 | >4 | 4.4 | 94.7 | 0 | 97.5 | 6.8 | 93.2 |
piperacillin/tazobactam | >64 | >64 | 0 | 99.1 | 0 | 100.0 | 0 | 98.6 |
P. aeruginosa (n) | (3567) | (1310) | (2257) | |||||
meropenem/vaborbactam | 0.5 | 32 | 82.1 | 17.9 | 69.2 | 30.8 | 89.7 | 10.3 |
meropenem | 0.5 | 32 | 67.3 | 17.8 | 49.7 | 30.3 | 77.5 | 10.6 |
imipenem | 1 | >8 | b | 31.1 | b | 48.9 | b | 20.8 |
amikacin | 4 | >32 | 86.0c | 14 | 72.8c | 27.2 | 93.7c | 6.3 |
aztreonam | 8 | >16 | b | 22.5 | b | 26.4 | b | 20.2 |
cefepime | 4 | 16 | b | 23.7 | b | 33.8 | b | 17.8 |
ceftazidime | 2 | >32 | b | 27 | b | 37.4 | b | 21 |
colistin | 1 | 2 | 99.4 | 0.6 | 99.1 | 0.9 | 99.6 | 0.4 |
gentamicin | 2 | >8 | ||||||
levofloxacin | 1 | >4 | b | 42 | b | 57.2 | b | 33.2 |
piperacillin/tazobactam | 8 | >64 | b | 30.6 | b | 40.9 | b | 24.5 |
MDR P. aeruginosa (n) | (972) | (542) | (430) | |||||
meropenem/vaborbactam | 16 | >32 | 41.0 | 59.0 | 31.5 | 68.5 | 53.0 | 47.0 |
meropenem | 16 | >32 | 13.0 | 59.5 | 8.3 | 67.9 | 18.8 | 48.8 |
imipenem | >8 | >8 | b | 79.8 | b | 87.8 | b | 69.8 |
amikacin | 16 | >32 | 53.1c | 46.9 | 38.6c | 61.4 | 71.4c | 28.6 |
aztreonam | >16 | >16 | b | 55.5 | b | 48.3 | b | 64.4 |
cefepime | 16 | >16 | b | 76.4 | b | 78 | b | 74.4 |
ceftazidime | 32 | >32 | b | 82 | b | 83 | b | 80.7 |
colistin | 1 | 2 | 99.0 | 1.0 | 98.7 | 1.3 | 99.3 | 0.7 |
gentamicin | >8 | >8 | ||||||
levofloxacin | >4 | >4 | b | 90.9 | b | 94.6 | b | 86.3 |
piperacillin/tazobactam | 64 | >64 | b | 93.3 | b | 91.7 | b | 95.3 |
Criteria as published by EUCAST.11
An arbitrary susceptible breakpoint of ≤0.001 mg/L and/or >50 mm has been published by EUCAST indicating that susceptible should not be reported for this organism/agent combination and intermediate should be interpreted as ‘susceptible increased exposure’.11 For imipenem with Enterobacterales, this decision applies to M. morgannii, Proteus spp. and Providencia spp.
For infections originating from the urinary tract. For systemic infections, aminoglycosides must be used in combination with another active therapy.