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. 2021 Jun;13(3):294–302. doi: 10.18502/ijm.v13i3.6389

Table 3.

Resistance to antimicrobial agents in the ESBL producers

Antimicrobial agents No. (%) of isolates p- value of
CIPR CIPS


ST131
(n= 33)
non-ST131
(n= 27)
ST131
(n= 15)
non-ST131
(n= 19)
CIPR
(ST131 vs. non-ST131)
CIPS
(ST131 vs. non-ST131)
AS
(CIPR non-ST131 vs. CIPS non-ST131)
AS
(CIPR ST131 vs. CIPS ST131)
AUG 24 (73) 14 (52) 8 (53) 12 (63) 0.095 0.728 0.446 0.186
SAM 23 (70) 12 (44) 2 (13) 7 (37) 0.048 0.123 0.606 < 0.0001
PTZ 11 (33) 8 (29) 1 (7) 4 (21) 0.759 0.240 0.514 0.048
ATM 32 (97) 21 (77) 13 (87) 13 (68) 0.047 0.312 0.477 0.172
SXT 26 (79) 22 (81) 11 (73) 15 (79) 0.795 0.732 0.831 0.677
GM 20 (61) 8 (30) 3 (20) 1 (5) 0.017 0.185 0.040 0.009
AN 5 (15) 3 (11) 1 (7) 2 (10) 0.647 0.694 0.950 0.410
IN 3 (9) 5 (18) 3 (20) 2 (10) 0.265 0.439 0.457 0.289

AS, Antimicrobial susceptibility; AUG, amoxicillin-clavulanic acid; SAM, ampicillin-sulbactam; PTZ, piperacillin-tazobactam; ATM, aztreonam; SXT, trimethoprim-sulfamethoxazole; GM, gentamicin; AN, amikacin; IN, nitrofurantoin; CIPR, fluoroquinolone resistant; CIPS, fluoroquinolone sensitive. The CIPR isolates studied were defined as resistant isolates to ciprofloxacin. The ESBL positive isolates studied were confirmed by the combined disk test (CDT) as ESBL producers. All the isolates were susceptible to carbapenems and resistant to cefotaxime and nalidixic acid.

A p-value ≤ 0.05 was consideredstatistically significant.