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. 2017 Apr 6;12(4):e0175224. doi: 10.1371/journal.pone.0175224

Table 3. Changes in antimicrobial susceptibility to eight antimicrobials before and after the PCV13 introduction.

Antimicrobial pre-PCV13 (2008–2009) PCV13 (2012–2013) p*
S# I R S I R
n (%) n (%) n (%) n (%) n (%) n (%)
Penicillin 734 (77.3) 155 (16.3) 61 (6.4) 446 (73.2) 107 (17.6) 56 (9.2) 0.043
Cefotaxime 852 (89.8) 83 (8.7) 14 (1.5) 533 (87.5) 54 (8.9) 22 (3.6) 0.006
Erythromycin 748 (78.8) 0 (0) 201 (21.2) 463 (76.1) 0 (0) 146 (23.9) 0.219
Clindamycin 770 (81.1) 0 (0) 179 (18.9) 483 (79.3) 0 (0) 126 (20.7) 0.399
Tetracycline 741 (78.1) 74 (7.8) 134 (14.1) 463 (76.1) 38 (6.2) 108 (17.7) 0.350
Chloramphenicol 880 (92.7) 69 (7.3) 571 (93.7) 38 (6.3) 0.415
Co-trimoxazole 675 (71.1) 54 (5.7) 220 (23.2) 441 (72.4) 21 (3.5) 147 (24.1) 0.607
Levofloxacin 926 (97.6) 23 (2.4) 601 (98.7) 8 (1.3) 0.147

* p-value comparing resistant isolates between periods. CLSI breakpoints were used.

# S: susceptible; I: intermediate; R: Resistant. Classical CLSI breakpoints for penicillin (oral: susceptible≤0.06mg/L; intermediate 0.12-1mg/L; and resistant ≥2mg/L) and cefotaxime (meningeal: susceptible≤0.5mg/L; intermediate 1mg/L; and resistant ≥2mg/L) were used.