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. 2019 Apr 16;43:338–346. doi: 10.1016/j.ebiom.2019.04.021

Table 1.

Clinical characteristics, age group, sex, clinical manifest and sample source, PCV period.

Category ≤2 3–5 6–15 16–24 25–44 45–65 >65 Total
Total 7179 2790 1061 398 982 602 442 13,454
Sex
 F 2863 972 440 214 502 173 89 5253
 M 3288 1067 486 150 343 209 117 5660
 Missing 1028 751 135 34 137 220 236 2541
Manifest
 Carriage 2841 935 646 223 173 25 6 4849
 Disease 4338 1855 415 175 809 577 436 8605
Source
 Blood 2998 1234 256 93 471 404 332 5788
 CSF 1070 444 135 67 290 132 55 2193
 Nasopharynx 2841 934 646 223 173 25 6 4848
 Other disease (non-invasive) 256 173 24 15 45 38 46 597
 Missing 14 5 0 0 3 3 3 28
PCV period
 Pre-PCV 3925 1439 671 250 418 230 177 7110
 Post-PCV7 1355 547 153 52 211 143 113 2574
 Post-PCV10 131 44 13 7 22 44 12 273
 Post-PCV13 1592 671 210 86 314 177 131 3181
 No universal introduction of PCV 176 89 14 3 17 8 9 316

Isolates were classified by PCV use in the country and year of their isolation. The pre-PCV period was defined as the years when no conjugate vaccine was used and the year of first PCV introduction, the post-PCV7 period from the second year of PCV7 introduction through to the first year of PCV10 introduction, the post-PCV10 period from the second year of PCV10 introduction through to the first year of PCV13 introduction and the post-PCV13 period from the second year of PCV13 introduction through to the last collection year. No universal introduction of PCV denotes years in which a nationwide immunisation policy did not exist.