Table 1.
Characteristics | N = 112 | % |
---|---|---|
Age range | ||
|
35 | 31.3 |
|
22 | 19.6 |
|
4 | 3.6 |
|
20 | 17.9 |
|
27 | 24.1 |
|
4 | 3.6 |
Male range (%) | 39.1–73.8% | |
Period of inclusion of participants; range | January 2015–December 2022 | |
Year of publication; range | 2017–2023 | |
Study design | ||
|
75 | 67 |
|
37 | 33 |
Sampling method | ||
|
110 | 98.2 |
|
2 | 1.8 |
Timing of data collection | ||
|
4 | 3.6 |
|
58 | 51.8 |
|
50 | 44.6 |
Study bias | ||
|
71 | 63.4 |
|
41 | 36.6 |
WHO region | ||
|
7 | 6.3 |
|
13 | 11.6 |
|
3 | 2.7 |
|
47 | 42 |
|
8 | 7.1 |
|
34 | 30.4 |
Type of assay | ||
|
22 | 19.6 |
|
85 | 75.9 |
|
5 | 4.5 |
Diagnostic technique $ | ||
|
6 | 5.4 |
|
16 | 14.3 |
|
5 | 4.5 |
|
14 | 12.5 |
|
18 | 16.1 |
|
16 | 14.3 |
|
2 | 1.8 |
|
31 | 27.7 |
|
4 | 3.6 |
Sample type | ||
|
7 | 6.3 |
|
9 | 8 |
|
62 | 55.4 |
|
11 | 9.8 |
|
8 | 7.1 |
|
7 | 6.3 |
|
3 | 2.7 |
|
5 | 4.5 |
¥ Immune assays: antigen testing or direct immunofluorescence. ¥¥ Molecular assays: multiplex PCR, multiplex RT–PCR, PCR, qPCR, RT–PCR, or RT–qPCR. ¥¥¥ Mixed assays: antigen testing/RT–PCR, direct immunofluorescence/RT–qPCR/antigen testing, direct immunofluorescence/RT–PCR, or indirect immunofluorescence/PCR. $ The indicated diagnostic technique is according to the authors’ description. * Mixed specimens: nasopharyngeal secretions and nasal secretions or nasal and throat secretions. Abbreviations: WHO, World Health Organization; BLF, bronchoalveolar lavage fluid.