Characteristics | Number of studies (%) |
---|---|
Continent | |
Europe | 41 (62.1) |
Asia | 18 (27.3) |
North America | 5 (7.6) |
South America | 2 (3.0) |
Study design | |
Prospective cohort | 25 (37.9) |
Retrospective cohort | 24 (36.4) |
Retrospective case–control | 2 (3.0) |
Cross-sectional | 2 (3.0) |
Not specified | 13 (19.7) |
Clinical setting where LUS was performed | |
ED | 22 (33.3) |
Hospital (wards and ICU) | 13 (19.7) |
Wards | 12 (18.2) |
ICU | 11 (16.7) |
ED and ICU | 1 (1.5) |
Pregnancy wards | 3 (4.5) |
Home | 1 (1.5) |
Nursing home | 2 (3.0) |
Rehabilitation unit | 1 (1.5) |
Number of COVID-19 patients included | |
10–29 | 23 (34.8) |
30–99 | 31 (47.0) |
100–500 | 12 (18.2) |
Time of LUS acquisition | |
Withing 24 h of admission | 40 (60.6) |
Withing 5 days of admission | 6 (9.1) |
After a median time of >5 days | 5 (7.6) |
At discharge | 1 (1.5) |
Following fetal assessment | 1 (1.5) |
Not specified | 13 (19.7) |
Blinded operators | |
Yes | 34 (51.5) |
No | 32 (48.5) |
Type of blinding | |
To clinical data | 16 (47.1) |
To PCR status | 15 (44.1) |
To CT scan or chest radiography | 12 (35.3) |
Not specified | 4 (11.8) |
Chest anatomical areas scanned | |
<12 | 16 (24.2) |
12 | 35 (53.0) |
>12 | 8 (12.1) |
Not specified | 7 (10.6) |
Main type of ultrasound probe used | |
Convex | 41 (62.1) |
Linear | 7 (10.6) |
Phased array | 4 (6.1) |
Not specified | 14 (21.2) |
*ED: Emergency Department, ICU: Intensive Care Unit specified