Table 5:
Duration of Hospitalisation, ICU, Mechanical Ventilation, ECMO, and ARDS Among Those Requiring the Support at Randomisation, and Escalation of Clinical Support Measures During the Study.
High-titre (n=91) | Low-titre (n=47) | p value | |
---|---|---|---|
Duration of initial in-hospital treatment (days) | |||
Patients receiving intervention at randomisation (n) | 91 | 47 | ·· |
Median (IQR) | 5 (3–12) | 6 (4–12) | 0·30 |
Duration of initial intensive care treatment (days) | |||
Patients receiving intervention at randomisation (n) | 40 | 20 | ·· |
Median (IQR) | 5·0 (3·0–12·5) | 8 (4–25) | 0·32 |
Duration of initial mechanical ventilation (days) | |||
Patients receiving intervention at randomisation (n) | 25 | 14 | ·· |
Median (IQR) | 9 (4–16) | 15·5 (7·0–29·0) | 0·22 |
Duration of extracorporeal membrane oxygenation (days)* | |||
Patients receiving intervention at randomisation (n) | 5 | 1 | ·· |
Median (IQR) | 16 (14–18) | 20 (20–20) | ·· |
Duration of acute respiratory distress syndrome (days)* | |||
Patients with condition at randomisation (n) | 15 | 3 | ·· |
Median (IQR) | 9 (4–15) | 8 (4–29) | ·· |
p values were calculated with Wilcoxon’s test.
Estimates from Wilcoxon’s test are not provided because of the small population size of the low-titre group.