For the primary analysis, we compared I and F to R and no AKI.
For the primary analysis, we examined current irritability dichotomized according to the presence or absence of any irritability.
For the primary analysis of the intervention, delirium was considered a binary outcome (absent or present) according to its earliest occurrence.
The study was powered for the primary analysis.
For the primary analysis, we assumed a 'most likely scenario' for assigning transmission to one patient.
For the primary analysis, all randomized mother-infant pairs in either the intervention and control group were combined.
For the primary analysis, we defined TB as present if a patient had ≥1 positive sputum or BAL mycobacterial culture.
For the primary analysis, polymorphisms of candidate genes were classified as exposures and ASB or urine inflammatory markers (chemokines or neutrophils) were treated as the outcomes.
For the primary analysis, two time points were considered, days 0 and 14, yielding 5,679 genes with a 1.5 fold or greater increase in expression.
The initial imaging reports were used for the primary analysis.
The ITT population will be used for the primary analysis.
