TABLE 2.
Study period | Medication profile | Summary statistic | |
---|---|---|---|
First 24 h | Number of RASS measurements per participant, median [IQR] | 12 [12, 12] | |
Time on sedatives/analgesics with a potentially relevant pharmacogene, hours median [IQR] | 24 [22, 24] | ||
Number of altered phenotypes per patient, median [IQR] | 2 [1, 3] | ||
Fentanyl weight normalized cumulative 24‐h dose, median [IQR] (mcg/h/kg) | 6.81 [3.8, 12.3] | ||
Propofol weight normalized cumulative 24‐h dose, median [IQR] (mcg/min/kg) | 260 [162, 405] | ||
Dexmedetomidine weight normalized cumulative 24‐h dose, median [IQR] (mcg/h/kg) | 3 [1.15, 4.6] | ||
Midazolam weight normalized cumulative 24‐h dose, median [IQR] (mg/kg) | 0.198 [0.03, 0.34] | ||
Fentanyl, n (%) | Did not receive medication | 11 (14.1) | |
Low weight normalized cumulative dose | 33 (42.3) | ||
High weight normalized cumulative dose | 34 (43.6) | ||
Propofol, n (%) | Did not receive medication | 11 (14.1) | |
Low weight normalized cumulative dose | 33 (42.3) | ||
High weight normalized cumulative dose | 34 (43.6) | ||
Dexmedetomidine, n (%) | Did not receive medication | 43 (55.1) | |
Low weight normalized cumulative dose | 17 (21.8) | ||
High weight normalized cumulative dose | 18 (23.1) | ||
Midazolam, n (%) | Did not receive medication | 60 (76.9) | |
Low weight normalized cumulative dose | 9 (11.5) | ||
High weight normalized cumulative dose | 9 (11.5) |
Abbreviations: IQR, interquartile range; RASS, Richmond Agitation‐sedation scale.
Low cumulative dose is below the median cumulative dose and high is above the median cumulative dose in the first 24 h.