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Fortunately, the actual time of sampling was recorded, and we were able to adjust for this variability in sampling time by only comparing bevacizumab concentrations collected within a relatively narrow time window around the end of a dosing cycle (21 days after dose), such as days 19 to 23, which is adequate given that bevacizumab has a long half life of 20 days.
Patients with septic shock (37) and non-septic shock controls (40) were recruited and were well matched for demographic characteristics; clinical status at the time of blood sampling was recorded and represented in Table 1 with clinical outcome data.
Time of sampling was recorded.
The exact time of sampling was recorded.
The exact time of blood sampling was recorded by the medical staff.
Antimicrobial therapy at the time of sampling was recorded e.g. azithromycin, inhaled therapies.
Similar(43)
Ejaculation abstinence period and time of blood sampling were recorded.
The location where the sample was recorded.
Impact response of the samples was recorded and compared.
An average of five measurements for each sample was recorded.
The fresh weight of each litter sample was recorded.
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