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All adverse events and subsequent treatment adjustments were recorded.
All decisions regarding dosage were left to individual clinicians, as in routine clinical practice, and all dosage adjustments were recorded throughout the study.
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Chair height and position, backrest adjustment, dynamometer position and resistance arm adjustment were recorded to standardize each subject's individual position.
The mean propofol dosage before and after the examination, the times of propofol dosage adjustment, and the interval from the beginning of the FB to the first propofol dosage adjustment were recorded.
Periods of significant landscape instability and fluvial re-adjustment are recorded for the periods ca 4800 3800, 3000 2500, and 1000 800 cal BP.
The operated orientation adjustment is recorded as a value of the P_FLPROT keyword in the header of the HDU in the FITS file.
Any medication adjustment recommendations were recorded, which included the patient's medical record number, the pharmacist, the type and daily dose of the medication, and the prescribing physician (GP or clinician).
The LOS on the ICU, the time at which the patient was eligible for weaning or extubation and the actual time of weaning and extubation, plus all study drugs with all adjustments in dosage, were recorded.
Any adjustments to the intensity were recorded.
All sequential physiologic values taken on by the virtual patients, as well as the sequential adjustments made by the subjects, were recorded.
We assumed, therefore, that the mortality of patients who transferred was the same as for those who remained in their practice, given adjustment for the characteristics that were recorded.
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