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Differences between the analysis datasets were found in the development of the trough and the horizontal distribution of moisture.
Finally 976 participants were included in the analysis datasets.
The method defines an efficient data interface between the clinical/administrative databases and the analysis datasets [ 61, 62].
As a result of the analysis, datasets 5, 6, and 15 have been classified as inconsistent with both methods.
After these analyses were completed, the health plan discovered that some clinical data were missing in master files from which the analysis datasets were created.
All dosing records for any formulation containing levodopa-carbidopa (morning, continuous and extra-doses of LCIG, doses associated with LCIG tube flush, night-time, rescue and unclassified LC tablets and LC-oral capsules) were included in the analysis datasets.
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The analysis dataset consisted of 910 matched pairs.
For each survey, the analysis dataset contained a record for every enumerated household member.
Since the laboratory dataset was based on distinct patient encounters, individuals may have been included in the analysis dataset more than once (i.e., if they had multiple blood collection events).
The analysis dataset was as treated and with the relevant safety data measured.
Figure 1 provides an overview of the creation of the analysis dataset.
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