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This prospective observational study was conducted in a 19-bed polyvalent adult intensive care unit of the "Attikon" University Hospital, between November 2012 and June 2013.TF and TFPA levels were recorded on day of study entry (protocol day 0) and further followed once a week (days 7 and 14 or until they were discharged from ICU or until death).
The data entry protocol included separate quality review of each survey against the entered data to ensure accuracy.
As part of the data entry protocol, CMS and NCQA allowed vendors to use either optical character recognition (scanning) technology or manual data entry.
Participants were highly compliant with diary entry protocol and schedule, found the methodology to be acceptable, enjoyed and felt comfortable participating in the study, and did not alter their risk behaviors as a result of frequent reporting.
Participants were highly compliant with diary entry protocol and schedule: over the entire 12 study weeks, participants submitted 89.7% (54,914/61,236) of the expected diary entries, with an average of 18.86 of the 21 expected diaries (85.7%) each week.
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Even when PRMs are administered through self-administered surveys (e.g., mailed to the patients), data entry protocols to reduce error are recommended, and these require training.
For those who know anything about the technology that underpins the current market, and order entry protocols, you recognize that this proposal is straightforward.
However, quality control documentation supports data collection and entry protocols.
Data recorders were trained in data entry protocols.
However, data collection and entry protocols were well documented and quality control guidelines were implemented during the oral health screening process throughout the time span reported.
Data from returned surveys were entered using a double-entry protocol and compared using an automated procedure to identify discordant values.
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