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Information for all serious adverse events was sought at each visit and further documentation was collected on events of interest (including initiation of renal replacement therapy and all deaths) by study staff.
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Documentation was collected from May 2011 to September 2012.
Documentation was collected over the lifespan of the study.
Images were collected on a Fluorchem 8900 gel documentation system (Alpha Innotech).
Photographic documentation of each one was collected and laryngeal injuries were evaluated.
Information specifying lack of consent documentation as the reason for test rejection was collected when available.
Documentation from 36 monthly rotations per resident was collected.
Documentation of postoperative sepsis/septic shock, demographics, surgical variables, and preoperative comorbidities was collected.
All documentation related to the intervention and implementation at the two sections was collected.
Their documentation will be collected after the end of the study.
Figure 2 shows the photo documentation to be collected as the standard recommended by the EPHect Working Group.
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