The PERSEUS research program acquired ED bedside patient monitor datastreams continuously from the study area and displayed specific elements on a remote-mirroring dashboard display in the ED research office. Research assistants used this setup to screen for potential subjects based on whether they met inclusion criteria, as follows: A patient who did not trigger any of the standard, study-selected red alarms was enrolled into the no alarm [NA] group (with checks of the electronic medical record to additionally confirm the absence of alarm triggering vital signs during their ED care, in case of non-monitored patient, undetected failure of datastream or research pipeline infrastructure).
Notes:
This research was supported by the Agency for Healthcare, Research and Quality (AHRQ) under award number R18HS022860.
Kobayashi L., Oyalowo A., Agrawal U., et al.,
"ATOMICS Clinical Correlate (ATOMICS-CC) No Alarms (NAs)"
(2019).
Brown University Open Data Collection.
Brown Digital Repository. Brown University Library.
https://doi.org/10.26300/yzsy-s794
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