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ATOMICS Clinical Correlate (ATOMICS-CC) No Alarms (NAs)


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).
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.



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