Ann & Robert H Lurie Children's Hospital of Chicago
The purpose of this study is to develop biocompatible wireless electronic devices that will allow continuous, non-invasive hemodynamic and physiology measurements in the ICU.
Screening: All ICU patients will be screened by the study team based on inclusion and exclusion criteria through review of electronic medical records. For screening at Prentice Women's Hospital, screening criteria will be automatically applied through the use of the electronic data warehouse, and information from infants meeting this screening criteria will be transferred to the study team through electronic data warehouse. A screening and enrollment log will be kept to track ICU patients/parents who have been approached and agreed or declined to participate in the study. The screening and enr…
Inclusion Criteria-ICU Population: * Admitted to one of the four ICUs at Lurie Children's or Prentice Women's Hospital * Under 18 years of age Inclusion Criteria-Non-ICU Population * Under 18 years of age * Willing to visit the Center for Autonomic Medicine in Pediatrics (CAMP) for a one time study visit Exclusion Criteria-ICU Population: * A skin abnormality that would potentially increase the risk of device * 18 years of age or older * Determined by an attending physician or bedside care team to be too unstable (patient) or experiencing too much stress (family) Exclusion Criteria-Non-I…
Placement of wireless wearable vital sign monitors on patients limbs for up to 48 hours
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