Cardiac Surgery, Myocardial Infarction
Conditions
Keywords
telemonitoring
Brief summary
The aims of the present study are to evaluate the information obtained by the EarlySenese monitoring system and examine correlation of the obtained data and clinical events.
Detailed description
The EarlySense Home Care System developed by EarlySense, Ltd., is a contact-less tele-monitoring system. The system is intended for continuous monitoring of patients' respiration rate, heart rate and patient's motion. The system, which monitors the patient while in bed, consists of a piezoelectric sensor that produces an electrical signal in response to physiological stimulation, and a microprocessor control unit that analyzes the recorded signal and identifies respiratory and heart rates and patient motion, while patient is in bed,. In addition, the system indicates patient's in or out of bed status. The system also provides alerts if either of the physiological parameters cross predefined threshold settings (e.g., high/ low heart rate or respiratory rate, or motion or time in bed). The system saves patient's parameters and then flags the patients, as those to have changes in their vital signs and motion, or those that do not have noteworthy changes during recent hours of monitoring. Flagging of the patients are based on changes detected in patients' baseline vital signs (heart and respiratory rates and patterns) and well as recognition of changes in patients motion and in and out of bed status in comparison to set thresholds. The aim of this study is to evaluate relevance of the information (vital sign trends, alerts and flags) as provided by the EarlySense Home Care Tele-monitoring system to medical staff in Sheba Medical Center's Heart Rehabilitation Institute (Shelev) in order proactively monitor patients at home. The correlation between the EarlySense system alerts and flags to patient deterioration and hospital readmission will be studied.
Interventions
OTHERHome Monitoring
Non invasive nocturnal monitoring of heart and respiratory rate and subjects movement out of bed.
Sponsors
EarlySense Ltd.
Sheba Medical Center
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
21 Years to No maximum
Healthy volunteers
No
Inclusion criteria
1. Patients who resided in Shelev following a cardiac event (cardiac surgery, myocardial infarction, pacemaker implantation or other cardiac interventions ) 2. Age ≥ 21 years 3. Any patient hosted in Shelev with geographically resident within 50 Km from Sheba Medical Center 4. Patients agrees to sign the consent form and able to comply with study protocol. 5. Sleeps on a mattress
Exclusion criteria
1. Planned readmission within 30 days of discharge from hospital 2. Discharge to hospice care. 3. Patients with cognitive disabilities 4. Patient's major treating hospital is not the Sheba Medical Center
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Diagnositic Utility | 30 days following enrollment | Positive percent agreement between the EarlySense device and clinical events as adjudicated by health-care personal |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| System Acceptance | 30 days following enrollment | Assess the acceptability of the EarlySense Home care device by clinicians and by patients and their families in their own home as determined by a provided questioner. |
Countries
Israel
Contacts
Primary ContactRobert Klempfner, MD
Backup ContactMeirav Moreno, Msc
Outcome results
None listed