This study aims to provide myriad of physiological parameters in patients admitted in an internal medicine department, and which are defined as being in an increased risk of clinical deterioration within the first 72-hours after admission. The investigators will also conduct a retrospective comparison between physiological changes in patients who did deteriorate to those who did not. This will form the basis for the development of an algorithm for early prediction and warning of physiological and clinical deterioration during the first 72-hours of admission.
Study Type
OBSERVATIONAL
Enrollment
410
Prospective monitoring with retrospective big-data analysis
The Sheba Medical Center, Tel Hashomer
Ramat Gan, Israel
Monitoring blood pressure changes in high-risk patients
The investigators will record blood pressure measurements using a non-invasive wireless monitoring device working continuously for 72 hours in high-risk patients.
Time frame: 72 hours per individual
Monitoring early heart rate changes in high-risk patients
The investigators will record heart rate using a non-invasive wireless monitoring device working continuously for 72 hours in high-risk patients.
Time frame: 72 hours per individual
Monitoring respiratory rate changes in high-risk patients
The investigators will record respiratory rate using a non-invasive wireless monitoring device working continuously for 72 hours in high-risk patients.
Time frame: 72 hours per individual
Monitoring blood oxygen saturation changes in high-risk patients
The investigators will record blood oxygen saturation using a non-invasive wireless monitoring device working continuously for 72 hours in high-risk patients.
Time frame: 72 hours per individual
Monitoring stroke volume changes in high-risk patients
The investigators will record stroke volume measurements using a non-invasive wireless monitoring device working continuously for 72 hours in high-risk patients.
Time frame: 72 hours per individual
Monitoring cardiac output changes in high-risk patients
The investigators will record cardiac output measurements using a non-invasive wireless monitoring device working continuously for 72 hours in high-risk patients.
Time frame: 72 hours per individual
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