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A prospective observational study in patients admitted with an acute cardiac disease, in which the PPG-based device will be attached to them on admission, for frequent monitoring of their vitals during hospitalization and interventional procedures. in parallel to currently-used and approved devices. Data will be crossed with gathered clinical and laboratory data, to study the device's ability to detect acute hemodynamic and respiratory changes during hospitalization, and gathering workflow information from the nursing staff.
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Non-invasive Monitoring | Device | Wearable, wireless, non-invasive chest-patch devices will be attached to the patients following recruitment and aigning an informed consent form, and from that moment on, vitals will be collected automatically and analyzed retrospectively. |
| Measure | Description | Time Frame |
|---|---|---|
| Detection of cardio-respiratory changes | Detection of acute cardio-respiratory/hemodynamic changes during hospitalization and during interventional procedures conducted in the cardiac ICU. | Through study completion, an average of 1 year. |
| Measure | Description | Time Frame |
|---|---|---|
| Workflow assessment. | Nursing staff will be asked - using questionnaires - to assess whether the use of these devices helps in reducing burden of work and increase other interactions with the patients. | Through study completion, an average of 1 year. |
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Inclusion Criteria:
Exclusion Criteria:
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200 men and women admitted to the cardiac ICU with acute caridac event.
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| Name | Affiliation | Role |
|---|---|---|
| Ronen Rubinshtein, MD | The Edith Wolfson Medical Center | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| The Edith Wolfson Medical Center | Holon | 58100 | Israel |
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