Bronchopulmonary Dysplasia
Conditions
Keywords
newborn, ballistocardiograph, pressure sensor, unobtrusive sensing
Brief summary
This study aims to explore the correlation between using ballistocardiography for monitoring respiration and heart rate in neonates under invasive and non-invasive respiratory support.
Detailed description
Background: Traditional physiological measurement methods often require subjects to remain immobile or have various devices attached to their bodies, causing discomfort, especially unsuitable for neonatal care. However, with the development of electronic technologies, these methods have improved. ballistocardiography (BCG) presents a possible solution for monitoring neonates' physiological signals. BCG is a non-invasive and non-contact instrument that measures the body's reactive motion pressure changes caused by cardiac contraction. These sensors do not require direct attachment, allowing for long-term physiological signal measurement without disturbing the subject. Methods: The study will be conducted in the neonatal intensive care unit on the seventh floor of Fu Jen Catholic University Hospital, with an expected enrollment of 60 participants. The subjects will be grouped and stratified based on weight and the use of invasive respiratory support. During the hospitalization, daily output of ventilator data and physiological monitor data will be collected and analyzed for correlation. Effect: This trial is expected to confirm the application of BCG in the neonatal population, demonstrate its correlation with current conventional physiological monitors, and assess its applicability in low-weight preterm infants. Additionally, the study will investigate whether continuous BCG monitoring during hospitalization can predict the possibility of bronchopulmonary dysplasia.
Interventions
using ballistocardiography (BCG) for monitoring respiration and heart rate in neonates
Sponsors
Study design
Eligibility
Inclusion criteria
* Using invasive ventilation support with flow sensors or non-invasive ventilation support * The legal representative signs the informed consent form
Exclusion criteria
* Refusal to participate in the study
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| ballistocardiography waveform | through study completion, an average of 2 weeks | the correlation between using Ballistocardiography (BCG) for monitoring respiration and heart rate |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| tidal volume | through study completion, an average of 2 weeks | the correlation between using Ballistocardiography (BCG) for tidal volume |
Countries
Taiwan
Contacts
Fu Jen Catholic University Hospital