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Noninvasive Point of Care Device for Assessing Cardiac Response to Acute Volume Changes
Harry A Silber1, Nisha A Gilotra1, Thomas L Miller2,3
1Department of Medicine, Division of Cardiology, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Medical Devices (Auckland, N.Z.)
|November 1, 2023
Summary
The Indicor device accurately measures the Valsalva pulse response (VPR) and detects changes in central blood volume. This noninvasive tool shows promise for assessing fluid status at the bedside.
Area of Science:
- Cardiovascular Physiology
- Medical Device Technology
- Diagnostic Tools
Background:
- The Valsalva maneuver alters peripheral pulse amplitude, offering insights into volume status.
- Automated quantification of the Valsalva pulse response (VPR) can aid bedside assessment.
- A novel device, Indicor, aims to standardize and automate VPR measurement.
Purpose of the Study:
- To evaluate if the Indicor device's VPR measurement can detect acute central volume changes induced by passive leg raise (PLR).
- To assess the sensitivity of automated VPR in healthy volunteers during a standardized Valsalva maneuver.
Main Methods:
- Healthy volunteers underwent a standardized Valsalva maneuver guided by the Indicor device.
- Photoplethysmography (PPG) signals were recorded during a 10-second expiratory effort (20 mmHg).
- VPR was calculated as the ratio of end-Valsalva to baseline pulse amplitude.
Main Results:
- VPR significantly increased from baseline (0.34 ± 0.13) to PLR (0.60 ± 0.14) in all 30 participants (p < 0.0001).
- Upon returning to upright, VPR decreased significantly (0.33 ± 0.10) compared to PLR (p < 0.0001).
- The device demonstrated sensitivity to acute central volume loading via PLR.
Conclusions:
- The Indicor device reliably and automatically quantifies VPR using PPG during a standardized Valsalva maneuver.
- Automated VPR measurement is sensitive to acute increases in central volume load from PLR in healthy individuals.
- Further research is needed to explore VPR in patient populations with heart failure and altered fluid status.
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