This is a prospective longitudinal cohort study to determine the value of HRV obtained using noninvasive actigraphy to quantify the response to pulmonary vasodilator therapy in newly diagnosed PAH patients
This single center prospective longitudinal cohort study will take place at the University of Cincinnati (UC). We will screen adult patients newly diagnosed with PAH and placed on targeted pulmonary vasodilator therapy by their treating physician for enrollment. We will enroll 35 eligible participants over a two-year period. HRV will be measured using the Polar™ H10 wearable chest actigraphy device in conjunction with analytic software to capture HRV data. After enrollment and completion of the baseline visit, study participants will receive chest actigraphy device to measure their heart rate for a two hour period twice a week during study participation. Follow up research visits will be conducted at one-month, 3-months, and 6-months to sync the actigraphy device and assess any AE's. In-between these visits, study staff will communicate with participants at two weeks, two months, 4 months, and 5 months, to identify and address any issues with study actigraphic device, assess any adverse events and maintain regular contact with study participants. Throughout study participation, subjects will continue routine clinical care at the direction of their treating physician as needed.
Study Type
OBSERVATIONAL
Enrollment
24
Noninvasive chest-mounted actigraphic device to be worn for 2 hour intervals two times per week during the six month study participation.
University of Cincinnati
Cincinnati, Ohio, United States
Change from baseline in HRV via RMSSD
Change from baseline in Root Mean Squared Successive Differences (RMSSD) measure of Heart Rate variability in patients on targeted therapy
Time frame: 6 months
Change from baseline in HRV via SDNN
Change from baseline in Standard Deviation of N-to-N (SDNN) measure of Heart Rate Variability in patients on targeted therapy
Time frame: 6 months
Correlation with Cardiac Magnetic Resonance Imaging Variables
Correlation between RMSSD and SDNN with key cardiac Magnetic Resonance Imaging Variables of PAH disease, the Right Ventricular Stroke Volume
Time frame: 6 months
Correlation with NTproBNP
Correlation between RMSSD and SDNN with N-terminal Pro-B-Type Natriuretic Peptide (NTproBNP), a marker of PAH disease severity and treatment response
Time frame: 6 months
Correlation with REVEAL 2.0 Risk Score
Correlation between RMSSD and SDNN with the REVEAL 2.0 Risk score, a measure of PAH prognosis
Time frame: 6 months
Correlation with CAMPHOR Quality of Life Score
Correlation between RMSSD and SDNN with the Cambridge Pulmonary Hypertension Outcome Review (CAMPHOR) score, a 3-domain quality of life assessment tool specific to PAH patients
Time frame: 6 months
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