External baroreflex activation for assessment and treatment
Devices, systems and methods for non-invasive modulation of the baroreflex system of a patient. In embodiments, the present disclosure may be used to measure and monitor baroreflex function for diagnostic purposes in patients acutely or chronically to inform and guide medical treatment, assess disease severity, or assess morbidity/mortality risk. In embodiments, the present disclosure may be used to provide non-invasive baroreflex activation therapy acutely or chronically to treat a variety of disease conditions through rebalancing of the sympathetic and parasympathetic limbs of the autonomic nervous system and their connections to higher brain centers.
1 . A method for modulating autonomic nervous system activity in a patient, comprising:
positioning a wearable collar device externally on the neck of the patient, such that one or more pressure ports are aligned with a carotid sinus region;
delivering a baroreflex activation regimen to the patient using the wearable collar device, wherein the regimen comprises application of pneumatic pressure through the pressure ports; and
modifying autonomic nervous system function by selectively activating or deactivating baroreceptors via controlled external mechanical stimulation.
2 . The method of claim 1 , wherein the baroreflex activation regimen comprises application of external positive or negative pneumatic pressure, generated by an integrated pressure generator.
3 . The method of claim 2 , wherein the integrated pressure generator comprises a miniaturized pump assembly and control unit housed within the wearable collar device, configured to deliver pneumatic pressure locally without requiring external tubing or separate hardware.
4 . The method of claim 1 , wherein the wearable collar device includes a plurality of independently actuatable pressure ports, each pressure port in communication with a dedicated conduit and valve, configured to map and deliver the baroreflex activation regimen based on differential patient response.
5 . The method of claim 1 , wherein the wearable collar device includes a left-side pressure port and a right-side pressure port, each independently controllable to deliver unilateral or bilateral stimulation to the carotid sinus region.
6 . The method of claim 1 , further comprising recording a physiological response to the applied pressure to assess baroreflex function, including baroreflex sensitivity and gain.
7 . The method of claim 6 , further comprising generating a lateralized baroreflex response map to identify optimal stimulation parameters based on side-specific autonomic responses.
8 . The method of claim 1 , wherein the baroreflex activation regimen includes delivery of graded pressure stimuli at multiple predefined intensities to generate a dose-response profile.
9 . The method of claim 1 , wherein the method is used to deliver therapeutic modulation for a disease state characterized by sympathetic overactivity or parasympathetic underactivity.
10 . The method of claim 9 , wherein the disease condition comprises one or more of: resistant hypertension, systolic or diastolic heart failure, pulmonary hypertension, epilepsy, migraine, chronic pain syndrome, major depressive disorder, cardiac arrhythmia, or systemic inflammatory conditions.
11 . The method of claim 1 , wherein the baroreflex activation regimen is delivered to a patient undergoing dialysis to stabilize blood pressure fluctuations and reduce dialysis-associated symptoms.
12 . The method of claim 1 , wherein the baroreflex activation regimen is delivered to a patient with acute decompensated heart failure to improve pulmonary congestion and stability circulatory function.
13 . The method of claim 1 , further comprising measuring a physiological parameter in response to the baroreflex activation regimen using one or more onboard or auxiliary sensors.
14 . The method of claim 13 , wherein the physiological parameter comprises one or more of: arterial blood pressure, heart rate, heart rate variability, cardiac output, vascular resistance, respiratory rate, seizure activity, or autonomic tone indices.
15 . The method of claim 13 , further comprising dynamically adjusting the baroreflex activation regimen in real time in response to the measured physiological parameter.
16 . The method of claim 1 , wherein the wearable device includes at least one biosensor configured to detect changes in autonomic nervous system function, and further comprising storing biosensor data in a local or remote memory storage device for review or clinical interpretation and wirelessly transmitting the data to a clinician interface, electronic health record system, or remote monitoring server.
17 . The method of claim 1 , wherein the wearable device includes a programmable controller configured to operate the device in a closed loop control mode, and wherein the closed loop control mode includes modifying the pressure delivery pattern based on real-time feedback from one or more physiological sensors.
18 . The method of claim 1 , wherein the baroreflex activation regimen comprises delivery of pressure waveforms selected from continuous, pulsatile, or alternating sequences of positive and negative pressures.