© Copyright 2026 American Medical Association. All rights reserved.
The CPT® Code 0273T refers to an in-person interrogation device evaluation specifically for a carotid sinus baroreflex activation system. This procedure is essential for patients suffering from refractory hypertension, where the body's ability to regulate blood pressure and heart rate through the carotid sinus baroreflex is compromised. The implanted baroreflex activation device works by enhancing the electrical activity in the carotid baroreceptor afferent nerves. This increased activity is interpreted by the brainstem as a signal of elevated arterial blood pressure, prompting the central nervous system to adjust sympathetic and vagal nerve outputs. As a result, this modulation leads to a decrease in both blood pressure and heart rate. During the evaluation, the patient is connected to an electrocardiogram (ECG) monitor, allowing for real-time assessment of cardiac function. A connection is established between the carotid sinus baroreflex activation device and the interrogation device, enabling the physician to perform a thorough interrogation of the device. The physician reviews the data obtained from the device to evaluate its functionality and the current programmed parameters. This includes a detailed analysis of stored device data, which is compared to previous data acquisitions to assess any changes in the patient's condition. The evaluation also involves monitoring the number and duration of events indicated by variations in blood pressure and heart rate, as well as reviewing exercise and physiological stress data to observe how the patient’s blood pressure and heart rate adapt under different conditions. Additionally, the mechanical integrity of the device, including the leads and battery status, is assessed. Unlike the routine evaluation described in CPT® Code 0272T, which does not involve programming, the procedure associated with CPT® Code 0273T includes programming adjustments to the device. These adjustments may involve modifications to pulse amplitude, pulse width, therapy frequency, pathway mode, burst mode, and daily therapy start/stop times, ensuring that the device is optimized for the patient's therapeutic needs.
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