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Wearable electrocardiographic rhythm-derived monitoring, as described by CPT® Code 93233, involves the collection of electrocardiographic (ECG) data over a continuous 24-hour period. This procedure is performed using a specialized device, commonly referred to as a Holter monitor, which is worn by the patient during their normal daily activities. The device is equipped with electrodes or leads that are strategically placed on the patient's chest to capture the electrical activity of the heart. Throughout the monitoring period, the device records original ECG waveforms continuously, ensuring that all relevant heart rhythm data is collected without interruption. The recorded data is stored on a medium such as magnetic tape or a digital format, allowing for later analysis. Upon completion of the monitoring period, the patient returns the device, and the stored data is analyzed to assess various cardiac parameters, including heart rhythm and rate, ST segment analysis, heart rate variability, and T-wave alternans. A miniaturized printout of the entire recording is generated, accompanied by a microprocessor-based analysis report that includes selective sampling of rhythm strips. The physician is responsible for reviewing and interpreting this data to identify any potential heart arrhythmias. It is important to note that while CPT® Code 93233 specifically pertains to the physician's review and interpretation of the data, other related codes exist for the complete procedure, recording, and analysis components, ensuring comprehensive billing and documentation for the entire monitoring process.
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The wearable electrocardiographic rhythm-derived monitoring procedure is indicated for various clinical scenarios where continuous heart rhythm assessment is necessary. The following conditions may warrant the use of this monitoring technique:
The procedure for wearable electrocardiographic rhythm-derived monitoring involves several key steps to ensure accurate data collection and analysis. The following outlines the procedural steps:
After the completion of the wearable electrocardiographic rhythm-derived monitoring, the patient may be provided with instructions regarding any follow-up care or additional testing that may be necessary based on the results of the monitoring. The physician will typically discuss the findings with the patient, including any identified arrhythmias or other significant cardiac events. Depending on the results, further diagnostic testing or treatment options may be recommended to address any identified issues. It is essential for the patient to maintain communication with their healthcare provider regarding any ongoing symptoms or concerns following the procedure.
Short Descr | ECG MONITOR/REVIEW, 24 HRS | Medium Descr | WR ECG 24 HR W/O SUPIMPOS WMINI TRACG PHYS R&I | Long Descr | WR ECG 24 HR W/O SUPIMPOS WMINI TRACG PHYS R&I | Status Code | Active Code | Global Days | XXX - Global Concept Does Not Apply | PC/TC Indicator (26, TC) | 2 - Professional Component Only Code | Multiple Procedures (51) | 0 - No payment adjustment rules for multiple procedures apply. | Bilateral Surgery (50) | 0 - 150% payment adjustment for bilateral procedures does NOT apply. | Physician Supervisions | 09 - Concept does not apply. | Assistant Surgeon (80, 82) | 0 - Payment restriction for assistants at surgery applies to this procedure... | Co-Surgeons (62) | 0 - Co-surgeons not permitted for this procedure. | Team Surgery (66) | 0 - Team surgeons not permitted for this procedure. | Diagnostic Imaging Family | 99 - Concept Does Not Apply | APC Status Indicator | Type of Service (TOS) | 5 - Diagnostic Laboratory | Berenson-Eggers TOS (BETOS) | T2C - Other tests - EKG monitoring | MUE | Not applicable/unspecified. | CCS Clinical Classification | 203 - Electrographic cardiac monitoring |
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