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The CPT® Code 0528T refers to a specific procedure known as the programming device evaluation of an intracardiac ischemia monitoring system. This evaluation is conducted in person and involves an iterative adjustment of programmed values. Typically performed a few weeks after the insertion of the monitoring device, this procedure is often carried out during a stress test to assess the device's functionality and effectiveness. During the evaluation, the device is wirelessly connected to a computer, allowing healthcare professionals to view the current settings and monitor the patient's heart activity in real-time. The procedure captures data at various stages: while the patient is at rest, during the stress test, and throughout the recovery period following the test. This comprehensive data collection enables the determination of normal heart rate ranges and ischemic detection thresholds, which are critical for accurate monitoring of intracardiac ischemia. After thorough analysis and review of the collected data, healthcare providers make necessary adjustments to the programmed values to ensure optimal sensing and detection capabilities of the device. Upon completion of the programming process, the device is disconnected from the computer, and a detailed written report is generated to document the findings and adjustments made during the evaluation.
© Copyright 2025 Coding Ahead. All rights reserved.
The programming device evaluation of an intracardiac ischemia monitoring system is indicated for patients who have undergone the insertion of such a device and require assessment of its functionality and performance. This procedure is typically performed to ensure that the device is accurately detecting ischemic events and to optimize its programmed settings based on the patient's physiological responses during stress testing.
The procedure begins with the patient being prepared for the evaluation, which includes connecting the intracardiac ischemia monitoring device wirelessly to a computer system. This connection allows for real-time monitoring and display of the device's current settings. The healthcare provider then initiates the data capture process, which occurs in three distinct phases: while the patient is at rest, during the stress test, and in the recovery period following the test. During the resting phase, baseline heart activity is recorded to establish normal heart rate ranges. Next, the patient undergoes a stress test, which may involve physical exertion or pharmacological stimulation, to provoke cardiac responses that are critical for assessing the device's performance. Data collected during this phase is crucial for determining ischemic detection thresholds. After the stress test, the recovery phase allows for additional data collection as the patient's heart rate returns to baseline levels. Following the completion of data capture, the healthcare provider conducts a thorough analysis and review of the collected information. Based on this analysis, iterative adjustments are made to the programmed values of the device to optimize its sensing capabilities. Once the programming is finalized, the device is disconnected from the computer, and a comprehensive written report is generated, summarizing the findings and any adjustments made during the evaluation.
After the programming device evaluation is completed, the patient may be monitored for any immediate reactions or complications related to the stress test or device adjustments. The written report generated during the procedure serves as a critical document for ongoing patient management and follow-up care. It outlines the adjustments made to the device settings and provides insights into the patient's cardiac responses during the evaluation. Healthcare providers may schedule follow-up appointments to reassess the device's performance and make further adjustments if necessary. Patients are typically advised on any specific post-procedure care instructions, including monitoring for symptoms of ischemia or other cardiac events, and to report any unusual symptoms to their healthcare provider promptly.
Short Descr | PRGRMG DEV EVAL IIMS IP | Medium Descr | PRGRMG DEVICE EVAL IIMS IN PERSON | Long Descr | Programming device evaluation (in person) of intracardiac ischemia monitoring system with iterative adjustment of programmed values, with analysis, review, and report | Status Code | Carriers Price the Code | Global Days | XXX - Global Concept Does Not Apply | PC/TC Indicator (26, TC) | 1 - Diagnostic Tests for Radiology Services | Multiple Procedures (51) | 9 - Concept does not apply. | Bilateral Surgery (50) | 9 - Concept does not apply. | Physician Supervisions | 09 - Concept does not apply. | Assistant Surgeon (80, 82) | 9 - Concept does not apply. | Co-Surgeons (62) | 9 - Concept does not apply. | Team Surgery (66) | 9 - Concept does not apply. | Diagnostic Imaging Family | 99 - Concept Does Not Apply | APC Status Indicator | STV-Packaged Codes | Berenson-Eggers TOS (BETOS) | none | MUE | 1 |
59 | Distinct procedural service: under certain circumstances, it may be necessary to indicate that a procedure or service was distinct or independent from other non-e/m services performed on the same day. modifier 59 is used to identify procedures/services, other than e/m services, that are not normally reported together, but are appropriate under the circumstances. documentation must support a different session, different procedure or surgery, different site or organ system, separate incision/excision, separate lesion, or separate injury (or area of injury in extensive injuries) not ordinarily encountered or performed on the same day by the same individual. however, when another already established modifier is appropriate it should be used rather than modifier 59. only if no more descriptive modifier is available, and the use of modifier 59 best explains the circumstances, should modifier 59 be used. note: modifier 59 should not be appended to an e/m service. to report a separate and distinct e/m service with a non-e/m service performed on the same date, see modifier 25. |
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