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Hyperthermia generated by intracavitary probe(s) is a specialized medical procedure aimed at increasing the temperature of tumor cells while minimizing damage to surrounding healthy tissue. This technique utilizes probes that are inserted into body cavities, where they generate heat through various methods such as microwave, radiofrequency, or ultrasound. The fundamental principle behind this procedure is that tumor cells exhibit a higher sensitivity to elevated temperatures compared to normal cells. By raising the temperature of the tumor cells, the procedure can enhance the efficacy of concurrent treatments like radiation and chemotherapy, as well as potentially stimulate the immune system to target and destroy abnormal cells more effectively. Intracavitary hyperthermia is particularly applicable for tumors that are accessible through natural body openings, including the vagina for cervical and uterine tumors, the anus for prostate tumors, the nose for nasopharyngeal tumors, and the mouth for esophageal tumors. During the procedure, a specially designed probe that conforms to the shape of the cavity is carefully inserted, with its placement often confirmed through imaging techniques such as x-ray or ultrasound. Once positioned, a heat source is introduced into the probe, elevating the temperature of the targeted area to the predetermined therapeutic level. Upon completion of the hyperthermia session, the probe and heat source are removed from the body cavity. This CPT® code encompasses not only the hyperthermia treatment itself but also includes the management of the treatment course, physics planning, insertion of temperature sensors, and the utilization of heat-generating devices.
© Copyright 2025 Coding Ahead. All rights reserved.
The procedure of hyperthermia generated by intracavitary probe(s) is indicated for various tumor types that can be accessed through natural body orifices. The following conditions are explicitly mentioned as suitable for this treatment:
The procedure for hyperthermia generated by intracavitary probe(s) involves several critical steps to ensure effective treatment. Each step is designed to maximize the therapeutic benefits while ensuring patient safety.
After the hyperthermia treatment, patients may require monitoring for any immediate post-procedure effects. Expected recovery may vary based on individual patient factors and the extent of the procedure. Patients are typically advised to follow up with their healthcare provider to assess the treatment's effectiveness and to discuss any further management or additional therapies that may be necessary. It is essential to monitor for any potential complications, such as discomfort or localized reactions at the site of probe insertion. Comprehensive post-procedure care instructions will be provided to ensure optimal recovery and ongoing management of the underlying condition.
| Short Descr | HYPERTHERMIA GEN INTRCV PRB | Medium Descr | HYPERTHERMIA GENERATED BY INTRACAVITARY PROBES | Long Descr | Hyperthermia generated by intracavitary probe(s) | Status Code | Restricted Coverage | Global Days | XXX - Global Concept Does Not Apply | PC/TC Indicator (26, TC) | 1 - Diagnostic Tests for Radiology Services | 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 | Procedure or Service, Not Discounted when Multiple | ASC Payment Indicator | Radiology service paid separately when provided integral to a surgical procedure on ASC list; payment based on OPPS relative payment weight. | Type of Service (TOS) | 6 - Therapeutic Radiology | Berenson-Eggers TOS (BETOS) | P7B - Oncology - other | MUE | 1 | CCS Clinical Classification | 211 - Therapeutic radiology |
| 26 | Professional component: certain procedures are a combination of a physician or other qualified health care professional component and a technical component. when the physician or other qualified health care professional component is reported separately, the service may be identified by adding modifier 26 to the usual procedure number. | 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. | GC | This service has been performed in part by a resident under the direction of a teaching physician |
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| 2025-01-01 | Changed | Short and Medium Descriptions changed. |
| Pre-1990 | Added | Code added. |
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