© Copyright 2025 American Medical Association. All rights reserved.
The procedure described by CPT® Code 0661T involves the removal and reimplantation of a nonbiodegradable drug-eluting implant specifically designed for the anterior segment of the eye. This innovative approach utilizes a drug-eluting implant that delivers targeted therapy for various ocular conditions, particularly glaucoma. The implant is engineered to provide a continuous and controlled release of travoprost, a medication that effectively lowers intraocular pressure, which is crucial for managing glaucoma. By bypassing the corneal barrier, this method eliminates the need for patients to adhere to a regimen of eye drops, thereby enhancing treatment compliance and efficacy. The titanium implant consists of a scleral anchor that secures it to the trabecular meshwork, a drug reservoir that holds the medication, and a titrating elution membrane that regulates the release of the drug into the anterior chamber. The procedure is performed through a micro-invasive technique, involving a 2.4 mm incision, allowing for a minimally invasive approach to ocular surgery. The scleral anchor is positioned within the trabecular meshwork and is secured by gentle nudging. When the implant's drug reservoir is depleted, the titanium implant can be removed and replaced using a similar surgical technique, ensuring ongoing treatment for the patient.
© Copyright 2025 Coding Ahead. All rights reserved.
The removal and reimplantation of the anterior segment intraocular nonbiodegradable drug-eluting implant is indicated for patients requiring sustained intraocular pressure management due to glaucoma or other ocular conditions that necessitate targeted drug delivery. This procedure is particularly beneficial for individuals who may struggle with adherence to traditional eye drop regimens, as the implant provides a continuous release of medication directly into the anterior chamber.
The procedure for the removal and reimplantation of the drug-eluting implant involves several key steps that ensure the effective management of intraocular pressure. Initially, a 2.4 mm incision is made in the eye to access the anterior chamber. This incision is strategically placed to facilitate an ab interno approach, allowing the surgeon to visualize the anterior chamber angle. Once access is obtained, the scleral anchor of the titanium implant is carefully positioned within the trabecular meshwork. The surgeon secures the anchor by gently nudging it into place, ensuring a stable attachment that will allow for effective drug delivery. After the implant has been properly seated, the next step involves the removal of the depleted titanium implant. This is performed using a similar micro-invasive technique, ensuring minimal trauma to the surrounding ocular structures. Following the removal, a new drug-eluting implant is then inserted into the same location, allowing for the continuation of therapy. This reimplantation process is crucial for maintaining the therapeutic effects of the medication and managing intraocular pressure effectively.
After the removal and reimplantation of the drug-eluting implant, patients may experience a recovery period that typically involves monitoring for any signs of complications, such as infection or inflammation. It is essential for healthcare providers to provide appropriate post-operative care instructions, which may include the use of topical medications to reduce inflammation and prevent infection. Patients should be advised to attend follow-up appointments to assess the effectiveness of the implant and monitor intraocular pressure. The expected recovery time may vary depending on individual patient factors, but most patients can resume normal activities within a short period following the procedure. Continuous evaluation of intraocular pressure will be necessary to ensure the ongoing effectiveness of the treatment.
Short Descr | RMVL&RIMPLTJ ANT SGM IMPLT | Medium Descr | RMVL&RIMPLTJ ANT SGM IO NBIODGRD RX ELUT IMPLT | Long Descr | Removal and reimplantation of anterior segment intraocular nonbiodegradable drug-eluting implant | Status Code | Carriers Price the Code | Global Days | YYY - Carrier Determines Whether Global Concept Applies | PC/TC Indicator (26, TC) | 0 - Physician Service Code | Multiple Procedures (51) | 2 - Standard payment adjustment rules for multiple procedures apply. | Bilateral Surgery (50) | 1 - 150% payment adjustment for bilateral procedures applies. | Physician Supervisions | 09 - Concept does not apply. | Assistant Surgeon (80, 82) | 1 - Statutory 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 | Hospital Part B services paid through a comprehensive APC | ASC Payment Indicator | Non office-based surgical procedure added in CY 2008 or later; payment based on OPPS relative payment weight. | Berenson-Eggers TOS (BETOS) | none | MUE | 1 |
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2022-01-01 | Added | First appearance in codebook. |
2021-07-01 | Added | Code added. |
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