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Official Description

Temporary female intraurethral valve-pump (ie, voiding prosthesis); replacement

© Copyright 2025 American Medical Association. All rights reserved.

Common Language Description

The CPT® Code 0597T refers to the replacement of a temporary female intraurethral valve-pump, specifically designed as a voiding prosthesis. This device, known as the inFlow™ intraurethral valve pump, is intended for use in females aged 18 years and older who experience permanent urinary retention due to neurologic impairment affecting the detrusor muscle. The detrusor muscle is responsible for bladder contraction, and when its contractility is insufficient, individuals are unable to urinate independently, leading to significant urinary complications. This condition is often chronic and can arise from various causes, including spinal cord injuries, diseases, or other neurologic conditions. The inFlow™ system provides a solution that allows for near-normal voiding without the need for external assistance, tubes, or urinary bags, thereby enhancing the quality of life for affected individuals. The device is designed for replacement every 29 days or less, ensuring optimal functionality. The initial insertion of the device requires prior sizing, which is performed using a plastic sizing device that helps determine the appropriate urethral length. The intraurethral device itself is constructed from silicone and features flexible fins that secure it in place at the bladder neck, while an internal magnetically activated miniature valve-pump facilitates bladder emptying. The system also includes a handheld remote control activator that allows the user to operate the valve pump conveniently. This innovative approach to managing urinary retention represents a significant advancement in urological care for women facing these challenges.

© Copyright 2025 Coding Ahead. All rights reserved.

1. Indications

The inFlow™ intraurethral valve pump is indicated for use in females aged 18 years and older who suffer from permanent urinary retention due to neurologic impairment of the detrusor muscle. This condition may arise from various underlying causes, including:

  • Spinal Cord Injury - Damage to the spinal cord that affects nerve signals to the bladder.
  • Neurologic Conditions - Disorders that impair the function of the nervous system, impacting bladder control.
  • Detrusor Muscle Dysfunction - Insufficient contractility of the detrusor muscle, leading to an inability to urinate independently.

2. Procedure

The procedure for replacing the inFlow™ intraurethral valve pump involves several key steps to ensure proper placement and functionality of the device. The initial step is to perform device sizing, which is crucial for determining the appropriate length of the urethra. This is accomplished by inserting a plastic sizing device that features gradient markings corresponding to urethral length. The adjustable tab on the sizing device is moved back until it touches the meatus, allowing the physician to accurately measure the urethral length.

  • Step 1: Device Sizing - The physician inserts the plastic sizing device into the urethra and adjusts the tab to measure the length accurately.
  • Step 2: Insertion of the Intraurethral Device - Once sizing is complete, the intraurethral device, which is 3-7 cm long and housed in silicone, is inserted. The device features flexible petal-like fins that open to secure it at the bladder neck and hold it in place within the urethra.
  • Step 3: Activation of the Valve-Pump - The internal miniature valve-pump, which is magnetically activated, is now positioned within the housing tube of the device. The user will utilize a handheld remote control activator to operate the valve pump.
  • Step 4: Bladder Emptying - To empty the bladder, the user holds the remote control activator over her pelvis and presses the button to activate the pump. Releasing the button stops the urine flow.
  • Step 5: Device Replacement - When it is time for replacement, the device can be removed by grasping the external tab and pulling it out, making the process straightforward and manageable.

3. Post-Procedure

After the replacement of the inFlow™ intraurethral valve pump, patients can expect to resume normal activities with minimal downtime. It is important to monitor for any signs of complications, such as discomfort or leakage, and to follow up with healthcare providers as necessary. The device is designed for ease of use, allowing for self-management or assistance from a trained caregiver at home. Regular replacement of the device every 29 days or less is essential to maintain optimal function and prevent urinary complications.

Short Descr TEMP FML IU VALVE-PMP RPLCMT
Medium Descr TEMP FEMALE INTRAURETHRAL VALVE-PUMP REPLACEMENT
Long Descr Temporary female intraurethral valve-pump (ie, voiding prosthesis); replacement
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) 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 Hospital Part B services paid through a comprehensive APC
ASC Payment Indicator Office-based surgical procedure added to ASC list in CY 2008 or later without MPFS nonfacility PE RVUs; payment based on OPPS relative payment weight.
Berenson-Eggers TOS (BETOS) none
MUE 1
Date
Action
Notes
2021-01-01 Added First appearance of code in code book.
2020-07-01 Added Code added.
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