Displacement of esophageal anti-reflux device, sequela

This code signifies a long-term complication where an anti-reflux device, such as a LINX device or a fundoplication wrap, has shifted from its intended position within the esophagus. This displacement is not an acute event but rather a persistent issue or a consequence of an earlier acute displacement. It indicates an ongoing problem related to the device's stability and function.

Use this code when documenting a patient presenting with symptoms or findings directly attributable to a previously displaced esophageal anti-reflux device, where the displacement is no longer acute but a chronic or residual issue. This applies to follow-up encounters for persistent symptoms or for planning corrective procedures related to the long-term effects of the displacement. It is appropriate for situations where the initial displacement occurred in the past and is now being addressed as a sequela.

• Always assign an additional code to specify the type of esophageal anti-reflux device involved, if known.
• Do not use this code for acute displacement; reserve it for chronic or residual issues.
• Ensure documentation clearly supports the "sequela" aspect, indicating a past event with ongoing consequences.