047M35Z
Dilation Popliteal Artery, Right to No Qualifier with Intraluminal Device, Drug-eluting, Two, Percutaneous Approach
Procedural Specifications
| Clinical Axis | Detail Definition |
|---|---|
| Section | 0 Medical and Surgical |
| Body System | 4 Lower Arteries |
| Operation | 7 Dilation |
| Body Part | M Popliteal Artery, Right |
| Approach | 3 Percutaneous |
| Device | 5 Intraluminal Device, Drug-eluting, Two |
| Qualifier | Z No Qualifier |
Operation Definition
Expanding an orifice or the lumen of a tubular body part
Procedure Overview
This family describes procedures that widen a narrowed or blocked segment of an artery in the leg, pelvis, or abdomen so blood can flow more freely to the tissues those vessels supply. Narrowing in these arteries is commonly caused by atherosclerotic plaque buildup, and when it becomes severe enough, patients may experience leg pain with walking, poor wound healing, or in serious cases, tissue at risk of loss.
The procedure is typically performed using a catheter threaded through the vascular system to the narrowed spot, where a balloon is inflated to press the plaque outward and reopen the lumen. A stent is often left behind to help hold the artery open, though the dilation itself refers to the widening action rather than the device placement. Open surgical techniques that stretch a vessel are also included in this family.
These procedures are generally performed to relieve symptoms of peripheral artery disease, restore circulation to a limb, or address a stenosis found on vascular imaging, and are chosen based on how severe the narrowing is and how much of the artery is affected.
Anatomy & Axis Detail
Popliteal Artery, Right
The right popliteal artery, the continuation of the femoral artery behind the knee, supplies the lower leg and is notable for its vulnerability to both atherosclerotic disease and entrapment or aneurysmal degeneration given its confined anatomic course through the popliteal fossa. Dilation is performed to relieve stenosis or occlusion causing claudication or, in more advanced disease, critical limb ischemia threatening tissue loss, typically via balloon angioplasty since stent placement in this segment carries added risk of fracture from the repetitive flexion stresses at the knee. Because the popliteal artery is a common site of chronic total occlusion, particularly in diabetic patients with distal disease patterns, procedural approach and any adjunctive device use should be clearly documented, as these details affect both the completeness of coding and understanding of expected durability.
Approach: Percutaneous
Percutaneous describes entry by needle or instrument puncture through the skin or mucous membrane to reach the site of the procedure, without cutting the tissue open or using a visualizing scope. It differs from Open in that the site itself is never exposed, and from Percutaneous Endoscopic in that no endoscope is used to see internal structures. Common examples include needle biopsies and injections.
Device: Intraluminal Device, Drug-eluting, Two
This value specifies that exactly two drug-eluting intraluminal devices, such as coronary stents, were deployed within the same body part during one procedure. The device count matters for procedural coding because it reflects added technical complexity compared to a single drug-eluting device, and it is distinguished from the Three and Four or More counts by the specific number placed.
Coding & Documentation
Coders need documentation identifying the specific lower artery segment dilated, the approach used (open, percutaneous, or percutaneous endoscopic), and whether a device such as a stent or an intraluminal device was left in place, since that determines the device value appended to the code. The number of separate lesions treated in different named vessels can also affect how many codes are reported.
A common error is failing to code a separate Dilation for each distinct body part when multiple sites along the same limb are treated, since ICD-10-PCS defines body part values by specific artery segment. Another frequent mistake is omitting or misselecting the device value when a drug-eluting stent, a bare stent, or no device at all was used, since the operative note's wording on device type must be matched precisely to the code table options.