# Concomitant Venous Disease in Patients with Advanced Peripheral Arterial Disease: A Patient- and Limb-Level Analysis

**Authors:** Daniela Marinescu, Laurențiu Augustus Barbu, Tiberiu Stefăniță Țenea Cojan, Ștefan Pătrascu, Marius Bică, Răzvan Alexandru Marinescu, Sarmis Marian Săndulescu, Valeriu Șurlin, Ana-Maria Ciurea

PMC · DOI: 10.3390/life16020312 · 2026-02-11

## TL;DR

This study finds that venous disease commonly coexists with severe peripheral arterial disease and is linked to worse arterial disease markers, suggesting a need for combined arterial and venous assessments.

## Contribution

The study introduces a clinically oriented composite definition for venous disease and demonstrates its significant association with advanced peripheral arterial disease severity.

## Key findings

- Concomitant venous disease was present in 68.9% of patients with advanced peripheral arterial disease.
- Venous disease at the limb level was associated with severe arterial markers like inflow disease and impaired tibial runoff.
- Patients with venous disease had a lower unadjusted rate of major amputation despite greater arterial severity.

## Abstract

Background: Advanced stages of peripheral arterial disease, particularly chronic limb-threatening ischemia, are characterized by unfavorable limb outcomes and a substantial risk of major amputation. Clinical evaluation traditionally focuses on arterial obstruction; however, venous dysfunction may coexist and contribute to local limb pathophysiology in advanced PAD, remaining insufficiently recognized in routine practice. Methods: We performed a retrospective cohort analysis of consecutive patients with advanced peripheral arterial disease managed at the First Surgical Clinic of the Emergency County Clinical Hospital of Craiova over a five-year period (January 2020 to December 2024). Venous disease was defined using a clinically oriented composite definition incorporating imaging-confirmed venous pathology, prior deep venous thrombosis, and persistent lower-limb edema attributable to venous dysfunction. Arterial disease severity was assessed using multimodal imaging. Analyses were performed at both patient and limb levels to evaluate associations between venous disease, arterial severity markers, and clinical outcomes. Results: Among 241 patients (482 limbs), concomitant venous disease was identified in 68.9% at the patient level and was predominantly unilateral. At the limb level, venous disease was significantly associated with markers of severe arterial involvement, including inflow disease, higher segment occlusion scores, impaired tibial runoff, and absence of a patent pedal arch. Despite greater arterial severity, patients with venous disease exhibited a lower unadjusted rate of major amputation compared with those without venous involvement. Conclusions: Concomitant venous disease is highly prevalent in patients with advanced PAD and is closely linked to arterial disease severity. These findings suggest that venous dysfunction represents an integral component of advanced limb-threatening ischemia rather than an isolated comorbidity. Incorporating clinically oriented venous assessment may improve understanding of limb pathophysiology and support a more integrated arterio-venous approach to advanced PAD management.

## Linked entities

- **Diseases:** peripheral arterial disease (MONDO:0005386)

## Full-text entities

- **Diseases:** frailty (MESH:D000073496), Acute limb ischemia (MESH:D000208), outflow disease (MESH:D014694), obstruction (MESH:D000402), ischemia (MESH:D007511), Venous hypertension (MESH:D014647), stroke (MESH:D020521), thrombophilia (MESH:D019851), obesity (MESH:D009765), arterio-venous disease (MESH:D001159), Lower-limb edema (MESH:D004487), chronic kidney disease (MESH:D051436), CLTI (MESH:D000089802), malignancy (MESH:D009369), ischemic (MESH:D002545), diabetes mellitus (MESH:D003920), chronic venous insufficiency (MESH:D014689), arterial insufficiency (MESH:D014715), pelvic malignancies (MESH:D010386), Hyperlipidemia (MESH:D006949), Arterial Disease (MESH:D002539), inflammatory (MESH:D007249), liver disease (MESH:D008107), , and infrapopliteal disease (MESH:D004194), injury to (MESH:D014947), systemic infection (MESH:D012141), tissue loss (MESH:D017695), Lipid abnormalities (MESH:D011017), congestive heart failure (MESH:D006333), PAD (MESH:D058729), deep venous thrombosis (MESH:D020246), involvement (MESH:C564676), end-stage vascular disease (MESH:D007676), cardiovascular disease (MESH:D002318), arterial (MESH:D012078), infection (MESH:D007239), atherosclerotic disease (MESH:D050197), death (MESH:D003643), limb (MESH:D001259), hypertension (MESH:D006973), arterial obstruction (MESH:D001157)
- **Chemicals:** oxygen (MESH:D010100), lipid (MESH:D008055)
- **Species:** Homo sapiens (human, species) [taxon 9606]

---
Source: https://tomesphere.com/paper/PMC12941635