# Early experience with a composite ovine forestomach matrix graft in chronic lower extremity wounds: a multi-center retrospective case series

**Authors:** James E Geiger, Anthony J LaLama, Alpash K Patel

PMC · DOI: 10.1093/jscr/rjag129 · Journal of Surgical Case Reports · 2026-03-07

## TL;DR

A new outpatient treatment using a composite bioscaffold with ovine forestomach matrix and hyaluronic acid showed effectiveness and safety in healing chronic lower extremity wounds.

## Contribution

This study presents early evidence of a novel composite bioscaffold (OFM-HA) for treating chronic lower extremity wounds in an outpatient setting.

## Key findings

- The mean time to 50% wound area reduction was 3.2 weeks, and mean time to full closure was 9.9 weeks.
- OFM-HA was applied a median of 4 times with no complications or recurrences observed.
- The bioscaffold proved durable and effective for complex chronic wounds in elderly patients with comorbidities.

## Abstract

Chronic wounds place a significant burden on patients and healthcare. A newer outpatient treatment is a composite bioscaffold that contains ovine forestomach matrix and hyaluronic acid (OFM-HA). This multi-center retrospective case series investigated OFM-HA in the treatment of lower extremity chronic wounds. Medical records of 10 patients were reviewed and patient and wound characteristics were documented. Time to 50% percent area reduction (%PAR), time to closure, and complications were evaluated. Patients were primarily elderly with several comorbidities. The mean time to 50% PAR was 3.2 ± 2.3 weeks, and the mean time to closure was 9.9 ± 5.1 weeks. Patients received a median of 4 (IQR: 2, 5) applications. No complications or recurrences occurred. OFM-HA was effective and safe to treat complex lower extremity chronic wounds in the outpatient setting. Moreover, OFM-HA proved to be a durable material, with full closure requiring few applications.

## Full-text entities

- **Diseases:** diabetes (MESH:D003920), DM (MESH:D009223), chronic kidney disease (MESH:D051436), inflammatory (MESH:D007249), Chronic lower extremity wounds (MESH:D014947), NSTI (MESH:D018461), OFM (MESH:D012757), obesity (MESH:D009765), Wagner (MESH:C536075), VLUs (MESH:D014647), CVA (MESH:D020521), CKD (MESH:D012080), infection (MESH:D007239), calciphylaxis (MESH:D002115), ulcer (MESH:D014456), Charcot arthropathy (MESH:D007592), PIs (MESH:D003668), DFUs (MESH:D017719), hypertension (MESH:D006973), cellulitis (MESH:D002481), peripheral artery disease (MESH:D058729), coronary artery disease (MESH:D003324), peripheral venous disease (MESH:D010523), thrombotic microangiopathy (MESH:D057049)
- **Chemicals:** hypochlorous acid (MESH:D006997), saline (MESH:D012965), oxygen (MESH:D010100), HA (MESH:D006820), Myriad Matrix (-)
- **Species:** Human immunodeficiency virus 1 (no rank) [taxon 11676], Homo sapiens (human, species) [taxon 9606], Human immunodeficiency virus (species) [taxon 12721]

## Full text

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## Figures

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## References

25 references — full list in the complete paper: https://tomesphere.com/paper/PMC12966786/full.md

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Source: https://tomesphere.com/paper/PMC12966786