A Two-Stage Approach Integrating Provisional Biomaterial-Mediated Stabilization Followed by a Definitive Treatment for Managing Volumetric Muscle Loss Injuries

Author:

Clark Andrew R.123ORCID,Kulwatno Jonathan12ORCID,Kanovka Sergey S.12ORCID,Klarmann George J.45ORCID,Hernandez Claudia E.126,Natoli Roman M.7ORCID,McKinley Todd O.7,Potter Benjamin K.28ORCID,Dearth Christopher L.12ORCID,Goldman Stephen M.12ORCID

Affiliation:

1. Extremity Trauma and Amputation Center of Excellence, Defense Health Agency, Falls Church, VA 22042, USA

2. Department of Surgery, Uniformed Services University of the Health Sciences, Bethesda, MD 20814, USA

3. The Henry M. Jackson Foundation for the Advancement of Military Medicine, Bethesda, MD 20817, USA

4. 4D Bio3 Center for Biotechnology and Department of Radiology and Radiological Sciences, Uniformed Services University of the Health Sciences, Bethesda, MD 20817, USA

5. The Geneva Foundation, Tacoma, WA 98402, USA

6. C2 Alaska, LLC, San Antonio, TX 78249, USA

7. Department of Orthopaedic Surgery, Indiana University School of Medicine, Indianapolis, IN 46202, USA

8. Department of Orthopaedic Surgery, Walter Reed National Military Medical Center, Bethesda, MD 20889, USA

Abstract

Treatment of volumetric muscle loss (VML) faces challenges due to its unique pathobiology and lower priority in severe musculoskeletal injury management. Consequently, a need exists for multi-stage VML treatment strategies to accommodate delayed interventions owing to comorbidity management or prolonged casualty care in combat settings. To this end, polyvinyl alcohol (PVA) was used at concentrations of 5%, 7.5%, and 10% to generate provisional muscle void fillers (MVFs) of varying stiffness values (1.125 kPa, 3.700 kPa, and 7.699 kPa) to stabilize VML injuries as part of a two-stage approach. These were implanted into a rat model for a duration of 4 weeks, then explanted and either left untreated (control) or treated through minced muscle grafting (MMG). Additional benchmarks included acute MMG and unrepaired groups. At the MVF explant, the 7.5% PVA group exhibited superior neuromuscular function compared to the 5% and 10% PVA groups, the least fibrosis, and the largest median myofiber size among all groups at the 12-week endpoint. Despite the 7.5% PVA’s superiority amongst the two-stage treatment groups, neuromuscular function was neither improved nor impaired relative to acute treatment benchmarks. This suggests that the future success of a two-stage VML treatment strategy will necessitate a more effective definitive intervention.

Funder

United States Army Medical Research and Development Command

Publisher

MDPI AG

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