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A Two-Stage Approach Integrating Provisional Biomaterial-Mediated Stabilization Followed by a Definitive Treatment for Managing Volumetric Muscle Loss Injuries.
Clark, Andrew R; Kulwatno, Jonathan; Kanovka, Sergey S; Klarmann, George J; Hernandez, Claudia E; Natoli, Roman M; McKinley, Todd O; Potter, Benjamin K; Dearth, Christopher L; Goldman, Stephen M.
Afiliação
  • Clark AR; Extremity Trauma and Amputation Center of Excellence, Defense Health Agency, Falls Church, VA 22042, USA.
  • Kulwatno J; Department of Surgery, Uniformed Services University of the Health Sciences, Bethesda, MD 20814, USA.
  • Kanovka SS; The Henry M. Jackson Foundation for the Advancement of Military Medicine, Bethesda, MD 20817, USA.
  • Klarmann GJ; Extremity Trauma and Amputation Center of Excellence, Defense Health Agency, Falls Church, VA 22042, USA.
  • Hernandez CE; Department of Surgery, Uniformed Services University of the Health Sciences, Bethesda, MD 20814, USA.
  • Natoli RM; Extremity Trauma and Amputation Center of Excellence, Defense Health Agency, Falls Church, VA 22042, USA.
  • McKinley TO; Department of Surgery, Uniformed Services University of the Health Sciences, Bethesda, MD 20814, USA.
  • Potter BK; 4D Bio3 Center for Biotechnology and Department of Radiology and Radiological Sciences, Uniformed Services University of the Health Sciences, Bethesda, MD 20817, USA.
  • Dearth CL; The Geneva Foundation, Tacoma, WA 98402, USA.
  • Goldman SM; Extremity Trauma and Amputation Center of Excellence, Defense Health Agency, Falls Church, VA 22042, USA.
J Funct Biomater ; 15(6)2024 Jun 06.
Article em En | MEDLINE | ID: mdl-38921533
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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article