Evidence map›Paper›PMID 38921533›Full record

ArticleJournal of functional biomaterials2024

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

Andrew R Clark, Jonathan Kulwatno, Sergey S Kanovka, George J Klarmann, Claudia E Hernandez, Roman M Natoli, Todd O McKinley, Benjamin K Potter, Christopher L Dearth, Stephen M Goldman

Abstract read
In one paragraph

Article in Journal of functional biomaterials, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Review
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Andrew R ClarkExtremity Trauma and Amputation Center of Excellence, Defense Health Agency, Falls Church, VA 22042, USA.ORCID 0000-0003-1273-9630
Jonathan KulwatnoExtremity Trauma and Amputation Center of Excellence, Defense Health Agency, Falls Church, VA 22042, USA.ORCID 0000-0002-3851-0298
Sergey S KanovkaExtremity Trauma and Amputation Center of Excellence, Defense Health Agency, Falls Church, VA 22042, USA.ORCID 0000-0002-2637-8824
George J Klarmann4D Bio3 Center for Biotechnology and Department of Radiology and Radiological Sciences, Uniformed Services University of the Health Sciences, Bethesda, MD 20817, USA.ORCID 0000-0001-9614-9464
Claudia E HernandezExtremity Trauma and Amputation Center of Excellence, Defense Health Agency, Falls Church, VA 22042, USA.
Roman M NatoliDepartment of Orthopaedic Surgery, Indiana University School of Medicine, Indianapolis, IN 46202, USA.ORCID 0000-0002-4182-3244
Todd O McKinleyDepartment of Orthopaedic Surgery, Indiana University School of Medicine, Indianapolis, IN 46202, USA.
Benjamin K PotterDepartment of Surgery, Uniformed Services University of the Health Sciences, Bethesda, MD 20814, USA.ORCID 0000-0002-8771-0317
Christopher L DearthExtremity Trauma and Amputation Center of Excellence, Defense Health Agency, Falls Church, VA 22042, USA.ORCID 0000-0003-3701-0950
Stephen M GoldmanExtremity Trauma and Amputation Center of Excellence, Defense Health Agency, Falls Church, VA 22042, USA.ORCID 0000-0002-2244-1443

Funding

United States Army Medical Research and Development Command W81XWH-20-2-0009
6 · The paper itself

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.

Indexed as

military medicineorthopedicspolymersskeletal muscletrauma

Identifiers

PMID38921533
PMCPMC11204500

What OpenQuestion holds

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Read underepoch 390

Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.