Nonoperative and Operative Soft-Tissue and Cartilage Regeneration and Orthopaedic Biologics of the Foot and Ankle: An Orthoregeneration Network Foundation Review.


Journal

Arthroscopy : the journal of arthroscopic & related surgery : official publication of the Arthroscopy Association of North America and the International Arthroscopy Association
ISSN: 1526-3231
Titre abrégé: Arthroscopy
Pays: United States
ID NLM: 8506498

Informations de publication

Date de publication:
07 2022
Historique:
received: 06 04 2022
accepted: 07 04 2022
pubmed: 24 5 2022
medline: 14 7 2022
entrez: 23 5 2022
Statut: ppublish

Résumé

Orthoregeneration is defined as a solution for orthopaedic conditions that harnesses the benefits of biology to improve healing, reduce pain, improve function, and optimally, provide an environment for tissue regeneration. Options include drugs, surgical intervention, scaffolds, biologics as a product of cells, and physical and electromagnetic stimuli. The goal of regenerative medicine is to enhance the healing of tissue after musculoskeletal injuries as both isolated treatment and adjunct to surgical management, using novel therapies to improve recovery and outcomes. Various orthopaedic biologics (orthobiologics) have been investigated for the treatment of pathology involving the foot and ankle (including acute traumatic injuries and fractures, tumor, infection, osteochondral lesions, arthritis, and tendinopathy) and procedures, including osteotomy or fusion. Promising and established treatment modalities include 1) bone-based therapies (such as cancellous or cortical autograft from the iliac crest, proximal tibia, and/or calcaneus, fresh-frozen or freeze-dried cortical or cancellous allograft, including demineralized bone matrix putty or powder combined with growth factors, and synthetic bone graft substitutes, such as calcium sulfate, calcium phosphate, tricalcium phosphate, bioactive glasses (often in combination with bone marrow aspirate), and polymers; proteins such as bone morphogenic proteins; and platelet-derived growth factors; 2) cartilage-based therapies such as debridement, bone marrow stimulation (such as microfracture or drilling), scaffold-based techniques (such as autologous chondrocyte implantation [ACI] and matrix-induced ACI, autologous matrix-induced chondrogenesis, matrix-associated stem cell transplantation, particulated juvenile cartilage allograft transplantation, and minced local cartilage cells mixed with fibrin and platelet rich plasma [PRP]); and 3) blood, cell-based, and injectable therapies such as PRP, platelet-poor plasma biomatrix loaded with mesenchymal stromal cells, concentrated bone marrow aspirate, hyaluronic acid, and stem or stromal cell therapy, including mesenchymal stem cell allografts, and adipose tissue-derived stem cells, and micronized adipose tissue injections. LEVEL OF EVIDENCE: Level V, expert opinion.

Identifiants

pubmed: 35605840
pii: S0749-8063(22)00286-9
doi: 10.1016/j.arthro.2022.04.018
pii:
doi:

Substances chimiques

Biological Products 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

2350-2358

Informations de copyright

Copyright © 2022 The Author(s). Published by Elsevier Inc. All rights reserved.

Auteurs

Richard Danilkowicz (R)

Department of Orthopaedic Surgery, Duke University Medical Center, Durham, North Carolina, U.S.A.

Christopher Murawski (C)

Department of Orthopaedic Surgery, Duke University Medical Center, Durham, North Carolina, U.S.A.

Manuel Pellegrini (M)

Department of Orthopaedic Surgery, Duke University Medical Center, Durham, North Carolina, U.S.A.

Markus Walther (M)

Department of Orthopaedic Surgery, Duke University Medical Center, Durham, North Carolina, U.S.A.

Victor Valderrabano (V)

Department of Orthopaedic Surgery, Duke University Medical Center, Durham, North Carolina, U.S.A.

Chayanin Angthong (C)

Department of Orthopaedic Surgery, Duke University Medical Center, Durham, North Carolina, U.S.A.

Samuel Adams (S)

Department of Orthopaedic Surgery, Duke University Medical Center, Durham, North Carolina, U.S.A. Electronic address: Samuel.adams@duke.edu.

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Classifications MeSH