Does the Choice of Acellular Scaffold and Augmentation With Bone Marrow Aspirate Concentrate Affect Short-term Outcomes in Cartilage Repair? A Systematic Review and Meta-analysis.


Journal

The American journal of sports medicine
ISSN: 1552-3365
Titre abrégé: Am J Sports Med
Pays: United States
ID NLM: 7609541

Informations de publication

Date de publication:
05 2023
Historique:
medline: 2 5 2023
pubmed: 1 3 2022
entrez: 28 2 2022
Statut: ppublish

Résumé

Matrix-induced chondrogenesis (MIC) is a promising treatment option for critical-size cartilage lesions of the knee; however, there exists substantial heterogeneity in the choice of acellular scaffold matrix for MIC cartilage repairs. The choice of acellular matrix will not affect patient outcomes after MIC cartilage repair procedures, and the addition of concentrated bone marrow aspirate (cBMA) will improve short-term patient outcomes regardless of matrix choice. Meta-analysis; Level of evidence, 4. Studies were stratified by matrix type: multilayered, single layered, and gel based. Continuous outcomes were analyzed with pairwise meta-analysis using the inverse variance model with random effects applied. Binary outcomes were analyzed as pooled proportions in a single-arm fashion; after which, reconstruction of relative risks (RRs) with confidence intervals was performed using the Katz logarithmic method. A total of 876 patients were included: 469 received multilayered bioscaffolds; 238, gel-based scaffolds; and 169, single-layered scaffolds. The mean age of patients was 36.2 years (95% CI, 33.9 to 38.4), while the mean lesion size was 3.91 cm While cartilage repair with acellular scaffolds provides significant improvements in pain and function for patients, there is insufficient clinical evidence to suggest which scaffold material is the most superior in influencing such improvements. The enhancement of cartilage repair procedures with cBMA may provide further functional improvements and improve defect filling; however, more long-term evidence is required to evaluate the effects.

Sections du résumé

BACKGROUND
Matrix-induced chondrogenesis (MIC) is a promising treatment option for critical-size cartilage lesions of the knee; however, there exists substantial heterogeneity in the choice of acellular scaffold matrix for MIC cartilage repairs.
HYPOTHESIS
The choice of acellular matrix will not affect patient outcomes after MIC cartilage repair procedures, and the addition of concentrated bone marrow aspirate (cBMA) will improve short-term patient outcomes regardless of matrix choice.
STUDY DESIGN
Meta-analysis; Level of evidence, 4.
METHODS
Studies were stratified by matrix type: multilayered, single layered, and gel based. Continuous outcomes were analyzed with pairwise meta-analysis using the inverse variance model with random effects applied. Binary outcomes were analyzed as pooled proportions in a single-arm fashion; after which, reconstruction of relative risks (RRs) with confidence intervals was performed using the Katz logarithmic method.
RESULTS
A total of 876 patients were included: 469 received multilayered bioscaffolds; 238, gel-based scaffolds; and 169, single-layered scaffolds. The mean age of patients was 36.2 years (95% CI, 33.9 to 38.4), while the mean lesion size was 3.91 cm
CONCLUSION
While cartilage repair with acellular scaffolds provides significant improvements in pain and function for patients, there is insufficient clinical evidence to suggest which scaffold material is the most superior in influencing such improvements. The enhancement of cartilage repair procedures with cBMA may provide further functional improvements and improve defect filling; however, more long-term evidence is required to evaluate the effects.

Identifiants

pubmed: 35225004
doi: 10.1177/03635465211069565
doi:

Types de publication

Meta-Analysis Systematic Review Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1622-1633

Auteurs

Zachariah Gene Wing Ow (ZGW)

Yong Loo Lin School of Medicine, National University of Singapore, Singapore.

Hannah Li Xin Cheang (HLX)

Yong Loo Lin School of Medicine, National University of Singapore, Singapore.

Jin Hean Koh (JH)

Yong Loo Lin School of Medicine, National University of Singapore, Singapore.

Joshua Zhi En Koh (JZE)

Yong Loo Lin School of Medicine, National University of Singapore, Singapore.

Katelyn Kaye-Ling Lim (KK)

Yong Loo Lin School of Medicine, National University of Singapore, Singapore.

Dean Wang (D)

Department of Orthopaedic Surgery, University of California, Irvine, California, USA.

Tom Minas (T)

Cartilage Repair Center, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts, USA.

James L Carey (JL)

McKay Orthopaedic Research Laboratory, University of Pennsylvania, Philadelphia, Pennsylvania, USA.

Heng An Lin (HA)

Department of Orthopaedic Surgery, Sengkang General Hospital, Singapore.

Keng Lin Wong (KL)

Yong Loo Lin School of Medicine, National University of Singapore, Singapore.
Department of Orthopaedic Surgery, Sengkang General Hospital, Singapore.
Musculoskeletal Sciences Academic Clinical Programme, Duke-NUS Graduate Medical School, Singapore.

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Classifications MeSH