Evidence map›Paper›PMID 33331973›Full record

ArticleKnee surgery, sports traumatology, arthroscopy : official journal of the ESSKA2021

Mesenchymal stromal cells and platelet-rich plasma promote tendon allograft healing in ovine anterior cruciate ligament reconstruction.

Adam T Hexter, Anita Sanghani-Kerai, Nima Heidari, Deepak M Kalaskar, Ashleigh Boyd, Catherine Pendegrass, Scott A Rodeo, Fares S Haddad, Gordon W Blunn

Open access · hybridAbstract read
In one paragraph

Article in Knee surgery, sports traumatology, arthroscopy : official journal of the ESSKA, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
2.2field-weighted citation impact, top 11% of its field
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

7 citing papers in PubMed, 14 citations in OpenAlex.

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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

9 authors at 6 institutions in 2 countries.

Adam T HexterDivision of Surgery and Interventional Science, University College London (UCL), London, UK. a.hexter@ucl.ac.uk.ORCID http://orcid.org/0000-0002-0478-7811
Anita Sanghani-KeraiDivision of Surgery and Interventional Science, University College London (UCL), London, UK.
Nima HeidariRoyal London Hospital and Orthopaedic Specialists (OS), London, UK.
Deepak M KalaskarDivision of Surgery and Interventional Science, University College London (UCL), London, UK.
Ashleigh BoydDivision of Surgery and Interventional Science, University College London (UCL), London, UK.
Catherine PendegrassDivision of Surgery and Interventional Science, University College London (UCL), London, UK.
Scott A RodeoHospital of Special Surgery (HSS), New York, USA.
Fares S HaddadUniversity College London Hospitals, London, UK.
Gordon W BlunnUniversity of Portsmouth, Portsmouth, UK.
University College London · GBHospital for Special Surgery · USRoyal London Hospital · GBRoyal National Orthopaedic Hospital · GBUniversity College Hospital · GBUniversity of Portsmouth · GB

Funding

Biotechnology Institute (BTI) Project grantRoyal College of Surgeons of England Surgical Research Fellowship
6 · The paper itself

Abstract

purposeThe effect of bone marrow mesenchymal stromal cells (BMSCs) and platelet-rich plasma (PRP) on tendon allograft maturation in a large animal anterior cruciate ligament (ACL) reconstruction model was reported for the first time. It was hypothesised that compared with non-augmented ACL reconstruction, BMSCs and PRP would enhance graft maturation after 12 weeks and this would be detected using magnetic resonance imaging (MRI).

methodsFifteen sheep underwent unilateral tendon allograft ACL reconstruction using aperture fixation and were randomised into three groups (n = 5). Group 1 received 10 million allogeneic BMSCs in 2 ml fibrin sealant; Group 2 received 12 ml PRP in a plasma clot injected into the graft and bone tunnels; and Group 3 (control) received no adjunctive treatment. At autopsy at 12 weeks, a graft maturation score was determined by the sum for graft integrity, synovial coverage and vascularisation, graft thickness and apparent tension, and synovial sealing at tunnel apertures. MRI analysis (n = 2 animals per group) of the signal-noise quotient (SNQ) and fibrous interzone (FIZ) was used to evaluate intra-articular graft maturation and tendon-bone healing, respectively. Spearman's rank correlation coefficient (r) of SNQ, autopsy graft maturation score and bone tunnel diameter were analysed.

resultsThe BMSC group (p = 0.01) and PRP group (p = 0.03) had a significantly higher graft maturation score compared with the control group. The BMSC group scored significantly higher for synovial sealing at tunnel apertures (p = 0.03) compared with the control group. The graft maturation score at autopsy significantly correlated with the SNQ (r = - 0.83, p < 0.01). The tunnel diameter of the femoral tunnel at the aperture (r = 0.883, p = 0.03) and mid-portion (r = 0.941, p = 0.02) positively correlated with the SNQ.

conclusionsBMSCs and PRP significantly enhanced graft maturation, which indicates that orthobiologics can accelerate the biologic events in tendon allograft incorporation. Femoral tunnel expansion significantly correlated with inferior maturation of the intra-articular graft. The clinical relevance of this study is that BMSCs and PRP enhance allograft healing in a translational model, and biological modulation of graft healing can be evaluated non-invasively using MRI.

Indexed as

Anterior Cruciate Ligament InjuriesAnterior Cruciate Ligament ReconstructionMesenchymal Stem CellsPlatelet-Rich PlasmaAllograftsAnimalsAnterior Cruciate LigamentSheepTendonsAnterior cruciate ligament (ACL) reconstructionAutopsyBiological modulationBone marrow-derived mesenchymal stromal cells (BMSCs)Magnetic resonance imaging (MRI)Platelet-rich plasma (PRP)

Identifiers

PMID33331973
PMCPMC8514355
OpenAlexW3110814292

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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.