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Journal of Orthopaedics and Traumatology : Official Journal of the Italian Society of Orthopaedics and Traumatology logoLink to Journal of Orthopaedics and Traumatology : Official Journal of the Italian Society of Orthopaedics and Traumatology
. 2021 Oct 6;22:39. doi: 10.1186/s10195-021-00603-w

Reliability of the MOCART score: a systematic review

Filippo Migliorini 1,, Nicola Maffulli 2,3,4, Jörg Eschweiler 1, Arne Driessen 1, Markus Tingart 1, Alice Baroncini 1
PMCID: PMC8494868  PMID: 34613499

Abstract

Background

The present systematic review analysed the available literature to assess reliability of the Magnetic Resonance Observation of Cartilage Repair Tissue (MOCART) score in the evaluation of knee and ankle osteochondral lesions.

Methods

All the studies using the MOCART score for knee and/or talus chondral defects were accessed in March 2021. A multivariate analysis was performed to assess associations between the MOCART score at last follow-up and data of patients at baseline, clinical scores and complications. A multiple linear model regression analysis was used.

Results

The MOCART score evidenced no association with patient age (P = 0.6), sex (P = 0.1), body mass index (P = 0.06), defect size (P = 0.9), prior length of symptoms (P = 0.9) or visual analogue scale (P = 0.07). For chondral defects of the knee, no statistically significant association was found between the MOCART score and the International Knee Documentation Committee (P = 0.9) and with the Lysholm Knee Scoring Scales (P = 0.2), Tegner Activity Scale (P = 0.2), visual analogue scale P = 0.07), rate of failure (P = 0.2) and revision (P = 0.9). For chondral defect of the talus, no statistically significant associations were found between the MOCART score and the American Orthopedic Foot and Ankle Score (P = 0.3), Tegner Activity Scale (P = 0.4), visual analogue scale (P = 0.1), rate of failure (P = 0.1) and revision (P = 0.7).

Conclusion

The MOCART score demonstrated no association with patient characteristics and with the surgical outcome in patients who underwent surgical management for knee and talus chondral defects.

Level of evidence

Level IV.

Keywords: Chondral defect, Knee, Talus, MOCART

Introduction

Acute injuries, repeated strains or joint instability can produce osteochondral lesions (OL), with damage to the hyaline cartilage of the joint and to the subchondral bone [1, 2]. Typically, these lesions lead to a decrease in daily activities from pain on weight bearing and exercise [3]. Several surgical techniques are available for the operative management of OL of the knee and ankle: it necessary to have reliable evaluation tools to compare the outcomes of the different techniques and offer clinically meaningful feedback to patients. Arthroscopy remains the gold standard for the evaluation of the cartilage after treatment [4], but non-invasive follow-up methods are required for post-operative assessment. Plain radiography and computed tomography are inadequate for the analysis of cartilage layers, and the ionizing radiations required are of concern [5]. Magnetic resonance imaging (MRI), on the other hand, allows a detailed analysis of the cartilage and does not require ionizing radiation [6], and has thus become a widespread tool for post-operative evaluation of the outcome of OL [7]. To assess and quantify possible changes after treatment, Marlovits and colleagues introduced the Magnetic Resonance Observation of Cartilage Repair Tissue (MOCART) score [8]. However, its role in the evaluation of the treated cartilage and its clinical value are still debated [1, 2, 9, 10]. The MOCART Score analyses different MRI variables that should correlate with the success of the operative management of OL lesions. These include degree of repair and filling of the OL, integration to border zone, surface, structure and signal intensity of the repair tissue, aspect of the subchondral lamina and bone and presence of adhesions or effusion (CIT).

The present systematic review analysed the available literature regarding the use of the MOCART score in the evaluation of osteochondral lesions of the knee and ankle. We wished to ascertain possible associations between the MOCART and other evaluation tools, which would highlight the association of the MOCART score with clinical outcomes, and support the use of this score for clinical use.

Methods

Search strategy

This systematic review was conducted according to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses: the PRISMA statement [11]. The PICO framework was followed:

  • P (Problem): knee and talus chondral defect;

  • I (Intervention): surgical management;

  • C (Control): MOCART score at last follow-up;

  • O (Outcomes): clinical scores and complications.

Data source

The literature search was conducted independently by two authors (**;**). In June 2021, the following databases were accessed: PubMed, Google scholar, Embase and Scopus with no time constrains. The following keywords were used in combination using the Boolean operators AND/OR: chondral, cartilage, articular, damage, defect, injury, chondropathy, knee, pain, matrix-induced, periosteal, periosteum, collagen, autologous, chondrocyte, transplantation, implantation, MFX, microfractures, mosaicplasty, mACI, cACI, pACI, AMIC, OAT, osteochondral transplantation, allograft, autograft, membrane, therapy, management, surgery, outcomes, revision, hypertrophy, failure. The resulting articles were screened by the same authors. The full text of the articles of interest were accessed. The bibliography of the full-text articles was also screened. Disagreements were debated and solved by a third author (**).

Eligibility criteria

All the studies using the MOCART score for knee and/or talus chondral defects were accessed. Given the authors language abilities, articles in English, German, Italian, French and Spanish were eligible. Studies with level I–IV of evidence, according to Oxford Centre of Evidence-Based Medicine [12], were considered. Studies which reported data on patients with end-stage joint degeneration were not considered. Abstracts, reviews, comments, editorials and opinions were non considered. Animals, biomechanics or in vitro studies were not considered. Only studies which clearly stated the nature of the surgical intervention were included. Only articles reporting quantitative data under the outcomes of interest were considered for inclusion. Missing data under the outcomes of interest warranted the exclusion from this study.

Data extraction

Data extraction was performed separately by two authors (**;**). Data concerning author, year, journal, type of study and length of the follow-up was extracted. Data of the MOCART score at last follow-up was collected. The following data at baseline was collected: number of samples with related mean body mass index (BMI) and age, duration of symptoms, percentage of female, size of the defect. Data concerning the following scores at last follow-up were retrieved according to their localisation (knee and talus): visual analogue scale (VAS), American Orthopedic Foot and Ankle Score (AOFAS) [13], Tegner Activity Scale [14], Lysholm Knee Scoring Scale [15], and International Knee Documentation Committee (IKDC) [16] scores. Data on complications (rate of hypertrophy, failure and revision) were also retrieved.

Methodology quality assessment

The methodological quality assessment was performed by two independent authors (**;**). The risk of bias graph tool of the Review Manager Software (The Nordic Cochrane Collaboration, Copenhagen) was used. The following risk of bias were evaluated: selection, detection, attrition and other source of bias.

Statistical analyses

All statistical analyses were performed by one author (F.M.) using the software STATA/MP 14.1 (StataCorp, College Station, TX). The Shapiro–Wilk test was performed to investigate data distribution. For normal data, mean and standard deviation were calculated. For non-parametric data, median and interquartile range were calculated. The Student t-test was used to assess significance for parametric data, while the Mann–Whitney U-test for non-parametric variables. Values of P < 0.05 considered statistically significant. A multivariate analysis was performed to assess associations between the values of the MOCART score at last follow-up and data of patients at baseline, clinical scores at last follow-up and the rate of complications. A multiple linear model regression analysis through the Pearson product-moment correlation coefficient (r) was used. The Cauchy–Schwarz formula was used for inequality: +1 is considered as positive linear correlation, while −1 is considered a negative one. Values of 0.1 < |r| < 0.3, 0.3 < |r| < 0.5, and |r| > 0.5 were considered to have weak, moderate and strong correlation, respectively. The overall significance was performed through the χ2 test, with values of P < 0.05 considered statistically significant.

Results

Search result

The literature search identified 688 articles. Of them, 207 were duplicates. A further 481 articles were excluded as they did not match the eligibility criteria: not reporting data over the MOCART score (N = 301), not focusing on knee or ankle (N = 22), study design (N = 92), not reporting quantitative data under the outcomes of interest (N = 21), other (N = 9), language limitations (N = 2). This left 34 articles for the present study. The literature search results are shown in Fig. 1.

Fig. 1.

Fig. 1

Flow chart of the literature search

Methodological quality assessment

Given the limited number of randomised clinical studies (2 of 34) and the great number of retrospective studies (21 of 34), the risk of selection bias was moderate. The risk of detection bias was high, since most of studies lacked of blinding. The risk of attrition and reporting bias were estimated as moderate, as was the risk of other bias. In conclusion, the overall review authors’ judgements about each risk of bias item scored moderate, attesting to this study fair methodological assessment. The risk of bias graph is shown in Fig. 2.

Fig. 2.

Fig. 2

Methodological quality assessment

Patient demographics

Data from 1017 procedures were retrieved. The mean duration of symptoms before the index surgery was 30.1 ± 17.7 months. Forty percent (407 of 1017) were women. The mean age of the patients was 34.6 ± 6.1 years, the mean BMI was 25.7 ± 1.7 kg/m2. The mean defect size was 2.8 ± 2 cm2. The median follow-up was 37.1 (24 to 59.9) months. Generalities and demographic of the study are presented in Table 1.

Table 1.

Generalities and patients baseline of the included studies

Author, year Journal Design Follow-up (months) Place Type of treatment Procedures (n) Female (%) Mean age
Albano et al. 2017 [21] BMC Musculos Dis Retrospective 30.0 Talus AMIC 16 50.0 42.6
Anders et al. 2012 [22] Int Orthop Prospective 63.5 Talus MACI 22 22.7 23.9
Apprich et al. 2012 [23] Osteoarthritis Cartilage Retrospective 48.0 Talus MACT 10 60.0 31.0
59.6 Talus MFX 10 40.0 32.4
Astur et al. 2018 [24] Rev Bras Orthop Prospective 12.0 Knee AMIC 7 14.3 37.2
Aurich et al. 2010 [25] Am J Sports Med Retrospective 24.5 Talus MACI 19 27.8 29.2
Baumfeld et al. 2018 [26] Foot Retrospective 10.8 Talus AMIC 17 47.1 37.5
Becher et al. 2015 [27] Arch Orthop Trauma Surg Prospective 21.0 Knee MFX 5 40.0 27.0
DeSandis et al. 2018 [28] J Foot Ankle Surg Retrospective 16.7 Talus Allo-transplantation 46 54.4 37.6
Dhollander et al. 2012 [29] Knee Surg Sports Traumatol Arthrosc Prospective 36.0 Knee cACI 32 31.0 30.0
Di Cave et al. 2017 [30] The Foot Retrospective 90.0 Talus Scaffold 12 25.0 38.6
Galla et al. 2018 [31] Knee Surg Sports Traumatol Arthrosc Retrospective 33.5 Talus AMIC 23 34.8 35.6
Gottschalk et al. 2017 [32] J Foot Ankle Surg Retrospective 60.0 Talus AMIC 21 38.1 37.0
Halem et al. 2014 [33] Am J Sports Med Retrospective 93.0 Talus OAT 14 50.0 42.8
85.3 Talus OAT 28 39.3 44.1
Hoburg et al. 2019 [34] Orthop J Sports Med Prospective 63.0 Knee mACI 29 48.0 16.0
48.0 Knee mACI 42 29.0 27.0
Karnovski et al. 2018 [35] Foot Ankle Int Retrospective 38.2 Talus MFX 30 50.0 37.7
19.4 Talus Allo- transplantation 20 65.0 36.6
Koh et al. 2016 [36] Arthroscopy Prospective, Randomised 27.0 Knee MFX 40 65.0 38.0
Knee MFX 40 60.0 39.0
Kubosch et al. 2015 [9] Int Orthop Retrospective 39.5 Talus AMIC 17 47.1 38.8
Magnan et al. 2012 [37] Advance Orthop Retrospective 45.0 Talus MACI 30 50.0 28.9
Marlovits et al. 2012 [38] Am J Sports Med Prospective 60.0 Knee mACI 24 12.0 35.0
Niemeyer et al. 2013 [39] Am J Sports Med Prospective 131.0 Knee pACI 70 64.0 33.0
Ogura et al. 2019 [40] Orthop J Sports Med Prospective 24.0 Knee pACI, cACI 15 20.0 31.0
Perdisa et al. 2017 [41] Am J Sports Med Prospective 24.0 Knee Scaffold 34 47.0 30.0
Quirbach et al. 2009 [42] Skeletal Radiol Retrospective 19.8 Talus MACT 12 33.3 32.8
Rosa et al. 2015 [43] J Orthop Traumatol Retrospective 148.0 Knee pACI 15 40.0 21.0
Sadlik et al. 2017 [44] Foot Ankle Surg Retrospective 46.4 Talus OAT 10 40.0 37.0
Schneider et al. 2016 [45] J Orthop Surg Prospective, Randomised 12.0 Knee MFX 13 50.0 47.0
Knee MFX 4 50.0 37.0
Schüttler et al. 2019 [46] Arch Orthop Trauma Surg Prospective 60.0 Knee mACI 23 34.0
Siebold et al. 2018 [47] Knee Surg Sports Traumatol Arthrosc Prospective 34.8 Knee mACI 30 36.0 36.0
Shimozono et al. 2018 [48] Am J Sports Med Retrospective 52.0 Talus OAT 63 42.9 36.0
45.0 Talus OAT 31 32.3 34.0
Shimozono et al. 2018 [49] Bone Joint Surg Retrospective 26.3 Talus OAT 25 64.0 38.4
22.3 Talus OAT 16 37.5 43.6
Usuelli et al. 2018 [50] Knee Surg Sports Traumatol Arthrosc Retrospective 24.0 Talus AMIC 20 45.0 36.1
Valderrabano et al. 2013 [51] Am J Sports Med Retrospective 30.9 Talus AMIC 26 30.8 34.6
Weigelt et al. 2019 [52] Am J Sports Med Retrospective 56.4 Talus AMIC 33 4.2 35.1
Wiewiorski et al. 2013 [53] Clin Radiology Retrospective 23.3 Talus AMIC 23 30.4 34.2

Outcomes of interest

The MOCART score at last follow-up evidenced no association with patients’ age (P = 0.6), sex (P = 0.1), BMI (P = 0.06), defect size (P = 0.9) or prior length of symptoms (P = 0.9). For chondral defects of the knee, no association was found between the MOCART score and IKDC (P = 0.9), the Lysholm Knee Scoring Scale (P = 0.2), Tegner Activity Scale (P = 0.2), VAS (P = 0.07), rate of failure (P = 0.2) and revision (P = 0.9). For chondral defect of the talus, no significant associations were found between the MOCART score and the AOFAS (P = 0.3), Tegner Activity Scale (P = 0.4), VAS (P = 0.1), rate of failure (P = 0.1) and revision (P = 0.7) (Table 2).

Table 2.

Overall results of the analyses

Endpoint r P
Patient characteristics
 Sex −0.22 0.1
 Mean age 0.08 0.6
 BMI −0.54 0.06
 Defect size (cm2) −0.02 0.9
 Prior symptoms (months) −0.01 0.9
Knee chondral defects
 VAS −0.45 0.07
 Tegner −0.55 0.2
 Lysholm −0.71 0.2
 IKD 0.00 0.9
 Rate of failure −0.30 0.2
 Rate of revision 0.01 0.9
Talus chondral defects
 VAS −0.33 0.1
 Tegner −0.24 0.4
 AOFAS 0.29 0.3
 Rate of failure −0.44 0.1
 Rate of revision 0.10 0.7

Discussion

According to the main findings of this systematic review, the MOCART score showed no evidence of a statistically significant association with patient characteristics and surgical outcome in patients who underwent surgical management for knee and talus OL.

The MOCART score did not correlate with any of the other considered scores, namely VAS, AOFAS, IKD, Tegner and Lysholm. This finding corroborates the hypothesis that the MOCART is not a reliable tool for clinical assessment in the setting of osteochondral lesions of the knee and talus, as it does not reflect or associates to any other clinical finding. Similar results were obtained by Casari et al., who did not observe correlations between the MOCART score and other variables such as age, AOFAS score and Tegner score in patients with OL of the talus [2]. While a correlation between VAS and/or the knee injury and osteoarthritis outcome score (KOOS) and different items of the MOCART score was observed in a previous study [17], in particular ‘filling the defect’, ‘structure’ and ‘subchondral bone’ [17], no evaluation of the MOCART score as a whole and VAS or KOOS was performed in that study. In addition, the overall MOCART score was not associated with the trabecular bone parameters in the injured and contralateral knee [18].

Notably, we did not observe any association between the MOCART score and the rate of failure and revision. This finding suggests that the MOCART score does not have a prognostic value in the assessment of the outcomes of surgical management of OL in the knee and talus. Also, the MOCART score did not have sufficient inter-rater reproducibility to allow reliable and univocal use in clinical practice [1].

Three modified versions of the MOCART score are presently available, namely the MOCART 2.0 [19], the modified MOCART [20] and the MOCART 3D [10]. The modified MOCART showed inhomogeneous inter-class correlation coefficients, and no strong correlation could be established between the score and the arthroscopic findings in OL of the talus [20]. The MOCART 2.0 also did not show any association with clinical parameters [2]. On the other hand, however, many items of the MOCART and MOCART 3D showed good correlations with histological scoring systems [10]. Given these limitations, it is difficult to interpret the lack of relationship between age, sex, BMI and defect size and the MOCART score. One possible key is that the MOCART score is not influenced by these factors, or that age, sex and BMI do not influence the extent of OL lesions. The available data do not allow clarification of this issue.

Overall, the question arises whether MRI is a reliable enough tool to assess chondral damage and to follow-up OL treatment, or whether the MOCART score is not a powerful enough tool to allow association of imaging and clinical data. Numerous studies support the use of MRI when following patients with OL of the knee and of the talus. MRI changes of the chondral surface correlate with the structure of the underlying trabecular bone [18], and the combination of clinical parameters with specific MR imaging acquisition represents a promising tool in the follow-up of OL treatment [4, 10]. These findings, combined with the findings of a present study, support the hypothesis that the MOCART score, more than the MRI itself, is not a reliable tool in the follow-up of patients who underwent surgical treatment of OL lesions. However, strong evidence supporting the use of MRI as gold standard in the assessment of OL and its treatment is still lacking [7].

This study does not come without limitations. First, only the evaluation of the MOCART score and not of its successive implementation was possible given the lack of data available for the analysis. Although several studies focused on the management of chondral defects of the knee and talus, relevant quantitative data available for inclusion and analysis were limited. The lack of RCTs also represent an inevitable bias in the interpretation of the results.

Conclusion

The MOCART score demonstrated no association with patient characteristics and surgical outcome in patients who underwent surgical management for chondral defects of the knee and talus.

Acknowledgements

None.

Abbreviations

MOCART

Magnetic Resonance Observation of Cartilage Repair Tissue

VAS

Visual analogue scale

OL

Osteochondral lesions

MRI

Magnetic resonance imaging

PRISMA

Preferred Reporting Items for Systematic Reviews and Meta-Analyses

AOFAS

American Orthopedic Foot and Ankle Score

IKDC

International Knee Documentation Committee

BMI

Body mass index

Authors’ contributions

F.M.: conception and design of the study, literature search, data extraction, methodological quality assessment, writing, analysis, interpretation of data and final approval; A.B.: literature search, data extraction, methodological quality assessment, writing and final approval; N.M.: revision and final approval; J.E., M.T.: supervision and final approval. All authors read and approved the final manuscript.

Funding

Open Access funding enabled and organized by Projekt DEAL. No external source of funding was used.

Availability of data and materials

The data underlying this article are available in the article and in its online supplementary material.

Declarations

Ethics approval consent to participate

Not applicable.

Consent for publication

Not applicable.

Competing interests

The authors declare that they have no conflict of interest.

Footnotes

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

References

  • 1.Albano D, Martinelli N, Bianchi A, Giacalone A, Sconfienza LM. Evaluation of reproducibility of the MOCART score in patients with osteochondral lesions of the talus repaired using the autologous matrix-induced chondrogenesis technique. Radiol Med. 2017;122:909–917. doi: 10.1007/s11547-017-0794-y. [DOI] [PubMed] [Google Scholar]
  • 2.Casari FA, Germann C, Weigelt L, Wirth S, Viehofer A, Ackermann J. The role of magnetic resonance imaging in autologous matrix-induced chondrogenesis for osteochondral lesions of the talus: analyzing MOCART 1 and 2.0. Cartilage 2020: 1947603520946382. [DOI] [PMC free article] [PubMed]
  • 3.van Dijk CN, Reilingh ML, Zengerink M, van Bergen CJ. Osteochondral defects in the ankle: why painful? Knee Surg Sports Traumatol Arthrosc. 2010;18:570–580. doi: 10.1007/s00167-010-1064-x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4.Liu YW, Tran MD, Skalski MR, Patel DB, White EA, Tomasian A, et al. MR imaging of cartilage repair surgery of the knee. Clin Imaging. 2019;58:129–139. doi: 10.1016/j.clinimag.2019.07.004. [DOI] [PubMed] [Google Scholar]
  • 5.Schuman L, Struijs PA, van Dijk CN. Arthroscopic treatment for osteochondral defects of the talus. Results at follow-up at 2 to 11 years. J Bone Joint Surg Br. 2002;84:364–368. doi: 10.1302/0301-620X.84B3.0840364. [DOI] [PubMed] [Google Scholar]
  • 6.Recht M, White LM, Winalski CS, Miniaci A, Minas T, Parker RD. MR imaging of cartilage repair procedures. Skeletal Radiol. 2003;32:185–200. doi: 10.1007/s00256-003-0631-3. [DOI] [PubMed] [Google Scholar]
  • 7.de Windt TS, Welsch GH, Brittberg M, Vonk LA, Marlovits S, Trattnig S, et al. Is magnetic resonance imaging reliable in predicting clinical outcome after articular cartilage repair of the knee? A systematic review and meta-analysis. Am J Sports Med. 2013;41:1695–1702. doi: 10.1177/0363546512473258. [DOI] [PubMed] [Google Scholar]
  • 8.Marlovits S, Striessnig G, Resinger CT, Aldrian SM, Vecsei V, Imhof H, et al. Definition of pertinent parameters for the evaluation of articular cartilage repair tissue with high-resolution magnetic resonance imaging. Eur J Radiol. 2004;52:310–319. doi: 10.1016/j.ejrad.2004.03.014. [DOI] [PubMed] [Google Scholar]
  • 9.Kubosch EJ, Erdle B, Izadpanah K, Kubosch D, Uhl M, Sudkamp NP, et al. Clinical outcome and T2 assessment following autologous matrix-induced chondrogenesis in osteochondral lesions of the talus. Int Orthop. 2016;40:65–71. doi: 10.1007/s00264-015-2988-z. [DOI] [PubMed] [Google Scholar]
  • 10.Goebel L, Zurakowski D, Muller A, Pape D, Cucchiarini M, Madry H. 2D and 3D MOCART scoring systems assessed by 9.4 T high-field MRI correlate with elementary and complex histological scoring systems in a translational model of osteochondral repair. Osteoarthr Cartil. 2014;22:1386–1395. doi: 10.1016/j.joca.2014.05.027. [DOI] [PubMed] [Google Scholar]
  • 11.Moher D, Liberati A, Tetzlaff J, Altman DG, Group P. Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement. BMJ. 2009;339:b2535. doi: 10.1136/bmj.b2535. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 12.Howick J CI, Glasziou P, Greenhalgh T, Carl Heneghan, Liberati A, Moschetti I, Phillips B, Thornton H, Goddard O, Hodgkinson M. The 2011 Oxford CEBM Levels of Evidence. Oxford Centre for Evidence-Based Medicine. https://www.cebm.net/index.aspx?o=5653 2011.
  • 13.Kitaoka HB, Alexander IJ, Adelaar RS, Nunley JA, Myerson MS, Sanders M. Clinical rating systems for the ankle-hindfoot, midfoot, hallux, and lesser toes. Foot Ankle Int. 1994;15:349–353. doi: 10.1177/107110079401500701. [DOI] [PubMed] [Google Scholar]
  • 14.Briggs KK, Lysholm J, Tegner Y, Rodkey WG, Kocher MS, Steadman JR. The reliability, validity, and responsiveness of the Lysholm score and Tegner activity scale for anterior cruciate ligament injuries of the knee: 25 years later. Am J Sports Med. 2009;37:890–897. doi: 10.1177/0363546508330143. [DOI] [PubMed] [Google Scholar]
  • 15.Lysholm J, Gillquist J. Evaluation of knee ligament surgery results with special emphasis on use of a scoring scale. Am J Sports Med. 1982;10:150–154. doi: 10.1177/036354658201000306. [DOI] [PubMed] [Google Scholar]
  • 16.Higgins LD, Taylor MK, Park D, Ghodadra N, Marchant M, Pietrobon R, et al. Reliability and validity of the International Knee Documentation Committee (IKDC) Subjective Knee Form. Joint Bone Spine. 2007;74:594–599. doi: 10.1016/j.jbspin.2007.01.036. [DOI] [PubMed] [Google Scholar]
  • 17.Marlovits S, Singer P, Zeller P, Mandl I, Haller J, Trattnig S. Magnetic resonance observation of cartilage repair tissue (MOCART) for the evaluation of autologous chondrocyte transplantation: determination of interobserver variability and correlation to clinical outcome after 2 years. Eur J Radiol. 2006;57:16–23. doi: 10.1016/j.ejrad.2005.08.007. [DOI] [PubMed] [Google Scholar]
  • 18.Gersing AS, Feuerriegel G, Holwein C, Suchowierski J, Karampinos DC, Haller B, et al. T2-relaxation time of cartilage repair tissue is associated with bone remodeling after spongiosa-augmented matrix-associated autologous chondrocyte implantation. Osteoarthr Cartil. 2019;27:90–98. doi: 10.1016/j.joca.2018.08.023. [DOI] [PubMed] [Google Scholar]
  • 19.Schreiner MM, Raudner M, Marlovits S, Bohndorf K, Weber M, Zalaudek M, et al. The MOCART (Magnetic Resonance Observation of Cartilage Repair Tissue) 2.0 Knee Score and Atlas. Cartilage 2019: 1947603519865308. [DOI] [PMC free article] [PubMed]
  • 20.Lee KT, Choi YS, Lee YK, Cha SD, Koo HM. Comparison of MRI and arthroscopy in modified MOCART scoring system after autologous chondrocyte implantation for osteochondral lesion of the talus. Orthopedics. 2011;34:e356–362. doi: 10.3928/01477447-20110627-10. [DOI] [PubMed] [Google Scholar]
  • 21.Albano D, Martinelli N, Bianchi A, Messina C, Malerba F, Sconfienza LM. Clinical and imaging outcome of osteochondral lesions of the talus treated using autologous matrix-induced chondrogenesis technique with a biomimetic scaffold. BMC Musculoskelet Disord. 2017;18:306. doi: 10.1186/s12891-017-1679-x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 22.Anders S, Goetz J, Schubert T, Grifka J, Schaumburger J. Treatment of deep articular talus lesions by matrix associated autologous chondrocyte implantation–results at five years. Int Orthop. 2012;36:2279–2285. doi: 10.1007/s00264-012-1635-1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 23.Apprich S, Trattnig S, Welsch GH, Noebauer-Huhmann IM, Sokolowski M, Hirschfeld C, et al. Assessment of articular cartilage repair tissue after matrix-associated autologous chondrocyte transplantation or the microfracture technique in the ankle joint using diffusion-weighted imaging at 3 Tesla. Osteoarthr Cartil. 2012;20:703–711. doi: 10.1016/j.joca.2012.03.008. [DOI] [PubMed] [Google Scholar]
  • 24.Astur DC, Lopes JC, Santos MA, Kaleka CC, Amaro JT, Cohen M. Surgical treatment of chondral knee defects using a collagen membrane—autologus matrix-induced chondrogenesis. Rev Bras Ortop. 2018;53:733–739. doi: 10.1016/j.rbo.2017.06.019. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 25.Aurich M, Bedi HS, Smith PJ, Rolauffs B, Muckley T, Clayton J, et al. Arthroscopic treatment of osteochondral lesions of the ankle with matrix-associated chondrocyte implantation: early clinical and magnetic resonance imaging results. Am J Sports Med. 2011;39:311–319. doi: 10.1177/0363546510381575. [DOI] [PubMed] [Google Scholar]
  • 26.Baumfeld T, Baumfeld D, Prado M, Nery C. All-arthroscopic AMIC((R)) (AT-AMIC) for the treatment of talar osteochondral defects: a short follow-up case series. Foot. 2018;37:23–27. doi: 10.1016/j.foot.2018.07.006. [DOI] [PubMed] [Google Scholar]
  • 27.Becher C, Ettinger M, Ezechieli M, Kaps C, Ewig M, Smith T. Repair of retropatellar cartilage defects in the knee with microfracture and a cell-free polymer-based implant. Arch Orthop Trauma Surg. 2015;135:1003–1010. doi: 10.1007/s00402-015-2235-5. [DOI] [PubMed] [Google Scholar]
  • 28.DeSandis BA, Haleem AM, Sofka CM, O'Malley MJ, Drakos MC. Arthroscopic treatment of osteochondral lesions of the talus using juvenile articular cartilage allograft and autologous bone marrow aspirate concentration. J Foot Ankle Surg. 2018;57:273–280. doi: 10.1053/j.jfas.2017.09.009. [DOI] [PubMed] [Google Scholar]
  • 29.Dhollander AA, Verdonk PC, Lambrecht S, Verdonk R, Elewaut D, Verbruggen G, et al. Short-term outcome of the second generation characterized chondrocyte implantation for the treatment of cartilage lesions in the knee. Knee Surg Sports Traumatol Arthrosc. 2012;20:1118–1127. doi: 10.1007/s00167-011-1759-7. [DOI] [PubMed] [Google Scholar]
  • 30.Di Cave E, Versari P, Sciarretta F, Luzon D, Marcellini L. Biphasic bioresorbable scaffold (TruFit Plug((R))) for the treatment of osteochondral lesions of talus: 6- to 8-year follow-up. Foot. 2017;33:48–52. doi: 10.1016/j.foot.2017.05.005. [DOI] [PubMed] [Google Scholar]
  • 31.Galla M, Duensing I, Kahn TL, Barg A. Open reconstruction with autologous spongiosa grafts and matrix-induced chondrogenesis for osteochondral lesions of the talus can be performed without medial malleolar osteotomy. Knee Surg Sports Traumatol Arthrosc. 2019;27:2789–2795. doi: 10.1007/s00167-018-5063-7. [DOI] [PubMed] [Google Scholar]
  • 32.Gottschalk O, Altenberger S, Baumbach S, Kriegelstein S, Dreyer F, Mehlhorn A, et al. Functional medium-term results after autologous matrix-induced chondrogenesis for osteochondral lesions of the talus: a 5-year prospective cohort study. J Foot Ankle Surg. 2017;56:930–936. doi: 10.1053/j.jfas.2017.05.002. [DOI] [PubMed] [Google Scholar]
  • 33.Haleem AM, Ross KA, Smyth NA, Duke GL, Deyer TW, Do HT, et al. Double-plug autologous osteochondral transplantation shows equal functional outcomes compared with single-plug procedures in lesions of the talar dome: a minimum 5-year clinical follow-up. Am J Sports Med. 2014;42:1888–1895. doi: 10.1177/0363546514535068. [DOI] [PubMed] [Google Scholar]
  • 34.Hoburg A, Loer I, Korsmeier K, Siebold R, Niemeyer P, Fickert S, et al. Matrix-associated autologous chondrocyte implantation is an effective treatment at midterm follow-up in adolescents and young adults. Orthop J Sports Med. 2019;7:2325967119841077. doi: 10.1177/2325967119841077. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 35.Karnovsky SC, DeSandis B, Haleem AM, Sofka CM, O'Malley M, Drakos MC. Comparison of juvenile allogenous articular cartilage and bone marrow aspirate concentrate versus microfracture with and without bone marrow aspirate concentrate in arthroscopic treatment of talar osteochondral lesions. Foot Ankle Int. 2018;39:393–405. doi: 10.1177/1071100717746627. [DOI] [PubMed] [Google Scholar]
  • 36.Koh YG, Kwon OR, Kim YS, Choi YJ, Tak DH. Adipose-derived mesenchymal stem cells with microfracture versus microfracture alone: 2-year follow-up of a prospective randomized trial. Arthroscopy. 2016;32:97–109. doi: 10.1016/j.arthro.2015.09.010. [DOI] [PubMed] [Google Scholar]
  • 37.Magnan B, Samaila E, Bondi M, Vecchini E, Micheloni GM, Bartolozzi P. Three-dimensional matrix-induced autologous chondrocytes implantation for osteochondral lesions of the talus: midterm results. Adv Orthop. 2012;2012:942174. doi: 10.1155/2012/942174. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 38.Marlovits S, Aldrian S, Wondrasch B, Zak L, Albrecht C, Welsch G, et al. Clinical and radiological outcomes 5 years after matrix-induced autologous chondrocyte implantation in patients with symptomatic, traumatic chondral defects. Am J Sports Med. 2012;40:2273–2280. doi: 10.1177/0363546512457008. [DOI] [PubMed] [Google Scholar]
  • 39.Niemeyer P, Porichis S, Steinwachs M, Erggelet C, Kreuz PC, Schmal H, et al. Long-term outcomes after first-generation autologous chondrocyte implantation for cartilage defects of the knee. Am J Sports Med. 2014;42:150–157. doi: 10.1177/0363546513506593. [DOI] [PubMed] [Google Scholar]
  • 40.Ogura T, Merkely G, Bryant T, Winalski CS, Minas T. Autologous chondrocyte implantation "segmental-sandwich" technique for deep osteochondral defects in the knee: clinical outcomes and correlation with magnetic resonance imaging findings. Orthop J Sports Med. 2019;7:2325967119847173. doi: 10.1177/2325967119847173. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 41.Perdisa F, Filardo G, Sessa A, Busacca M, Zaffagnini S, Marcacci M, et al. One-step treatment for patellar cartilage defects with a cell-free osteochondral scaffold: a prospective clinical and MRI evaluation. Am J Sports Med. 2017;45:1581–1588. doi: 10.1177/0363546517694159. [DOI] [PubMed] [Google Scholar]
  • 42.Quirbach S, Trattnig S, Marlovits S, Zimmermann V, Domayer S, Dorotka R, et al. Initial results of in vivo high-resolution morphological and biochemical cartilage imaging of patients after matrix-associated autologous chondrocyte transplantation (MACT) of the ankle. Skeletal Radiol. 2009;38:751–760. doi: 10.1007/s00256-009-0682-1. [DOI] [PubMed] [Google Scholar]
  • 43.Rosa D, Balato G, Ciaramella G, Soscia E, Improta G, Triassi M. Long-term clinical results and MRI changes after autologous chondrocyte implantation in the knee of young and active middle aged patients. J Orthop Traumatol. 2016;17:55–62. doi: 10.1007/s10195-015-0383-6. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 44.Sadlik B, Kolodziej L, Blasiak A, Szymczak M, Warchal B. Biological reconstruction of large osteochondral lesions of the talar dome with a modified "sandwich" technique-midterm results. Foot Ankle Surg. 2017;23:290–295. doi: 10.1016/j.fas.2016.09.001. [DOI] [PubMed] [Google Scholar]
  • 45.Schneider U. Controlled, randomized multicenter study to compare compatibility and safety of ChondroFiller liquid (cell free 2-component collagen gel) with microfracturing of patients with focal cartilage defects of the knee joint. J Ortop Surg. 2016;1:1–8. [Google Scholar]
  • 46.Schuttler KF, Gotschenberg A, Klasan A, Stein T, Pehl A, Roessler PP, et al. Cell-free cartilage repair in large defects of the knee: increased failure rate 5 years after implantation of a collagen type I scaffold. Arch Orthop Trauma Surg. 2019;139:99–106. doi: 10.1007/s00402-018-3028-4. [DOI] [PubMed] [Google Scholar]
  • 47.Siebold R, Suezer F, Schmitt B, Trattnig S, Essig M. Good clinical and MRI outcome after arthroscopic autologous chondrocyte implantation for cartilage repair in the knee. Knee Surg Sports Traumatol Arthrosc. 2018;26:831–839. doi: 10.1007/s00167-017-4491-0. [DOI] [PubMed] [Google Scholar]
  • 48.Shimozono Y, Donders JCE, Yasui Y, Hurley ET, Deyer TW, Nguyen JT, et al. Effect of the containment type on clinical outcomes in osteochondral lesions of the talus treated with autologous osteochondral transplantation. Am J Sports Med. 2018;46:2096–2102. doi: 10.1177/0363546518776659. [DOI] [PubMed] [Google Scholar]
  • 49.Shimozono Y, Hurley ET, Nguyen JT, Deyer TW, Kennedy JG. Allograft compared with autograft in osteochondral transplantation for the treatment of osteochondral lesions of the talus. J Bone Joint Surg Am. 2018;100:1838–1844. doi: 10.2106/JBJS.17.01508. [DOI] [PubMed] [Google Scholar]
  • 50.Usuelli FG, D'Ambrosi R, Maccario C, Boga M, de Girolamo L. All-arthroscopic AMIC((R)) (AT-AMIC((R))) technique with autologous bone graft for talar osteochondral defects: clinical and radiological results. Knee Surg Sports Traumatol Arthrosc. 2018;26:875–881. doi: 10.1007/s00167-016-4318-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 51.Valderrabano V, Miska M, Leumann A, Wiewiorski M. Reconstruction of osteochondral lesions of the talus with autologous spongiosa grafts and autologous matrix-induced chondrogenesis. Am J Sports Med. 2013;41:519–527. doi: 10.1177/0363546513476671. [DOI] [PubMed] [Google Scholar]
  • 52.Weigelt L, Hartmann R, Pfirrmann C, Espinosa N, Wirth SH. Autologous matrix-induced chondrogenesis for osteochondral lesions of the talus: a clinical and radiological 2- to 8-year follow-up study. Am J Sports Med. 2019;47:1679–1686. doi: 10.1177/0363546519841574. [DOI] [PubMed] [Google Scholar]
  • 53.Wiewiorski M, Miska M, Kretzschmar M, Studler U, Bieri O, Valderrabano V. Delayed gadolinium-enhanced MRI of cartilage of the ankle joint: results after autologous matrix-induced chondrogenesis (AMIC)-aided reconstruction of osteochondral lesions of the talus. Clin Radiol. 2013;68:1031–1038. doi: 10.1016/j.crad.2013.04.016. [DOI] [PubMed] [Google Scholar]

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