Skip to main content
Download PDF
  • Systematic Review
  • Open access
  • Published:

The efficacy of autologous matrix-induced chondrogenesis (AMIC) for osteochondral lesions of the talus in the mid-long term: a systematic review and meta-analysis

Journal of Orthopaedic Surgery and Research volume 19, Article number: 373 (2024) Cite this article

Abstract

Purpose

The objective of this study was to provide a comprehensive review of the existing literature regarding the treatment of osteochondral lesions of the talus (OLT) using autologous matrix-induced chondrogenesis (AMIC), while also discussing the mid-long term functional outcomes, complications, and surgical failure rate.

Methods

We searched Embase, PubMed, and Web of Science for studies on OLT treated with AMIC with an average follow-up of at least 2 years. Publication information, patient data, functional scores, surgical failure rate, and complications were extracted.

Results

A total of 15 studies were screened and included, with 12 case series selected for meta-analysis and 3 non-randomized controlled studies chosen for descriptive analysis. The improvements in the Visual Analog Scale (VAS), the American Orthopaedic Foot & Ankle Society (AOFAS) ankle-hindfoot, and Tegner scores at the last follow-up were (SMD = − 2.825, 95% CI − 3.343 to  − 2.306, P < 0.001), (SMD = 2.73, 95% CI 1.60 to 3.86, P < 0.001), (SMD = 0.85, 95% CI 0.5 to 1.2, P < 0.001) respectively compared to preoperative values. The surgery failure rate was 11% (95% CI 8–15%), with a total of 12 patients experiencing complications.

Conclusion

The use of AMIC demonstrates a positive impact on pain management, functional improvement, and mobility enhancement in patients with OLT. It is worth noting that the choice of stent for AMIC, patient age, and OLT size can influence the ultimate clinical outcomes. This study provides evidences supporting the safety and efficacy of AMIC as a viable treatment option in real-world medical practice.

Introduction

Osteochondral lesion of the talus (OLT) primarily affects the articular surface and subchondral bone of the talus. As there is no soft tissue attachment to the talus surface, approximately 70% of primary OLT cases are associated with ankle injuries, such as sprains and fractures [1, 2]. Additionally, vascular diseases, infections, hormone disorders, and ossification disorders can also contribute to the development of OLT [3]. Due to inadequate blood supply to the talus osteochondral, the limited regenerative capacity following injury often renders conservative treatment ineffective, ultimately necessitating surgical intervention.

Microfracture (MF) is the most commonly employed surgical intervention for OLT. This procedure utilizes a special MF tool to create small perforations in the subchondral bone, facilitating the egress of bone marrow and blood, ultimately leading to fibrocartilage formation. While short-term symptom improvement can be achieved by treating OLT with a diameter less than 15 mm, it should be noted that fibrocartilage generated through MF exhibits limited mechanical elasticity and undergoes degradation over time [4,5,6]. In cases involving soft bone lesions with intact superficial cartilage, Retrograde Drilling presents distinct advantages as it allows for preservation of superficial cartilage integrity; however, careful control over drill bit positioning and depth is crucial to prevent any damage while achieving optimal depth [7, 8]. For OLT with large defects and associated subchondral bone cysts, both autologous osteochondral transplantation (AOT) and osteochondral allograft transplantation (OAT) can be considered as treatment options. The clinical efficacy of these two approaches is comparable; however, when compared to AOT, the use of OAT implants has been found to result in higher rates of cartilage wear and cyst formation on imaging [9]. Biological agents such as platelet-rich plasma and hyaluronic acid have emerged as novel treatments for OLT. Although there have been positive short-term outcomes reported in the literature, it is important to note that there is currently a lack of high-quality research supporting their long-term effectiveness [10, 11]. Additionally, there exist various chondrocyte implantation techniques such as autologous/allogeneic osteochondral transplantation, autologous chondrocyte implantation, and matrix-induced autologous chondrocyte implantation [12,13,14]. This technique involves a two-step process: Step 1 entails harvesting healthy cartilage tissue from non-weight-bearing areas and cultivating cartilage cells in vitro, while Step 2 involves implanting the in vitro-cultivated cartilage cells at the site of the cartilage defect. Although the outcomes are favorable, it is important to note that this technique necessitates two surgeries, leading to increased treatment costs and requiring a high level of surgical expertise. Consequently, it is not recommended as the primary choice for initial OLT treatment. A new technique for repairing cartilage defects by combining MF with collagen matrix scaffolds, called autologous matrix-induced chondrogenesis (AMIC), was introduced in 2003.AMIC allows the implantation of scaffolds with mesenchymalstem cells in a single operation, avoiding the need for laboratory culture of cells and a second implantation [15]. Behrens first introduced AMIC into OLT surgery in 2005 [16]. In the past few decades, some studies have reported that the AMIC technique has shown satisfactory results in treating primary OLT, secondary OLT (after initial surgical failure) and OLT with subchondral bone cysts [17,18,19,20]. Recently, several studies have integrated AMIC with autogenous bone grafting, particularly for the concurrent presence of subchondral cysts. These combined techniques aim to eradicate necrotic subchondral bone and employ bone grafting(BG) to uphold local vascular reconstruction and cartilage regeneration in the subchondral region of the talus [21,22,23]. Consequently, the fundamental surgical approaches for AMIC employed in this systematic review encompass not only MF but also BG. The previous systematic reviews on AMIC for the treatment of OLT have not specifically addressed mid-long term outcomes [17, 18]. The present study establishes a 2-year follow-up period as the designated threshold for intermediate follow-up.

This study aims to investigate the mid-long term efficacy of AMIC in treating OLT through a comprehensive literature review and meta-analysis. Our objective is to evaluate patient pain and functional outcomes, as well as surgical failure rate and complications. We hypothesize that AMIC treatment for OLT will continue to improve patient pain and function while demonstrating lower complication rates and surgical failures during mid-long term follow-up.

Materials and methods

Search strategy

The PubMed, Embase, and Web of Science databases were comprehensively searched up until November 11, 2023.The language used is exclusively English and there are no limitations on the publication date.Additionally, we scrutinized the reference lists of the included literature and early reviews to ensure that any studies overlooked during the electronic database searches were included. The following are the keywords utilized for conducting searches: AMIC or Autologous Matrix-Induced Chondrogenesis or collagen scaffold and osteochondral or cartilage and talus or talar.

Eligibility criteria

The inclusion criteria for this meta-analysis were as follows: (1) patients diagnosed with osteochondral injury of the talus requiring autologous matrix-induced chondrogenesis treatment, (2) an average follow-up duration of 2 years or longer, and (3) one or more postoperative outcomes of interest such as visual analog scale (VAS), American Orthopaedic Foot & Ankle Society ankle-hindfoot score (AOFAS), Tegner, failure rate and complication. The exclusion criteria included: (1) incomplete data reports; (2) animal experiments, cell studies, reviews, meta-analyses, case reports, or conference abstracts.

Data extraction and management

Two authors (Jiang and Li) screened a comprehensive screening of titles and abstracts, followed by a thorough examination of the full text based on predetermined inclusion criteria. Disagreement was resolved by consensus or a third author. They independently extracted relevant clinical information in a standardized format, encompassing: (1) author and publication year; (2) country; (3) study design; (4) patient characteristics such as age, gender, BMI, and lesion size; (5) sample size; (6) follow-up duration; (7) assessment measures including VAS score, AOFAS score, Tegner score, complications, surgical failure rate. The collected data were duplicated and systematically arranged in a Microsoft Excel spreadsheet.

Assessment of methodological quality

Two senior authors (Jiang and Li) independently assessed the methodological quality of the selected studies.The risk of bias of cohort studies was assessed according to the Newcastle Ottawa Quality Assessment Scale (NOS) [24], which has a maximum score of 9 points attributed to the quality of selection (4 points), comparability(2 points), exposure(3 points), or outcome of study participants(3 points). Scores of 0–3, 4–6, and 7–9 were regarded as high, moderate, and low risk of bias, respectively. The risk of bias in the case series study was evaluated using the Joanna Briggs Institute (JBI) evaluation manual [25], which consists of 10 questions with response options including yes, no, unclear or not applicable.

Statistical analysis

The extracted data were analyzed using Stata/MP 16.0(StataCorp). Continuous variables were presented as means and standard deviations. If partial continuous variables represented raw data, the calculations were converted to means and standard deviations for consistent result summarization. If mean or standard deviation values was not provided, they were derived from the median, minimum, and maximum values [26, 27]. The I2 statistic was employed to assess the heterogeneity among the included studies. Heterogeneity is considered insignificant when ranging from 0 to 40%, moderate between 30 and 60%, substantial between 50 and 90%, and considerable between 75 and 100%. Consequently, a fixed effect model is utilized when heterogeneity is below 60%; otherwise, a random effect model is employed. Significance tests were conducted with two-tailed criteria, considering P < 0.05 as statistically significant.

Results

Search results and characteristics of the included studies

A search of three major databases yielded a total of 297 studies (77 in Pubmed, 106 in Embase, and 144 in Web of Science). The exclusion process was conducted using Endnote20 software to remove 140 duplicate studies. Two investigators independently screened the remaining 157 articles by reviewing titles and abstracts, resulting in the exclusion of 103 irrelevant studies. Subsequently, the remaining 54 articles were assessed for full-text availability. Among them, five studies could not be obtained for full text, while another 28 studies were excluded based on the predefined inclusion and exclusion criteria. Additionally, four studies were identified as duplicates and two were not written in English. Finally, a total of fifteen eligible studies were included in the meta-analysis. The screening flow chart is in Fig. 1.

Fig. 1
figure 1

Flow diagram of the meta-analysis for the inclusion/exclusion of studies

Full size image

A total of 15 articles were included in this meta-analysis, comprising 12 case series involving 372 patients and 3 cohort studies involving 196 patients. These studies were categorized into the non-AMIC group (82 cases) and the AMIC group (114 cases). The characteristics of the included studies are available in Table 1.

Table 1 Basic characteristics of the included studies
Full size table

Study quality assessment

The JBI scoring methodology was employed in 12 case series, while the NOS scoring methodology was utilized in 3 cohort studies. All included studies demonstrated good methodological quality. The details of the included studies are listed in Tables 2 and 3

Table 2 JBI critical appraisal quality assessment of the case series study
Full size table
Table 3 Quality assessment according to the Newcastle–Ottawa scale
Full size table

Meta‑analysis results

VAS score

The VAS scores were reported in 9 studies involving 305 patients, with an average follow-up duration of 37 months. Utilizing a random-effects model (I2 = 79.4%, P < 0.001), the analysis revealed a significant disparity in VAS scores between the final follow-up and preoperative assessments (SMD = − 2.825, 95% CI − 3.343 to − 2.306, P < 0.001), as displayed in Fig. 2.

Fig. 2
figure 2

Forest plots for the change in VAS scores compared to baseline

Full size image

AOFAS score

The AOFAS score was reported in 5 studies involving a total of 142 patients, with an average follow-up duration of 29 months. Utilizing a random-effects model (I2 = 92.0%, P < 0.001), the analysis revealed a significant disparity in AOFAS scores between the final follow-up and preoperative scores (SMD = 2.73, 95% CI 1.60 to 3.86, P < 0.001), as shown in Fig. 3

Fig. 3
figure 3

Forest plots for the change in AOFAS scores compared to baseline

Full size image

Tegner score

The Tegner score was reported in four studies involving a total of 141 patients, with an average follow-up time of 52 months. Utilizing the random effect model (I2 = 71.8%, P = 0.014), the analysis revealed a significant disparity in Tegner scores at the last follow-up compared to preoperative scores (SMD = 0.49, 95% CI 0.01 to 0.96, P = 0.046). Sensitivity results demonstrated that the combined outcomes of the meta-analysis remained robust and reliable even after excluding any individual study from consideration. Subsequent subgroup analysis based on age indicated no discrepancy in Tegner scores between preoperative and last follow-up among individuals under 50 years old (SMD = 0.07, 95% CI − 0.25 to 0.39, P = 0.673), with minimal heterogeneity within this group (I2 = 0%, P = 0.771). Conversely, there was a notable difference in Tegner scores between preoperative and last follow-up among individuals over 50 years old (SMD = 0.85, 95% CI 0.5 to 1, P < 0.001), also exhibiting low heterogeneity within this group (I2 = 0.0%, P = 0.513) (Fig. 4).

Fig. 4
figure 4

Forest plots for the change in Tegner scores and subgroup analysis

Full size image

Failure rate

All 7 studies included in this meta-analysis, which included 283 patients, with an average follow-up time of 37 months, reported surgical failure. The level of heterogeneity between studies was low (I2 = 32.9%, P = 0.177); therefore, a fixed-effects model was used. As shown, the surgical failure rate was 11% (95% CI 8–15%) (Fig. 5).

Fig. 5
figure 5

Forest plots for the failure rate

Full size image

AMIC vs non-AMIC

The VAS and AOFAS scores were compared between the AMIC group and non-AMIC group in 3 studies at the last follow-up. The AMIC group included 114 patients, with an average follow-up of 60 months, while the non-AMIC group had 82 patients with an average follow-up of 59 months. Significant heterogeneity was observed in VAS scores between the two groups (I2 = 81.8%, P = 0.004). Subsequent sensitivity analysis revealed that the meta-analysis results were influenced by 2 studies [34, 36]. Consequently, a decision was made to abandon the meta-analysis and only perform descriptive analysis (Fig. 6).

Fig. 6
figure 6

Results of sensitivity analysis

Full size image

Complications

Complications were reported in 5 studies involving 12 patients. 1 patient had delayed incision healing and no treatment was given; one patient had hypertrophic hyperplasia and underwent arthroscopic debridement;5 patients had persistent pain and underwent revision surgery, 2 patients with superficial portal skin infection received oral anti-inflammatory drugs, and 3 patients developed early arthritis and underwent arthrodesis, as shown in Table 4.

Table 4 The list of complications among the studies
Full size table

Discussion

A total of 15 studies were included through literature retrieval and screening, with 12 case series being subjected to meta-analysis, while the remaining 3 cohort studies were descriptively analyzed. The findings demonstrated that AMIC treatment for OLT effectively alleviated pain symptoms, improved functional outcomes, and enhanced exercise capacity during medium to long-term follow-up. Furthermore, a less of complications were observed. However, this systematic review did not yield sufficient evidence to support the superiority of AMIC over simple MF.

The technique of MF involves the use of a specialized tool to create small holes in the subchondral bone at intervals of 3–4 mm. This allows for the release of bone marrow and blood, which then form blood clots to fill the defect site and promote fibrocartilage formation. However, it should be noted that these blood clots formed after MF lack sufficient mechanical resistance to remain in place [43]. In contrast, AMIC utilizes MF as part of a single-stage operation, followed by the application of a resorbable membrane over the treatment site. This membrane serves to protect and stabilize the blood clots containing factors stimulated by bone marrow release [44]. Although there are currently no comparative studies on the short-term efficacy of AMIC and MF, previous retrospective studies have demonstrated significant improvements in ankle function and pain symptoms in the short term for AMIC cases [33, 45, 46]. A recent systematic review [17] involving 323 patients also revealed significant improvements in patient prognosis between 1 and 2 years. Based on these aforementioned studies, it can be inferred that AMIC exhibits comparable short-term clinical efficacy to MF. Therefore, this systematic review primarily focused on evaluating long-term efficacy. On the one hand, we discussed the results of meta-analysis encompassing clinical scores, surgical failure rates, and complications; on the other hand, due to limited literature comparing AMIC and MF available at present, we extensively reviewed previous studies during our discussion to explore the clinical outcomes of both procedures.

Although MF can achieve favorable early outcomes for OLT [47, 48], its long-term efficacy remains unsatisfactory [5, 49, 50]. This may be attributed to the fact that the fibrocartilage formed after MF primarily consists of type I collagen, while chondrocytes in the ankle joint cavity are scarce and exhibit poor regenerative capacity. Consequently, achieving complete integration between fibrocartilage and primary cartilage becomes challenging, with fibrocartilage being structurally and biomechanically inferior to hyaline cartilage [4]. As a result, fibrocartilage undergoes degradation over time, as evidenced by increasing pain levels, revision rates, complication incidence, and extent of cartilage injury. As for the mid-long term efficacy of AMIC, our studies showed good clinical outcomes, with 3 studies with an average follow-up time of more than 4 years and 3 studies with an average follow-up time of more than 5 years, and all studies with a follow-up time ranging from 2 to 10 years. In addition, through the analysis of the existing literature, we found that the efficacy of AMIC would gradually increase over a period of time and remain stable for a long time after reaching a peak. Walther [17] posited that AMIC could significantly enhance the clinical outcomes of patients within a 5-year postoperative period. Efrimma [51], in 62 OLT patients with a median follow-up of 84 months, observed substantial improvements in VAS and AOFAS scores during the first 2 years after OLT surgery, while no significant changes were noted in clinical outcomes between the 24th and 60th month. This finding aligns with Gottschalk's study [52], which reported significant enhancements in pain relief and functional recovery following AMIC, particularly within the initial year and peaking at two years. Moreover, these improvements were sustained for at least five years, accompanied by notable restoration of mobility and further enhancement of patient satisfaction at the five-year follow-up point. Collectively, The findings of these studies demonstrate that AMIC exhibit a consistently positive long-term outcome. However, due to the low quality of these studies, further high-quality research is needed to validate them.

As for postoperative complications and surgical failure rate, Walther's systematic review [17] included 4 studies with a total of 6 patients who underwent revision surgery due to persistent pain caused by articular fibrosis, hypertrophic scar tissue, or progression of degenerative arthritis. Migliorini's systematic review [18] reported that 7.8% of patients required revision surgery. In our meta-analysis of 7 studies, we observed similar complications as in other systematic reviews. However, when it comes to the surgical failure rate, our meta-analysis yielded a final result of 11%, which significantly differs from previously published systematic reviews. Through analysis, on one hand, the definition of surgical failure in this study is relatively broad. For studies that have not clearly reported the failure rate, we also include the dissatisfaction rate in the category of failure rate. On the other hand, our study did not provide a clear definition for OLT's nature. For instance, Yontar's study included primary OLT [28], primary with tumor-related OLT, and revision OLT. The surgical failure rates were 4.8%, 11.8%, and 38% respectively for these categories. Additionally, Albano's study reported a surgical failure rate as high as 38% [40]. It should be noted that MaioRegen® scaffold was used in this particular study (a cell-free biomimetic scaffold composed of type I collagen and hydroxyapatite), while most published studies on AMIC utilized Chondro-Gide® scaffold (a bilayer collagen I/III matrix scaffold). Another author observed through MRI and CT scans that incomplete cartilage repair and poor subchondral bone repair were induced by the MaioRegen® scaffold [53], which contributed to its high failure rate. In conclusion, we think that the choice of scaffold material can impact clinical outcomes; therefore we recommend using Chondro-Gide® scaffold based on the above research.

In terms of the efficacy of AMIC and MF, Migliorini et al.[34]reported that after an average follow-up period of 43.5 months for OLT defects measuring 27.1 ± 6.4 cm2, the clinical scores (AOFAS, VAS, Tegner) in the AMIC group were significantly superior to those in the MF group, with a notably lower failure rate compared to the latter group. Becher et al. [38], on the other hand, investigated OLT defects measuring 1.06 ± 0.47cm2 and found that although the average score in the AMIC group was better than that in the bone marrow stimulation(BMS) alone group at a five-year follow-up, this difference did not reach statistical significance. Upon analysis, it appears that one potential factor contributing to these divergent findings could be lesion size; thus prompting us to inquire whether lesion size influences the efficacy of AMIC. The study conducted by Chuckpaiwong et al. [54] examined 105 OLT patients who underwent MF treatment and observed that all patients with treatment failure had lesions larger than 15 mm, leading to the conclusion that membrane scaffolds were necessary for OLT > 1.5 cm2 [55]. However, a systematic review indicated that BMS as the sole treatment should be limited to osteochondral lesions smaller than 1 cm2 [56]. For surgical treatment of OLT > 1 cm2, the International Consensus Group on Cartilage Repair agreed that implanting scaffolds would yield superior and more reliable outcomes [57]. In 2024, the latest guidelines issued by the German Society of Orthopedics and Traumatology (DGOU) stated that the long-term benefits of scaffolds were proportional to the size of the lesion; in other words, larger areas exhibited more significant effects [58]. Therefore, based on existing research [23, 27], DGOU recommended adding additional scaffolds when OLT > 1 cm2 (instead of 1.5 cm2).

Another point of interest for us was age. Ayyaswamy [39] observed in his study that there was no significant correlation between age and AOFAS score, and the correlation between age and VAS score was only weak to moderate, but not statistically significant. Therefore, he concluded that age did not have a significant impact on outcome scores. However, another scholar presented a different perspective. Efrima [51] discovered significant differences in the Short Form-12, Halasi, and the University of California at Los Angeles scores between patients younger than 33 years old and those older than 33 years old at the 60-month follow-up period, suggesting that increasing age was significantly associated with poorer outcomes. D'Ambrosii [59] also found in his study that younger patients had significantly better functional recovery compared to older patients. Interestingly though, we subgrouped the Tegner scores of 141 patients from four studies based on their ages (with 50 years old as the threshold). At the final follow-up assessment, we observed that the exercise level of patients younger than 50 years old remained unchanged compared to pre-surgery levels; however, the exercise level of patients older than 50 years old showed a positive improvement after undergoing AMIC treatment, indicating its effectiveness in restoring exercise capacity among older individuals.

Despite these significant findings, the study has certain limitations. Firstly, the sample size of the studies included in this analysis was small and there was a lack of control groups. Therefore, our evaluation focused on efficacy and risk, without clear evidence demonstrating AMIC's superiority over simple MF. Secondly, the majority of our included studies are case series, which would indicate a high risk for bias and these studies were conducted in European countries such as Switzerland and Germany, which resulted in homogeneity in geographical origin and medical institutions. Hence, caution is required when extrapolating these results to a broader population.

Conclusion

The present meta-analysis revealed that the choice of stent utilized in the AMIC procedure, along with patient age and OLT area size, exerted an impact on the ultimate clinical outcome. To a certain extent, it substantiated a good mid-long term therapeutic efficacy of AMIC in ameliorating pain, function, and exercise levels among OLT patients. Nevertheless, future endeavors should focus on conducting further high-quality research to more comprehensively evaluate its effectiveness in treating OLT.

Availability of data and materials

Data and materials will be available on reasonable request.

References

  1. Leontaritis N, Hinojosa L, Panchbhavi VK. Arthroscopically detected intra-articular lesions associated with acute ankle fractures. J Bone Joint Surg Am. 2009;91(2):333–9.

    Article  PubMed  Google Scholar 

  2. McCollum GA, Calder JDF, Longo UG, et al. Talus osteochondral bruises and defects: diagnosis and differentiation. Foot Ankle Clin. 2013;18(1):35–47.

    Article  PubMed  Google Scholar 

  3. Schachter AK, Chen AL, Reddy PD, et al. Osteochondral lesions of the Talus. J Am Acad Orthop Surg. 2005;13(3):152.

    Article  PubMed  Google Scholar 

  4. Bae DK, Yoon KH, Song SJ. Cartilage healing after microfracture in osteoarthritic knees. Arthroscopy. 2006;22(4):367–74.

    Article  PubMed  Google Scholar 

  5. Park JH, Park KH, Cho JY, et al. Bone marrow stimulation for osteochondral lesions of the talus: are clinical outcomes maintained 10 years later? Am J Sports Med. 2021;49(5):1220–6.

    Article  PubMed  Google Scholar 

  6. Hannon CP, Bayer S, Murawski CD, et al. Debridement curettage and bone marrow stimulation: proceedings of the international consensus meeting on cartilage repair of the ankle. Foot Ankle Int. 2018;39(1_Suppl):16S-22S.

    Article  PubMed  Google Scholar 

  7. Saxena A, Maffulli N, Jin A, et al. Outcomes of talar osteochondral and transchondral lesions using an algorithmic approach based on size, location, and subchondral plate integrity: a 10-year study on 204 lesions. J Foot Ankle Surg. 2022;61(3):442–7.

    Article  PubMed  Google Scholar 

  8. Artioli E, Mazzotti A, Gerardi S, et al. Retrograde drilling for ankle joint osteochondral lesions: a systematic review. J Orthop Traumatol. 2023;24(1):37.

    Article  PubMed  PubMed Central  Google Scholar 

  9. Migliorini F, Maffulli N, Baroncini A, et al. Allograft versus autograft osteochondral transplant for chondral defects of the talus: systematic review and meta-analysis. Am J Sports Med. 2022;50(12):3447–55.

    Article  PubMed  Google Scholar 

  10. Mei-Dan O, Carmont MR, Laver L, et al. Platelet-rich plasma or hyaluronate in the management of osteochondral lesions of the talus. Am J Sports Med. 2012;40(3):534–41.

    Article  PubMed  Google Scholar 

  11. Woo I, Park JJ, Seok H-G. The efficacy of platelet-rich plasma augmentation in microfracture surgery osteochondral lesions of the talus: a systematic review and meta-analysis. J Clin Med. 2023;12(15):4998.

    Article  PubMed  PubMed Central  Google Scholar 

  12. Bruns J, Habermann C, Werner M. Osteochondral Lesions of the Talus: A Review on Talus Osteochondral, Injuries Including Osteochondritis Dissecans. Cartilage. 2021;13(11):1380–401.

    Article  Google Scholar 

  13. Qgh R, Gmmj K. Osteochondral Lesions of the talus: an individualized treatment paradigm from the amsterdam perspective. Foot Ankle Clin, Foot Ankle Clin. 2021;26(1):121–36.

    Article  Google Scholar 

  14. Powers RT, Dowd TC, Giza E. Surgical Treatment for Osteochondral Lesions of the Talus. Arthroscopy. 2021;37(12):3393–6.

    Article  PubMed  Google Scholar 

  15. Gille J, Schuseil E, Wimmer J, et al. Mid-term results of Autologous Matrix-Induced Chondrogenesis for treatment of focal cartilage defects in the knee. Knee Surg Sports Traumatol Arthrosc. 2010;18(11):1456–64.

    Article  CAS  PubMed  Google Scholar 

  16. Behrens P. Matrixgekoppelte Mikrofrakturierung]. Arthroskopie. 2005;18(3):193–7.

    Article  Google Scholar 

  17. Walther M, Valderrabano V, Wiewiorski M, et al. Is there clinical evidence to support autologous matrix-induced chondrogenesis (AMIC) for chondral defects in the talus? A systematic review and meta-analysis. Foot Ankle Surg. 2021;27(3):236–45.

    Article  PubMed  Google Scholar 

  18. Migliorini F, Maffulli N, Bell A, et al. Autologous matrix-induced chondrogenesis (AMIC) for osteochondral defects of the talus: a systematic review. Life (Basel). 2022;12(11):1738.

    PubMed  Google Scholar 

  19. Migliorini F, Maffulli N, Schenker H, et al. Surgical management of focal chondral defects of the talus: a bayesian network meta-analysis. Am J Sports Med. 2022;50(10):2853–9.

    Article  PubMed  Google Scholar 

  20. Migliorini F, Schenker H, Maffulli N, et al. Autologous matrix induced chondrogenesis (AMIC) as revision procedure for failed AMIC in recurrent symptomatic osteochondral defects of the talus. Sci Rep. 2022;12(1):16244.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  21. Usuelli FG, Maccario C, Ursino C, et al. The impact of weight on arthroscopic osteochondral talar reconstruction. Foot Ankle Int. 2017;38(6):612–20.

    Article  PubMed  Google Scholar 

  22. Götze C, Nieder C, Felder H, et al. AMIC for traumatic focal osteochondral defect of the talar shoulder: a 5 years follow-up prospective cohort study. BMC Musculoskelet Disord. 2021. https://doi.org/10.1186/s12891-021-04506-z.

    Article  PubMed  PubMed Central  Google Scholar 

  23. D’Ambrosi R, Maccario C, Ursino C, et al. Combining microfractures, autologous bone graft, and autologous matrix-induced chondrogenesis for the treatment of juvenile osteochondral talar lesions. Foot Ankle Int. 2017;38(5):485–95.

    Article  PubMed  Google Scholar 

  24. Stang A. Critical evaluation of the Newcastle-Ottawa scale for the assessment of the quality of nonrandomized studies in meta-analyses. Eur J Epidemiol. 2010;25(9):603–5.

    Article  PubMed  Google Scholar 

  25. Munn Z, Barker TH, Moola S, et al. Methodological quality of case series studies: an introduction to the JBI critical appraisal tool. JBI Evid Synth. 2020;18(10):2127–33.

    PubMed  Google Scholar 

  26. Hozo SP, Djulbegovic B, Hozo I. Estimating the mean and variance from the median, range, and the size of a sample. BMC Med Res Methodol. 2005;5:13.

    Article  PubMed  PubMed Central  Google Scholar 

  27. Wan X, Wang W, Liu J, et al. Estimating the sample mean and standard deviation from the sample size, median, range and/or interquartile range. BMC Med Res Methodol. 2014;14:135.

    Article  PubMed  PubMed Central  Google Scholar 

  28. Yontar NS, Aslan L, Öğüt T. Functional outcomes of autologous matrix-related chondrogenesis to treat large osteochondral lesions of the talus. Foot Ankle Int. 2022;43(6):783–9.

    Article  PubMed  Google Scholar 

  29. Wiewiorski M, Werner L, Paul J, et al. Sports activity after reconstruction of osteochondral lesions of the talus with autologous spongiosa grafts and autologous matrix-induced chondrogenesis. Am J Sports Med. 2016;44(10):2651–8.

    Article  PubMed  Google Scholar 

  30. Weigelt L, Hartmann R, Pfirrmann C, et al. 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(7):1679–86.

    Article  PubMed  Google Scholar 

  31. Viehöfer AF, Casari F, Waibel FWA, et al. Smoking is associated with anterior ankle impingement after isolated autologous matrix-induced chondrogenesis for osteochondral lesions of the talus. Cartilage. 2021;13(1_Suppl):1366s–72s.

    Article  PubMed  Google Scholar 

  32. Valderrabano V, Miska M, Leumann A, et al. Reconstruction of osteochondral lesions of the talus with autologous spongiosa grafts and autologous matrix-induced chondrogenesis. Am J Sports Med. 2013;41(3):519–27.

    Article  PubMed  Google Scholar 

  33. Usuelli FG, D’Ambrosi R, Maccario C, et al. All-arthroscopic AMIC® (AT-AMIC®) technique with autologous bone graft for talar osteochondral defects: clinical and radiological results[J]. Knee Surg Sports Traumatol Arthrosc. 2018;26(3):875–81.

    Article  PubMed  Google Scholar 

  34. Migliorini F, Eschweiler J, Maffulli N, et al. Autologous Matrix Induced Chondrogenesis (AMIC) compared to microfractures for chondral defects of the talar shoulder: a five-year follow-up prospective cohort study. Life (Basel). 2021. https://doi.org/10.3390/life11030244.

    Article  PubMed  Google Scholar 

  35. Kubosch EJ, Erdle B, Izadpanah K, et al. Clinical outcome and T2 assessment following autologous matrix-induced chondrogenesis in osteochondral lesions of the talus. Int Orthop. 2016;40(1):65–71.

    Article  PubMed  Google Scholar 

  36. Gorgun B, Gamlı A, Duran ME, et al. Collagen Scaffold Application in Arthroscopic Reconstruction of Osteochondral Lesions of the Talus With Autologous Cancellous Bone Grafts. Orthop J Sports Med. 2023. https://doi.org/10.1177/23259671221145733.

    Article  PubMed  PubMed Central  Google Scholar 

  37. D’Ambrosi R, Villafañe JH, Indino C, et al. Return to Sport After Arthroscopic Autologous Matrix-Induced Chondrogenesis for Patients With Osteochondral Lesion of the Talus. Clin J Sport Med. 2019;29(6):470.

    Article  Google Scholar 

  38. Becher C, Malahias MA, Ali MM, et al. Arthroscopic microfracture vs arthroscopic autologous matrix-induced chondrogenesis for the treatment of articular cartilage defects of the talus. Knee Surg Sports Traumatol Arthrosc. 2019;27(9):2731–6.

    Article  PubMed  Google Scholar 

  39. Ayyaswamy B, Salim M, Sidaginamale R, et al. Early to medium term outcomes of osteochondral lesions of the talus treated by autologous matrix induced chondrogenesis (AMIC). Foot Ankle Surg. 2021;27(2):207–12.

    Article  PubMed  Google Scholar 

  40. Albano D, Martinelli N, Bianchi A, et al. 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(1):306.

    Article  PubMed  PubMed Central  Google Scholar 

  41. Ackermann J, Casari FA, Germann C, et al. Autologous matrix-induced chondrogenesis with lateral ligament stabilization for osteochondral lesions of the talus in patients with ankle instability. Orthop J Sports Med. 2021;9(5):23259671211007440.

    PubMed  PubMed Central  Google Scholar 

  42. Götze C, Nieder C, Felder H, et al. AMIC for focal osteochondral defect of the Talar shoulder. Life (Basel). 2020;10(12):328.

    PubMed  Google Scholar 

  43. Miyahira MKC, Novaretti JV, Astur DC, et al. Larger chondral lesions treated with collagen membrane - matrix-induced autologous chondrogenesis - show larger increase in clinical scores. Rev Bras Ortop (Sao Paulo). 2021;56(3):333–9.

    PubMed  Google Scholar 

  44. Benthien JP, Behrens P. The treatment of chondral and osteochondral defects of the knee with autologous matrix-induced chondrogenesis (AMIC): method description and recent developments. Knee Surg Sports Traumatol Arthrosc. 2011;19(8):1316–9.

    Article  PubMed  Google Scholar 

  45. Baumfeld T, Baumfeld D, Prado M, et al. All-arthroscopic AMIC® (AT-AMIC) for the treatment of talar osteochondral defects: a short follow-up case series. Foot. 2018;37:23–7.

    Article  PubMed  Google Scholar 

  46. Yontar NS, Aslan L, Can A, et al. One step treatment of talus osteochondral lesions with microfracture and cell free hyaluronic acid based scaffold combination. Acta Orthop Traumatol Turc. 2019;53(5):372–5.

    Article  PubMed  PubMed Central  Google Scholar 

  47. Guelfi M, DiGiovanni CW, Calder J, et al. Large variation in management of talar osteochondral lesions among foot and ankle surgeons: results from an international survey. Knee Surg Sports Traumatol Arthrosc. 2021;29(5):1593–603.

    Article  PubMed  Google Scholar 

  48. Barbier O, Amouyel T, De l’Escalopier N, et al. Osteochondral lesion of the talus: What are we talking about? Orthop Traumatol Surg Res. 2021;107(81):103068.

    Article  PubMed  Google Scholar 

  49. Toale J, Shimozono Y, Mulvin C, et al. Midterm outcomes of bone marrow stimulation for primary osteochondral lesions of the talus: a systematic review. Orthop J Sports Med. 2019;7(10):2325967119879127.

    PubMed  PubMed Central  Google Scholar 

  50. Fu S, Yang K, Li X, et al. Radiographic and clinical outcomes after arthroscopic microfracture for osteochondral lesions of the talus: 5-year results in 355 consecutive ankles. Orthop J Sports Med. 2022;10(10):23259671221128772.

    PubMed  PubMed Central  Google Scholar 

  51. Efrima B, Barbero A, Maccario C, et al. Significant clinical improvement after arthroscopic autologous matrix-induced chondrogenesis for osteochondral lesions of the talus: a 5-year follow-up. Cartilage. 2024. https://doi.org/10.1177/19476035241240341.

    Article  PubMed  Google Scholar 

  52. Gottschalk O, Altenberger S, Baumbach S, 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(5):930–6.

    Article  PubMed  Google Scholar 

  53. Christensen BB, Foldager CB, Jensen J, et al. Poor osteochondral repair by a biomimetic collagen scaffold: 1- to 3-year clinical and radiological follow-up. Knee Surg Sports Traumatol Arthrosc. 2016;24(7):2380–7.

    Article  PubMed  Google Scholar 

  54. Chuckpaiwong B, Berkson EM, Theodore GH. Microfracture for osteochondral lesions of the ankle: outcome analysis and outcome predictors of 105 cases. Arthroscopy. 2008;24(1):106–12.

    Article  PubMed  Google Scholar 

  55. Choi WJ, Park KK, Kim BS, et al. Osteochondral lesion of the talus: is there a critical defect size for poor outcome? Am J Sports Med. 2009;37(10):1974–80.

    Article  PubMed  Google Scholar 

  56. Ramponi L, Yasui Y, Murawski CD, et al. Lesion size is a predictor of clinical outcomes after bone marrow stimulation for osteochondral lesions of the talus: a systematic review. Am J Sports Med. 2017;45(7):1698–705.

    Article  PubMed  Google Scholar 

  57. Rothrauff BB, Murawski CD, Angthong C, et al. Scaffold-based therapies: proceedings of the international consensus meeting on cartilage repair of the ankle. Foot Ankle Int. 2018;39(1_Suppl):41S-47S.

    Article  PubMed  Google Scholar 

  58. Walther M, Gottschalk O. M Aurich 2024 Operative management of osteochondral lesions of the talus: 2024 recommendations of the working group “clinical tissue regeneration” of the German Society of Orthopedics and Traumatology (DGOU). EFORT Open Rev. 2024;9(3):217–34.

    Article  PubMed  PubMed Central  Google Scholar 

  59. D’Ambrosi R, Maccario C, Serra N, et al. Osteochondral lesions of the talus and autologous matrix-induced chondrogenesis: is age a negative predictor outcome? Arthroscopy. 2017;33(2):428–35.

    Article  PubMed  Google Scholar 

Download references

Acknowledgements

Not applicable.

Funding

No funding was received.

Author information

Authors and Affiliations

  1. Foot and Ankle Surgery, Tianjin Hospital, Tianjin, 300211, China

    Ning Jiang, Haomin Li, Jia Wang, Lin Shen & Xiantie Zeng

  2. Graduate School, Tianjin University of Traditional Chinese Medicine, Tianjin, 301617, China

    Ning Jiang

Authors
  1. Ning Jiang
    View author publications

    You can also search for this author in PubMed Google Scholar

  2. Haomin Li
    View author publications

    You can also search for this author in PubMed Google Scholar

  3. Jia Wang
    View author publications

    You can also search for this author in PubMed Google Scholar

  4. Lin Shen
    View author publications

    You can also search for this author in PubMed Google Scholar

  5. Xiantie Zeng
    View author publications

    You can also search for this author in PubMed Google Scholar

Contributions

NJ conceived the study, designed, performed, and wrote the paper. HML carried out the data collection, JW LS TXZ carried out revised the paper. All authors reviewed the results and approved the final version of the manuscript. The authors read and approved the final manuscript.

Corresponding author

Correspondence to Xiantie Zeng.

Ethics declarations

Ethics approval and consent to participate

This article does not contain any studies with human participants or animals performed by any of the authors.

Consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.

Additional information

Publisher's Note

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

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Jiang, N., Li, H., Wang, J. et al. The efficacy of autologous matrix-induced chondrogenesis (AMIC) for osteochondral lesions of the talus in the mid-long term: a systematic review and meta-analysis. J Orthop Surg Res 19, 373 (2024). https://doi.org/10.1186/s13018-024-04864-z

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/s13018-024-04864-z

Keywords

Journal of Orthopaedic Surgery and Research

ISSN: 1749-799X