The menisci of the knee are semi-lunar fibrocartilaginous structures critical in load bearing, shock absorption, stability, and lubrication. Loss of meniscal tissue can lead to pain and decreased function and activity. Current methods of treating repairable meniscal tears include standard suture, meniscal tacks, darts, and arrow devices. Individuals with meniscal tears that cannot be repaired by these methods typically receive partial or total meniscectomy. However, several investigators believe that degenerative processes in adjacent articular cartilage surfaces may be associated with partial or total meniscectomy and could influence knee function over time (Hede et al., 1992; Schimmer et al., 1998).
Allografts or synthetic meniscus scaffolds have been used for meniscus tears to prevent early degenerative joint disease with varying success, although problems related to reduced initial and long-term stability, as well as immunological reactions prevent wide-spread clinical use (Sandmann et al., 2009).
CMIs, also known as collagen scaffolds or Menaflex, are implantable porous meniscus scaffolds composed of collagen fibers, enriched with glycosaminoglycan, used as a template and support for generation of new tissue to replace the lost menisci.
In December 2008, Menaflex (ReGen Biologics, Inc., Hackensack, NJ), previously known as CMI, received US Food and Drug Administration (FDA) 510(k) marketing clearance as a collagen scaffold for repair and reinforcement of the medial meniscus of the knee. It is a synthetic resorbable collagen matrix implant composed of bovine type I collagen and is intended for the reinforcement and repair of soft tissue injuries of the medial meniscus where weakness exists, such as defects that result from prior surgeries to the involved meniscus (e.g., partial meniscectomy). The implant is a crescent-shaped device that can be trimmed to fit the defect in the meniscal tissue and is sutured to the remaining native meniscus during arthroscopic surgery. The device provides a sponge-like scaffold that is replaced by the individual's own meniscal tissue over time.
In its 510(k) submission, the manufacturer provided the FDA with data from a prospective, randomized, controlled, multicenter study that compared the Menaflex with partial meniscectomy. Individuals (n=311) with an irreparable injury of the medial meniscus or a previous partial medial meniscectomy (PMM) were enrolled in the study. There were two study arms:
1. Individuals (n = 157) with no prior surgery on the involved meniscus (the "acute" arm of the study), and
2. Individuals (n = 154) with prior (one to three) meniscal surgical procedures (the "chronic" arm).
Individuals were randomly assigned either to receive the CMI or to serve as a control subject treated with a partial meniscectomy only. Subjects underwent frequent clinical follow-up examinations during 2 years and completed validated outcomes questionnaires during 7 years. Individuals who had received a CMI were required by protocol to have second-look arthroscopy at 1 year to determine the amount of new tissue growth and to perform a biopsy to assess tissue quality. Re-operation and survival rates were determined. In the acute group, 75 individuals received a CMI and 82 were controls. In the chronic group, 85 individuals received the implant and 69 were controls. The mean duration of follow-up was 59 months (range, 16–92). The 141 repeat arthroscopies done at 1 year showed that the CMIs had resulted in significantly (P=0.001) increased meniscal tissue compared with that seen after the original index partial meniscectomy. The implant supported meniscus-like matrix production and integration as it was assimilated and resorbed. In the chronic group, individuals who had received an implant regained significantly more of their lost activity than did controls (P=0.02) and they underwent significantly fewer nonprotocol re-operations (P=0.04). No differences were detected between the two treatment groups in the acute arm of the study. Of the 12 documented serious complications in individuals with the Menaflex, seven were classified as probably or at least possibly related to the Menaflex. In one individual, a skin infection developed at a portal site requiring joint irrigation and debridement and the Menaflex was removed. Pain scores, Lysholm scores, and individual self-assessment scores improved between the preoperative and latest follow-up evaluations in all treatment groups and were similar regardless of treatment or chronicity. The authors concluded that the Menaflex device supports new tissue ingrowth and that the new tissue ingrowth is adequate to enhance meniscal function in individuals with a chronic meniscal injury; however, it does not have any benefit for patients with an acute injury (Rodkey et al., 2008).
In 2008, the FDA made the following observations during their analysis of the Rodkey et al. study data: the majority of the Menaflex devices were firmly attached to the host rim; however, 16% were not firmly attached and 18% of knee compartments were determined to be worse than during the operative procedure at the time of the re-look arthroscopic procedure, the investigators reported that 5 years after receiving a Menaflex implant, 22.7% of control individuals required further meniscal surgery, compared to only 9.5% of the Menaflex recipients, however, if additional operations that were performed during the second arthroscopy are included, the re-operation rate among Menaflex recipients was 19.7%, and the Tegner Index is meant to complement other functional scores (e.g., the Lysholm knee score) for individuals with ligamentous injuries, however, the investigators reported the Tegner Index in isolation and there was no pre-specified hypothesis for its use in the study design, thus, it is unclear how this endpoint should be interpreted given that there is no defined clinical significance for the Tegner Score when used in isolation.
The majority of the Menaflex devices were firmly attached to the host rim, however, 16% were not firmly attached and 18% of knee compartments were determined to be worse than during the operative procedure at the time of the re-look arthroscopic procedure, the investigators reported that 5 years after receiving a Menaflex implant, 22.7% of control individuals required further meniscal surgery, compared to only 9.5% of the Menaflex recipients, however, if additional operations that were performed during the second arthroscopy are included, the re-operation rate among Menaflex recipients was 19.7%, and the Tegner Index is meant to complement other functional scores (e.g., the Lysholm knee score) for individuals with ligamentous injuries, however, the investigators reported the Tegner Index in isolation and there was no pre-specified hypothesis for its use in the study design, thus, it is unclear how this endpoint should be interpreted given that there is no defined clinical significance for the Tegner Score when used in isolation. In addition, there is a noted difference in the rehabilitation necessary for individuals receiving the Menaflex implant versus partial meniscectomy. During the first 6 months following implantation, the individual's activity level is restricted to reduce the stress on the mesh-reinforced meniscus, allowing tissue in-growth and maturation to take place. In contrast, the rehabilitation program for a partial meniscectomy is to return to full activities by 2 to 3 weeks post-operatively since there is no period of meniscal healing required.
At the 75th annual meeting of the American Academy of Orthopaedic Surgeons in March 2008, histologic findings were presented from individuals who had received the Menaflex implant (n=128). Biopsies taken 1 year after implantation found residual implant material in 63% of cases and all cases showed infiltration of the implant matrix with new meniscal tissue. Inflammation was noted around the implant in 9% of individuals (Choi, 2008).
Systematic evidence reviews have not evaluated the Menaflex device. A Cochrane review (Howell and Handoll, 2000) on the effects of common surgical interventions in the treatment of meniscal injuries of the knee concluded, "[t]he lack of randomised trials means that no conclusions can be drawn on the issue of surgical versus non-surgical treatment of meniscal injuries, nor meniscal tear repair versus excision. In randomised trials so far reported, there is no evidence of difference in radiological or long term clinical outcomes between arthroscopic and open meniscal surgery, or between total and partial meniscectomy. Partial meniscectomy seems preferable to the total removal of the meniscus in terms of recovery and overall functional outcome in the short term."
Although some clinical studies have demonstrated improvement with the CMI, the number of individuals have been small in all studies and the positive effect on the prevention of progression of osteoarthritis was not compared with control groups (Bumam, 2007).
An assessment by the California Technology Assessment Forum (CTAF) (Tice, 2010) concluded that the CMI does not meet CTAF criteria. The CTAF assessment found that the pivotal randomized clinical trial (citing Rodkey et al., 2008) failed to demonstrate any improvement in pain or symptoms in either arm of the trial and the trial has substantial risk for selection bias, confounding, and reporting bias because of the large number of individuals lost to follow-up after randomization and the lack of blinding for subjective outcomes. In addition, no data on osteoarthritis were presented. The CTAF assessment concluded that the trial "presents evidence that the CMI offers no important clinical benefits, requires longer and more intensive post-operative rehabilitation, and some uncertainty remains about the potential for long-term harm from the device."
The Centers for Medicare & Medicaid Services (CMS, 2010) has concluded that the CMA does not improve health outcomes in the Medicare population. Therefore, CMS has determined that the CMI is not reasonable and necessary for the treatment of meniscal injury/tear. Furthermore, on October 14, 2010, the FDA announced that the Menaflex Collagen Scaffold should not have been cleared for marketing in the United States. The FDA has now concluded that the Menaflex device is intended to be used for different purposes and is technologically dissimilar from devices already on the market known as “predicate devices.” These differences can affect the safety and effectiveness of the Menaflex device. For example, instead of simply repairing or reinforcing damaged tissue like predicate devices, Menaflex is intended to stimulate the growth of new tissue to replace tissue that was surgically removed. Because of these differences, the Menaflex device should not have been cleared by the agency. The announcement follows a re-evaluation of the scientific evidence that was undertaken after a September 2009 agency report identified problems in the agency’s review of the device. To correct this error, the agency will begin the process to rescind the product’s marketing clearance.
In a case-series study, Monllau et al. (2011) evaluated the clinical outcome of a CMI in an injured medial meniscus after a minimum of 10 years' follow-up. Twenty-five individuals underwent arthroscopic CMI. They had either persistent compartmental joint line pain due to a previous medial meniscus resection (five cases) or a large irreparable meniscus tear at arthroscopy (20 cases). Implant failure was defined as infection due to the implant or mechanical failure of the device. Twenty-two individuals returned for clinical, functional, and radiographic evaluation. MRI was also performed and was analyzed with the criteria of Genovese et al. (in which type 3 indicates normal and type 1 indicates completely abnormal). All the aforementioned evaluations were carried out at a minimum of 10 years (range of 10.1 to 12.5 years) after the procedure. The mean Lysholm score improved from 59.9 preoperatively to 89.6 at 1 year (P<0.001), and it was 87.5 at final follow-up (P<0.001). The results were good or excellent in 83% of the population. No differences were observed between the Lysholm score at 1 year of follow-up with the score at final follow-up (P>0.05). The mean pain score on a VAS improved by 3.5 points at final follow-up. Individual satisfaction with the procedure was 3.4 of 4 points. Radiographic evaluation showed either minimal or no narrowing of the joint line. MRI showed type 2 in 64% of cases and type 3 in 21%. All cases showed less volume than expected (size type 2 in 89%). The failure rate in the patient population was 8% (2 of 25). There were no complications related to the device. The authors concluded that although there were several different types of individuals and acute and chronic tears were treated in a limited number of individuals, meniscal substitution with CMI provides significant pain relief and functional improvement after a minimum of 10 years' follow-up. The implant generally diminished in size, but the procedure proved to be safe and had a low rate of implant failure on a long-term basis. No development or progression of degenerative knee joint disease was observed in most cases (Level IV evidence).
In a cohort study, Zaffagnini et al (2011) compared the long-term outcomes of the medial collagen meniscus implant (MCMI) versus PMM. A total of 33 non-consecutive individuals (men; mean age of 40 years) with meniscal injuries were enrolled in the study to receive MCMI or to serve as a control individual treated with PMM. The choice of treatment was decided by the individual. All individuals were clinically evaluated at time 0 and at 5 years and a minimum of 10 years after surgery (mean follow-up of 133 months) by Lysholm, VAS for pain, objective IKDC knee form, and Tegner activity level scores. The SF-36 score was performed pre-operatively and at final follow-up. Bilateral weight-bearing radiographs were completed before the index surgery and at final follow-up. Minimum 10-year follow-up MRI images were compared with pre-operative MRI images by means of the Yulish score. The Genovese score was also used to evaluate MCMI MRI survivorship. The MCMI group, compared with the PMM group, showed significantly lower VAS for pain (1.2 ± 0.9 versus 3.3 ± 1.8; P=0.004) and higher objective IKDC (7A and 10B for MCMI, 4B and 12C for PMM; P=0.0001), Teger index (75 ± 27.5 versus 50 ± 11.67; P=0.026), and SF-36 (53.9 ± 4.0 versus 44.1 ± 9.2; P=0.026 for Physical Health Index; 54.7 ± 3.8 versus 43.8 ± 6.5; P=0.004 for Mental Health Index) scores. Radiographic evaluation showed significantly less medial joint space narrowing in the MCMI group than in the PMM group (0.48 ± 0.63 mm versus 2.13 ± 0.79 mm; P=0.0003). No significant differences between groups were reported regarding Lysholm (P=0.062) and Yulish (P=0.122) scores. Genovese score remained constant between 5 and 10 years after surgery (P=0.5). The MRI evaluation of the MCMI individuals revealed 11 cases of myxoid degeneration signal: four had a normal signal with reduced size, and two had no recognizable implant. The authors concluded that pain, activity level, and radiological outcomes are significantly improved with use of the MCMI at a minimum 10-year follow-up compared with PMM alone. Moreover, they stated that randomized controlled trials (RCTs) on a larger population are needed to confirm MCMI benefits at long-term.
Harston et al. (2012) examined CMI effectiveness for improving individual function, symptoms, and activity level. Study methodologies, rehabilitation, and return-to-sport guidelines were also reviewed. MedLine, Embase, CINAHL, Life Science Citations, and Cochrane Central Register of Controlled Trials databases were searched from January 1995 to May 2011 using the term collagen meniscal or meniscus implant. Only human studies with English language abstracts that reported individual outcomes were included. Modified Coleman Methodology Score (CMS) were used to score research quality. Eleven studies with 520 subjects (men = 428; women = 92; 17.7% women) of 38.2 ± 3.7 years of age met the inclusion criteria. Of these subjects, 321 (men = 263, women = 58; 18.1% women) received a CMI. Based primarily on Lysholm Knee Score, Tegner Activity Scale, pain scales and self-assessment measurements, knee function, symptoms, and activity level generally improved by 46.6 ± 39.9 months post-surgery. Rehabilitation was described in nine of 11 (81.8%) studies and four released individuals to full activities at 6 months post-surgery. No study described how advanced rehabilitation or function testing contributed to return to activity decision-making. Research quality was generally low (67.1 ± 18.6) with widely ranging (29 to 97) scores. Reduced CMI size at last follow-up was reported in six of 11 (54.5%) studies, but the significance of this finding is unknown. The authors concluded that knee function, symptoms, and activity level generally improved following CMI use, but poor research report quality was common. They stated that additional well-designed long-term prospective studies are needed to better determine knee osteoarthrosis prevention efficacy and appropriate patient selection.
Furthermore, the Work Loss Data Institute's guideline on "Knee and leg (acute and chronic)" (2011; updated November 2013) does not recommend the use of CMI/Menaflex.
Spencer et al. (2012) presented their early experience on meniscal scaffolds and performed a review of the literature. Twenty-three individuals underwent meniscal scaffold implantation (14 medial, nine lateral) with either the Menaflex (ReGen Biologics) (n=12) or Actifit (Orteq) (n=11) scaffolds. Minimum follow-up was 1 year with a mean of 24.1 months (18–27) for the Menaflex and 14.7 months (12–18) for the Actifit groups. Mean age at surgery was 35 years (17–47) with a mean Outerbridge grade of 1.9 in the affected compartment. Eight (36%) underwent concurrent osteotomy, ligament reconstruction, or microfracture of the tibial plateau. KOOS, Lysholm, Tegner activity and IKDC scores were collected preoperatively and at 6-month interval post-surgery. Assessment of the reconstruction was obtained with MRI scanning and arthroscopy. One scaffold tore and was revised at 19 months postoperatively. A total of 21 of 23 (91.3%) had a significant improvement in knee scores when compared to pre-surgery levels at latest follow-up. Second-look arthroscopy in 14 at 1-year postimplantation showed variable amounts of regenerative tissue. There was no progression in chondral wear noted on repeat MRI scanning. The authors concluded that treatment with meniscal scaffold implants can provide good pain relief for the post-meniscectomy knee following partial meniscectomy. Moreover, they stated that longer follow-up is needed to examine if they also prevent the progressive chondral wear associated with a post-meniscectomy knee.
The National Institute for Health and Clinical Excellence's guideline on "Partial replacement of the meniscus of the knee using a biodegradable scaffold" (NICE, 2012) states that "Current evidence on partial replacement of the meniscus of the knee using a biodegradable scaffold raises no major safety concerns. Evidence for any advantage of the procedure over standard surgery, for symptom relief in the short-term, or for any reduction in further operations in the long-term, is limited in quantity. Therefore, this procedure should only be used with special arrangements for clinical governance, consent and audit or research."
Brophy and Matava (2012) stated that as a result of biologic issues and technical limitations, repair of the meniscus is indicated for unstable, peripheral vertical tears; most other types of meniscal tears that are degenerative, significantly traumatized, and/or located in an avascular area of the meniscus are managed with partial meniscectomy. Options to restore the meniscus range from allograft transplantation to the use of synthetic technologies. Recent studies demonstrated good long-term outcomes from MAT, although the indications and techniques continue to evolve and the long-term chondroprotective potential has yet to be determined. Several synthetic implants, none of which has FDA approval, have shown some promise for replacing part or all of the meniscus, including the collagen meniscal implant, hydrogels, and polymer scaffolds.
Papalia et al. (2013) systematically reviewed the literature on clinical outcomes following partial meniscal replacement using different scaffolds. These investigators performed a comprehensive search of Medline, CINAHL, Embase and the Cochrane Central Registry of Controlled Trials. The reference lists of the selected articles were then examined by hand. Only studies focusing on investigation of clinical outcomes on individuals undergoing a partial meniscal replacement using a scaffold were selected. These researchers then evaluated the methodological quality of each article using the CMS, a 10-criteria scoring list assessing the methodological quality of the selected studies. Fifteen studies were included, all prospective studies, but only two were RCTs. Biological scaffolds were involved in 12 studies, two studies investigated synthetic scaffolds, whereas one remaining article presented data from the use of both classes of device. The mean modified CMS was 64.6. Several demographic and biomechanical factors could influence the outcomes of this treatment modality. Partial replacement using both classes of scaffolds achieved significant and encouraging improved clinical results when compared with baseline values or with controls when present, with no adverse reaction related to the device. The authors concluded that there is a need for more and better designed RCTs, to confirm with a stronger level of evidence the promising preliminary results achieved by the current research.
Although originally cleared for marketing in 2008, the FDA rescinded the marketing clearance for Menaflex as it concluded that the device is intended to be used for different purposes and is technologically dissimilar from devices already on the market.
In April 2013, a Washington DC federal judge upheld the FDA in the Menaflex case (Thompson, 2013). The court noted that the FDA acted properly and within its statutory authority when it re-classified ReGen Biologics Menaflex knee repair device and rescinded the company’s 510(k). The company filed a lawsuit in 2011 charging that the FDA’s decision to withdraw the device’s clearance was arbitrary and capricious. The FDA's Center for Devices and Radiological Health (CDRH) cleared the device in 2008 over objections of some reviewers that it provided little or no benefit to individuals. The new agency leadership brought in by the Obama administration reviewed the earlier decision and determined that the device should not have been cleared because the FDA’s review was influenced by outside pressure, including congressional lobbying. Ivy Sports Medicine subsequently became the successor in interest to ReGen, according to the court.
Hirschmann et al. (2013) evaluated the clinical and radiological outcomes after medial/lateral CMI at 12 months postoperatively. A total of 67 individuals (47 male individuals, mean age of 36 ± 10 years) underwent arthroscopic CMI after previous subtotal medial (n=55) or lateral meniscectomy (n=12) due to persistent joint line pain (n=25) or for prophylactic reasons (n=42). Clinical follow-up consisted of IKDC score, Tegner score, Lysholm score, and VAS for pain and satisfaction (pre-injury, preoperatively, and 12 months postoperatively; follow-up rate, 90%); MRI scans were analyzed according to the Genovese criteria. Nineteen individuals (29%) showed a normal (A), 35 nearly normal (B), five abnormal (C), and one individual severely abnormal total IKDC score (D). The median Tegner pre-injury score was 7 (range, 2–10) and at follow-up 6 (range, 2–10). The mean Lysholm score before surgery was 68 ± 20 and 93 ± 9 at follow-up. Preoperatively, the mean VAS for pain was 4.4 ± 3.1 and 2.0 ± 1.0 at follow-up. Clinical failure of the CMI occurred in three individuals (one infection, one failure of the implant, one chronic synovitis). On MRI, the CMI was completely resorbed in three individuals (5%), partially resorbed in 55 (92%), and entirely preserved in three (5%) individuals. In five individuals (8%), the CMI was iso-intense, in 54 (90%) slightly, and in one (2%) highly hyper-intense; 43 (72%) individuals showed an extrusion of the CMI implant of more than 3 mm. The authors concluded that significant pain relief and functional improvement throughout all scores at 1 year was noted. The CMI undergoes significant re-modeling, degradation, resorption, and extrusion in most of the individuals. No difference in outcomes between the medial and lateral CMI was observed.
Bulgheroni et al. (2014) compared the clinical, objective, and radiographic long-term results of individuals with ACL lesion and partial medial meniscus defects, treated with ACLR and PMM or medial CMI implant. Seventeen individuals treated with combined ACLR and medial CMI and 17 individuals treated with ACL reconstruction and PMM were evaluated with mean follow-up 9.6 years with Lysholm, Tegner, objective and subjective IKDC scores, and VAS for pain. Arthrometric evaluation was performed with KT 2000. Weight-bearing radiographs, anteroposterior and Rosenberg view, were also performed and evaluated with Kellgren-Lawrence score, Ahlbäck score, and joint space narrowing. Preoperative demographic parameters and clinical scores between individuals treated with CMI and PMM revealed no significant differences. A significant improvement of all the clinical scores was detected in both groups from preoperative status to final follow-up. No significant differences between groups were found for clinical and radiographic scores; however, the chronic subgroup of individuals treated with CMI showed a significantly lower level of postoperative knee pain compared to individuals treated with PMM, and the acute subgroup of medial CMI showed better arthrometric scores. The authors concluded that good long-term clinical results in terms of stability, subjective outcomes, and objective evaluation were reported both for medial CMI implant and PMM, combined with ACL reconstruction for the treatment of partial medial meniscus tears combined with ACL lesions. Individuals with chronic meniscal tears treated with medial CMI reported lower levels of postoperative pain compared to meniscectomy, whereas those with acute lesions treated with medial CMI showed less knee laxity. Therefore, the use of CMI in the case of anterior knee instability with a meniscal defect appears justified and able to improve long-term clinical outcomes. The findings of this small study need to be validated by well-designed studies.
Kaleka et al. (2014) stated that the preservation of meniscal tissue is paramount for long-term joint function, especially in younger individuals who are athletically active. Many studies have reported encouraging results following the repair of meniscus tears, including both simple longitudinal tears located in the periphery and complex multiplanar tears that extend into the central third avascular region. However, most types of meniscal lesions are managed with a partial meniscectomy. Options to restore the meniscus range from an allograft transplantation to the use of synthetic and biological technologies. Recent studies have demonstrated good long-term outcomes with MAT, although the indications and techniques continue to evolve, and the long-term chondroprotective potential of this approach has yet to be determined. Several synthetic implants, most of which are approved in the European market, have shown some promise for replacing part of or the entire meniscus, including CMIs, hydrogels, and polymer scaffolds. The authors concluded that currently, there is no ideal implant generated by means of tissue engineering. However, meniscus tissue engineering is a fast-developing field that promises the development of an implant that mimics the histologic and biomechanical properties of a native meniscus.
Myers et al. (2014) noted that there are two scaffold products designed for meniscal reconstruction or substitution of partial meniscal defects that are currently available in the Europe: the collagen meniscal implant (CMI; Ivy Sports Medicine, Gräfelfing, Germany) and the polymer scaffold (PS; Actifit, Orteq Bioengineering, London, United Kingdom).
There are also several comparative studies that reported improved clinical scores in individuals with chronic medial meniscus symptoms treated with CMI versus repeat partial meniscectomy, and a lower reoperation rate. Recently, polymer scaffold insertion was shown to result in improved clinical outcomes in individuals with chronic post-meniscectomy symptoms of the medial or lateral meniscus at short-term follow-up. However, the authors stated that there are currently no medium- or long-term data available for the polymer scaffold, and that the use of meniscal scaffolds in the acute setting has not been found to result in improved outcomes in most studies.
In a multicenter study, Zaffagnini et al. (2015) presented the 2-year results of the use of the lateral CMI for the treatment of irreparable lateral meniscal lesions or partial lateral meniscal defects, investigated the potential predictors of clinical results, and monitored device safety. A total of 43 individuals with a mean age of 30.1 ± 12.0 years were clinically evaluated 24 months after treatment of partial lateral meniscal defects with the CMI. These investigators used the Lysholm score, the Tegner Activity Scale, a VAS for pain (during strenuous activity, during routine activity, and at rest), a functional questionnaire, and a satisfaction questionnaire for the evaluation. All demographic and surgical parameters were used for multiple regression analysis to find outcome predictors. Serious adverse events and reoperations were monitored. All clinical scores significantly improved from preoperatively to final evaluation at 24.2 ± 1.9 months' follow-up. The Lysholm score improved significantly from 64.3 ± 18.4 preoperatively to 93.2 ± 7.2 at final follow-up (P=0.0001). Functional improvement was detected from 6 months after surgery, whereas strenuous activities and knee swelling reached optimal results after 12 months. The highest pain ratings experienced during strenuous activity, during routine activity, and at rest significantly improved from 59 ± 29, 29 ± 25, and 20 ± 25, respectively, preoperatively, to 14 ± 18, 3 ± 5, and 2 ± 6, respectively, at 2 years' follow-up (P=0.0001). At final follow-up, 58% of individuals reported activity levels similar to their pre-injury values whereas 95% of individuals reported that they were satisfied with the procedure. A higher body mass index (BMI), the presence of concomitant procedures, and a chronic injury pattern seemed to negatively affect the final outcomes. Serious adverse events with a known or unknown relation to the scaffold, such as pain, swelling, and scaffold resorption, were reported in 6% of individuals, leading to CMI explantation, debridement, or synovectomy. The authors concluded that the lateral CMI scaffold could be considered a potentially safe and effective procedure to treat both irreparable lateral meniscal tears and post-meniscectomy syndrome in appropriately selected individuals. Chronic injury, high BMI, and concomitant procedures have been shown to negatively affect the short-term results; however, the results appeared to slowly improve through the 24-month follow-up period. This case-series study provided Level IV evidence; its major drawbacks were small sample size (n=430 and short-term follow-up of 24 months).
Mutsaerts et al. (2016) compared the outcomes of various surgical treatments for meniscal injuries including:
1. total and partial meniscectomy;
2. meniscectomy and meniscal repair;
3. meniscectomy and meniscal transplantation;
4. open and arthroscopic meniscectomy; and
5. various different repair techniques.
The Bone, Joint and Muscle Trauma Group Register, Cochrane Database, Medline, Embase and CINAHL were searched for all (quasi) RCTs comparing various surgical techniques for meniscal injuries. Primary outcomes of interest included patient-reported outcomes scores, return to pre-injury activity level, level of sports participation and persistence of pain using the VAS. Where possible, data were pooled and a meta-analysis was performed. Nine studies were included, involving a combined 904 subjects; 330 individuals underwent a meniscal repair, 402 meniscectomy, and 160 a CMI. The only surgical treatments that were compared in homogeneous fashion across more than one study were the arrow and inside-out technique, which showed no difference for re-tear or complication rate. Strong evidence-based recommendations regarding the other surgical treatments that were compared could not be made. The authors concluded that the findings of this meta-analysis illustrated the lack of level I evidence to guide the surgical management of meniscal tears.
Bulgheroni et al. (2016) compared the effectiveness of two different meniscal scaffolds in treating individuals with irreparable partial medial meniscal tear and individuals complaining of pain in the medial compartment of the knee due to a previous partial medial meniscal tear. Based on previous studies, these researchers hypothesized that both the scaffolds are effective in improving clinical outcomes in these patient populations. Twenty-eight individuals underwent collagen-based medial meniscus implantation (CMI-Menaflex) and 25 with a second-generation scaffold (Actifit). All individuals were assessed with Lysholm, Tegner scale, and MRI evaluation: preoperatively, at 6 months, at 12 months, and were followed-up for a minimum of 2 years. Second-look arthroscopy and concomitant biopsy were performed in seven and 12 individuals of CMI and Actifit groups, respectively. The CMI group at final follow-up showed improvement in Lysholm score from 58.4 ± 17.3 to 94.5 ± 6.0, while the Actifit group showed improvement from 67.0 ± 15.7 to 90.3 ± 13.1; the improvement was statistically significant in both the groups, but inter-group difference was not statistically significant (P=0.1061). Tegner Activity Scale score improved in both the groups, but inter-group difference was not statistically significant (P=0.5918). MRI evaluation showed in situ scaffold and no progression of degenerative arthritis in both the groups at final follow-up. Histological evaluation showed more fibrous tissue with blood vessels in the CMI group and the Actift group showed avascular cartilaginous features. The authors concluded that both the scaffolds were effective in improving individuals' symptoms and joint function at short-term follow-up. The main drawbacks of this study were its small sample size (n=28 for the Menaflex group) and short-term follow-up (2 years).
Lin et al. (2017) reported that meniscal injury is a common problem among sportsmen and increasingly seen in the older and more active population. The traditional treatment options include a partial meniscectomy, which provides good mechanical and pain relief to the individual. However, the focus of treatment is shifting towards repairing meniscal tears where possible and replacement of the lost meniscal tissue where appropriate. Replacement can be total or partial. Total meniscal replacement using an allograft is usually reserved for young individuals who meet certain criteria and who have undergone several subtotal meniscectomies or a single-stage total meniscectomy and are still symptomatic. Partial meniscal replacement can be utilized in conjunction with a partial meniscectomy to fill the resulting space left by the resection. The authors noted that collagen-based implants and synthetic scaffolds have entered the European market but have demonstrated mixed results in clinical trials. They stated that tissue engineering to create an implant that mimics the biomechanical properties holds much potential for future research.
According to Sun et al. (2017), current surgical treatments for meniscal tears lead to subsequent degeneration of knee joints, limited donor organs, and inconsistent post-treatment results. Three clinical scaffolds (Menaflex CMI, Actifit scaffold, and NUsurface Meniscus Implant) are available on the market. Menaflex CMI and Actifit scaffold are partial meniscal substitutes with equivalents in histological, radiological, and clinical evaluations. They have received the Conformité Européene (CE) mark in Europe, whereas the FDA believes that additional data are needed to confirm their efficacy on chondral degradation and prevention of osteoarthritis development. Thus, many scaffold-based research activities have been carried out to develop new materials, structures, and fabrication technologies to mimic native meniscus for cell attachment and subsequent tissue development, and restore functionalities of injured meniscus for long-term effects. This review began with a synopsis of relevant structural features of meniscus and went on to describe the critical considerations. Promising advances made in the field of meniscal scaffolding technology, in terms of biocompatible materials, fabrication methods, structure design and their impact on mechanical and biological properties were discussed in detail. Among all the scaffolding technologies, additive manufacturing (AM) is very promising because of its ability to precisely control fiber diameter, orientation, and pore network microarchitecture to mimic the native meniscus microenvironment.
SUMMARY
MAT appears to improve symptoms in select individuals with a prior meniscectomy who are considered too young to undergo total knee replacement. Short- to intermediate-term results are promising. However, the current available peer-reviewed literature does not permit conclusions concerning the effect of MAT on the long-term progression of degenerative changes and joint space narrowing.
MAT is associated with a reoperation rate of up to 32% and a high number of complications, including tears of the transplanted meniscus, displacement, or arthrofibrosis. Therefore, careful patient selection appears to be critical for successful surgical outcomes. MAT is considered a salvage procedure and is not recommended to be performed by surgeons without extensive experience and expertise in complex knee reconstruction. Based on the available evidence, clinical input, and recommendations from relevant medical societies, MAT may be considered medically necessary in individuals younger than 55 years of age with disabling knee pain who have not shown an adequate response to physical therapy and analgesic medications.
Although MAT can be performed by itself to meet clinical needs, MAT may be clinically indicated when performed in combination, either concurrently or sequentially, with treatment of focal articular cartilage lesions using procedures of autologous chondrocyte implantation, osteochondral allografting, or osteochondral autografting; when the latter treatments are also medically necessary.
Evidence evaluating the safety and efficacy of collagen meniscal implants generally involve small patient populations. Some of the preliminary results are encouraging, suggesting meniscus regeneration occurs with an associated reduction in individuals' symptoms (Zaffagnini et al., 2007). One prospective randomized trial (n=311) conducted by Rodkey et al. (2008) demonstrated that the use of a CMI appeared safe, supported new tissue ingrowth, and improved clinical outcomes (e.g., pain scores, Lysholm scores, and patient assessment scores) in individuals with chronic meniscal injury at an average follow-up of 59 months. The authors noted that individuals who received the implant regained significantly more of their lost activity when compared to a group of individuals who underwent repeat partial meniscectomy. A technology assessment conducted by the CTAF (2010) concluded that the collagen meniscal implant for irreparable medial meniscus injury did not meet CTAF technology assessment criterion. The published evidence did not support improvement in health outcomes or that clinical improvement was attainable outside of the investigational setting. Although promising, long-term data supporting safety, efficacy, and improved clinical outcomes, including prevention of osteoarthritis, are not yet available to support widespread use of this bioactive scaffold for meniscal regeneration. There is a paucity of evidence in the peer-reviewed published scientific literature evaluating meniscal scaffolds and implants (Zaffagnini et al., 2007; Rodkey et al., 2008; CTAF, 2010). For other emerging technologies, much of the evidence is in the form of animal, cadaveric or short-term clinical trials and does not support safety and efficacy. Additionally there is no consensus opinion with regard to their widespread clinical application.