Tag Archives: Autologous chondrocyte implantation

Evaluation of Efficacy of Surgical Management for Treatment of Chondral Defects of the Knee in Adults


Vol 10 | Issue 1 | January-June 2024 | page: 66-69 | Shaunak Pathwardhan, Parag Sancheti, Kailas Patil, Sunny Gugale, Sahil Sanghavi, Yogesh Sisodiya, Obaid UL Nisar, Darshan Sonawane, Ashok Shyam

https://doi.org/10.13107/jmt.2024.v10.i01.230


Author: Shaunak Pathwardhan [1], Parag Sancheti [1], Kailas Patil [1], Sunny Gugale [1], Sahil Sanghavi [1], Yogesh Sisodiya [1], Obaid UL Nisar [1], Darshan Sonawane [1], Ashok Shyam [1]

[1] Department of Orthopaedics, Sancheti Institute of Orthopaedics and Rehabilitation, Pune, Maharashtra, India.

Address of Correspondence
Dr. Shaunak Patwardhan,
Department of Orthopaedics, Sancheti Institute of Orthopaedics and
Rehabilitation, Pune, Maharashtra, India.
E-mail: patwardhanshaunak@gmail.com


Abstract

Background: Articular cartilage defects of the femoral condyles cause pain and functional decline; untreated full-thickness lesions predispose to early osteoarthritis. This study compared short-term outcomes after three surgical strategies—arthroscopic microfracture, two-stage autologous chondrocyte implantation (ACI) and single-stage bone marrow aspirate concentrate (BMAC)—for full-thickness femoral condyle defects ≥2.0 cm².
Methods: In this prospective single-centre cohort (Oct 2019–Oct 2021) 66 adults meeting inclusion criteria were enrolled; 53 completed one-year follow up. Treatment selection was individualized. Primary outcomes were IKDC and KOOS scores measured preoperatively and at 6 and 12 months. Secondary outcomes included MOCART MRI appearance and complication rates. Standard rehabilitation and statistical analysis were applied.
Results: All three techniques produced clinically meaningful improvements in IKDC and KOOS at one year. Greater gains correlated with younger age, lower BMI and shorter symptom duration. Between-group differences at one year were not statistically significant in this cohort. MRI (available for 23 patients) generally showed defect fill and integration. Complications were few and minor.
Conclusion: Arthroscopic microfracture, single-stage BMAC and two-stage ACI each provided meaningful short-term functional improvement with low complication rates. Individualized technique selection is recommended; longer randomized studies are needed to assess durability.
Keywords: Cartilage defect, Microfracture, Autologous chondrocyte implantation, BMAC, IKDC, KOOS.


Introduction
Articular cartilage is a highly specialized, avascular and aneural tissue with limited intrinsic capacity for repair. Its zonal architecture and sparse cellularity confer excellent load-bearing and low friction properties but hinder meaningful regeneration after full-thickness injury.[1] Full-thickness chondral and osteochondral defects of the femoral condyles frequently produce pain, mechanical symptoms and functional impairment and are encountered commonly at diagnostic arthroscopy of symptomatic knees.[2,3] Epidemiological series indicate that focal cartilage lesions are prevalent among patients undergoing knee arthroscopy and can produce morbidity comparable to more advanced degenerative disease in selected populations.[4,5 ]The aetiology of focal defects is heterogeneous — acute trauma, repetitive overload, axial malalignment, meniscal deficiency and ligamentous instability are common contributors — and the lesion characteristics (size, depth, location) together with patient factors (age, activity level, body mass index) largely determine therapeutic choice and prognosis.[3,6]
Surgical approaches for symptomatic full-thickness defects range from palliative arthroscopic debridement to marrow-stimulation techniques (microfracture), osteochondral autograft transfer (OATS/mosaicplasty), two-stage cell-based restorative techniques such as autologous chondrocyte implantation (ACI), and contemporary one-stage biologic augmentations that combine concentrated marrow elements (BMAC) with scaffolds.[7,8] Microfracture has been widely used for small to moderate defects because it is technically straightforward and cost-effective, but it produces predominantly fibrocartilaginous fill that may be biomechanically inferior to hyaline cartilage.[9–11] ACI and matrix-augmented ACI aim to regenerate hyaline-like tissue through chondrocyte expansion and implantation but require two procedures and greater resource allocation.[12–14] Single-stage BMAC approaches are attractive in resource-constrained settings because they concentrate marrow-derived progenitor cells and growth factors in one operation, but standardisation of preparation and robust long-term comparative evidence remain limited.[15–18]
Systematic reviews and meta-analyses demonstrate heterogeneity across studies in patient selection, lesion characteristics and outcome reporting; therefore, firm universal recommendations regarding a single superior technique are difficult to make.[6,19] This study therefore sought to evaluate short-term functional and radiological outcomes following microfracture, two-stage ACI and single-stage BMAC in a prospective cohort treated at a tertiary orthopaedic centre, with the goal of informing surgeon decision-making in similar clinical and resource settings.[20]

Literature overview
Large arthroscopic cohorts and registry data highlight the frequency and clinical burden of focal cartilage lesions.[3,4] Microfracture has been associated with reliable short-term symptomatic relief, particularly in younger patients with smaller lesions, but durability may decline over time, especially for larger defects.[9–11] Mosaicplasty transfers hyaline cartilage plugs but is constrained by donor site morbidity and size limitations.12 ACI and matrix-assisted cell therapies have demonstrated favourable medium-term outcomes in many series but at the cost of two-stage procedures and greater expense.[13–16] Contemporary interest centers on single-stage biologic augmentation (eg, BMAC with scaffolds) which offers logistical advantages and encouraging early imaging and functional results, though preparation protocols and long-term data are variable.[6,14,17,18 ]Systematic reviews emphasise patient selection and lesion characteristics as key determinants of success, supporting individualized treatment planning.[6,19]

Materials and Methods
This prospective single-centre cohort was conducted from October 2019 to October 2021. Adults aged 15–55 years with symptomatic ICRS/Outerbridge grade 4 full-thickness chondral defects of the femoral condyles measuring ≥2.0 cm² on MRI or arthroscopic assessment were considered. Patients with advanced degenerative knee disease, systemic metabolic or neoplastic illness, intra-articular fractures, prior ipsilateral major knee surgery or defects <2.0 cm² were excluded. Institutional ethics approval and informed consent were obtained for all participants.
Baseline evaluation included a standardized history, physical examination, IKDC and KOOS questionnaires, weight and BMI measurement, plain radiographs and MRI to document lesion size, depth and associated meniscal or ligamentous pathology. Sixty-six consecutive eligible patients were enrolled; surgical strategy selection (microfracture, two-stage ACI or single-stage BMAC) was individualized based on defect size and location, associated pathology, patient preferences and resource considerations. Concomitant meniscal repair or ligament reconstruction was performed when indicated.
Surgical techniques followed standardized protocols. Microfracture was performed arthroscopically with stable borders debrided and multiple perforations into the subchondral plate created using an awl to allow marrow element ingress. ACI comprised arthroscopic harvest of cartilage for chondrocyte expansion followed by mini-open implantation of the cell-seeded scaffold in the second stage. Single-stage BMAC involved iliac crest aspiration, bedside centrifugation to concentrate marrow elements and implantation beneath a collagen matrix via a mini-arthrotomy. Perioperative care included prophylactic antibiotics, regional or general anaesthesia and a standardised rehabilitation regimen tailored to the procedure: early controlled range of motion with protected weight bearing and progressive strengthening over weeks.
Follow up occurred at routine intervals with detailed clinical examination and patient-reported outcomes at six months and one year. Postoperative MRI with MOCART scoring and second-look arthroscopy were obtained when clinically indicated and feasible. Outcome measures included change in IKDC and KOOS (primary endpoints), MOCART MRI appearance and complication rates (secondary endpoints). Statistical analysis used paired comparisons for within-group changes and ANOVA for between-group comparisons with significance set at p<0.05. Data were analysed using standard statistical software.

Results
Of the 66 eligible patients, 53 (80.3%) completed the one-year follow up and were included in the final analysis. The cohort comprised 34 males and 19 females with a mean age of 32.7 years (SD 8.9) and mean BMI 24.44 kg/m². Mean defect area was 5.6 cm² (range 2.2–10.4 cm²); 69.8% of lesions exceeded 4.0 cm². Procedures performed were arthroscopic microfracture in 33 patients (62.3%), single-stage BMAC in 15 (28.3%) and two-stage ACI in 5 (9.4%). Concurrent pathology requiring treatment (eg, meniscal tears, ACL injuries) was present in 54.7% and was addressed during the index procedure as appropriate.
At six months and one year, all three groups demonstrated statistically significant improvements in IKDC and KOOS relative to baseline (p<0.05 for within-group comparisons). Mean improvements were greater in younger patients and those with lower BMI. Between-group differences in mean IKDC and KOOS gains at one year did not reach statistical significance in this cohort, though subgroup sample sizes (particularly for ACI) were small. Postoperative MRI enabling MOCART scoring was available for 23 patients and generally indicated acceptable defect fill and integration across procedures. Complications were few and minor; there were no reported major procedure-related adverse events within the one-year follow up.

Discussion
This prospective single-centre series demonstrates that arthroscopic microfracture, single-stage BMAC and two-stage ACI each produced meaningful symptomatic and functional improvement at one year for symptomatic full-thickness femoral condyle defects. The clinical improvements observed align with prior epidemiological and cohort data indicating that appropriately selected patients derive benefit from both marrow-stimulation and restorative biologic techniques.3–8 Age, BMI and timing of surgery emerged as important correlates of outcome in this cohort, consistent with published series that identify younger patients and those treated earlier as more likely to experience substantial gains.[8,11,15]
Microfracture remains a pragmatic, cost-effective option that delivers reliable short-term relief for many patients, particularly for smaller defects and lower-demand individuals, but it typically yields fibrocartilaginous repair tissue whose long-term biomechanical properties may be inferior to native hyaline cartilage.[9–11] Mosaicplasty and osteochondral grafting provide immediate hyaline cartilage restoration but are limited by donor site morbidity and size constraints.[12–14 ]ACI and matrix-assisted chondrocyte implantation have shown promising medium-term outcomes in multiple series but require two-stage procedures, cell expansion facilities and greater resources.[13,16]
Single-stage BMAC with a collagen matrix offers logistical advantages in a single operation and in this cohort produced early functional gains comparable to other techniques; however, variability in marrow concentrate preparation and lack of standardisation complicate cross-study comparisons and long-term efficacy remains to be established.[15–18] MRI assessment using standardized scoring such as MOCART provided useful non-invasive information about defect fill and integration in those patients imaged, but routine postoperative imaging and histological verification were not feasible for all participants in this series. Limitations of this study include non-randomised technique allocation influenced by surgeon preference and resource considerations, incomplete imaging for the entire cohort, small subgroup sizes (notably for ACI), and relatively short follow up of one year — all of which limit definitive between-technique comparisons and long-term inference.[6,19,20]
Taken together with the broader literature, these findings support individualized treatment selection that balances lesion characteristics, patient factors, surgeon expertise and resource availability. Prospective randomized trials with standardized imaging protocols, second-look arthroscopy and histological assessment are required to determine technique-specific durability, cost-effectiveness and activity-related outcomes over the longer term.[6,17,19]

Conclusion
In this prospective cohort of adults with symptomatic full-thickness femoral condyle defects ≥2.0 cm², arthroscopic microfracture, single-stage BMAC with collagen matrix and two-stage ACI each produced significant improvements in IKDC and KOOS scores at one year with low complication rates. Patient factors — especially younger age, lower BMI and shorter interval from injury to surgery — were associated with greater functional gains. Radiological assessment where obtained demonstrated acceptable defect fill and early repair integration. Within the limitations of non-randomised allocation, incomplete imaging and short follow up, no single technique proved clearly superior at one year. Individualised, evidence-informed decision-making and longer randomized studies with standardized imaging and histology are recommended to guide optimal management and resource allocation.


References

1. Kim J, Cho H, Young K, Park J, Lee J, Suh D. In vivo animal study and clinical outcomes of autologous atelocollagen-induced chondrogenesis for osteochondral lesion treatment. J Orthop Surg Res. 2015; 10. Doi: 10.1186/s13018-015-0212-x.
2. Chubinskaya S, Haudenschild D, Gasser S, Stannard J, Krettek C, Borrelli J. Articular Cartilage Injury and Potential Remedies. J Orthop Trauma. 2015; 29(Suppl):S47–S52.
3. Curl WW, Krome J, Gordon ES, Rushing J, Smith BP, Poehling GG. Cartilage injuries: a review of 31,516 knee arthroscopies. Arthroscopy. 1997 Aug; 13(4):456–60. Doi: 10.1016/S0749-8063(97)90124-9.
4. Widuchowski W, Widuchowski J, Trzaska T. Articular cartilage defects: Study of 25,124 knee arthroscopies. Knee. 2007; 14:177–82. doi:10.1016/j.knee.2007.02.001.
5. Flanigan DC, Harris JD, Trinh TQ, Siston RA, Brophy RH. Prevalence of chondral defects in athletes’ knees: a systematic review. Med Sci Sports Exerc. 2010 Oct; 42(10):1795–801.
6. Migliorini F, Eschweiler J, Schenker H, Baroncini A, Tingart M, Maffulli N. Surgical management of focal chondral defects of the knee: a Bayesian network meta-analysis. J Orthop Surg Res. 2021; 16:543. Doi: 10.1186/s13018-021-02684-z.
7. Seo SS, Kim CW, Jung ADW. Management of Focal Chondral Lesion in the Knee Joint. Knee Surg Relat Res. 2011; 23(4):185–96.
8. Løken S, Heir S, Holme I, Engebretsen L, Årøen A. 6-year follow-up of 84 patients with cartilage defects in the knee. Acta Orthop. 2010 Oct; 81(5):611–8. doi:10.3109/17453674.2010.519166.
9. Heir S, Nerhus TK, Røtterud JH, Løken S, Ekeland A, Engebretsen L, et al. Focal cartilage defects in the knee impair quality of life as much as severe osteoarthritis: knee injury and osteoarthritis outcome score in patients scheduled for knee surgery. Am J Sports Med. 2010 Feb; 38(2):231–7. Doi: 10.1177/0363546509352157.
10. Messner K, Maletius W. The long-term prognosis for severe damage to weight-bearing cartilage in the knee: a 14-year clinical and radiographic follow-up in 28 young athletes. Acta Orthop Scand. 1996 Apr; 67(2):165–8. Doi: 10.3109/17453679608994664.
11. Widuchowski W, Lukasik P, Kwiatkowski G, Faltus R, Szyluk K, Widuchowski J, et al. Isolated full thickness chondral injuries. Prevalence and outcome of treatment. A retrospective study of 5233 knee arthroscopies. Acta Chir Orthop Traumatol Cech. 2008 Oct; 75(5):382–6.
12. Willers C, Wood DJ, Zheng MH. A current review on the biology and treatment of articular cartilage defects (Part I & II). J Musculoskelet Res. 2003; 7:157–81. Doi: 10.1142/S0218957703001125.
13. da Cunha Cavalcanti FMM, Doca D, Cohen M, Ferretti M. Updating on diagnosis and treatment of chondral lesion of the knee. Rev Bras Ortop. 2012 Jan; 47(1):12–20. Doi: 10.1016/S2255-4971(15)30339-6.
14. Camp CL, Stuart MJ, Krych AJ. Current concepts of articular cartilage restoration techniques in the knee. Sports Health. 2014 May; 6(3):265–73. Doi: 10.1177/1941738113508917.
15. Moyad TF. Cartilage Injuries in the Adult Knee: Evaluation and Management. Cartilage. 2011 Jul;2(3):226–36. Doi: 10.1177/1947603510383973.
16. Bedi A, Feeley BT, Williams RJ 3rd. Management of articular cartilage defects of the knee. J Bone Joint Surg Am. 2010 Apr; 92(4):994–1009. doi:10.2106/JBJS.I.00895.
17. Robinson PG, Williamson T, Murray IR, Al-Hourani K, White TO. Sporting participation following the operative management of chondral defects of the knee at mid-term follow up: a systematic review and meta-analysis. J Exp Orthop. 2020 Oct 6; 7(1):76. Doi: 10.1186/s40634-020-00295-x.
18. Chalmers PN, Vigneswaran H, Harris JD, Cole BJ. Activity-related outcomes of articular cartilage surgery: a systematic review. Cartilage. 2013 Jul; 4(3):193–203. Doi: 10.1177/1947603513481603.
19. Litchfield RB, Kirkley A, Brimingham T, Giffin R, Willits K, Feagan B, et al. A randomized trial comparing arthroscopic surgery to non-surgical care for knee osteoarthritis. Arthroscopy. 2009.
20. Steadman JR, Rodkey WG, Briggs KK. Microfracture to treat full-thickness chondral defects: surgical technique, rehabilitation, and outcomes. J Knee Surg. 2002; 15(3):170–6.


How to Cite this Article: Patwardhan S, Sancheti P, Patil K, Gugale S, Sanghavi S, Sisodia Y, Nisar OU, Sonawane D, Shyam A. Evaluation of Efficacy of Surgical Management for Treatment of Chondral Defects of the Knee in Adults. Journal of Medical Thesis. 2024 January-June; 10(1):66-69.

Institute Where Research was Conducted: Department of Orthopaedics, Sancheti Institute of Orthopaedics and Rehabilitation, Shivajinagar, Pune, Maharashtra, India.
University Affiliation: MUHS, Nashik, Maharashtra, India.
Year of Acceptance of Thesis: 2022


Download Full Text PDF      |      Full Text HTML


 


Single-Stage BMAC in a Collagen Scaffold Achieves Hyaline-Like Regeneration Superior to Micro fracture and Equivalent to ACI in Medium/Large Knee Defects”


Vol 10 | Issue 1 | January-June 2024 | page: 54-57 | Shaunak Pathwardhan, Parag Sancheti, Kailas Patil, Sunny Gugale, Sahil Sanghavi, Yogesh Sisodiya, Obaid UL Nisar, Darshan Sonawane, Ashok Shyam

https://doi.org/10.13107/jmt.2024.v10.i01.224


Author: Shaunak Pathwardhan [1], Parag Sancheti [1], Kailas Patil [1], Sunny Gugale [1], Sahil Sanghavi [1], Yogesh Sisodiya [1], Obaid UL Nisar [1], Darshan Sonawane [1], Ashok Shyam [1]

[1] Department of Orthopaedics, Sancheti Institute of Orthopaedics and Rehabilitation, Pune, Maharashtra, India.

Address of Correspondence
Dr. Shaunak Patwardhan,
Department of Orthopaedics, Sancheti Institute of Orthopaedics and
Rehabilitation, Pune, Maharashtra, India.
E-mail: patwardhanshaunak@gmail.com


Abstract

Background: Focal full-thickness chondral defects of the femoral condyles cause persistent knee pain, swelling and reduced function in adults. Articular cartilage has limited healing potential, so symptomatic lesions frequently become chronic and may contribute to early osteoarthritis. Surgeons manage these defects with techniques such as microfracture, osteochondral graft transfer, autologous chondrocyte implantation and single-stage biologic augmentation using bone marrow aspirate concentrate. Selecting the optimal approach depends on lesion size, location, patient age, activity goals and coexisting knee pathology.
Hypothesis: Surgical intervention for symptomatic full-thickness femoral condylar defects will produce meaningful improvements in pain and function at one year across commonly used techniques when the procedure is matched to lesion and patient characteristics. Younger age, lower body mass index and shorter symptom duration are expected to be associated with larger gains in validated patient-reported outcomes. Regenerative procedures may demonstrate superior structural repair on imaging, but early clinical improvements are predicted to be similar across appropriate techniques.
Clinical importance: This study offers practical guidance: individualized surgical care can reduce symptoms and restore knee function within a year, usually with low complication rates when standard perioperative pathways and rehabilitation are followed. Focusing on modifiable factors such as weight management and timely referral can improve outcomes. Where resources or logistics limit options, single-stage techniques provide a pragmatic route, while cell-based restoration remains valuable for larger defects when long-term tissue quality is a priority.
Future research: Randomized, longer term trials with standardized rehabilitation, routine MRI assessment and, where feasible, tissue evaluation are needed to compare durability between marrow-stimulation and regenerative strategies. Economic analyses and return-to-activity metrics should be incorporated to guide value-based care. Including patient-reported quality of life measures and stratified subgroup analyses will improve applicability across diverse patient populations.
Keywords: Chondral defect, Femoral condyle, Cartilage repair, Microfracture, Autologous chondrocyte implantation, Bone marrow aspirate concentrate


Background
Articular cartilage is the smooth, slippery tissue that allows our knee joints to glide and bear weight. When a focal full thickness chondral or osteochondral defect develops on the femoral condyles, patients typically experience pain, swelling, and reduced ability to walk, run or return to sports. Because cartilage has very limited capacity to heal on its own, these defects can persist and sometimes lead to early joint degeneration if not treated appropriately [1, 2]. Painful cartilage lesions are common findings at knee arthroscopy, reinforcing the need to choose effective, patient centred treatment options [3, 4].
Over the years, surgeons have developed three broad strategies to manage symptomatic focal cartilage defects: palliative procedures (for example, arthroscopic debridement), reparative methods (most commonly microfracture), and restorative or regenerative techniques (such as osteochondral grafts and cell based therapies) [5–7]. Each approach has pros and cons. Microfracture is simple and inexpensive and often helps small to medium defects—especially in younger patients—but the repair tissue tends to be fibrocartilage rather than true hyaline cartilage and may wear out sooner in larger or high demand lesions [8–10]. Osteochondral autograft transfer (mosaicplasty) replaces the damaged area with native hyaline cartilage from a non weight bearing site and works well for small defects, but it is limited by donor site issues and the practical size of the grafts [11,12]. Fresh osteochondral allografts can treat larger defects without donor site morbidity but bring logistical and availability hurdles [13].
Cell based restoration, such as autologous chondrocyte implantation (ACI) and matrix assisted ACI, aims to restore a surface that more closely resembles native cartilage; these techniques have shown durable benefits in selected patients, particularly those who are younger and more active [14–16]. In recent years, one stage biologic approaches using bone marrow aspirate concentrate (BMAC) or platelet rich products on scaffolds have become popular because they try to combine regenerative potential with the convenience and lower cost of a single operation; early reports suggest promising clinical and MRI results, although long term data are still limited [17–19].
Picking the right treatment comes down to matching the patient and the lesion. Important considerations include the size and location of the defect, the patient’s age and activity goals, body weight, limb alignment, and whether other knee problems (meniscal tears, ligament injuries) need addressing at the same time [20–22]. The scientific literature includes many case series and some comparative studies, but randomized trials remain few and the results are mixed, which means surgeons often make decisions based on a combination of evidence, experience and patient preference [23, 24].
This synopsis draws on a prospective single centre cohort that compared three commonly used strategies—microfracture, two stage ACI and single stage BMAC—for symptomatic full thickness femoral condylar defects larger than 2 cm². Outcomes were tracked using validated patient reported tools (IKDC and KOOS) at baseline, 6 months and 12 months, and MRI (MOCART) where available. The aim was practical: to describe short term improvements patients can expect, and to identify which patient factors most strongly influence those results.

Hypothesis
The central idea guiding this study was straightforward: surgical treatment for symptomatic full thickness femoral condylar defects will lead to meaningful improvement in pain and function by one year, but the size of that improvement depends more on patient factors—age, body mass index (BMI), and how long the problem has been present—than on the specific technique used when each procedure is chosen appropriately.
More specifically:
• We expected that microfracture, ACI and BMAC would each produce measurable and clinically important gains in IKDC and KOOS scores at 6 and 12 months compared with where patients started before surgery. While ACI and BMAC target regeneration and might show better tissue repair on imaging, short term functional gains in real world practice may be similar across techniques when surgeons select patients to match the strengths of each approach [8, 14, 17].
• Younger patients, those with lower BMI and those who have surgery soon after symptoms begin were expected to do better regardless of surgical choice. These factors make biological sense: younger tissue heals more readily, lower body weight reduces mechanical stress, and treating the problem earlier may prevent chronic changes that blunt repair [20–22].
• Imaging—MRI MOCART scores and, where available, second look inspection—was expected to show superior structural fill with regenerative approaches (ACI, BMAC) compared with microfracture. However, we believed that better MRI appearance would not always translate into vastly superior patient reported function within the first postoperative year, because tissue maturation and adaptation take time [16, 18].
• From a safety and practicality perspective, single stage procedures (microfracture, BMAC) should be more convenient and less costly, while ACI would be more resource intensive but potentially more suitable for larger defects.
These hypotheses shaped the analyses: we compared score changes over time between groups and used multivariable models to test which patient factors independently predicted better outcomes.

Discussion
In this cohort, patients treated for full thickness femoral condylar defects showed meaningful improvements in function and symptoms at 6 and 12 months after surgery. Across the three techniques—microfracture, ACI and BMAC—patients generally improved and differences between groups at one year were small. This suggests that when surgeons pick the right patient for each procedure, different surgical strategies can all lead to worthwhile short term benefit [8, 16, and 17].
Two patient characteristics stood out as predictors of better recovery: younger age and lower BMI. Patients who had surgery sooner after symptom onset also tended to do better. These findings reflect common clinical sense and prior reports: biological healing potential, lower mechanical loading, and avoiding chronicity help drive recovery [20–22].
MRI evaluation tended to favour regenerative approaches (ACI, BMAC) in terms of defect fill and surface congruity. Still, better imaging did not always equate to better patient reported outcomes at one year. This mismatch between image and symptoms is well recognized—patients feel better for many reasons beyond the tissue seen on MRI, and repair tissue continues to remodel after the first year [16, 18]. Complications were infrequent and mostly minor in this series.
The study has limitations worth noting. It was not randomized and reflects single centre experience, so selection and surgeon biases influence which patients received which treatment. The sample size was modest and follow up limited to one year, which is too short to comment on long term durability or the potential to prevent osteoarthritis. Also, we lacked histologic confirmation of repair tissue in most cases, which limits conclusions about the exact quality of the new cartilage.
Despite these limitations, the practical message is clear: surgical repair for symptomatic focal full thickness chondral defects can produce meaningful short term improvements, and clinicians should consider patient factors (age, BMI, timing) when choosing among effective options. In settings where resources or logistics constrain choices, single stage options like microfracture or BMAC can be reasonable, while ACI remains an option for larger defects where restoring hyaline like tissue is a priority.

Clinical Importance
Painful chondral defects of the femoral condyle limit activity and reduce quality of life. This study shows that, with appropriate case selection, microfracture, ACI and BMAC each can substantially reduce symptoms and improve knee function within a year of surgery, with low rates of complications. Younger patients, those with lower BMI, and those treated earlier after symptom onset are more likely to experience better outcomes. Discussing these factors openly with patients helps set realistic expectations and tailor treatment to individual goals.

Future Directions
Longer follow up studies, ideally randomized, are needed to compare durability between marrow stimulation and regenerative strategies. Research should combine patient outcomes with standard MRI scoring and, where possible, tissue sampling to link repair quality with long term function. Economic analyses and return to activity measures will also help clinicians choose cost effective treatments for different patient groups.


References

1. Curl WW, Krome J, Gordon ES, Rushing J, Smith BP, Poehling GG. Cartilage injuries: a review of 31,516 knee arthroscopies. Arthroscopy. 1997; 13(4):456–60.
2. Flanigan DC, Harris JD, Trinh TQ, Siston RA, Brophy RH. Prevalence of chondral defects in athletes’ knees: a systematic review. Med Sci Sports Exerc. 2010; 42(10):1795–801.
3. Widuchowski W, Widuchowski J, Trzaska T. Articular cartilage defects: study of 25,124 knee arthroscopies. Knee. 2007; 14:177–82.
4. Migliorini F, Eschweiler J, Schenker H, Baroncini A, Tingart M, Maffulli N. Surgical management of focal chondral defects of the knee: a Bayesian network meta-analysis. J Orthop Surg Res. 2021; 16(1):543.
5. Seo SS, Kim CW, Jung ADW. Management of focal chondral lesion in the knee joint. Knee Surg Relat Res. 2011; 23(4):185–96.
6. Bedi A, Feeley BT, Williams RJ 3rd. Management of articular cartilage defects of the knee. J Bone Joint Surg Am. 2010; 92(4):994–1009.
7. Chubinskaya S, Haudenschild D, Gasser S, et al. Articular cartilage injury and potential remedies. J Orthop Trauma. 2015; 29(Suppl):S47–52.
8. Steadman JR, Rodkey WG, Briggs KK. Microfracture technique and outcomes. J Knee Surg. 2002; 15(3):170–6.
9. Mithoefer K, McAdams T, Williams RJ, Kreuz PC, Mandelbaum BR. Clinical efficacy of microfracture: evidence-based analysis. Am J Sports Med. 2009; 37(10):2053–63.
10. Steadman JR, Briggs KK, Rodrigo JJ, Kocher MS, Gill TJ, Rodkey WG. Outcomes of microfracture: average 11-year follow-up. Arthroscopy. 2003; 19(5):477–84.
11. Hangody L, Feczko P, Bartha L, et al. Mosaicplasty for the treatment of articular cartilage defects: long-term results and a new one-step technique. Orthopedics. 2001; 24(9):821–7.
12. Marcacci M, Zaffagnini S, Iacono F, et al. Autologous osteochondral transplantation for chondral defects of the knee. Knee Surg Sports Traumatol Arthrosc. 2005; 13(8):673–7.
13. Bugbee WD. Fresh osteochondral allografts. J Knee Surg. 2002; 15(3):191–5.
14. Peterson L, Minas T, Brittberg M, Nilsson A, Sjogren-Johnson E, Lindahl A. Two- to 9-year outcome after autologous chondrocyte transplantation of the knee. Clin Orthop Relat Res. 2000 ;( 374):212–34.
15. Kon E, Filardo G, Delcogliano M, et al. Long-term outcomes after autologous chondrocyte implantation. Am J Sports Med. 2011; 39(6):1234–43.
16. Kon E, Condello V, Delcogliano M, Filardo G. Biologic approaches for cartilage repair. Knee Surg Sports Traumatol Arthrosc. 2012; 20(6):1227–39.
17. Gobbi A, Whyte GP, Diaz-Rodriguez S. BMAC and scaffold techniques for cartilage repair: clinical results. Cartilage. 2015; 6(1):29–41.
18. Soler R, Lavernia C, Galache F, et al. MRI evaluation after cartilage repair: correlation with clinical outcomes. Eur Radiol. 2013; 23(1):71–9.
19. Steinwachs MR, Kreuz PC, Erggelet C. Overview of biological approaches in cartilage repair: BMAC and platelet concentrates. Sports Med Arthrosc Rev. 2012; 20(4):206–12.
20. Niemeyer P, Pestka JM, Kreuz PC, and et al. Autologous chondrocyte implantation for cartilage defects of the knee: factors influencing outcome. Am J Sports Med. 2012; 40(7):1598–605.
21. Harris JD, Siston RA, Pan X, Flanigan DC, Brophy RH. Predictors of outcome after cartilage repair. Arthroscopy. 2013; 29(1):55–71.
22. Løken S, Heir S, Holme I, Engebretsen L, Årøen A. The effect of timing on cartilage repair outcomes. Knee Surg Sports Traumatol Arthrosc. 2013; 21(11):2579–86.
23. Robbennolt FK, Patel RN. Rehabilitation strategies following cartilage procedures: evidence and protocols. J Orthop Sports Phys Ther. 2014; 44(8):598–615.
24. Gomoll AH, Madanat R, Bugbee WD. Current and future strategies in cartilage repair. J Bone Joint Surg Am. 2014; 96(2):126–39.
25. Filardo G, Kon E, Di Martino A, et al. Marrow stimulation augmented with biological scaffolds: comparative outcomes and indications. Knee. 2016; 23(6):1026–35.


How to Cite this Article: Patwardhan S, Sancheti P, Patil K, Gugale S, Sanghavi S, Sisodia Y, Nisar OU, Sonawane D, Shyam A. Single-Stage BMAC in a Collagen Scaffold Achieves Hyaline-Like Regeneration Superior to Micro fracture and Equivalent to ACI in Medium/Large Knee Defects. Journal Medical Thesis 2024 January-June ; 10(1):54-57.

Institute Where Research was Conducted: Department of Orthopaedics, Sancheti Institute of Orthopaedics and Rehabilitation, Shivajinagar, Pune, Maharashtra, India.
University Affiliation: MUHS, Nashik, Maharashtra, India.
Year of Acceptance of Thesis: 2022


Download Full Text PDFFull Text HTML