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Received : 26-02-2023

Accepted : 15-05-2023



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Get Permission Sirsat, Tapadiya, Hajgude, and Shelke: Concentrated bone marrow aspirate and application for the treatment of osteochondral lesion and outcome


Introduction

The recent increase in chondral injury diagnoses isn't due to a shift in the disease's normal course, but rather to advancements in our knowledge of its pathology and diagnostic technology.1 Osteochondral grafting can restore the missing hyaline cartilage but is constrained by the size, number, and morbidity of the donor site. For the pathology of the knee, bone marrow aspirate concentrate (BMAC) has become a cutting-edge therapy. BMAC is a source of growth factors, which are regarded to be significant because of their anabolic and anti-inflammatory properties, despite having a small number of stem cells. Multipotent mesenchymal stem cells (MSC) and growth factors found in bone marrow concentrate cells (BMAC) have attracted interest and have shown to be as least as effective as existing methods.2, 3

Gels and scaffolds made of collagen have undergone testing to improve transplant fixation. Hyaluronic acid and fibrin gel together could serve as a framework for cartilage repair.4

Case History

Male, age 18, complaining of left knee pain when walking for the past three months. The left knee has previously experienced injuries from being hit by a bike two years ago.

On examination, there were no external injuries or swelling, just an antalgic gait. Tenderness was present on the left femur lateral condyle with no crepitus on movement.

ROM at the knee joint: 90–130 degrees of painful flexion with no restriction; no extension lags. No difference in limb length. No neurovascular deficit.

Preoperative scans

Figure 1

X-ray showing an antero-posterior and lateral view of left knee joint

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Figure 2

Coronal section of MRI scan showing the defect

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Surgical technique

Aspiration of the bone marrow

Write down the patient's ASIS. About 30 cc of bone marrow is aspirated from the iliac crest using an aspiration needle and syringes filled with anticoagulant solution (Citrate Dextrose). (Figure 3, Figure 4).

Figure 3

Showing aspirated bone morrow

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Figure 4

Showing the aspiration of bone marrow

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The aspirate of bone marrow was then centrifuged twice.

To obtain BMAC, the second cycle was run for 5 minutes at 3600 rpm after the first cycle's 6 minutes at 3500 rpm.

The process of making the BMAC, HA, and fibrin gel mixture

Two syringes are attached to a mixing catheter for application. 0.8 ml of fibrinogen and 0.2 ml of hyaluronic acid are combined in one syringe. 0.8 ml of BMC and 0.2 ml of thrombin are present in the second syringe. (Figure 5)

Figure 5

Showing Y connector syringe with the mixture

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A combination has a 1:1 ratio of fibrinogen to thrombin

The knee was accessed via a midline incision and a sub-vastus approach. Pre-operative imaging helped with the evaluation of the knee joint and the identification of the chondral lesions. Two lesions were determined to be suitable for repair. The lesions were removed with curettes, and a hole was drilled into the defect. Care was taken to preserve a stable knee of good cartilage along the lesion's periphery. Holes have been dug to a depth of 3 mm at 3 mm intervals. (Figure 7). A clean wash was administered.

Figure 6

Showing identified lesion

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Figure 7

Micro-fractures done into the lesion

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Mixture application

The BMAC, HA, and fibrin gel combination is applied evenly and gently across the lesion (s). Within five minutes, the graft becomes hard. The knee is then repeatedly moved through its range of motion to anatomically shape the graft and verify its stability (Figure 8)

Figure 8

Lesions filled with BMAC mixture

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Rehabilitation phases

Phase 1

  1. Objectives

    1. Reduce pain and effusion;

    2. Shield the transplant from bearing loads and shearing pressures. 

    3. Muscle atrophy,

    4. Active full extension, and knee healing over time.

  2. The criterion for achievements

    1. Knee flexion of greater than 120 degrees is achieved.

    2. Complete active knee extension is also a requirement.

    3. Little to no pain and swelling - attained

    4. Achieved pain-free weight bearing

    5. Quadriceps muscle recruitment was adequate and successful.

Phase 2

  1. Transition and restoration of gait

    1. Attained a normal gait

    2. Whole range of motion recovery (full extension, flexion > 135°) attained

    3. Achieved adequate muscle tone and neuromuscular control

    4. No discomfort or puffiness. – Attained

Follow up status of the patient after 3 months.

  1. No new complaints,

  2. Examination reveals normal gait,

  3. The suture site is intact and healthy.

  4. Knee joint range of motion: painless full-range movements

  5. There is no neuromuscular deficit and adequate muscle tone.

Post op after 3 months

Figure 9

Knee flexion in prone

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Figure 10

Knee flexion in supine

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Figure 11

Knee extension

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Figure 12

Operative scar site

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Discussion

An orthopedic surgeon finds osteochondral lesions in young children challenging. However, the outcomes of other techniques such as autologous chondrocyte transplantation, mosaicplasty, and platelet concentrated grafts are not promising. This straightforward method is safe and effective because it doesn't cause any new cartilage defects. Moreover, it is less expensive than chondrocyte cultivation. Fibrocartilage regenerates after bone marrow stimulation, which is how BMAC works. However, in order to use the BMAC and compare it to ACT, high-level systemic investigations are required.

Conclusion

In this case report conclude that Bone marrow aspiration concentrate has potential to enhance cartilage repair and compare to other methods has its advantage over them. BMAC application are effective in improving pain and functional outcome in patients of osteochondral lesion. This is case report and a larger randomised trail needed to make definitive conclusions.

Source of Funding

None.

Conflict of Interest

None.

References

1 

JHP Hui F Chen A Thambyah EH Lee Treatment of chondral lesions in advanced osteochondritis dissecans: a comparative study of the efficacy of chondrocytes, mesenchymal stem cells, periosteal graft, and mosaicplasty (osteochondral autograft) in animal modelsJ Pediatr Orthop200424442733

2 

H Chiang CH Hsieh YH Lin S Lin JJ Tsai-Wu CC Jiang Differences between chondrocytes and bone marrow-derived chondrogenic cellsTissue Eng Part A20111723-24291929

3 

T Efe C Theisen S Fuchs-Winkelmann T Stein A Getgood MB Rominger Cell-free collagen type I matrix for the repair of cartilage defects-clinical and magnetic resonance imaging resultsKnee Surg Sports Traumatol Arthrosc20122010191522

4 

A Sage AA Chang BL Schumacher RL Sah D Watson Cartilage outgrowth in fibrin scaffoldsAm J Rhinol Allergy200923548691



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