Bone Grafting around an Articular Joint

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Chapter 15 Bone Grafting around an Articular Joint

Introduction

No substitute has been proven to be better than autograft. Bone is formed by stem cells, and most arrive in the circulation and migrate to an injured surface of bone, attach, and begin to form bone.

The contribution of stem cells in the graft is thought to be small, but the scaffold of bone and its contained growth factors is ideal for the formation of new bone. William Macewen of Glasgow proved the ability of bone graft to regenerate a humerus, and this followed an exemplary series of studies and research.1

Circulating monocytes also migrate through the endothelium of adjacent capillaries and become either alternatively activated (AA) macrophages or, under the influence of receptor activator of nuclear factor-кβ (RANK), osteoclasts. These three cell types are the basis of repair, bone regeneration, and remodeling.

The early hematoma forming around an injured bone surface (whether the result of your osteotomy or a fracture) immediately contains stem cells.2 These multiply rapidly in the hematoma and are in the right place to contribute to healing.

Of note, only the first bleeding from an injured bony surface provides these cells, so the initial hematoma is particularly precious; it should not be thrown away but should be used to amalgamate your bone graft or mix into bone graft substitutes.

The osteoblasts are particularly sensitive to the mechanical environment.

Stability is defined as the maintenance of reduction and correlates with strength. Stiffness is a distinctly different parameter from strength and in fracture or osteotomy fixation is defined as the rigidity of the construct.

Osteoblasts are evolved for a rigid environment with cyclic strains of less than 1% to 2% of their length.

It is particularly useful for graft to be packed tight, for early callus to be bulky, and to limit cyclic movements or a rigid plate be applied while an osteotomy or cancellous fracture is healing.

Weight bearing is good for the maintenance of bone and muscle and the prevention of deep vein thrombosis, but the biological plate of callus or the internal or external fixation must be able to sustain these loads, otherwise weight-bearing loads will need to be limited.

Flexible fixation and early cyclic movements are appropriate for the bulky callus formation needed in diaphyseal fractures.3

This external callus is rarely needed in the metaphysic or epiphysis where there is sufficient bulk and well vascularized cancellous bone that will allow rapid union. John Charnley took biopsies at 6 weeks following knee arthrodesis to prove that union is achieved in this time.4

Taking Autograft

Cancellous Graft

Before surgery, and even if the possibility is remote, explain to your patient that he or she may need a bone graft and that this will be taken from the iliac crest.

It is useful to know if the patient always sleeps on one side, as you should warn the patient that the donor site will be tender for some time.

When possible, a small sandbag behind the hip is useful.

Prepare the area of the iliac crest with antiseptic, and use adherent paper drapes with an adherent plastic sheet to prevent the drapes from moving around while you are operating on the knee.

Use a skin incision that ends 2 cm from the anterior superior iliac spine to avoid cutting the lateral cutaneous nerve of the thigh. This happens in 10% of cases, and it is of note that in 10% of cases the nerve passes through the bone of the iliac crest.

If there is no spinal anesthetic, it is useful to infiltrate bupivacaine or a similar long-acting anesthetic in the tissues around your incision at this time to prevent painful stimuli reaching the brain.

Cut the fibers of gluteus maximus as they arise from the lip of the iliac crest.

Hemostasis will be needed at the posterior part of your incision.

Use a saw to cut the outer table of the iliac crest and then a broad osteotome to lift a lid. This exposes the cancellous layer (see Fig. 15-1, A-C).

Use a sharp, long-handled curette to remove cancellous bone from between the cortical sheets (Fig. 15-2).

Keep the hematoma that gathers in the wound with your graft.

Tricortical Graft

Expose the iliac crest as descried, and then strip all periosteum from the bone to be taken; otherwise it will not expand in the months and years following incorporation. Macewen described periosteum as the limiting membrane of bone. He undertook many studies on bone and was the first person to use allograft successfully.1

Use a saw to cut an accurately sized block including both inner and outer walls of the iliac crest. There is a risk of herniation through the iliac crest, so for large blocks of bone greater than about 4 × 4 cm I would advise suturing a suitable membrane such as one used for inguinal hernia repair across the inner table to reduce this risk.

For closure after harvest of the different bone grafts described earlier in the text, follow these steps:

Allograft: Fresh Frozen

Allograft bone will carry a small risk of infection, despite all the screening measures used. All nonautologous graft does, however, carry the advantages of avoiding the complications of an autologous graft.6

Bone Graft Substitutes

These are numerous in composition, and handling has greatly improved. Table 15-1 lists only a selection.

TABLE 15-1 Examples of Bone Graft Substitutes

Demineralized Bone Matrix Grafton, Allomatrix
rhBMP-2 OP-1 Implant
rhBMP-2 INFUSE
β-tri-calcium phosphate (TCP) Allogran-R
Calcium sulphate Stimulan
Hydroxyapatite Actifuse, Allogran-N
Bi-phasic calcium based ceramics geneX
Bioglass Vitoss, NovaBone

There are few reports of histology or of clinical trials against autogenous bone graft demonstrating successful incorporation of bone graft substitutes, but even the simple calcium sulphate is in widespread use.

We use Allogran-N for load bearing in impaction grafting,7 geneX for tibial, and femoral tensegrity osteotomies,9 and for cultured stem cells in nonunion.10 Stimulan is used with added antibiotic for chronic osteomyelitis.

Autologous bone graft is now only used for osteochondral defects in combination in autologous chondrocyte implantation.

References

1. Macewen W. The growth of bone. Observations on osteogenesis. An experimental inquiry into the development and reproduction of diaphyseal bone. Glasgow: James Maclehose & Sons; 1912.

2. Oe K., Miwa M., Sakai, Lee S.Y., Kuroda R., Kurosaka M. An in vitro study demonstrating that haematomas found at the site of human fractures contain progenitor cells with multilineage capacity. J Bone Joint Surg Br. 2007 Jan;89-B(1):133-138.

3. Kenwright J., Richardson J.B., Goodship A.E., et al. Effect of controlled axial micromovement on healing of tinial fractures. Lancet. 1986 Nov 22;2(8517):1185-1187.

4. Charnley J., Baker S.L. Compression arthrodesis of the knee; a clinical and histological study. J Bone Joint Surg Br. 1952 May;34-B(2):187-199.

5. Website: www.kaltec.com.au/Precision Bone Grafting Kit.

6. Younger E.M., Chapman M.W. Morbidity at bone graft donor sites. J Orthop Trauma. 1989;3(3):192-195.

7. Aulakh T.S., Jayasekera N., Kuiper J.H., Richardson J.B. Long-term clinical outcomes following the use of synthetic hydroxyapatite and bone graft in impaction in revision hip. Biomaterials. 2009;30:1732-1738.

8. Pearsall A.W.I.V., Tucker J.A., Hester R.B., Heitman R.J. Chondrocyte Viability in refrigerated osteochondral allografts used for transplantation within the knee. Am J Sports Med. 2004 Jan-Feb;32(1):125-131.

9. Richardson JB, Cooper JJ, Waters R D. Tensegrity Osteotomy System US Patent 2007/0233145.

10. Bajada S., Harrison P.E., Ashton B.A., Cassar-Pullicino V.N., Ashammakhi N., Richardson J.B. Successful treatment of refractory tibial non-union using calcium sulphate and bone marrow stromal cell implantation. J Bone Joint Surg Br. 2007;89(10):1382-1386.