Should Bio-Oss Be Used as an Onlay Bone Substitute?
by Dr. Abdullah Al-Harkan
Often times,
dental implant placement is complicated by inadequacy of bone volume due to
tooth loss, periodontal disease, pathology, or trauma. However, more
challenging implant cases are being performed due to the advancement in bone
augmentation procedures and materials to augment deficient alveolar bone.1
Autogenous bone is considered to be
the “gold standard”, for alveolar ridge regeneration, due to its osteogenicity.1,2
However, autogenous bone grafts are associated with rapid rate of resorbtion3
and donor site morbidity1. This has led scientists to investigate
allogenic and xenogenic bone grafts, as well as alloplastic materials, such as
Hydroxyapatite and Calcium Phosphate Compounds.4
An alternative to autogenous bone is
xenograft. Although xenografts have provided acceptable results, they are considered
to be inferior in bone generation potential when compared to autografts.
However, the supply of xenograft is unlimited. Xenografts are usually derived
from bovine origin.5
Bio-Oss®
(Geistlich Pharmaceutical, Walhusen, Switzerland) is a natural bovine bone
derivative that lacks the organic component.6 Bio-Oss® and
mineralized human bone are similar in their chemical and morphological
structures.2 Bio-Oss® granules are 0.25 to 1.00 mm in diameter.6
Due to its porous structure, Bio-Oss® occupies 25-30% of the defect space
initially.7 This facilitates angiogenesis (penetration of the bone
augmentation material by blood vessels) and osteoblast migration.8
Along with all of its potential properties,
the osteoconductive nature of Bio-Oss® when used as an onlay graft is not well
established. The Osteoconductivity of Bio-Oss® has been a topic of debate in
the literature.
It is well known
that an onlay bone graft is more challenging to maintain clinically than an
inlay bone graft. Rosenthal
el al demonstrated that onlay bone grafts showed resorption with time, while
inlay bone grafts showed increased volumes overtime.9 Increased bone
to bone contact between the inlay bone graft and the native bone is one
explanation to this difference. Another explanation is the fact that inlay bone
grafts are surrounded by biological boundaries. This shields them from recoil
forces of the surrounding soft tissue. In addition, inlay bone grafts receive
identical physical stresses to those received by the surrounding bone.9
Some studies
described Bio-Oss® as having osteoconductive properties. In an experiment
involving the skull of the rabbit, using histomorphometric analysis, Slotte et al examined the bone formation in
titanium cylinders filled with either autogenous bone or Bio-Oss® as compared
to empty titanium cylinders as controls. Significantly more bone tissue was
found in the two test groups than the control group.10
Other studies
claimed that Bio-Oss® is not osteoconductive when used as an onlay. In an
experiment involving the skull of the rat, Slotte and Lundgren studied,
histomorphometrically, the bone generation potential of silicone domes grafted
with Bio-Oss® compared to empty ones.11 The study demonstrated that
Bio-Oss® arrested bone formation.
In
two different studies using the mandible of the rat, Stavropoulos et al studied the amount of bone
generation in Teflon capsules grafted with Bio-Oss® as compared to empty
(control) capsules. The capsules were fixed to the mandible using suture
material. In both experiments, it was shown that Bio-Oss® had an inhibitory
effect on bone formation.12,13
Such results and
the results of other studies have lead some authors to suggest that dental
implant survival in grafted sites may be owed mainly to the function of the
native bone rather than the bone graft itself.14
Araújo et al found
that Bio-Oss resulted in less bone generation than autogenous bone when used as
an onlay in dogs’ mandibles.15 However, they found that Bio-Oss
maintained more volume than autogenous bone did. Due to this fact, some authors
suggested the use of Bio-Oss mainly to preserve the architecture of the soft
tissue.16
From the discussion
above, in my opinion, the use of Bio-Oss an onlay bone substitute may not have
a significant value in bone generation potential, but it may add some value to
the way it supports the soft tissue profile. This feature may give the implant
a better esthetic outcome.
References
1- Norton M, Odell EW, Thompson ID,
Cook RJ. Efficacy of bovine bone mineral for alveolar augmentation: a human
histologic study. Clinical Oral Implant Research. 2003; 14: 775-783
2- Ewers R, Goriwoda W, Schopper C, Moser D, Spassova E.
Histologic findings at augmented bone areas supplied with different bone
substitute materials combined with sinus floor lifting. Report of one case.
Clinical Implant Research. 2004; 15: 96-100.
3- Johansson, B., Grepe, A., Wannfors, K. & Hirsch, J-M.
(2001) A clinical study of changes in the volume of bone grafts in the atrophic
maxilla. Dentomaxillofacial Radiology 30: 157-161.
4- Hämmerle,
C.H., Chiantella, G.C., Karring, T. &
Lang, N.P.
(1998) The effect of a deproteinized bovine bone mineral on bone regeneration
around titanium dental implants. Clinical
Oral Implants Research 3:
151-162.
5- Tuominen, T., Jäsmä, T., Tuukkanen, J., Marttinen, A.,
Lindholm, T.S. & Jalovaara, P. (2001) Bovine bone implant with bovine bone
morphogenetic protein in healing a canine ulnar defect. International Orthopaedics 25(1):
5-8.
6- Hising, P., Bolin, A. & Branting, C. (2001)
Reconstruction of severely resorbed alveolar ridge crests with dental implants
using a bovine bone mineral for augmentation. The International Journal of Oral & Maxillofacial Implants 16(1): 90-97.
7- Peetz, M (1997) Characterization
of xenogenic bone material. In: Boyne, P.J., ed. Osseous reconstruction of the
maxilla and the mandible – surgical techniques using titanium mesh and bone
mineral, 87-100. Chicago, Berlin: Quintessence.
8- Yildirim M, Spiekermann H,
Biesterfeld S, Edelhoff D. Maxillary sinus augmentation using xenogenic bone
substitute material Bio-Oss® in combination with venous blood. A histologic and
histomorphometric study in humans. Clinical Oral Implant Research 2000:
11:217-229
9- Rosenthal, A.H. and S.R. Buchman,
Volume maintenance of inlay bone grafts in the craniofacial skeleton. Plastic
and reconstructiove surgey, 2003. 112(3) p.802811.
10- Slotte C, Lundgren D, Burgos PM. Placement of autogenic
bone chips or bovine bone mineral in guided bone augmentation: A rabbit skull
study. The International Journal of Oral & Maxillofacial implants, 2003;
18: 795-806
11- Slotte C, Lundgren D.
Augmentation of calvarial tissue using non-permeable silicone domes and bovine
bone mineral. An experimental study in the rat. Clinical Oral Implant Research
1999: 10: 468-476
12- Stavropoulos A, Kostopoulos L,
Mardas N, Nyengaard JR, Karring T. Deproteinized bovine bone used as an adjunct
to guided bone augmentation (GBA) An experimental study in the rat. Clinical
Implant Dentistry and Related Research, 2001a; 3: 156-165
13- Stavropoulos A, Kostopoulos L,
Nyengaard J R, Karring T. Deproteinized bovine bone (Bio-Oss®) and bioactive
glass (Biogran®) arrest bone formation when used as an adjunct to guided tissue
regeneration (GTR). An experimental study in the rat. Journal of Clinical Periodontology
2003; 30: 636-643
14- Aghaloo TL, Moy PK, Which
hard tissue augmentation techniques are the most successful in furnishing bony
support for implant placement? Int J Oral
Maxillofac Implants. 2007; 22 Suppl:49-70.
15-
Araújo MG,
Sonohara M,
Hayacibara R,
Cardaropoli G,
Lindhe J,
Lateral ridge augmentation by the use of grafts comprised of autologous bone or
a biomaterial. An experiment in the dog. J Clin Periodontol. 2002
Dec; 29(12):1122-31.
16- Schlee M,
Esposito M,
Aesthetic and patient preference using a bone substitute to preserve extraction
sockets under pontics. A cross-sectional survey. Eur J Oral
Implantol. 2009 Autumn; 2(3):209-17.

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