H. Mittelmeier et al., XENOGENIC DEPROTEINIZED BONE SUBSTITUTE P YROST - EXPERIMENTAL BASICSAND 13 YEARS OF CLINICAL-EXPERIENCE IN MORE THAN 1000 CASES, Der Orthopade, 27(2), 1998, pp. 126-135
In different animal investigations Pyrost demonstrated osteoconductive
and osteostimulative effects. In ectopic tissues and especially in co
nditions of low osteogenetic potency, the combination of Pyrost and au
togenic bone marrow effects bone formation. In a clinical prospective
study, Pyrost was implanted in 1117 cases in the following indications
: Donor site defects after bone transplantation, bone defects after tu
mor resection, revision of THA, acetabuloplasty, fracture treatment, p
seudarthrosis and lengthening osteotomy, spondylodesis. In 87.3 % the
regeneration of the bone defects was complete, in 8 % a partial regene
ration was found. Excessive bone formation took place in 2.7 %, insuff
icient regeneration in 2.0 % in cases of instability or infection. Acc
ording to the clinical results Pyrost is a suitable bone substitute in
small bone defects and it is a valuable completion to the autogenic b
one graft in large defects. In disadvantageous bone bed Pyrost has to
be augmented with bone marrow and in large segmental defects the combi
nation with autogenic bone grafts is recommendable. Pre-supposition fo
r the application of bone substitutes like Pyrost in large defects is
a sufficiant primary stability of the bone bed. The application in inf
ected tissue is not favorable.