TY - JOUR
T1 - Reverse dynamisation
T2 - A modern perspective on stephan perren’s strain theory
AU - Glatt, V.
AU - Evans, C. H.
AU - Tetsworth, K.
N1 - Funding Information:
We would like to thank Dr Anna Woloszyk (The University of Texas Health Science Centre, San Antonio, TX, USA) for making Fig. 3. Furthermore, we would also like to thank Miva Stock Photography (Boston, MA, USA) for creating illustrations for Fig. 1 and 3. Dr Evans's research is supported in part by the John and Posy Krehbiel Professorship in Orthopedics.
Publisher Copyright:
© 2021, AO Research Institute Davos. All rights reserved.
PY - 2021/6
Y1 - 2021/6
N2 - The present review acknowledges the tremendous impact of Stephan Perren’s strain theory, considered with respect to the earlier contributions of Roux and Pauwels. Then, it provides further insight by examining how the concept of reverse dynamisation extended Perren’s theory within a modern context. A key factor of this more contemporary theory is that it introduces variable mechanical conditions at different time points during bone healing, opening the possibility of manipulating biology through mechanics to achieve the desired clinical outcome. The discussion focusses on the current state of the art and the most recent advances made towards optimising and accelerating bone regeneration, by actively controlling the mechanical environment as healing progresses. Reverse dynamisation utilises a very specific mechanical manipulation regimen, with conditions initially flexible to encourage and expedite early callus formation. Once callus has formed, the mechanical conditions are intentionally modified to create a rigid environment under which the soft callus is quickly converted to hard callus, bridging the fracture site and leading to a more rapid union. The relevant literature, principally animal studies, was surveyed to provide ample evidence in support of the effectiveness of reverse dynamisation. By providing a modern perspective on Stephan Perren’s strain theory, reverse dynamisation perhaps holds the key to tipping the balance in favour of a more rapid and reliable union when treating acute fractures, osteotomies, non-unions and other circumstances where it is necessary to regenerate bone.
AB - The present review acknowledges the tremendous impact of Stephan Perren’s strain theory, considered with respect to the earlier contributions of Roux and Pauwels. Then, it provides further insight by examining how the concept of reverse dynamisation extended Perren’s theory within a modern context. A key factor of this more contemporary theory is that it introduces variable mechanical conditions at different time points during bone healing, opening the possibility of manipulating biology through mechanics to achieve the desired clinical outcome. The discussion focusses on the current state of the art and the most recent advances made towards optimising and accelerating bone regeneration, by actively controlling the mechanical environment as healing progresses. Reverse dynamisation utilises a very specific mechanical manipulation regimen, with conditions initially flexible to encourage and expedite early callus formation. Once callus has formed, the mechanical conditions are intentionally modified to create a rigid environment under which the soft callus is quickly converted to hard callus, bridging the fracture site and leading to a more rapid union. The relevant literature, principally animal studies, was surveyed to provide ample evidence in support of the effectiveness of reverse dynamisation. By providing a modern perspective on Stephan Perren’s strain theory, reverse dynamisation perhaps holds the key to tipping the balance in favour of a more rapid and reliable union when treating acute fractures, osteotomies, non-unions and other circumstances where it is necessary to regenerate bone.
KW - Animal models
KW - Bone healing
KW - Dynamisation
KW - Fixation stability
KW - Fracture healing
KW - Interfragmentary strain theory
KW - Mechanical environment
KW - Reverse dynamisation
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U2 - 10.22203/eCM.v041a43
DO - 10.22203/eCM.v041a43
M3 - Article
C2 - 34111297
AN - SCOPUS:85108038163
VL - 41
SP - 668
EP - 679
JO - European Cells and Materials
JF - European Cells and Materials
SN - 1473-2262
ER -