Published 2013
| Version v1
Publication
Thoracic cage plasticity in prepubertal New Zealand white rabbits submitted to T1-T12 dorsal arthrodesis: computed tomography evaluation, echocardiographic assessment and cardio-pulmonary measurements
Contributors
Description
Purpose We aimed to describe the morphological changes
in the thoracic cage and spinal column induced in New
Zealand White (NZW) prepubertal rabbits subjected to
dorsal arthrodesis and observed at skeletal maturity by
computed tomography (CT) scans. This was done to
evaluate the plasticity of the thoracic cage of rabbits with
non-deformed spine, by highlighting its modifications after
spinal arthrodesis. Emogas data analysis, echocardiographic
assessment and cardio-pulmonary measurements
completed the evaluation.
Methods Surgery was performed in 16 female rabbits,
6 weeks old. Nine were subjected to T1–T12 dorsal
arthrodesis, while seven were sham-operated. Surgery
involved the implant of two C-shaped stainless steel bars
and heterologous bone graft. CT scans were performed
before surgery, 2, 6 and 12 months after surgery. One week
after the last CT scan, echocardiographic and emogas
evaluations were performed.
Results Chest depth (8 %), thoracic kyphosis (ThK)
(23 %), dorsal and ventral length of the thoracic spine
(11 %) and sternal length (7 %) were significantly reduced
in operated compared to sham-operated rabbits. Mean
values ± standard deviation (SD) of PaCO2, PaO2 and sO2
were not significantly different. Mean values ± SD of
echocardiographic measurements were not significantly
different between the two groups of rabbits, except for
thickness of the interventricular septum in systole, contractile
capacity of the left ventricle and ejection fraction.
Conclusions T1–T12 dorsal arthrodesis in prepubertal
NZW rabbits with non-deformed spine induced changes of
the thoracic cage morphology. However, those changes are
source of cardio-pulmonary complications not severe
enough to reproduce a clinical picture comparable to thoracic
insufficiency syndrome in humans.
Additional details
Identifiers
- URL
- https://hdl.handle.net/11567/1187423
- URN
- urn:oai:iris.unige.it:11567/1187423
Origin repository
- Origin repository
- UNIGE