Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/97844
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dc.contributor.advisorWormald, Peter-John-
dc.contributor.authorRajiv, Sukanya-
dc.date.issued2015-
dc.identifier.urihttp://hdl.handle.net/2440/97844-
dc.description.abstractINTRODUCTION Haemostasis and adhesion prevention in surgery is of paramount importance to prevent complications. It is even more important in neurosurgical procedures where even minor complications can lead to devastating consequences. There is constant work in the direction of development of both haemostatic and anti-adhesion agents with recent research with the use of chitosan dextran gel and autologous muscle tissue showing promise. Normal wound healing following surgery may lead to adhesion formation with the development of adhesions correlating to the presence and amount of blood clot. This linking of bleeding and adhesion formation is key to adhesion prevention. The amount and site of adhesion formation will often influence the postoperative course of the patient. While there have been many substances developed in an attempt to prevent adhesions, this thesis will examine Chitosan dextran (CD) gel and muscle for their potential role in neurological surgery. CD gel has previously been shown to be effective as a haemostat and as an anti- adhesion agent in endoscopic sinus surgery while autologous muscle has been shown to be effective with major vascular injury. This thesis will examine Chitosan Dextran gel in central nervous system and also try to explore the potential mechanisms of action of muscle tissue in bleeding control. METHODS The haemostatic and anti adhesion potential of Chitosan Dextran gel was studied with the help of sheep models. A neurosurgical burr hole model was used to assess the safety and efficacy of Chitosan Dextran gel on the dura and brain tissue. Bleeding control was tested at the level of bone, dura and brain separately with both Chitosan Dextran gel and Gelfoam paste on separate burr holes. Baseline bleeding was measured at the time of injury using the Boezaart scale, and then every two minutes after the application of each agent until complete haemostasis or 10 minutes, whichever was earlier. Safety was assessed through MRI scans and histopathological analysis. To further assess the antiadhesion potential of Chitosan Dextran gel, a sheep model of spinal laminectomy was used. Gelfoam paste was again used as the control agent. Following the laminectomy procedure and exposure of dura, the test agent, i.e, Chitosan Dextran gel or Gelfoam or normal saline wash was applied on the dura and the wound was closed. Healing was allowed for three months. The efficacy of adhesion prevention was assessed by Peel test and MRI scans. Histopathology was performed to assess safety of the agent. In vitro studies were performed to evaluate the haemostatic action of muscle tissue. Muscle extracts were prepared by dissolving crushed snap-frozen muscle tissue in saline. Plain saline was used as control. Prothrombin time, activated partial thromboplastin time (APTT), thrombin time, and platelet aggregation studies were performed on both muscle extract and saline. Prothrombin time and APTT were repeated using factor VII–deficient plasma, factor X–deficient plasma, lupus plasma, and contact pathway inhibited plasma. RESULTS 1. The efficacy and safety profiles of Chitosan Dextran gel were comparable to those of Gelfoam in the neurosurgical burr hole study. The logistic regression model suggested that Chitosan Dextran gel was more effective at stopping bleeding after two minutes, the clinical significance may be small and this should be tested in a model with greater volume of bleeding with more intervention numbers. 2. With regards to antiadhesion efficacy of Chitosan Dextran gel in the sheep model of laminectomy there was a significant reduction in adhesions when compared to the untreated (normal saline) group. However when compared to the Gelfoam treated group there was no significant difference. MRI did not show any difference in the overall epidural fibrosis among the three groups. 3. In vitro muscle coagulation studies did not show any significant difference between muscle and saline except in the APTT using factor X-deficient plasma. Higher concentrations of muscle extract showed an increase in platelet aggregation. CONCLUSION Chitosan Dextran gel is an effective safe haemostatic and anti-adhesive agent in the central nervous system. Further work is needed to extend its use in neurosurgical procedures in humans. Platelet aggregation appears to play an important role in the haemostatic action of muscle tissue and further study of this mechanism may improve the development of new topical haemostatic agents.en
dc.subjectchitosanen
dc.subjectdextranen
dc.subjectskeletal muscleen
dc.subjecthaemostasisen
dc.subjectanti adhesionen
dc.subjectsheepen
dc.subjectlaminectomyen
dc.subjectnervous systemen
dc.titleThe effect of Chitosan Dextran gel as a haemostatic and anti adhesion agent in the central nervous system and evaluation of haemostatic mechanism of skeletal muscle tissueen
dc.typeThesesen
dc.contributor.schoolSchool of Medicineen
dc.provenanceThis electronic version is made publicly available by the University of Adelaide in accordance with its open access policy for student theses. Copyright in this thesis remains with the author. This thesis may incorporate third party material which has been used by the author pursuant to Fair Dealing exceptions. If you are the owner of any included third party copyright material you wish to be removed from this electronic version, please complete the take down form located at: http://www.adelaide.edu.au/legals-
dc.description.dissertationThesis (Ph.D.) -- University of Adelaide, School of School of Medicine, 2015en
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