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1.
Lab Anim ; 39(3): 308-13, 2005 Jul.
Article in English | MEDLINE | ID: mdl-16004690

ABSTRACT

It is well documented that pigs frequently die from postoperative acute gastric dilatation, and proximal gastric 'stress' ulceration. Three cases of gastric mucosal 'de-gloving' are reported. This was secondary to acute gastric dilatation and resulted in death from acute haemorrhage. All animals had undergone major abdominal surgery. Histology confirmed that the proximal gastric mucosa had been 'de-gloved', or torn from the gastro-oesophageal junction, leaving exposed muscle fibres. This syndrome has not been reported previously. The postmortem appearances of this mechanical injury could easily be mistaken for extensive oesophago-gastric peptic ulceration. This has major implications for prevention.


Subject(s)
Esophagus/pathology , Gastric Dilatation/pathology , Stomach Ulcer/pathology , Stomach/pathology , Sus scrofa/surgery , Animals , Fatal Outcome , Female , Gastric Dilatation/etiology , Gastric Dilatation/mortality , Postoperative Period , Specific Pathogen-Free Organisms , Stomach Ulcer/etiology , Stomach Ulcer/mortality , Viscera/surgery
2.
Dig Dis ; 23(1): 83-91, 2005.
Article in English | MEDLINE | ID: mdl-15920329

ABSTRACT

BACKGROUND: Palliation of pancreatic cancer remains the only option for the majority of patients. Palliative techniques such as surgical bypass and endoscopic retrograde cholangiopancreatography (ERCP) with stenting are not ideal. The 'ideal' palliative technique would combine the efficacy of surgery with the minimal complications of an endoscopic procedure. Endoscopically delivered perductal electrolytic ablation of pancreatic lesions has the potential to meet these criteria. METHODS: Fifteen pigs were used. The pancreatic duct was cannulated with an electrolysis catheter. Animals were randomised to either: controls, treatment 2-week survivor or treatment 8-week survivor. An electrolytic dose was administered to the treatment animals. Post-operatively, serum amylase and leucocyte count were assessed. Pancreata were histologically examined to detect evidence of acute pancreatitis. RESULTS: Electrolysis was well tolerated. There was no difference in post-operative hyperamylasaemia and leucocyte count between the groups. Histological examination showed inflammation at the ablation site at 2 weeks, by 8 weeks this was replaced by scarring. CONCLUSION: The results of this study suggest that endoscopic perductal electrolytic ablation of the pancreas is feasible and safe. Biochemical and histological findings indicate self-limiting localised inflammation of the pancreas. This technique may have a role in the palliation of pancreatic cancer and warrants further investigation.


Subject(s)
Carcinoma/therapy , Electrolysis/adverse effects , Electrolysis/methods , Pancreatic Neoplasms/therapy , Animals , Carcinoma/veterinary , Disease Models, Animal , Electrolysis/veterinary , Endoscopy/methods , Endoscopy/veterinary , Female , Morbidity , Pancreatic Ducts , Pancreatic Neoplasms/veterinary , Random Allocation , Swine
3.
Br J Surg ; 91(2): 178-83, 2004 Feb.
Article in English | MEDLINE | ID: mdl-14760665

ABSTRACT

BACKGROUND: Local ablation has been proposed for treatment of liver tumours. Cryoshock, a variant of the systemic inflammatory response syndrome (SIRS), is a potentially fatal complication of cryoablation caused by systemic release of necrotic breakdown products from ablated liver. The proinflammatory cytokines tissue necrosis factor (TNF) alpha and interleukin (IL) 1 are important mediators of this response. This study assessed the risk of SIRS complicating electrolytic liver ablation by measuring circulating levels of inflammatory cytokines, other inflammatory markers and clinical markers of organ function. METHODS: Electrolytic liver ablation was performed in 16 pigs and four pigs served as controls. Platelet count, and serum levels of urea, creatinine, liver enzymes, C-reactive protein (CRP), TNF-alpha and IL-1beta were measured before treatment and for 72 h after the procedure. RESULTS: There were significant dose-related increases in CRP and alanine aminotransferase levels with liver electrolysis. There was no significant derangement in renal function or platelet count following ablation. A rise in serum TNF-alpha and IL-1beta levels was not associated with liver electrolysis. CONCLUSION: There was no evidence of organ failure or significantly raised levels of proinflammatory cytokines as a result of liver electrolysis, suggesting that this is a safe procedure for liver ablation.


Subject(s)
Catheter Ablation/methods , Electrolysis/methods , Liver Neoplasms/surgery , Systemic Inflammatory Response Syndrome/etiology , Alanine Transaminase/metabolism , Alkaline Phosphatase/metabolism , Animals , C-Reactive Protein/analysis , Female , Interleukin-1/blood , Liver/enzymology , Platelet Count , Risk Factors , Serum , Swine , Systemic Inflammatory Response Syndrome/blood , Systemic Inflammatory Response Syndrome/enzymology , Tumor Necrosis Factor-alpha/analysis
4.
Surg Endosc ; 18(10): 1435-41, 2004 Oct.
Article in English | MEDLINE | ID: mdl-15791365

ABSTRACT

BACKGROUND: Pancreatic cancer has a dismal prognosis. Few patients are suitable for surgical resection, leaving the majority requiring symptom palliation. Current palliative techniques such as surgical bypass and endoscopic retrograde cholangiopancreatography (ERCP) are imperfect. A novel palliative therapy combining the symptom control of surgical bypass with the minimally invasive nature of ERCP is required. METHODS: Perductal electrolytic ablation of pancreatic tissue, in a porcine model, was performed. There were two survival groups of 2 weeks (n = 4) and 8 weeks (n = 4). Postoperatively, serum biochemistry, amylase and C-reactive protein (CRP) were assessed. Histological examination of the pancreas, lungs, and kidneys was performed to determine the presence of acute pancreatitis or systemic inflammatory response. RESULTS: An immediate transient increase in both amylase and CRP was seen. Although pancreatic histology demonstrated localised necrosis at the electrolytic site at 2 weeks, there was no evidence of generalized pancreatitis or a systemic inflammatory response at either 2 or 8 weeks. CONCLUSIONS: This study suggests that, although there is localized pancreatic necrosis and transient hyperamylasemia, perductal pancreatic electrolytic ablation is safe, with neither generalized pancreatitis nor a systemic inflammatory response, in the medium and long term. Although performed in normal porcine pancreas, because of the absence of a large-animal model of pancreatic cancer, this study suggests that electrolytic pancreatic ablation is safe. This technique may have a role in the palliation of pancreatic cancer, especially if delivered via a minimally, invasive approach, and warrants further investigation.


Subject(s)
Electrolysis , Palliative Care , Pancreatectomy/methods , Animals , Endoscopy, Gastrointestinal , Female , Pancreas/pathology , Swine , Time Factors
5.
Br J Surg ; 90(4): 440-4, 2003 Apr.
Article in English | MEDLINE | ID: mdl-12673745

ABSTRACT

BACKGROUND: In-depth knowledge of pig liver anatomy allows potential research into segmental liver resections and hepatic regeneration, as well as liver transplantation techniques. The segmental anatomy, however, remains largely unknown. This study aimed to delineate the segmental anatomy of the porcine liver in comparison with that of the human. METHODS: The segmental anatomy of the porcine liver was determined using acrylic injection casting of ex vivo pig livers, allowing the arterial, venous and biliary supply to be visualized directly. This was correlated using multi-slice computed tomography (CT) and three-dimensional reconstructions. RESULTS: Although the external morphology of the porcine liver differs from that of the human, the segmental anatomy is remarkably similar in term of its vascularity and biliary tree. CONCLUSION: Acrylic casting of the porcine liver accurately delineates the vascular and biliary anatomy, and is a useful tool for performing experimental liver surgery. The similarities between porcine and human segmental anatomy allow domestic swine to be used as a comparable model. Three-dimensional CT reconstructions can also accurately visualize the anatomy and may be used to perform virtual surgery, or to assess segmental volumes.


Subject(s)
Hepatectomy/methods , Liver/anatomy & histology , Animals , Biliary Tract/anatomy & histology , Female , Hepatic Artery/anatomy & histology , Hepatic Veins/anatomy & histology , Liver/blood supply , Portal Vein/anatomy & histology , Swine , Tomography, X-Ray Computed/methods
6.
Surg Endosc ; 17(2): 207-11, 2003 Feb.
Article in English | MEDLINE | ID: mdl-12399852

ABSTRACT

BACKGROUND: Inoperable pancreatic cancer has a dismal prognosis. Palliation involves either stenting or surgical bypass. Stenting does not relieve gastric outlet obstruction, and surgical bypass is a major procedure. A minimally invasive procedure is needed that relieves both gastric outlet and biliary obstruction, with the potential for relieving pain. METHODS: In an experimental model, pancreatic electrolysis was investigated. The pancreatic duct was cannulated via a transduodenal approach with an electrode catheter. In 6 animals an electrolytic "lesion" was created using a direct current generator. Six animals were controls. The local and systemic effects of electrolysis were assessed using histological and biochemical parameters. RESULTS: The pancreatic duct was cannulated in all animals and treatment was uneventful. Electrolytic lesions comprised a central area of necrosis with a sharp demarcation between necrotic and viable pancreas. All animals developed transient hyperamylasemia after electrolysis. There was no significant difference between treatment and controls. Importantly, no animal had clinical, biochemical, or histological evidence of pancreatitis. CONCLUSIONS: This experimental study suggested that electrolytic palliation of inoperable pancreatic cancer via the gastrointestinal tract is potentially safe. In patients, this treatment could be performed during endoscopic retrograde cholangiopancreatography and may have therapeutic advantages when compared to stenting or biliary bypass.


Subject(s)
Catheter Ablation/methods , Palliative Care/methods , Pancreatic Neoplasms/surgery , Amylases/blood , Animals , C-Reactive Protein/metabolism , Feasibility Studies , Female , Laparotomy , Necrosis , Pancreas/metabolism , Pancreas/pathology , Swine , Treatment Outcome
8.
Br J Surg ; 89(9): 1089-95, 2002 Sep.
Article in English | MEDLINE | ID: mdl-12190672

ABSTRACT

BACKGROUND: Partial hepatectomy is the strongest stimulator of hepatic regeneration. The process of initiation and the control of the final size of the regenerated liver have been the subject of research for many years. A better understanding of this process and the effect of disease may allow better selection of patients for partial hepatectomy. It may also allow an insight into the possible application of clinical stimulation of regeneration. METHODS: Data were reviewed from the published literature using the Medline database. RESULTS: Most knowledge comes from in vitro studies and the study of resection in the rat model. A variety of cytokines, hormones and growth factors are involved in regeneration but very few have been found capable of stimulating regeneration in vitro. The exact interactions are not known, but there is probably a cascade involving different factors at differing stages of regeneration. CONCLUSION: Further in vivo research should allow greater understanding of liver regeneration, thereby providing a potential therapeutic tool in patients for whom regeneration has failed, or is likely to fail. Such research is also important in respect of liver support devices, which may inhibit liver regeneration by filtration of many of the factors involved.


Subject(s)
Liver Regeneration/physiology , Liver/anatomy & histology , Cytokines/physiology , Epidermal Growth Factor/physiology , Growth Substances/physiology , Hepatocyte Growth Factor/physiology , Hepatocytes/physiology , Humans , Intercellular Signaling Peptides and Proteins , Mitogens/physiology , Peptides/physiology , Transforming Growth Factor alpha/physiology , Transforming Growth Factor beta/physiology
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