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| ==Description== | | ==Description== |
− | '''Peritonitis''' is defined as [[Inflammation - Pathology|inflammation]] of the [[Peritoneal Cavity - Anatomy & Physiology|peritoneum]]. The inflammatory response involves vasodilation, [[Exudate|exudation]] of protein-rich fluid, cellular infiltration, pain and, chronically, formation of fibrous adhesion. The disease can be classified into primary and secondary cases. | + | '''Peritonitis''' is defined as inflammation of the [[Peritoneal Cavity - Anatomy & Physiology|peritoneum]]. The inflammatory response involves vasodilation, [[Exudate|exudation]] of protein-rich fluid, cellular infiltration, pain and, chronically, formation of fibrous adhesion. The disease can be classified into primary and secondary cases. |
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− | '''Primary peritonitis''' occurs spontaneously without any pre-existing pathological process in the abdomen. In cats, [[Feline Infectious Peritonitis |feline infectious peritonitis]] is the most common cause of primary peritonitis. | + | '''Primary peritonitis''' occurs spontaneously without any pre-existing pathological process in the abdomen. In cats, [[Feline Infectious Peritonitis |feline infectious peritonitis]] is the most common cause of primary peritonitis. |
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− | '''Secondary peritonitis''' occurs as the result of a pre-existing pathological process within the abdomen. It can be further classified into '''septic''' or '''non-septic''' peritonitis, where septic peritonitis results from direct bacterial infection of the peritoneal cavity. Septic peritonitis is the most common form in the dog and its causes include: | + | '''Secondary peritonitis''' occurs as the result of a pre-existing pathological process within the abdomen. It can be further classified into '''septic''' or '''non-septic''' peritonitis, where septic peritonitis results from direct bacterial infection of the peritoneal cavity. Septic peritonitis is the most common form in the dog and its causes include: |
− | *'''Perforation of the gastro-intestinal tract''' due to foreign bodies, [[Intussusception|intussuscepta]], invasive [[Neoplasia - Pathology|neoplasia]], deep ulceration or dehiscence of surgical wounds or biopsy sites. Peritonitis as a result of wound dehiscence is most likely to occur 3-5 days post-operatively. | + | *'''Perforation of the gastro-intestinal tract''' due to foreign bodies, [[Intussusception|intussuscepta]], invasive [[Neoplasia - Pathology|neoplasia]], deep ulceration or dehiscence of surgical wounds or biopsy sites. Peritonitis as a result of wound dehiscence is most likely to occur 3-5 days post-operatively. |
| *'''Penetration of the abdomen''' by a stick, gunshot or other foreign body. | | *'''Penetration of the abdomen''' by a stick, gunshot or other foreign body. |
− | *Rupture of an infected uterus ('''pyometra'''), biliary tract or urinary tract. | + | *Rupture of an infected uterus ('''pyometra'''), [[Biliary Tract - Rupture|biliary tract]] or urinary tract. |
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| The bacteria causing septic peritonitis or their products may spread systemically causing sepsis or endotoxaemia. | | The bacteria causing septic peritonitis or their products may spread systemically causing sepsis or endotoxaemia. |
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− | '''Non-septic''' peritonitis may occur due to the leakage of bile, urine or pancreatic enzymes ('''chemical peritonitis''') or due to the presence of foreign substances such as barium or glove powder ('''physical peritonitis'''). In some cases of urinary tract or biliary tract rupture however, septic peritonitis may occur if the tracts were previously infected. | + | '''Non-septic''' peritonitis may occur due to the leakage of bile, urine or pancreatic enzymes ('''chemical peritonitis''') or due to the presence of foreign substances such as barium or glove powder ('''physical peritonitis'''). In some cases of urinary tract or biliary tract rupture however, septic peritonitis may occur if the tracts were previously infected. |
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− | ==Diagnosis==
| + | ==Clinical Signs== |
− | ===Clinical Signs===
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| The clinical signs are related to the presence of severe inflammation within the body cavity, with or without systemic infection. | | The clinical signs are related to the presence of severe inflammation within the body cavity, with or without systemic infection. |
| *'''Abdominal pain''', manifesting as a reluctance to move due to inflammation of the parietal peritoneum. | | *'''Abdominal pain''', manifesting as a reluctance to move due to inflammation of the parietal peritoneum. |
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| *'''Hypothermia''' or '''hyperthermia'''. | | *'''Hypothermia''' or '''hyperthermia'''. |
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− | ===Laboratory Tests===
| + | ==Laboratory Tests== |
− | ====Haematology====
| + | ===Haematology=== |
− | As with any severe inflammatory process, '''leucocytosis''' will occur. Initially, this is caused by '''neutrophilia''' which may have a left shift or, if very severe, a degenerative right shift. Severe localised inflammation may stimulate a '''leukaemoid response''' with massive mobilisation of neutrophils from the bone marrow pools. | + | As with any severe inflammatory process, '''leucocytosis''' will occur. Initially, this is caused by '''[[neutrophilia]]''' which may have a left shift or, if very severe, a degenerative right shift. Severe localised inflammation may stimulate a '''leukaemoid response''' with massive mobilisation of neutrophils from the bone marrow pools. |
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| '''Haemoconcentration''' (causing a raised packed cell volume (PCV) and total protein concentration) may occur due to loss of extracellular fluid. | | '''Haemoconcentration''' (causing a raised packed cell volume (PCV) and total protein concentration) may occur due to loss of extracellular fluid. |
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− | ====Biochemistry====
| + | ===Biochemistry=== |
| '''Hypoproteinaemia''' may occur due to loss of plasma proteins into the inflammatory [[Exudate|exudate]]. | | '''Hypoproteinaemia''' may occur due to loss of plasma proteins into the inflammatory [[Exudate|exudate]]. |
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| '''Hypokalaemia''' may occur as a result of chronic vomiting and it may contribute to the intestinal ileus which often develops in cases of peritonitis. | | '''Hypokalaemia''' may occur as a result of chronic vomiting and it may contribute to the intestinal ileus which often develops in cases of peritonitis. |
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− | ===Diagnostic Imaging===
| + | ==Diagnostic Imaging== |
− | ====Radiography====
| + | ===Radiography=== |
− | '''Plain radiographs of the abdomen''' may reveal the presence of free gas in the abdomen ('''pneumoperitoneum''') due to intestinal perforation or bacterial production. The normal serosal detail may be effaced due to the presence of an abdominal effusion and, if a horizontal beam decubitus radiograph is made, a '''fluid line''' may be apparent. | + | '''Plain radiographs of the abdomen''' may reveal the presence of free gas in the abdomen ('''pneumoperitoneum''') due to intestinal perforation or bacterial production. The normal serosal detail may be effaced due to the presence of an abdominal effusion and, if a horizontal beam decubitus radiograph is made, a '''fluid line''' may be apparent. |
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| In cases where neoplasia is thought to be the cause of the inflammatory process, thoracic radiograph should be assessed for signs of metastatic disease. | | In cases where neoplasia is thought to be the cause of the inflammatory process, thoracic radiograph should be assessed for signs of metastatic disease. |
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− | ====Ultrasonography====
| + | ===Ultrasonography=== |
− | This modality has a high sensitivity for the detection of free fluid in the abdomen and it may be used to identify some specific causes of peritonitis, including abscesses of organs or rupture of the [[Biliary Tract - Rupture|biliary tract]]. | + | This modality has a high sensitivity for the detection of free fluid in the abdomen and it may be used to identify some specific causes of peritonitis, including abscesses of organs or [[Biliary Tract - Rupture|rupture of the biliary tract]]. |
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| Ultrasound scans can also be used to guide '''abdominocentesis'''. | | Ultrasound scans can also be used to guide '''abdominocentesis'''. |
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| ===Other Tests=== | | ===Other Tests=== |
− | Free abdominal fluid can be collected under ultrasound guidance and submitted for cytological analysis. If fluid cannot be obtained on aspiration, '''diagnostic peritoneal lavage''' can be performed by istilling a small volume (~20 ml/kg) of warmed isotonic crystalloid into the abdomen, agitating the abdomen and then re-aspirating this fluid. Grossly, the fluid may contain vegetable fibres if the gastro-intestinal tract has ruptured or it may be evidently green (indicating the presence of bile) or haemorrhagic. On cytological examaintion, the sample should be assessed for the presence of neutrophils (and other leucocytes) with intracellular bacteria. | + | Free abdominal fluid can be collected under ultrasound guidance and submitted for cytological analysis. If fluid cannot be obtained on aspiration, '''diagnostic peritoneal lavage''' can be performed by instilling a small volume (~20 ml/kg) of warmed isotonic crystalloid into the abdomen, agitating the abdomen and then re-aspirating this fluid. Grossly, the fluid may contain vegetable fibres if the gastro-intestinal tract has ruptured or it may be evidently green (indicating the presence of bile) or haemorrhagic. On cytological examination, the sample should be assessed for the presence of neutrophils (and other leucocytes) with intracellular bacteria. |
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| Further possible tests include: | | Further possible tests include: |
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| *'''Creatinine''' and '''potassium''' if the effusion is thought to be a uroabdomen. | | *'''Creatinine''' and '''potassium''' if the effusion is thought to be a uroabdomen. |
| *'''Glucose''' (<2.8 mmol/l) and '''lactate''' (>5.5 mmol/l) should be measured and, where their values are below those shown, the inflammation is likely to be septic. | | *'''Glucose''' (<2.8 mmol/l) and '''lactate''' (>5.5 mmol/l) should be measured and, where their values are below those shown, the inflammation is likely to be septic. |
| + | <font color = 'green'> Where the difference between blood and peritoneal fluid glucose concentration is greater then 2.8mmol/l and blood and peritoneal fluid lactate concentration is less than 5.5mmol/l, the inflammation is likely to be septic. - Peritoneal fluid has less glucose and more lactate than blood.</font color> |
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| In cats with [[Feline Infectious Peritonitis]], the effusion usually has a high protein content (>35g/l) with a high globulin: albumin ratio. There is a variably high cellularity mainly composed of lymphocytes. | | In cats with [[Feline Infectious Peritonitis]], the effusion usually has a high protein content (>35g/l) with a high globulin: albumin ratio. There is a variably high cellularity mainly composed of lymphocytes. |
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| ==Treatment== | | ==Treatment== |
− | It is vital to identify severe cases promptly as these will require emergency surgical intervention. Any of the following criteria is a major indication for surgery: | + | It is vital to identify severe cases promptly as these will require emergency surgical intervention. Any of the following criteria is a major indication for surgery: |
| *Presence of intracellular bacteria in leucocytes in the abdominal exudate | | *Presence of intracellular bacteria in leucocytes in the abdominal exudate |
| *Pneumoperitoneum | | *Pneumoperitoneum |
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| ===Medical Management=== | | ===Medical Management=== |
| ====Fluid Therapy==== | | ====Fluid Therapy==== |
− | Aggressive fluid therapy with [[Crystalloids|crystalloid]] and [[Colloids|colloid]] should be given on initial presentation to improve haemodynamic parameters and this should be mainatined into the peri- and post-operative periods where appropriate and until the patient is normotensive. If the patient remaines hypotensive, the use of a vasopressor such as [[Interventional_Agents#Dobutamine|dobutamine]], [[Interventional_Agents#Dopamine|dopamine]] or even [[Interventional_Agents#Vasopressin|vasopressin]] should be considered as animals in septic shock are likely to have systemic peripheral vasodilation. | + | Aggressive [[Principles of Fluid Therapy|fluid therapy]] with [[Crystalloids|crystalloid]] and [[Colloids|colloid]] should be given on initial presentation to improve haemodynamic parameters and this should be maintained into the peri- and post-operative periods where appropriate and until the patient is normotensive. If the patient remains hypotensive, the use of a vasopressor such as [[Interventional_Agents#Dobutamine|dobutamine]], [[Interventional_Agents#Dopamine|dopamine]] or even [[Interventional_Agents#Vasopressin|vasopressin]] should be considered as animals in septic shock are likely to have systemic peripheral vasodilation. |
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− | Glucose and potassium should be supplemented where these parameters are found to be abnormal and, in cases of severe metabolic acidosis, the use of sodium bicarbonate may be considered. This product should be used with care as overdoses may result in overshoot metabolic alkalosis, tissue anoxia due to a left-shift of the haemoglobin-oxygen dissociation curve and paradoxical cerebral acidosis as carbon dioxide (not bicarbonate) crosses the blood brain barrier. | + | Glucose and potassium should be supplemented where these parameters are found to be abnormal and, in cases of severe metabolic acidosis, the use of sodium bicarbonate may be considered. This product should be used with care as overdoses may result in overshoot metabolic alkalosis, tissue anoxia due to a left-shift of the haemoglobin-oxygen dissociation curve and paradoxical cerebral acidosis as carbon dioxide (not bicarbonate) crosses the blood brain barrier. |
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− | Septic peritonitis can cause [[Disseminated Intravascular Coagulation|disseminated intravascular coagulation (DIC)]] which represents a very large therapeutic challenge. Plasma my be administered to replace used clotting factors and some authors advocate the use of low doses of heparin to prevent further coagulation. | + | Septic peritonitis can cause [[Disseminated Intravascular Coagulation|disseminated intravascular coagulation (DIC)]] which represents a very large therapeutic challenge. Plasma my be administered to replace used clotting factors and some authors advocate the use of low doses of heparin to prevent further coagulation. |
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| ====Antimicrobial Drugs==== | | ====Antimicrobial Drugs==== |
− | Broad spectrum bactericidal antibiotics should be administered and, where possible, the choice of product should then be guided by culture and sensitivity of samples of peritoneal fluid. [[Escherichia coli|''Escherichia coli'']], [[:Category:Clostridium species|''Clostridium spp.'']] and ''[[Enterococcus faecalis]]'' are the species most commonly isolated in cases of septic peritonitis. | + | Broad spectrum bactericidal antibiotics should be administered and, where possible, the choice of product should then be guided by culture and sensitivity of samples of peritoneal fluid. [[Escherichia coli|''Escherichia coli'']], [[:Category:Clostridium species|''Clostridium spp.'']] and ''[[Enterococcus faecalis]]'' are the species most commonly isolated in cases of septic peritonitis. |
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| ===Surgical Management=== | | ===Surgical Management=== |
− | Surgical intervention is indicated if the cause of peritonitis is undetermined or if it has been caused by intestinal rupture, intestinal obstruction or mesenteric avulsion. Abdominal lavage is a controversial procedure as it carries a risk of disseminating infection throughout the body and it is therefore indicated in cases of generalised peritonitis but should be used with care in cases of localised peritonitis. A volume of around 200 ml/k fluid should be used to lavage the abdomen and as much of this fluid as possible should be re-aspirated as its continued presence will hinder the immune system by diluting bactericidal factor and preventing leucocyte migration. | + | Surgical intervention is indicated if the cause of peritonitis is undetermined or if it has been caused by intestinal rupture, intestinal obstruction or mesenteric avulsion. Abdominal lavage is a controversial procedure as it carries a risk of disseminating infection throughout the body and it is therefore indicated in cases of generalised peritonitis but should be used with care in cases of localised peritonitis. A volume of around 200 ml/kg fluid should be used to lavage the abdomen and as much of this fluid as possible should be re-aspirated as its continued presence will hinder the immune system by diluting bactericidal factor and preventing leucocyte migration. |
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− | It is beneficial to maintain peritoneal drainage after lavage by either '''open''' or '''closed''' drainage. Open drainage involves leaving part of the abdominal wall loosely sutured so that peritoneal fluid can leak out under gravity. The wound must be dressed under sterile conditions and there is a high risk of ascending infection and of continued protein loss with this technique. | + | It is beneficial to maintain peritoneal drainage after lavage by either '''open''' or '''closed''' drainage. Open drainage involves leaving part of the abdominal wall loosely sutured so that peritoneal fluid can leak out under gravity. The wound must be dressed under sterile conditions and there is a high risk of ascending infection and of continued protein loss with this technique. |
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− | Closed drainage involves implanting a drain into the abdomen (often a '''Jackson Pratt drain''') to which suction can be applied to aspirate fluid from the peritoneal cavity. The drain usually has multiple fenestrations along its length so that it does not become blocked by omentum or fat. | + | Closed drainage involves implanting a drain into the abdomen (often a '''Jackson Pratt drain''') to which suction can be applied to aspirate fluid from the peritoneal cavity. The drain usually has multiple fenestrations along its length so that it does not become blocked by omentum or fat. |
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| ==Prognosis== | | ==Prognosis== |
− | Guarded. Peritonitis is a multifactorial disease and the consequence is fatal in most cases. A rapid diagnosis and treatment may improve the prognosis but it is generally poor in cases of septic peritonitis. | + | Guarded. Peritonitis is a multifactorial disease and the consequence is fatal in most cases. A rapid diagnosis and treatment may improve the prognosis but it is generally poor in cases of septic peritonitis. |
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| + | ==Literature Search== |
| + | [[File:CABI logo.jpg|left|90px]] |
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| + | Use these links to find recent scientific publications via CAB Abstracts (log in required unless accessing from a subscribing organisation). |
| + | <br><br><br> |
| + | [http://www.cabdirect.org/search.html?q=title%3A%28peritonitis%29+AND+od%3A%28cats%29+ Peritonitis in cats publications] |
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| + | [http://www.cabdirect.org/search.html?q=title%3A%28peritonitis%29+AND+od%3A%28dogs%29+ Peritonitis in dogs publications] |
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| ==References== | | ==References== |
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| For further information on peritonitis see: [http://inpractice.bvapublications.com/cgi/reprint/26/7/358 maxtoshow=&HITS=10&hits=10&RESULTFORMAT=&fulltext=haemoabdomen&searchid=1&FIRSTINDEX=0&sortspec=relevance&resourcetype=HWCIT] In Practice article | | For further information on peritonitis see: [http://inpractice.bvapublications.com/cgi/reprint/26/7/358 maxtoshow=&HITS=10&hits=10&RESULTFORMAT=&fulltext=haemoabdomen&searchid=1&FIRSTINDEX=0&sortspec=relevance&resourcetype=HWCIT] In Practice article |
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| [[Category:Peritoneal_Cavity_-_Inflammatory_Pathology]] | | [[Category:Peritoneal_Cavity_-_Inflammatory_Pathology]] |
− | | + | [[Category:Expert Review]][[Category:Cat]][[Category:Dog]] |
− | [[Category:To Do - Review]] | |
− | [[Category:To_Do_-_James]] | |