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Intra-abdominal Sepsis and Abscesses

Introduction
Terminology
Primary peritonitis: this is a term used for a condition in which inflammation occurs in the peritoneum itself
rather than as a result of pathology arising in another organ. Bacterial infection arising from intraperitoneal dialysis is a typical example. Spontaneous bacterial peritonitis (SBP) is a specific condition which occurs in patients with ascites secondary to chronic liver disease; it is seen mainly in hospitalised patients and is rare in asymptomatic outpatients. [1]

Secondary peritonitis: this occurs when a pathological process adjacent to the peritoneum causes
inflammation. Perforation of a viscus is a typical example.

Localised peritonitis: this term is used when the inflammation is in a limited area, such as adjacent to an
inflamed appendix or diverticulum prior to rupture.

Generalised peritonitis: as one might suspect, this term is used when the inflammation is widespread, eg after
the rupture of a viscus.

Intra-abdominal sepsis: this is a term is used for any intra-abdominal infection and encompasses both localised
and generalised peritonitis.

Abscesses: [2] these are localised collections of infected fluid. Approximately 50% of patients have simple
abscesses, with the remainder having complex multiloculated abscesses, which are divided by fibrous tissue and organisation of infected material. The most common areas are subhepatic, pelvic and paracolic gutters but abscesses can also develop in the lesser sac, perisplenic area and between small loops of bowel and their omentum.

Histopathology of peritonitis
The pathological process underpinning peritonitis involves the omentum (the 'abdominal policeman') which attempts to confine the area by wrapping around the infection. Adjacent bowel and fibrinous adhesions are also involved. It is thought that chemical mechanisms such as the release of cytokines and antimicrobial peptides also contribute to the process. If this process fails, generalised life-threatening peritonitis occurs. [3]

Causes

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Causes of Intra-abdominal Sepsis and Abscesses [2] Source
Oesophagus

Causes
Boerhaave's syndrome (spontaneous rupture of oesophagus - usually after forced emesis. Malignancy. Trauma (mostly penetrating). Iatrogenic (usually endoscopy). Peptic ulcer perforation. Malignancy (eg adenocarcinoma, lymphoma, gastrointestinal stromal tumour). Trauma (mostly penetrating). Iatrogenic (usually endoscopy). Peptic ulcer perforation. Trauma (blunt and penetrating). Iatrogenic (usually endoscopy). Cholecystitis. Stone perforation from gallbladder (ie gallstone ileus) or common duct. Malignancy. Choledochal cyst (rare). Trauma (mostly penetrating). Iatrogenic (usually endoscopy). Pancreatitis (eg alcohol, drugs, gallstones). Trauma (blunt and penetrating). Iatrogenic (usually endoscopy). Ischaemic bowel. Incarcerated hernia (internal and external). Closed loop obstruction. Crohn's disease. Malignancy (rare). Meckel's diverticulum Trauma (mostly penetrating) Ischaemic bowel. Diverticulitis. Malignancy. Ulcerative colitis and Crohn's disease. Appendicitis. Colonic volvulus. Trauma (mostly penetrating). Iatrogenic (usually mechanical or thermal damage, or dehiscence of an anastamosis). Pelvic inflammatory disease (eg salpingo-oophoritis, tubo-ovarian abscess, ovarian cyst). Malignancy (rare). Trauma (uncommon).

Stomach

Duodenum

Biliary tract

Pancreas

Small bowel

Large bowel and appendix

Uterus, salpinx, and ovaries

Epidemiology
The incidence depends on the cause. 10-30% of patients with cirrhosis develop spontaneous bacterial peritonitis (SBP). [4] Three studies of patients with perforated appendicitis found an incidence of postoperative abscess formation of 20%. Another study of patients undergoing appendectomy found an incidence of localised and generalised peritonitis of 26.4% and 14.0% respectively. [5]

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Presentation
Symptoms
Abscess - the symptoms are highly variable but may include fever, pain anywhere in the abdomen, diarrhoea or
ileus. A subphrenic abscess can cause pulmonary symptoms and a pelvic abscess can cause urinary symptoms. [2]

Peritonitis - the principle feature is abdominal pain. Depending on the site of the infection and the underlying
pathology it may be insidious, dull and poorly localised from the outset, getting gradually worse and more localised as the infection spreads. More generalised pain may develop if the condition is not contained. In some cases (eg gastric perforation) acute generalised pain is present from the onset. Anorexia, nausea and vomiting may precede the pain, particularly if a degree of obstruction is present. [4]

Signs
Abscess- the temperature chart is typically described as 'swinging' or 'spikey' (swinging pyrexia). There may be
palpable abdominal inflammatory mass or hot tender mass on rectal examination (typical after appendectomy). In the early stages, the clinical picture may be one of an ill patient with few physical signs. There may be little or no abdominal tenderness, particularly if the abscess is deep-seated. [2]

Peritonitis - the patient usually appears unwell and distressed. A high fever is present in the initial stages but in
severe peritonitis there may be hypothermia. Tachycardia is usually present. The classic abdominal signs are tenderness on palpation, guarding and rebound tenderness. The tenderness will be maximal over the area of pathology. Severely ill patients will have rigidity and may lie with their knees flexed to minimise movement of the abdominal wall. They may be hypotensive due to dehydration and show signs of septic shock. Bowel sounds may be absent. Rectal examination may increase the abdominal pain (typically to the right if the appendix is involved and anteriorly if there is pelvic inflammation). [4]

Investigations [2]
These will depend on the suspected pathology but the following are likely to be contributory in most cases. FBC - there is usually a leukocytosis. LFTs, amylase and lipase - particularly if pancreatitis is suspected. Blood cultures - aerobic and anaerobic to exclude blood sepsis. Peritoneal fluid - for culture and amylase level. Urinalysis - to exclude renal tract pathology. Imaging - this may include straight abdominal X-ray, upright CXR, ultrasound, CT scanning, MRI and contrast studies.

Management [2] [4]

Abscess
Drugs - antibiotics are usually required parenterally. Treatment should be based on the results of blood or
abscess culture material. Both aerobic and anaerobic organisms need to be dealt with, so a combination of two agents or a broad spectrum antibiotic (eg ciprofloxacin plus metronidazole) is required.

Surgery - 'To drain or not to drain' is a question which has been raging in the literature for many years, The
question has to a large extent been answered with the advent of percutaneous drainage under CT or ultrasound guidance. This is relatively low-risk and effective in the majority of patients. Failure is usually due to other complicating factors, such as immune deficiency (the abscess is often tubercular) or multilocular abscesses. [6] [7]

Peritonitis

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Drugs - spontaneous bacterial peritonitis (SBP) will initially require a third-generation cefalosporin, with further
therapy guided by microbiological culture results. In secondary peritonitis, the patient is likely to require medical treatment to stabilise renal, haemodynamic and pulmonary function, nutritional and metabolic support and systemic antibiotic therapy. Best results are achieved when antibiotics are started early, before culture results are received, with a second- or third-generation cefalosporin (eg cefotaxime) or a quinolone (eg ciprofloxacin) with or without metronidazole.

Surgery - an attempt to identify the cause of the infection should be made prior to surgery if possible. In the early
stages it may be possible to adopt a 'wait and see' approach (particularly if pancreatitis is suspected); otherwise the options are localised percutaneous drainage of abscesses, open surgery or laparoscopy. The choice will depend on the likely pathology and the clinical state of the patient. Emergency exploratory surgery will be required if the patient is rapidly deteriorating, even if the underlying cause cannot be found. Open surgery is also indicated if there is significant intestinal distension or extensive oedema of the abdominal wall, or organ oedema. In such circumstances, primary fascial closure under tension may be difficult and is associated with multiple organ failure, necrotising abdominal wall infection and increased mortality. An initial operation may be required for drainage and to remove necrotic tissue. A second operation may be required to deal with the underlying pathology and provide further clearance of infection. Studies suggest that further surgery after this point is less beneficial. [4] Pancreatitis-associated peritonitis often needs intensive medical treatment for 12-24 hours before any surgical procedures are contemplated. Surgical debridement and repeated exploration are preferred and a percutaneous approach should be avoided unless defined collections of fluid around the pancreas require drainage in stable patients.

Prognosis
Abscess [2]
The prognosis has improved considerably with the advent of drainage under CT scanning. Deaths are generally due to the underlying disease process or unsuspected foci of infection. Risk factors for adverse clinical outcomes include age over 50 and multiple surgical procedures.

Peritonitis
The main prognostic factor in spontaneous bacterial peritonitis (SBP) in cirrhotic patients is renal dysfunction. One study reported that the mortality rate among patients with renal dysfunction was 67%, compared with only 11% of patients who maintained normal renal function. [8] Various scoring systems have been used to predict the prognosis of peritonitis, most of which rely on systemic signs of the patient and the degree, if any, of organ failure. One of the most commonly used is the Acute Physiology and Chronic Health Evaluation II (APACHE II) scoring system. [9] One study found that the prognosis in secondary peritonitis was more related to the organisms present in peritoneal fluid than in the cause of the peritonitis. Thus, whereas there was no difference in incidence of shock and outcome between patients with postoperative and those with community-acquired peritonitis, enterococci and yeast in the peritoneal fluid were associated with worse outcome. Biliary origin of peritonitis was an independent risk factor for mortality. [10]

Further reading & references

1. Mohan P, Venkataraman J; Prevalence and risk factors for unsuspected spontaneous ascitic fluid infection Indian J Gastroenterol. 2011 Sep;30(5):221-4. Epub 2011 Sep 29. 2. Saber AAet al , Abdominal Abscess, Medscape, May 2009 3. Chandra A, Srivastava RK, Kashyap MP, et al; The anti-inflammatory and antibacterial basis of human omental defense: selective PLoS One. 2011;6(5):e20446. Epub 2011 May 24. 4. Peralta R et al, Surgical Approach to Peritonitis and Abdominal Sepsis, Medscape, Mar 2011 5. Chamisa I; Aclinicopathological review of 324 appendices removed for acute appendicitis in Ann R Coll Surg Engl. 2009 Nov;91(8):688-92. 6. Slater B, Acute Abdomen and HIV/AIDS, Mount Sinai School of Medicine, 2003 7. Sia IG, Wieland ML; Current concepts in the management of tuberculosis. Mayo Clin Proc. 2011 Apr;86(4):348-61. 8. Tandon P, Garcia-Tsao G; Renal dysfunction is the most important independent predictor of mortality in Clin Gastroenterol Hepatol. 2011 Mar;9(3):260-5. Epub 2010 Dec 8. 9. Delibegovic S, Markovic D, Hodzic S; APACHE II scoring system is superior in the prediction of the outcome in Med Arh. 2011;65(2):82-5.

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10. Riche FC, Dray X, Laisne MJ, et al; Factors associated with septic shock and mortality in generalized peritonitis: Crit Care. 2009;13(3):R99. Epub 2009 Jun 24.

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Original Author: Dr Huw Thomas Last Checked: 19/01/2012 Current Version: Dr Laurence Knott Document ID: 4138 (v22) Peer Reviewer: Prof Cathy Jackson EMIS

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