One should have a high index of suspicion for SBP in all patients presenting with ascites, and this is especially true if the patient has an acute history of clinical deterioration. The majority of patients with SBP will present with fever, chills, and abdominal pain, although some patients may be asymptomatic,, and SBP is an incidental finding. Temperature is the most common symptom encountered in patients with SBP, which is a particularly useful clinical symptom as patients with cirrhosis are typically hypothermic. Additional signs and symptoms include diarrhea, paralytic ileus, new-onset or worsening encephalopathy (e.g., altered mental status) without any other identifiable cause, new-onset or worsening renal failure, or presence of ascites that does not improve with the use of diuretic medications.

On physical examination, most patients will have a tender abdomen, although patient response can vary from mild discomfort to the presence of guarding and rebound tenderness. The absence of fever does not rule out SBP.

There is a short window of opportunity for treating SBP before it progresses to septic shock or multisystem organ failure; therefore, rapid assessment and diagnosis are critical (i.e., treatment is much more successful if antibiotics are started before the development of shock).[2][8][9]

Peritoneal fluid analysis (e.g., cell count, differential, culture, lactate level, pH) should be performed in all patients with suspected SBP. This may be achieved either by diagnostic paracentesis or withdrawal of fluid through a peritoneal catheter, which is sometimes present in patients undergoing peritoneal dialysis. In patients with only a small amount of ascites, ultrasonography should be employed to help guide the paracentesis procedure.

Additionally, blood and urine cultures should be obtained before initiation of antibiotic therapy as the results of these may help point towards a source of infection and guide antibiotic therapy.

The most accurate predictor of SBP is a polymorphonuclear leukocyte (PMN or granulocytes such as neutrophils, basophils, and eosinophils) count of greater than 500 cells/uL in a sample of ascitic fluid with a sensitivity and specificity of 86% and 98%, respectively. At a PMN count of higher than 250cells/uL, sensitivity increases to 93%, while specificity declines to 94%. This is the widely accepted number of PMNs needed to form a possible diagnosis of SBP, before beginning empiric antibiotic therapy.

If the perforation is suspected within the abdomen, imaging is warranted, and computed tomography (CT) should be strongly considered, as it is more sensitive for detecting smaller perforations than a plain radiograph.

More recently, proposed tests for SBP include a rapid reagent strip that evaluates for the presence of leukocyte esterase in ascitic fluid, which is shown to have a sensitivity of 100% in the diagnosis of SBP when compared to manual PMN counting. Though this may prove to be a much more efficient method of SBP diagnosis than those previously used, the test still needs to undergo a large-scale comprehensive evaluation. 

Patients who are at high risk for SBP include: 

• Patients with gastrointestinal bleed and cirrhosis.
• Patients who already had SBP one or more times in the past.
• Cirrhotic patients with ascites in which ascitic fluid protein is < 1.5 g/dl along with renal failure (Creatinine > 1.2mg/dl).
• Cirrhotic patients who are hospitalized for a cause other than SBP and have an ascitic protein concentration of < 1 g/dl (10g/L).

Empiric antibiotic therapy, such as intravenous third-generation cephalosporin, should be started in all patients with suspected SBP and a PMN count of greater than 250 cell/uL on ascitic fluid analysis. Exceptions to this rule include patients with recent beta-lactam antibiotic exposure or diagnosis of SBP in a nosocomial setting. Antibiotics should be chosen based on the results of susceptibility testing in these cases.[10][11][12]

Patients with an ascitic fluid PMN count of greater than 500cells/uL should be admitted and treated with empiric antibiotic therapy as soon as possible, and the antibiotics adjusted later based on the results of susceptibility testing. A follow-up analysis of ascitic fluid to assess PMN count should be performed to ensure the patient is receiving adequate and appropriate antibiotic therapy. This is important, as lack of improvement after 48 hours of therapy may indicate an underlying perforation or abscess formation, such as secondary bacterial peritonitis, that may require surgery. In general, ascitic fluid PMN count should be reduced by at least 25% after 48 hours of antibiotic therapy.

Some cirrhotic patients with SBP and either a serum creatinine higher than 1mg/dL, a blood urea nitrogen (BUN) higher than 30mg/dL, or total bilirubin greater than 4mg/dL should be given adjunctive (i.e., in addition to antibiotics) albumin intravenously. This has been shown to reduce both in-hospital mortality and renal damage when compared to the use of antibiotic therapy alone. 

Certain high-risk patients may benefit from outpatient antibiotic prophylactic therapy, including norfloxacin, ciprofloxacin, or trimethoprim-sulfamethoxazole. These individuals have had a prior episode of SBP, or ascitic fluid with either a low protein count (< 1g/dL) or is associated with a GI bleed.

A common related concern to antibiotic prophylaxis is antibiotic resistance, especially in those centers which particularly use fluoroquinolone as SBP prophylaxis. In these patients, cefotaxime is the treatment of choice. Piperacillin-tazobactam or a carbapenem can also be used as an alternative empirically if cefotaxime can not be utilized.[13]

Renal failure is the major cause of death in the patients of SBP and develops in 30-40 percent of the patients. The risk can be minimized by giving IV albumin. IV albumin should be given when the creatinine is > 1 mg/dl, the blood urea nitrogen is > 30 mg/dl, or the total bilirubin is > 4 mg/dl. Treatment with octreotide or midodrine is helpful if the renal failure develops.[14]

• Perforated viscus
• Perinephric abscess
• Pyelonephritis
• Diverticulitis
• Appendicitis
• Mesenteric ischemia

The infection-related mortality in SBP is very low with appropriate treatment. However, the mortality rate is quite high in those patients who develop sepsis. But with appropriate antibiotic therapy, better outcomes can be achieved. In hospital settings, the non-infection related mortality in SBP patients can be as high as 20-40 percent, and one to two years of mortality rates are 70 and 80 percent, respectively.[15] Regardless of the short term outcome of SBP, patients who have liver disease severe enough to develop SBP usually have a terrible long term prognosis. Moreover, liver transplantation should be considered for the survivors of SBP, who are otherwise good transplantation candidates.

• Renal failure 
• Sepsis
• Liver failure/insufficiency
• Tense ascites
• Bleeding after paracentesis 
• Bowel perforation after paracentesis 
• Spontaneous fungal peritonitis

• Treat Acute GI bleeding aggressively.
• Patients with ascitic fluid levels with protein concentration less than 1g/dl should be managed as inpatients.
• Patients who have a history of SBP in the past year should be given appropriate antibiotic prophylaxis for a longer duration.
• For patients with a history of SBP, prolonged out-patient treatment with either Trimethoprim-sulphamethoxazole or ciprofloxacin/norfloxacin should be used.

When patients develop ascites from whatever cause, the treatment usually involves a team of healthcare professionals, including nurses, pharmacists, physicians, and other allied healthcare workers. These patients not only need to be treated for the acute infection but also the primary disorder causing the fluid build-up. The patients are often emaciated and need a dietary consultation. A physical therapy consult is required in order to increase mobility and muscle function.  The pharmacist must ensure that the patient is on no medications that can worsen liver or renal function and must abstain from alcohol use. The nurse has to monitor the patient's abdomen circumference, body weight, and vital signs regularly to make sure that the treatment is working. The family has to be educated on the signs and symptoms of bacterial peritonitis and when to bring the patient back to the hospital. There is a small margin for errors, and any delay in seeking help can lead to mortality. [16][17] (Level V)

Outcomes

Spontaneous bacterial peritonitis carries a mortality rate of 30-70% in patients with end-stage liver and kidney disease. The mortality rates are lower in children with nephrosis. Recently the mortality rates have shown a slight decrease because of earlier diagnosis and advances in treatment. For the patient who develops septic shock secondary to bacterial peritonitis, the mortality increases each hour until antibiotic therapy is started. [18][7](Level V)