SBP should be suspected in a patient with ascites and any of the following:
1.
Temperature greater than 37.8ºC
(100ºF)
2.
Abdominal pain and/or
tenderness
3.
A change in mental status
4.
Ascitic fluid PMN count ≥250
cells/mm
Most cases of SBP are due to gut bacteria
such as Escherichia coli and Klebsiella, though streptococcal and
staphylococcal infections can also occur.
For patients with suspected SBP, while
awaiting culture results, treat with a third-generation cephalosporin:
-Cefotaxime (2 g intravenously every eight
hours) or a similar third-generation cephalosporin provides appropriate
microbial coverage and attains good ascitic fluid levels.
-A fluoroquinolone (eg, levofloxacin) is an
alternative in patients who are allergic to penicillin.
Antibiotic therapy should be tailored once
the results of sensitivity testing are available. (See 'Choice of antibiotic' above.)
After five days of treatment, reassess the
patient:
-Treatment is discontinued if there has been
the usual dramatic improvement.
-If fever or pain persists, paracentesis is
repeated, and the decision to continue or discontinue treatment is determined
by the PMN response:
· If the PMN count is more than 250
cells/mm3, treatment is stopped
·
If the PMN count is greater
than the pretreatment value, a search for a surgical source of infection is
undertaken
·
If the PMN count is elevated
but less than the pretreatment value, antibiotics are continued for another 48
hours, and the paracentesis is repeated
Patients at high risk for SBP include:
-Patients with cirrhosis and
gastrointestinal bleeding.
-Patients who have had one or more episodes
of SBP (among whom recurrence of SBP within one year has been reported to be
close to 70 percent)
-Patients with cirrhosis and ascites if the
ascitic fluid protein is less than 1.5 g/dL (15 g/L) along with either impaired renal
function or liver failure.
-Patients with cirrhosis who are
hospitalized for other reasons and have an ascitic protein concentration of
less than 1 g/dL (10 g/L)
For patients with a history of SBP, use
prolonged outpatient fluoroquinolone therapy (norfloxacin 400 mg/day).
In settings where norfloxacin is
unavailable, ciprofloxacin (500 mg orally once daily) or
trimethoprim-sulfamethoxazole (one double-strength tablet daily) is an
acceptable alternative.
In patients with cirrhosis who are hospitalized
for other reasons and have an ascitic protein concentration of less than 1 g/dL
(10 g/L), use oral norfloxacin (400 mg per day) ortrimethoprim-sulfamethoxazole
(one double-strength tablet once daily) with discontinuation of the drug at the
time of discharge.
SBP is a frequent complication of the ascites of cirrhosis. It is diagnosed by ascitic fluid examination which reveals a PMN count of >250/ml. SBP has poor prognostic significance with a one year survival after a diagnosis of between 30-50%. It is, as the name suggests a spontaneous event that is not a consequence of intestinal perforation.
ReplyDeleteIt is speculated that the infective organism may leak into the ascitic fluid via the blood or from intestinal overgrowth. Organisms should be cultured by directly collecting into blood culture bottles. It is typically caused by aerobic gram negative bacteria. Hence, antibiotics such as co-amoxiclav, tazoscin or ciprofloxacin are typically used as first line treatment.
E. coli and Klebsiella should be considered aerobic organisms. They are more precisely defined as facultative anaerobes, that is to say they reproduce best in aerobic conditions but can also reproduce in anaerobic conditions. Obligate anaerobes (e.g. Clostridia) are killed by the presence of oxygen as opposed to aerotolerant anaerobes (e.g. Lactobacillus) which have exclusively fermentative (anaerobic) metabolism but are not sensitive to the presence of oxygen.
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