Spontaneous bacterial peritonitis medical therapy
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Aditya Govindavarjhulla, M.B.B.S. [2], Chetan Lokhande, M.B.B.S [3], Guillermo Rodriguez Nava, M.D. [4], Alejandro Lemor, M.D. [5]
Overview
Empiric broad-spectrum intravenous antibiotic, preferably with a third generation cephalosporin such as cefotaxime, is warranted for suspected or established spontaneous bacterial peritonitis (SBP) to cover the most common isolates including Escherichia coli, Klebsiella pneumoniae, and Streptococcus pneumoniae. Oral ofloxacin may be considered in selected cases. Albumin should be reserved for patients with ascitic fluid PMN counts greater than or equal to 250 cells/mm3 and clinical suspicion of SBP, who also have a serum creatinine >1 mg/dL, blood urea nitrogen >30 mg/dL, or total bilirubin >4 mg/dL.
Medical Therapy Adapted from AASLD Practice Guidelines: Management of Adult Patients with Ascites Due to Cirrhosis.[1]
Spontaneous Bacterial Peritonitis, Empiric Therapy |
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Preferred Regimen |
▸ Cefotaxime 2 g IV q8h (or 2 g IV q4h if life-threatening) x 5–10 days |
Alternative Regimen |
▸ Ofloxacin 400 mg PO bid x 5–10 days† OR ▸ Ciprofloxacin 200 mg IV q12h x 7 days† OR ▸ Ciprofloxacin 200 mg IV q12h x 2 days, then 500 mg PO bid x 5 days† |
† Fluoroquinolones should not be administered in a patient who had been receiving a fluoroquinolone for SBP prophylaxis.[2][3][4] |
- Empiric antibiotic therapy should be administered to patients with ascitic fluid PMN counts greater than or equal to 250 cells/mm3 in a clinical setting compatible with ascitic fluid infection or those who have convincing signs or symptoms of infection (fever, abdominal pain, or unexplained encephalopathy) regardless of the PMN count in the ascitic fluid.[5][6]
- The most common isolates from the ascitic fluid are Escherichia coli, Klebsiella pneumoniae, and Streptococcus pneumoniae.
- Relatively broad-spectrum therapy, preferably with cefotaxime, is warranted until the results of susceptibility testing are available.
- Infection with multiresistant organism including Extended-spectrum β-lactamase (ESBL)-producing Enterobacteriaceae, Pseudomonas aeruginosa, methicillin-resistant Staphylococcus aureus (MRSA), and Enterococcus faecium is associated with an increased mortality. Risk factors for multiresistant infections include:[7]
- Nosocomial origin of infection
- Long-term norfloxacin prophylaxis
- Recent infection with multiresistant bacteria
- Recent use of beta-lactams
- Oral ofloxacin may be used alternatively in selected cases such as patients without vomiting, shock, grade II (or higher) hepatic encephalopathy, or serum creatinine greater than 3 mg/dL.[8]
- The optimal duration of therapy remains unclear, although most patients respond to a treatment course of five days. Infection-related mortality, bacteriologic cure, and recurrence of ascitic fluid infection were not significantly different between the 5- and 10-day treatment groups in a randomized trial.[9]
- Albumin infusion should be administered to cirrhotic patients with spontaneous bacterial peritonitis in the following conditions:[10]
- Serum creatinine> 1 mg/dL
- Blood urea nitrogen >30 mg/dL
- Total bilirubin >4 mg/dL
- Adjunctive intravenous albumin at a dose of 1.5 g/kg at the time of diagnosis, followed by 1 g/kg on day 3 is associated with a reduced incidence of renal impairment and death in comparison with treatment with an antibiotic alone.[11]
- The use of non-selective beta blockers in cirrhotic patients with SBP should be discouraged since it is associated with an increased risk for hemodynamic compromise, prolonged hospitalization, hepatorenal syndrome, acute kidney injury.[12]
Recommendations for the Management of Spontaneous Bacterial Peritonitis (2013 AASLD Practice Guideline)
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References
- ↑ "AASLD Practice Guidelines: Management of Adult Patients with Ascites Due to Cirrhosis" (PDF).
- ↑ Navasa, M (1996-10). "Randomized, comparative study of oral ofloxacin versus intravenous cefotaxime in spontaneous bacterial peritonitis". Gastroenterology. 111 (4): 1011–1017. ISSN 0016-5085. PMID 8831596. Unknown parameter
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(help) - ↑ Terg, R (2000-10). "Oral ciprofloxacin after a short course of intravenous ciprofloxacin in the treatment of spontaneous bacterial peritonitis: results of a multicenter, randomized study". Journal of hepatology. 33 (4): 564–569. ISSN 0168-8278. PMID 11059861. Unknown parameter
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(help) - ↑ European Association for the Study of the Liver (2010-09). "EASL clinical practice guidelines on the management of ascites, spontaneous bacterial peritonitis, and hepatorenal syndrome in cirrhosis". Journal of hepatology. 53 (3): 397–417. doi:10.1016/j.jhep.2010.05.004. ISSN 1600-0641. PMID 20633946. Check date values in:
|date=
(help) - ↑ Runyon, Bruce A (2013-04). "Introduction to the revised American Association for the Study of Liver Diseases Practice Guideline management of adult patients with ascites due to cirrhosis 2012". Hepatology (Baltimore, Md.). 57 (4): 1651–1653. doi:10.1002/hep.26359. ISSN 1527-3350. PMID 23463403. Unknown parameter
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(help) - ↑ Hoefs, J C (1982-08). "Spontaneous bacterial peritonitis". Hepatology (Baltimore, Md.). 2 (4): 399–407. ISSN 0270-9139. PMID 7095741. Unknown parameter
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(help) - ↑ Fernández, Javier (2012-05). "Prevalence and risk factors of infections by multiresistant bacteria in cirrhosis: a prospective study". Hepatology (Baltimore, Md.). 55 (5): 1551–1561. doi:10.1002/hep.25532. ISSN 1527-3350. PMID 22183941. Unknown parameter
|coauthors=
ignored (help); Check date values in:|date=
(help) - ↑ Navasa, M (1996-10). "Randomized, comparative study of oral ofloxacin versus intravenous cefotaxime in spontaneous bacterial peritonitis". Gastroenterology. 111 (4): 1011–1017. ISSN 0016-5085. PMID 8831596. Unknown parameter
|coauthors=
ignored (help); Check date values in:|date=
(help) - ↑ Runyon, B A (1991-06). "Short-course versus long-course antibiotic treatment of spontaneous bacterial peritonitis. A randomized controlled study of 100 patients". Gastroenterology. 100 (6): 1737–1742. ISSN 0016-5085. PMID 2019378. Unknown parameter
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(help) - ↑ Sigal, Samuel H (2007-04). "Restricted use of albumin for spontaneous bacterial peritonitis". Gut. 56 (4): 597–599. doi:10.1136/gut.2006.113050. ISSN 0017-5749. PMC 1856861. PMID 17369392. Unknown parameter
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(help) - ↑ Sort, P (1999-08-05). "Effect of intravenous albumin on renal impairment and mortality in patients with cirrhosis and spontaneous bacterial peritonitis". The New England journal of medicine. 341 (6): 403–409. doi:10.1056/NEJM199908053410603. ISSN 0028-4793. PMID 10432325. Unknown parameter
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ignored (help) - ↑ Mandorfer, Mattias (2014-06). "Nonselective β Blockers Increase Risk for Hepatorenal Syndrome and Death in Patients With Cirrhosis and Spontaneous Bacterial Peritonitis". Gastroenterology. 146 (7): 1680–1690.e1. doi:10.1053/j.gastro.2014.03.005. ISSN 1528-0012. PMID 24631577. Unknown parameter
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(help)